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.

56 matches for Hu Z, showing the first 20.

Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci
Human molecular genetics · 2015 · PMID 25429064
12 pages+
rs7184046 rs3755206 rs3771381 rs1865760 rs11970475 rs10448080
Genome-wide association study identifies 74 loci associated with educational attainment
LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
12 pages+
rs56044892 rs12410444 rs12754946 rs1008078 rs17372140 rs78365243
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
SpiroMeta Consortium
Nature genetics · 2017 · PMID 28604730 · open access
12 pages+
rs116826541 rs139244745 rs115870917 rs147680653 rs116480994 rs116418332
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes
eQTLGen Consortium
Nature communications · 2018 · PMID 30054458 · open access
12 pages+
rs12088739 rs2493394 rs17334919 rs12617659 rs7561798 rs2292662
Shared genetics of asthma and mental health disorders: a large-scale genome-wide cross-trait analysis
The European respiratory journal · 2019 · PMID 31619474
12 pages+
rs827637 rs801429 rs12722502 rs72782676 rs146597587 rs34986765
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration
Nature communications · 2020 · PMID 32242144 · open access
12 pages+
rs12794714 rs8121940 rs10832254 rs12278461 rs59536295 rs7784802
High Blood Pressure and Intraocular Pressure: A Mendelian Randomization Study
Investigative ophthalmology & visual science · 2022 · PMID 35762941 · open access
12 pages+
rs62051558 rs72740613 rs78058068 rs80222951 rs9974014 rs11832510
The correlates of neonatal complement component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders
Cell genomics · 2023 · PMID 38116117 · open access
12 pages+
rs7769158 rs3130321 rs9469058 rs2535300 rs11751198 rs61229539
Genetic landscape and functional exploration of kidney cancer predisposition in cross-ancestral populations
Nature communications · 2026 · PMID 42000752 · open access
12 pages+
rs932826 rs33925946 rs28607501 rs1007934 rs73073561 rs139729777
Genome-wide association analyses of gestational phenotypes identify context-specific genetic effects
Nature genetics · 2026 · PMID 42509370
12 pages+
rs2251056 rs77833165 rs7783398 rs79328581 rs6127091 rs147740307
A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic aetiology with obesity
The European respiratory journal · 2021 · PMID 33766948
11 pages
rs16828537 rs73995038 rs801170 rs6696174 rs1482675 rs78732306
Genome-wide association analysis of left ventricular imaging-derived phenotypes identifies 72 risk loci and yields genetic insights into hypertrophic cardiomyopathy
Nature communications · 2023 · PMID 38036550 · open access
8 pages
rs62250980 rs7928419 rs9462210 rs117742247 rs35630683 rs79548216
Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations
Nature genetics · 2011 · PMID 21642993
6 pages
rs10058728 rs8030672 rs2274223 rs11066015 rs10052657 Oesophageal Cancer
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations
Ovarian Cancer Association Consortium (OCAC) · PRACTICAL Consortium and 3 more consortia
Cancer research · 2016 · PMID 27197191
6 pages
rs11844632 rs4808075 rs56084662 rs11571833 rs186507655 rs148883465
Shared genetic and experimental links between obesity-related traits and asthma subtypes in UK Biobank
The Journal of allergy and clinical immunology · 2020 · PMID 31669095
6 pages
rs12493005 rs73086541 rs73084574 rs1787663 rs9275570 rs8089834
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
Genome-wide meta-analysis across East Asian and European populations provides insights into the molecular basis of lung cancer
Genome medicine · 2026 · PMID 42152146 · open access
6 pages
rs4887067 rs13167280 rs4291686 rs36108040 rs1039766 rs12822733
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
Genomewide association study of leprosy
The New England journal of medicine · 2009 · PMID 20018961
4 pages
rs602875 rs40457 rs42490 Leprosy
Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions
Nature genetics · 2012 · PMID 22960999
3 pages
rs4785204 rs4822983 Oesophageal Cancer

Showing 20 of 56 · page 1 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.