For researchers

Is your paper here?

2,673 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.

27 matches for Denny JC, showing the first 20.

Genetics of rheumatoid arthritis contributes to biology and drug discovery
RACI consortium · GARNET consortium
Nature · 2014 · PMID 24390342 · open access
12 pages+
rs9653442 rs71508903 rs9372120 rs72634030 rs11933540 rs2561477
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
CARe Consortium · COGENT Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24952745 · open access
12 pages+
rs1983546 rs12930096 rs12444261 rs1052536 rs1396515 rs1805128
Defining the role of common variation in the genomic and biological architecture of adult human height
Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25282103 · open access
12 pages+
rs6485978 rs4332428 rs1562975 rs17807185 rs12120956 rs3739707
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
ICBP Consortium · AGEN Consortium and 3 more consortia
Nature communications · 2016 · PMID 26831199 · open access
12 pages+
rs6795744 rs228611 rs3750082 rs10491967 rs11666497 rs1800615
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
METASTROKE Consortium of the ISGC · Neurology Working Group of the CHARGE Consortium and 1 more consortia
Nature genetics · 2017 · PMID 28416818
12 pages+
rs60848348 rs1454934 rs36004974 rs577676 rs11598047 rs10800507
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
CHD Exome+ Consortium · EPIC-CVD Consortium and 9 more consortia
Nature genetics · 2018 · PMID 29273807 · open access
12 pages+
rs2277598 rs295322 rs62623713 rs11555762 rs9891146 rs13447324
Multi-ethnic genome-wide association study for atrial fibrillation
Nature genetics · 2018 · PMID 29892015
12 pages+
rs10027347 rs10165883 rs1044258 rs10479177 rs10760361 rs10842383
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity
Nature communications · 2018 · PMID 30046033 · open access
12 pages+
rs17767398 rs13018106 rs12678719 rs11465506 rs397637 rs4430933
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
Understanding Society Scientific Group · International Consortium for Blood Pressure and 2 more consortia
Nature genetics · 2019 · PMID 30578418 · open access
12 pages+
rs10926991 rs2764043 rs10088725 rs12951622 rs147202915 rs34797797
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
rs10494217 rs1051860 rs141845046 rs145878042 rs1715919 rs62266958
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
BioBank Japan Project
Nature genetics · 2022 · PMID 36333501
12 pages+
rs4341355 rs10872479 rs6495979 rs73005423 rs798000 rs56750287
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs3742636 rs74387263 rs10758321 rs11023938 rs116257126 rs144589448
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Million Veteran Program · Lifelines Cohort Study and 2 more consortia
Nature genetics · 2024 · PMID 38689001 · open access
12 pages+
rs11639335 rs2374457 rs35745897 rs57244721 rs75488436 rs73022874
Genome-wide meta-analysis identifies novel risk loci for uterine fibroids within and across multiple ancestry groups
Nature communications · 2025 · PMID 40050615 · open access
12 pages+
rs117424499 rs143479908 rs10751644 rs2145763 rs60702155 rs11008552
Multi-ancestry genome-wide association analyses provide insights into the genetic basis of Hashimoto's thyroiditis
Biobank Japan Project
Nature genetics · 2026 · PMID 42527560 · open access
12 pages+
rs9267665 rs41519545 rs142170016 rs115686299 rs150084830 rs746708
Exome-wide association study of plasma lipids in >300,000 individuals
Charge Diabetes Working Group · EPIC-InterAct Consortium and 3 more consortia
Nature genetics · 2017 · PMID 29083408 · open access
11 pages
rs10861661 rs201596848 rs900399 rs7157785 rs3927680 rs7946
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations
PLoS genetics · 2017 · PMID 28498854 · open access
8 pages
rs115795127 rs7651190 rs11563582 rs62434120 rs113866309 rs76987554
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
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) QRS Group
Circulation · 2013 · PMID 23463857
3 pages
rs1805126 rs6906287 rs1321313
Identification of unique venous thromboembolism-susceptibility variants in African-Americans
Thrombosis and haemostasis · 2017 · PMID 28203683
3 pages
rs3804476 rs142143628 rs138916004

Showing 20 of 27 · 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.