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Caroline Hayward

Showing results (121-130 of 527) with videos related to

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European Journal of Human Genetics : EJHG|March 7, 2008
Quantifying the increase in average human heterozygosity due to urbanisationIgor Rudan, Andrew D Carothers, Ozren Polasek, et al.
Circulation|June 24, 2022
Socioeconomic Deprivation: An Important, Largely Unrecognized Risk Factor in Primary Prevention of Cardiovascular DiseaseDorien M Kimenai, Leah Pirondini, John Gregson, et al.
Nature Communications|September 8, 2017
Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylationXia Shen, Lucija Klarić, Sodbo Sharapov, et al.
Human Molecular Genetics|January 16, 2007
Effects of genome-wide heterozygosity on a range of biomedically relevant human quantitative traitsHarry Campbell, Andrew D Carothers, Igor Rudan, et al.
Translational Psychiatry|October 3, 2022
Investigating the contributions of circadian pathway and insomnia risk genes to autism and sleep disturbancesRackeb Tesfaye, Guillaume Huguet, Zoe Schmilovich, et al.
Neurology|December 24, 2015
Polygenic risk of ischemic stroke is associated with cognitive abilitySarah E Harris, Rainer Malik, Riccardo Marioni, et al.
Human Molecular Genetics|August 29, 2003
Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degenerationCaroline Hayward, Xinhua Shu, Artur V Cideciyan, et al.
Clinical Chemistry|December 9, 2023
Multiple Cardiac Biomarkers to Improve Prediction of Cardiovascular Events: Findings from the Generation Scotland Scottish Family Health StudyPaul Welsh, Dorien M Kimenai, Anoop S V Shah, et al.
Epigenetics|March 8, 2012
Epigenetic silencing of HNF1A associates with changes in the composition of the human plasma N-glycomeVlatka Zoldoš, Tomislav Horvat, Mislav Novokmet, et al.
Scientific Reports|September 24, 2017
Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degenerationChloe M Stanton, Shyamanga Borooah, Camilla Drake, et al.
Pageof 53

Showing results (121-130 of 527) with videos related to

Sort By:
Pageof 53
European Journal of Human Genetics : EJHG|March 7, 2008
Quantifying the increase in average human heterozygosity due to urbanisationIgor Rudan, Andrew D Carothers, Ozren Polasek, et al.
Circulation|June 24, 2022
Socioeconomic Deprivation: An Important, Largely Unrecognized Risk Factor in Primary Prevention of Cardiovascular DiseaseDorien M Kimenai, Leah Pirondini, John Gregson, et al.
Nature Communications|September 8, 2017
Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylationXia Shen, Lucija Klarić, Sodbo Sharapov, et al.
Human Molecular Genetics|January 16, 2007
Effects of genome-wide heterozygosity on a range of biomedically relevant human quantitative traitsHarry Campbell, Andrew D Carothers, Igor Rudan, et al.
Translational Psychiatry|October 3, 2022
Investigating the contributions of circadian pathway and insomnia risk genes to autism and sleep disturbancesRackeb Tesfaye, Guillaume Huguet, Zoe Schmilovich, et al.
Neurology|December 24, 2015
Polygenic risk of ischemic stroke is associated with cognitive abilitySarah E Harris, Rainer Malik, Riccardo Marioni, et al.
Human Molecular Genetics|August 29, 2003
Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degenerationCaroline Hayward, Xinhua Shu, Artur V Cideciyan, et al.
Clinical Chemistry|December 9, 2023
Multiple Cardiac Biomarkers to Improve Prediction of Cardiovascular Events: Findings from the Generation Scotland Scottish Family Health StudyPaul Welsh, Dorien M Kimenai, Anoop S V Shah, et al.
Epigenetics|March 8, 2012
Epigenetic silencing of HNF1A associates with changes in the composition of the human plasma N-glycomeVlatka Zoldoš, Tomislav Horvat, Mislav Novokmet, et al.
Scientific Reports|September 24, 2017
Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degenerationChloe M Stanton, Shyamanga Borooah, Camilla Drake, et al.
Pageof 53