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.
Anderson C에 대해
19건.
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+
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
Anderson CA,
Boucher G,
Lees CW,
Franke A,
D'Amato M,
Taylor KD,
Lee JC,
Goyette P,
Imielinski M,
Latiano A,
Lagacé C,
Scott R
외 101명 — 모두 보기
Amininejad L,
Bumpstead S,
Baidoo L,
Baldassano RN,
Barclay M,
Bayless TM,
Brand S,
Büning C,
Colombel JF,
Denson LA,
De Vos M,
Dubinsky M,
Edwards C,
Ellinghaus D,
Fehrmann RS,
Floyd JA,
Florin T,
Franchimont D,
Franke L,
Georges M,
Glas J,
Glazer NL,
Guthery SL,
Haritunians T,
Hayward NK,
Hugot JP,
Jobin G,
Laukens D,
Lawrance I,
Lémann M,
Levine A,
Libioulle C,
Louis E,
McGovern DP,
Milla M,
Montgomery GW,
Morley KI,
Mowat C,
Ng A,
Newman W,
Ophoff RA,
Papi L,
Palmieri O,
Peyrin-Biroulet L,
Panés J,
Phillips A,
Prescott NJ,
Proctor DD,
Roberts R,
Russell R,
Rutgeerts P,
Sanderson J,
Sans M,
Schumm P,
Seibold F,
Sharma Y,
Simms LA,
Seielstad M,
Steinhart AH,
Targan SR,
van den Berg LH,
Vatn M,
Verspaget H,
Walters T,
Wijmenga C,
Wilson DC,
Westra HJ,
Xavier RJ,
Zhao ZZ,
Ponsioen CY,
Andersen V,
Torkvist L,
Gazouli M,
Anagnou NP,
Karlsen TH,
Kupcinskas L,
Sventoraityte J,
Mansfield JC,
Kugathasan S,
Silverberg MS,
Halfvarson J,
Rotter JI,
Mathew CG,
Griffiths AM,
Gearry R,
Ahmad T,
Brant SR,
Chamaillard M,
Satsangi J,
Cho JH,
Schreiber S,
Daly MJ,
Barrett JC,
Parkes M,
Annese V,
Hakonarson H,
Radford-Smith G,
Duerr RH,
Vermeire S,
Weersma RK,
Rioux JD
Nature genetics · 2011 · PMID 21297633 · open access
페이지 12개+
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Jostins L,
Ripke S,
Weersma RK,
Duerr RH,
McGovern DP,
Hui KY,
Lee JC,
Schumm LP,
Sharma Y,
Anderson CA,
Essers J,
Mitrovic M
외 94명 — 모두 보기
Ning K,
Cleynen I,
Theatre E,
Spain SL,
Raychaudhuri S,
Goyette P,
Wei Z,
Abraham C,
Achkar JP,
Ahmad T,
Amininejad L,
Ananthakrishnan AN,
Andersen V,
Andrews JM,
Baidoo L,
Balschun T,
Bampton PA,
Bitton A,
Boucher G,
Brand S,
Büning C,
Cohain A,
Cichon S,
D'Amato M,
De Jong D,
Devaney KL,
Dubinsky M,
Edwards C,
Ellinghaus D,
Ferguson LR,
Franchimont D,
Fransen K,
Gearry R,
Georges M,
Gieger C,
Glas J,
Haritunians T,
Hart A,
Hawkey C,
Hedl M,
Hu X,
Karlsen TH,
Kupcinskas L,
Kugathasan S,
Latiano A,
Laukens D,
Lawrance IC,
Lees CW,
Louis E,
Mahy G,
Mansfield J,
Morgan AR,
Mowat C,
Newman W,
Palmieri O,
Ponsioen CY,
Potocnik U,
Prescott NJ,
Regueiro M,
Rotter JI,
Russell RK,
Sanderson JD,
Sans M,
Satsangi J,
Schreiber S,
Simms LA,
Sventoraityte J,
Targan SR,
Taylor KD,
Tremelling M,
Verspaget HW,
De Vos M,
Wijmenga C,
Wilson DC,
Winkelmann J,
Xavier RJ,
Zeissig S,
Zhang B,
Zhang CK,
Zhao H,
Silverberg MS,
Annese V,
Hakonarson H,
