For researchers

Is your paper here?

3,082 papers hold this site up. Every variant and condition page names the research it was written from, and this is that list, gathered from the pages themselves. Search your name, your journal, or a PMID.

22 matches for Vermeulen S, showing the first 20.

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Nature genetics · 2013 · PMID 23563607 · open access
12 pages+
rs11205303 rs798554 rs6662509 rs1885486 rs2280470 rs2744971
Defining the role of common variation in the genomic and biological architecture of adult human height
Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25282103 · open access
12 pages+
rs8102380 rs2854207 rs9650315 rs7870753 rs2278483 rs4735677
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
CHARGE Consortium · DIAGRAM Consortium and 4 more consortia
PLoS genetics · 2015 · PMID 26426971 · open access
12 pages+
rs13011109 rs38902 rs7081678 rs4721902 rs2820443 rs12955983
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
CHD Exome+ Consortium · EPIC-CVD Consortium and 9 more consortia
Nature genetics · 2018 · PMID 29273807 · open access
12 pages+
rs284860 rs1131877 rs2277598 rs295322 rs62623713 rs11555762
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
rs10494217 rs1051860 rs141845046 rs145878042 rs1715919 rs62266958
Multi-population GWAS meta-analysis identifies bladder cancer susceptibility loci and highlights genetic regulation of smoking-related risk
UROMOL Consortium
Nature communications · 2026 · PMID 42706231 · open access
12 pages+
rs72826305 rs112204664 rs7076867 rs7937265 rs6910215 rs7145592
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
PLoS genetics · 2013 · PMID 23408906 · open access
10 pages
rs9497965 rs7860634 rs7240777 rs10799824 rs9472138 rs11755845
Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease
The American journal of clinical nutrition · 2013 · PMID 23824729
8 pages
rs2275565 rs7130284 rs154657 rs234709 rs548987 rs12780845
Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations
PloS one · 2019 · PMID 31136621 · open access
8 pages
rs9974927 rs113740363 rs202062355 rs202227463 rs201778907 rs75287757
Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights
UROMOL Consortium
European urology · 2023 · PMID 37210288
4 pages
rs4743687 rs17863783 rs1414253 rs411482
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
PLoS genetics · 2012 · PMID 22693459 · open access
3 pages
rs2073963 rs12565727 Androgenetic Alopecia (Male Pattern Baldness)
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
PLoS genetics · 2014 · PMID 24586183 · open access
3 pages
rs1230666 rs10944479 Thyroid Autoimmunity (TPO Antibodies)
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
Nature communications · 2017 · PMID 29030599 · open access
3 pages
rs34831921 rs55730499 Human Lifespan and Longevity
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
Nature genetics · 2010 · PMID 20972438 · open access
2 pages
rs8102137 rs798766
Common variants in DGKK are strongly associated with risk of hypospadias
Nature genetics · 2011 · PMID 21113153
2 pages
rs1934179 Hypospadias
Genetic studies of body mass index yield new insights for obesity biology
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
2 pages
rs16851483 rs2121279
Two newly identified genetic determinants of pigmentation in Europeans
Nature genetics · 2008 · PMID 18488028
1 page
rs1408799
FTO genotype is associated with phenotypic variability of body mass index
Nature · 2012 · PMID 22982992
1 page
rs7202116
Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder
Genetics of Personality Consortium
JAMA psychiatry · 2015 · PMID 25993607
1 page
rs35855737
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms
Aneurysm Consortium; Vascular Research Consortium of New Zealand
Journal of the American Heart Association · 2016 · PMID 27418160 · open access
1 page
rs595244

Showing 20 of 22 · page 1 of 2

Questions about this list

Why is my paper here? I never gave you permission.

Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page cites your work, and links to the paper on PubMed — which is what a citation is. Your title and author list come from Europe PMC, the same public record a library catalogue uses.

Why are all the authors listed instead of "et al."?

Because a study that needed 622 people is a different kind of study from one that needed four, and "et al." erases that. Twelve names show and the rest are one click away. Everyone is searchable, including the 187th name on a consortium paper — that person exists and may be looking for it.

My name is misspelt, or the paper is wrong.

Tell us and it is fixed. Names come from the public record and initials are inconsistent across databases; where two people share a form of a name we cannot separate them, and we would rather be corrected than guess.

My paper is not here. Does that mean you rejected it?

No. This catalogue is assembled from what a small team could read, and it is thinnest outside European-ancestry cohorts. A paper is absent because nobody has got to it, not because it was assessed and turned down.

Which pages rest on a paper?

Each row lists them, up to six, and links to each one. The count beside a row is how many pages cite it in total.

How often does this change?

It is rebuilt from the pages every hour. A paper appears the moment a page starts resting on it and disappears if that page stops — there is no separate list to keep in step, because the citation lives on the page that makes the claim.