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.

15 matches for Crawford DC.

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+
rs7692995 rs17556750 rs9392918 rs6919534 rs17721822 rs7154721
New genetic loci link adipose and insulin biology to body fat distribution
ADIPOGen Consortium · CARDIOGRAMplusC4D Consortium and 11 more consortia
Nature · 2015 · PMID 25673412 · open access
12 pages+
rs6088619 rs12143789 rs798528 rs6060717 rs11989744 rs4646404
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
Nature genetics · 2021 · PMID 33398198 · open access
12 pages+
rs143745027 rs4842687 rs10122990 rs7011138 rs1048374 rs9978557
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
12 pages+
rs940526 rs11264734 rs7236307 rs4848397 rs11055891 rs74179816
Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries
VA Million Veteran Program · International AMD Genomics Consortium (IAMDGC)
Nature genetics · 2024 · PMID 39623103
12 pages+
rs9973159 rs334362 rs56123646 rs1137776 rs7803454 rs9821337
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) QRS Group
Circulation · 2013 · PMID 23463857
3 pages
rs1805126 rs6906287 rs1321313
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci
Circulation research · 2017 · PMID 27899403 · open access
3 pages
rs12133641 rs9316871 Abdominal Aortic Aneurysm
Genetic variation associated with circulating monocyte count in the eMERGE Network
CHARGE Hematology Working Group · electronic Medical Records and Genomics (eMERGE) Network
Human molecular genetics · 2013 · PMID 23314186
2 pages
rs2124440 Monocyte Count
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 Novel Susceptibility Loci for Prostate Cancer in Men of African Ancestry
PRACTICAL/ELLIPSE Consortium
Journal of the National Cancer Institute · 2017 · PMID 29117387 · open access
2 pages
rs75823044 rs78554043
Genome-wide association analysis of common genetic variants of resistant hypertension
eMERGE network
The pharmacogenomics journal · 2019 · PMID 30237584
2 pages
rs11749255 Resistant Hypertension
Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study
G3 (Bethesda, Md.) · 2013 · PMID 23696099 · open access
1 page
rs7120391
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
Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program
VA Million Veteran Program COVID-19 Science Initiative
Frontiers in genetics · 2021 · PMID 35222515 · open access
1 page
rs73062389
Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry
European urology · 2023 · PMID 36872133
1 page
rs150947563

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.