---
_id: '8125'
abstract:
- lang: eng
  text: Context, such as behavioral state, is known to modulate memory formation and
    retrieval, but is usually ignored in associative memory models. Here, we propose
    several types of contextual modulation for associative memory networks that greatly
    increase their performance. In these networks, context inactivates specific neurons
    and connections, which modulates the effective connectivity of the network. Memories
    are stored only by the active components, thereby reducing interference from memories
    acquired in other contexts. Such networks exhibit several beneficial characteristics,
    including enhanced memory capacity, high robustness to noise, increased robustness
    to memory overloading, and better memory retention during continual learning.
    Furthermore, memories can be biased to have different relative strengths, or even
    gated on or off, according to contextual cues, providing a candidate model for
    cognitive control of memory and efficient memory search. An external context-encoding
    network can dynamically switch the memory network to a desired state, which we
    liken to experimentally observed contextual signals in prefrontal cortex and hippocampus.
    Overall, our work illustrates the benefits of organizing memory around context,
    and provides an important link between behavioral studies of memory and mechanistic
    details of neural circuits.</jats:p><jats:sec><jats:title>SIGNIFICANCE</jats:title><jats:p>Memory
    is context dependent — both encoding and recall vary in effectiveness and speed
    depending on factors like location and brain state during a task. We apply this
    idea to a simple computational model of associative memory through contextual
    gating of neurons and synaptic connections. Intriguingly, this results in several
    advantages, including vastly enhanced memory capacity, better robustness, and
    flexible memory gating. Our model helps to explain (i) how gating and inhibition
    contribute to memory processes, (ii) how memory access dynamically changes over
    time, and (iii) how context representations, such as those observed in hippocampus
    and prefrontal cortex, may interact with and control memory processes.
article_processing_charge: No
author:
- first_name: William F.
  full_name: Podlaski, William F.
  last_name: Podlaski
  orcid: 0000-0001-6619-7502
- first_name: Everton J.
  full_name: Agnes, Everton J.
  last_name: Agnes
  orcid: 0000-0001-7184-7311
- first_name: Tim P
  full_name: Vogels, Tim P
  id: CB6FF8D2-008F-11EA-8E08-2637E6697425
  last_name: Vogels
  orcid: 0000-0003-3295-6181
citation:
  ama: Podlaski WF, Agnes EJ, Vogels TP. High capacity and dynamic accessibility in
    associative memory networks with context-dependent neuronal and synaptic gating.
    <i>bioRxiv</i>. 2022. doi:<a href="https://doi.org/10.1101/2020.01.08.898528">10.1101/2020.01.08.898528</a>
  apa: Podlaski, W. F., Agnes, E. J., &#38; Vogels, T. P. (2022). High capacity and
    dynamic accessibility in associative memory networks with context-dependent neuronal
    and synaptic gating. <i>bioRxiv</i>. Cold Spring Harbor Laboratory. <a href="https://doi.org/10.1101/2020.01.08.898528">https://doi.org/10.1101/2020.01.08.898528</a>
  chicago: Podlaski, William F., Everton J. Agnes, and Tim P Vogels. “High Capacity
    and Dynamic Accessibility in Associative Memory Networks with Context-Dependent
    Neuronal and Synaptic Gating.” <i>BioRxiv</i>. Cold Spring Harbor Laboratory,
    2022. <a href="https://doi.org/10.1101/2020.01.08.898528">https://doi.org/10.1101/2020.01.08.898528</a>.
  ieee: W. F. Podlaski, E. J. Agnes, and T. P. Vogels, “High capacity and dynamic
    accessibility in associative memory networks with context-dependent neuronal and
    synaptic gating,” <i>bioRxiv</i>. Cold Spring Harbor Laboratory, 2022.
  ista: Podlaski WF, Agnes EJ, Vogels TP. 2022. High capacity and dynamic accessibility
    in associative memory networks with context-dependent neuronal and synaptic gating.
    bioRxiv, <a href="https://doi.org/10.1101/2020.01.08.898528">10.1101/2020.01.08.898528</a>.
  mla: Podlaski, William F., et al. “High Capacity and Dynamic Accessibility in Associative
    Memory Networks with Context-Dependent Neuronal and Synaptic Gating.” <i>BioRxiv</i>,
    Cold Spring Harbor Laboratory, 2022, doi:<a href="https://doi.org/10.1101/2020.01.08.898528">10.1101/2020.01.08.898528</a>.
  short: W.F. Podlaski, E.J. Agnes, T.P. Vogels, BioRxiv (2022).
date_created: 2020-07-16T12:24:28Z
date_published: 2022-12-21T00:00:00Z
date_updated: 2024-03-06T12:03:59Z
day: '21'
department:
- _id: TiVo
doi: 10.1101/2020.01.08.898528
language:
- iso: eng
locked: '1'
main_file_link:
- open_access: '1'
  url: 'https://doi.org/10.1101/2020.01.08.898528 '
month: '12'
oa: 1
oa_version: Preprint
publication: bioRxiv
publication_status: published
publisher: Cold Spring Harbor Laboratory
status: public
title: High capacity and dynamic accessibility in associative memory networks with
  context-dependent neuronal and synaptic gating
type: preprint
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2022'
...
---
_id: '7577'
abstract:
- lang: eng
  text: Weak convergence of inertial iterative method for solving variational inequalities
    is the focus of this paper. The cost function is assumed to be non-Lipschitz and
    monotone. We propose a projection-type method with inertial terms and give weak
    convergence analysis under appropriate conditions. Some test results are performed
    and compared with relevant methods in the literature to show the efficiency and
    advantages given by our proposed methods.
acknowledgement: The project of the first author has received funding from the European
  Research Council (ERC) under the European Union's Seventh Framework Program (FP7
  - 2007-2013) (Grant agreement No. 616160).
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Yekini
  full_name: Shehu, Yekini
  id: 3FC7CB58-F248-11E8-B48F-1D18A9856A87
  last_name: Shehu
  orcid: 0000-0001-9224-7139
- first_name: Olaniyi S.
  full_name: Iyiola, Olaniyi S.
  last_name: Iyiola
citation:
  ama: Shehu Y, Iyiola OS. Weak convergence for variational inequalities with inertial-type
    method. <i>Applicable Analysis</i>. 2022;101(1):192-216. doi:<a href="https://doi.org/10.1080/00036811.2020.1736287">10.1080/00036811.2020.1736287</a>
  apa: Shehu, Y., &#38; Iyiola, O. S. (2022). Weak convergence for variational inequalities
    with inertial-type method. <i>Applicable Analysis</i>. Taylor &#38; Francis. <a
    href="https://doi.org/10.1080/00036811.2020.1736287">https://doi.org/10.1080/00036811.2020.1736287</a>
  chicago: Shehu, Yekini, and Olaniyi S. Iyiola. “Weak Convergence for Variational
    Inequalities with Inertial-Type Method.” <i>Applicable Analysis</i>. Taylor &#38;
    Francis, 2022. <a href="https://doi.org/10.1080/00036811.2020.1736287">https://doi.org/10.1080/00036811.2020.1736287</a>.
  ieee: Y. Shehu and O. S. Iyiola, “Weak convergence for variational inequalities
    with inertial-type method,” <i>Applicable Analysis</i>, vol. 101, no. 1. Taylor
    &#38; Francis, pp. 192–216, 2022.
  ista: Shehu Y, Iyiola OS. 2022. Weak convergence for variational inequalities with
    inertial-type method. Applicable Analysis. 101(1), 192–216.
  mla: Shehu, Yekini, and Olaniyi S. Iyiola. “Weak Convergence for Variational Inequalities
    with Inertial-Type Method.” <i>Applicable Analysis</i>, vol. 101, no. 1, Taylor
    &#38; Francis, 2022, pp. 192–216, doi:<a href="https://doi.org/10.1080/00036811.2020.1736287">10.1080/00036811.2020.1736287</a>.
  short: Y. Shehu, O.S. Iyiola, Applicable Analysis 101 (2022) 192–216.
date_created: 2020-03-09T07:06:52Z
date_published: 2022-01-01T00:00:00Z
date_updated: 2024-03-05T14:01:52Z
day: '01'
ddc:
- '510'
- '515'
- '518'
department:
- _id: VlKo
doi: 10.1080/00036811.2020.1736287
ec_funded: 1
external_id:
  arxiv:
  - '2101.08057'
  isi:
  - '000518364100001'
file:
- access_level: open_access
  checksum: 869efe8cb09505dfa6012f67d20db63d
  content_type: application/pdf
  creator: dernst
  date_created: 2020-10-12T10:42:54Z
  date_updated: 2021-03-16T23:30:06Z
  embargo: 2021-03-15
  file_id: '8648'
  file_name: 2020_ApplicAnalysis_Shehu.pdf
  file_size: 4282586
  relation: main_file
file_date_updated: 2021-03-16T23:30:06Z
has_accepted_license: '1'
intvolume: '       101'
isi: 1
issue: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Submitted Version
page: 192-216
project:
- _id: 25FBA906-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '616160'
  name: 'Discrete Optimization in Computer Vision: Theory and Practice'
publication: Applicable Analysis
publication_identifier:
  eissn:
  - 1563-504X
  issn:
  - 0003-6811
publication_status: published
publisher: Taylor & Francis
quality_controlled: '1'
scopus_import: '1'
status: public
title: Weak convergence for variational inequalities with inertial-type method
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 101
year: '2022'
...
---
_id: '14355'
abstract:
- lang: eng
  text: 'Purpose: The mediator (MED) multisubunit-complex modulates the activity of
    the transcriptional machinery, and genetic defects in different MED subunits (17,
    20, 27) have been implicated in neurologic diseases. In this study, we identified
    a recurrent homozygous variant in MED11 (c.325C>T; p.Arg109Ter) in 7 affected
    individuals from 5 unrelated families. Methods: To investigate the genetic cause
    of the disease, exome or genome sequencing were performed in 5 unrelated families
    identified via different research networks and Matchmaker Exchange. Deep clinical
    and brain imaging evaluations were performed by clinical pediatric neurologists
    and neuroradiologists. The functional effect of the candidate variant on both
    MED11 RNA and protein was assessed using reverse transcriptase polymerase chain
    reaction and western blotting using fibroblast cell lines derived from 1 affected
    individual and controls and through computational approaches. Knockouts in zebrafish
    were generated using clustered regularly interspaced short palindromic repeats/Cas9.
    Results: The disease was characterized by microcephaly, profound neurodevelopmental
    impairment, exaggerated startle response, myoclonic seizures, progressive widespread
    neurodegeneration, and premature death. Functional studies on patient-derived
    fibroblasts did not show a loss of protein function but rather disruption of the
    C-terminal of MED11, likely impairing binding to other MED subunits. A zebrafish
    knockout model recapitulates key clinical phenotypes. Conclusion: Loss of the
    C-terminal of MED subunit 11 may affect its binding efficiency to other MED subunits,
    thus implicating the MED-complex stability in brain development and neurodegeneration.
    (C) 2022 The Authors. Published by Elsevier Inc. on behalf of American College
    of Medical Genetics and Genomics.'
article_processing_charge: No
article_type: original
author:
- first_name: Elisa
  full_name: Cali, Elisa
  last_name: Cali
- first_name: Sheng-Jia
  full_name: Lin, Sheng-Jia
  last_name: Lin
- first_name: Clarissa
  full_name: Rocca, Clarissa
  last_name: Rocca
- first_name: Yavuz
  full_name: Sahin, Yavuz
  last_name: Sahin
- first_name: Aisha
  full_name: Al Shamsi, Aisha
  last_name: Al Shamsi
- first_name: Salima
  full_name: El Chehadeh, Salima
  last_name: El Chehadeh
- first_name: Myriam
  full_name: Chaabouni, Myriam
  last_name: Chaabouni
- first_name: Kshitij
  full_name: Mankad, Kshitij
  last_name: Mankad
- first_name: Evangelia
  full_name: Galanaki, Evangelia
  last_name: Galanaki
- first_name: Stephanie
  full_name: Efthymiou, Stephanie
  last_name: Efthymiou
- first_name: Sniya
  full_name: Sudhakar, Sniya
  last_name: Sudhakar
- first_name: Alkyoni
  full_name: Athanasiou-Fragkouli, Alkyoni
  last_name: Athanasiou-Fragkouli
- first_name: Tamer
  full_name: Celik, Tamer
  last_name: Celik
- first_name: Nejat
  full_name: Narli, Nejat
  last_name: Narli
- first_name: Sebastiano
  full_name: Bianca, Sebastiano
  last_name: Bianca
- first_name: David
  full_name: Murphy, David
  last_name: Murphy
- first_name: Francisco Martins De Carvalho
  full_name: Moreira, Francisco Martins De Carvalho
  last_name: Moreira
- first_name: Andrea
  full_name: Accogli, Andrea
  last_name: Accogli
- first_name: Cassidy
  full_name: Petree, Cassidy
  last_name: Petree
- first_name: Kevin
  full_name: Huang, Kevin
  id: 3b3d2888-1ff6-11ee-9fa6-8f209ca91fe3
  last_name: Huang
  orcid: 0000-0002-2512-7812
- first_name: Kamel
  full_name: Monastiri, Kamel
  last_name: Monastiri
- first_name: Masoud
  full_name: Edizadeh, Masoud
  last_name: Edizadeh
- first_name: Rosaria
  full_name: Nardello, Rosaria
  last_name: Nardello
- first_name: Marzia
  full_name: Ognibene, Marzia
  last_name: Ognibene
- first_name: Patrizia
  full_name: De Marco, Patrizia
  last_name: De Marco
- first_name: Martino
  full_name: Ruggieri, Martino
  last_name: Ruggieri
- first_name: Federico
  full_name: Zara, Federico
  last_name: Zara
- first_name: Pasquale
  full_name: Striano, Pasquale
  last_name: Striano
- first_name: Yavuz
  full_name: Sahin, Yavuz
  last_name: Sahin
- first_name: Lihadh
  full_name: Al-Gazali, Lihadh
  last_name: Al-Gazali
- first_name: Marie Therese Abi
  full_name: Warde, Marie Therese Abi
  last_name: Warde
- first_name: Benedicte
  full_name: Gerard, Benedicte
  last_name: Gerard
- first_name: Giovanni
  full_name: Zifarelli, Giovanni
  last_name: Zifarelli
- first_name: Christian
  full_name: Beetz, Christian
  last_name: Beetz
- first_name: Sara
  full_name: Fortuna, Sara
  last_name: Fortuna
- first_name: Miguel
  full_name: Soler, Miguel
  last_name: Soler
- first_name: Enza Maria
  full_name: Valente, Enza Maria
  last_name: Valente
- first_name: Gaurav
  full_name: Varshney, Gaurav
  last_name: Varshney
- first_name: Reza
  full_name: Maroofian, Reza
  last_name: Maroofian
- first_name: Vincenzo
  full_name: Salpietro, Vincenzo
  last_name: Salpietro
- first_name: Henry
  full_name: Houlden, Henry
  last_name: Houlden
- first_name: SYNaPS Study
  full_name: Grp, SYNaPS Study
  last_name: Grp
citation:
  ama: Cali E, Lin S-J, Rocca C, et al. A homozygous MED11 C-terminal variant causes
    a lethal neurodegenerative disease. <i>Genetics in Medicine</i>. 2022;24(10):2194-2203.
