For researchers

Is your paper here?

2,677 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.

70 matches for Wang C, showing the first 20.

Cross-ancestry genome-wide association studies of brain imaging phenotypes
CHIMGEN Consortium
Nature genetics · 2024 · PMID 38811844
12 pages+
rs1163297 rs12030374 rs919445 rs3744349 rs60865161 rs7302114
Proteogenomic analysis of human cerebrospinal fluid identifies neurologically relevant regulation and implicates causal proteins for Alzheimer's disease
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528825
12 pages+
rs188243493 rs192695415 rs62207047 rs72856699 rs9791 rs11778107
Genetic architecture of cerebrospinal fluid and brain metabolite levels and the genetic colocalization of metabolites with human traits
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528826
12 pages+
rs10820726 rs1847530 rs150303712 rs9554707 rs1015998 rs71352704
Cross-ancestry and sex-stratified genome-wide association analyses of amygdala and subnucleus volumes
CHIMGEN Consortium
Nature genetics · 2025 · PMID 40097784
12 pages+
rs56390130 rs62329462 rs12679702 rs11133310 rs150434736 rs201081507
Low overlap of plasma and CSF protein quantitative trait loci affects protein discovery for neurological disease
Science translational medicine · 2026 · PMID 42054495
12 pages+
rs75787047 rs797027774 rs570212 rs7223939 rs885303 rs149412438
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Australian Asthma Genetics Consortium (AAGC)
Nature genetics · 2015 · PMID 26482879 · open access
11 pages
rs112111458 rs10214237 rs6473227 rs6602364 rs7127307 rs2143950
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
Communications biology · 2023 · PMID 37402774 · open access
11 pages
rs12132335 rs11029963 rs11993347 rs12107945 rs113622822 rs34814687
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
Early Growth Genetics (EGG) Consortium
Nature genetics · 2023 · PMID 37798380 · open access
10 pages
rs6040436 rs10486660 rs7783810 rs12529634 rs140691414 rs1434836
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 meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes
Nature genetics · 2025 · PMID 40962958
9 pages
rs7708883 rs4462678 rs9959583 rs4131786 rs1435746 rs7100410
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Nature communications · 2024 · PMID 38233393 · open access
8 pages
rs12382607 rs4328011 rs139036121 rs5933079 rs181497961 rs111410539
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma
Frontiers of medicine · 2021 · PMID 32889700
6 pages
rs465498 rs1200399 rs2517873 rs4573350 rs1264308 rs17038564
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4
Australian Asthma Genetics Consortium (AAGC)
Nature communications · 2021 · PMID 34785669 · open access
6 pages
rs2844594 rs3848669 rs13208697 rs4372325 rs12334935 rs2918299
Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy
Nature genetics · 2015 · PMID 25642632
5 pages
rs13220141 rs10817758 rs58600253 rs10414149 Leprosy
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero
23andMe Research Team
Human molecular genetics · 2018 · PMID 29659830 · open access
5 pages
rs4927012 rs12474669 rs847158 rs10790969 rs1080014
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity
Early Growth Genetics Consortium
Human molecular genetics · 2019 · PMID 31504550
5 pages
rs6567160 rs4077678 rs10493544 rs114670539 rs74583214
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
Nature communications · 2023 · PMID 37236969 · open access
5 pages
rs75031349 rs137884934 rs682888 rs10901793 rs71467682
Trans-ancestry meta-analysis of genome-wide association study identifies eight novel genetic loci in type 1 diabetes: A multi-population study
Diabetic medicine : a journal of the British Diabetic Association · 2026 · PMID 42594184
5 pages
rs9934969 rs2395639 rs28464459 rs117520198 rs9981704
Genomewide association study of leprosy
The New England journal of medicine · 2009 · PMID 20018961
4 pages
rs602875 rs40457 rs42490 Leprosy

Showing 20 of 70 · 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.