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성함이나 학술지명, PMID로 찾아보십시오.
Lee J에 대해
111건, 그중 20건 표시.
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
Law MH,
Bishop DT,
Lee JE,
Brossard M,
Martin NG,
Moses EK,
Song F,
Barrett JH,
Kumar R,
Easton DF,
Pharoah PDP,
Swerdlow AJ
외 63명 — 모두 보기
Kypreou KP,
Taylor JC,
Harland M,
Randerson-Moor J,
Akslen LA,
Andresen PA,
Avril MF,
Azizi E,
Scarrà GB,
Brown KM,
Dębniak T,
Duffy DL,
Elder DE,
Fang S,
Friedman E,
Galan P,
Ghiorzo P,
Gillanders EM,
Goldstein AM,
Gruis NA,
Hansson J,
Helsing P,
Hočevar M,
Höiom V,
Ingvar C,
Kanetsky PA,
Chen WV,
Landi MT,
Lang J,
Lathrop GM,
Lubiński J,
Mackie RM,
Mann GJ,
Molven A,
Montgomery GW,
Novaković S,
Olsson H,
Puig S,
Puig-Butille JA,
Qureshi AA,
Radford-Smith GL,
van der Stoep N,
van Doorn R,
Whiteman DC,
Craig JE,
Schadendorf D,
Simms LA,
Burdon KP,
Nyholt DR,
Pooley KA,
Orr N,
Stratigos AJ,
Cust AE,
Ward SV,
Hayward NK,
Han J,
Schulze HJ,
Dunning AM,
Bishop JAN,
Demenais F,
Amos CI,
MacGregor S,
Iles MM
GenoMEL Consortium · Essen-Heidelberg Investigators 외 컨소시엄 4곳
Nature genetics · 2015 · PMID 26237428 · open access
페이지 2개
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
외 233명 — 모두 보기
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 외 컨소시엄 2곳
Nature genetics · 2015 · PMID 26390057
페이지 2개
Korean atrial fibrillation network genome-wide association study for early-onset atrial fibrillation identifies novel susceptibility loci
Lee JY,
Kim TH,
Yang PS,
Lim HE,
Choi EK,
Shim J,
Shin E,
Uhm JS,
Kim JS,
Joung B,
Oh S,
Lee MH
외 2명 — 모두 보기
European heart journal · 2017 · PMID 28460022
페이지 2개
Population-specific genetic modification of Huntington's disease in Venezuela
Chao MJ,
Kim KH,
Shin JW,
Lucente D,
Wheeler VC,
Li H,
Roach JC,
Hood L,
Wexler NS,
Jardim LB,
Holmans P,
Jones L
외 5명 — 모두 보기
PLoS genetics · 2018 · PMID 29750799 · open access
페이지 2개
Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women
Lawrenson K,
Song F,
Hazelett DJ,
Kar SP,
Tyrer J,
Phelan CM,
Corona RI,
Rodríguez-Malavé NI,
Seo JH,
Adler E,
Coetzee SG,
Segato F
외 40명 — 모두 보기
Fonseca MAS,
Amos CI,
Carney ME,
Chenevix-Trench G,
Choi J,
Doherty JA,
Jia W,
Jin GJ,
Kim BG,
Le ND,
Lee J,
Li L,
Lim BK,
Adenan NA,
Mizuno M,
Park B,
Pearce CL,
Shan K,
Shi Y,
Shu XO,
Sieh W,
Thompson PJ,
Wilkens LR,
Wei Q,
Woo YL,
Yan L,
Karlan BY,
Freedman ML,
Noushmehr H,
Goode EL,
Berchuck A,
Sellers TA,
Teo SH,
Zheng W,
Matsuo K,
Park S,
Chen K,
Pharoah PDP,
Gayther SA,
Goodman MT
Australian Ovarian Cancer Study Group
Gynecologic oncology · 2019 · PMID 30898391
페이지 2개
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
외 152명 — 모두 보기
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 외 컨소시엄 8곳
Nature · 2019 · PMID 31118516 · open access
페이지 2개
Association of an IGHV3-66 gene variant with Kawasaki disease
Johnson TA,
Mashimo Y,
Wu JY,
Yoon D,
Hata A,
Kubo M,
Takahashi A,
Tsunoda T,
Ozaki K,
Tanaka T,
Ito K,
Suzuki H
외 18명 — 모두 보기
Hamada H,
Kobayashi T,
Hara T,
Chen CH,
Lee YC,
Liu YM,
Chang LC,
Chang CP,
Hong YM,
Jang GY,
Yun SW,
Yu JJ,
Lee KY,
Kim JJ,
Park T,
Lee JK,
Chen YT,
Onouchi Y
Korean Kawasaki Disease Genetics Consortium, Taiwan Kawasaki Disease Genetics Consortium, Taiwan Pediatric ID Alliance, Japan Kawasaki Disease Genome Consortium
Journal of human genetics · 2021 · PMID 33106546 · open access
페이지 2개
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations
Loh M,
Zhang W,
Ng HK,
Schmid K,
Lamri A,
Tong L,
Ahmad M,
Lee JJ,
Ng MCY,
Petty LE,
Spracklen CN,
Takeuchi F
외 35명 — 모두 보기
Islam MT,
Jasmine F,
Kasturiratne A,
Kibriya M,
Mohlke KL,
Paré G,
Prasad G,
Shahriar M,
Chee ML,
de Silva HJ,
Engert JC,
Gerstein HC,