    doi:<a href="https://doi.org/10.1016/j.gim.2022.07.013">10.1016/j.gim.2022.07.013</a>
  apa: Cali, E., Lin, S.-J., Rocca, C., Sahin, Y., Al Shamsi, A., El Chehadeh, S.,
    … Grp, Syn. S. (2022). A homozygous MED11 C-terminal variant causes a lethal neurodegenerative
    disease. <i>Genetics in Medicine</i>. Elsevier. <a href="https://doi.org/10.1016/j.gim.2022.07.013">https://doi.org/10.1016/j.gim.2022.07.013</a>
  chicago: Cali, Elisa, Sheng-Jia Lin, Clarissa Rocca, Yavuz Sahin, Aisha Al Shamsi,
    Salima El Chehadeh, Myriam Chaabouni, et al. “A Homozygous MED11 C-Terminal Variant
    Causes a Lethal Neurodegenerative Disease.” <i>Genetics in Medicine</i>. Elsevier,
    2022. <a href="https://doi.org/10.1016/j.gim.2022.07.013">https://doi.org/10.1016/j.gim.2022.07.013</a>.
  ieee: E. Cali <i>et al.</i>, “A homozygous MED11 C-terminal variant causes a lethal
    neurodegenerative disease,” <i>Genetics in Medicine</i>, vol. 24, no. 10. Elsevier,
    pp. 2194–2203, 2022.
  ista: Cali E, Lin S-J, Rocca C, Sahin Y, Al Shamsi A, El Chehadeh S, Chaabouni M,
    Mankad K, Galanaki E, Efthymiou S, Sudhakar S, Athanasiou-Fragkouli A, Celik T,
    Narli N, Bianca S, Murphy D, Moreira FMDC, Accogli A, Petree C, Huang K, Monastiri
    K, Edizadeh M, Nardello R, Ognibene M, De Marco P, Ruggieri M, Zara F, Striano
    P, Sahin Y, Al-Gazali L, Warde MTA, Gerard B, Zifarelli G, Beetz C, Fortuna S,
    Soler M, Valente EM, Varshney G, Maroofian R, Salpietro V, Houlden H, Grp SynS.
    2022. A homozygous MED11 C-terminal variant causes a lethal neurodegenerative
    disease. Genetics in Medicine. 24(10), 2194–2203.
  mla: Cali, Elisa, et al. “A Homozygous MED11 C-Terminal Variant Causes a Lethal
    Neurodegenerative Disease.” <i>Genetics in Medicine</i>, vol. 24, no. 10, Elsevier,
    2022, pp. 2194–203, doi:<a href="https://doi.org/10.1016/j.gim.2022.07.013">10.1016/j.gim.2022.07.013</a>.
  short: E. Cali, S.-J. Lin, C. Rocca, Y. Sahin, A. Al Shamsi, S. El Chehadeh, M.
    Chaabouni, K. Mankad, E. Galanaki, S. Efthymiou, S. Sudhakar, A. Athanasiou-Fragkouli,
    T. Celik, N. Narli, S. Bianca, D. Murphy, F.M.D.C. Moreira, A. Accogli, C. Petree,
    K. Huang, K. Monastiri, M. Edizadeh, R. Nardello, M. Ognibene, P. De Marco, M.
    Ruggieri, F. Zara, P. Striano, Y. Sahin, L. Al-Gazali, M.T.A. Warde, B. Gerard,
    G. Zifarelli, C. Beetz, S. Fortuna, M. Soler, E.M. Valente, G. Varshney, R. Maroofian,
    V. Salpietro, H. Houlden, Syn.S. Grp, Genetics in Medicine 24 (2022) 2194–2203.
date_created: 2023-09-20T20:57:18Z
date_published: 2022-10-01T00:00:00Z
date_updated: 2023-09-25T08:57:07Z
day: '01'
ddc:
- '570'
department:
- _id: GradSch
doi: 10.1016/j.gim.2022.07.013
extern: '1'
file:
- access_level: open_access
  checksum: 8117175a89129eb5022d81ffe7625f9f
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-25T08:56:06Z
  date_updated: 2023-09-25T08:56:06Z
  file_id: '14371'
  file_name: 2022_GeneticsMedicine_Calin.pdf
  file_size: 1434037
  relation: main_file
  success: 1
file_date_updated: 2023-09-25T08:56:06Z
has_accepted_license: '1'
intvolume: '        24'
issue: '10'
keyword:
- Human mediator complex
- MED11
- MEDopathies
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: 2194-2203
publication: Genetics in Medicine
publication_identifier:
  issn:
  - 1098-3600
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 24
year: '2022'
...
---
_id: '14356'
abstract:
- lang: eng
  text: Aminoacyl-tRNA synthetases (ARSs) are essential enzymes for faithful assignment
    of amino acids to their cognate tRNA. Variants in ARS genes are frequently associated
    with clinically heterogeneous phenotypes in humans and follow both autosomal dominant
    or recessive inheritance patterns in many instances. Variants in tryptophanyl-tRNA
    synthetase 1 (WARS1) cause autosomal dominantly inherited distal hereditary motor
    neuropathy and Charcot-Marie-Tooth disease. Presently, only one family with biallelic
    WARS1 variants has been described. We present three affected individuals from
    two families with biallelic variants (p.Met1? and p.(Asp419Asn)) in WARS1, showing
    varying severities of developmental delay and intellectual disability. Hearing
    impairment and microcephaly, as well as abnormalities of the brain, skeletal system,
    movement/gait, and behavior were variable features. Phenotyping of knocked down
    wars-1 in a Caenorhabditis elegans model showed depletion is associated with defects
    in germ cell development. A wars1 knockout vertebrate model recapitulates the
    human clinical phenotypes, confirms variant pathogenicity, and uncovers evidence
    implicating the p.Met1? variant as potentially impacting an exon critical for
    normal hearing. Together, our findings provide consolidating evidence for biallelic
    disruption of WARS1 as causal for an autosomal recessive neurodevelopmental syndrome
    and present a vertebrate model that recapitulates key phenotypes observed in patients.
article_processing_charge: No
article_type: original
author:
- first_name: Sheng-Jia
  full_name: Lin, Sheng-Jia
  last_name: Lin
- first_name: Barbara
  full_name: Vona, Barbara
  last_name: Vona
- first_name: Hillary M.
  full_name: Porter, Hillary M.
  last_name: Porter
- first_name: Mahmoud
  full_name: Izadi, Mahmoud
  last_name: Izadi
- first_name: Kevin
  full_name: Huang, Kevin
  id: 3b3d2888-1ff6-11ee-9fa6-8f209ca91fe3
  last_name: Huang
  orcid: 0000-0002-2512-7812
- first_name: Yves
  full_name: Lacassie, Yves
  last_name: Lacassie
- first_name: Jill A.
  full_name: Rosenfeld, Jill A.
  last_name: Rosenfeld
- first_name: Saadullah
  full_name: Khan, Saadullah
  last_name: Khan
- first_name: Cassidy
  full_name: Petree, Cassidy
  last_name: Petree
- first_name: Tayyiba A.
  full_name: Ali, Tayyiba A.
  last_name: Ali
- first_name: Nazif
  full_name: Muhammad, Nazif
  last_name: Muhammad
- first_name: Sher A.
  full_name: Khan, Sher A.
  last_name: Khan
- first_name: Noor
  full_name: Muhammad, Noor
  last_name: Muhammad
- first_name: Pengfei
  full_name: Liu, Pengfei
  last_name: Liu
- first_name: Marie-Louise
  full_name: Haymon, Marie-Louise
  last_name: Haymon
- first_name: Franz
  full_name: Rueschendorf, Franz
  last_name: Rueschendorf
- first_name: Il-Keun
  full_name: Kong, Il-Keun
  last_name: Kong
- first_name: Linda
  full_name: Schnapp, Linda
  last_name: Schnapp
- first_name: Natasha
  full_name: Shur, Natasha
  last_name: Shur
- first_name: Lynn
  full_name: Chorich, Lynn
  last_name: Chorich
- first_name: Lawrence
  full_name: Layman, Lawrence
  last_name: Layman
- first_name: Thomas
  full_name: Haaf, Thomas
  last_name: Haaf
- first_name: Ehsan
  full_name: Pourkarimi, Ehsan
  last_name: Pourkarimi
- first_name: Hyung-Goo
  full_name: Kim, Hyung-Goo
  last_name: Kim
- first_name: Gaurav K.
  full_name: Varshney, Gaurav K.
  last_name: Varshney
citation:
  ama: Lin S-J, Vona B, Porter HM, et al. Biallelic variants in WARS1 cause a highly
    variable neurodevelopmental syndrome and implicate a critical exon for normal
    auditory function. <i>Human Mutation</i>. 2022;43(10):1472-1489. doi:<a href="https://doi.org/10.1002/humu.24435">10.1002/humu.24435</a>
  apa: Lin, S.-J., Vona, B., Porter, H. M., Izadi, M., Huang, K., Lacassie, Y., …
    Varshney, G. K. (2022). Biallelic variants in WARS1 cause a highly variable neurodevelopmental
    syndrome and implicate a critical exon for normal auditory function. <i>Human
    Mutation</i>. Wiley. <a href="https://doi.org/10.1002/humu.24435">https://doi.org/10.1002/humu.24435</a>
  chicago: Lin, Sheng-Jia, Barbara Vona, Hillary M. Porter, Mahmoud Izadi, Kevin Huang,
    Yves Lacassie, Jill A. Rosenfeld, et al. “Biallelic Variants in WARS1 Cause a
    Highly Variable Neurodevelopmental Syndrome and Implicate a Critical Exon for
    Normal Auditory Function.” <i>Human Mutation</i>. Wiley, 2022. <a href="https://doi.org/10.1002/humu.24435">https://doi.org/10.1002/humu.24435</a>.
  ieee: S.-J. Lin <i>et al.</i>, “Biallelic variants in WARS1 cause a highly variable
    neurodevelopmental syndrome and implicate a critical exon for normal auditory
    function,” <i>Human Mutation</i>, vol. 43, no. 10. Wiley, pp. 1472–1489, 2022.
  ista: Lin S-J, Vona B, Porter HM, Izadi M, Huang K, Lacassie Y, Rosenfeld JA, Khan
    S, Petree C, Ali TA, Muhammad N, Khan SA, Muhammad N, Liu P, Haymon M-L, Rueschendorf
    F, Kong I-K, Schnapp L, Shur N, Chorich L, Layman L, Haaf T, Pourkarimi E, Kim
    H-G, Varshney GK. 2022. Biallelic variants in WARS1 cause a highly variable neurodevelopmental
    syndrome and implicate a critical exon for normal auditory function. Human Mutation.
