Improving estimation and prediction of common complex disease risk

Project Period: 2020-05-01 – 2024-10-31
Funding Organisation: SNF
Principal Investigator
Department(s)
Grant Number
PCEGP3_181181
Funding Organisation
SNF

3 Publications

2022 | Published | Journal Article | IST-REx-ID: 12142 | OA
Liability-scale heritability estimation for biobank studies of low-prevalence disease
S.E. Ojavee, Z. Kutalik, M.R. Robinson, The American Journal of Human Genetics 109 (2022) 2009–2017.
[Published Version] View | Files available | DOI | WoS
 
2022 | Published | Journal Article | IST-REx-ID: 10702 | OA
Blood-based epigenome-wide analyses of cognitive abilities
McCartney DL, Hillary RF, Conole ELS, Banos DT, Gadd DA, Walker RM, Nangle C, Flaig R, Campbell A, Murray AD, Maniega SM, Valdés-Hernández MDC, Harris MA, Bastin ME, Wardlaw JM, Harris SE, Porteous DJ, Tucker-Drob EM, McIntosh AM, Evans KL, Deary IJ, Cox SR, Robinson MR, Marioni RE. 2022. Blood-based epigenome-wide analyses of cognitive abilities. Genome Biology. 23(1), 26.
[Published Version] View | Files available | DOI | WoS
 
2021 | Published | Journal Article | IST-REx-ID: 8430 | OA
Genomic architecture and prediction of censored time-to-event phenotypes with a Bayesian genome-wide analysis
S.E. Ojavee, A. Kousathanas, D. Trejo Banos, E.J. Orliac, M. Patxot, K. Lall, R. Magi, K. Fischer, Z. Kutalik, M.R. Robinson, Nature Communications 12 (2021).
[Published Version] View | Files available | DOI | WoS
 

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