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2,673 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
Cho YS,
showing the first 12.
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
Cho YS,
Go MJ,
Kim YJ,
Heo JY,
Oh JH,
Ban HJ,
Yoon D,
Lee MH,
Kim DJ,
Park M,
Cha SH,
Kim JW
and 20 more — show all
Han BG,
Min H,
Ahn Y,
Park MS,
Han HR,
Jang HY,
Cho EY,
Lee JE,
Cho NH,
Shin C,
Park T,
Park JW,
Lee JK,
Cardon L,
Clarke G,
McCarthy MI,
Lee JY,
Lee JK,
Oh B,
Kim HL
Nature genetics · 2009 · PMID 19396169
3 pages
Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits
Kim YJ,
Go MJ,
Hu C,
Hong CB,
Kim YK,
Lee JY,
Hwang JY,
Oh JH,
Kim DJ,
Kim NH,
Kim S,
Hong EJ
and 21 more — show all
Kim JH,
Min H,
Kim Y,
Zhang R,
Jia W,
Okada Y,
Takahashi A,
Kubo M,
Tanaka T,
Kamatani N,
Matsuda K,
Park T,
Oh B,
Kimm K,
Kang D,
Shin C,
Cho NH,
Kim HL,
Han BG,
Lee JY,
Cho YS
MAGIC consortium
Nature genetics · 2011 · PMID 21909109
3 pages
Meta-analysis identifies common variants associated with body mass index in east Asians
Wen W,
Cho YS,
Zheng W,
Zheng W,
Dorajoo R,
Kato N,
Qi L,
Chen CH,
Delahanty RJ,
Okada Y,
Tabara Y,
Gu D
and 52 more — show all
Zhu D,
Haiman CA,
Mo Z,
Gao YT,
Saw SM,
Go MJ,
Takeuchi F,
Chang LC,
Kokubo Y,
Liang J,
Hao M,
Le Marchand L,
Zhang Y,
Hu Y,
Wong TY,
Long J,
Han BG,
Kubo M,
Yamamoto K,
Su MH,
Miki T,
Henderson BE,
Song H,
Tan A,
He J,
Ng DP,
Cai Q,
Tsunoda T,
Tsai FJ,
Iwai N,
Chen GK,
Shi J,
Xu J,
Sim X,
Xiang YB,
Maeda S,
Ong RT,
Li C,
Nakamura Y,
Aung T,
Kamatani N,
Liu JJ,
Lu W,
Yokota M,
Seielstad M,
Fann CS,
Wu JY,
Lee JY,
Hu FB,
Tanaka T,
Tai ES,
Shu XO
Genetic Investigation of ANthropometric Traits (GIANT) Consortium
Nature genetics · 2012 · PMID 22344219 · open access
2 pages
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Flannick J,
Mercader JM,
Fuchsberger C,
Udler MS,
Mahajan A,
Wessel J,
Teslovich TM,
Caulkins L,
Koesterer R,
Barajas-Olmos F,
Blackwell TW,
Boerwinkle E
and 152 more — show all
Brody JA,
Centeno-Cruz F,
Chen L,
Chen S,
Contreras-Cubas C,
Córdova E,
Correa A,
Cortes M,
DeFronzo RA,
Dolan L,
Drews KL,
Elliott A,
Floyd JS,
Gabriel S,
Garay-Sevilla ME,
García-Ortiz H,
Gross M,
Han S,
Heard-Costa NL,
Jackson AU,
Jørgensen ME,
Kang HM,
Kelsey M,
Kim BJ,
Koistinen HA,
Kuusisto J,
Leader JB,
Linneberg A,
Liu CT,
Liu J,
Lyssenko V,
Manning AK,
Marcketta A,
Malacara-Hernandez JM,
Martínez-Hernández A,
Matsuo K,
Mayer-Davis E,
Mendoza-Caamal E,
Mohlke KL,
Morrison AC,
Ndungu A,
Ng MCY,
O'Dushlaine C,
Payne AJ,
Pihoker C,
Post WS,
Preuss M,
Psaty BM,
Vasan RS,
Rayner NW,
Reiner AP,
Revilla-Monsalve C,
Robertson NR,
Santoro N,
Schurmann C,
So WY,
Soberón X,
Stringham HM,
Strom TM,
Tam CHT,
Thameem F,
Tomlinson B,
Torres JM,
