For researchers

Is your paper here?

2,663 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.

13 matches for Vernooij MW.

Cerebral small vessel disease genomics and its implications across the lifespan
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 pages+
rs4843553 rs11685652 rs7157599 rs73923006 rs6797002 rs7603972
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
9 pages
rs10217651 rs35200015 rs3133370 rs2206656 rs4784256 rs196807
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate
Brain : a journal of neurology · 2022 · PMID 35511193 · open access
6 pages
rs3744027 rs6503417 rs12149643 rs73191849 rs13403122 Cerebral Small Vessel Disease
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI
Circulation. Cardiovascular genetics · 2015 · PMID 25663218
4 pages
rs7894407 rs72848980 rs7909791 rs7214628
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
CHARGE consortium
Nature medicine · 2023 · PMID 37069360 · open access
3 pages
rs6011998 rs112407396 rs72485816
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504421 · open access
2 pages
rs17178006 rs6581612
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
Stroke · 2020 · PMID 32517579
2 pages
rs2598420 rs3758575
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Nature genetics · 2023 · PMID 37770635
2 pages
rs62555371 rs10899970
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium
Annals of neurology · 2011 · PMID 21681796
1 page
rs1055129
Identification of common variants associated with human hippocampal and intracranial volumes
Alzheimer's Disease Neuroimaging Initiative · EPIGEN Consortium and 4 more consortia
Nature genetics · 2012 · PMID 22504417
1 page
rs10784502
Common variants at 6q22 and 17q21 are associated with intracranial volume
Early Growth Genetics Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504418
1 page
rs4273712
Common variants at 12q15 and 12q24 are associated with infant head circumference
Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium and 1 more consortia
Nature genetics · 2012 · PMID 22504419
1 page
rs1042725
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
Nature communications · 2018 · PMID 30258056 · open access
1 page
rs34113929

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.