Skip to Main Content
CKG
Home
Home
Home
TKG
Author details
Breadcrumb
Author Details
Full Name
Veikko Salomaa
Affiliation
ORCID
Career Start Year
2007
Papers
16
H Index
14
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36240095
Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke.
Neurology
2022
31152163
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
Nat Genet
2019
31686056
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power.
Nature
2019
31367044
Exome sequencing of Finnish isolates enhances rare-variant association power.
Nature
2019
29531354
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
Nat Genet
2018
29973585
Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.
Nat Commun
2018
30140049
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.
Nat Commun
2018
27355579
Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
PLoS Genet
2016
23381943
Ischemic stroke is associated with the ABO locus: the EuroCLOT study.
Ann Neurol
2013
22238593
A genome-wide association search for type 2 diabetes genes in African Americans.
PLoS One
2012
21597005
An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemia.
Arterioscler Thromb Vasc Biol
2011
20657596
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
Nat Genet
2010
20190752
Multiple common variants for celiac disease influencing immune gene expression.
Nat Genet
2010
19198609
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
Nat Genet
2009
19222087
Systematically missing confounders in individual participant data meta-analysis of observational cohort studies.
Stat Med
2009
17876711
The Emerging Risk Factors Collaboration: analysis of individual data on lipid, inflammatory and other markers in over 1.1 million participants in 104 prospective studies of cardiovascular diseases.
Eur J Epidemiol
2007
1 - 16 of 16
Column Actions
Search
Recommended Authors
Collaborators
Bruce M Psaty
Co-authored papers
7
Braxton D Mitchell
Co-authored papers
7
Kari Stefansson
University of Iceland
Co-authored papers
6
Jerome I Rotter
Co-authored papers
6
John Danesh
Co-authored papers
5
Michael Boehnke
Co-authored papers
5
Gudmar Thorleifsson
deCODE genetics/Amgen Inc.
Co-authored papers
5
Markku Laakso
Co-authored papers
5
Philippe Amouyel
Co-authored papers
5
Heather M Stringham
Co-authored papers
5
Paul M Ridker
Co-authored papers
5
Samuli Ripatti
Co-authored papers
5
Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
Co-authored papers
4
Vilmundur Gudnason
Co-authored papers
4
Steven A McCarroll
Co-authored papers
4
Anne U Jackson
Co-authored papers
4
Erik Ingelsson
Stanford University School of Medicine
Co-authored papers
4
Benjamin F Voight
Perelman School of Medicine, University of Pennsylvania
Co-authored papers
4
Cornelia M van Duijn
University of Oxford
Co-authored papers
4
Andres Metspalu
Co-authored papers
4
Unnur Thorsteinsdottir
University of Iceland
Co-authored papers
4
Albert Hofman
Harvard T.H. Chan School of Public Health
Co-authored papers
4
Mark J Daly
Massachusetts General Hospital
Co-authored papers
4
Aarno Palotie
Co-authored papers
4
Christian Gieger
German Research Center for Cardiovascular Disease (DZHK)
Co-authored papers
4
Kenneth Rice
Co-authored papers
4
Sekar Kathiresan
Co-authored papers
4
James G Wilson
Beth Israel Deaconess Medical Center
Co-authored papers
3
Laura J Scott
Co-authored papers
3
Veikko Salomaa
Co-authored papers
3
1 - 30