For researchers

Is your paper here?

2,663 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.

56 matches for Hu Z, showing the first 16.

Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer
PLoS genetics · 2012 · PMID 22383897 · open access
1 page
rs9485372
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
New loci associated with chronic hepatitis B virus infection in Han Chinese
Nature genetics · 2013 · PMID 24162738
1 page
rs3130542
A genome-wide association study identifies susceptibility loci of silica-related pneumoconiosis in Han Chinese
Human molecular genetics · 2014 · PMID 24986923
1 page
rs73329476
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Human molecular genetics · 2016 · PMID 26732429
1 page
rs7741164
Genome-wide association study identifies 8p21.3 associated with persistent hepatitis B virus infection among Chinese
Nature communications · 2016 · PMID 27244555 · open access
1 page
rs7000921
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
Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility
International journal of cancer · 2019 · PMID 30714141
1 page
rs10842893
Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis
Hepatology (Baltimore, Md.) · 2019 · PMID 30854688 · open access
1 page
rs1794280
Identification of Novel T1D Risk Loci and Their Association With Age and Islet Function at Diagnosis in Autoantibody-Positive T1D Individuals: Based on a Two-Stage Genome-Wide Association Study
Diabetes care · 2019 · PMID 31152121
1 page
rs4320356
Meta-analysis of genome-wide association studies and functional assays decipher susceptibility genes for gastric cancer in Chinese populations
Gut · 2020 · PMID 31383772
1 page
rs10029005
Genetic risk, incident gastric cancer, and healthy lifestyle: a meta-analysis of genome-wide association studies and prospective cohort study
The Lancet. Oncology · 2020 · PMID 33002439
1 page
rs10074991
Unique motif shared by HLA-B*59:01 and HLA-B*55:02 is associated with methazolamide-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Han Chinese
Journal of the European Academy of Dermatology and Venereology : JEADV · 2022 · PMID 35122707
1 page
rs2074494
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population
Parkinson’s Disease & Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC)
NPJ Parkinson's disease · 2023 · PMID 36759515 · open access
1 page
rs34594498
Genome-wide discovery and integrative genomic characterization of insulin resistance loci using serum triglycerides to HDL-cholesterol ratio as a proxy
Nature communications · 2024 · PMID 39277575 · open access
1 page
rs61905108

Showing 16 of 56 · page 3 of 3

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.