For researchers

Is your paper here?

2,675 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.

9 matches for Kang S.

Genomic Variations in Susceptibility to Intracranial Aneurysm in the Korean Population
Journal of clinical medicine · 2019 · PMID 30823506 · open access
12 pages+
rs17688188 rs72835045 rs76855873 rs74115822 rs3737926 rs11646803
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 rs672769 rs10071837 rs4899520 rs75823898 rs112226333
Regulatory Variants on the Leukocyte Immunoglobulin-Like Receptor Gene Cluster are Associated with Crohn's Disease and Interact with Regulatory Variants for TAP2
Journal of Crohn's & colitis · 2024 · PMID 37523193
5 pages
rs224135 rs12033764 rs56211063 rs10786560 rs73243351
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis
International PSC Study Group
Nature communications · 2023 · PMID 36828809 · open access
3 pages
rs2523593 rs3094210 rs6905775
Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease
Molecular psychiatry · 2023 · PMID 37198259 · open access
3 pages
rs74825460 rs117807585 rs9394766
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
Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6
Genes, brain, and behavior · 2012 · PMID 22554406
1 page
rs2835872
A genome wide association study of fast beta EEG in families of European ancestry
International journal of psychophysiology : official journal of the International Organization of Psychophysiology · 2017 · PMID 28040410
1 page
rs2252790
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

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.