For researchers

Is your paper here?

2,665 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.

41 matches for Wang M, showing the first 20.

Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
Human molecular genetics · 2017 · PMID 28334899
12 pages+
rs2188380 rs2144300 rs11984636 rs3786247 rs11208004 rs2244608
Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia
Nature genetics · 2017 · PMID 28991256
12 pages+
rs61041384 rs6846161 rs10510653 rs2383377 rs13164092 rs867743
Interethnic analyses of blood pressure loci in populations of East Asian and European descent
International Genomics of Blood Pressure (iGEN-BP) Consortium
Nature communications · 2018 · PMID 30487518 · open access
12 pages+
rs58244401 rs6590816 rs6712094 rs2270860 rs1004467 rs4684242
The genetic architecture of the human cerebral cortex
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
rs2358483 rs149142 rs78155705 rs62005276 rs639016 rs34322452
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs28599782 rs111246699 rs11205766 rs3735567 rs12403994 rs60054445
Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus
Japanese Research Committee on Idiopathic Osteonecrosis of the Femoral Head
Annals of the rheumatic diseases · 2021 · PMID 33272962 · open access
12 pages+
rs116785379 rs12120358 rs76107698 rs2039982 rs4143303 rs218174
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs118164457 rs7063597 rs3752435 rs4317621 rs4731113 rs4674280
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+
rs111859808 rs17209803 rs74705598 rs10082867 rs12358424 rs78186330
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs4267865 rs57634870 rs11196296 rs3825801 rs79495865 rs1871045
Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots
Nature communications · 2022 · PMID 35773277 · open access
12 pages+
rs11199845 rs13410987 rs4872393 rs72810972 rs11057402 rs6903044
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+
rs12787013 rs17036665 rs17040476 rs174348 rs17617811 rs17712993
The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians
Nature communications · 2022 · PMID 36333282 · open access
12 pages+
rs2926700 rs11216916 rs3858910 rs4992759 rs520688 rs117887821
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Biobank Japan · EPIC-CVD and 1 more consortia
Nature genetics · 2022 · PMID 36474045 · open access
12 pages+
rs28867400 rs77787671 rs10928241 rs2067831 rs11752218 rs17086617
Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes
CHIMGEN Consortium
Nature genetics · 2023 · PMID 37337106
12 pages+
rs10850725 rs74712405 rs10479662 rs6478240 rs7636254 rs13084097
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs290490 rs3742636 rs74387263 rs10758321 rs11023938 rs116257126
Large-scale cross-ancestry genome-wide meta-analysis of serum urate
Nature communications · 2024 · PMID 38658550 · open access
12 pages+
rs12364994 rs2236270 rs76227013 rs36163299 rs2770807 rs62585352
Cross-ancestry genome-wide association studies of brain imaging phenotypes
CHIMGEN Consortium
Nature genetics · 2024 · PMID 38811844
12 pages+
rs1163297 rs12030374 rs919445 rs3744349 rs60865161 rs7935166
Cross-ancestry and sex-stratified genome-wide association analyses of amygdala and subnucleus volumes
CHIMGEN Consortium
Nature genetics · 2025 · PMID 40097784
12 pages+
rs12565378 rs35166705 rs56390130 rs62329462 rs12679702 rs150434736
Trans-ancestry GWAS identifies 59 loci and improves risk prediction and fine-mapping for kidney stone disease
Nature communications · 2025 · PMID 40216741 · open access
12 pages+
rs42085 rs2459380 rs9516602 rs77759957 rs113831804 rs10051765
Genome-wide association studies reveal new insights into the genetic basis of IgG4-related disease in the Chinese Han population
Annals of the rheumatic diseases · 2026 · PMID 41298177
10 pages
rs28371251 rs116353692 rs9348878 rs2233964 rs57235233 rs4717156

Showing 20 of 41 · 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.