For researchers

Is your paper here?

2,683 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.

121 matches for Wang Y, showing the first 20.

Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
Nature genetics · 2014 · PMID 24880342 · open access
1 page
rs13314271
A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese
PloS one · 2014 · PMID 24940741 · open access
1 page
rs9366816
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
Scientific reports · 2016 · PMID 26785701 · open access
1 page
rs10051787
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Nature genetics · 2016 · PMID 27064256
1 page
rs3739821
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders
Nature genetics · 2017 · PMID 27918536
1 page
rs6481128
Genetic Polymorphisms of CFH and ARMS2 Do Not Predict Response to Antioxidants and Zinc in Patients with Age-Related Macular Degeneration: Independent Statistical Evaluations of Data from the Age-Related Eye Disease Study
Ophthalmology · 2018 · PMID 29032853
1 page
AREDS2 Eye Formula
CETP (Cholesteryl Ester Transfer Protein) Concentration: A Genome-Wide Association Study Followed by Mendelian Randomization on Coronary Artery Disease
Circulation. Genomic and precision medicine · 2018 · PMID 29728394
1 page
rs117427818
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · open access
1 page
rs492571
Meta-analysis of genome-wide association studies and functional assays decipher susceptibility genes for gastric cancer in Chinese populations
Gut · 2020 · PMID 31383772
1 page
rs10029005
Genome-Wide Association Study of Brain Alzheimer's Disease-Related Metabolic Decline as Measured by [18F] FDG-PET Imaging
Alzheimer’s Disease Neuroimaging Initiative
Journal of Alzheimer's disease : JAD · 2020 · PMID 32804141
1 page
rs13387360
Genetic risk, incident gastric cancer, and healthy lifestyle: a meta-analysis of genome-wide association studies and prospective cohort study
The Lancet. Oncology · 2020 · PMID 33002439
1 page
rs10074991
Interaction between <i>G</i><i>ALNT12</i> and <i>C1GALT1</i> Associates with Galactose-Deficient IgA1 and IgA Nephropathy
Journal of the American Society of Nephrology : JASN · 2021 · PMID 33593824
1 page
rs10238682
Genome-wide association study reveals susceptibility loci for self-reported headache in a large community-based Asian population
Cephalalgia : an international journal of headache · 2022 · PMID 34404248
1 page
rs10493859
Identification of Shared and Asian-Specific Loci for Systemic Lupus Erythematosus and Evidence for Roles of Type III Interferon Signaling and Lysosomal Function in the Disease: A Multi-Ancestral Genome-Wide Association Study
Arthritis & rheumatology (Hoboken, N.J.) · 2022 · PMID 34783190
1 page
rs76596471
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information
Biological psychiatry · 2022 · PMID 34865855 · open access
1 page
rs10821140
COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection
PLoS genetics · 2022 · PMID 36327221 · open access
1 page
rs4792891
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population
Parkinson’s Disease & Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC)
NPJ Parkinson's disease · 2023 · PMID 36759515 · open access
1 page
rs34594498
Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry
European urology · 2023 · PMID 36872133
1 page
rs150947563
Genome-wide association study on coordination and agility in 461 Chinese Han males
Heliyon · 2023 · PMID 37654465 · open access
1 page
rs77038481
Genome-wide discovery and integrative genomic characterization of insulin resistance loci using serum triglycerides to HDL-cholesterol ratio as a proxy
Nature communications · 2024 · PMID 39277575 · open access
1 page
rs61905108

Showing 20 of 121 · page 6 of 7

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.