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.

34 matches for Kim H, showing the first 14.

Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia
Nature genetics · 2012 · PMID 23143601
2 pages
rs4488809 rs7086803
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
Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
Nature · 2010 · PMID 20596022
1 page
Alopecia Areata
Identification of new genetic risk variants for type 2 diabetes
PLoS genetics · 2010 · PMID 20862305 · open access
1 page
rs10906115
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
DIAGRAM Consortium · MuTHER Consortium
Nature genetics · 2011 · PMID 22158537
1 page
rs9470794
A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study
Breast cancer research : BCR · 2012 · PMID 22452962 · open access
1 page
rs13393577
Genome-wide association study of ulcerative colitis in Koreans suggests extensive overlapping of genetic susceptibility with Caucasians
Inflammatory bowel diseases · 2013 · PMID 23511034
1 page
rs16940202
Immunochip analysis identification of 6 additional susceptibility loci for Crohn's disease in Koreans
Inflammatory bowel diseases · 2015 · PMID 25489960
1 page
rs224143
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Human molecular genetics · 2016 · PMID 26732429
1 page
rs7741164
A coding variant in <i>FTO</i> confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBD
Gut · 2017 · PMID 27558924
1 page
rs79206939
Genomewide Association Study of Platelet Reactivity and Cardiovascular Response in Patients Treated With Clopidogrel: A Study by the International Clopidogrel Pharmacogenomics Consortium
ICPC Investigators
Clinical pharmacology and therapeutics · 2020 · PMID 32472697
1 page
rs28399513
Variants in NEB and RIF1 genes on chr2q23 are associated with skeletal muscle index in Koreans: genome-wide association study
Scientific reports · 2021 · PMID 33674626 · open access
1 page
rs138684936
A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages
Alzheimer’s Disease Neuroimaging Initiative
Translational psychiatry · 2021 · PMID 34785643 · open access
1 page
rs77359862
Cross-ancestry genome-wide association study identifies implications of SORL1 in cerebral beta-amyloid deposition
Nature communications · 2025 · PMID 40175353 · open access
1 page
rs76490923

Showing 14 of 34 · page 2 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.