For researchers

Is your paper here?

2,673 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.

39 matches for Lin D, showing the first 19.

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
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese
PLoS genetics · 2013 · PMID 23341777 · open access
2 pages
rs12296850 Lung Squamous Cell Carcinoma
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12
Nature genetics · 2013 · PMID 23817570
2 pages
rs13117307 Cervical Cancer
A genome-wide association study of polycystic ovary syndrome identified from electronic health records
American journal of obstetrics and gynecology · 2020 · PMID 32289280
2 pages
rs17186366 rs113168128
Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network
eMERGE Consortium
Genetic epidemiology · 2021 · PMID 32964493 · open access
2 pages
rs2526620 Carotid Artery Stenosis
Identification of Novel, Replicable Genetic Risk Loci for Suicidal Thoughts and Behaviors Among US Military Veterans
Million Veteran Program Suicide Exemplar Workgroup, the International Suicide Genetics Consortium, the Veterans Affairs Mid-Atlantic Mental Illness Research, Education, and Clinical Center Workgroup, and the Veterans Affairs Million Veteran Program
JAMA psychiatry · 2023 · PMID 36515925
2 pages
rs35675346 rs3757323
GWAS meta-analysis identifies five susceptibility loci for endometrial cancer
Estonian Biobank Research Team
EBioMedicine · 2025 · PMID 40633141 · open access
2 pages
rs148261157 rs7579014
Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus
Nature genetics · 2009 · PMID 19838193
1 page
rs1167796
A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese
Nature genetics · 2011 · PMID 21725308
1 page
rs753955
Genome-wide association study of B cell non-Hodgkin lymphoma identifies 3q27 as a susceptibility locus in the Chinese population
Nature genetics · 2013 · PMID 23749188
1 page
rs6773854
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects
Human genetics · 2014 · PMID 24026423
1 page
rs9900280
A genome wide association study identifies common variants associated with lipid levels in the Chinese population
PloS one · 2013 · PMID 24386095 · open access
1 page
rs2043085
A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population
BMC medical genomics · 2014 · PMID 24513273 · open access
1 page
rs4148152
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Human molecular genetics · 2016 · PMID 26732429
1 page
rs7741164
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
Scientific reports · 2016 · PMID 26785701 · open access
1 page
rs10051787
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 analyses of diverse populations improves discovery for complex traits
Nature · 2019 · PMID 31217584
1 page
Obesity and Body Weight
Systematic review and meta-analysis of the moderating effect of rs1799971 in OPRM1, the mu-opioid receptor gene, on response to naltrexone treatment of alcohol use disorder
Addiction (Abingdon, England) · 2020 · PMID 31961981
1 page
Opioid Receptor Sensitivity (OPRM1)
Genetic Factors Associated with Prostate Cancer Conversion from Active Surveillance to Treatment
HGG advances · 2022 · PMID 34993496 · open access
1 page
rs1404610

Showing 19 of 39 · page 2 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.