For researchers

Is your paper here?

2,671 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.

32 matches for Park S, showing the first 20.

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
BOCS · kConFab Investigators and 3 more consortia
Nature genetics · 2015 · PMID 25751625 · open access
12 pages+
rs2012709 rs12048493 rs72755295 rs4593472 rs13267382 rs745570
Association analysis identifies 65 new breast cancer risk loci
NBCS Collaborators · ABCTB Investigators and 1 more consortia
Nature · 2017 · PMID 29059683 · open access
12 pages+
rs6904031 rs56387622 rs11624333 rs1895062 rs13294895 rs2223621
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs62098013 rs17638867 rs3811038 rs11773992 rs13383034 rs9517908
Genome-wide association study and fine-mapping on Korean biobank to discover renal trait-associated variants
Kidney research and clinical practice · 2024 · PMID 37919891 · open access
12 pages+
rs78069066 rs11871637 rs795230 rs11748165 rs12478841 rs4666000
Genetic Architecture of Trans-Laminar Cribrosa Pressure Difference and Primary Open-Angle Glaucoma
Investigative ophthalmology & visual science · 2026 · PMID 42017308 · open access
12 pages+
rs62279163 rs10201197 rs1423422 rs2478873 rs9573609 rs68192516
Novel Association of Genetic Markers Affecting CYP2A6 Activity and Lung Cancer Risk
Cancer research · 2016 · PMID 27488534
10 pages
rs113029345 rs76935404 rs10425738 rs11878604 rs7247903 rs2316205
Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants
Nature communications · 2020 · PMID 32139696 · open access
10 pages
rs17268829 rs10760444 rs71559437 rs6964587 rs4496150 rs9833888
The contribution of common genetic variation to nicotine and cotinine glucuronidation in multiple ethnic/racial populations
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2015 · PMID 25293881
9 pages
rs141360540 rs115219551 rs6832720 rs6952407 rs60634637 rs76513344
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
AOCS study group · EMBRACE Study and 4 more consortia
Nature genetics · 2017 · PMID 28346442
9 pages
rs1400482 rs1879586 rs7207826 rs11651755 rs688187 rs7902587
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
ABCTB Investigators · EMBRACE and 4 more consortia
Nature genetics · 2017 · PMID 29058716
5 pages
rs10995201 rs9397437 rs6562760 rs6678914 rs67397200
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
GEMO Study Collaborators · EMBRACE Collaborators and 3 more consortia
Nature communications · 2021 · PMID 33597508 · open access
5 pages
rs7222250 rs60882887 rs12470785 rs79183898 rs736596
Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations
Gut · 2014 · PMID 23850713
3 pages
rs11235667 rs10947261 rs6856616
Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1
DRIVE GAME-ON Consortium
Nature genetics · 2014 · PMID 25038754 · open access
3 pages
rs4951011 rs10474352 rs2290203
HLA-C*01 is a Risk Factor for Crohn's Disease
Inflammatory bowel diseases · 2016 · PMID 26891255
3 pages
rs114985235 rs6478109 rs140068907
Genome-wide association study in East Asians identifies two novel breast cancer susceptibility loci
Human molecular genetics · 2016 · PMID 27354352
3 pages
rs2981582 rs12118297 rs16992204
Identification of Genetic Loci Associated with Facial Wrinkles in a Large Korean Population
The Journal of investigative dermatology · 2022 · PMID 35421404
3 pages
rs13005242 rs36015125 rs749810
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
Mapping and annotating genomic loci to prioritize genes and implicate distinct polygenic adaptations for skin color
Nature communications · 2024 · PMID 38849341 · open access
3 pages
rs77310623 rs800884 rs33932559
Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women
Australian Ovarian Cancer Study Group
Gynecologic oncology · 2019 · PMID 30898391
2 pages
rs7748275 rs1934363
Identification of shared loci associated with both Crohn's disease and leprosy in East Asians
Human molecular genetics · 2022 · PMID 35512355
2 pages
rs10817678 rs9271011

Showing 20 of 32 · 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.