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.

15 matches for Sharma P.

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+
rs4674124 rs4702131 rs2304098 rs6912005 rs183421746 rs35419901
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
Penn Medicine Biobank
Nature genetics · 2025 · PMID 40195560
12 pages+
rs12724121 rs2904129 rs6779426 rs7873569 rs2837993 rs56289631
Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits
DIAMANTE Hispanic/Latino Consortium · Global Hispanic Lipids Consortium
Nature communications · 2025 · PMID 40210677 · open access
12 pages+
rs16989540 rs536240710 rs181676594 rs6974288 rs3846663 rs12939051
Ischemic stroke is associated with the ABO locus: the EuroCLOT study
EuroCLOT Investigators · Wellcome Trust Case Control Consortium 2 and 3 more consortia
Annals of neurology · 2013 · PMID 23381943 · open access
11 pages
rs2022309 rs10922162 rs3211770 rs1318606 rs555212 rs10982156
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
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs6015450 rs11191548 rs7129220 rs1173771 rs13139571
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
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
rs60882887 rs12470785 rs79183898 rs736596 rs7222250
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
4 pages
rs2107595 rs879324 rs13407662 Ischaemic Stroke
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
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
LifeLines Cohort Study · CARDIoGRAM Consortium and 3 more consortia
Nature genetics · 2013 · PMID 23263486
3 pages
rs1481012 rs4475146 Gout
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
kConFab Investigators · ABCTB Investigators and 2 more consortia
Nature genetics · 2020 · PMID 32424353 · open access
2 pages
rs17743054 rs11065822
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants
METASTROKE Consortium · CARDIoGRAM Consortium and 2 more consortia
Stroke · 2014 · PMID 24262325
1 page
rs12646447
Genetic variation at 16q24.2 is associated with small vessel stroke
METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
Annals of neurology · 2017 · PMID 27997041 · open access
1 page
rs12445022
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies
Helsinki Stroke, Study Dutch Parelsnoer Institute-Cerebrovascular Accident (CVA) Study Group · National Institute of Neurological Disorders and Stroke (NINDS) Stroke Genetics Network and 2 more consortia
The Lancet. Neurology · 2021 · PMID 33773637 · open access
1 page
rs72934535

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.