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성함이나 학술지명, PMID로 찾아보십시오.
Im C에 대해
17건.
Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases
Li YR,
Li J,
Zhao SD,
Bradfield JP,
Mentch FD,
Maggadottir SM,
Hou C,
Abrams DJ,
Chang D,
Gao F,
Guo Y,
Wei Z
외 54명 — 모두 보기
Connolly JJ,
Cardinale CJ,
Bakay M,
Glessner JT,
Li D,
Kao C,
Thomas KA,
Qiu H,
Chiavacci RM,
Kim CE,
Wang F,
Snyder J,
Richie MD,
Flatø B,
Førre Ø,
Denson LA,
Thompson SD,
Becker ML,
Guthery SL,
Latiano A,
Perez E,
Resnick E,
Russell RK,
Wilson DC,
Silverberg MS,
Annese V,
Lie BA,
Punaro M,
Dubinsky MC,
Monos DS,
Strisciuglio C,
Staiano A,
Miele E,
Kugathasan S,
Ellis JA,
Munro JE,
Sullivan KE,
Wise CA,
Chapel H,
Cunningham-Rundles C,
Grant SF,
Orange JS,
Sleiman PM,
Behrens EM,
Griffiths AM,
Satsangi J,
Finkel TH,
Keinan A,
Prak ET,
Polychronakos C,
Baldassano RN,
Li H,
Keating BJ,
Hakonarson H
Nature medicine · 2015 · PMID 26301688
페이지 12개+
Korea4K: whole genome sequences of 4,157 Koreans with 107 phenotypes derived from extensive health check-ups
Jeon S,
Choi H,
Jeon Y,
Choi WH,
Choi H,
An K,
Ryu H,
Bhak J,
Lee H,
Kwon Y,
Ha S,
Kim YJ
외 18명 — 모두 보기
Blazyte A,
Kim C,
Kim Y,
Kang Y,
Woo YJ,
Lee C,
Seo J,
Yoon C,
Bolser D,
Biro O,
Shin ES,
Kim BC,
Kim SY,
Park JH,
Jeon J,
Jung D,
Lee S,
Bhak J
GigaScience · 2024 · PMID 38626723 · open access
페이지 12개+
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Sawcer S,
Hellenthal G,
Pirinen M,
Spencer CC,
Patsopoulos NA,
Moutsianas L,
Dilthey A,
Su Z,
Freeman C,
Hunt SE,
Edkins S,
Gray E
외 230명 — 모두 보기
Booth DR,
Potter SC,
Goris A,
Band G,
Oturai AB,
Strange A,
Saarela J,
Bellenguez C,
Fontaine B,
Gillman M,
Hemmer B,
Gwilliam R,
Zipp F,
Jayakumar A,
Martin R,
Leslie S,
Hawkins S,
Giannoulatou E,
D'alfonso S,
Blackburn H,
Martinelli Boneschi F,
Liddle J,
Harbo HF,
Perez ML,
Spurkland A,
Waller MJ,
Mycko MP,
Ricketts M,
Comabella M,
Hammond N,
Kockum I,
McCann OT,
Ban M,
Whittaker P,
Kemppinen A,
Weston P,
Hawkins C,
Widaa S,
Zajicek J,
Dronov S,
Robertson N,
Bumpstead SJ,
Barcellos LF,
Ravindrarajah R,
Abraham R,
Alfredsson L,
Ardlie K,
Aubin C,
Baker A,
Baker K,
Baranzini SE,
Bergamaschi L,
Bergamaschi R,
Bernstein A,
Berthele A,
Boggild M,
Bradfield JP,
Brassat D,
Broadley SA,
Buck D,
Butzkueven H,
Capra R,
Carroll WM,
Cavalla P,
Celius EG,
Cepok S,
Chiavacci R,
Clerget-Darpoux F,
Clysters K,
Comi G,
Cossburn M,
Cournu-Rebeix I,
Cox MB,
Cozen W,
Cree BA,
Cross AH,
Cusi D,
Daly MJ,
Davis E,
de Bakker PI,
Debouverie M,
D'hooghe MB,
Dixon K,
Dobosi R,
Dubois B,
Ellinghaus D,
Elovaara I,
Esposito F,
Fontenille C,
Foote S,
Franke A,
Galimberti D,
Ghezzi A,
Glessner J,
Gomez R,
Gout O,
Graham C,
Grant SF,
Guerini FR,
Hakonarson H,
Hall P,
Hamsten A,
Hartung HP,
Heard RN,
Heath S,
Hobart J,
Hoshi M,
Infante-Duarte C,
Ingram G,
Ingram W,
Islam T,
Jagodic M,
Kabesch M,
