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.

184 matches for Psaty BM, showing the first 20.

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
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
Nature communications · 2023 · PMID 36918541 · open access
12 pages+
rs72825047 rs11195260 rs10793848 rs2066626 rs1873164 rs2762049
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
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+
rs9463706 rs13206305 rs3807095 rs729639 rs11264871 rs41394446
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Genes & Health Research Team · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2025 · PMID 40038546 · open access
12 pages+
rs67377357 rs149780392 rs3794752 rs62233286 rs7095308 rs73048654
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
BioBank Japan Project · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2025 · PMID 40050429
12 pages+
rs12211167 rs34216626 rs2030653 rs58952060 rs3734215 rs9928077
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium
Bone Mineral Density in Childhood Study (BMDCS) Group
PLoS genetics · 2017 · PMID 28430825 · open access
11 pages
rs62105306 rs17057164 rs149352150 rs56330886 rs112778462 rs378854
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
rs201596848 rs900399 rs7157785 rs3927680 rs7946 rs3947
Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Inflammation Working Group
Human molecular genetics · 2024 · PMID 38747556
11 pages
rs519064 rs144007943 rs6588153 rs74479543 rs370370301 rs144067869
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
PLoS genetics · 2013 · PMID 23408906 · open access
10 pages
rs9497965 rs7860634 rs7240777 rs10799824 rs9472138 rs11755845
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
10 pages
rs2206656 rs4784256 rs196807 rs9505301 rs9818981 rs2410767
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels
Circulation · 2011 · PMID 21300955
9 pages
rs6734238 rs13233571 rs1183910 rs1800961 rs10521222 rs2847281
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
VTE Consortium · STROKE Consortium and 3 more consortia
Circulation · 2013 · PMID 23969696
9 pages
rs434943 rs2106854 rs7968440 rs1938492 rs1019670 rs4817986
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans
CHARGE QRS Consortium
Human molecular genetics · 2016 · PMID 27577874
9 pages
rs7907361 rs1362212 rs2207791 rs9573330 rs13185595 rs7756236
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
CHD Exome+ Consortium · ExomeBP Consortium and 4 more consortia
Nature genetics · 2016 · PMID 27618448
9 pages
rs2493292 rs11639856 rs1925153 rs3755652 rs11014166 rs11024074
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders
Nature human behaviour · 2019 · PMID 31358974
9 pages
rs10496076 rs71414193 rs57281063 rs227179 rs4794015 rs988748
New insights into the genetic etiology of Alzheimer's disease and related dementias
EADB · GR@ACE and 7 more consortia
Nature genetics · 2022 · PMID 35379992 · open access
9 pages
rs3848143 rs62374257 rs3851179 rs6605556 rs7767350 rs6586028
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
LifeLines Cohort Study
Nature genetics · 2012 · PMID 22267201 · open access
8 pages
rs1635501 rs10183486 rs2153157 rs12294104 rs10852344 rs12461110
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Nature genetics · 2012 · PMID 22504420 · open access
8 pages
rs7953528 rs163879 rs1864325 rs7084921 rs344081 rs3905706
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
Global BPgen Consortium · CARDIoGRAM Consortium and 4 more consortia
Nature genetics · 2013 · PMID 23583979
8 pages
rs4140885 rs180242 rs17796783 rs17287293 rs11118555 rs13030174

Showing 20 of 184 · page 3 of 10

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.