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.

Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations
KidneyGen Consortium · CKDGen Consortium and 1 more consortia
Nature genetics · 2012 · PMID 22797727
6 pages
rs17730281 rs11868441 rs10767873 rs2074356 rs17730436 rs11864909
Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese
Circulation. Cardiovascular genetics · 2013 · PMID 24165912
6 pages
rs10930597 rs2030114 rs16890334 rs17135875 rs1330225 rs8002688
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
Nature communications · 2016 · PMID 26818947 · open access
6 pages
rs1116357 rs1575972 rs9309245 rs67156297 rs7107784 rs78627331
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations
The Journal of clinical endocrinology and metabolism · 2018 · PMID 29325163
6 pages
rs1526692 rs719700 rs1410656 rs13107347 rs17767445 Vitamin D Deficiency and the GC Gene
Polygenic risk score for atopic dermatitis in the Canadian population
The Journal of allergy and clinical immunology · 2021 · PMID 32439431
6 pages
rs213549 rs1841513 rs6799780 rs1438119 rs10053502 rs10512169
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension
Human molecular genetics · 2015 · PMID 25249183
5 pages
rs9810888 rs2021783 rs1902859 rs13143871 rs4409766
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function
The Journal of clinical investigation · 2017 · PMID 28394258
5 pages
rs6702619 rs17696696 rs7127129 rs2649 rs11207426
Identification of six new genetic loci associated with atrial fibrillation in the Japanese population
AFGen Consortium
Nature genetics · 2017 · PMID 28416822
5 pages
rs17059534 rs3853445 rs2540953 rs2296610 rs60572254
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Gut · 2021 · PMID 33632709 · open access
5 pages
rs73161913 rs62131228 rs6014965 rs61975764 rs80158569
Multi-Trait Genetic Analysis Identifies Autoimmune Loci Associated with Cutaneous Melanoma
23andMe Research Team
The Journal of investigative dermatology · 2022 · PMID 34813871
5 pages
rs6737159 rs7943603 rs1888621 rs112761681 rs9322309
Risk of Revision After Arthroplasty Associated with Specific Gene Loci: A Genomewide Association Study of Single-Nucleotide Polymorphisms in 1,130 Twins Treated with Arthroplasty
The Journal of bone and joint surgery. American volume · 2022 · PMID 34982741
5 pages
rs77149046 rs17309567 rs62233562 rs73546868 rs114355846
Stroke genetics informs drug discovery and risk prediction across ancestries
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
rs76110445 rs12415501 rs60401382 rs72934589 Cardioembolic Stroke
Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis
DBDS Consortium · Regeneron Genetics Center
The Journal of clinical investigation · 2022 · PMID 36194491 · open access
5 pages
rs9704688 rs56172805 rs2633313 rs2633321 rs925411
Gene discovery and biological insights into anxiety disorders from a large-scale multi-ancestry genome-wide association study
Nature genetics · 2024 · PMID 39294497
5 pages
rs10171148 rs17408393 rs2510682 rs10138360 rs4870060
Multi-ancestry meta-analysis identifies genetic modifiers of age-at-onset of Alzheimer's disease at known and novel loci
Alzheimer's Disease Genetics Consortium (ADGC)
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025 · PMID 40883957 · open access
5 pages
rs1284402 rs7920721 rs9640386 rs9395285 rs62377696
Multiomics analyses prioritize disease genes and pathways in hidradenitis suppurativa
The Journal of investigative dermatology · 2026 · PMID 41548865
5 pages
rs116212806 rs11545042 rs3129879 rs150315199 Hidradenitis Suppurativa
Matching heterogeneous cohorts by projected principal components reveals two novel Alzheimer's disease-associated genes in the Hispanic population
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026 · PMID 41755704 · open access
5 pages
rs182804071 rs192423465 rs2120001636 rs985256115 rs374043832
Hirsutism beyond PCOS: Genome-wide evidence for genetic factors
FinnGen · Estonian Biobank Research Team
The Journal of investigative dermatology · 2026 · PMID 42190866
5 pages
rs150735020 rs199649605 rs180731645 rs544265360 Hirsutism
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians
Nature genetics · 2011 · PMID 21572416
4 pages
rs35444 rs17249754 rs6825911 Blood Pressure
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population
Journal of human genetics · 2011 · PMID 21900946
4 pages
rs3893464 rs4313034 rs4248154 Graves' Disease

Showing 20 of 145 · page 3 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.