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.

33 matches for Wen W, showing the first 20.

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
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+
rs114846969 rs6029549 rs556107 rs117753190 rs6489786 rs217358
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+
rs1080066 rs73313052 rs9375477 rs117461235 rs68175985 rs71471500
Cerebral small vessel disease genomics and its implications across the lifespan
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 pages+
rs17205972 rs7596872 rs55940034 rs2303655 rs55897749 rs72934583
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
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
Blood metabolic biomarkers and colorectal cancer risk: results from large prospective cohort and Mendelian randomisation analyses
British journal of cancer · 2025 · PMID 40307439 · open access
12 pages+
rs9370162 rs17052058 rs12692735 rs144972973 rs9457827 rs62222988
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
9 pages
rs2410767 rs10439607 rs10217651 rs35200015 rs3133370 rs2206656
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
InterAct Consortium · Lifelines Cohort, Groningen, The Netherlands (Lifelines Cohort Study)
American journal of epidemiology · 2019 · PMID 30698716
8 pages
rs79624003 rs55809639 rs4847240 rs4660303 rs7298909 rs56204645
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
CHARGE Neurology Working Group · COGENT-Kidney Consortium and 2 more consortia
American journal of human genetics · 2018 · PMID 29455858
7 pages
rs115234772 rs62319742 rs148772934 rs138973557 rs148753653 rs12135881
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation
International HIV Controllers Study
Science (New York, N.Y.) · 2010 · PMID 21051598
6 pages
rs4418214 rs2523590 rs2255221 rs2395029 rs9262632 HIV-1 Viral Control
Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer
Gastroenterology · 2019 · PMID 30529582
6 pages
rs7542665 rs201395236 rs113569514 rs3830041 rs77969132 rs1886450
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index
Human molecular genetics · 2014 · PMID 24861553
4 pages
rs2535633 rs11030104 rs574367 rs591166
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
Lifelines Cohort Study
Molecular psychiatry · 2021 · PMID 32372009 · open access
4 pages
rs9308788 rs141962517 rs75535814 rs113809930
Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1
DRIVE GAME-ON Consortium
Nature genetics · 2014 · PMID 25038754 · open access
3 pages
rs4951011 rs10474352 rs2290203
Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk
Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO) · Colorectal Transdisciplinary (CORECT) Study and 1 more consortia
Gastroenterology · 2016 · PMID 26965516
3 pages
rs2450115 rs4919687 rs6061231
Genome-wide association study in East Asians identifies two novel breast cancer susceptibility loci
Human molecular genetics · 2016 · PMID 27354352
3 pages
rs2981582 rs12118297 rs16992204
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
CHARGE consortium
Nature medicine · 2023 · PMID 37069360 · open access
3 pages
rs6011998 rs112407396 rs72485816
Meta-analysis identifies common variants associated with body mass index in east Asians
Genetic Investigation of ANthropometric Traits (GIANT) Consortium
Nature genetics · 2012 · PMID 22344219 · open access
2 pages
rs9356744 rs261967
Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations
GIANT consortium
Nature genetics · 2012 · PMID 22344221
2 pages
rs12149832 rs11671664

Showing 20 of 33 · 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.