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Author Details

Vincent Mooser
McGill University
1987
224
74
PMIDPaper TitleJournal TitlePublished Year
36805566Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity.Nat Metab2023
37612393From target discovery to clinical drug development with human genetics.Nature2023
37131148HostSeq: a Canadian whole genome sequencing and clinical data resource.BMC Genom Data2023
37069249Circulating proteins to predict COVID-19 severity.Sci Rep2023
36805566Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity.Nat Metab2023
37612393From target discovery to clinical drug development with human genetics.Nature2023
37069249Circulating proteins to predict COVID-19 severity.Sci Rep2023
37131148HostSeq: a Canadian whole genome sequencing and clinical data resource.BMC Genom Data2023
36376796Correction: The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals.Clin Proteomics2022
36376796Correction: The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals.Clin Proteomics2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
35856777Pharmacogenetics-guided dalcetrapib therapy after an acute coronary syndrome: the dal-GenE trial.Eur Heart J2022
35856777Pharmacogenetics-guided dalcetrapib therapy after an acute coronary syndrome: the dal-GenE trial.Eur Heart J2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
32989287Genome-wide association study identifies 48 common genetic variants associated with handedness.Nat Hum Behav2021
33633408A Neanderthal OAS1 isoform protects individuals of European ancestry against COVID-19 susceptibility and severity.Nat Med2021
34010280The Biobanque québécoise de la COVID-19 (BQC19)-A cohort to prospectively study the clinical and biological determinants of COVID-19 clinical trajectories.PLoS One2021
34061844Vitamin D and COVID-19 susceptibility and severity in the COVID-19 Host Genetics Initiative: A Mendelian randomization study.PLoS Med2021
34043590Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.J Clin Invest2021
32989287Genome-wide association study identifies 48 common genetic variants associated with handedness.Nat Hum Behav2021
33349849The effect of angiotensin-converting enzyme levels on COVID-19 susceptibility and severity: a Mendelian randomization study.Int J Epidemiol2021
34461734Utility of Genetically Predicted Lp(a) (Lipoprotein [a]) and ApoB Levels for Cardiovascular Risk Assessment.Circ Genom Precis Med2021
33633408A Neanderthal OAS1 isoform protects individuals of European ancestry against COVID-19 susceptibility and severity.Nat Med2021
34461734Utility of Genetically Predicted Lp(a) (Lipoprotein [a]) and ApoB Levels for Cardiovascular Risk Assessment.Circ Genom Precis Med2021
34043590Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.J Clin Invest2021
34061844Vitamin D and COVID-19 susceptibility and severity in the COVID-19 Host Genetics Initiative: A Mendelian randomization study.PLoS Med2021
34010280The Biobanque québécoise de la COVID-19 (BQC19)-A cohort to prospectively study the clinical and biological determinants of COVID-19 clinical trajectories.PLoS One2021
33349849The effect of angiotensin-converting enzyme levels on COVID-19 susceptibility and severity: a Mendelian randomization study.Int J Epidemiol2021
32511779A Polygenic Risk Score as a Risk Factor for Medication-Associated Fractures.J Bone Miner Res2020
32087417Study design of Dal-GenE, a pharmacogenetic trial targeting reduction of cardiovascular events with dalcetrapib.Am Heart J2020
32511779A Polygenic Risk Score as a Risk Factor for Medication-Associated Fractures.J Bone Miner Res2020
32728465Modeling consent in the time of COVID-19.J Law Biosci2020
32675199The undiagnosed disease burden associated with alpha-1 antitrypsin deficiency genotypes.Eur Respir J2020
33398295Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19.medRxiv2020
32087417Study design of Dal-GenE, a pharmacogenetic trial targeting reduction of cardiovascular events with dalcetrapib.Am Heart J2020
33398295Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19.medRxiv2020
32675199The undiagnosed disease burden associated with alpha-1 antitrypsin deficiency genotypes.Eur Respir J2020
32728465Modeling consent in the time of COVID-19.J Law Biosci2020
30004884Protecting Privacy and Security of Genomic Data in i2b2 with Homomorphic Encryption and Differential Privacy.IEEE/ACM Trans Comput Biol Bioinform2018
30004884Protecting Privacy and Security of Genomic Data in i2b2 with Homomorphic Encryption and Differential Privacy.IEEE/ACM Trans Comput Biol Bioinform2018
28703510[Precision medicine : a required approach for the general internist].Rev Med Suisse2017
28703510[Precision medicine : a required approach for the general internist].Rev Med Suisse2017
29063527High participation rate among 25 721 patients with broad age range in a hospital-based research project involving whole-genome sequencing - the Lausanne Institutional Biobank.Swiss Med Wkly2017
29063527High participation rate among 25 721 patients with broad age range in a hospital-based research project involving whole-genome sequencing - the Lausanne Institutional Biobank.Swiss Med Wkly2017
27497240Identification and molecular characterisation of Lausanne Institutional Biobank participants with familial hypercholesterolaemia - a proof-of-concept study.Swiss Med Wkly2016
28696621[Genomic medicine : the challenges of information in clinical practice].Rev Med Suisse2016
27141948Low birth weight leads to obesity, diabetes and increased leptin levels in adults: the CoLaus study.Cardiovasc Diabetol2016
27497240Identification and molecular characterisation of Lausanne Institutional Biobank participants with familial hypercholesterolaemia - a proof-of-concept study.Swiss Med Wkly2016
28696621[Genomic medicine : the challenges of information in clinical practice].Rev Med Suisse2016
27141948Low birth weight leads to obesity, diabetes and increased leptin levels in adults: the CoLaus study.Cardiovasc Diabetol2016
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Collaborators

G??rard Waeber
Centre hospitalier universitaire vaudois
Co-authored papers 101
Peter Vollenweider
Lausanne University Hospital and University of Lausanne
Co-authored papers 88
Dawn M Waterworth
Co-authored papers 57
Murielle Bochud
University of Lausanne
Co-authored papers 37
Nicholas J Wareham
Co-authored papers 31
Kijoung Song
Co-authored papers 30
Ruth J F Loos
Co-authored papers 28
H-Erich Wichmann
Co-authored papers 27
Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 26
Toby Johnson
Co-authored papers 26
Nicole Soranzo
Wellcome Sanger Institute
Co-authored papers 25
Nilesh J Samani
Co-authored papers 25
Tim D Spector
King's College London
Co-authored papers 24
Jacques S Beckmann
University of Lausanne
Co-authored papers 24
Jing Hua Zhao
Co-authored papers 23
Inês Barroso
Co-authored papers 23
Kari Stefansson
University of Iceland
Co-authored papers 23
Cornelia M van Duijn
University of Oxford
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Sven Bergmann
University of Lausanne
Co-authored papers 22
Marjo-Riitta Järvelin
Co-authored papers 22
Leena Peltonen
Co-authored papers 22
Christian Gieger
German Research Center for Cardiovascular Disease (DZHK)
Co-authored papers 22
John Brent Richards
Lady Davis Institute for Medical Research, Jewish General Hospital
Co-authored papers 22
Unnur Thorsteinsdottir
University of Iceland
Co-authored papers 21
Mark I McCarthy
Co-authored papers 21
Jian'an Luan
Co-authored papers 20
Paul Elliott
Co-authored papers 20
Luigi Ferrucci
National Institute on Aging, National Institutes of Health
Co-authored papers 20
Veikko Salomaa
Co-authored papers 19
Massimo Mangino
Co-authored papers 19
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