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성함이나 학술지명, PMID로 찾아보십시오.
Wang K에 대해
11건.
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Franke A,
McGovern DP,
Barrett JC,
Wang K,
Radford-Smith GL,
Ahmad T,
Lees CW,
Balschun T,
Lee J,
Roberts R,
Anderson CA,
Bis JC
외 84명 — 모두 보기
Bumpstead S,
Ellinghaus D,
Festen EM,
Georges M,
Green T,
Haritunians T,
Jostins L,
Latiano A,
Mathew CG,
Montgomery GW,
Prescott NJ,
Raychaudhuri S,
Rotter JI,
Schumm P,
Sharma Y,
Simms LA,
Taylor KD,
Whiteman D,
Wijmenga C,
Baldassano RN,
Barclay M,
Bayless TM,
Brand S,
Büning C,
Cohen A,
Colombel JF,
Cottone M,
Stronati L,
Denson T,
De Vos M,
D'Inca R,
Dubinsky M,
Edwards C,
Florin T,
Franchimont D,
Gearry R,
Glas J,
Van Gossum A,
Guthery SL,
Halfvarson J,
Verspaget HW,
Hugot JP,
Karban A,
Laukens D,
Lawrance I,
Lemann M,
Levine A,
Libioulle C,
Louis E,
Mowat C,
Newman W,
Panés J,
Phillips A,
Proctor DD,
Regueiro M,
Russell R,
Rutgeerts P,
Sanderson J,
Sans M,
Seibold F,
Steinhart AH,
Stokkers PC,
Torkvist L,
Kullak-Ublick G,
Wilson D,
Walters T,
Targan SR,
Brant SR,
Rioux JD,
D'Amato M,
Weersma RK,
Kugathasan S,
Griffiths AM,
Mansfield JC,
Vermeire S,
Duerr RH,
Silverberg MS,
Satsangi J,
Schreiber S,
Cho JH,
Annese V,
Hakonarson H,
Daly MJ,
Parkes M
Nature genetics · 2010 · PMID 21102463
페이지 12개+
Multi-population GWAS meta-analysis identifies bladder cancer susceptibility loci and highlights genetic regulation of smoking-related risk
Prokunina-Olsson L,
Florez-Vargas O,
Levin MG,
Dutta D,
Breeze CE,
Hurwitz LM,
Yan W,
Lamy P,
Papenberg BW,
Wang K,
Lee CH,
Milne RL
외 45명 — 모두 보기
Gu J,
Um CY,
Joseph V,
Furberg H,
Le Calvez-Kelm F,
Lori A,
Choudhury PP,
Afshar N,
Kogevinas M,
Offit K,
Vermeulen SH,
López de Maturana E,
Albanes D,
Purdue MP,
Cortessis VK,
Karagas MR,
Kooperberg C,
Bjurlin M,
Tadesse DA,
Moore SC,
Huang WY,
Haiman CA,
Stern MC,
Eliassen AH,
Mucci LA,
Aben KK,
Galesloot TE,
Verma A,
Yoshino S,
Hikino K,
Terao C,
Rafnar T,
Matsuda K,
Shuin T,
Garcia-Closas M,
Real FX,
Kiemeney LA,
Chanock SJ,
Malats N,
Silverman DT,
Dyrskjot L,
Rothman N,
Damrauer SM,
Koutros S,
Damrauer JS
UROMOL Consortium
Nature communications · 2026 · PMID 42706231 · 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
Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study
Duan L,
Wei L,
Tian Y,
Zhang Z,
Hu P,
Wei Q,
Liu S,
Zhang J,
Wang Y,
Li D,
Yang W,
Zong R
외 25명 — 모두 보기
Xian P,
Han C,
Bao X,
Zhao F,
Feng J,
Liu W,
Cao W,
Zhou G,
Zhu C,
Yu F,
Yang W,
Meng Y,
Wang J,
Chen X,
Wang Y,
Shen B,
Zhao B,
Wan J,
Zhang F,
Zhao G,
Xu A,
Zhang X,
Liu J,
Zuo X,
Wang K
Stroke · 2018 · PMID 29273593
페이지 6개
Genomewide association study of leprosy
Zhang FR,
Huang W,
Chen SM,
Sun LD,
Liu H,
Li Y,
Cui Y,
Yan XX,
Yang HT,
Yang RD,
Chu TS,
Zhang C
외 55명 — 모두 보기
Zhang L,
Han JW,
Yu GQ,
Quan C,
Yu YX,
Zhang Z,
Shi BQ,
Zhang LH,
Cheng H,
Wang CY,
Lin Y,
Zheng HF,
Fu XA,
Zuo XB,
Wang Q,
Long H,
Sun YP,
Cheng YL,
Tian HQ,
Zhou FS,
Liu HX,
Lu WS,
He SM,
Du WL,
Shen M,
Jin QY,
Wang Y,
Low HQ,
Erwin T,
Yang NH,
Li JY,
Zhao X,
Jiao YL,
Mao LG,
Yin G,
Jiang ZX,
Wang XD,
Yu JP,
Hu ZH,
Gong CH,
Liu YQ,
