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.

88 matches for Hao J, showing the first 20.

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution
Wellcome Trust Case Control Consortium · Procardis Consortia and 1 more consortia
PLoS genetics · 2009 · PMID 19557161 · open access
3 pages
rs987237 rs7826222 rs2605100
Genome-wide association study identifies five loci associated with lung function
Wellcome Trust Case Control Consortium · NSHD Respiratory Study Team
Nature genetics · 2010 · PMID 20010834
3 pages
rs12899618 rs10516526 rs12504628
Genetic variants influencing circulating lipid levels and risk of coronary artery disease
Wellcome Trust Case Control Consortium
Arteriosclerosis, thrombosis, and vascular biology · 2010 · PMID 20864672
3 pages
rs964184 rs2304130 rs10105606
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
MAGIC
Nature genetics · 2010 · PMID 20935629
3 pages
rs1055144 rs6784615 rs6861681
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
LifeLines Cohort Study · CARDIoGRAM Consortium and 3 more consortia
Nature genetics · 2013 · PMID 23263486
3 pages
rs4475146 rs1481012 Gout
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia
LifeLines Cohort Study
American journal of human genetics · 2014 · PMID 24954895
3 pages
rs12416687 rs16833934 rs4842666
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Nature communications · 2016 · PMID 26833246 · open access
3 pages
rs6738627 rs4788099 rs693839
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference
Proceedings of the National Academy of Sciences of the United States of America · 2016 · PMID 27911795
3 pages
rs12599112 rs11940694 Alcohol Consumption
Discovery of 42 genome-wide significant loci associated with dyslexia
23andMe Research Team · Quantitative Trait Working Group of the GenLang Consortium
Nature genetics · 2022 · PMID 36266505 · open access
3 pages
rs3735260 rs72916919 rs4696277
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
Proceedings of the National Academy of Sciences of the United States of America · 2011 · PMID 21471458
2 pages
rs6943555 Alcohol Consumption
Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA
Australian Asthma Genetics Consortium Collaborators
PloS one · 2012 · PMID 23028483 · open access
2 pages
rs13408661 rs9268516
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function
PLoS genetics · 2012 · PMID 23284291 · open access
2 pages
rs7764819 rs11654749
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
rs348495 rs10261878
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Consortium for Refractive Error and Myopia · Fuchs' Genetics Multi-Center Study Group and 2 more consortia
American journal of human genetics · 2013 · PMID 24144296
2 pages
rs9811920 rs12193446
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
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) and 2 more consortia
Molecular psychiatry · 2015 · PMID 25288136
2 pages
rs9902453 rs7800944
Genetic studies of body mass index yield new insights for obesity biology
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
2 pages
rs16851483 rs2121279
Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome
Scientific reports · 2015 · PMID 26190474 · open access
2 pages
rs2857281 Trichloroethylene-Induced Hypersensitivity Syndrome
Variants in MTNR1B influence fasting glucose levels
Nature genetics · 2009 · PMID 19060907
1 page
rs560887
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Wellcome Trust Case Control Consortium · Genetic Investigation of ANthropometric Traits Consortium
Nature genetics · 2009 · PMID 19079261
1 page
rs10838738

Showing 20 of 88 · page 4 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.