For researchers

Is your paper here?

2,671 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.

90 matches for Zheng W, showing the first 20.

Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Breast and Ovarian Cancer Susceptibility Collaboration · Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON) and 3 more consortia
Nature genetics · 2013 · PMID 23535729
12 pages+
rs16857609 rs6762644 rs9790517 rs6828523 rs204247 rs720475
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci
Human molecular genetics · 2015 · PMID 25429064
12 pages+
rs6823268 rs7153027 rs2271266 rs6728302 rs2401171 rs7250071
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
BOCS · kConFab Investigators and 3 more consortia
Nature genetics · 2015 · PMID 25751625 · open access
12 pages+
rs2012709 rs12048493 rs72755295 rs4593472 rs13267382 rs745570
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
PRACTICAL consortium · kConFab Investigators and 4 more consortia
Nature genetics · 2015 · PMID 26414677 · open access
12 pages+
rs12142240 rs2236918 rs704795 rs930036 rs6856693 rs11738223
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
Association analysis identifies 65 new breast cancer risk loci
NBCS Collaborators · ABCTB Investigators and 1 more consortia
Nature · 2017 · PMID 29059683 · open access
12 pages+
rs6904031 rs56387622 rs11624333 rs1895062 rs13294895 rs2223621
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
InterAct Consortium
PloS one · 2018 · PMID 29912962 · open access
12 pages+
rs4886640 rs7125196 rs259983 rs11725969 rs1894400 rs34063670
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+
rs11044991 rs8084192 rs3774427 rs751985 rs6590811 rs62501779
Discovery of common and rare genetic risk variants for colorectal cancer
Nature genetics · 2019 · PMID 30510241 · open access
12 pages+
rs12144319 rs116353863 rs117079142 rs11884596 rs12708491 rs4901473
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Lifelines Cohort Study
Nature communications · 2019 · PMID 30670697 · open access
12 pages+
rs72834327 rs116376114 rs114846969 rs6029549 rs556107 rs117753190
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs186568031 rs117267808 rs4711389 rs75536691 rs7787720 rs1955163
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
Nature genetics · 2021 · PMID 33398198 · open access
12 pages+
rs2028900 rs339351 rs9306894 rs28441558 rs76765083 rs4714485
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+
rs58680090 rs12332985 rs146576224 rs10180829 rs672769 rs10071837
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+
rs7063597 rs3752435 rs4317621 rs4731113 rs4674280 rs138245006
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
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+
rs7819706 rs1473781 rs6876198 rs3743140 rs3806155 rs7313668
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+
rs3967200 rs7156625 rs12463674 rs12136856 rs4282339 rs823114
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Nature genetics · 2023 · PMID 36539618
12 pages+
rs117042741 rs35564340 rs1919364 rs11108175 rs78341008 rs9983528
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+
rs78416326 rs17804499 rs72725734 rs11228580 rs7336001 rs77541621
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs11466334 rs12555274 rs13094957 rs76675804 rs2056857 rs72802365

Showing 20 of 90 · page 1 of 5

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.