For researchers

Is your paper here?

2,665 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 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+
rs2744971 rs10843164 rs10182181 rs1412239 rs1421085 rs538656
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci
Human molecular genetics · 2015 · PMID 25429064
12 pages+
rs7184046 rs13072744 rs3755206 rs3771381 rs1865760 rs11970475
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+
rs2277598 rs295322 rs62623713 rs11555762 rs9891146 rs13447324
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Profile Study · Australian Prostate Cancer BioResource (APCB) and 7 more consortia
Nature genetics · 2018 · PMID 29892016
12 pages+
rs4962416 rs684232 rs182314334 rs2121875 rs17021918 rs11859370
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
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+
rs73909841 rs10788167 rs3787099 rs371707439 rs12701838 rs565189650
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study
Blood Cell Consortium
BMC genomics · 2021 · PMID 34107879 · open access
12 pages+
rs72981097 rs2900727 rs6326 rs61787890 rs7529274 rs4847150
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+
rs10886810 rs1037137 rs11892008 rs6151589 rs4713343 rs78416326
Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations
Nature genetics · 2011 · PMID 21642993
6 pages
rs10058728 rs8030672 rs2274223 rs11066015 rs10052657 Oesophageal Cancer
The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype
eMERGE Network
Genetic epidemiology · 2019 · PMID 30298529 · open access
5 pages
rs9810195 rs541558502 rs147482218 rs142765674 Shingles
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
Nature communications · 2023 · PMID 37236969 · open access
5 pages
rs71467682 rs75031349 rs137884934 rs682888 rs10901793
Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions
Nature genetics · 2012 · PMID 22960999
3 pages
rs4785204 rs4822983 Oesophageal Cancer
Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies
Gut · 2017 · PMID 26701879 · open access
3 pages
rs80142782 rs13361707 Non-Cardia Gastric Cancer
Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk
Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO) · Colorectal Transdisciplinary (CORECT) Study and 1 more consortia
Gastroenterology · 2016 · PMID 26965516
3 pages
rs2450115 rs4919687 rs6061231
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
Medical Records-Based Genetic Studies of the Complement System
Journal of the American Society of Nephrology : JASN · 2021 · PMID 33941608
3 pages
rs16869834 rs3135353 rs17208153
Genome-wide association study identifies 1p36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers
Nature genetics · 2010 · PMID 20676096
2 pages
rs17401966 HBV-Related Hepatocellular Carcinoma
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations
Nature genetics · 2011 · PMID 22158540
2 pages
rs372883 Pancreatic Cancer
Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese
American journal of human genetics · 2012 · PMID 23103227
2 pages
rs2494938 rs2285947
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia
Nature genetics · 2012 · PMID 23143601
2 pages
rs4488809 rs7086803

Showing 20 of 39 · 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.