For researchers

Is your paper here?

2,681 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.

25 matches for Nadkarni G, showing the first 20.

Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
Understanding Society Scientific Group · Geisinger-Regeneron DiscovEHR Collaboration
Nature genetics · 2017 · PMID 28166213 · open access
12 pages+
rs7872188 rs10870202 rs10515750 rs113745635 rs11658500 rs1458979
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Nature genetics · 2018 · PMID 30297969
12 pages+
rs3772071 rs11699802 rs231349 rs35913461 rs3845281 rs6063048
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies
Nature communications · 2019 · PMID 30604766 · open access
12 pages+
rs231889 rs10066990 rs10851885 rs11039221 rs111449836 rs12722725
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
rs10096421 rs57126710 rs6833292 rs6589750 rs271679 rs16942713
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
rs77951490 rs78863347 rs9271585 rs4807003 rs4766898 rs56106601
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Nature communications · 2020 · PMID 32439900 · open access
12 pages+
rs17099893 rs7803297 rs11214037 rs922000 rs3784192 rs3794809
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
rs59611499 rs62369630 rs6937957 rs72829173 rs7393251 rs75404152
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs6045639 rs632497 rs6458375 rs72803383 rs8078668 rs9270186
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
rs149165710 rs145441283 rs187207161 rs767105335 rs77357563 rs2306899
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs118164457 rs182859029 rs7063597 rs3752435 rs4317621 rs4731113
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+
rs111589301 rs12992267 rs141350130 rs7410608 rs186398347 rs3135688
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs57634870 rs11196296 rs3825801 rs79495865 rs1871045 rs80102379
Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease
Nature genetics · 2022 · PMID 35710981
12 pages+
rs35165944 rs74183052 rs62480403 rs7752602 rs11063188 rs12057768
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
rs6632109 rs8049403 rs2048528 rs1518760 rs78475244 rs76668186
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+
rs6539283 rs6885658 rs12906348 rs12724121 rs2904129 rs6779426
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
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
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
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
Cell genomics · 2024 · PMID 38190104 · open access
6 pages
rs10993435 rs2016708 rs13392691 rs35790011 rs11753349 rs73392143
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Regeneron Genetics Center
Nature communications · 2022 · PMID 36376295 · open access
3 pages
rs981150 rs17513625 rs10738604

Showing 20 of 25 · page 1 of 2

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.