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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.
67 matches for
Kim Y,
showing the first 7.
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Wang Z,
Seow WJ,
Shiraishi K,
Hsiung CA,
Matsuo K,
Liu J,
Chen K,
Yamji T,
Yang Y,
Chang IS,
Wu C,
Hong YC
and 138 more — show all
Burdett L,
Wyatt K,
Chung CC,
Li SA,
Yeager M,
Hutchinson A,
Hu W,
Caporaso N,
Landi MT,
Chatterjee N,
Song M,
Fraumeni JF Jr,
Kohno T,
Yokota J,
Kunitoh H,
Ashikawa K,
Momozawa Y,
Daigo Y,
Mitsudomi T,
Yatabe Y,
Hida T,
Hu Z,
Dai J,
Ma H,
Jin G,
Song B,
Wang Z,
Cheng S,
Yin Z,
Li X,
Ren Y,
Guan P,
Chang J,
Tan W,
Chen CJ,
Chang GC,
Tsai YH,
Su WC,
Chen KY,
Huang MS,
Chen YM,
Zheng H,
Li H,
Cui P,
Guo H,
Xu P,
Liu L,
Iwasaki M,
Shimazu T,
Tsugane S,
Zhu J,
Jiang G,
Fei K,
Park JY,
Kim YH,
Sung JS,
Park KH,
Kim YT,
Jung YJ,
Kang CH,
Park IK,
Kim HN,
Jeon HS,
Choi JE,
Choi YY,
Kim JH,
Oh IJ,
Kim YC,
Sung SW,
Kim JS,
Yoon HI,
Kweon SS,
Shin MH,
Seow A,
Chen Y,
Lim WY,
Liu J,
Wong MP,
Lee VH,
Bassig BA,
Tucker M,
Berndt SI,
Chow WH,
Ji BT,
Wang J,
Xu J,
Sihoe AD,
Ho JC,
Chan JK,
Wang JC,
Lu D,
Zhao X,
Zhao Z,
Wu J,
Chen H,
Jin L,
Wei F,
Wu G,
An SJ,
Zhang XC,
Su J,
Wu YL,
Gao YT,
Xiang YB,
He X,
Li J,
Zheng W,
Shu XO,
Cai Q,
Klein R,
Pao W,
Lawrence C,
Hosgood HD 3rd,
Hsiao CF,
Chien LH,
Chen YH,
Chen CH,
Wang WC,
Chen CY,
Wang CL,
Yu CJ,
Chen HL,
Su YC,
Tsai FY,
Chen YS,
Li YJ,
Yang TY,
Lin CC,
Yang PC,
Wu T,
Lin D,
Zhou B,
Yu J,
Shen H,
Kubo M,
Chanock SJ,
Rothman N,
Lan Q
Human molecular genetics · 2016 · PMID 26732429
1 page
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
Wen W,
Kato N,
Hwang JY,
Guo X,
Tabara Y,
Li H,
Dorajoo R,
Yang X,
Tsai FJ,
Li S,
Wu Y,
Wu T
and 64 more — show all
Kim S,
Guo X,
Liang J,
Shungin D,
Adair LS,
Akiyama K,
Allison M,
Cai Q,
Chang LC,
Chen CH,
Chen YT,
Cho YS,
Choi BY,
Gao Y,
Go MJ,
Gu D,
Han BG,
He M,
Hixson JE,
Hu Y,
Huang T,
Isono M,
Jung KJ,
Kang D,
Kim YJ,
Kita Y,
Lee J,
Lee NR,
Lee J,
Wang Y,
Liu JJ,
Long J,
Moon S,
Nakamura Y,
Nakatochi M,
Ohnaka K,
Rao D,
Shi J,
Sull JW,
Tan A,
Ueshima H,
Wu C,
Xiang YB,
Yamamoto K,
Yao J,
Ye X,
Yokota M,
Zhang X,
Zheng Y,
Qi L,
Rotter JI,
Jee SH,
Lin D,
Mohlke KL,
He J,
Mo Z,
Wu JY,
Tai ES,
Lin X,
Miki T,
Kim BJ,
Takeuchi F,
Zheng W,
Shu XO
Scientific reports · 2016 · PMID 26785701 · open access
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
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
Watson HJ,
Yilmaz Z,
Thornton LM,
Hübel C,
Coleman JRI,
Gaspar HA,
Bryois J,
Hinney A,
Leppä VM,
Mattheisen M,
Medland SE,
Ripke S
and 198 more — show all
Yao S,
Giusti-Rodríguez P,
Hanscombe KB,
Purves KL,
Adan RAH,
Alfredsson L,
Ando T,
Andreassen OA,
Baker JH,
Berrettini WH,
Boehm I,
Boni C,
Perica VB,
Buehren K,
Burghardt R,
Cassina M,
Cichon S,
Clementi M,
Cone RD,
Courtet P,
Crow S,
Crowley JJ,
Danner UN,
Davis OSP,
de Zwaan M,
Dedoussis G,
Degortes D,
DeSocio JE,
Dick DM,
Dikeos D,
Dina C,
Dmitrzak-Weglarz M,
Docampo E,
Duncan LE,
Egberts K,
Ehrlich S,
Escaramís G,
Esko T,
Estivill X,
Farmer A,
Favaro A,
Fernández-Aranda F,
Fichter MM,
Fischer K,
Föcker M,
Foretova L,
Forstner AJ,
Forzan M,
Franklin CS,
Gallinger S,
Giegling I,
Giuranna J,
Gonidakis F,
Gorwood P,
Mayora MG,
Guillaume S,
Guo Y,
Hakonarson H,
Hatzikotoulas K,
Hauser J,
Hebebrand J,
Helder SG,
Herms S,
Herpertz-Dahlmann B,
Herzog W,
Huckins LM,
Hudson JI,
Imgart H,
