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2,673 papers hold this site up. Every variant and condition page names
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32 matches for
Kim BJ,
showing the first 12.
Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians
Chen P,
Takeuchi F,
Lee JY,
Li H,
Wu JY,
Liang J,
Long J,
Tabara Y,
Goodarzi MO,
Pereira MA,
Kim YJ,
Go MJ
and 59 more — show all
Stram DO,
Vithana E,
Khor CC,
Liu J,
Liao J,
Ye X,
Wang Y,
Lu L,
Young TL,
Lee J,
Thai AC,
Cheng CY,
van Dam RM,
Friedlander Y,
Heng CK,
Koh WP,
Chen CH,
Chang LC,
Pan WH,
Qi Q,
Isono M,
Zheng W,
Zheng W,
Cai Q,
Gao Y,
Yamamoto K,
Ohnaka K,
Takayanagi R,
Kita Y,
Ueshima H,
Hsiung CA,
Cui J,
Sheu WH,
Rotter JI,
Chen YD,
Hsu C,
Okada Y,
Kubo M,
Takahashi A,
Tanaka T,
van Rooij FJ,
Ganesh SK,
Huang J,
Huang T,
Yuan J,
Hwang JY,
Gross MD,
Assimes TL,
Miki T,
Shu XO,
Qi L,
Chen YT,
Lin X,
Aung T,
Wong TY,
Teo YY,
Kim BJ,
Kato N,
Tai ES
CHARGE Hematology Working Group
Diabetes · 2014 · PMID 24647736 · open access
4 pages
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index
Wen W,
Zheng W,
Zheng W,
Okada Y,
Takeuchi F,
Tabara Y,
Hwang JY,
Dorajoo R,
Li H,
Tsai FJ,
Yang X,
He J
and 98 more — show all
Wu Y,
He M,
Zhang Y,
Liang J,
Guo X,
Sheu WH,
Delahanty R,
Guo X,
Kubo M,
Yamamoto K,
Ohkubo T,
Go MJ,
Liu JJ,
Gan W,
Chen CC,
Gao Y,
Li S,
Lee NR,
Wu C,
Zhou X,
Song H,
Yao J,
Lee IT,
Long J,
Tsunoda T,
Akiyama K,
Takashima N,
Cho YS,
Ong RT,
Lu L,
Chen CH,
Tan A,
Rice TK,
Adair LS,
Gui L,
Allison M,
Lee WJ,
Cai Q,
Isomura M,
Umemura S,
Kim YJ,
Seielstad M,
Hixson J,
Xiang YB,
Isono M,
Kim BJ,
Sim X,
Lu W,
Nabika T,
Lee J,
Lim WY,
Gao YT,
Takayanagi R,
Kang DH,
Wong TY,
Hsiung CA,
Wu IC,
Juang JM,
Shi J,
Choi BY,
Aung T,
Hu F,
Kim MK,
Lim WY,
Wang TD,
Shin MH,
Lee J,
Ji BT,
Lee YH,
Young TL,
Shin DH,
Chun BY,
Cho MC,
Han BG,
Hwu CM,
Assimes TL,
Absher D,
Yan X,
Kim E,
Kuo JZ,
Kwon S,
Taylor KD,
Chen YD,
Rotter JI,
Qi L,
Zhu D,
Wu T,
Mohlke KL,
Gu D,
Mo Z,
Wu JY,
Lin X,
Miki T,
Tai ES,
Lee JY,
Kato N,
Shu XO,
Tanaka T
Human molecular genetics · 2014 · PMID 24861553
4 pages
Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures
Styrkarsdottir U,
Thorleifsson G,
Gudjonsson SA,
Sigurdsson A,
Center JR,
Lee SH,
Nguyen TV,
Kwok TCY,
Lee JSW,
Ho SC,
Woo J,
Leung PC
and 11 more — show all
Kim BJ,
Rafnar T,
Kiemeney LA,
Ingvarsson T,
Koh JM,
Tang NLS,
Eisman JA,
Christiansen C,
Sigurdsson G,
Thorsteinsdottir U,
Stefansson K
Nature communications · 2016 · PMID 26733130 · open access
3 pages
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Kato N,
Loh M,
Takeuchi F,
Verweij N,
Wang X,
Zhang W,
Kelly TN,
Saleheen D,
Lehne B,
Leach IM,
Drong AW,
Abbott J
and 233 more — show all
Wahl S,
Tan ST,
Scott WR,
Campanella G,
Chadeau-Hyam M,
Afzal U,
Ahluwalia TS,
Bonder MJ,
Chen P,
Dehghan A,
Edwards TL,
Esko T,
Go MJ,
Harris SE,
Hartiala J,
Kasela S,
Kasturiratne A,
Khor CC,
Kleber ME,
Li H,
Yu Mok Z,
Nakatochi M,
Sapari NS,
Saxena R,
Stewart AFR,
Stolk L,
Tabara Y,
Teh AL,
Wu Y,
Wu JY,
Zhang Y,
Aits I,
Da Silva Couto Alves A,
Das S,
Dorajoo R,
Hopewell JC,
Kim YK,
Koivula RW,
Luan J,
Lyytikäinen LP,
Nguyen QN,
Pereira MA,
Postmus I,
Raitakari OT,
Scannell Bryan M,
Scott RA,
Sorice R,
Tragante V,
Traglia M,
