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.

81 matches for Zhang Y, showing the first 20.

Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia
Nature communications · 2017 · PMID 28165464 · open access
12 pages+
rs58055674 rs34004493 rs3755397 rs7690934 rs9392504 rs2267708
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
Human molecular genetics · 2017 · PMID 28334899
12 pages+
rs2188380 rs2144300 rs11984636 rs3786247 rs11208004 rs2244608
Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups
Nature communications · 2021 · PMID 33536424 · open access
12 pages+
rs1016140 rs7815944 rs405858 rs9630991 rs9899849 rs12093154
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
arcOGEN Consortium · HUNT All-In Pain and 2 more consortia
Cell · 2021 · PMID 34450027 · open access
12 pages+
rs17288390 rs216175 rs7212908 rs747952496 rs3993110 rs781661531
Whole exome sequencing analyses reveal novel genes in telomere length and their biomedical implications
GeroScience · 2024 · PMID 38837026
12 pages+
rs75544730 rs79253753 rs147978211 rs77610594 rs558886548 rs145967304
Networks of human milk microbiota are associated with host genomics, childhood asthma, and allergic sensitization
Cell host & microbe · 2024 · PMID 39293435
12 pages+
rs7560183 rs355570 rs987023 rs112238348 rs112292550 rs142596319
Translational genomics of osteoarthritis in 1,962,069 individuals
arcOGEN Consortium · ARGO Consortium and 7 more consortia
Nature · 2025 · PMID 40205036 · open access
12 pages+
rs12350099 rs1480637 rs2095140 rs13118508 rs2015110 rs509236
Shared genetic architecture between the topology of brain white matter structural connectome and fluid intelligence
Communications biology · 2026 · PMID 42092107 · open access
12 pages+
rs6943986 rs6467499 rs2647230 rs62253605 rs66868086 rs201882079
Development and validation of a multiancestry and multitrait polygenic risk score for lung cancer
Nature communications · 2026 · PMID 42364979 · open access
12 pages+
rs1138373 rs705698 rs7638643 rs750608 rs74231870 rs951984
Multiscale analysis and functional validation of the cellular and genetic determinants of skeletal disease
International Federation of Musculoskeletal Research Societies (IFMRS) Big Data Working Group
Nature genetics · 2026 · PMID 42432248 · open access
12 pages+
rs566836317 rs1772720 rs148243584 rs189567770 rs73400424 rs61872090
Exome-wide association study of plasma lipids in >300,000 individuals
Charge Diabetes Working Group · EPIC-InterAct Consortium and 3 more consortia
Nature genetics · 2017 · PMID 29083408 · open access
11 pages
rs201596848 rs900399 rs7157785 rs3927680 rs7946 rs3947
Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci
Clinical and translational medicine · 2021 · PMID 33634981 · open access
11 pages
rs73365860 rs117445861 rs6497488 rs74716564 rs8073361 rs76199614
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation
Nature genetics · 2017 · PMID 27918534
7 pages
rs2434264 rs7374732 rs6689335 rs912056 rs10060123 rs2123685
The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders
Translational psychiatry · 2023 · PMID 37236919 · open access
7 pages
rs10980625 rs11621425 rs12552125 rs1110339 rs7616662 rs12369969
Human milk oligosaccharides are associated with maternal genetics and respiratory health of human milk-fed children
Nature communications · 2024 · PMID 39232002 · open access
7 pages
rs485186 rs546308 rs16982241 rs1132054 rs4015 rs10414887
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Veterans Affairs Million Veteran Program†
Circulation · 2020 · PMID 32981348 · open access
6 pages
rs10808546 rs35254673 rs4401144 rs118039278 rs73149487 Abdominal Aortic Aneurysm
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 multiple susceptibility loci for pulmonary fibrosis
Nature genetics · 2013 · PMID 23583980 · open access
5 pages
rs1278769 rs2609255 rs11191865 rs1981997 Interstitial Lung Disease
Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma
Nature genetics · 2014 · PMID 25261932 · open access
5 pages
rs79480871 rs116446171 rs13255292 rs4733601 Diffuse Large B Cell Lymphoma
Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region
American journal of human genetics · 2014 · PMID 25279986
5 pages
rs12195582 rs4937362 rs17749561 rs13254990 Follicular Lymphoma

Showing 20 of 81 · page 1 of 5

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.