Brant SR,
Radford-Smith G,
Mathew CG,
Rioux JD,
Schadt EE,
Daly MJ,
Franke A,
Parkes M,
Vermeire S,
Barrett JC,
Cho JH
International IBD Genetics Consortium (IIBDGC)
Nature · 2012 · PMID 23128233 · 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+
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
Liu JZ,
van Sommeren S,
Huang H,
Ng SC,
Alberts R,
Takahashi A,
Ripke S,
Lee JC,
Jostins L,
Shah T,
Abedian S,
Cheon JH
외 28명 — 모두 보기
Cho J,
Dayani NE,
Franke L,
Fuyuno Y,
Hart A,
Juyal RC,
Juyal G,
Kim WH,
Morris AP,
Poustchi H,
Newman WG,
Midha V,
Orchard TR,
Vahedi H,
Sood A,
Sung JY,
Malekzadeh R,
Westra HJ,
Yamazaki K,
Yang SK,
Barrett JC,
Alizadeh BZ,
Parkes M,
Bk T,
Daly MJ,
Kubo M,
Anderson CA,
Weersma RK
International Multiple Sclerosis Genetics Consortium · International IBD Genetics Consortium
Nature genetics · 2015 · PMID 26192919
페이지 12개+
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease
de Lange KM,
Moutsianas L,
Lee JC,
Lamb CA,
Luo Y,
Kennedy NA,
Jostins L,
Rice DL,
Gutierrez-Achury J,
Ji SG,
Heap G,
Nimmo ER
외 20명 — 모두 보기
Edwards C,
Henderson P,
Mowat C,
Sanderson J,
Satsangi J,
Simmons A,
Wilson DC,
Tremelling M,
Hart A,
Mathew CG,
Newman WG,
Parkes M,
Lees CW,
Uhlig H,
Hawkey C,
Prescott NJ,
Ahmad T,
Mansfield JC,
Anderson CA,
Barrett JC
Nature genetics · 2017 · PMID 28067908 · open access
페이지 12개+
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
Christophersen IE,
Rienstra M,
Roselli C,
Yin X,
Geelhoed B,
Barnard J,
Lin H,
Arking DE,
Smith AV,
Albert CM,
Chaffin M,
Tucker NR
외 150명 — 모두 보기
Li M,
Klarin D,
Bihlmeyer NA,
Low SK,
Weeke PE,
Müller-Nurasyid M,
Smith JG,
Brody JA,
Niemeijer MN,
Dörr M,
Trompet S,
Huffman J,
Gustafsson S,
Schurmann C,
Kleber ME,
Lyytikäinen LP,
Seppälä I,
Malik R,
Horimoto ARVR,
Perez M,
Sinisalo J,
Aeschbacher S,
Thériault S,
Yao J,
Radmanesh F,
Weiss S,
Teumer A,
Choi SH,
Weng LC,
Clauss S,
Deo R,
Rader DJ,
Shah SH,
Sun A,
Hopewell JC,
Debette S,
Chauhan G,
Yang Q,
Worrall BB,
Paré G,
Kamatani Y,
Hagemeijer YP,
Verweij N,
Siland JE,
Kubo M,
Smith JD,
Van Wagoner DR,
Bis JC,
Perz S,
Psaty BM,
Ridker PM,
Magnani JW,
Harris TB,
Launer LJ,
Shoemaker MB,
Padmanabhan S,
Haessler J,
Bartz TM,
Waldenberger M,
Lichtner P,
Arendt M,
Krieger JE,
Kähönen M,
Risch L,
Mansur AJ,
Peters A,
Smith BH,
Lind L,
Scott SA,
Lu Y,
Bottinger EB,
Hernesniemi J,
Lindgren CM,
Wong JA,
Huang J,
Eskola M,
Morris AP,
Ford I,
Reiner AP,
Delgado G,
Chen LY,
Chen YI,
Sandhu RK,
Li M,
Boerwinkle E,
Eisele L,
Lannfelt L,
Rost N,
Anderson CD,
Taylor KD,
Campbell A,
Magnusson PK,
Porteous D,
Hocking LJ,
Vlachopoulou E,
Pedersen NL,
Nikus K,
Orho-Melander M,
Hamsten A,
Heeringa J,
Denny JC,
Kriebel J,
Darbar D,
