For researchers
Is your paper here?
2,683 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 12.
A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population
Yoon KA,
Park JH,
Han J,
Park S,
Lee GK,
Han JY,
Zo JI,
Kim J,
Lee JE,
Takahashi A,
Kubo M,
Nakamura Y
and 1 more — show all
Human molecular genetics · 2010 · PMID 20876614
1 page
Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer
Long J,
Cai Q,
Sung H,
Shi J,
Zhang B,
Choi JY,
Wen W,
Delahanty RJ,
Lu W,
Gao YT,
Shen H,
Park SK
and 40 more — show all
Chen K,
Shen CY,
Ren Z,
Haiman CA,
Matsuo K,
Kim MK,
Khoo US,
Iwasaki M,
Zheng Y,
Xiang YB,
Gu K,
Rothman N,
Wang W,
Hu Z,
Liu Y,
Yoo KY,
Noh DY,
Han BG,
Lee MH,
Zheng H,
Zhang L,
Wu PE,
Shieh YL,
Chan SY,
Wang S,
Xie X,
Kim SW,
Henderson BE,
Le Marchand L,
Ito H,
Kasuga Y,
Ahn SH,
Kang HS,
Chan KY,
Iwata H,
Tsugane S,
Li C,
Shu XO,
Kang DH,
Zheng W
PLoS genetics · 2012 · PMID 22383897 · open access
1 page
A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study
Kim HC,
Lee JY,
Sung H,
Choi JY,
Park SK,
Lee KM,
Kim YJ,
Go MJ,
Li L,
Cho YS,
Park M,
Kim DJ
and 27 more — show all
Oh JH,
Kim JW,
Jeon JP,
Jeon SY,
Min H,
Kim HM,
Park J,
Yoo KY,
Noh DY,
Ahn SH,
Lee MH,
Kim SW,
Lee JW,
Park BW,
Park WY,
Kim EH,
Kim MK,
Han W,
Lee SA,
Matsuo K,
Shen CY,
Wu PE,
Hsiung CN,
Lee JY,
Kim HL,
Han BG,
Kang D
Breast cancer research : BCR · 2012 · PMID 22452962 · open access
1 page
Genome-wide association study of ulcerative colitis in Koreans suggests extensive overlapping of genetic susceptibility with Caucasians
Yang SK,
Hong M,
Zhao W,
Jung Y,
Tayebi N,
Ye BD,
Kim KJ,
Park SH,
Lee I,
Shin HD,
Cheong HS,
Kim LH
and 6 more — show all
Inflammatory bowel diseases · 2013 · PMID 23511034
1 page
Immunochip analysis identification of 6 additional susceptibility loci for Crohn's disease in Koreans
Yang SK,
Hong M,
Choi H,
Zhao W,
Jung Y,
Haritunians T,
Ye BD,
Kim KJ,
Park SH,
Lee I,
Kim WH,
Cheon JH
and 15 more — show all
Kim YH,
Jang BI,
Kim HS,
Choi JH,
Koo JS,
Lee JH,
Jung SA,
Shin HD,
Kang D,
Youn HS,
Taylor KD,
Rotter JI,
Liu J,
McGovern DP,
Song K
Inflammatory bowel diseases · 2015 · PMID 25489960
1 page
Identification of Ten Additional Susceptibility Loci for Ulcerative Colitis Through Immunochip Analysis in Koreans
Ye BD,
Choi H,
Hong M,
Yun WJ,
Low HQ,
Haritunians T,
Kim KJ,
Park SH,
Lee I,
Bang SY,
Kim TH,
Shin HD
and 7 more — show all
Inflammatory bowel diseases · 2016 · PMID 26398853
1 page
A coding variant in <i>FTO</i> confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBD
Kim HS,
Cheon JH,
Jung ES,
Park J,
Aum S,
Park SJ,
Eun S,
Lee J,
Rüther U,
Yeo GSH,
Ma M,
Park KS
and 5 more — show all
Gut · 2017 · PMID 27558924
1 page
Identification of Loci at 1q21 and 16q23 That Affect Susceptibility to Inflammatory Bowel Disease in Koreans
Yang SK,
Hong M,
Oh H,
Low HQ,
Jung S,
Ahn S,
Kim Y,
Baek J,
Lee CH,
Kim E,
Kim KM,
Ye BD
and 9 more — show all
Gastroenterology · 2016 · PMID 27569725
1 page
BRCA1/2-negative, high-risk breast cancers (BRCAX) for Asian women: genetic susceptibility loci and their potential impacts
Lee JY,
Kim J,
Kim SW,
Park SK,
Ahn SH,
Lee MH,
Suh YJ,
Noh DY,
Son BH,
Cho YU,
Lee SB,
Lee JW