Liu RY,
Wang DM,
Wei D,
Liu JX,
Cao WK,
Cao HZ,
Li YP,
Yan WG,
Wei SY,
Wang KJ,
Hibberd ML,
Yang S,
Zhang XJ,
Liu JJ
The New England journal of medicine · 2009 · PMID 20018961
페이지 4개
Two Novel Susceptibility Loci for Prostate Cancer in Men of African Ancestry
Conti DV,
Wang K,
Sheng X,
Bensen JT,
Hazelett DJ,
Cook MB,
Ingles SA,
Kittles RA,
Strom SS,
Rybicki BA,
Nemesure B,
Isaacs WB
외 77명 — 모두 보기
Stanford JL,
Zheng W,
Zheng W,
Sanderson M,
John EM,
Park JY,
Xu J,
Stevens VL,
Berndt SI,
Huff CD,
Wang Z,
Yeboah ED,
Tettey Y,
Biritwum RB,
Adjei AA,
Tay E,
Truelove A,
Niwa S,
Sellers TA,
Yamoah K,
Murphy AB,
Crawford DC,
Gapstur SM,
Bush WS,
Aldrich MC,
Cussenot O,
Petrovics G,
Cullen J,
Neslund-Dudas C,
Stern MC,
Jarai ZK,
Govindasami K,
Chokkalingam AP,
Hsing AW,
Goodman PJ,
Hoffmann T,
Drake BF,
Hu JJ,
Clark PE,
Van Den Eeden SK,
Blanchet P,
Fowke JH,
Casey G,
Hennis AJM,
Han Y,
Lubwama A,
Thompson IM Jr,
Leach R,
Easton DF,
Schumacher F,
Van den Berg DJ,
Gundell SM,
Stram A,
Wan P,
Xia L,
Pooler LC,
Mohler JL,
Fontham ETH,
Smith GJ,
Taylor JA,
Srivastava S,
Eeles RA,
Carpten J,
Kibel AS,
Multigner L,
Parent ME,
Menegaux F,
Cancel-Tassin G,
Klein EA,
Brureau L,
Stram DO,
Watya S,
Chanock SJ,
Witte JS,
Blot WJ,
Henderson BE,
Haiman CA
PRACTICAL/ELLIPSE Consortium
Journal of the National Cancer Institute · 2017 · PMID 29117387 · open access
페이지 2개
Genome-wide association study provides insights into the genetic basis of Lewy body dementia
Zhu P,
Jin Z,
Wu S,
Gao S,
He Y,
Hu S,
Liu F,
Chen Y,
Wang M,
Wang K,
Liu G
Molecular psychiatry · 2025 · PMID 41068259
페이지 2개
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
Benjamin EJ,
Rice KM,
Arking DE,
Pfeufer A,
van Noord C,
Smith AV,
Schnabel RB,
Bis JC,
Boerwinkle E,
Sinner MF,
Dehghan A,
Lubitz SA
외 44명 — 모두 보기
D'Agostino RB Sr,
Lumley T,
Ehret GB,
Heeringa J,
Aspelund T,
Newton-Cheh C,
Larson MG,
Marciante KD,
Soliman EZ,
Rivadeneira F,
Wang TJ,
Eiríksdottir G,
Levy D,
Psaty BM,
Li M,
Chamberlain AM,
Hofman A,
Vasan RS,
Harris TB,
Rotter JI,
Kao WH,
Agarwal SK,
Stricker BH,
Wang K,
Launer LJ,
Smith NL,
Chakravarti A,
Uitterlinden AG,
Wolf PA,
Sotoodehnia N,
Köttgen A,
van Duijn CM,
Meitinger T,
Mueller M,
Perz S,
Steinbeck G,
Wichmann HE,
Lunetta KL,
Heckbert SR,
Gudnason V,
Alonso A,
Kääb S,
Ellinor PT,
Witteman JC
Nature genetics · 2009 · PMID 19597492 · open access
페이지 1개
Common variants in KCNN3 are associated with lone atrial fibrillation
Ellinor PT,
Lunetta KL,
Glazer NL,
Pfeufer A,
Alonso A,
Chung MK,
Sinner MF,
de Bakker PI,
Mueller M,
Lubitz SA,
Fox E,
Darbar D
외 50명 — 모두 보기
Smith NL,
Smith JD,
Schnabel RB,
Soliman EZ,
Rice KM,
Van Wagoner DR,
Beckmann BM,
van Noord C,
Wang K,
Ehret GB,
Rotter JI,
Hazen SL,
Steinbeck G,
Smith AV,
Launer LJ,
Harris TB,
Makino S,
Nelis M,
Milan DJ,
Perz S,
Esko T,
Köttgen A,
Moebus S,
Newton-Cheh C,
Li M,
Möhlenkamp S,
Wang TJ,
Kao WH,
Vasan RS,
Nöthen MM,
MacRae CA,
Stricker BH,
Hofman A,
Uitterlinden AG,
Levy D,
Boerwinkle E,
Metspalu A,
Topol EJ,
Chakravarti A,
Gudnason V,
Psaty BM,
Roden DM,
Meitinger T,
Wichmann HE,
Witteman JC,
Barnard J,
Arking DE,
Benjamin EJ,
