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성함이나 학술지명, PMID로 찾아보십시오.
Bellenguez C에 대해
17건.
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Beecham AH,
Patsopoulos NA,
Xifara DK,
Davis MF,
Kemppinen A,
Cotsapas C,
Shah TS,
Spencer C,
Booth D,
Goris A,
Oturai A,
Saarela J
외 181명 — 모두 보기
Fontaine B,
Hemmer B,
Martin C,
Zipp F,
D'Alfonso S,
Martinelli-Boneschi F,
Taylor B,
Harbo HF,
Kockum I,
Hillert J,
Olsson T,
Ban M,
Oksenberg JR,
Hintzen R,
Barcellos LF,
Agliardi C,
Alfredsson L,
Alizadeh M,
Anderson C,
Andrews R,
Søndergaard HB,
Baker A,
Band G,
Baranzini SE,
Barizzone N,
Barrett J,
Bellenguez C,
Bergamaschi L,
Bernardinelli L,
Berthele A,
Biberacher V,
Binder TM,
Blackburn H,
Bomfim IL,
Brambilla P,
Broadley S,
Brochet B,
Brundin L,
Buck D,
Butzkueven H,
Caillier SJ,
Camu W,
Carpentier W,
Cavalla P,
Celius EG,
Coman I,
Comi G,
Corrado L,
Cosemans L,
Cournu-Rebeix I,
Cree BA,
Cusi D,
Damotte V,
Defer G,
Delgado SR,
Deloukas P,
di Sapio A,
Dilthey AT,
Donnelly P,
Dubois B,
Duddy M,
Edkins S,
Elovaara I,
Esposito F,
Evangelou N,
Fiddes B,
Field J,
Franke A,
Freeman C,
Frohlich IY,
Galimberti D,
Gieger C,
Gourraud PA,
Graetz C,
Graham A,
Grummel V,
Guaschino C,
Hadjixenofontos A,
Hakonarson H,
Halfpenny C,
Hall G,
Hall P,
Hamsten A,
Harley J,
Harrower T,
Hawkins C,
Hellenthal G,
Hillier C,
Hobart J,
Hoshi M,
Hunt SE,
Jagodic M,
Jelčić I,
Jochim A,
Kendall B,
Kermode A,
Kilpatrick T,
Koivisto K,
Konidari I,
Korn T,
Kronsbein H,
Langford C,
Larsson M,
Lathrop M,
Lebrun-Frenay C,
Lechner-Scott J,
Lee MH,
Leone MA,
Leppä V,
Liberatore G,
Lie BA,
Lill CM,
Lindén M,
Link J,
Luessi F,
Lycke J,
Macciardi F,
Männistö S,
Manrique CP,
Martin R,
Martinelli V,
Mason D,
Mazibrada G,
McCabe C,
Mero IL,
Mescheriakova J,
Moutsianas L,
Myhr KM,
Nagels G,
Nicholas R,
Nilsson P,
Piehl F,
Pirinen M,
Price SE,
Quach H,
Reunanen M,
Robberecht W,
Robertson NP,
Rodegher M,
Rog D,
Salvetti M,
Schnetz-Boutaud NC,
Sellebjerg F,
Selter RC,
Schaefer C,
Shaunak S,
Shen L,
Shields S,
Siffrin V,
Slee M,
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Sorosina M,
Sospedra M,
Spurkland A,
Strange A,
Sundqvist E,
Thijs V,
Thorpe J,
Ticca A,
Tienari P,
van Duijn C,
Visser EM,
Vucic S,
Westerlind H,
Wiley JS,
Wilkins A,
Wilson JF,
Winkelmann J,
Zajicek J,
Zindler E,
Haines JL,
Pericak-Vance MA,
Ivinson AJ,
Stewart G,
Hafler D,
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Compston A,
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McCauley JL
International Multiple Sclerosis Genetics Consortium (IMSGC) · Wellcome Trust Case Control Consortium 2 (WTCCC2) 외 컨소시엄 1곳
Nature genetics · 2013 · PMID 24076602 · open access
페이지 12개+
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Tedja MS,
Wojciechowski R,
Hysi PG,
Eriksson N,
Furlotte NA,
Verhoeven VJM,
Iglesias AI,
Meester-Smoor MA,
Tompson SW,
Fan Q,
Khawaja AP,
Cheng CY
외 86명 — 모두 보기
Höhn R,
Yamashiro K,
Wenocur A,
Grazal C,
Haller T,
Metspalu A,
Wedenoja J,
Jonas JB,
Wang YX,
Xie J,
Mitchell P,
Foster PJ,
Klein BEK,
Klein R,
Paterson AD,
Hosseini SM,
Shah RL,
Williams C,
Teo YY,
Tham YC,
Gupta P,
Zhao W,
Shi Y,
Saw WY,
Tai ES,
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Huffman JE,
Polašek O,
Hayward C,
Bencic G,
Rudan I,
Wilson JF,
Joshi PK,
Tsujikawa A,
Matsuda F,
Whisenhunt KN,
Zeller T,
van der Spek PJ,
Haak R,
Meijers-Heijboer H,
van Leeuwen EM,
Iyengar SK,
Lass JH,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Vingerling JR,
Lehtimäki T,
Raitakari OT,
Biino G,
Concas MP,
Schwantes-An TH,
Igo RP Jr,
Cuellar-Partida G,
Martin NG,
Craig JE,
Gharahkhani P,
Williams KM,
Nag A,
Rahi JS,
Cumberland PM,
Delcourt C,
Bellenguez C,
Ried JS,
Bergen AA,
Meitinger T,
Gieger C,
Wong TY,
Hewitt AW,
Mackey DA,
Simpson CL,
Pfeiffer N,
Pärssinen O,
Baird PN,
Vitart V,
Amin N,
van Duijn CM,
Bailey-Wilson JE,
Young TL,
Saw SM,
Stambolian D,
MacGregor S,
Guggenheim JA,
Tung JY,
Hammond CJ,
Klaver CCW
CREAM Consortium · 23andMe Research Team 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 29808027 · 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,
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Capra R,
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Celius EG,
Cepok S,
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Clerget-Darpoux F,
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Comi G,
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Cournu-Rebeix I,
Cox MB,
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Compston A
International Multiple Sclerosis Genetics Consortium · Wellcome Trust Case Control Consortium 2
Nature · 2011 · PMID 21833088 · open access
페이지 11개
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Ripke S,
O'Dushlaine C,