Kermode AG,
Kilpatrick TJ,
Kim C,
Klopp N,
Koivisto K,
Larsson M,
Lathrop M,
Lechner-Scott JS,
Leone MA,
Leppä V,
Liljedahl U,
Bomfim IL,
Lincoln RR,
Link J,
Liu J,
Lorentzen AR,
Lupoli S,
Macciardi F,
Mack T,
Marriott M,
Martinelli V,
Mason D,
McCauley JL,
Mentch F,
Mero IL,
Mihalova T,
Montalban X,
Mottershead J,
Myhr KM,
Naldi P,
Ollier W,
Page A,
Palotie A,
Pelletier J,
Piccio L,
Pickersgill T,
Piehl F,
Pobywajlo S,
Quach HL,
Ramsay PP,
Reunanen M,
Reynolds R,
Rioux JD,
Rodegher M,
Roesner S,
Rubio JP,
Rückert IM,
Salvetti M,
Salvi E,
Santaniello A,
Schaefer CA,
Schreiber S,
Schulze C,
Scott RJ,
Sellebjerg F,
Selmaj KW,
Sexton D,
Shen L,
Simms-Acuna B,
Skidmore S,
Sleiman PM,
Smestad C,
Sørensen PS,
Søndergaard HB,
Stankovich J,
Strange RC,
Sulonen AM,
Sundqvist E,
Syvänen AC,
Taddeo F,
Taylor B,
Blackwell JM,
Tienari P,
Bramon E,
Tourbah A,
Brown MA,
Tronczynska E,
Casas JP,
Tubridy N,
Corvin A,
Vickery J,
Jankowski J,
Villoslada P,
Markus HS,
Wang K,
Mathew CG,
Wason J,
Palmer CN,
Wichmann HE,
Plomin R,
Willoughby E,
Rautanen A,
Winkelmann J,
Wittig M,
Trembath RC,
Yaouanq J,
Viswanathan AC,
Zhang H,
Wood NW,
Zuvich R,
Deloukas P,
Langford C,
Duncanson A,
Oksenberg JR,
Pericak-Vance MA,
Haines JL,
Olsson T,
Hillert J,
Ivinson AJ,
De Jager PL,
Peltonen L,
Stewart GJ,
Hafler DA,
Hauser SL,
McVean G,
Donnelly P,
Compston A
International Multiple Sclerosis Genetics Consortium · Wellcome Trust Case Control Consortium 2
Nature · 2011 · PMID 21833088 · open access
페이지 11개
GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children
Li J,
Glessner JT,
Zhang H,
Hou C,
Wei Z,
Bradfield JP,
Mentch FD,
Guo Y,
Kim C,
Xia Q,
Chiavacci RM,
Thomas KA
외 5명 — 모두 보기
Human molecular genetics · 2013 · PMID 23263863
페이지 4개
A genome-wide analysis of the response to inhaled β2-agonists in chronic obstructive pulmonary disease
Hardin M,
Cho MH,
McDonald ML,
Wan E,
Lomas DA,
Coxson HO,
MacNee W,
Vestbo J,
Yates JC,
Agusti A,
Calverley PM,
Celli B
외 13명 — 모두 보기
Crim C,
Rennard S,
Wouters E,
Bakke P,
Bhatt SP,
Kim V,
Ramsdell J,
Regan EA,
Make BJ,
Hokanson JE,
Crapo JD,
Beaty TH,
Hersh CP
ECLIPSE and COPDGene Investigators · COPDGene Investigators—clinical centers
The pharmacogenomics journal · 2016 · PMID 26503814 · open access
페이지 3개
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
Hakonarson H,
Grant SF,
Bradfield JP,
Marchand L,
Kim CE,
Glessner JT,
Grabs R,
Casalunovo T,
Taback SP,
Frackelton EC,
Lawson ML,
Robinson LJ
외 11명 — 모두 보기
Skraban R,
Lu Y,
Chiavacci RM,
Stanley CA,
Kirsch SE,
Rappaport EF,
Orange JS,
Monos DS,
Devoto M,
Qu HQ,
Polychronakos C
Nature · 2007 · PMID 17632545
페이지 2개
Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease
Kugathasan S,
Baldassano RN,
Bradfield JP,
Sleiman PM,
Imielinski M,
Guthery SL,
Cucchiara S,
Kim CE,
Frackelton EC,
Annaiah K,
Glessner JT,
Santa E
