연구자에게
내 논문이 여기 있나요?
논문 2,657편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Strange A에 대해
7건.
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
Tsoi LC,
Spain SL,
Knight J,
Ellinghaus E,
Stuart PE,
Capon F,
Ding J,
Li Y,
Tejasvi T,
Gudjonsson JE,
Kang HM,
Allen MH
외 53명 — 모두 보기
McManus R,
Novelli G,
Samuelsson L,
Schalkwijk J,
Ståhle M,
Burden AD,
Smith CH,
Cork MJ,
Estivill X,
Bowcock AM,
Krueger GG,
Weger W,
Worthington J,
Tazi-Ahnini R,
Nestle FO,
Hayday A,
Hoffmann P,
Winkelmann J,
Wijmenga C,
Langford C,
Edkins S,
Andrews R,
Blackburn H,
Strange A,
Band G,
Pearson RD,
Vukcevic D,
Spencer CC,
Deloukas P,
Mrowietz U,
Schreiber S,
Weidinger S,
Koks S,
Kingo K,
Esko T,
Metspalu A,
Lim HW,
Voorhees JJ,
Weichenthal M,
Wichmann HE,
Chandran V,
Rosen CF,
Rahman P,
Gladman DD,
Griffiths CE,
Reis A,
Kere J,
Nair RP,
Franke A,
Barker JN,
Abecasis GR,
Elder JT,
Trembath RC
Collaborative Association Study of Psoriasis (CASP) · Genetic Analysis of Psoriasis Consortium 외 컨소시엄 2곳
Nature genetics · 2012 · PMID 23143594 · open access
페이지 12개+
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,
Sorensen PS,
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,
Hauser SL,
Compston A,
McVean G,
De Jager P,
Sawcer SJ,
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+
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
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,
Maier W,
Mallet J,
Nertney DA,
Nestadt G,
Norton N,
O'Neill FA,
Papadimitriou GN,
Ribble R,
Sanders AR,
Silverman JM,
Walsh D,
Williams NM,
Wormley B,
Arranz MJ,
Bakker S,
Bender S,
Bramon E,
Collier D,
Crespo-Facorro B,
Hall J,
Iyegbe C,
Jablensky A,
Kahn RS,
Kalaydjieva L,
Lawrie S,
Lewis CM,
Lin K,
Linszen DH,
Mata I,
McIntosh A,
Murray RM,
Ophoff RA,
Powell J,
Rujescu D,
Van Os J,
Walshe M,
Weisbrod M,
Wiersma D,
Donnelly P,
Barroso I,
Blackwell JM,
Bramon E,
Brown MA,
Casas JP,
Corvin AP,
Deloukas P,
Duncanson A,
Jankowski J,
Markus HS,
Mathew CG,
Palmer CN,
Plomin R,
Rautanen A,
Sawcer SJ,
Trembath RC,
Viswanathan AC,
Wood NW,
Spencer CC,
Band G,
Bellenguez C,
Freeman C,
Hellenthal G,
Giannoulatou E,
Pirinen M,
Pearson RD,
Strange A,
Su Z,
Vukcevic D,
Donnelly P,
Langford C,
Hunt SE,
Edkins S,
Gwilliam R,
Blackburn H,
Bumpstead SJ,
Dronov S,
Gillman M,
Gray E,
Hammond N,
Jayakumar A,
McCann OT,
Liddle J,
Potter SC,
Ravindrarajah R,
Ricketts M,
Tashakkori-Ghanbaria A,
Waller MJ,
Weston P,
Widaa S,
Whittaker P,
Barroso I,
Deloukas P,
Mathew CG,
Blackwell JM,
Brown MA,
Corvin AP,
McCarthy MI,
Spencer CC,
Bramon E,
Corvin AP,
O'Donovan MC,
Stefansson K,
Scolnick E,
Purcell S,
McCarroll SA,
Sklar P,
Hultman CM,
Sullivan PF
Multicenter Genetic Studies of Schizophrenia Consortium · Psychosis Endophenotypes International Consortium 외 컨소시엄 1곳
Nature genetics · 2013 · PMID 23974872 · open access
페이지 10개
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility
Evans DM,
Spencer CC,
Pointon JJ,
Su Z,
Harvey D,
Kochan G,
Oppermann U,
Dilthey A,
Pirinen M,
