For researchers

Is your paper here?

2,665 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.

14 matches for Verma A.

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+
rs111859808 rs17209803 rs74705598 rs10082867 rs12358424 rs78186330
Leveraging deep phenotyping from health check-up cohort with 10,000 Korean individuals for phenome-wide association study of 136 traits
Scientific reports · 2022 · PMID 35121771 · open access
12 pages+
rs72810954 rs192385957 rs79945097 rs182483569 rs76731854 rs77162552
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs147660927 rs7209222 rs9272456 rs4515883 rs6743072 rs35073727
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
12 pages+
rs13115816 rs144564964 rs34731601 rs4648884 rs4925094 rs62134679
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium and 4 more consortia
Nature genetics · 2026 · PMID 41644669 · open access
12 pages+
rs57831860 rs12196336 rs542166863 rs7606251 rs1030964 rs73191621
Multi-population GWAS meta-analysis identifies bladder cancer susceptibility loci and highlights genetic regulation of smoking-related risk
UROMOL Consortium
Nature communications · 2026 · PMID 42706231 · open access
12 pages+
rs72826305 rs112204664 rs7076867 rs7937265 rs6910215 rs7145592
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Regeneron Genetics Center · Geisinger-Regeneron DiscovEHR Collaboration and 2 more consortia
Nature genetics · 2022 · PMID 35654975
8 pages
rs3935942 rs1626329 rs6059896 rs168144 rs74816838 rs3810367
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
Genetic drivers of etiologic heterogeneity in thyroid cancer
Nature communications · 2026 · PMID 42431967 · open access
6 pages
rs17089782 rs1979221 rs143459581 rs17767904 rs4733129 rs11245983
The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype
eMERGE Network
Genetic epidemiology · 2019 · PMID 30298529 · open access
5 pages
rs9810195 rs541558502 rs147482218 rs142765674 Shingles
Whole-genome sequencing reveals host factors underlying critical COVID-19
GenOMICC investigators · 23andMe investigators and 1 more consortia
Nature · 2022 · PMID 35255492 · open access
5 pages
rs8178521 rs28368148 rs3848456 rs9271609 rs2532300
Cross-definition GWAS of IBS in 2.8 million individuals reveals cardiometabolic and triglyceride-linked mechanisms
Colorado Center for Personalized Medicine · Estonian Biobank Research Team and 3 more consortia
Gut · 2026 · PMID 42425734
5 pages
rs2195110 rs72700810 rs10184811 rs12221193 Irritable Bowel Syndrome
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci
Circulation research · 2017 · PMID 27899403 · open access
3 pages
rs12133641 rs9316871 Abdominal Aortic Aneurysm
Genetic risk factors for COVID-19 and influenza are largely distinct
Colorado Center for Precision Medicine · Mayo Clinic Project Generation and 2 more consortia
Nature genetics · 2024 · PMID 39103650 · open access
1 page
rs2837112

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.