Mani KR,
Sabanayagam C,
Vujkovic M,
Wickremasinghe AR,
Wong TY,
Yajnik CS,
Yusuf S,
Ahsan H,
Bharadwaj D,
Anand SS,
Below JE,
Boehnke M,
Bowden DW,
Chandak GR,
Cheng CY,
Kato N,
Mahajan A,
Sim X,
McCarthy MI,
Morris AP,
Kooner JS,
Saleheen D,
Chambers JC
Communications biology · 2022 · PMID 35393509 · open access
페이지 2개
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
외 19명 — 모두 보기
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
페이지 1개
Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations
Miki D,
Kubo M,
Takahashi A,
Yoon KA,
Kim J,
Lee GK,
Zo JI,
Lee JS,
Hosono N,
Morizono T,
Tsunoda T,
Kamatani N
외 5명 — 모두 보기
Nature genetics · 2010 · PMID 20871597
페이지 1개
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
외 1명 — 모두 보기
Human molecular genetics · 2010 · PMID 20876614
페이지 1개
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
외 56명 — 모두 보기
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
페이지 1개
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
외 27명 — 모두 보기
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
페이지 1개
Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans
Zhang M,
Song F,
Liang L,
Nan H,
Zhang J,
Liu H,
Wang LE,
Wei Q,
Lee JE,
Amos CI,
Kraft P,
Qureshi AA
외 1명 — 모두 보기
Human molecular genetics · 2013 · PMID 23548203
페이지 1개
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
외 1명 — 모두 보기
Journal of human genetics · 2013 · PMID 23575436
페이지 1개
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
페이지 1개
HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants
Heap GA,
Weedon MN,
Bewshea CM,
Singh A,
Chen M,
Satchwell JB,
Vivian JP,
So K,
Dubois PC,
Andrews JM,
Annese V,
Bampton P
외 44명 — 모두 보기
Barnardo M,
Bell S,
Cole A,
Connor SJ,
Creed T,
Cummings FR,
D'Amato M,
Daneshmend TK,
Fedorak RN,
Florin TH,
Gaya DR,
Greig E,
Halfvarson J,
Hart A,
Irving PM,
Jones G,
Karban A,
Lawrance IC,
Lee JC,
Lees C,
Lev-Tzion R,
Lindsay JO,
Mansfield J,
Mawdsley J,
Mazhar Z,
Parkes M,
Parnell K,
Orchard TR,
Radford-Smith G,
Russell RK,
Reffitt D,
Satsangi J,
Silverberg MS,
Sturniolo GC,
Tremelling M,
Tsianos EV,
van Heel DA,
Walsh A,
Watermeyer G,
Weersma RK,
Zeissig S,
Rossjohn J,
Holden AL,
Ahmad T
International Serious Adverse Events Consortium · IBD Pharmacogenetics Study Group
Nature genetics · 2014 · PMID 25217962
페이지 1개
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
외 15명 — 모두 보기
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
페이지 1개
Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations
Hayes MG,
Urbanek M,
Ehrmann DA,
Armstrong LL,
Lee JY,
Sisk R,
Karaderi T,
Barber TM,
McCarthy MI,
Franks S,
Lindgren CM,
Welt CK
외 11명 — 모두 보기
Diamanti-Kandarakis E,
Panidis D,
Goodarzi MO,
Azziz R,
Zhang Y,
James RG,
Olivier M,
Kissebah AH,
Stener-Victorin E,
Legro RS,
Dunaif A
Reproductive Medicine Network
Nature communications · 2015 · PMID 26284813 · open access
페이지 1개
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왜 "외 몇 명"이 아니라 저자를 다 적습니까?
622명이 필요했던 연구는 4명이 한 연구와 다른 종류의 연구인데, "et al."은 그것을 지우기
때문입니다. 12명을 먼저 보여 주고 나머지는 한 번 눌러 펼칩니다. 검색은 전원을 대상으로
합니다. 컨소시엄 논문의 187번째 이름도 실재하는 사람이고, 그 사람이 자기 이름을 찾고 있을
수 있습니다.
제 이름이 틀렸거나 논문 정보가 잘못되었습니다.
알려 주시면 고칩니다. 이름은 공개 기록에서 가져오는데 데이터베이스마다 이니셜 표기가
다르고, 같은 형태의 이름을 쓰는 두 사람을 저희가 구분할 수 없는 경우도 있습니다. 추측하기
보다 지적을 받는 편이 낫습니다.
제 논문이 없습니다. 탈락시킨 것입니까?
아닙니다. 이 카탈로그는 작은 팀이 읽을 수 있었던 것으로 모은 것이고, 유럽계 조상 코호트
바깥이 가장 얇습니다. 논문이 없는 것은 아직 아무도 거기까지 가지 못했기 때문이지 검토해서
제외한 것이 아닙니다.
어떤 페이지가 그 논문 위에 서 있는지 볼 수 있습니까?
각 줄에 최대 여섯 개까지 표시되며 각각 링크되어 있습니다. 줄 옆의 숫자는 그 논문을
인용하는 페이지가 모두 몇 개인지입니다.
얼마나 자주 갱신됩니까?
페이지들에서 매시간 다시 만들어집니다. 어떤 페이지가 그 논문 위에 서기 시작하면 그
순간 나타나고 그만두면 사라집니다. 따로 관리하는 목록이 없기 때문인데, 인용은 그 주장을
하는 페이지에 붙어 있어야 하기 때문입니다.