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.

81 matches for Zhang Y, showing the first 20.

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
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
Meta-analysis identifies common variants associated with body mass index in east Asians
Genetic Investigation of ANthropometric Traits (GIANT) Consortium
Nature genetics · 2012 · PMID 22344219 · open access
2 pages
rs9356744 rs261967
Genetic determinants of haemolysis in sickle cell anaemia
Walk-PHAAST Investigators
British journal of haematology · 2013 · PMID 23406172
2 pages
rs7948471 Haemolysis Severity in Sickle Cell Anaemia
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12
Nature genetics · 2013 · PMID 23817570
2 pages
rs13117307 Cervical Cancer
Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne
Nature communications · 2014 · PMID 24399259
2 pages
rs7531806 Severe Acne
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study
The Lancet. Respiratory medicine · 2013 · PMID 24429156
2 pages
rs17690703 Idiopathic Pulmonary Fibrosis
Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk
Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO) · Colorectal Transdisciplinary (CORECT) Study and 1 more consortia
Nature genetics · 2014 · PMID 24836286 · open access
2 pages
rs704017 rs1800469
Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B
Hepatology (Baltimore, Md.) · 2015 · PMID 25802187
2 pages
rs2856718 rs2853953
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
rs9687065 rs1563788
Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia
Nature communications · 2016 · PMID 26956414 · open access
2 pages
rs9270750 rs72742684
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
Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis
American journal of respiratory and critical care medicine · 2020 · PMID 31710517 · open access
2 pages
rs59424629 rs41308092
A genome-wide association study of polycystic ovary syndrome identified from electronic health records
American journal of obstetrics and gynecology · 2020 · PMID 32289280
2 pages
rs17186366 rs113168128
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Lifelines Cohort Study · Regeneron Genetics Center
Kidney international · 2021 · PMID 33137338
2 pages
rs56012466 rs141809766
A genetic variant in IL-6 lowering its expression is protective for critical patients with COVID-19
Signal transduction and targeted therapy · 2022 · PMID 35368020 · open access
2 pages
rs7598285 rs7422259
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
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

Showing 20 of 81 · page 3 of 5

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.