For researchers

Is your paper here?

2,660 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.

36 matches for Hao Y, 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 rs13072744 rs3755206 rs3771381 rs1865760 rs11970475
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use
CHD Exome+ Consortium · Consortium for Genetics of Smoking Behaviour
Biological psychiatry · 2019 · PMID 30679032
12 pages+
rs1727284 rs442467 rs11135030 rs11210887 rs12053870 rs1264322
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
American journal of human genetics · 2021 · PMID 33713608
12 pages+
rs10180829 rs10071837 rs4899520 rs75823898 rs112226333 rs2553033
Using human genetics to understand the phenotypic association between chronotype and breast cancer
Journal of sleep research · 2024 · PMID 37380357
12 pages+
rs9475034 rs2075881 rs72807264 rs115356840 rs139909 rs695459
Genetic landscape and functional exploration of kidney cancer predisposition in cross-ancestral populations
Nature communications · 2026 · PMID 42000752 · open access
12 pages+
rs73113855 rs10015491 rs932826 rs33925946 rs28607501 rs1007934
Development and validation of a multiancestry and multitrait polygenic risk score for lung cancer
Nature communications · 2026 · PMID 42364979 · open access
12 pages+
rs1138373 rs705698 rs7638643 rs750608 rs74231870 rs951984
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium
Bone Mineral Density in Childhood Study (BMDCS) Group
PLoS genetics · 2017 · PMID 28430825 · open access
11 pages
rs62105306 rs17057164 rs149352150 rs56330886 rs112778462 rs378854
Genetic correlation, shared loci, but no causality between bipolar disorder and inflammatory bowel disease: A genome-wide pleiotropic analysis
Journal of affective disorders · 2024 · PMID 38154582
10 pages
rs7612624 rs401763 rs28653100 rs380571 rs3732385 rs2844697
New insights into the genetic etiology of Alzheimer's disease and related dementias
EADB · GR@ACE and 7 more consortia
Nature genetics · 2022 · PMID 35379992 · open access
9 pages
rs3848143 rs62374257 rs3851179 rs6605556 rs7767350 rs6586028
Unprocessed Red Meat and Processed Meat Consumption, Plasma Metabolome, and Risk of Ischemic Heart Disease: A Prospective Cohort Study of UK Biobank
Journal of the American Heart Association · 2023 · PMID 36974753 · open access
9 pages
rs3094621 rs3106165 rs6760497 rs71401819 rs55888687 rs178803
Investigating the shared genetic architecture of uterine leiomyoma and breast cancer: A genome-wide cross-trait analysis
American journal of human genetics · 2022 · PMID 35803233
8 pages
rs12555322 rs56083805 rs851981 rs851982 rs9611271 rs12217370
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
rs6692219 rs11971186 rs1937455 rs6738833 rs13026471 rs6883351
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension
Human molecular genetics · 2015 · PMID 25249183
5 pages
rs9810888 rs2021783 rs1902859 rs13143871 rs4409766
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
Nature genetics · 2011 · PMID 21151128
4 pages
rs13429458 rs10818854 rs12478601 Polycystic Ovary Syndrome
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome
Nature genetics · 2012 · PMID 22885925
4 pages
rs3802457 rs1894116 rs2272046 rs6022786
Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations
Circulation. Cardiovascular genetics · 2016 · PMID 26582766
4 pages
rs1260333 rs2575876 rs7525649 rs9357121
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese
PLoS genetics · 2013 · PMID 23341777 · open access
2 pages
rs12296850 Lung Squamous Cell Carcinoma
Genome-wide association study in Han Chinese identifies three novel loci for human height
Human genetics · 2013 · PMID 23456168
2 pages
rs3816804 rs3751599
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans
Arthritis & rheumatology (Hoboken, N.J.) · 2014 · PMID 24782177
2 pages
rs12525220 rs1854853
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

Showing 20 of 36 · page 1 of 2

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.