외 18명 — 모두 보기
Willson T,
Eckert AW,
Bonkowski E,
Shaner JL,
Smith RM,
Otieno FG,
Peterson N,
Abrams DJ,
Chiavacci RM,
Grundmeier R,
Mamula P,
Tomer G,
Piccoli DA,
Monos DS,
Annese V,
Denson LA,
Grant SF,
Hakonarson H
Nature genetics · 2008 · PMID 18758464
페이지 2개
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia
Lan Q,
Hsiung CA,
Matsuo K,
Hong YC,
Seow A,
Wang Z,
Hosgood HD 3rd,
Chen K,
Wang JC,
Chatterjee N,
Hu W,
Wong MP
외 119명 — 모두 보기
Zheng W,
Caporaso N,
Park JY,
Chen CJ,
Kim YH,
Kim YT,
Landi MT,
Shen H,
Lawrence C,
Burdett L,
Yeager M,
Yuenger J,
Jacobs KB,
Chang IS,
Mitsudomi T,
Kim HN,
Chang GC,
Bassig BA,
Tucker M,
Wei F,
Yin Z,
Wu C,
An SJ,
Qian B,
Lee VH,
Lu D,
Liu J,
Jeon HS,
Hsiao CF,
Sung JS,
Kim JH,
Gao YT,
Tsai YH,
Jung YJ,
Guo H,
Hu Z,
Hutchinson A,
Wang WC,
Klein R,
Chung CC,
Oh IJ,
Chen KY,
Berndt SI,
He X,
Wu W,
Chang J,
Zhang XC,
Huang MS,
Zheng H,
Wang J,
Zhao X,
Li Y,
Choi JE,
Su WC,
Park KH,
Sung SW,
Shu XO,
Chen YM,
Liu L,
Kang CH,
Hu L,
Chen CH,
Pao W,
Kim YC,
Yang TY,
Xu J,
Guan P,
Tan W,
Su J,
Wang CL,
Li H,
Sihoe AD,
Zhao Z,
Chen Y,
Choi YY,
Hung JY,
Kim JS,
Yoon HI,
Cai Q,
Lin CC,
Park IK,
Xu P,
Dong J,
Kim C,
He Q,
Perng RP,
Kohno T,
Kweon SS,
Chen CY,
Vermeulen R,
Wu J,
Lim WY,
Chen KC,
Chow WH,
Ji BT,
Chan JK,
Chu M,
Li YJ,
Yokota J,
Li J,
Chen H,
Xiang YB,
Yu CJ,
Kunitoh H,
Wu G,
Jin L,
Lo YL,
Shiraishi K,
Chen YH,
Lin HC,
Wu T,
Wu YL,
Yang PC,
Zhou B,
Shin MH,
Fraumeni JF Jr,
Lin D,
Chanock SJ,
Rothman N
Nature genetics · 2012 · PMID 23143601
페이지 2개
Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk
Chang X,
Zhao Y,
Hou C,
Glessner J,
McDaniel L,
Diamond MA,
Thomas K,
Li J,
Wei Z,
Liu Y,
Guo Y,
Mentch FD
외 9명 — 모두 보기
Nature communications · 2017 · PMID 28924153 · open access
페이지 2개
First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes
Cousminer DL,
Ahlqvist E,
Mishra R,
Andersen MK,
Chesi A,
Hawa MI,
Davis A,
Hodge KM,
Bradfield JP,
Zhou K,
Guy VC,
Åkerlund M
외 41명 — 모두 보기
Wod M,
Fritsche LG,
Vestergaard H,
Snyder J,
Højlund K,
Linneberg A,
Käräjämäki A,
Brandslund I,
Kim CE,
Witte D,
Sørgjerd EP,
Brillon DJ,
Pedersen O,
Beck-Nielsen H,
Grarup N,
Pratley RE,
Rickels MR,
Vella A,
Ovalle F,
Melander O,
Harris RI,
Varvel S,
Grill VER,
Hakonarson H,
Froguel P,
Lonsdale JT,
Mauricio D,
Schloot NC,
Khunti K,
Greenbaum CJ,
Åsvold BO,
Yderstræde KB,
Pearson ER,
Schwartz S,
Voight BF,
Hansen T,
Tuomi T,
Boehm BO,
Groop L,
Leslie RD,
Grant SFA
Bone Mineral Density in Childhood Study
Diabetes care · 2018 · PMID 30254083 · open access
페이지 2개
A type 1 diabetes genetic risk score discriminates between type 1 diabetes and type 2 diabetes in a Chinese population
Hu J,
Jiang G,
Qin J,
Luo S,
Fan B,
Xie Z,
Wan R,
Li X,
Tam CHT,
Wang Z,
Ding J,
Xia Y
외 16명 — 모두 보기
Yang Y,
Lin J,
Yu G,
Jin P,
Lim CKP,
Luk AOY,
So WY,
Chan JCN,
Wang C,
Huang J,
