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.

14 matches for Shi H.

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
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
GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcγ receptor region
Nature communications · 2024 · PMID 38296975 · open access
7 pages
rs7355798 rs2021408 rs844663 rs10912594 rs11851053 rs10892286
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
Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population
American journal of human genetics · 2012 · PMID 23000144
3 pages
rs6890853 rs4938534 Primary Biliary Cholangitis
Genetic determinants and an epistasis of <i>LILRA3</i> and HLA-B*52 in Takayasu arteritis
Proceedings of the National Academy of Sciences of the United States of America · 2018 · PMID 30498034
3 pages
rs1713450 rs4817988 Takayasu Arteritis
Genome-wide association analyses using machine learning-based phenotyping reveal genetic architecture of occupational creativity and overlap with psychiatric disorders
Psychiatry research · 2024 · PMID 38335777
3 pages
rs73079014 rs34427167 rs35800293
A genome-wide association study identified PTPN2 as a population-specific susceptibility gene locus for primary biliary cholangitis
Hepatology (Baltimore, Md.) · 2024 · PMID 38652555
3 pages
rs8098858 rs9268641 rs1889341
IgG4-related disease in the Japanese population: a whole-genome sequencing study
Japanese IgG4-Related Disease Working Consortium
The Lancet. Rheumatology · 2026 · PMID 41197642
3 pages
rs894063168 rs66917126 IgG4-Related Disease
A SNP in the ABCC11 gene is the determinant of human earwax type
Nature genetics · 2006 · PMID 16444273
1 page
rs17822931
Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C
Human molecular genetics · 2011 · PMID 21659334
1 page
rs6139030
Worldwide incidence and prevalence of inflammatory bowel disease in the 21st century: a systematic review of population-based studies
Lancet (London, England) · 2017 · PMID 29050646
1 page
Crohn's Disease
CCDC102B confers risk of low vision and blindness in high myopia
Nagahama Study group
Nature communications · 2018 · PMID 29725004 · open access
1 page
rs11873439
Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy
Communications biology · 2019 · PMID 31872073 · open access
1 page
rs6061548

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.