For researchers

Is your paper here?

2,673 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.

68 matches for Wang X, showing the first 20.

Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese
American journal of human genetics · 2012 · PMID 23103227
2 pages
rs2494938 rs2285947
Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries
Caries research · 2014 · PMID 24556642
2 pages
rs17236529 Dental Caries
Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract
Human molecular genetics · 2014 · PMID 24951543
2 pages
rs11911275 Age-Related Nuclear Cataracts
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
rs9687065 rs1563788
HLA-B*57:01 Confers Susceptibility to Pazopanib-Associated Liver Injury in Patients with Cancer
Clinical cancer research : an official journal of the American Association for Cancer Research · 2016 · PMID 26546620
2 pages
rs1800625 Pazopanib-Associated Liver Injury
Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth
Nature communications · 2017 · PMID 28598419 · open access
2 pages
rs8029754 rs11161721
An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels
Circulation · 2018 · PMID 29593015
2 pages
rs17573010 Cholesterol (LDL, HDL and Total)
Identification of new susceptibility loci associated with rheumatoid arthritis
Annals of the rheumatic diseases · 2020 · PMID 32868391
2 pages
rs770667 rs2201584
Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes
Nature communications · 2023 · PMID 37696869 · open access
2 pages
rs4769312 rs6121609
GWAS meta-analysis identifies five susceptibility loci for endometrial cancer
Estonian Biobank Research Team
EBioMedicine · 2025 · PMID 40633141 · open access
2 pages
rs148261157 rs7579014
Body Mass Index, Clinical Outcomes, and Mortality in Heart Failure: A Mendelian Randomization Study
Journal of the American College of Cardiology · 2026 · PMID 42017882 · open access
2 pages
rs62576378 Heart Failure Progression
A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese
Nature genetics · 2011 · PMID 21725308
1 page
rs753955
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
Gene Environment Interaction and Breast Cancer in Germany (GENICA) Consortium
Nature genetics · 2011 · PMID 22037553
1 page
rs10069690
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11
Australian Breast Cancer Tissue Bank Investigators · Familial Breast Cancer Study and 1 more consortia
Human molecular genetics · 2012 · PMID 22976474
1 page
rs9383938
Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4
Nature genetics · 2012 · PMID 23023329
1 page
rs103294
A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations
Nature genetics · 2013 · PMID 23708190
1 page
rs1531070
Association of 3q13.32 variants with hip trochanter and intertrochanter bone mineral density identified by a genome-wide association study
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2016 · PMID 27311723
1 page
rs7839059
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity
Nature communications · 2017 · PMID 28232668 · open access
1 page
rs12229892
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
1 page
rs139967528
Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy
Nature communications · 2017 · PMID 29051540 · open access
1 page
rs12964116

Showing 20 of 68 · page 3 of 4

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.