Weedon MN,
Hagopian WA,
Oram RA,
Ma RCW,
Xiao Y,
Zhou Z
Hong Kong Diabetes Biobank Study Group
Diabetologia · 2025 · PMID 40569436 · open access
페이지 2개
Genome-wide association study of childhood B-cell acute lymphoblastic leukemia reveals novel African ancestry-specific susceptibility loci
Im C,
Raduski AR,
Mills LJ,
Bhattarai KR,
Mobley RJ,
Barnett KR,
Lu Z,
Liao K,
Anderson N,
Johnson RA,
Langer E,
Hooten AJ
외 31명 — 모두 보기
Seif AE,
Bernt KM,
Tsang M,
Mamou BA,
Gil-de-Gómez L,
Wolfson JA,
Friedman DN,
Shukla N,
Klesse LJ,
Marcotte EL,
Ji L,
Dang A,
Luo M,
Zhong Y,
Langie J,
Chiang CWK,
de Smith A,
Wiemels JL,
DeWan A,
Ma X,
Metayer C,
Wang Z,
Nelson HH,
Pankratz N,
Yang T,
Basu S,
Turcotte LM,
Yang JJ,
Savic D,
Scheurer ME,
Spector LG
Nature communications · 2025 · PMID 41125582 · open access
페이지 2개
Common variants at 12q15 and 12q24 are associated with infant head circumference
Taal HR,
Pourcain BS,
Thiering E,
Das S,
Mook-Kanamori DO,
Warrington NM,
Kaakinen M,
Kreiner-Møller E,
Bradfield JP,
Freathy RM,
Geller F,
Guxens M
외 74명 — 모두 보기
Cousminer DL,
Kerkhof M,
Timpson NJ,
Ikram MA,
Beilin LJ,
Bønnelykke K,
Buxton JL,
Charoen P,
Chawes BLK,
Eriksson J,
Evans DM,
Hofman A,
Kemp JP,
Kim CE,
Klopp N,
Lahti J,
Lye SJ,
McMahon G,
Mentch FD,
Müller M,
O'Reilly PF,
Prokopenko I,
Rivadeneira F,
Steegers EAP,
Sunyer J,
Tiesler C,
Yaghootkar H,
Breteler MMB,
Debette S,
Fornage M,
Gudnason V,
Launer LJ,
van der Lugt A,
Mosley TH,
Seshadri S,
Smith AV,
Vernooij MW,
Blakemore AI,
Chiavacci RM,
Feenstra B,
Fernandez-Benet J,
Grant SFA,
Hartikainen AL,
van der Heijden AJ,
Iñiguez C,
Lathrop M,
McArdle WL,
Mølgaard A,
Newnham JP,
Palmer LJ,
Palotie A,
Palotie A,
Pouta A,
Ring SM,
Sovio U,
Standl M,
Uitterlinden AG,
Wichmann HE,
Vissing NH,
DeCarli C,
van Duijn CM,
McCarthy MI,
Koppelman GH,
Estivill X,
Hattersley AT,
Melbye M,
Bisgaard H,
Pennell CE,
Widen E,
Hakonarson H,
Smith GD,
Heinrich J,
Jarvelin MR,
Jaddoe VWV
Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium 외 컨소시엄 1곳
Nature genetics · 2012 · PMID 22504419
페이지 1개
Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease
McDonald ML,
Cho MH,
Sørheim IC,
Lutz SM,
Castaldi PJ,
Lomas DA,
Coxson HO,
Edwards LD,
MacNee W,
Vestbo J,
Yates JC,
Agusti A
외 19명 — 모두 보기
Calverley PM,
Celli B,
Crim C,
Rennard SI,
Wouters EF,
Bakke P,
Tal-Singer R,
Miller BE,
Gulsvik A,
Casaburi R,
Wells JM,
Regan EA,
Make BJ,
Hokanson JE,
Lange C,
Crapo JD,
Beaty TH,
Silverman EK,
Hersh CP
Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints and COPDGene Investigators
American journal of respiratory cell and molecular biology · 2014 · PMID 24825563
페이지 1개
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Khor CC,
Do T,
Jia H,
Nakano M,
George R,
Abu-Amero K,
Duvesh R,
Chen LJ,
Li Z,
Nongpiur ME,
Perera SA,
Qiao C
외 217명 — 모두 보기
Wong HT,
Sakai H,