Newton-Cheh C,
Shaffer C,
Macfarlane PW,
Heilmann-Heimbach S,
Almgren P,
Huang PL,
Sotoodehnia N,
Soliman EZ,
Uitterlinden AG,
Hofman A,
Franco OH,
Völker U,
Jöckel KH,
Sinner MF,
Lin HJ,
Guo X,
Dichgans M,
Ingelsson E,
Kooperberg C,
Melander O,
Loos RJF,
Laurikka J,
Conen D,
Rosand J,
van der Harst P,
Lokki ML,
Kathiresan S,
Pereira A,
Jukema JW,
Hayward C,
Rotter JI,
März W,
Lehtimäki T,
Stricker BH,
Chung MK,
Felix SB,
Gudnason V,
Alonso A,
Roden DM,
Kääb S,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Tanaka T,
Lunetta KL,
Lubitz SA,
Ellinor PT
METASTROKE Consortium of the ISGC · Neurology Working Group of the CHARGE Consortium 외 컨소시엄 1곳
Nature genetics · 2017 · PMID 28416818
페이지 12개+
Multi-ethnic genome-wide association study for atrial fibrillation
Roselli C,
Chaffin MD,
Weng LC,
Aeschbacher S,
Ahlberg G,
Albert CM,
Almgren P,
Alonso A,
Anderson CD,
Aragam KG,
Arking DE,
Barnard J
외 206명 — 모두 보기
Bartz TM,
Benjamin EJ,
Bihlmeyer NA,
Bis JC,
Bloom HL,
Boerwinkle E,
Bottinger EB,
Brody JA,
Calkins H,
Campbell A,
Cappola TP,
Carlquist J,
Chasman DI,
Chen LY,
Chen YI,
Choi EK,
Choi SH,
Christophersen IE,
Chung MK,
Cole JW,
Conen D,
Cook J,
Crijns HJ,
Cutler MJ,
Damrauer SM,
Daniels BR,
Darbar D,
Delgado G,
Denny JC,
Dichgans M,
Dörr M,
Dudink EA,
Dudley SC,
Esa N,
Esko T,
Eskola M,
Fatkin D,
Felix SB,
Ford I,
Franco OH,
Geelhoed B,
Grewal RP,
Gudnason V,
Guo X,
Gupta N,
Gustafsson S,
Gutmann R,
Hamsten A,
Harris TB,
Hayward C,
Heckbert SR,
Hernesniemi J,
Hocking LJ,
Hofman A,
Horimoto ARVR,
Huang J,
Huang PL,
Huffman J,
Ingelsson E,
Ipek EG,
Ito K,
Jimenez-Conde J,
Johnson R,
Jukema JW,
Kääb S,
Kähönen M,
Kamatani Y,
Kane JP,
Kastrati A,
Kathiresan S,
Katschnig-Winter P,
Kavousi M,
Kessler T,
Kietselaer BL,
Kirchhof P,
Kleber ME,
Knight S,
Krieger JE,
Kubo M,
Launer LJ,
Laurikka J,
Lehtimäki T,
Leineweber K,
Lemaitre RN,
Li M,
Lim HE,
Lin HJ,
Lin H,
Lind L,
Lindgren CM,
Lokki ML,
London B,
Loos RJF,
Low SK,
Lu Y,
Lyytikäinen LP,
Macfarlane PW,
Magnusson PK,
Mahajan A,
Malik R,
Mansur AJ,
Marcus GM,
Margolin L,
Margulies KB,
März W,
McManus DD,
Melander O,
Mohanty S,
Montgomery JA,
Morley MP,
Morris AP,
Müller-Nurasyid M,
Natale A,
Nazarian S,
Neumann B,
Newton-Cheh C,
Niemeijer MN,
Nikus K,
Nilsson P,
Noordam R,
Oellers H,
Olesen MS,
Orho-Melander M,
Padmanabhan S,
Pak HN,
Paré G,
Pedersen NL,
Pera J,
Pereira A,
Porteous D,
Psaty BM,
Pulit SL,
Pullinger CR,
Rader DJ,
Refsgaard L,
Ribasés M,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rosand J,
Rosenberg MA,
Rost N,
Rotter JI,
Saba S,
Sandhu RK,
Schnabel RB,
Schramm K,
Schunkert H,
Schurman C,
Scott SA,
Seppälä I,
Shaffer C,
Shah S,
Shalaby AA,
Shim J,
Shoemaker MB,
Siland JE,
