For researchers

Is your paper here?

2,663 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.

21 matches for Chang KM, showing the first 20.

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+
rs3800406 rs75393320 rs71559014 rs2362529 rs10275712 rs10177080
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+
rs9563574 rs146886108 rs9859406 rs9384 rs10407429 rs10305420
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes
Lifelines Cohort Study · VA Million Veteran Program
Nature communications · 2021 · PMID 33972514 · open access
12 pages+
rs35013847 rs77707292 rs6684154 rs8046061 rs4712253 rs7450517
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+
rs3211938 rs151235402 rs73339979 rs114139997 rs10184673 rs117139027
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+
rs1983864 rs145350287 rs9317002 rs7715256 rs6234 rs13109980
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs12789028 rs11466334 rs12555274 rs13094957 rs76675804 rs2056857
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+
rs739846 rs12824533 rs6879279 rs1862069 rs1047912 rs12318598
CXCL12 drives natural variation in coronary artery anatomy across diverse populations
Million Veteran Program
Cell · 2025 · PMID 40049164
12 pages+
rs61855737 rs142539486 rs906943 rs268274 rs800331 rs7083186
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
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease
INVENT Consortium · Veterans Affairs’ Million Veteran Program
Nature genetics · 2019 · PMID 31676865 · open access
7 pages
rs9411377 rs6083037 rs10747514 rs7051718 rs16867574 rs57328376
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs139120857 rs5942972 rs7063103 rs62603531 rs151113194 rs762517
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Veterans Affairs Million Veteran Program†
Circulation · 2020 · PMID 32981348 · open access
6 pages
rs10808546 rs35254673 rs4401144 rs118039278 rs73149487 Abdominal Aortic Aneurysm
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
6 pages
rs1867073 rs7622417 rs2715879 rs7884019 rs56210063 rs78532451
A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program
VA Million Veteran Program
PLoS genetics · 2022 · PMID 35653334 · open access
5 pages
rs139405583 rs2197973 rs1840086 rs3812813 rs12143563
Genetic variants affect diurnal glucose levels throughout the day
FinnGen · Estonian Biobank Research Team and 1 more consortia
Nature communications · 2026 · PMID 42173832 · open access
4 pages
rs77464186 rs34942927 rs2282456 rs35323862
Genome-wide association study of peripheral artery disease in the Million Veteran Program
VA Million Veteran Program
Nature medicine · 2019 · PMID 31285632 · open access
3 pages
rs138294113 rs4722172 rs7476
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience
FinnGen · VA Million Veteran Program and 1 more consortia
Nature genetics · 2024 · PMID 39572784 · open access
3 pages
rs17226476 rs4731517 Dilated Cardiomyopathy
Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies
VA Million Veteran Program
American journal of human genetics · 2019 · PMID 31564439
1 page
rs17097556
Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci
Frontiers in genetics · 2021 · PMID 35186008 · open access
1 page
rs1531817
Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program
Veterans Affairs’ Million Veteran Program
PloS one · 2022 · PMID 35613103 · open access
1 page
rs244417

Showing 20 of 21 · 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.