    43(10), 1472–1489.
  mla: Lin, Sheng-Jia, et al. “Biallelic Variants in WARS1 Cause a Highly Variable
    Neurodevelopmental Syndrome and Implicate a Critical Exon for Normal Auditory
    Function.” <i>Human Mutation</i>, vol. 43, no. 10, Wiley, 2022, pp. 1472–89, doi:<a
    href="https://doi.org/10.1002/humu.24435">10.1002/humu.24435</a>.
  short: S.-J. Lin, B. Vona, H.M. Porter, M. Izadi, K. Huang, Y. Lacassie, J.A. Rosenfeld,
    S. Khan, C. Petree, T.A. Ali, N. Muhammad, S.A. Khan, N. Muhammad, P. Liu, M.-L.
    Haymon, F. Rueschendorf, I.-K. Kong, L. Schnapp, N. Shur, L. Chorich, L. Layman,
    T. Haaf, E. Pourkarimi, H.-G. Kim, G.K. Varshney, Human Mutation 43 (2022) 1472–1489.
date_created: 2023-09-20T20:58:24Z
date_published: 2022-10-01T00:00:00Z
date_updated: 2023-09-25T08:54:14Z
day: '01'
ddc:
- '570'
doi: 10.1002/humu.24435
extern: '1'
file:
- access_level: open_access
  checksum: 74b01d4e4084b2f64c30ed32b18ee928
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-25T08:52:54Z
  date_updated: 2023-09-25T08:52:54Z
  file_id: '14370'
  file_name: 2022_HumanMutation_Lin.pdf
  file_size: 12131312
  relation: main_file
  success: 1
file_date_updated: 2023-09-25T08:52:54Z
has_accepted_license: '1'
intvolume: '        43'
issue: '10'
keyword:
- autosomal recessive
- biallelic variants
- C
- elegans
- translation initiation sites
- tryptophanyl-tRNA synthetase 1 (WARS1)
- WHEP domain
- zebrafish
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: 1472-1489
publication: Human Mutation
publication_identifier:
  issn:
  - 1059-7794
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome
  and implicate a critical exon for normal auditory function
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 43
year: '2022'
...
---
_id: '14357'
abstract:
- lang: eng
  text: 'Aminoacylation of transfer RNA (tRNA) is a key step in protein biosynthesis,
    carried out by highly specific aminoacyl-tRNA synthetases (ARSs). ARSs have been
    implicated in autosomal dominant and autosomal recessive human disorders. Autosomal
    dominant variants in tryptophanyl-tRNA synthetase 1 (WARS1) are known to cause
    distal hereditary motor neuropathy and Charcot-Marie-Tooth disease, but a recessively
    inherited phenotype is yet to be clearly defined. Seryl-tRNA synthetase 1 (SARS1)
    has rarely been implicated in an autosomal recessive developmental disorder. Here,
    we report five individuals with biallelic missense variants in WARS1 or SARS1,
    who presented with an overlapping phenotype of microcephaly, developmental delay,
    intellectual disability, and brain anomalies. Structural mapping showed that the
    SARS1 variant is located directly within the enzyme’s active site, most likely
    diminishing activity, while the WARS1 variant is located in the N-terminal domain.
    We further characterize the identified WARS1 variant by showing that it negatively
    impacts protein abundance and is unable to rescue the phenotype of a CRISPR/Cas9
    wars1 knockout zebrafish model. In summary, we describe two overlapping autosomal
    recessive syndromes caused by variants in WARS1 and SARS1, present functional
    insights into the pathogenesis of the WARS1-related syndrome and define an emerging
    disease spectrum: ARS-related developmental disorders with or without microcephaly.'
article_processing_charge: No
article_type: original
author:
- first_name: Nina
  full_name: Boegershausen, Nina
  last_name: Boegershausen
- first_name: Hannah E.
  full_name: Krawczyk, Hannah E.
  last_name: Krawczyk
- first_name: Rami A.
  full_name: Jamra, Rami A.
  last_name: Jamra
- first_name: Sheng-Jia
  full_name: Lin, Sheng-Jia
  last_name: Lin
- first_name: Goekhan
  full_name: Yigit, Goekhan
  last_name: Yigit
- first_name: Irina
  full_name: Huening, Irina
  last_name: Huening
- first_name: Anna M.
  full_name: Polo, Anna M.
  last_name: Polo
- first_name: Barbara
  full_name: Vona, Barbara
  last_name: Vona
- first_name: Kevin
  full_name: Huang, Kevin
  id: 3b3d2888-1ff6-11ee-9fa6-8f209ca91fe3
  last_name: Huang
  orcid: 0000-0002-2512-7812
- first_name: Julia
  full_name: Schmidt, Julia
  last_name: Schmidt
- first_name: Janine
  full_name: Altmueller, Janine
  last_name: Altmueller
- first_name: Johannes
  full_name: Luppe, Johannes
  last_name: Luppe
- first_name: Konrad
  full_name: Platzer, Konrad
  last_name: Platzer
- first_name: Beate B.
  full_name: Doergeloh, Beate B.
  last_name: Doergeloh
- first_name: Andreas
  full_name: Busche, Andreas
  last_name: Busche
- first_name: Saskia
  full_name: Biskup, Saskia
  last_name: Biskup
- first_name: Marisa
  full_name: Mendes, I, Marisa
  last_name: Mendes, I
- first_name: Desiree E. C.
  full_name: Smith, Desiree E. C.
  last_name: Smith
- first_name: Gajja S.
  full_name: Salomons, Gajja S.
  last_name: Salomons
- first_name: Arne
  full_name: Zibat, Arne
  last_name: Zibat
- first_name: Eva
  full_name: Bueltmann, Eva
  last_name: Bueltmann
- first_name: Peter
  full_name: Nuernberg, Peter
  last_name: Nuernberg
- first_name: Malte
  full_name: Spielmann, Malte
  last_name: Spielmann
- first_name: Johannes R.
  full_name: Lemke, Johannes R.
  last_name: Lemke
- first_name: Yun
  full_name: Li, Yun
  last_name: Li
- first_name: Martin
  full_name: Zenker, Martin
  last_name: Zenker
- first_name: Gaurav K.
  full_name: Varshney, Gaurav K.
  last_name: Varshney
- first_name: Hauke S.
  full_name: Hillen, Hauke S.
  last_name: Hillen
- first_name: Christian P.
  full_name: Kratz, Christian P.
  last_name: Kratz
- first_name: Bernd
  full_name: Wollnik, Bernd
  last_name: Wollnik
citation:
  ama: 'Boegershausen N, Krawczyk HE, Jamra RA, et al. WARS1 and SARS1: Two tRNA synthetases
    implicated in autosomal recessive microcephaly. <i>Human Mutation</i>. 2022;43(10):1454-1471.
    doi:<a href="https://doi.org/10.1002/humu.24430">10.1002/humu.24430</a>'
  apa: 'Boegershausen, N., Krawczyk, H. E., Jamra, R. A., Lin, S.-J., Yigit, G., Huening,
    I., … Wollnik, B. (2022). WARS1 and SARS1: Two tRNA synthetases implicated in
    autosomal recessive microcephaly. <i>Human Mutation</i>. Wiley. <a href="https://doi.org/10.1002/humu.24430">https://doi.org/10.1002/humu.24430</a>'
  chicago: 'Boegershausen, Nina, Hannah E. Krawczyk, Rami A. Jamra, Sheng-Jia Lin,
    Goekhan Yigit, Irina Huening, Anna M. Polo, et al. “WARS1 and SARS1: Two TRNA
    Synthetases Implicated in Autosomal Recessive Microcephaly.” <i>Human Mutation</i>.
    Wiley, 2022. <a href="https://doi.org/10.1002/humu.24430">https://doi.org/10.1002/humu.24430</a>.'
  ieee: 'N. Boegershausen <i>et al.</i>, “WARS1 and SARS1: Two tRNA synthetases implicated
    in autosomal recessive microcephaly,” <i>Human Mutation</i>, vol. 43, no. 10.
    Wiley, pp. 1454–1471, 2022.'
  ista: 'Boegershausen N, Krawczyk HE, Jamra RA, Lin S-J, Yigit G, Huening I, Polo
    AM, Vona B, Huang K, Schmidt J, Altmueller J, Luppe J, Platzer K, Doergeloh BB,
    Busche A, Biskup S, Mendes, I M, Smith DEC, Salomons GS, Zibat A, Bueltmann E,
    Nuernberg P, Spielmann M, Lemke JR, Li Y, Zenker M, Varshney GK, Hillen HS, Kratz
    CP, Wollnik B. 2022. WARS1 and SARS1: Two tRNA synthetases implicated in autosomal
    recessive microcephaly. Human Mutation. 43(10), 1454–1471.'
  mla: 'Boegershausen, Nina, et al. “WARS1 and SARS1: Two TRNA Synthetases Implicated
    in Autosomal Recessive Microcephaly.” <i>Human Mutation</i>, vol. 43, no. 10,
    Wiley, 2022, pp. 1454–71, doi:<a href="https://doi.org/10.1002/humu.24430">10.1002/humu.24430</a>.'
  short: N. Boegershausen, H.E. Krawczyk, R.A. Jamra, S.-J. Lin, G. Yigit, I. Huening,
    A.M. Polo, B. Vona, K. Huang, J. Schmidt, J. Altmueller, J. Luppe, K. Platzer,
    B.B. Doergeloh, A. Busche, S. Biskup, M. Mendes, I, D.E.C. Smith, G.S. Salomons,
    A. Zibat, E. Bueltmann, P. Nuernberg, M. Spielmann, J.R. Lemke, Y. Li, M. Zenker,
    G.K. Varshney, H.S. Hillen, C.P. Kratz, B. Wollnik, Human Mutation 43 (2022) 1454–1471.
date_created: 2023-09-20T20:59:33Z
date_published: 2022-10-01T00:00:00Z
date_updated: 2023-09-25T08:43:06Z
day: '01'
ddc:
- '570'
doi: 10.1002/humu.24430
extern: '1'
external_id:
  pmid:
  - '35790048'
file:
- access_level: open_access
  checksum: c31fc91e0445c35b9da83eb911a9b552
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-25T08:41:23Z
  date_updated: 2023-09-25T08:41:23Z
  file_id: '14367'
  file_name: 2022_HumanMutation_Boegershausen.pdf
  file_size: 4863605
  relation: main_file
  success: 1
file_date_updated: 2023-09-25T08:41:23Z
has_accepted_license: '1'
intvolume: '        43'
issue: '10'
keyword:
- aminoacylation
- aminoacyl-tRNA synthetase
- ARS
- CRISPR
- Cas9
- intellectual disability
- microcephaly
- SARS1
- tRNA
- WARS1
- zebrafish
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '10'
oa: 1
oa_version: Published Version
page: 1454-1471
pmid: 1
publication: Human Mutation
publication_identifier:
  issn:
  - 1059-7794
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'WARS1 and SARS1: Two tRNA synthetases implicated in autosomal recessive microcephaly'
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 43
year: '2022'
...
---
_id: '14520'
abstract:
- lang: eng
  text: 'This dataset comprises all data shown in the figures of the submitted article
    "Compact vacuum gap transmon qubits: Selective and sensitive probes for superconductor
    surface losses" at arxiv.org/abs/2206.14104. Additional raw data are available
    from the corresponding author on reasonable request.'
article_processing_charge: No
author:
- first_name: Martin
  full_name: Zemlicka, Martin
  id: 2DCF8DE6-F248-11E8-B48F-1D18A9856A87
  last_name: Zemlicka
- first_name: Elena
  full_name: Redchenko, Elena
  id: 2C21D6E8-F248-11E8-B48F-1D18A9856A87
  last_name: Redchenko
- first_name: Matilda
  full_name: Peruzzo, Matilda
  id: 3F920B30-F248-11E8-B48F-1D18A9856A87
  last_name: Peruzzo
  orcid: 0000-0002-3415-4628
- first_name: Farid
  full_name: Hassani, Farid
  id: 2AED110C-F248-11E8-B48F-1D18A9856A87
  last_name: Hassani
  orcid: 0000-0001-6937-5773
- first_name: Andrea
  full_name: Trioni, Andrea
  id: 42F71B44-F248-11E8-B48F-1D18A9856A87
  last_name: Trioni
- first_name: Shabir
  full_name: Barzanjeh, Shabir
  id: 2D25E1F6-F248-11E8-B48F-1D18A9856A87
  last_name: Barzanjeh
  orcid: 0000-0003-0415-1423
- first_name: Johannes M
  full_name: Fink, Johannes M
  id: 4B591CBA-F248-11E8-B48F-1D18A9856A87
  last_name: Fink
  orcid: 0000-0001-8112-028X
citation:
  ama: 'Zemlicka M, Redchenko E, Peruzzo M, et al. Compact vacuum gap transmon qubits:
    Selective and sensitive probes for superconductor surface losses. 2022. doi:<a
    href="https://doi.org/10.5281/ZENODO.8408897">10.5281/ZENODO.8408897</a>'
  apa: 'Zemlicka, M., Redchenko, E., Peruzzo, M., Hassani, F., Trioni, A., Barzanjeh,
    S., &#38; Fink, J. M. (2022). Compact vacuum gap transmon qubits: Selective and
    sensitive probes for superconductor surface losses. Zenodo. <a href="https://doi.org/10.5281/ZENODO.8408897">https://doi.org/10.5281/ZENODO.8408897</a>'
  chicago: 'Zemlicka, Martin, Elena Redchenko, Matilda Peruzzo, Farid Hassani, Andrea
    Trioni, Shabir Barzanjeh, and Johannes M Fink. “Compact Vacuum Gap Transmon Qubits:
    Selective and Sensitive Probes for Superconductor Surface Losses.” Zenodo, 2022.