White J,
Yamamoto K,
Zhang Y,
Adair LS,
Ahmed A,
Akiyama K,
Asif R,
Aung T,
Barroso I,
Bjonnes A,
Braun TR,
Cai H,
Chang LC,
Chen CH,
Cheng CY,
Chong YS,
Collins R,
Courtney R,
Davies G,
Delgado G,
Do LD,
Doevendans PA,
Gansevoort RT,
Gao YT,
Grammer TB,
Grarup N,
Grewal J,
Gu D,
Wander GS,
Hartikainen AL,
Hazen SL,
He J,
Heng CK,
Hixson JE,
Hofman A,
Hsu C,
Huang W,
Husemoen LLN,
Hwang JY,
Ichihara S,
Igase M,
Isono M,
Justesen JM,
Katsuya T,
Kibriya MG,
Kim YJ,
Kishimoto M,
Koh WP,
Kohara K,
Kumari M,
Kwek K,
Lee NR,
Lee J,
Liao J,
Lieb W,
Liewald DCM,
Matsubara T,
Matsushita Y,
Meitinger T,
Mihailov E,
Milani L,
Mills R,
Mononen N,
Müller-Nurasyid M,
Nabika T,
Nakashima E,
Ng HK,
Nikus K,
Nutile T,
Ohkubo T,
Ohnaka K,
Parish S,
Paternoster L,
Peng H,
Peters A,
Pham ST,
Pinidiyapathirage MJ,
Rahman M,
Rakugi H,
Rolandsson O,
Ann Rozario M,
Ruggiero D,
Sala CF,
Sarju R,
Shimokawa K,
Snieder H,
Sparsø T,
Spiering W,
Starr JM,
Stott DJ,
Stram DO,
Sugiyama T,
Szymczak S,
Tang WHW,
Tong L,
Trompet S,
Turjanmaa V,
Ueshima H,
Uitterlinden AG,
Umemura S,
Vaarasmaki M,
van Dam RM,
van Gilst WH,
van Veldhuisen DJ,
Viikari JS,
Waldenberger M,
Wang Y,
Wang A,
Wilson R,
Wong TY,
Xiang YB,
Yamaguchi S,
Ye X,
Young RD,
Young TL,
Yuan JM,
Zhou X,
Asselbergs FW,
Ciullo M,
Clarke R,
Deloukas P,
Franke A,
Franks PW,
Franks S,
Friedlander Y,
Gross MD,
Guo Z,
Hansen T,
Jarvelin MR,
Jørgensen T,
Jukema JW,
Kähönen M,
Kajio H,
Kivimaki M,
Lee JY,
Lehtimäki T,
Linneberg A,
Miki T,
Pedersen O,
Samani NJ,
Sørensen TIA,
Takayanagi R,
Toniolo D,
Ahsan H,
Allayee H,
Chen YT,
Danesh J,
Deary IJ,
Franco OH,
Franke L,
Heijman BT,
Holbrook JD,
Isaacs A,
Kim BJ,
Lin X,
Liu J,
März W,
Metspalu A,
Mohlke KL,
Sanghera DK,
Shu XO,
van Meurs JBJ,
Vithana E,
Wickremasinghe AR,
Wijmenga C,
Wolffenbuttel BHW,
Yokota M,
Zheng W,
Zheng W,
Zhu D,
Vineis P,
Kyrtopoulos SA,
Kleinjans JCS,
McCarthy MI,
Soong R,
Gieger C,
Scott J,
Teo YY,
He J,
Elliott P,
Tai ES,
van der Harst P,
Kooner JS,
Chambers JC
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
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
Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus
Suetsugu H,
Kim K,
Yamamoto T,
Bang SY,
Sakamoto Y,
Shin JM,
Sugano N,
Kim JS,
Mukai M,
Lee YK,
Ohmura K,
Park DJ
and 43 more — show all
Takahashi D,
Ahn GY,
Karino K,
Kwon YC,
Miyamura T,
Kim J,
Nakamura J,
Motomura G,
Kuroda T,
Niiro H,
Miyamoto T,
Takeuchi T,
Ikari K,
Amano K,
Tada Y,
Yamaji K,
Shimizu M,
Atsumi T,
Seki T,
Tanaka Y,
Kubo T,
Hisada R,
Yoshioka T,
Yamazaki M,
Kabata T,
Kajino T,
Ohta Y,
Okawa T,
Naito Y,
Kaneuji A,
Yasunaga Y,
Ohzono K,
Tomizuka K,
Koido M,
Matsuda K,
Okada Y,
Suzuki A,
Kim BJ,
Kochi Y,
Lee HS,
Ikegawa S,
Bae SC,
Terao C
Human molecular genetics · 2022 · PMID 34850884
2 pages
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
Identification of a genetic variant at 2q12.1 associated with blood pressure in East Asians by genome-wide scan including gene-environment interactions
Kim YK,
Kim Y,
Hwang MY,
Shimokawa K,
Won S,
Kato N,
Tabara Y,
Yokota M,
Han BG,
Lee JH,
Kim BJ
BMC medical genetics · 2014 · PMID 24903457 · open access
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
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.