For researchers

Is your paper here?

2,657 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.

23 matches for Han T, showing the first 20.

Association analysis identifies 65 new breast cancer risk loci
NBCS Collaborators · ABCTB Investigators and 1 more consortia
Nature · 2017 · PMID 29059683 · open access
12 pages+
rs71557345 rs6904031 rs56387622 rs11624333 rs1895062 rs13294895
Association analyses identify 31 new risk loci for colorectal cancer susceptibility
PRACTICAL consortium
Nature communications · 2019 · PMID 31089142 · open access
12 pages+
rs77776598 rs16969681 rs75686861 rs10849438 rs12143541 rs17816465
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+
rs2527927 rs704417 rs117042741 rs35564340 rs1919364 rs11108175
Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes
CHIMGEN Consortium
Nature genetics · 2023 · PMID 37337106
12 pages+
rs12504966 rs7020341 rs3800232 rs4762080 rs16856156 rs9829866
New role of fat-free mass in cancer risk linked with genetic predisposition
Scientific reports · 2024 · PMID 38538606 · open access
12 pages+
rs9538147 rs9840500 rs11041809 rs11062555 rs11684373 rs11823264
Cross-ancestry genome-wide association studies of brain imaging phenotypes
CHIMGEN Consortium
Nature genetics · 2024 · PMID 38811844
12 pages+
rs3744349 rs60865161 rs7935166 rs145628449 rs180960063 rs2286184
Cross-ancestry and sex-stratified genome-wide association analyses of amygdala and subnucleus volumes
CHIMGEN Consortium
Nature genetics · 2025 · PMID 40097784
12 pages+
rs62329462 rs150434736 rs201081507 rs11941622 rs2195243 rs2200225
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+
rs6862531 rs13280929 rs3912827 rs7241605 rs7641768 rs2141907
Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants
Nature communications · 2020 · PMID 32139696 · open access
10 pages
rs17268829 rs10760444 rs71559437 rs6964587 rs4496150 rs9833888
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium
Diabetes · 2011 · PMID 21386085 · open access
7 pages
rs173539 rs11820589 rs301 rs11823543 rs2954033 rs1919128
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis
23andMe Research team · Esophageal cancer consortium
Gut · 2022 · PMID 34187846 · open access
7 pages
rs9372625 rs10982622 rs2145318 rs2597301 rs1431196 rs2106353
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis
Barrett's and Esophageal Adenocarcinoma Consortium (BEACON) · Esophageal Adenocarcinoma GenEtics Consortium (EAGLE) and 1 more consortia
The Lancet. Oncology · 2016 · PMID 27527254 · open access
6 pages
rs2464469 rs17451754 rs9918259 rs1979654 rs75783973 Oesophageal Cancer
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
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
COGENT Consortium · CORGI Consortium and 2 more consortia
Nature genetics · 2010 · PMID 20972440 · open access
4 pages
rs6687758 rs4925386 rs6691170 Colorectal Cancer
Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases
BEACON · 23andMe Research Team
Nature communications · 2019 · PMID 31527586 · open access
4 pages
rs7282609 rs10940767 rs4676893 Gastroesophageal Reflux Disease
Heterogeneous genetic architectures of prostate cancer susceptibility in sub-Saharan Africa
Nature genetics · 2024 · PMID 39358599
4 pages
rs147567323 rs6983515 rs339321 rs16902043
ELF1 is associated with systemic lupus erythematosus in Asian populations
Human molecular genetics · 2011 · PMID 21044949
2 pages
rs7329174 Systemic Lupus Erythematosus
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504421 · open access
2 pages
rs17178006 rs6581612
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer
Scientific reports · 2015 · PMID 25990418 · open access
2 pages
rs11255841 rs2293582
GWAS meta-analysis of 16 790 patients with Barrett's oesophagus and oesophageal adenocarcinoma identifies 16 novel genetic risk loci and provides insights into disease aetiology beyond the single marker level
Wellcome Trust Case Control Consortium 2 (WTCCC2) · Esophageal Adenocarcinoma Genetics Consortium (EAGLE) and 1 more consortia
Gut · 2023 · PMID 35882562
2 pages
rs72760500 rs2687197

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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.