    <a href="https://doi.org/10.5281/ZENODO.8408897">https://doi.org/10.5281/ZENODO.8408897</a>.'
  ieee: 'M. Zemlicka <i>et al.</i>, “Compact vacuum gap transmon qubits: Selective
    and sensitive probes for superconductor surface losses.” Zenodo, 2022.'
  ista: 'Zemlicka M, Redchenko E, Peruzzo M, Hassani F, Trioni A, Barzanjeh S, Fink
    JM. 2022. Compact vacuum gap transmon qubits: Selective and sensitive probes for
    superconductor surface losses, Zenodo, <a href="https://doi.org/10.5281/ZENODO.8408897">10.5281/ZENODO.8408897</a>.'
  mla: 'Zemlicka, Martin, et al. <i>Compact Vacuum Gap Transmon Qubits: Selective
    and Sensitive Probes for Superconductor Surface Losses</i>. Zenodo, 2022, doi:<a
    href="https://doi.org/10.5281/ZENODO.8408897">10.5281/ZENODO.8408897</a>.'
  short: M. Zemlicka, E. Redchenko, M. Peruzzo, F. Hassani, A. Trioni, S. Barzanjeh,
    J.M. Fink, (2022).
date_created: 2023-11-13T08:09:10Z
date_published: 2022-06-28T00:00:00Z
date_updated: 2024-09-10T12:23:57Z
day: '28'
ddc:
- '530'
department:
- _id: JoFi
doi: 10.5281/ZENODO.8408897
has_accepted_license: '1'
license: https://creativecommons.org/publicdomain/zero/1.0/
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5281/ZENODO.8408897
month: '06'
oa: 1
oa_version: Published Version
publisher: Zenodo
related_material:
  record:
  - id: '14517'
    relation: used_in_publication
    status: public
status: public
title: 'Compact vacuum gap transmon qubits: Selective and sensitive probes for superconductor
  surface losses'
tmp:
  image: /images/cc_0.png
  legal_code_url: https://creativecommons.org/publicdomain/zero/1.0/legalcode
  name: Creative Commons Public Domain Dedication (CC0 1.0)
  short: CC0 (1.0)
type: research_data_reference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2022'
...
---
_id: '14597'
abstract:
- lang: eng
  text: "Phase-field models such as the Allen-Cahn equation may give rise to the formation
    and evolution of geometric shapes, a phenomenon that may be analyzed rigorously
    in suitable scaling regimes. In its sharp-interface limit, the vectorial Allen-Cahn
    equation with a potential with N≥3 distinct minima has been conjectured to describe
    the evolution of branched interfaces by multiphase mean curvature flow.\r\nIn
    the present work, we give a rigorous proof for this statement in two and three
    ambient dimensions and for a suitable class of potentials: As long as a strong
    solution to multiphase mean curvature flow exists, solutions to the vectorial
    Allen-Cahn equation with well-prepared initial data converge towards multiphase
    mean curvature flow in the limit of vanishing interface width parameter ε↘0. We
    even establish the rate of convergence O(ε1/2).\r\nOur approach is based on the
    gradient flow structure of the Allen-Cahn equation and its limiting motion: Building
    on the recent concept of \"gradient flow calibrations\" for multiphase mean curvature
    flow, we introduce a notion of relative entropy for the vectorial Allen-Cahn equation
    with multi-well potential. This enables us to overcome the limitations of other
    approaches, e.g. avoiding the need for a stability analysis of the Allen-Cahn
    operator or additional convergence hypotheses for the energy at positive times."
article_processing_charge: No
arxiv: 1
author:
- first_name: Julian L
  full_name: Fischer, Julian L
  id: 2C12A0B0-F248-11E8-B48F-1D18A9856A87
  last_name: Fischer
  orcid: 0000-0002-0479-558X
- first_name: Alice
  full_name: Marveggio, Alice
  id: 25647992-AA84-11E9-9D75-8427E6697425
  last_name: Marveggio
citation:
  ama: Fischer JL, Marveggio A. Quantitative convergence of the vectorial Allen-Cahn
    equation towards multiphase mean curvature flow. <i>arXiv</i>. doi:<a href="https://doi.org/10.48550/ARXIV.2203.17143">10.48550/ARXIV.2203.17143</a>
  apa: Fischer, J. L., &#38; Marveggio, A. (n.d.). Quantitative convergence of the
    vectorial Allen-Cahn equation towards multiphase mean curvature flow. <i>arXiv</i>.
    <a href="https://doi.org/10.48550/ARXIV.2203.17143">https://doi.org/10.48550/ARXIV.2203.17143</a>
  chicago: Fischer, Julian L, and Alice Marveggio. “Quantitative Convergence of the
    Vectorial Allen-Cahn Equation towards Multiphase Mean Curvature Flow.” <i>ArXiv</i>,
    n.d. <a href="https://doi.org/10.48550/ARXIV.2203.17143">https://doi.org/10.48550/ARXIV.2203.17143</a>.
  ieee: J. L. Fischer and A. Marveggio, “Quantitative convergence of the vectorial
    Allen-Cahn equation towards multiphase mean curvature flow,” <i>arXiv</i>. .
  ista: Fischer JL, Marveggio A. Quantitative convergence of the vectorial Allen-Cahn
    equation towards multiphase mean curvature flow. arXiv, <a href="https://doi.org/10.48550/ARXIV.2203.17143">10.48550/ARXIV.2203.17143</a>.
  mla: Fischer, Julian L., and Alice Marveggio. “Quantitative Convergence of the Vectorial
    Allen-Cahn Equation towards Multiphase Mean Curvature Flow.” <i>ArXiv</i>, doi:<a
    href="https://doi.org/10.48550/ARXIV.2203.17143">10.48550/ARXIV.2203.17143</a>.
  short: J.L. Fischer, A. Marveggio, ArXiv (n.d.).
date_created: 2023-11-23T09:30:02Z
date_published: 2022-03-31T00:00:00Z
date_updated: 2023-11-30T13:25:02Z
day: '31'
department:
- _id: JuFi
doi: 10.48550/ARXIV.2203.17143
ec_funded: 1
external_id:
  arxiv:
  - '2203.17143'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/2203.17143
month: '03'
oa: 1
oa_version: Preprint
project:
- _id: 0aa76401-070f-11eb-9043-b5bb049fa26d
  call_identifier: H2020
  grant_number: '948819'
  name: Bridging Scales in Random Materials
publication: arXiv
publication_status: submitted
related_material:
  record:
  - id: '14587'
    relation: dissertation_contains
    status: public
status: public
title: Quantitative convergence of the vectorial Allen-Cahn equation towards multiphase
  mean curvature flow
type: preprint
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2022'
...
---
_id: '14600'
abstract:
- lang: eng
  text: We study the problem of learning controllers for discrete-time non-linear
    stochastic dynamical systems with formal reach-avoid guarantees. This work presents
    the first method for providing formal reach-avoid guarantees, which combine and
    generalize stability and safety guarantees, with a tolerable probability threshold
    $p\in[0,1]$ over the infinite time horizon. Our method leverages advances in machine
    learning literature and it represents formal certificates as neural networks.
    In particular, we learn a certificate in the form of a reach-avoid supermartingale
    (RASM), a novel notion that we introduce in this work. Our RASMs provide reachability
    and avoidance guarantees by imposing constraints on what can be viewed as a stochastic
    extension of level sets of Lyapunov functions for deterministic systems. Our approach
    solves several important problems -- it can be used to learn a control policy
    from scratch, to verify a reach-avoid specification for a fixed control policy,
    or to fine-tune a pre-trained policy if it does not satisfy the reach-avoid specification.
    We validate our approach on $3$ stochastic non-linear reinforcement learning tasks.
article_processing_charge: No
arxiv: 1
author:
- first_name: Dorde
  full_name: Zikelic, Dorde
  id: 294AA7A6-F248-11E8-B48F-1D18A9856A87
  last_name: Zikelic
  orcid: 0000-0002-4681-1699
- first_name: Mathias
  full_name: Lechner, Mathias
  id: 3DC22916-F248-11E8-B48F-1D18A9856A87
  last_name: Lechner
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000-0002-2985-7724
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
citation:
  ama: Zikelic D, Lechner M, Henzinger TA, Chatterjee K. Learning control policies
    for stochastic systems with reach-avoid guarantees. <i>arXiv</i>. doi:<a href="https://doi.org/10.48550/ARXIV.2210.05308">10.48550/ARXIV.2210.05308</a>
  apa: Zikelic, D., Lechner, M., Henzinger, T. A., &#38; Chatterjee, K. (n.d.). Learning
    control policies for stochastic systems with reach-avoid guarantees. <i>arXiv</i>.
    <a href="https://doi.org/10.48550/ARXIV.2210.05308">https://doi.org/10.48550/ARXIV.2210.05308</a>
  chicago: Zikelic, Dorde, Mathias Lechner, Thomas A Henzinger, and Krishnendu Chatterjee.
    “Learning Control Policies for Stochastic Systems with Reach-Avoid Guarantees.”
    <i>ArXiv</i>, n.d. <a href="https://doi.org/10.48550/ARXIV.2210.05308">https://doi.org/10.48550/ARXIV.2210.05308</a>.
  ieee: D. Zikelic, M. Lechner, T. A. Henzinger, and K. Chatterjee, “Learning control
    policies for stochastic systems with reach-avoid guarantees,” <i>arXiv</i>. .
  ista: Zikelic D, Lechner M, Henzinger TA, Chatterjee K. Learning control policies
    for stochastic systems with reach-avoid guarantees. arXiv, <a href="https://doi.org/10.48550/ARXIV.2210.05308">10.48550/ARXIV.2210.05308</a>.
  mla: Zikelic, Dorde, et al. “Learning Control Policies for Stochastic Systems with
    Reach-Avoid Guarantees.” <i>ArXiv</i>, doi:<a href="https://doi.org/10.48550/ARXIV.2210.05308">10.48550/ARXIV.2210.05308</a>.
  short: D. Zikelic, M. Lechner, T.A. Henzinger, K. Chatterjee, ArXiv (n.d.).
date_created: 2023-11-24T13:10:09Z
date_published: 2022-11-29T00:00:00Z
date_updated: 2025-07-14T09:10:02Z
day: '29'
department:
- _id: KrCh
- _id: ToHe
doi: 10.48550/ARXIV.2210.05308
ec_funded: 1
external_id:
  arxiv:
  - '2210.05308'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-sa/4.0/
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/2210.05308
month: '11'
oa: 1
oa_version: Preprint
project:
- _id: 0599E47C-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '863818'
  name: 'Formal Methods for Stochastic Models: Algorithms and Applications'
- _id: 62781420-2b32-11ec-9570-8d9b63373d4d
  call_identifier: H2020
  grant_number: '101020093'
  name: Vigilant Algorithmic Monitoring of Software
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication: arXiv
publication_status: submitted
related_material:
  record:
  - id: '14539'
    relation: dissertation_contains
    status: public
  - id: '14830'
    relation: later_version
    status: public
status: public
title: Learning control policies for stochastic systems with reach-avoid guarantees
tmp:
  image: /images/cc_by_sa.png
  legal_code_url: https://creativecommons.org/licenses/by-sa/4.0/legalcode
  name: Creative Commons Attribution-ShareAlike 4.0 International Public License (CC
    BY-SA 4.0)
  short: CC BY-SA (4.0)
type: preprint
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2022'
...
---
_id: '14601'
abstract:
- lang: eng
  text: "In this work, we address the problem of learning provably stable neural\r\nnetwork
    policies for stochastic control systems. While recent work has\r\ndemonstrated
    the feasibility of certifying given policies using martingale\r\ntheory, the problem
    of how to learn such policies is little explored. Here, we\r\nstudy the effectiveness
    of jointly learning a policy together with a martingale\r\ncertificate that proves
    its stability using a single learning algorithm. We\r\nobserve that the joint
    optimization problem becomes easily stuck in local\r\nminima when starting from
    a randomly initialized policy. Our results suggest\r\nthat some form of pre-training
    of the policy is required for the joint\r\noptimization to repair and verify the
    policy successfully."
article_processing_charge: No
arxiv: 1
author:
- first_name: Dorde
  full_name: Zikelic, Dorde
  id: 294AA7A6-F248-11E8-B48F-1D18A9856A87
  last_name: Zikelic
  orcid: 0000-0002-4681-1699
- first_name: Mathias
  full_name: Lechner, Mathias
  id: 3DC22916-F248-11E8-B48F-1D18A9856A87
  last_name: Lechner
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000-0002-2985-7724
citation:
  ama: Zikelic D, Lechner M, Chatterjee K, Henzinger TA. Learning stabilizing policies
    in stochastic control systems. <i>arXiv</i>. doi:<a href="https://doi.org/10.48550/arXiv.2205.11991">10.48550/arXiv.2205.11991</a>
  apa: Zikelic, D., Lechner, M., Chatterjee, K., &#38; Henzinger, T. A. (n.d.). Learning
    stabilizing policies in stochastic control systems. <i>arXiv</i>. <a href="https://doi.org/10.48550/arXiv.2205.11991">https://doi.org/10.48550/arXiv.2205.11991</a>
  chicago: Zikelic, Dorde, Mathias Lechner, Krishnendu Chatterjee, and Thomas A Henzinger.
    “Learning Stabilizing Policies in Stochastic Control Systems.” <i>ArXiv</i>, n.d.