Chambert K,
Moran JL,
Kähler AK,
Akterin S,
Bergen SE,
Collins AL,
Crowley JJ,
Fromer M,
Kim Y,
Lee SH
외 176명 — 모두 보기
Lee SH,
Magnusson PK,
Sanchez N,
Stahl EA,
Williams S,
Wray NR,
Xia K,
Bettella F,
Borglum AD,
Bulik-Sullivan BK,
Cormican P,
Craddock N,
de Leeuw C,
Durmishi N,
Gill M,
Golimbet V,
Hamshere ML,
Holmans P,
Hougaard DM,
Kendler KS,
Lin K,
Morris DW,
Mors O,
Mortensen PB,
Neale BM,
O'Neill FA,
Owen MJ,
Milovancevic MP,
Posthuma D,
Powell J,
Richards AL,
Riley BP,
Ruderfer D,
Rujescu D,
Sigurdsson E,
Silagadze T,
Smit AB,
Stefansson H,
Steinberg S,
Suvisaari J,
Tosato S,
Verhage M,
Walters JT,
Levinson DF,
Gejman PV,
Kendler KS,
Laurent C,
Mowry BJ,
O'Donovan MC,
Owen MJ,
Pulver AE,
Riley BP,
Schwab SG,
Wildenauer DB,
Dudbridge F,
Holmans P,
Shi J,
Albus M,
Alexander M,
Campion D,
Cohen D,
Dikeos D,
Duan J,
Eichhammer P,
Godard S,
Hansen M,
Lerer FB,
Liang KY,
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Nestadt G,
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Papadimitriou GN,
Ribble R,
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Silverman JM,
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Bakker S,
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Crespo-Facorro B,
Hall J,
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Mata I,
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Band G,
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Sklar P,
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Multicenter Genetic Studies of Schizophrenia Consortium · Psychosis Endophenotypes International Consortium 외 컨소시엄 1곳
Nature genetics · 2013 · PMID 23974872 · open access
페이지 10개
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
Fan Q,
Verhoeven VJ,
Wojciechowski R,
Barathi VA,
Hysi PG,
Guggenheim JA,
Höhn R,
Vitart V,
Khawaja AP,
Yamashiro K,
Hosseini SM,
Lehtimäki T
외 142명 — 모두 보기
Lu Y,
Haller T,
Xie J,
Delcourt C,
Pirastu M,
Wedenoja J,
Gharahkhani P,
Venturini C,
Miyake M,
Hewitt AW,
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Mazur J,
Huffman JE,
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Polasek O,
Campbell H,
Rudan I,
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Joshi PK,
McMahon G,
St Pourcain B,
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Mirshahi A,
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Bellenguez C,
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Raitakari O,
Kähönen M,
Seppala I,
Zeller T,
Meitinger T,
Ried JS,
Gieger C,
Portas L,
van Leeuwen EM,
Amin N,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
Vingerling JR,
Wang YX,
Wang X,
Tai-Hui Boh E,
Ikram MK,
Sabanayagam C,
Gupta P,
Tan V,
Zhou L,
Ho CE,
Lim W,
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Siantar R,
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Vithana E,
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Khor CC,
Hayward C,
Luben RN,
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Metspalu A,
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Young TL,
He M,
Pärssinen O,
van Duijn CM,
Jin Wang J,
Williams C,
Jonas JB,
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Mackey DA,
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Wong TY,
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Cheng CY,
Hammond CJ,
Klaver CC,
Saw SM,
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Korobelnik JF,
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Craig JE,
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Lass JH,
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Zhao JH,
Khaw KT,
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Rantanen T,
Kaprio J,
Pang CP,
Chen LJ,
Tam PO,
Jhanji V,
Young AL,
Döring A,
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Cotch MF,
Li X,
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Mizuki N,
Meguro A,
Mäkelä KM
Consortium for Refractive Error and Myopia
Nature communications · 2016 · PMID 27020472 · open access
페이지 10개
New insights into the genetic etiology of Alzheimer's disease and related dementias
Bellenguez C,
Küçükali F,
Jansen IE,
Kleineidam L,
Moreno-Grau S,
Amin N,
Naj AC,
Campos-Martin R,
Grenier-Boley B,
Andrade V,
Holmans PA,
Boland A
외 391명 — 모두 보기
Damotte V,
van der Lee SJ,
Costa MR,
Kuulasmaa T,
Yang Q,
de Rojas I,
Bis JC,
Yaqub A,
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페이지 3개
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페이지 2개
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외 39명 — 모두 보기
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페이지 1개
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ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
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