and 2 more — show all
Scientific reports · 2018 · PMID 30323354 · open access
1 page
Genetic analyses of diverse populations improves discovery for complex traits
Wojcik GL,
Graff M,
Nishimura KK,
Tao R,
Haessler J,
Gignoux CR,
Highland HM,
Patel YM,
Sorokin EP,
Avery CL,
Belbin GM,
Bien SA
and 74 more — show all
Cheng I,
Cullina S,
Hodonsky CJ,
Hu Y,
Huckins LM,
Jeff J,
Justice AE,
Kocarnik JM,
Lim U,
Lin BM,
Lu Y,
Nelson SC,
Park SL,
Poisner H,
Preuss MH,
Richard MA,
Schurmann C,
Setiawan VW,
Sockell A,
Vahi K,
Verbanck M,
Vishnu A,
Walker RW,
Young KL,
Zubair N,
Acuña-Alonso V,
Ambite JL,
Barnes KC,
Boerwinkle E,
Bottinger EP,
Bustamante CD,
Caberto C,
Canizales-Quinteros S,
Conomos MP,
Deelman E,
Do R,
Doheny K,
Fernández-Rhodes L,
Fornage M,
Hailu B,
Heiss G,
Henn BM,
Hindorff LA,
Jackson RD,
Laurie CA,
Laurie CC,
Li Y,
Lin DY,
Moreno-Estrada A,
Nadkarni G,
Norman PJ,
Pooler LC,
Reiner AP,
Romm J,
Sabatti C,
Sandoval K,
Sheng X,
Stahl EA,
Stram DO,
Thornton TA,
Wassel CL,
Wilkens LR,
Winkler CA,
Yoneyama S,
Buyske S,
Haiman CA,
Kooperberg C,
Le Marchand L,
Loos RJF,
Matise TC,
North KE,
Peters U,
Kenny EE,
Carlson CS
Nature · 2019 · PMID 31217584
1 page
Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions
Dareng EO,
Coetzee SG,
Tyrer JP,
Peng PC,
Rosenow W,
Chen S,
Davis BD,
Dezem FS,
Seo JH,
Nameki R,
Reyes AL,
Aben KKH
and 141 more — show all
Anton-Culver H,
Antonenkova NN,
Aravantinos G,
Bandera EV,
Beane Freeman LE,
Beckmann MW,
Beeghly-Fadiel A,
Benitez J,
Bernardini MQ,
Bjorge L,
Black A,
Bogdanova NV,
Bolton KL,
Brenton JD,
Budzilowska A,
Butzow R,
Cai H,
Campbell I,
Cannioto R,
Chang-Claude J,
Chanock SJ,
Chen K,
Chenevix-Trench G,
Chiew YE,
Cook LS,
DeFazio A,
Dennis J,
Doherty JA,
Dörk T,
du Bois A,
Dürst M,
Eccles DM,
Ene G,
Fasching PA,
Flanagan JM,
Fortner RT,
Fostira F,
Gentry-Maharaj A,
Giles GG,
Goodman MT,
Gronwald J,
Haiman CA,
Håkansson N,
Heitz F,
Hildebrandt MAT,
Høgdall E,
Høgdall CK,
Huang RY,
Jensen A,
Jones ME,
Kang D,
Karlan BY,
Karnezis AN,
Kelemen LE,
Kennedy CJ,
Khusnutdinova EK,
Kiemeney LA,
Kjaer SK,
Kupryjanczyk J,
Labrie M,
Lambrechts D,
Larson MC,
Le ND,
Lester J,
Li L,
Lubiński J,
Lush M,
Marks JR,
Matsuo K,
May T,
McLaughlin JR,
McNeish IA,
Menon U,
Missmer S,
Modugno F,
Moffitt M,
Monteiro AN,
Moysich KB,
Narod SA,
Nguyen-Dumont T,
Odunsi K,
Olsson H,
Onland-Moret NC,
Park SK,
Pejovic T,
Permuth JB,
Piskorz A,
Prokofyeva D,
Riggan MJ,
Risch HA,
Rodríguez-Antona C,
Rossing MA,
Sandler DP,
Setiawan VW,
Shan K,
Song H,
Southey MC,
Steed H,
Sutphen R,
Swerdlow AJ,
Teo SH,
Terry KL,
Thompson PJ,
Vestrheim Thomsen LC,
Titus L,
Trabert B,
Travis R,
Tworoger SS,
Valen E,
Van Nieuwenhuysen E,
Edwards DV,
Vierkant RA,
Webb PM,
Weinberg CR,
Weise RM,
Wentzensen N,
White E,
Winham SJ,
Wolk A,
Woo YL,
Wu AH,
Yan L,
Yannoukakos D,
Zeinomar N,
Zheng W,
Ziogas A,
Berchuck A,
Goode EL,
Huntsman DG,
Pearce CL,
Ramus SJ,
Sellers TA,
Freedman ML,
Lawrenson K,
Schildkraut JM,
Hazelett D,
Plummer JT,
Kar S,
Jones MR,
Pharoah PDP,
Gayther SA
AOCS Group · OPAL Study Group and 1 more consortia
American journal of human genetics · 2024 · PMID 38723632
1 page
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.