For researchers

Is your paper here?

2,682 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.

320 matches for Ng A, showing the first 20.

European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
23andMe Research Team · Estonian Biobank Research Team
Nature communications · 2023 · PMID 37794016 · open access
12 pages+
rs6023002 rs705699 rs117137535 rs11236813 rs56308324 rs10836538
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
12 pages+
rs4713343 rs2485662 rs78416326 rs17804499 rs72725734 rs11228580
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs12140915 rs11063029 rs321234 rs7080579 rs9561488 rs2283205
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+
rs6801151 rs78201023 rs2214230 rs7243332 rs6032660 rs10487459
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 pages+
rs57551109 rs501842 rs12113633 rs62169409 rs4140952 rs7629500
Whole exome sequencing analyses reveal novel genes in telomere length and their biomedical implications
GeroScience · 2024 · PMID 38837026
12 pages+
rs145943094 rs5748769 rs75010776 rs76382474 rs2009144 rs2396106
Developing an optimal stratification model for colorectal cancer screening and reducing racial disparities in multi-center population-based studies
Genome medicine · 2024 · PMID 38872215 · open access
12 pages+
rs72818736 rs181112261 rs77572134 rs7728240 rs6117251 rs73039433
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+
rs1275923 rs371071053 rs74315329 rs6762719 rs115378818 rs3015326
Novel risk loci for COVID-19 hospitalization among admixed American populations
SCOURGE Cohort Group
eLife · 2024 · PMID 39361370 · open access
12 pages+
rs4403445 rs2517723 rs9636867 rs17213127 rs7515509 rs34288077
Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes
Nature genetics · 2024 · PMID 39379762 · open access
12 pages+
rs10841867 rs7313918 rs6752053 rs2074314 rs72802352 rs12912777
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+
rs3781780 rs2501949 rs57580158 rs6755369 rs111961139 rs143497775
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+
rs181676594 rs6974288 rs3846663 rs12939051 rs58458113 rs58223766
A genome-wide association study of mass spectrometry proteomics using a nanoparticle enrichment platform
Nature genetics · 2025 · PMID 41310232 · open access
12 pages+
rs288296 rs73143813 rs7604812 rs9442970 rs8101725 rs12151742
Multiscale analysis and functional validation of the cellular and genetic determinants of skeletal disease
International Federation of Musculoskeletal Research Societies (IFMRS) Big Data Working Group
Nature genetics · 2026 · PMID 42432248 · open access
12 pages+
rs13280929 rs3912827 rs7241605 rs7641768 rs2141907 rs74521943
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
MAGIC · Procardis Consortium
Nature genetics · 2010 · PMID 20935630 · open access
11 pages
rs543874 rs10150332 rs2241423 rs2287019 rs12444979 rs206936
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
GIANT Consortium
Nature genetics · 2010 · PMID 21102462
11 pages
rs1364063 rs4840086 rs9939609 rs10980926 rs7642134 rs17188434
Ischemic stroke is associated with the ABO locus: the EuroCLOT study
EuroCLOT Investigators · Wellcome Trust Case Control Consortium 2 and 3 more consortia
Annals of neurology · 2013 · PMID 23381943 · open access
11 pages
rs2022309 rs10922162 rs3211770 rs1318606 rs555212 rs10982156
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · open access
11 pages
rs16982520 rs7406910 rs34591516 rs1126930 rs10407022 rs470113
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
rs900399 rs7157785 rs3927680 rs7946 rs3947 rs622082
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs
PBC Consortia · Canadian PBC Consortium and 5 more consortia
Journal of hepatology · 2021 · PMID 34033851 · open access
11 pages
rs34655300 rs12695386 rs589446 rs11742270 rs859767 rs6550965

Showing 20 of 320 · page 4 of 16

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.