    <a href="https://doi.org/10.48550/arXiv.2205.11991">https://doi.org/10.48550/arXiv.2205.11991</a>.
  ieee: D. Zikelic, M. Lechner, K. Chatterjee, and T. A. Henzinger, “Learning stabilizing
    policies in stochastic control systems,” <i>arXiv</i>. .
  ista: Zikelic D, Lechner M, Chatterjee K, Henzinger TA. Learning stabilizing policies
    in stochastic control systems. arXiv, <a href="https://doi.org/10.48550/arXiv.2205.11991">10.48550/arXiv.2205.11991</a>.
  mla: Zikelic, Dorde, et al. “Learning Stabilizing Policies in Stochastic Control
    Systems.” <i>ArXiv</i>, doi:<a href="https://doi.org/10.48550/arXiv.2205.11991">10.48550/arXiv.2205.11991</a>.
  short: D. Zikelic, M. Lechner, K. Chatterjee, T.A. Henzinger, ArXiv (n.d.).
date_created: 2023-11-24T13:22:30Z
date_published: 2022-05-24T00:00:00Z
date_updated: 2025-07-14T09:10:00Z
day: '24'
department:
- _id: KrCh
- _id: ToHe
doi: 10.48550/arXiv.2205.11991
ec_funded: 1
external_id:
  arxiv:
  - '2205.11991'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/2205.11991
month: '05'
oa: 1
oa_version: Preprint
project:
- _id: 62781420-2b32-11ec-9570-8d9b63373d4d
  call_identifier: H2020
  grant_number: '101020093'
  name: Vigilant Algorithmic Monitoring of Software
- _id: 0599E47C-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '863818'
  name: 'Formal Methods for Stochastic Models: Algorithms and Applications'
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication: arXiv
publication_status: submitted
related_material:
  record:
  - id: '14539'
    relation: dissertation_contains
    status: public
status: public
title: Learning stabilizing policies in stochastic control systems
type: preprint
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2022'
...
---
_id: '13064'
abstract:
- lang: eng
  text: Genetically informed, deep-phenotyped biobanks are an important research resource
    and it is imperative that the most powerful, versatile, and efficient analysis
    approaches are used. Here, we apply our recently developed Bayesian grouped mixture
    of regressions model (GMRM) in the UK and Estonian Biobanks and obtain the highest
    genomic prediction accuracy reported to date across 21 heritable traits. When
    compared to other approaches, GMRM accuracy was greater than annotation prediction
    models run in the LDAK or LDPred-funct software by 15% (SE 7%) and 14% (SE 2%),
    respectively, and was 18% (SE 3%) greater than a baseline BayesR model without
    single-nucleotide polymorphism (SNP) markers grouped into minor allele frequency–linkage
    disequilibrium (MAF-LD) annotation categories. For height, the prediction accuracy
    R 2 was 47% in a UK Biobank holdout sample, which was 76% of the estimated h SNP
    2 . We then extend our GMRM prediction model to provide mixed-linear model association
    (MLMA) SNP marker estimates for genome-wide association (GWAS) discovery, which
    increased the independent loci detected to 16,162 in unrelated UK Biobank individuals,
    compared to 10,550 from BoltLMM and 10,095 from Regenie, a 62 and 65% increase,
    respectively. The average χ2 value of the leading markers increased by 15.24 (SE
    0.41) for every 1% increase in prediction accuracy gained over a baseline BayesR
    model across the traits. Thus, we show that modeling genetic associations accounting
    for MAF and LD differences among SNP markers, and incorporating prior knowledge
    of genomic function, is important for both genomic prediction and discovery in
    large-scale individual-level studies.
article_processing_charge: No
author:
- first_name: Etienne
  full_name: Orliac, Etienne
  last_name: Orliac
- first_name: Daniel
  full_name: Trejo Banos, Daniel
  last_name: Trejo Banos
- first_name: Sven
  full_name: Ojavee, Sven
  last_name: Ojavee
- first_name: Kristi
  full_name: Läll, Kristi
  last_name: Läll
- first_name: Reedik
  full_name: Mägi, Reedik
  last_name: Mägi
- first_name: Peter
  full_name: Visscher, Peter
  last_name: Visscher
- first_name: Matthew Richard
  full_name: Robinson, Matthew Richard
  id: E5D42276-F5DA-11E9-8E24-6303E6697425
  last_name: Robinson
  orcid: 0000-0001-8982-8813
citation:
  ama: Orliac E, Trejo Banos D, Ojavee S, et al. Improving genome-wide association
    discovery and genomic prediction accuracy in biobank data. 2022. doi:<a href="https://doi.org/10.5061/DRYAD.GTHT76HMZ">10.5061/DRYAD.GTHT76HMZ</a>
  apa: Orliac, E., Trejo Banos, D., Ojavee, S., Läll, K., Mägi, R., Visscher, P.,
    &#38; Robinson, M. R. (2022). Improving genome-wide association discovery and
    genomic prediction accuracy in biobank data. Dryad. <a href="https://doi.org/10.5061/DRYAD.GTHT76HMZ">https://doi.org/10.5061/DRYAD.GTHT76HMZ</a>
  chicago: Orliac, Etienne, Daniel Trejo Banos, Sven Ojavee, Kristi Läll, Reedik Mägi,
    Peter Visscher, and Matthew Richard Robinson. “Improving Genome-Wide Association
    Discovery and Genomic Prediction Accuracy in Biobank Data.” Dryad, 2022. <a href="https://doi.org/10.5061/DRYAD.GTHT76HMZ">https://doi.org/10.5061/DRYAD.GTHT76HMZ</a>.
  ieee: E. Orliac <i>et al.</i>, “Improving genome-wide association discovery and
    genomic prediction accuracy in biobank data.” Dryad, 2022.
  ista: Orliac E, Trejo Banos D, Ojavee S, Läll K, Mägi R, Visscher P, Robinson MR.
    2022. Improving genome-wide association discovery and genomic prediction accuracy
    in biobank data, Dryad, <a href="https://doi.org/10.5061/DRYAD.GTHT76HMZ">10.5061/DRYAD.GTHT76HMZ</a>.
  mla: Orliac, Etienne, et al. <i>Improving Genome-Wide Association Discovery and
    Genomic Prediction Accuracy in Biobank Data</i>. Dryad, 2022, doi:<a href="https://doi.org/10.5061/DRYAD.GTHT76HMZ">10.5061/DRYAD.GTHT76HMZ</a>.
  short: E. Orliac, D. Trejo Banos, S. Ojavee, K. Läll, R. Mägi, P. Visscher, M.R.
    Robinson, (2022).
date_created: 2023-05-23T16:28:13Z
date_published: 2022-09-02T00:00:00Z
date_updated: 2023-08-03T12:40:37Z
day: '02'
ddc:
- '570'
department:
- _id: MaRo
doi: 10.5061/DRYAD.GTHT76HMZ
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5061/dryad.gtht76hmz
month: '09'
oa: 1
oa_version: Published Version
publisher: Dryad
related_material:
  record:
  - id: '11733'
    relation: used_in_publication
    status: public
status: public
title: Improving genome-wide association discovery and genomic prediction accuracy
  in biobank data
tmp:
  image: /images/cc_0.png
  legal_code_url: https://creativecommons.org/publicdomain/zero/1.0/legalcode
  name: Creative Commons Public Domain Dedication (CC0 1.0)
  short: CC0 (1.0)
type: research_data_reference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2022'
...
---
_id: '13066'
abstract:
- lang: eng
  text: Chromosomal inversions have been shown to play a major role in local adaptation
    by suppressing recombination between alternative arrangements and maintaining
    beneficial allele combinations. However, so far, their importance relative to
    the remaining genome remains largely unknown. Understanding the genetic architecture
    of adaptation requires better estimates of how loci of different effect sizes
    contribute to phenotypic variation. Here, we used three Swedish islands where
    the marine snail Littorina saxatilis has repeatedly evolved into two distinct
    ecotypes along a habitat transition. We estimated the contribution of inversion
    polymorphisms to phenotypic divergence while controlling for polygenic effects
    in the remaining genome using a quantitative genetics framework. We confirmed
    the importance of inversions but showed that contributions of loci outside inversions
    are of similar magnitude, with variable proportions dependent on the trait and
    the population. Some inversions showed consistent effects across all sites, whereas
    others exhibited site-specific effects, indicating that the genomic basis for
    replicated phenotypic divergence is only partly shared. The contributions of sexual
    dimorphism as well as environmental factors to phenotypic variation were significant
    but minor compared to inversions and polygenic background. Overall, this integrated
    approach provides insight into the multiple mechanisms contributing to parallel
    phenotypic divergence.
article_processing_charge: No
author:
- first_name: Eva
  full_name: Koch, Eva
  last_name: Koch
- first_name: Mark
  full_name: Ravinet, Mark
  last_name: Ravinet
- first_name: Anja M
  full_name: Westram, Anja M
  id: 3C147470-F248-11E8-B48F-1D18A9856A87
  last_name: Westram
  orcid: 0000-0003-1050-4969
- first_name: Kerstin
  full_name: Jonannesson, Kerstin
  last_name: Jonannesson
- first_name: Roger
  full_name: Butlin, Roger
  last_name: Butlin
citation:
  ama: 'Koch E, Ravinet M, Westram AM, Jonannesson K, Butlin R. Data from: Genetic
    architecture of repeated phenotypic divergence in Littorina saxatilis ecotype
    evolution. 2022. doi:<a href="https://doi.org/10.5061/DRYAD.M905QFV4B">10.5061/DRYAD.M905QFV4B</a>'
  apa: 'Koch, E., Ravinet, M., Westram, A. M., Jonannesson, K., &#38; Butlin, R. (2022).
    Data from: Genetic architecture of repeated phenotypic divergence in Littorina
    saxatilis ecotype evolution. Dryad. <a href="https://doi.org/10.5061/DRYAD.M905QFV4B">https://doi.org/10.5061/DRYAD.M905QFV4B</a>'
  chicago: 'Koch, Eva, Mark Ravinet, Anja M Westram, Kerstin Jonannesson, and Roger
    Butlin. “Data from: Genetic Architecture of Repeated Phenotypic Divergence in
    Littorina Saxatilis Ecotype Evolution.” Dryad, 2022. <a href="https://doi.org/10.5061/DRYAD.M905QFV4B">https://doi.org/10.5061/DRYAD.M905QFV4B</a>.'
  ieee: 'E. Koch, M. Ravinet, A. M. Westram, K. Jonannesson, and R. Butlin, “Data
    from: Genetic architecture of repeated phenotypic divergence in Littorina saxatilis
    ecotype evolution.” Dryad, 2022.'
  ista: 'Koch E, Ravinet M, Westram AM, Jonannesson K, Butlin R. 2022. Data from:
    Genetic architecture of repeated phenotypic divergence in Littorina saxatilis
    ecotype evolution, Dryad, <a href="https://doi.org/10.5061/DRYAD.M905QFV4B">10.5061/DRYAD.M905QFV4B</a>.'
  mla: 'Koch, Eva, et al. <i>Data from: Genetic Architecture of Repeated Phenotypic
    Divergence in Littorina Saxatilis Ecotype Evolution</i>. Dryad, 2022, doi:<a href="https://doi.org/10.5061/DRYAD.M905QFV4B">10.5061/DRYAD.M905QFV4B</a>.'
  short: E. Koch, M. Ravinet, A.M. Westram, K. Jonannesson, R. Butlin, (2022).
date_created: 2023-05-23T16:33:12Z
date_published: 2022-07-28T00:00:00Z
date_updated: 2023-08-04T09:42:10Z
day: '28'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.5061/DRYAD.M905QFV4B
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5061/dryad.m905qfv4b
month: '07'
oa: 1
oa_version: Published Version
publisher: Dryad
related_material:
  record:
  - id: '12247'
    relation: used_in_publication
    status: public
status: public
title: 'Data from: Genetic architecture of repeated phenotypic divergence in Littorina
  saxatilis ecotype evolution'
tmp:
  image: /images/cc_0.png
  legal_code_url: https://creativecommons.org/publicdomain/zero/1.0/legalcode
  name: Creative Commons Public Domain Dedication (CC0 1.0)
  short: CC0 (1.0)
type: research_data_reference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2022'
...
