For researchers

Is your paper here?

2,657 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.

16 matches for Yang C.

A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses
Osteoarthritis and cartilage · 2023 · PMID 36889626
12 pages+
rs2681781 rs4858223 rs11753081 rs10846921 rs3731695 rs12200892
Using human genetics to understand the phenotypic association between chronotype and breast cancer
Journal of sleep research · 2024 · PMID 37380357
12 pages+
rs115356840 rs139909 rs695459 rs61863443 rs7907439 rs1242507
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+
rs77322067 rs78600547 rs12534190 rs150777747 rs4646605 rs958397
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+
rs2298840 rs55647329 rs73060324 rs11986259 rs16825455 rs7073937
Low overlap of plasma and CSF protein quantitative trait loci affects protein discovery for neurological disease
Science translational medicine · 2026 · PMID 42054495
12 pages+
rs2042782 rs1713566 rs9992989 rs351855 rs914187 rs144443274
Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft
PLoS genetics · 2019 · PMID 31609978 · open access
5 pages
rs6791526 rs730570 rs17820943 rs730643 rs4646211
Stroke genetics informs drug discovery and risk prediction across ancestries
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
rs12415501 rs60401382 rs72934589 rs76110445 Cardioembolic Stroke
Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function
Nature genetics · 2022 · PMID 35697868
4 pages
rs9856926 rs501740 rs55834511 rs78529941
Proteo-genomics of soluble TREM2 in cerebrospinal fluid provides novel insights and identifies novel modulators for Alzheimer's disease
Molecular neurodegeneration · 2024 · PMID 38172904 · open access
4 pages
rs142232675 rs12664332 rs73823326 rs11827324
GWAS meta-analysis of cerebrospinal fluid Alzheimer's biomarkers reveals loci regulating lipids, brain volume and autophagy
Nature communications · 2026 · PMID 42014397 · open access
4 pages
rs4843552 rs798560 rs35327527 rs7928895
Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus
Nature genetics · 2016 · PMID 27399966
3 pages
rs17321999 rs6762714 rs494003
Epidemiological and Genetic Analyses of Schizophrenia and Breast Cancer
Schizophrenia bulletin · 2024 · PMID 37467357
3 pages
rs2905432 rs2532363 rs7447717
Genome-wide association study identifies two new susceptibility loci for atopic dermatitis in the Chinese Han population
Nature genetics · 2011 · PMID 21666691
2 pages
rs3126085 Atopic Dermatitis
Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohorts
Communications biology · 2023 · PMID 37587153 · open access
2 pages
rs717894 rs57112407
Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus
Nature genetics · 2009 · PMID 19838193
1 page
rs1167796
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population
American journal of human genetics · 2011 · PMID 21640322
1 page
rs9318086

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.