For researchers

Is your paper here?

2,660 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.

44 matches for Zhang J, showing the first 20.

Co-regulatory networks of human serum proteins link genetics to disease
Science (New York, N.Y.) · 2018 · PMID 30072576
12 pages+
rs72651379 rs2069901 rs78183295 rs8026121 rs186872766 rs77546475
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs184980867 rs10248717 rs11672003 rs149590572 rs113920320 rs111589301
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
BioBank Japan Project
Nature genetics · 2022 · PMID 36333501
12 pages+
rs4341355 rs6495979 rs73005423 rs798000 rs56750287 rs16903108
Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes
CHIMGEN Consortium
Nature genetics · 2023 · PMID 37337106
12 pages+
rs74712405 rs10479662 rs6478240 rs7636254 rs13084097 rs751991
Cross-ancestry genome-wide association studies of brain imaging phenotypes
CHIMGEN Consortium
Nature genetics · 2024 · PMID 38811844
12 pages+
rs1163297 rs12030374 rs919445 rs3744349 rs60865161 rs7935166
Cross-ancestry and sex-stratified genome-wide association analyses of amygdala and subnucleus volumes
CHIMGEN Consortium
Nature genetics · 2025 · PMID 40097784
12 pages+
rs56390130 rs62329462 rs12679702 rs150434736 rs201081507 rs11941622
A genome-wide association study of neonatal metabolites
Cell genomics · 2024 · PMID 39389019 · open access
9 pages
rs75854125 rs12082305 rs1859000 rs10988200 rs1075650 rs695948
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
Bayesian Effect Size Ranking to Prioritise Genetic Risk Variants in Common Diseases for Follow-Up Studies
Genetic epidemiology · 2025 · PMID 39749473 · open access
7 pages
rs8013873 rs1048055 rs4804000 rs12130424 rs7545300 rs12506688
Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study
Stroke · 2018 · PMID 29273593
6 pages
rs9614159 rs74388387 rs9907978 rs10782008 rs117353193 Moyamoya Disease
Genome-wide meta-analysis across East Asian and European populations provides insights into the molecular basis of lung cancer
Genome medicine · 2026 · PMID 42152146 · open access
6 pages
rs1039766 rs12822733 rs4887067 rs13167280 rs4291686 rs36108040
Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians
American journal of human genetics · 2013 · PMID 23273568
5 pages
rs6705628 rs4852324 rs6804441 rs34330 rs729302
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome
Nature genetics · 2012 · PMID 22885925
4 pages
rs3802457 rs1894116 rs2272046 rs6022786
Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis
Vasculitis Clinical Research Consortium
Arthritis & rheumatology (Hoboken, N.J.) · 2017 · PMID 28029757 · open access
4 pages
rs62132293 rs7454108 rs35242582 ANCA-Associated Vasculitis
GWAS of Chronic Spontaneous Urticaria Reveals Genetic Overlap with Autoimmune Diseases, Not Atopic Diseases
The Journal of investigative dermatology · 2023 · PMID 35933036
4 pages
rs61986182 rs73075571 rs117754460 rs434124
Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia
Nature communications · 2016 · PMID 26853712 · open access
3 pages
rs17090300 rs11263613 rs13089920
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
Trans-ethnic genome-wide association study of blood metabolites in the Chronic Renal Insufficiency Cohort (CRIC) study
CKD Biomarkers Consortium and the Chronic Renal Insufficiency Cohort (CRIC) Study Investigators
Kidney international · 2022 · PMID 35120996
3 pages
rs6736866 rs74603482 rs61799988
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
CHARGE consortium
Nature medicine · 2023 · PMID 37069360 · open access
3 pages
rs112407396 rs72485816 rs6011998
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
Nature genetics · 2023 · PMID 37337107
3 pages
rs75413466 rs2075836 rs57917667

Showing 20 of 44 · page 1 of 3

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.