For researchers

Is your paper here?

2,677 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.

373 matches for An P, showing the first 20.

Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group and 3 more consortia
Nature genetics · 2024 · PMID 38177345 · open access
12 pages+
rs324901 rs534415 rs1526193 rs7415357 rs72786643 rs3091404
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs28475375 rs61748094 rs75640507 rs17489568 rs208311 rs6697896
Genome-wide characterization of circulating metabolic biomarkers
China Kadoorie Biobank Collaborative Group · Estonian Biobank Research Team and 1 more consortia
Nature · 2024 · PMID 38448586 · open access
12 pages+
rs1056265 rs1265103 rs73062380 rs4844565 rs12126767 rs35726795
Genetic determinants of plasma protein levels in the Estonian population
Estonian Biobank Research Team
Scientific reports · 2024 · PMID 38565889 · open access
12 pages+
rs4253536 rs420726 rs3135043 rs34266919 rs369634369 rs11465597
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
DBDS Genomic Consortium · Regeneron Genetics Center and 3 more consortia
Nature genetics · 2024 · PMID 38632349 · open access
12 pages+
rs554146 rs10517369 rs11815438 rs113469203 rs7280197 rs12552930
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
AURORA Study · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2024 · PMID 38637617
12 pages+
rs16948230 rs6801151 rs78201023 rs2214230 rs7243332 rs6032660
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 pages+
rs6916760 rs4506680 rs114427493 rs12274095 rs57551109 rs501842
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+
rs73022874 rs11007929 rs1155349 rs9463706 rs13206305 rs3807095
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+
rs557234063 rs181068683 rs183121790 rs183191767 rs189355347 rs189587536
Novel risk loci for COVID-19 hospitalization among admixed American populations
SCOURGE Cohort Group
eLife · 2024 · PMID 39361370 · open access
12 pages+
rs3828477 rs2834168 rs71325089 rs10066378 rs4403445 rs2517723
Multi-ancestry GWAS meta-analyses of lung cancer reveal susceptibility loci and elucidate smoking-independent genetic risk
VA Million Veteran Program
Nature communications · 2024 · PMID 39366959 · open access
12 pages+
rs398278 rs67824503 rs28557075 rs2271920 rs239935 rs36229791
Multi-trait association analysis reveals shared genetic loci between Alzheimer's disease and cardiovascular traits
Nature communications · 2024 · PMID 39537608 · open access
12 pages+
rs17836902 rs12758643 rs2348212 rs2488152 rs4961293 rs57740056
Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries
VA Million Veteran Program · International AMD Genomics Consortium (IAMDGC)
Nature genetics · 2024 · PMID 39623103
12 pages+
rs6073957 rs7663219 rs444189 rs11569415 rs9973159 rs334362
A genome-wide association study of high-sensitivity C-reactive protein in a large Korean population highlights its genetic relationship with cholesterol metabolism
Scientific reports · 2025 · PMID 39747571 · open access
12 pages+
rs117103761 rs74987345 rs75276031 rs208296 rs118011213 rs149156910
The X chromosome's influences on the human brain
Science advances · 2025 · PMID 39854466 · open access
12 pages+
rs3105280 rs5924922 rs781792327 rs11156600 rs5940512 rs57718759
Genome-wide association study of prostate-specific antigen levels in 392,522 men identifies new loci and improves prediction across ancestry groups
Nature genetics · 2025 · PMID 39930085 · open access
12 pages+
rs180674410 rs59085467 rs143092405 rs75249094 rs62599381 rs60907901
CXCL12 drives natural variation in coronary artery anatomy across diverse populations
Million Veteran Program
Cell · 2025 · PMID 40049164
12 pages+
rs11238779 rs1482472 rs61855695 rs2624682 rs61855737 rs142539486
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+
rs72797166 rs848189 rs61750827 rs17309887 rs12211167 rs34216626
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+
rs11008552 rs572179075 rs544934450 rs9549296 rs56073547 rs150323657
Translational genomics of osteoarthritis in 1,962,069 individuals
arcOGEN Consortium · ARGO Consortium and 7 more consortia
Nature · 2025 · PMID 40205036 · open access
12 pages+
rs79309042 rs2148677 rs3780325 rs7181536 rs72827088 rs12350099

Showing 20 of 373 · page 5 of 19

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.