Barbosa de Melo M,
Lee MC,
Chan AS,
Azhany Y,
Dao TL,
Ikeda Y,
Perez-Grossmann RA,
Zarnowski T,
Day AC,
Jonas JB,
Tam PO,
Tran TA,
Ayub H,
Akhtar F,
Micheal S,
Chew PT,
Aljasim LA,
Dada T,
Luu TT,
Awadalla MS,
Kitnarong N,
Wanichwecharungruang B,
Aung YY,
Mohamed-Noor J,
Vijayan S,
Sarangapani S,
Husain R,
Jap A,
Baskaran M,
Goh D,
Su DH,
Wang H,
Yong VK,
Yip LW,
Trinh TB,
Makornwattana M,
Nguyen TT,
Leuenberger EU,
Park KH,
Wiyogo WA,
Kumar RS,
Tello C,
Kurimoto Y,
Thapa SS,
Pathanapitoon K,
Salmon JF,
Sohn YH,
Fea A,
Ozaki M,
Lai JS,
Tantisevi V,
Khaing CC,
Mizoguchi T,
Nakano S,
Kim CY,
Tang G,
Fan S,
Wu R,
Meng H,
Nguyen TT,
Tran TD,
Ueno M,
Martinez JM,
Ramli N,
Aung YM,
Reyes RD,
Vernon SA,
Fang SK,
Xie Z,
Chen XY,
Foo JN,
Sim KS,
Wong TT,
Quek DT,
Venkatesh R,
Kavitha S,
Krishnadas SR,
Soumittra N,
Shantha B,
Lim BA,
Ogle J,
de Vasconcellos JP,
Costa VP,
Abe RY,
de Souza BB,
Sng CC,
Aquino MC,
Kosior-Jarecka E,
Fong GB,
Tamanaja VC,
Fujita R,
Jiang Y,
Waseem N,
Low S,
Pham HN,
Al-Shahwan S,
Craven ER,
Khan MI,
Dada R,
Mohanty K,
Faiq MA,
Hewitt AW,
Burdon KP,
Gan EH,
Prutthipongsit A,
Patthanathamrongkasem T,
Catacutan MA,
Felarca IR,
Liao CS,
Rusmayani E,
Istiantoro VW,
Consolandi G,
Pignata G,
Lavia C,
Rojanapongpun P,
Mangkornkanokpong L,
Chansangpetch S,
Chan JC,
Choy BN,
Shum JW,
Than HM,
Oo KT,
Han AT,
Yong VH,
Ng XY,
Goh SR,
Chong YF,
Hibberd ML,
Seielstad M,
Png E,
Dunstan SJ,
Chau NV,
Bei J,
Zeng YX,
Karkey A,
Basnyat B,
Pasutto F,
Paoli D,
Frezzotti P,
Wang JJ,
Mitchell P,
Fingert JH,
Allingham RR,
Hauser MA,
Lim ST,
Chew SH,
Ebstein RP,
Sakuntabhai A,
Park KH,
Ahn J,
Boland G,
Snippe H,
Stead R,
Quino R,
Zaw SN,
Lukasik U,
Shetty R,
Zahari M,
Bae HW,
Oo NL,
Kubota T,
Manassakorn A,
Ho WL,
Dallorto L,
Hwang YH,
Kiire CA,
Kuroda M,
Djamal ZE,
Peregrino JI,
Ghosh A,
Jeoung JW,
Hoan TS,
Srisamran N,
Sandragasu T,
Set SH,
Doan VH,
Bhattacharya SS,
Ho CL,
Tan DT,
Sihota R,
Loon SC,
Mori K,
Kinoshita S,
Hollander AI,
Qamar R,
Wang YX,
Teo YY,
Tai ES,
Hartleben-Matkin C,
Lozano-Giral D,
Saw SM,
Cheng CY,
Zenteno JC,
Pang CP,
Bui HT,
Hee O,
Craig JE,
Edward DP,
Yonahara M,
Neto JM,
Guevara-Fujita ML,
Xu L,
Ritch R,
Liza-Sharmini AT,
Wong TY,
Al-Obeidan S,
Do NH,
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Tham CC,
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Wang N,
Aung T
Nature genetics · 2016 · PMID 27064256
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A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
van Zuydam NR,
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외 69명 — 모두 보기
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Finnish Diabetic Nephropathy Study (FinnDiane) · Hong Kong Diabetes Registry Theme-based Research Scheme Project Group 외 컨소시엄 4곳
Diabetes · 2018 · PMID 29703844
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