For researchers

Is your paper here?

2,676 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.

145 matches for He J, showing the first 20.

Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors
The Journal of biological chemistry · 2022 · PMID 36395887 · open access
12 pages+
rs60591205 rs2322721 rs1832669 rs112062413 rs16952439 rs1438480
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs6708175 rs71483011 rs72875642 rs76942239 rs7705852 rs7901906
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Nature genetics · 2023 · PMID 36539618
12 pages+
rs6912214 rs2527927 rs704417 rs117042741 rs35564340 rs1919364
Identification of 16 novel Alzheimer's disease loci using multi-ancestry meta-analyses
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025 · PMID 39998322 · open access
12 pages+
rs368042471 rs115908094 rs1355274306 rs1265024412 rs140886023 rs1273071898
Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population
BioBank Japan Project
Nature communications · 2025 · PMID 41184235 · open access
12 pages+
rs1541596 rs73193820 rs3764351 rs7188250 rs59788391 rs2261787
Multi-ancestry genome-wide association and integrated multi-omics analyses of endometriosis and its clinical manifestations
Nature genetics · 2026 · PMID 42056605
12 pages+
rs2237257 rs2974396 rs10517343 rs55938609 rs17053711 rs10983311
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
NIDDK IBD Genetics Consortium · Belgian-French IBD Consortium and 1 more consortia
Nature genetics · 2008 · PMID 18587394
11 pages
rs3764147 rs2301436 rs9286879 rs1551398 rs7927894 rs11175593
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · open access
11 pages
rs16982520 rs7406910 rs34591516 rs1126930 rs10407022 rs470113
Genome- and exome-wide association study of serum lipoprotein (a) in the Jackson Heart Study
Journal of human genetics · 2015 · PMID 26377243
10 pages
rs9355814 rs9406316 rs9322428 rs17539620 rs149565105 rs185414370
Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling
CARDIoGRAM Consortium · CHARGE Inflammation Working Group and 1 more consortia
The Journal of clinical investigation · 2013 · PMID 23999434
9 pages
rs12999542 rs13019803 rs2302612 rs11693697 rs13029918 rs1014286
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population
Nature genetics · 2019 · PMID 30718926
9 pages
rs79407053 rs2908279 rs9505085 rs2844623 rs201597274 rs76550717
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype
Australian Asthma Genetics Consortium Collaborators
The Journal of allergy and clinical immunology · 2014 · PMID 24388013
8 pages
rs4833095 rs1438673 rs10197862 rs1837253 rs72699186 rs17294280
Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages
Alzheimer's Disease Neuroimaging Initiative
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2018 · PMID 29274321
8 pages
rs55644114 rs74442473 rs2378873 rs10775009 rs2819438 rs118130881
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Regeneron Genetics Center · Geisinger-Regeneron DiscovEHR Collaboration and 2 more consortia
Nature genetics · 2022 · PMID 35654975
8 pages
rs74816838 rs3810367 rs201082887 rs2763195 rs3935942 rs1626329
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population
Nature genetics · 2012 · PMID 22446963
7 pages
rs12529514 rs2233434 rs10821944 rs11900673 rs657075 rs3781913
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
CHARGE Neurology Working Group · COGENT-Kidney Consortium and 2 more consortia
American journal of human genetics · 2018 · PMID 29455858
7 pages
rs115234772 rs62319742 rs148772934 rs138973557 rs148753653 rs12135881
Shared genetic and experimental links between obesity-related traits and asthma subtypes in UK Biobank
The Journal of allergy and clinical immunology · 2020 · PMID 31669095
7 pages
rs112104755 rs12493005 rs73086541 rs73084574 rs1787663 rs9275570
Identifying Atopic Dermatitis Risk Loci in 1,094,060 Individuals with Subanalysis of Disease Severity and Onset
FinnGen · Estonian Biobank Research Team
The Journal of investigative dermatology · 2024 · PMID 38663478
7 pages
rs933905994 rs7481797 rs763581386 rs6064053 rs538763482 rs13275449
Genome-wide association studies for pelvic organ prolapse in the Japanese population
Biobank Japan project
Communications biology · 2024 · PMID 39349682 · open access
7 pages
rs1544637 rs251217 rs4944936 rs42400 rs12915554 rs4779863
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation
International HIV Controllers Study
Science (New York, N.Y.) · 2010 · PMID 21051598
6 pages
rs4418214 rs2523590 rs2255221 rs2395029 rs9262632 HIV-1 Viral Control

Showing 20 of 145 · page 2 of 8

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.