---
_id: '13076'
abstract:
- lang: eng
  text: "The source code for replicating experiments presented in the paper.\r\n\r\nThe
    implementation of the designed priority schedulers can be found in Galois-2.2.1/include/Galois/WorkList/:\r\nStealingMultiQueue.h
    is the StealingMultiQueue.\r\nMQOptimized/ contains MQ Optimized variants.\r\n\r\nWe
    provide images that contain all the dependencies and datasets. Images can be pulled
    from npostnikova/mq-based-schedulers repository, or downloaded from Zenodo. See
    readme for more detail."
article_processing_charge: No
author:
- first_name: Anastasiia
  full_name: Postnikova, Anastasiia
  last_name: Postnikova
- first_name: Nikita
  full_name: Koval, Nikita
  id: 2F4DB10C-F248-11E8-B48F-1D18A9856A87
  last_name: Koval
- first_name: Giorgi
  full_name: Nadiradze, Giorgi
  id: 3279A00C-F248-11E8-B48F-1D18A9856A87
  last_name: Nadiradze
- first_name: Dan-Adrian
  full_name: Alistarh, Dan-Adrian
  id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
  last_name: Alistarh
  orcid: 0000-0003-3650-940X
citation:
  ama: Postnikova A, Koval N, Nadiradze G, Alistarh D-A. Multi-queues can be state-of-the-art
    priority schedulers. 2022. doi:<a href="https://doi.org/10.5281/ZENODO.5733408">10.5281/ZENODO.5733408</a>
  apa: Postnikova, A., Koval, N., Nadiradze, G., &#38; Alistarh, D.-A. (2022). Multi-queues
    can be state-of-the-art priority schedulers. Zenodo. <a href="https://doi.org/10.5281/ZENODO.5733408">https://doi.org/10.5281/ZENODO.5733408</a>
  chicago: Postnikova, Anastasiia, Nikita Koval, Giorgi Nadiradze, and Dan-Adrian
    Alistarh. “Multi-Queues Can Be State-of-the-Art Priority Schedulers.” Zenodo,
    2022. <a href="https://doi.org/10.5281/ZENODO.5733408">https://doi.org/10.5281/ZENODO.5733408</a>.
  ieee: A. Postnikova, N. Koval, G. Nadiradze, and D.-A. Alistarh, “Multi-queues can
    be state-of-the-art priority schedulers.” Zenodo, 2022.
  ista: Postnikova A, Koval N, Nadiradze G, Alistarh D-A. 2022. Multi-queues can be
    state-of-the-art priority schedulers, Zenodo, <a href="https://doi.org/10.5281/ZENODO.5733408">10.5281/ZENODO.5733408</a>.
  mla: Postnikova, Anastasiia, et al. <i>Multi-Queues Can Be State-of-the-Art Priority
    Schedulers</i>. Zenodo, 2022, doi:<a href="https://doi.org/10.5281/ZENODO.5733408">10.5281/ZENODO.5733408</a>.
  short: A. Postnikova, N. Koval, G. Nadiradze, D.-A. Alistarh, (2022).
date_created: 2023-05-23T17:05:40Z
date_published: 2022-01-03T00:00:00Z
date_updated: 2023-08-03T06:48:34Z
day: '03'
ddc:
- '510'
department:
- _id: DaAl
doi: 10.5281/ZENODO.5733408
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5281/zenodo.5813846
month: '01'
oa: 1
oa_version: Published Version
publisher: Zenodo
related_material:
  link:
  - relation: software
    url: https://github.com/npostnikova/mq-based-schedulers/tree/v1.1
  record:
  - id: '11180'
    relation: used_in_publication
    status: public
status: public
title: Multi-queues can be state-of-the-art priority schedulers
type: research_data_reference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2022'
...
---
_id: '13239'
abstract:
- lang: eng
  text: Brains are thought to engage in predictive learning - learning to predict
    upcoming stimuli - to construct an internal model of their environment. This is
    especially notable for spatial navigation, as first described by Tolman’s latent
    learning tasks. However, predictive learning has also been observed in sensory
    cortex, in settings unrelated to spatial navigation. Apart from normative frameworks
    such as active inference or efficient coding, what could be the utility of learning
    to predict the patterns of occurrence of correlated stimuli? Here we show that
    prediction, and thereby the construction of an internal model of sequential stimuli,
    can bootstrap the learning process of a working memory task in a recurrent neural
    network. We implemented predictive learning alongside working memory match-tasks,
    and networks emerged to solve the prediction task first by encoding information
    across time to predict upcoming stimuli, and then eavesdropped on this solution
    to solve the matching task. Eavesdropping was most beneficial when neural resources
    were limited. Hence, predictive learning acts as a general neural mechanism to
    learn to store sensory information that can later be essential for working memory
    tasks.
acknowledgement: "The authors would like to thank members of the Vogels lab and Manohar
  lab, as well as Adam Packer, Andrew Saxe, Stefano Sarao Mannelli and Jacob Bakermans
  for fruitful discussions and comments on earlier versions of the manuscript.\r\nTLvdP
  was supported by funding from the Biotechnology and Biological Sciences Research
  Council (BBSRC) [grant number BB/M011224/1]. TPV was supported by an ERC Consolidator
  Grant (SYNAPSEEK). SGM was funded by a MRC Clinician Scientist Fellowship MR/P00878X
  and Leverhulme Grant RPG-2018-310."
article_processing_charge: No
author:
- first_name: Thijs L.
  full_name: Van Der Plas, Thijs L.
  last_name: Van Der Plas
- first_name: Tim P
  full_name: Vogels, Tim P
  id: CB6FF8D2-008F-11EA-8E08-2637E6697425
  last_name: Vogels
  orcid: 0000-0003-3295-6181
- first_name: Sanjay G.
  full_name: Manohar, Sanjay G.
  last_name: Manohar
citation:
  ama: 'Van Der Plas TL, Vogels TP, Manohar SG. Predictive learning enables neural
    networks to learn complex working memory tasks. In: <i>Proceedings of Machine
    Learning Research</i>. Vol 199. ML Research Press; 2022:518-531.'
  apa: Van Der Plas, T. L., Vogels, T. P., &#38; Manohar, S. G. (2022). Predictive
    learning enables neural networks to learn complex working memory tasks. In <i>Proceedings
    of Machine Learning Research</i> (Vol. 199, pp. 518–531). ML Research Press.
  chicago: Van Der Plas, Thijs L., Tim P Vogels, and Sanjay G. Manohar. “Predictive
    Learning Enables Neural Networks to Learn Complex Working Memory Tasks.” In <i>Proceedings
    of Machine Learning Research</i>, 199:518–31. ML Research Press, 2022.
  ieee: T. L. Van Der Plas, T. P. Vogels, and S. G. Manohar, “Predictive learning
    enables neural networks to learn complex working memory tasks,” in <i>Proceedings
    of Machine Learning Research</i>, 2022, vol. 199, pp. 518–531.
  ista: Van Der Plas TL, Vogels TP, Manohar SG. 2022. Predictive learning enables
    neural networks to learn complex working memory tasks. Proceedings of Machine
    Learning Research. vol. 199, 518–531.
  mla: Van Der Plas, Thijs L., et al. “Predictive Learning Enables Neural Networks
    to Learn Complex Working Memory Tasks.” <i>Proceedings of Machine Learning Research</i>,
    vol. 199, ML Research Press, 2022, pp. 518–31.
  short: T.L. Van Der Plas, T.P. Vogels, S.G. Manohar, in:, Proceedings of Machine
    Learning Research, ML Research Press, 2022, pp. 518–531.
date_created: 2023-07-16T22:01:12Z
date_published: 2022-12-01T00:00:00Z
date_updated: 2023-07-18T06:36:28Z
day: '01'
ddc:
- '000'
department:
- _id: TiVo
ec_funded: 1
file:
- access_level: open_access
  checksum: 7530a93ef42e10b4db1e5e4b69796e93
  content_type: application/pdf
  creator: dernst
  date_created: 2023-07-18T06:32:38Z
  date_updated: 2023-07-18T06:32:38Z
  file_id: '13243'
  file_name: 2022_PMLR_vanderPlas.pdf
  file_size: 585135
  relation: main_file
  success: 1
file_date_updated: 2023-07-18T06:32:38Z
has_accepted_license: '1'
intvolume: '       199'
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: 518-531
project:
- _id: 0aacfa84-070f-11eb-9043-d7eb2c709234
  call_identifier: H2020
  grant_number: '819603'
  name: Learning the shape of synaptic plasticity rules for neuronal architectures
    and function through machine learning.
publication: Proceedings of Machine Learning Research
publication_identifier:
  eissn:
  - 2640-3498
publication_status: published
publisher: ML Research Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Predictive learning enables neural networks to learn complex working memory
  tasks
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 199
year: '2022'
...
---
_id: '13240'
abstract:
- lang: eng
  text: Ustilago maydis is a biotrophic phytopathogenic fungus that causes corn smut
    disease. As a well-established model system, U. maydis is genetically fully accessible
    with large omics datasets available and subject to various biological questions
    ranging from DNA-repair, RNA-transport, and protein secretion to disease biology.
    For many genetic approaches, tight control of transgene regulation is important.
    Here we established an optimised version of the Tetracycline-ON (TetON) system
    for U. maydis. We demonstrate the Tetracycline concentration-dependent expression
    of fluorescent protein transgenes and the system’s suitability for the induced
    expression of the toxic protein BCL2 Associated X-1 (Bax1). The Golden Gate compatible
    vector system contains a native minimal promoter from the mating factor a-1 encoding
    gene, mfa with ten copies of the tet-regulated operator (tetO) and a codon optimised
    Tet-repressor (tetR*) which is translationally fused to the native transcriptional
    corepressor Mql1 (UMAG_05501). The metabolism-independent transcriptional regulator
    system is functional both, in liquid culture as well as on solid media in the
    presence of the inducer and can become a useful tool for toxin-antitoxin studies,
    identification of antifungal proteins, and to study functions of toxic gene products
    in Ustilago maydis.
acknowledgement: "The research leading to these results received funding from the
  European Research Council under the European Union’s Seventh Framework Programme
  ERC-2013-STG (grant agreement: 335691), the Austrian Science Fund (I 3033-B22),
  the Austrian Academy of Sciences, and the Deutsche Forschungsgemeinschaft (DFG,
  German Research Foundation) under Germany's Excellence Strategy EXC-2070-390732324
  (PhenoRob) and DFG grant (DJ 64/5-1).\r\nWe would like to thank the GMI/IMBA/IMP
  core facilities for their excellent technical support. We would like to acknowledge
  Dr. Sinéad A. O’Sullivan from DZNE, University of Bonn for providing anti-GFP antibodies.
  The authors are thankful to the Excellence University of Bonn for providing infrastructure
  and instrumentation facilities at the INRES-Plant Pathology department."
article_number: '1029114'
article_processing_charge: Yes
article_type: original
author:
- first_name: Kishor D.
  full_name: Ingole, Kishor D.
  last_name: Ingole
- first_name: Nithya
  full_name: Nagarajan, Nithya
  last_name: Nagarajan
- first_name: Simon
  full_name: Uhse, Simon
  last_name: Uhse
- first_name: Caterina
  full_name: Giannini, Caterina
  id: e3fdddd5-f6e0-11ea-865d-ca99ee6367f4
  last_name: Giannini
- first_name: Armin
  full_name: Djamei, Armin
  last_name: Djamei
citation:
  ama: Ingole KD, Nagarajan N, Uhse S, Giannini C, Djamei A. Tetracycline-controlled
    (TetON) gene expression system for the smut fungus Ustilago maydis. <i>Frontiers
    in Fungal Biology</i>. 2022;3. doi:<a href="https://doi.org/10.3389/ffunb.2022.1029114">10.3389/ffunb.2022.1029114</a>
  apa: Ingole, K. D., Nagarajan, N., Uhse, S., Giannini, C., &#38; Djamei, A. (2022).
    Tetracycline-controlled (TetON) gene expression system for the smut fungus Ustilago
    maydis. <i>Frontiers in Fungal Biology</i>. Frontiers Media. <a href="https://doi.org/10.3389/ffunb.2022.1029114">https://doi.org/10.3389/ffunb.2022.1029114</a>
  chicago: Ingole, Kishor D., Nithya Nagarajan, Simon Uhse, Caterina Giannini, and
    Armin Djamei. “Tetracycline-Controlled (TetON) Gene Expression System for the
    Smut Fungus Ustilago Maydis.” <i>Frontiers in Fungal Biology</i>. Frontiers Media,
    2022. <a href="https://doi.org/10.3389/ffunb.2022.1029114">https://doi.org/10.3389/ffunb.2022.1029114</a>.
  ieee: K. D. Ingole, N. Nagarajan, S. Uhse, C. Giannini, and A. Djamei, “Tetracycline-controlled
    (TetON) gene expression system for the smut fungus Ustilago maydis,” <i>Frontiers
    in Fungal Biology</i>, vol. 3. Frontiers Media, 2022.
  ista: Ingole KD, Nagarajan N, Uhse S, Giannini C, Djamei A. 2022. Tetracycline-controlled
    (TetON) gene expression system for the smut fungus Ustilago maydis. Frontiers
    in Fungal Biology. 3, 1029114.
  mla: Ingole, Kishor D., et al. “Tetracycline-Controlled (TetON) Gene Expression
    System for the Smut Fungus Ustilago Maydis.” <i>Frontiers in Fungal Biology</i>,
    vol. 3, 1029114, Frontiers Media, 2022, doi:<a href="https://doi.org/10.3389/ffunb.2022.1029114">10.3389/ffunb.2022.1029114</a>.
  short: K.D. Ingole, N. Nagarajan, S. Uhse, C. Giannini, A. Djamei, Frontiers in
    Fungal Biology 3 (2022).
date_created: 2023-07-16T22:01:12Z
date_published: 2022-10-19T00:00:00Z
date_updated: 2024-03-06T14:01:57Z
day: '19'
ddc:
- '579'
department:
- _id: JiFr
doi: 10.3389/ffunb.2022.1029114
file:
- access_level: open_access
  checksum: 2254e0119c0749d6f7237084fefcece6
  content_type: application/pdf
  creator: dernst
  date_created: 2023-07-17T11:46:34Z
  date_updated: 2023-07-17T11:46:34Z
  file_id: '13242'
  file_name: 2023_FrontiersFungalBio_Ingole.pdf
  file_size: 27966699
  relation: main_file
  success: 1
file_date_updated: 2023-07-17T11:46:34Z
has_accepted_license: '1'
intvolume: '         3'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
publication: Frontiers in Fungal Biology
publication_identifier:
  eissn:
  - 2673-6128
publication_status: published
publisher: Frontiers Media
quality_controlled: '1'
scopus_import: '1'
status: public
title: Tetracycline-controlled (TetON) gene expression system for the smut fungus
  Ustilago maydis
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 3
year: '2022'
...
