For researchers

Is your paper here?

2,663 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.

70 matches for Sen S, showing the first 20.

The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition
Communications biology · 2022 · PMID 36402844 · open access
10 pages
rs13083375 rs11892032 rs908611 rs2854152 rs60258355 rs6723391
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
AOCS study group · EMBRACE Study and 4 more consortia
Nature genetics · 2017 · PMID 28346442
9 pages
rs1879586 rs7207826 rs11651755 rs688187 rs7902587 rs9886651
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
DBDS Genetic Consortium · GO Consortium
Nature communications · 2022 · PMID 35110524 · open access
9 pages
rs751450 rs3135842 rs4757353 rs28487989 rs16934882 rs3010044
New insights into the genetic etiology of Alzheimer's disease and related dementias
EADB · GR@ACE and 7 more consortia
Nature genetics · 2022 · PMID 35379992 · open access
9 pages
rs62374257 rs3851179 rs6605556 rs7767350 rs6586028 rs7225151
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
DBDS Genomic Consortium · FinnGen Study and 3 more consortia
Nature genetics · 2023 · PMID 36914876
8 pages
rs71575922 rs1903068 rs3858429 rs4540228 rs57281976 rs2967684
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
COGS–Cancer Research UK GWAS–ELLIPSE (part of GAME-ON) Initiative · Australian Prostate Cancer Bioresource and 3 more consortia
Nature genetics · 2013 · PMID 23535732
7 pages
rs3850699 rs1894292 rs2273669 rs1270884 rs11650494 rs1218582
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
rs6692219 rs11971186 rs1937455 rs6738833 rs13026471 rs6883351
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity
HCMR Investigators
Nature genetics · 2021 · PMID 33495597
7 pages
rs7210446 rs118060942 rs4799426 rs142929136 rs139913353 rs74605438
Large-scale brainstem neuroimaging and genetic analyses provide new insights into the neuronal mechanisms of hypertension
HGG advances · 2025 · PMID 39663699 · open access
7 pages
rs12030641 rs111423688 rs13140033 rs783622 rs76344126 rs1863244
Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
ABCTB Investigators · AOCS Study Group & Australian Cancer Study (Ovarian Cancer) and 5 more consortia
Cancer discovery · 2016 · PMID 27432226
6 pages
rs2628317 rs17762342 rs739704 rs3802173 rs1469713 rs9657608
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
ExomeBP Consortium · MAGIC Consortium and 1 more consortia
Nature genetics · 2018 · PMID 29632382 · open access
6 pages
rs16826069 rs1127787 rs7572857 rs2233580 rs56200889 rs35658696
Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma
Frontiers of medicine · 2021 · PMID 32889700
6 pages
rs465498 rs1200399 rs2517873 rs4573350 rs1264308 rs17038564
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
ABCTB Investigators · EMBRACE and 4 more consortia
Nature genetics · 2017 · PMID 29058716
5 pages
rs10995201 rs9397437 rs6562760 rs6678914 rs67397200
Large-scale association analyses identify host factors influencing human gut microbiome composition
Nature genetics · 2021 · PMID 33462485
5 pages
rs7605229 rs7322849 rs11110281 rs61841503 rs71348714
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
GEMO Study Collaborators · EMBRACE Collaborators and 3 more consortia
Nature communications · 2021 · PMID 33597508 · open access
5 pages
rs12470785 rs79183898 rs736596 rs7222250 rs60882887
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
Nature communications · 2023 · PMID 37236969 · open access
5 pages
rs75031349 rs137884934 rs682888 rs10901793 rs71467682
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study
23andMe Research Team, China Kadoorie Biobank Collaborative Group, and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
JAMA psychiatry · 2021 · PMID 34586374 · open access
4 pages
rs1950829 rs4936272 rs17410557 rs112176860
Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function
Nature genetics · 2022 · PMID 35697868
4 pages
rs501740 rs55834511 rs78529941 rs9856926
Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer
NPJ genomic medicine · 2025 · PMID 41266372 · open access
4 pages
rs6979 rs768719522 rs1013698558 rs528577783
Multiple common variants for celiac disease influencing immune gene expression
Nature genetics · 2010 · PMID 20190752 · open access
3 pages
rs2327832 rs10806425 Celiac Disease

Showing 20 of 70 · page 2 of 4

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.