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.

28 matches for Ritchie MD, showing the first 20.

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
New genetic loci link adipose and insulin biology to body fat distribution
ADIPOGen Consortium · CARDIOGRAMplusC4D Consortium and 11 more consortia
Nature · 2015 · PMID 25673412 · open access
12 pages+
rs6060717 rs11989744 rs4646404 rs319564 rs2179129 rs16996700
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
23andMe Research Team · COGENT (Cognitive Genomics Consortium) and 1 more consortia
Nature genetics · 2018 · PMID 30038396
12 pages+
rs72673540 rs73648455 rs7754916 rs10509516 rs12693677 rs2221534
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+
rs13018106 rs12678719 rs11465506 rs397637 rs4430933 rs6599250
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
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
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs6058896 rs649523 rs6552828 rs3806325 rs7162940 rs7219047
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+
rs6743072 rs35073727 rs57631119 rs9380498 rs12187932 rs61208973
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs74627567 rs7851052 rs79190780 rs10849893 rs117526461 rs1109772
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 genome-wide association study of coronary artery disease in genetically diverse populations
Regeneron Genetics Center · CARDIoGRAMplusC4D Consortium and 2 more consortia
Nature medicine · 2022 · PMID 35915156
8 pages
rs56210063 rs78532451 rs17101521 rs11152953 rs1867073 rs7622417
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
8 pages
rs12012576 rs6527977 rs139120857 rs5942972 rs7063103 rs62603531
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
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development
American journal of human genetics · 2018 · PMID 29290336
4 pages
rs12614435 rs77831929 rs4404097 rs56202902
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Nature genetics · 2012 · PMID 22544366
3 pages
rs10821415 rs10824026 rs7164883
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
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
Identification of unique venous thromboembolism-susceptibility variants in African-Americans
Thrombosis and haemostasis · 2017 · PMID 28203683
3 pages
rs3804476 rs142143628 rs138916004
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 28 · 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.