Sinisalo J,
Sinner MF,
Slowik A,
Smith AV,
Smith BH,
Smith JG,
Smith JD,
Smith NL,
Soliman EZ,
Sotoodehnia N,
Stricker BH,
Sun A,
Sun H,
Svendsen JH,
Tanaka T,
Tanriverdi K,
Taylor KD,
Teder-Laving M,
Teumer A,
Thériault S,
Trompet S,
Tucker NR,
Tveit A,
Uitterlinden AG,
Van Der Harst P,
Van Gelder IC,
Van Wagoner DR,
Verweij N,
Vlachopoulou E,
Völker U,
Wang B,
Weeke PE,
Weijs B,
Weiss R,
Weiss S,
Wells QS,
Wiggins KL,
Wong JA,
Woo D,
Worrall BB,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Lubitz SA,
Lunetta KL,
Ellinor PT
Nature genetics · 2018 · PMID 29892015
페이지 12개+
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Roselli C,
Surakka I,
Olesen MS,
Sveinbjornsson G,
Marston NA,
Choi SH,
Holm H,
Chaffin M,
Gudbjartsson D,
Hill MC,
Aegisdottir H,
Albert CM
외 145명 — 모두 보기
Alonso A,
Anderson CD,
Arking DE,
Arnar DO,
Barnard J,
Benjamin EJ,
Braunwald E,
Brumpton B,
Campbell A,
Chami N,
Chasman DI,
Cho K,
Choi EK,
Christophersen IE,
Chung MK,
Conen D,
Crijns HJ,
Cutler MJ,
Czuba T,
Damrauer SM,
Dichgans M,
Dörr M,
Dudink E,
Duong T,
Erikstrup C,
Esko T,
Fatkin D,
Faul JD,
Ferreira M,
Freitag DF,
Ganesh SK,
Gaziano JM,
Geelhoed B,
Ghouse J,
Gieger C,
Giulianini F,
Graham SE,
Gudnason V,
Guo X,
Haggerty C,
Hayward C,
Heckbert SR,
Hveem K,
Ito K,
Johnson R,
Jukema JW,
Jurgens SJ,
Kääb S,
Kane JP,
Kany S,
Kardia SLR,
Kavousi M,
Khurshid S,
Kamanu FK,
Kirchhof P,
Kleber ME,
Knight S,
Komuro I,
Krieger JE,
Launer LJ,
Li D,
Lin H,
Lin HJ,
Loos RJF,
Lotta L,
Lubitz SA,
Lunetta KL,
Macfarlane PW,
Magnusson PKE,
Malik R,
Mantineo H,
Marcus GM,
März W,
McManus DD,
Melander O,
Melloni GEM,
Meyre PB,
Miyazawa K,
Mohanty S,
Monfort LM,
Müller-Nurasyid M,
Nafissi NA,
Natale A,
Nazarian S,
Ostrowski SR,
Pak HN,
Pang S,
Pedersen OB,
Pedersen NL,
Pereira AC,
Pirruccello JP,
Preuss M,
Psaty BM,
Pullinger CR,
Rader DJ,
Rämö JT,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rotter JI,
Sabatine MS,
Schunkert H,
Shah SH,
Shim J,
Shoemaker MB,
Simonson B,
Sinner MF,
Smit RAJ,
Smith JA,
Smith NL,
Smith JG,
Soliman EZ,
Sørensen E,
Sotoodehnia N,
Strbian D,
Stricker BH,
Teder-Laving M,
Sun YV,
Thériault S,
Thorolfsdottir RB,
Thorsteinsdottir U,
Tveit A,
van der Harst P,
van Meurs J,
Wang B,
Weiss S,
Wells QS,
Weng LC,
Wilson PW,
Xiao L,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Zhao W,
Zhao W,
Zhou X,
Zöllner S,
Ruff CT,
Bundgaard H,
Willer C,
Stefansson K,
Ellinor PT
BioBank Japan Project · Regeneron Genetics Center 외 컨소시엄 1곳
Nature genetics · 2025 · PMID 40050429
페이지 12개+
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
Barrett JC,
Hansoul S,
Nicolae DL,
Cho JH,
Duerr RH,
Rioux JD,
Brant SR,
Silverberg MS,
Taylor KD,
Barmada MM,
Bitton A,