Inoko H,
Janout V,
Jiménez-Murcia S,
Julià A,
Kalsi G,
Kaminská D,
Kaprio J,
Karhunen L,
Karwautz A,
Kas MJH,
Kennedy JL,
Keski-Rahkonen A,
Kiezebrink K,
Kim YR,
Klareskog L,
Klump KL,
Knudsen GPS,
La Via MC,
Le Hellard S,
Levitan RD,
Li D,
Lilenfeld L,
Lin BD,
Lissowska J,
Luykx J,
Magistretti PJ,
Maj M,
Mannik K,
Marsal S,
Marshall CR,
Mattingsdal M,
McDevitt S,
McGuffin P,
Metspalu A,
Meulenbelt I,
Micali N,
Mitchell K,
Monteleone AM,
Monteleone P,
Munn-Chernoff MA,
Nacmias B,
Navratilova M,
Ntalla I,
O'Toole JK,
Ophoff RA,
Padyukov L,
Palotie A,
Pantel J,
Papezova H,
Pinto D,
Rabionet R,
Raevuori A,
Ramoz N,
Reichborn-Kjennerud T,
Ricca V,
Ripatti S,
Ritschel F,
Roberts M,
Rotondo A,
Rujescu D,
Rybakowski F,
Santonastaso P,
Scherag A,
Scherer SW,
Schmidt U,
Schork NJ,
Schosser A,
Seitz J,
Slachtova L,
Slagboom PE,
Slof-Op 't Landt MCT,
Slopien A,
Sorbi S,
Świątkowska B,
Szatkiewicz JP,
Tachmazidou I,
Tenconi E,
Tortorella A,
Tozzi F,
Treasure J,
Tsitsika A,
Tyszkiewicz-Nwafor M,
Tziouvas K,
van Elburg AA,
van Furth EF,
Wagner G,
Walton E,
Widen E,
Zeggini E,
Zerwas S,
Zipfel S,
Bergen AW,
Boden JM,
Brandt H,
Crawford S,
Halmi KA,
Horwood LJ,
Johnson C,
Kaplan AS,
Kaye WH,
Mitchell JE,
Olsen CM,
Pearson JF,
Pedersen NL,
Strober M,
Werge T,
Whiteman DC,
Woodside DB,
Stuber GD,
Gordon S,
Grove J,
Henders AK,
Juréus A,
Kirk KM,
Larsen JT,
Parker R,
Petersen L,
Jordan J,
Kennedy M,
Montgomery GW,
Wade TD,
Birgegård A,
Lichtenstein P,
Norring C,
Landén M,
Martin NG,
Mortensen PB,
Sullivan PF,
Breen G,
Bulik CM
Anorexia Nervosa Genetics Initiative · Eating Disorders Working Group of the Psychiatric Genomics Consortium
Nature genetics · 2019 · PMID 31308545
1 page
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
Xie J,
Liu L,
Mladkova N,
Li Y,
Ren H,
Wang W,
Cui Z,
Lin L,
Hu X,
Yu X,
Xu J,
Liu G
and 108 more — show all
Caliskan Y,
Sidore C,
Balderes O,
Rosen RJ,
Bodria M,
Zanoni F,
Zhang JY,
Krithivasan P,
Mehl K,
Marasa M,
Khan A,
Ozay F,
Canetta PA,
Bomback AS,
Appel GB,
Sanna-Cherchi S,
Sampson MG,
Mariani LH,
Perkowska-Ptasinska A,
Durlik M,
Mucha K,
Moszczuk B,
Foroncewicz B,
Pączek L,
Habura I,
Ars E,
Ballarin J,
Mani LY,
Vogt B,
Ozturk S,
Yildiz A,
Seyahi N,
Arikan H,
Koc M,
Basturk T,
Karahan G,
Akgul SU,
Sever MS,
Zhang D,
Santoro D,
Bonomini M,
Londrino F,
Gesualdo L,
Reiterova J,
Tesar V,
Izzi C,
Savoldi S,
Spotti D,
Marcantoni C,
Messa P,
Galliani M,
Roccatello D,
Granata S,
Zaza G,
Lugani F,
Ghiggeri G,
Pisani I,
Allegri L,
Sprangers B,
Park JH,
Cho B,
Kim YS,
Kim DK,
Suzuki H,
Amoroso A,
Cattran DC,
Fervenza FC,
Pani A,
Hamilton P,
Harris S,
Gupta S,
Cheshire C,
Dufek S,
Issler N,
Pepper RJ,
Connolly J,
Powis S,
Bockenhauer D,
Stanescu HC,
Ashman N,
Loos RJF,
Kenny EE,
Wuttke M,
Eckardt KU,
Köttgen A,
Hofstra JM,
Coenen MJH,
Kiemeney LA,
Akilesh S,
Kretzler M,
Beck LH,
Stengel B,
Debiec H,
Ronco P,
Wetzels JFM,
Zoledziewska M,
Cucca F,
Ionita-Laza I,
Lee H,
Hoxha E,
Stahl RAK,
Brenchley P,
Scolari F,
Zhao MH,
Gharavi AG,
Kleta R,
Chen N,
Kiryluk K
Nature communications · 2020 · PMID 32231244 · open access
1 page
Shared genetic architectures of subjective well-being in East Asian and European ancestry populations
Kim S,
Kim K,
Hwang MY,
Ko H,
Jung SH,
Shim I,
Cha S,
Lee H,
Kim B,
Yoon J,
Ha TH,
Kim DK
and 7 more — show all
Nature human behaviour · 2022 · PMID 35589828
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.