Heckbert SR,
Kääb S
Nature genetics · 2010 · PMID 20173747 · open access
페이지 1개
Identification of common variants associated with human hippocampal and intracranial volumes
Stein JL,
Medland SE,
Vasquez AA,
Hibar DP,
Senstad RE,
Winkler AM,
Toro R,
Appel K,
Bartecek R,
Bergmann Ø,
Bernard M,
Brown AA
외 190명 — 모두 보기
Cannon DM,
Chakravarty MM,
Christoforou A,
Domin M,
Grimm O,
Hollinshead M,
Holmes AJ,
Homuth G,
Hottenga JJ,
Langan C,
Lopez LM,
Hansell NK,
Hwang KS,
Kim S,
Laje G,
Lee PH,
Liu X,
Loth E,
Lourdusamy A,
Mattingsdal M,
Mohnke S,
Maniega SM,
Nho K,
Nugent AC,
O'Brien C,
Papmeyer M,
Pütz B,
Ramasamy A,
Rasmussen J,
Rijpkema M,
Risacher SL,
Roddey JC,
Rose EJ,
Ryten M,
Shen L,
Sprooten E,
Strengman E,
Teumer A,
Trabzuni D,
Turner J,
van Eijk K,
van Erp TG,
van Tol MJ,
Wittfeld K,
Wolf C,
Woudstra S,
Aleman A,
Alhusaini S,
Almasy L,
Binder EB,
Brohawn DG,
Cantor RM,
Carless MA,
Corvin A,
Czisch M,
Curran JE,
Davies G,
de Almeida MA,
Delanty N,
Depondt C,
Duggirala R,
Dyer TD,
Erk S,
Fagerness J,
Fox PT,
Freimer NB,
Gill M,
Göring HH,
Hagler DJ,
Hoehn D,
Holsboer F,
Hoogman M,
Hosten N,
Jahanshad N,
Johnson MP,
Kasperaviciute D,
Kent JW Jr,
Kochunov P,
Lancaster JL,
Lawrie SM,
Liewald DC,
Mandl R,
Matarin M,
Mattheisen M,
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Nöthen MM,
Olvera RL,
Pandolfo M,
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Schnell K,
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Valdés Hernández MC,
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Westlye LT,
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Agartz I,
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Cavalleri GL,
Dale AM,
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Hagoort P,
Hall J,
Heinz A,
Jack CR Jr,
Foroud TM,
Le Hellard S,
Macciardi F,
Montgomery GW,
Poline JB,
Porteous DJ,
Sisodiya SM,
Starr JM,
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Gudnason V,
Tzourio C,
Vernooij MW,
Launer LJ,
DeCarli C,
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Apostolova LG,
Bastin ME,
Blangero J,
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Buckner RL,
Cichon S,
Coppola G,
de Zubicaray GI,
Deary IJ,
Donohoe G,
de Geus EJ,
Espeseth T,
Fernández G,
Glahn DC,
Grabe HJ,
Hardy J,
Hulshoff Pol HE,
Jenkinson M,
Kahn RS,
McDonald C,
McIntosh AM,
McMahon FJ,
McMahon KL,
Meyer-Lindenberg A,
Morris DW,
Müller-Myhsok B,
Nichols TE,
Ophoff RA,
Paus T,
Pausova Z,
Penninx BW,
Potkin SG,
Sämann PG,
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Wardlaw JM,
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Franke B,
Wright MJ,
Thompson PM
Alzheimer's Disease Neuroimaging Initiative · EPIGEN Consortium 외 컨소시엄 4곳
Nature genetics · 2012 · PMID 22504417
페이지 1개
Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence
St Pourcain B,
Skuse DH,
Mandy WP,
Wang K,
Hakonarson H,
Timpson NJ,
Evans DM,
Kemp JP,
Ring SM,
McArdle WL,
Golding J,
Smith GD
Molecular autism · 2014 · PMID 24564958 · open access
페이지 1개
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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.