---
_id: '13241'
abstract:
- lang: eng
  text: Addressing fairness concerns about machine learning models is a crucial step
    towards their long-term adoption in real-world automated systems. Many approaches
    for training fair models from data have been developed and an implicit assumption
    about such algorithms is that they are able to recover a fair model, despite potential
    historical biases in the data. In this work we show a number of impossibility
    results that indicate that there is no learning algorithm that can recover a fair
    model when a proportion of the dataset is subject to arbitrary manipulations.
    Specifically, we prove that there are situations in which an adversary can force
    any learner to return a biased classifier, with or without degrading accuracy,
    and that the strength of this bias increases for learning problems with underrepresented
    protected groups in the data. Our results emphasize on the importance of studying
    further data corruption models of various strength and of establishing stricter
    data collection practices for fairness-aware learning.
acknowledgement: "This paper is a shortened, workshop version of Konstantinov and
  Lampert (2021),\r\nhttps://arxiv.org/abs/2102.06004. For further results, including
  an analysis of algorithms achieving the lower bounds from this paper, we refer to
  the full version."
article_processing_charge: No
arxiv: 1
author:
- first_name: Nikola H
  full_name: Konstantinov, Nikola H
  id: 4B9D76E4-F248-11E8-B48F-1D18A9856A87
  last_name: Konstantinov
- first_name: Christoph
  full_name: Lampert, Christoph
  id: 40C20FD2-F248-11E8-B48F-1D18A9856A87
  last_name: Lampert
  orcid: 0000-0001-8622-7887
citation:
  ama: 'Konstantinov NH, Lampert C. On the impossibility of fairness-aware learning
    from corrupted data. In: <i>Proceedings of Machine Learning Research</i>. Vol
    171. ML Research Press; 2022:59-83.'
  apa: Konstantinov, N. H., &#38; Lampert, C. (2022). On the impossibility of fairness-aware
    learning from corrupted data. In <i>Proceedings of Machine Learning Research</i>
    (Vol. 171, pp. 59–83). ML Research Press.
  chicago: Konstantinov, Nikola H, and Christoph Lampert. “On the Impossibility of
    Fairness-Aware Learning from Corrupted Data.” In <i>Proceedings of Machine Learning
    Research</i>, 171:59–83. ML Research Press, 2022.
  ieee: N. H. Konstantinov and C. Lampert, “On the impossibility of fairness-aware
    learning from corrupted data,” in <i>Proceedings of Machine Learning Research</i>,
    2022, vol. 171, pp. 59–83.
  ista: Konstantinov NH, Lampert C. 2022. On the impossibility of fairness-aware learning
    from corrupted data. Proceedings of Machine Learning Research. vol. 171, 59–83.
  mla: Konstantinov, Nikola H., and Christoph Lampert. “On the Impossibility of Fairness-Aware
    Learning from Corrupted Data.” <i>Proceedings of Machine Learning Research</i>,
    vol. 171, ML Research Press, 2022, pp. 59–83.
  short: N.H. Konstantinov, C. Lampert, in:, Proceedings of Machine Learning Research,
    ML Research Press, 2022, pp. 59–83.
date_created: 2023-07-16T22:01:13Z
date_published: 2022-12-01T00:00:00Z
date_updated: 2023-09-26T10:44:37Z
day: '01'
department:
- _id: ChLa
external_id:
  arxiv:
  - '2102.06004'
intvolume: '       171'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/2102.06004
month: '12'
oa: 1
oa_version: Preprint
page: 59-83
publication: Proceedings of Machine Learning Research
publication_identifier:
  eissn:
  - 2640-3498
publication_status: published
publisher: ML Research Press
quality_controlled: '1'
related_material:
  record:
  - id: '10802'
    relation: extended_version
    status: public
scopus_import: '1'
status: public
title: On the impossibility of fairness-aware learning from corrupted data
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 171
year: '2022'
...
---
_id: '13345'
abstract:
- lang: eng
  text: The self-assembly of inorganic nanoparticles (NPs) into ordered structures
    (superlattices) has led to a wide range of nanomaterials with unique optical,
    magnetic, electronic, and catalytic properties. Various interactions have been
    employed to direct the crystallization of NPs, including van der Waals forces,
    hydrogen bonding, as well as electric and magnetic dipolar interactions. Among
    them, Coulombic interactions—ubiquitous in nature and the main driving force behind
    the formation of many minerals, such as fluorite or rock salt—have remained largely
    underexplored, owing to the rapid charge exchange between NPs bearing high densities
    of opposite charges (superionic NPs). Here, we worked with superionic NPs under
    conditions (room temperature, concentrated salt solutions) that preserved their
    native surface charge density. We demonstrate that under these conditions, the
    Coulombic interactions between superionic NPs are reminiscent of short-range intermolecular
    interactions. Our methodology was used to assemble oppositely charged NPs into
    high-quality superlattices exhibiting Catalan shapes. Depending on their size
    ratio, the NPs assembled into either rhombic dodecahedra or triakis tetrahedra
    with structures mimicking those of the ionic solids CsCl and Th3P4, respectively.
    We envision that the methodology described here can be applied to a wide range
    of charged NPs of various sizes, shapes, and compositions, thus facilitating the
    discovery of new nanomaterials.
article_processing_charge: No
author:
- first_name: Tong
  full_name: Bian, Tong
  last_name: Bian
- first_name: Ivan
  full_name: Lobato, Ivan
  last_name: Lobato
- first_name: Ji
  full_name: Wang, Ji
  last_name: Wang
- first_name: Tara A.
  full_name: Nitka, Tara A.
  last_name: Nitka
- first_name: Tzuf Shay
  full_name: Peled, Tzuf Shay
  last_name: Peled
- first_name: Byeongdu
  full_name: Lee, Byeongdu
  last_name: Lee
- first_name: Sandra
  full_name: Van Aert, Sandra
  last_name: Van Aert
- first_name: Sara
  full_name: Bals, Sara
  last_name: Bals
- first_name: Lela
  full_name: Vuković, Lela
  last_name: Vuković
- first_name: Thomas
  full_name: Altantzis, Thomas
  last_name: Altantzis
- first_name: Petr
  full_name: Král, Petr
  last_name: Král
- first_name: Rafal
  full_name: Klajn, Rafal
  id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
  last_name: Klajn
citation:
  ama: Bian T, Lobato I, Wang J, et al. Catalan solids from superionic nanoparticles.
    <i>ChemRxiv</i>. doi:<a href="https://doi.org/10.26434/chemrxiv-2022-klncg">10.26434/chemrxiv-2022-klncg</a>
  apa: Bian, T., Lobato, I., Wang, J., Nitka, T. A., Peled, T. S., Lee, B., … Klajn,
    R. (n.d.). Catalan solids from superionic nanoparticles. <i>ChemRxiv</i>. <a href="https://doi.org/10.26434/chemrxiv-2022-klncg">https://doi.org/10.26434/chemrxiv-2022-klncg</a>
  chicago: Bian, Tong, Ivan Lobato, Ji Wang, Tara A. Nitka, Tzuf Shay Peled, Byeongdu
    Lee, Sandra Van Aert, et al. “Catalan Solids from Superionic Nanoparticles.” <i>ChemRxiv</i>,
    n.d. <a href="https://doi.org/10.26434/chemrxiv-2022-klncg">https://doi.org/10.26434/chemrxiv-2022-klncg</a>.
  ieee: T. Bian <i>et al.</i>, “Catalan solids from superionic nanoparticles,” <i>ChemRxiv</i>.
    .
  ista: Bian T, Lobato I, Wang J, Nitka TA, Peled TS, Lee B, Van Aert S, Bals S, Vuković
    L, Altantzis T, Král P, Klajn R. Catalan solids from superionic nanoparticles.
    ChemRxiv, <a href="https://doi.org/10.26434/chemrxiv-2022-klncg">10.26434/chemrxiv-2022-klncg</a>.
  mla: Bian, Tong, et al. “Catalan Solids from Superionic Nanoparticles.” <i>ChemRxiv</i>,
    doi:<a href="https://doi.org/10.26434/chemrxiv-2022-klncg">10.26434/chemrxiv-2022-klncg</a>.
  short: T. Bian, I. Lobato, J. Wang, T.A. Nitka, T.S. Peled, B. Lee, S. Van Aert,
    S. Bals, L. Vuković, T. Altantzis, P. Král, R. Klajn, ChemRxiv (n.d.).
date_created: 2023-08-01T09:30:08Z
date_published: 2022-04-08T00:00:00Z
date_updated: 2023-08-02T06:48:27Z
day: '08'
doi: 10.26434/chemrxiv-2022-klncg
extern: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.26434/chemrxiv-2022-klncg
month: '04'
oa: 1
oa_version: Preprint
publication: ChemRxiv
publication_status: submitted
status: public
title: Catalan solids from superionic nanoparticles
type: preprint
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2022'
...
---
_id: '13347'
abstract:
- lang: eng
  text: Confining molecules within well-defined nanosized spaces can profoundly alter
    their physicochemical characteristics. For example, the controlled aggregation
    of chromophores into discrete oligomers has been shown to tune their optical properties
    whereas encapsulation of reactive species within molecular hosts can increase
    their stability. The resazurin/resorufin pair has been widely used for detecting
    redox processes in biological settings; yet, how tight confinement affects the
    properties of these two dyes remains to be explored. Here, we show that a flexible
    Pd<jats:sup>II</jats:sup><jats:sub>6</jats:sub>L<jats:sub>4</jats:sub> coordination
    cage can efficiently encapsulate both resorufin and resazurin in the form of dimers,
    dramatically modulating their optical properties. Furthermore, binding within
    the cage significantly decreases the reduction rate of resazurin to resorufin,
    and the rate of the subsequent reduction of resorufin to dihydroresorufin. During
    our studies, we also found that upon dilution, the Pd<jats:sup>II</jats:sup><jats:sub>6</jats:sub>L<jats:sub>4</jats:sub>
    cage disassembles to afford Pd<jats:sup>II</jats:sup><jats:sub>2</jats:sub>L<jats:sub>2</jats:sub>
    species, which lacks the ability to form inclusion complexes – a process that
    can be reversed upon the addition of the strongly binding resorufin/resazurin
    guests. We expect that the herein disclosed ability of a water-soluble cage to
    reversibly modulate the optical and chemical properties of a molecular redox probe
    will expand the versatility of synthetic fluorescent probes in biologically relevant
    environments.
article_number: '44'
article_processing_charge: No
article_type: original
author:
- first_name: Oksana
  full_name: Yanshyna, Oksana
  last_name: Yanshyna
- first_name: Michał J.
  full_name: Białek, Michał J.
  last_name: Białek
- first_name: Oleg V.
  full_name: Chashchikhin, Oleg V.
  last_name: Chashchikhin
- first_name: Rafal
  full_name: Klajn, Rafal
  id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
  last_name: Klajn
citation:
  ama: Yanshyna O, Białek MJ, Chashchikhin OV, Klajn R. Encapsulation within a coordination
    cage modulates the reactivity of redox-active dyes. <i>Communications Chemistry</i>.
    2022;5. doi:<a href="https://doi.org/10.1038/s42004-022-00658-8">10.1038/s42004-022-00658-8</a>
  apa: Yanshyna, O., Białek, M. J., Chashchikhin, O. V., &#38; Klajn, R. (2022). Encapsulation
    within a coordination cage modulates the reactivity of redox-active dyes. <i>Communications
    Chemistry</i>. Springer Nature. <a href="https://doi.org/10.1038/s42004-022-00658-8">https://doi.org/10.1038/s42004-022-00658-8</a>
  chicago: Yanshyna, Oksana, Michał J. Białek, Oleg V. Chashchikhin, and Rafal Klajn.
    “Encapsulation within a Coordination Cage Modulates the Reactivity of Redox-Active
    Dyes.” <i>Communications Chemistry</i>. Springer Nature, 2022. <a href="https://doi.org/10.1038/s42004-022-00658-8">https://doi.org/10.1038/s42004-022-00658-8</a>.
  ieee: O. Yanshyna, M. J. Białek, O. V. Chashchikhin, and R. Klajn, “Encapsulation
    within a coordination cage modulates the reactivity of redox-active dyes,” <i>Communications
    Chemistry</i>, vol. 5. Springer Nature, 2022.
  ista: Yanshyna O, Białek MJ, Chashchikhin OV, Klajn R. 2022. Encapsulation within
    a coordination cage modulates the reactivity of redox-active dyes. Communications
    Chemistry. 5, 44.
  mla: Yanshyna, Oksana, et al. “Encapsulation within a Coordination Cage Modulates
    the Reactivity of Redox-Active Dyes.” <i>Communications Chemistry</i>, vol. 5,
    44, Springer Nature, 2022, doi:<a href="https://doi.org/10.1038/s42004-022-00658-8">10.1038/s42004-022-00658-8</a>.
  short: O. Yanshyna, M.J. Białek, O.V. Chashchikhin, R. Klajn, Communications Chemistry
    5 (2022).
date_created: 2023-08-01T09:30:47Z
date_published: 2022-03-30T00:00:00Z
date_updated: 2023-08-02T06:41:54Z
day: '30'
doi: 10.1038/s42004-022-00658-8
extern: '1'
intvolume: '         5'
keyword:
- Materials Chemistry
- Biochemistry
- Environmental Chemistry
- General Chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1038/s42004-022-00658-8
month: '03'
oa: 1
oa_version: Published Version
publication: Communications Chemistry
publication_identifier:
  eissn:
  - 2399-3669
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Encapsulation within a coordination cage modulates the reactivity of redox-active
  dyes
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 5
year: '2022'
...