Stone MA,
Appleton L,
Moutsianas L
외 81명 — 모두 보기
Leslie S,
Wordsworth T,
Kenna TJ,
Karaderi T,
Thomas GP,
Ward MM,
Weisman MH,
Farrar C,
Bradbury LA,
Danoy P,
Inman RD,
Maksymowych W,
Gladman D,
Rahman P,
Morgan A,
Marzo-Ortega H,
Bowness P,
Gaffney K,
Gaston JS,
Smith M,
Bruges-Armas J,
Couto AR,
Sorrentino R,
Paladini F,
Ferreira MA,
Xu H,
Liu Y,
Jiang L,
Lopez-Larrea C,
Díaz-Peña R,
López-Vázquez A,
Zayats T,
Band G,
Bellenguez C,
Blackburn H,
Blackwell JM,
Bramon E,
Bumpstead SJ,
Casas JP,
Corvin A,
Craddock N,
Deloukas P,
Dronov S,
Duncanson A,
Edkins S,
Freeman C,
Gillman M,
Gray E,
Gwilliam R,
Hammond N,
Hunt SE,
Jankowski J,
Jayakumar A,
Langford C,
Liddle J,
Markus HS,
Mathew CG,
McCann OT,
McCarthy MI,
Palmer CN,
Peltonen L,
Plomin R,
Potter SC,
Rautanen A,
Ravindrarajah R,
Ricketts M,
Samani N,
Sawcer SJ,
Strange A,
Trembath RC,
Viswanathan AC,
Waller M,
Weston P,
Whittaker P,
Widaa S,
Wood NW,
McVean G,
Reveille JD,
Wordsworth BP,
Brown MA,
Donnelly P
Spondyloarthritis Research Consortium of Canada (SPARCC) · Australo-Anglo-American Spondyloarthritis Consortium (TASC) 외 컨소시엄 1곳
Nature genetics · 2011 · PMID 21743469
페이지 3개
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes
Zhou K,
Bellenguez C,
Spencer CC,
Bennett AJ,
Coleman RL,
Tavendale R,
Hawley SA,
Donnelly LA,
Schofield C,
Groves CJ,
Burch L,
Carr F
외 38명 — 모두 보기
Strange A,
Freeman C,
Blackwell JM,
Bramon E,
Brown MA,
Casas JP,
Corvin A,
Craddock N,
Deloukas P,
Dronov S,
Duncanson A,
Edkins S,
Gray E,
Hunt S,
Jankowski J,
Langford C,
Markus HS,
Mathew CG,
Plomin R,
Rautanen A,
Sawcer SJ,
Samani NJ,
Trembath R,
Viswanathan AC,
Wood NW,
Harries LW,
Hattersley AT,
Doney AS,
Colhoun H,
Morris AD,
Sutherland C,
Hardie DG,
Peltonen L,
McCarthy MI,
Holman RR,
Palmer CN,
Donnelly P,
Pearson ER
GoDARTS and UKPDS Diabetes Pharmacogenetics Study Group · Wellcome Trust Case Control Consortium 2 외 컨소시엄 1곳
Nature genetics · 2011 · PMID 21186350 · open access
페이지 2개
Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis
Fakiola M,
Strange A,
Cordell HJ,
Miller EN,
Pirinen M,
Su Z,
Mishra A,
Mehrotra S,
Monteiro GR,
Band G,
Bellenguez C,
Dronov S
외 39명 — 모두 보기
Edkins S,
Freeman C,
Giannoulatou E,
Gray E,
Hunt SE,
Lacerda HG,
Langford C,
Pearson R,
Pontes NN,
Rai M,
Singh SP,
Smith L,
Sousa O,
Vukcevic D,
Bramon E,
Brown MA,
Casas JP,
Corvin A,
Duncanson A,
Jankowski J,
Markus HS,
Mathew CG,
Palmer CN,
Plomin R,
Rautanen A,
Sawcer SJ,
Trembath RC,
Viswanathan AC,
Wood NW,
Wilson ME,
Deloukas P,
Peltonen L,
Christiansen F,
Witt C,
Jeronimo SM,
Sundar S,
Spencer CC,
Blackwell JM,
Donnelly P
LeishGEN Consortium · Wellcome Trust Case Control Consortium 2
Nature genetics · 2013 · PMID 23291585 · open access
페이지 1개
이 목록에 대한 질문
제 논문이 왜 여기 있습니까? 허락한 적이 없습니다.
논문의 내용은 여기에 전혀 옮겨져 있지 않습니다. 이 페이지가 기록하는 것은 MyGeneLog™의
어떤 페이지가 귀하의 연구를 인용하고 있다는 사실과 PubMed의 원문 링크뿐이며, 그것이 곧
인용입니다. 제목과 저자 목록은 도서관 목록이 쓰는 것과 같은 공개 기록인 Europe PMC에서
가져옵니다.
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.