For researchers

Is your paper here?

2,676 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.

69 matches for Zhang X, showing the first 20.

Identification of new susceptibility loci for IgA nephropathy in Han Chinese
Nature communications · 2015 · PMID 26028593 · open access
2 pages
rs2074038 IgA Nephropathy
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis
Nature communications · 2017 · PMID 28425483 · open access
2 pages
rs9501251 Primary Biliary Cholangitis
Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population
The Journal of investigative dermatology · 2018 · PMID 29857070
2 pages
rs11218708 Pemphigus Vulgaris
Exome-Wide Association Analysis Suggests LRP2BP as a Susceptibility Gene for Endothelial Injury in Systemic Sclerosis in the Han Chinese Population
The Journal of investigative dermatology · 2021 · PMID 33069728
2 pages
rs76285340 rs45471499
Genome-wide association analyses identified novel susceptibility loci for pulmonary embolism among Han Chinese population
China pUlmonary Thromboembolism REgistry Study (CURES) investigators
BMC medicine · 2023 · PMID 37076872 · open access
2 pages
rs35801946 rs4843804
A genome-wide association study of occupational creativity and its relations with well-being and career success
Communications biology · 2024 · PMID 39237691 · open access
2 pages
rs12130762 rs34034116
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · open access
2 pages
rs830463 rs62033408
Genome-wide association study identified novel loci and gene-environment interaction for refractive error in children
NPJ genomic medicine · 2025 · PMID 40410244 · open access
2 pages
rs17074027 rs6925312
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Alzheimer’s Disease Genetics Consortium (ADGC)
Genome biology · 2025 · PMID 40676597 · open access
2 pages
rs111486601 rs1898895
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
A genome-wide association study identifies two new risk loci for Graves' disease
China Consortium for Genetics of Autoimmune Thyroid Disease
Nature genetics · 2011 · PMID 21841780
1 page
rs12101261
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
Genome-wide significant association signals in IPO11-HTR1A region specific for alcohol and nicotine codependence
Alcoholism, clinical and experimental research · 2013 · PMID 23216389
1 page
rs7445832
A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population
Human molecular genetics · 2013 · PMID 23406873
1 page
rs4455882
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23
Nature genetics · 2013 · PMID 24097066
1 page
rs4282438
A genome wide association study identifies common variants associated with lipid levels in the Chinese population
PloS one · 2013 · PMID 24386095 · open access
1 page
rs2043085
A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population
BMC medical genomics · 2014 · PMID 24513273 · open access
1 page
rs4148152
Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations
China Consortium for Genetics of Autoimmune Thyroid Disease
Human molecular genetics · 2014 · PMID 24852370
1 page
rs2622590
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study
Molecular psychiatry · 2015 · PMID 25469926 · open access
1 page
rs1823125

Showing 20 of 69 · 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.