For researchers

Is your paper here?

2,676 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.

59 matches for Sun Y, showing the first 20.

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Million Veteran Program
Nature genetics · 2018 · PMID 30224653
12 pages+
rs10823136 rs2400509 rs7555285 rs76719272 rs72683923 rs34413141
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
Global Lipids Genetics Consortium · Myocardial Infarction Genetics (MIGen) Consortium and 2 more consortia
Nature genetics · 2018 · PMID 30275531 · open access
12 pages+
rs2489629 rs3843935 rs7316454 rs72653060 rs10513551 rs17615494
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+
rs7313782 rs7128382 rs414992 rs7766549 rs1155422 rs1036190
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
HPAP Consortium · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2020 · PMID 32541925 · open access
12 pages+
rs7026688 rs6438247 rs12918782 rs9913225 rs28712435 rs6714523
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
rs187207161 rs767105335 rs77357563 rs2306899 rs2273171 rs4846567
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
American journal of human genetics · 2021 · PMID 33713608
12 pages+
rs672769 rs10071837 rs4899520 rs75823898 rs112226333 rs2553033
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+
rs56881390 rs77631946 rs2010871 rs940922629 rs117047468 rs11758358
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+
rs7973282 rs11655686 rs6722682 rs6841071 rs6850035 rs7440928
Genomics and phenomics of body mass index reveals a complex disease network
VA Million Veteran Program
Nature communications · 2022 · PMID 36581621 · open access
12 pages+
rs58391909 rs6578300 rs76081634 rs1057227 rs12208543 rs17258507
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+
rs1457553 rs3765618 rs57917116 rs7003445 rs6964590 rs10819313
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+
rs576948131 rs577196812 rs577404626 rs57749711 rs577897177 rs587678021
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+
rs34216626 rs2030653 rs58952060 rs3734215 rs9928077 rs2266961
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+
rs2904129 rs6779426 rs7873569 rs2837993 rs56289631 rs79159857
GWAS and multi-omics integrative analysis reveal novel loci and their molecular mechanisms for circulating fatty acids
HGG advances · 2025 · PMID 40545721 · open access
12 pages+
rs3131045 rs6124746 rs10413669 rs2008915 rs7748382 rs10883462
Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population
BioBank Japan Project
Nature communications · 2025 · PMID 41184235 · open access
12 pages+
rs1541596 rs73193820 rs3764351 rs7188250 rs59788391 rs2261787
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
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Multiple Tissue Human Expression Resource (MUTHER) Consortium
Nature genetics · 2012 · PMID 22581228
8 pages
rs35747 rs4691380 rs2785980 rs1371614 rs13179048 rs6048205
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
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Regeneron Genetics Center · Geisinger-Regeneron DiscovEHR Collaboration and 2 more consortia
Nature genetics · 2022 · PMID 35654975
8 pages
rs74816838 rs3810367 rs201082887 rs2763195 rs3935942 rs1626329
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium
Diabetes · 2011 · PMID 21386085 · open access
7 pages
rs173539 rs11820589 rs301 rs11823543 rs2954033 rs1919128

Showing 20 of 59 · page 1 of 3

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.