---
_id: '13348'
abstract:
- lang: eng
  text: Molecular confinement effects can profoundly alter the physicochemical properties
    of the confined species. A plethora of organic molecules were encapsulated within
    the cavities of supramolecular hosts, and the impact of the cavity size and polarity
    was widely investigated. However, the extent to which the properties of the confined
    guests can be affected by the symmetry of the cage─which dictates the shape of
    the cavity─remains to be understood. Here we show that cage symmetry has a dramatic
    effect on the equilibrium between two isomers of the encapsulated spiropyran guests.
    Working with two Pd-based coordination cages featuring similarly sized but differently
    shaped hydrophobic cavities, we found a highly selective stabilization of the
    isomer whose shape matches that of the cavity of the cage. A Td-symmetric cage
    stabilized the spiropyrans’ colorless form and rendered them photochemically inert.
    In contrast, a D2h-symmetric cage favored the colored isomer, while maintaining
    reversible photoswitching between the two states of the encapsulated spiropyrans.
    We also show that the switching kinetics strongly depend on the substitution pattern
    on the spiropyran scaffold. This finding was used to fabricate a time-sensitive
    information storage medium with tunable lifetimes of the encoded messages.
article_processing_charge: No
article_type: original
author:
- first_name: Jinhua
  full_name: Wang, Jinhua
  last_name: Wang
- first_name: Liat
  full_name: Avram, Liat
  last_name: Avram
- first_name: Yael
  full_name: Diskin-Posner, Yael
  last_name: Diskin-Posner
- first_name: Michał J.
  full_name: Białek, Michał J.
  last_name: Białek
- first_name: Wojciech
  full_name: Stawski, Wojciech
  last_name: Stawski
- first_name: Moran
  full_name: Feller, Moran
  last_name: Feller
- first_name: Rafal
  full_name: Klajn, Rafal
  id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
  last_name: Klajn
citation:
  ama: Wang J, Avram L, Diskin-Posner Y, et al. Altering the properties of spiropyran
    switches using coordination cages with different symmetries. <i>Journal of the
    American Chemical Society</i>. 2022;144(46):21244-21254. doi:<a href="https://doi.org/10.1021/jacs.2c08901">10.1021/jacs.2c08901</a>
  apa: Wang, J., Avram, L., Diskin-Posner, Y., Białek, M. J., Stawski, W., Feller,
    M., &#38; Klajn, R. (2022). Altering the properties of spiropyran switches using
    coordination cages with different symmetries. <i>Journal of the American Chemical
    Society</i>. American Chemical Society. <a href="https://doi.org/10.1021/jacs.2c08901">https://doi.org/10.1021/jacs.2c08901</a>
  chicago: Wang, Jinhua, Liat Avram, Yael Diskin-Posner, Michał J. Białek, Wojciech
    Stawski, Moran Feller, and Rafal Klajn. “Altering the Properties of Spiropyran
    Switches Using Coordination Cages with Different Symmetries.” <i>Journal of the
    American Chemical Society</i>. American Chemical Society, 2022. <a href="https://doi.org/10.1021/jacs.2c08901">https://doi.org/10.1021/jacs.2c08901</a>.
  ieee: J. Wang <i>et al.</i>, “Altering the properties of spiropyran switches using
    coordination cages with different symmetries,” <i>Journal of the American Chemical
    Society</i>, vol. 144, no. 46. American Chemical Society, pp. 21244–21254, 2022.
  ista: Wang J, Avram L, Diskin-Posner Y, Białek MJ, Stawski W, Feller M, Klajn R.
    2022. Altering the properties of spiropyran switches using coordination cages
    with different symmetries. Journal of the American Chemical Society. 144(46),
    21244–21254.
  mla: Wang, Jinhua, et al. “Altering the Properties of Spiropyran Switches Using
    Coordination Cages with Different Symmetries.” <i>Journal of the American Chemical
    Society</i>, vol. 144, no. 46, American Chemical Society, 2022, pp. 21244–54,
    doi:<a href="https://doi.org/10.1021/jacs.2c08901">10.1021/jacs.2c08901</a>.
  short: J. Wang, L. Avram, Y. Diskin-Posner, M.J. Białek, W. Stawski, M. Feller,
    R. Klajn, Journal of the American Chemical Society 144 (2022) 21244–21254.
date_created: 2023-08-01T09:31:01Z
date_published: 2022-11-15T00:00:00Z
date_updated: 2023-08-02T06:39:50Z
day: '15'
doi: 10.1021/jacs.2c08901
extern: '1'
intvolume: '       144'
issue: '46'
keyword:
- Colloid and Surface Chemistry
- Biochemistry
- General Chemistry
- Catalysis
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1021/jacs.2c08901
month: '11'
oa: 1
oa_version: Published Version
page: 21244-21254
publication: Journal of the American Chemical Society
publication_identifier:
  eissn:
  - 1520-5126
  issn:
  - 0002-7863
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Altering the properties of spiropyran switches using coordination cages with
  different symmetries
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 144
year: '2022'
...
---
_id: '13350'
abstract:
- lang: eng
  text: Confinement within molecular cages can dramatically modify the physicochemical
    properties of the encapsulated guest molecules, but such host-guest complexes
    have mainly been studied in a static context. Combining confinement effects with
    fast guest exchange kinetics could pave the way toward stimuli-responsive supramolecular
    systems—and ultimately materials—whose desired properties could be tailored “on
    demand” rapidly and reversibly. Here, we demonstrate rapid guest exchange between
    inclusion complexes of an open-window coordination cage that can simultaneously
    accommodate two guest molecules. Working with two types of guests, anthracene
    derivatives and BODIPY dyes, we show that the former can substantially modify
    the optical properties of the latter upon noncovalent heterodimer formation. We
    also studied the light-induced covalent dimerization of encapsulated anthracenes
    and found large effects of confinement on reaction rates. By coupling the photodimerization
    with the rapid guest exchange, we developed a new way to modulate fluorescence
    using external irradiation.
article_processing_charge: No
article_type: original
author:
- first_name: Julius
  full_name: Gemen, Julius
  last_name: Gemen
- first_name: Michał J.
  full_name: Białek, Michał J.
  last_name: Białek
- first_name: Miri
  full_name: Kazes, Miri
  last_name: Kazes
- first_name: Linda J.W.
  full_name: Shimon, Linda J.W.
  last_name: Shimon
- first_name: Moran
  full_name: Feller, Moran
  last_name: Feller
- first_name: Sergey N.
  full_name: Semenov, Sergey N.
  last_name: Semenov
- first_name: Yael
  full_name: Diskin-Posner, Yael
  last_name: Diskin-Posner
- first_name: Dan
  full_name: Oron, Dan
  last_name: Oron
- first_name: Rafal
  full_name: Klajn, Rafal
  id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
  last_name: Klajn
citation:
  ama: Gemen J, Białek MJ, Kazes M, et al. Ternary host-guest complexes with rapid
    exchange kinetics and photoswitchable fluorescence. <i>Chem</i>. 2022;8(9):2362-2379.
    doi:<a href="https://doi.org/10.1016/j.chempr.2022.05.008">10.1016/j.chempr.2022.05.008</a>
  apa: Gemen, J., Białek, M. J., Kazes, M., Shimon, L. J. W., Feller, M., Semenov,
    S. N., … Klajn, R. (2022). Ternary host-guest complexes with rapid exchange kinetics
    and photoswitchable fluorescence. <i>Chem</i>. Elsevier. <a href="https://doi.org/10.1016/j.chempr.2022.05.008">https://doi.org/10.1016/j.chempr.2022.05.008</a>
  chicago: Gemen, Julius, Michał J. Białek, Miri Kazes, Linda J.W. Shimon, Moran Feller,
    Sergey N. Semenov, Yael Diskin-Posner, Dan Oron, and Rafal Klajn. “Ternary Host-Guest
    Complexes with Rapid Exchange Kinetics and Photoswitchable Fluorescence.” <i>Chem</i>.
    Elsevier, 2022. <a href="https://doi.org/10.1016/j.chempr.2022.05.008">https://doi.org/10.1016/j.chempr.2022.05.008</a>.
  ieee: J. Gemen <i>et al.</i>, “Ternary host-guest complexes with rapid exchange
    kinetics and photoswitchable fluorescence,” <i>Chem</i>, vol. 8, no. 9. Elsevier,
    pp. 2362–2379, 2022.
  ista: Gemen J, Białek MJ, Kazes M, Shimon LJW, Feller M, Semenov SN, Diskin-Posner
    Y, Oron D, Klajn R. 2022. Ternary host-guest complexes with rapid exchange kinetics
    and photoswitchable fluorescence. Chem. 8(9), 2362–2379.
  mla: Gemen, Julius, et al. “Ternary Host-Guest Complexes with Rapid Exchange Kinetics
    and Photoswitchable Fluorescence.” <i>Chem</i>, vol. 8, no. 9, Elsevier, 2022,
    pp. 2362–79, doi:<a href="https://doi.org/10.1016/j.chempr.2022.05.008">10.1016/j.chempr.2022.05.008</a>.
  short: J. Gemen, M.J. Białek, M. Kazes, L.J.W. Shimon, M. Feller, S.N. Semenov,
    Y. Diskin-Posner, D. Oron, R. Klajn, Chem 8 (2022) 2362–2379.
date_created: 2023-08-01T09:32:14Z
date_published: 2022-09-08T00:00:00Z
date_updated: 2023-08-02T09:39:35Z
day: '08'
doi: 10.1016/j.chempr.2022.05.008
extern: '1'
external_id:
  pmid:
  - '36133801'
intvolume: '         8'
issue: '9'
keyword:
- Materials Chemistry
- Biochemistry (medical)
- General Chemical Engineering
- Environmental Chemistry
- Biochemistry
- General Chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1016/j.chempr.2022.05.008
month: '09'
oa: 1
oa_version: Published Version
page: 2362-2379
pmid: 1
publication: Chem
publication_identifier:
  eissn:
  - 2451-9294
  issn:
  - 2451-9308
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Ternary host-guest complexes with rapid exchange kinetics and photoswitchable
  fluorescence
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2022'
...
---
_id: '13351'
abstract:
- lang: eng
  text: 'Molecular recognition is at the heart of the noncovalent synthesis of supramolecular
    assemblies and, at higher length scales, supramolecular materials. In a recent
    publication in Nature, Stoddart and co-workers demonstrate that the formation
    of host-guest complexes can be catalyzed by one of the simplest possible catalysts:
    the electron.'
article_processing_charge: No
article_type: original
author:
- first_name: Julius
  full_name: Gemen, Julius
  last_name: Gemen
- first_name: Rafal
  full_name: Klajn, Rafal
  id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
  last_name: Klajn
citation:
  ama: Gemen J, Klajn R. Electron catalysis expands the supramolecular chemist’s toolbox.
    <i>Chem</i>. 2022;8(5):1183-1186. doi:<a href="https://doi.org/10.1016/j.chempr.2022.04.022">10.1016/j.chempr.2022.04.022</a>
  apa: Gemen, J., &#38; Klajn, R. (2022). Electron catalysis expands the supramolecular
    chemist’s toolbox. <i>Chem</i>. Elsevier. <a href="https://doi.org/10.1016/j.chempr.2022.04.022">https://doi.org/10.1016/j.chempr.2022.04.022</a>
  chicago: Gemen, Julius, and Rafal Klajn. “Electron Catalysis Expands the Supramolecular
    Chemist’s Toolbox.” <i>Chem</i>. Elsevier, 2022. <a href="https://doi.org/10.1016/j.chempr.2022.04.022">https://doi.org/10.1016/j.chempr.2022.04.022</a>.
  ieee: J. Gemen and R. Klajn, “Electron catalysis expands the supramolecular chemist’s
    toolbox,” <i>Chem</i>, vol. 8, no. 5. Elsevier, pp. 1183–1186, 2022.
  ista: Gemen J, Klajn R. 2022. Electron catalysis expands the supramolecular chemist’s
    toolbox. Chem. 8(5), 1183–1186.
  mla: Gemen, Julius, and Rafal Klajn. “Electron Catalysis Expands the Supramolecular
    Chemist’s Toolbox.” <i>Chem</i>, vol. 8, no. 5, Elsevier, 2022, pp. 1183–86, doi:<a
    href="https://doi.org/10.1016/j.chempr.2022.04.022">10.1016/j.chempr.2022.04.022</a>.
  short: J. Gemen, R. Klajn, Chem 8 (2022) 1183–1186.
date_created: 2023-08-01T09:32:27Z
date_published: 2022-05-12T00:00:00Z
date_updated: 2023-08-02T07:24:57Z
day: '12'
doi: 10.1016/j.chempr.2022.04.022
extern: '1'
intvolume: '         8'
issue: '5'
keyword:
- Materials Chemistry
- Biochemistry (medical)
- General Chemical Engineering
- Environmental Chemistry
- Biochemistry
- General Chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1016/j.chempr.2022.04.022
month: '05'
oa: 1
oa_version: Published Version
page: 1183-1186
publication: Chem
publication_identifier:
  eissn:
  - 2451-9294
  issn:
  - 2451-9308
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Electron catalysis expands the supramolecular chemist’s toolbox
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2022'
...
