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.

67 matches for Wang X, showing the first 20.

Joint study of two genome-wide association meta-analyses identified 20p12.1 and 20q13.33 for bone mineral density
Bone · 2018 · PMID 29499414
10 pages
rs13194508 rs9479075 rs3779381 rs1286063 rs11631380 rs12719801
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 pages
rs6813195 rs17106184 rs849135 rs2261181 rs9936385 rs4458523
Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages
Alzheimer's Disease Neuroimaging Initiative
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2018 · PMID 29274321
8 pages
rs55644114 rs74442473 rs2378873 rs10775009 rs2819438 rs118130881
Novel genetic insight for psoriasis: integrative genome-wide analyses in 863 080 individuals and proteome-wide Mendelian randomization
Briefings in bioinformatics · 2024 · PMID 39883516 · open access
8 pages
rs9468487 rs1306395 rs34693947 rs6067293 rs6457109 rs74817271
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
Nature communications · 2016 · PMID 26818947 · open access
6 pages
rs78627331 rs1116357 rs1575972 rs9309245 rs67156297 rs7107784
Genome-wide association study of subclinical interstitial lung disease in MESA
Respiratory research · 2017 · PMID 28521775 · open access
6 pages
rs79441543 rs145855729 rs114571830 rs74361312 rs7852363 rs190432524
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs6015450 rs11191548 rs7129220 rs1173771 rs13139571
Detailed stratified GWAS analysis for severe COVID-19 in four European populations
COVICAT study group, Aachen Study (COVAS) · Norwegian SARS-CoV-2 Study group and 2 more consortia
Human molecular genetics · 2022 · PMID 35848942 · open access
5 pages
rs2269899 rs77534576 rs143334143 rs35731912 COVID-19 with Respiratory Failure Requiring Mechanical Ventilation
Genomewide association study of leprosy
The New England journal of medicine · 2009 · PMID 20018961
4 pages
rs602875 rs40457 rs42490 Leprosy
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Nature genetics · 2014 · PMID 24929828
4 pages
rs1430193 rs6923462 rs2863171 rs6501431
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
rs10088218 rs8170 rs9303542
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs
Scientific reports · 2016 · PMID 26780889 · open access
3 pages
rs138534124 rs2238675 rs8102280
A large-scale genome-wide association and meta-analysis identified four novel susceptibility loci for leprosy
Nature communications · 2016 · PMID 27976721 · open access
3 pages
rs10100465 rs6807915 Leprosy
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience
FinnGen · VA Million Veteran Program and 1 more consortia
Nature genetics · 2024 · PMID 39572784 · open access
3 pages
rs4731517 rs17226476 Dilated Cardiomyopathy
Large-scale meta- and cross-trait analyses uncover shared genetic risk factors for IBS and psychiatric disorders
Frontiers in psychiatry · 2026 · PMID 42221328 · open access
3 pages
rs7106434 rs20551 Irritable Bowel Syndrome
Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis
PLoS genetics · 2010 · PMID 20072603 · open access
2 pages
rs13182402 Osteoporosis
Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC
Nature genetics · 2010 · PMID 20526339
2 pages
rs2236313 Vitiligo
A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis
Nature genetics · 2011 · PMID 22138694
2 pages
rs17095830 Ankylosing Spondylitis
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations
Nature genetics · 2011 · PMID 22158540
2 pages
rs372883 Pancreatic Cancer
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

Showing 20 of 67 · page 2 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.