Tracy RP,
van Dam RM,
Vujkovic M,
Wang S,
Welch RP,
Witte DR,
Wong TY,
Atzmon G,
Barzilai N,
Blangero J,
Bonnycastle LL,
Bowden DW,
Chambers JC,
Chan E,
Cheng CY,
Cho YS,
Collins FS,
de Vries PS,
Duggirala R,
Glaser B,
Gonzalez C,
Gonzalez ME,
Groop L,
Kooner JS,
Kwak SH,
Laakso M,
Lehman DM,
Nilsson P,
Spector TD,
Tai ES,
Tuomi T,
Tuomilehto J,
Wilson JG,
Aguilar-Salinas CA,
Bottinger E,
Burke B,
Carey DJ,
Chan JCN,
Dupuis J,
Frossard P,
Heckbert SR,
Hwang MY,
Kim YJ,
Kirchner HL,
Lee JY,
Lee J,
Loos RJF,
Ma RCW,
Morris AD,
O'Donnell CJ,
Palmer CNA,
Pankow J,
Park KS,
Rasheed A,
Saleheen D,
Sim X,
Small KS,
Teo YY,
Haiman C,
Hanis CL,
Henderson BE,
Orozco L,
Tusié-Luna T,
Dewey FE,
Baras A,
Gieger C,
Meitinger T,
Strauch K,
Lange L,
Grarup N,
Hansen T,
Pedersen O,
Zeitler P,
Dabelea D,
Abecasis G,
Bell GI,
Cox NJ,
Seielstad M,
Sladek R,
Meigs JB,
Rich SS,
Rotter JI,
Altshuler D,
Burtt NP,
Scott LJ,
Morris AP,
Florez JC,
McCarthy MI,
Boehnke M
Broad Genomics Platform · DiscovEHR Collaboration and 8 more consortia
Nature · 2019 · PMID 31118516 · open access
2 pages
Identification of new genetic risk variants for type 2 diabetes
Shu XO,
Long J,
Cai Q,
Qi L,
Xiang YB,
Cho YS,
Tai ES,
Li X,
Lin X,
Chow WH,
Go MJ,
Seielstad M
and 19 more — show all
Bao W,
Li H,
Cornelis MC,
Yu K,
Wen W,
Shi J,
Han BG,
Sim XL,
Liu L,
Qi Q,
Kim HL,
Ng DP,
Lee JY,
Kim YJ,
Li C,
Gao YT,
Zheng W,
Zheng W,
Hu FB
PLoS genetics · 2010 · PMID 20862305 · open access
1 page
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
Cho YS,
Chen CH,
Hu C,
Long J,
Ong RT,
Sim X,
Takeuchi F,
Wu Y,
Go MJ,
Yamauchi T,
Chang YC,
Kwak SH
and 56 more — show all
Ma RC,
Yamamoto K,
Adair LS,
Aung T,
Cai Q,
Chang LC,
Chen YT,
Gao Y,
Hu FB,
Kim HL,
Kim S,
Kim YJ,
Lee JJ,
Lee NR,
Li Y,
Liu JJ,
Lu W,
Nakamura J,
Nakashima E,
Ng DP,
Tay WT,
Tsai FJ,
Wong TY,
Yokota M,
Zheng W,
Zheng W,
Zhang R,
Wang C,
So WY,
Ohnaka K,
Ikegami H,
Hara K,
Cho YM,
Cho NH,
Chang TJ,
Bao Y,
Hedman ÅK,
Morris AP,
McCarthy MI,
Takayanagi R,
Park KS,
Jia W,
Chuang LM,
Chuang LM,
Chan JC,
Maeda S,
Kadowaki T,
Lee JY,
Wu JY,
Teo YY,
Tai ES,
Shu XO,
Mohlke KL,
Kato N,
Han BG,
Seielstad M
DIAGRAM Consortium · MuTHER Consortium
Nature genetics · 2011 · PMID 22158537
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
New susceptibility loci in MYL2, C12orf51 and OAS1 associated with 1-h plasma glucose as predisposing risk factors for type 2 diabetes in the Korean population
Go MJ,
Hwang JY,
Kim YJ,
Hee Oh J,
Kim YJ,
Heon Kwak S,
Soo Park K,
Lee J,
Kim BJ,
Han BG,
Cho MC,
Cho YS
and 1 more — show all
Journal of human genetics · 2013 · PMID 23575436
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
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.