Dassopoulos T
외 49명 — 모두 보기
Datta LW,
Green T,
Griffiths AM,
Kistner EO,
Murtha MT,
Regueiro MD,
Rotter JI,
Schumm LP,
Steinhart AH,
Targan SR,
Xavier RJ,
Libioulle C,
Sandor C,
Lathrop M,
Belaiche J,
Dewit O,
Gut I,
Heath S,
Laukens D,
Mni M,
Rutgeerts P,
Van Gossum A,
Zelenika D,
Franchimont D,
Hugot JP,
de Vos M,
Vermeire S,
Louis E,
Cardon LR,
Anderson CA,
Drummond H,
Nimmo E,
Ahmad T,
Prescott NJ,
Onnie CM,
Fisher SA,
Marchini J,
Ghori J,
Bumpstead S,
Gwilliam R,
Tremelling M,
Deloukas P,
Mansfield J,
Jewell D,
Satsangi J,
Mathew CG,
Parkes M,
Georges M,
Daly MJ
NIDDK IBD Genetics Consortium · Belgian-French IBD Consortium 외 컨소시엄 1곳
Nature genetics · 2008 · PMID 18587394
페이지 11개
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis
Mells GF,
Floyd JA,
Morley KI,
Cordell HJ,
Franklin CS,
Shin SY,
Heneghan MA,
Neuberger JM,
Donaldson PT,
Day DB,
Ducker SJ,
Muriithi AW
외 8명 — 모두 보기
UK PBC Consortium · Wellcome Trust Case Control Consortium 3
Nature genetics · 2011 · PMID 21399635 · open access
페이지 11개
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease
Ji SG,
Juran BD,
Mucha S,
Folseraas T,
Jostins L,
Melum E,
Kumasaka N,
Atkinson EJ,
Schlicht EM,
Liu JZ,
Shah T,
Gutierrez-Achury J
외 58명 — 모두 보기
Boberg KM,
Bergquist A,
Vermeire S,
Eksteen B,
Durie PR,
Farkkila M,
Müller T,
Schramm C,
Sterneck M,
Weismüller TJ,
Gotthardt DN,
Ellinghaus D,
Braun F,
Teufel A,
Laudes M,
Lieb W,
Jacobs G,
Beuers U,
Weersma RK,
Wijmenga C,
Marschall HU,
Milkiewicz P,
Pares A,
Kontula K,
Chazouillères O,
Invernizzi P,
Goode E,
Spiess K,
Moore C,
Sambrook J,
Ouwehand WH,
Roberts DJ,
Danesh J,
Floreani A,
Gulamhusein AF,
Eaton JE,
Schreiber S,
Coltescu C,
Bowlus CL,
Luketic VA,
Odin JA,
Chopra KB,
Kowdley KV,
Chalasani N,
Manns MP,
Srivastava B,
Mells G,
Sandford RN,
Alexander G,
Gaffney DJ,
Chapman RW,
Hirschfield GM,
de Andrade M,
Rushbrook SM,
Franke A,
Karlsen TH,
Lazaridis KN,
Anderson CA
UK-PSC Consortium · International IBD Genetics Consortium 외 컨소시엄 1곳
Nature genetics · 2017 · PMID 27992413 · open access
페이지 8개
Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis
Liu JZ,
Almarri MA,
Gaffney DJ,
Mells GF,
Jostins L,
Cordell HJ,
Ducker SJ,
Day DB,
Heneghan MA,
Neuberger JM,
Donaldson PT,
Bathgate AJ
외 7명 — 모두 보기
UK Primary Biliary Cirrhosis (PBC) Consortium · Wellcome Trust Case Control Consortium 3
Nature genetics · 2012 · PMID 22961000 · open access
페이지 6개
Stroke genetics informs drug discovery and risk prediction across ancestries
Mishra A,
Malik R,
Hachiya T,
Jürgenson T,
Namba S,
Posner DC,
Kamanu FK,
Koido M,
Le Grand Q,
Shi M,
He Y,
Georgakis MK
외 175명 — 모두 보기
Caro I,
Krebs K,
Liaw YC,
Vaura FC,
Lin K,
Winsvold BS,
Srinivasasainagendra V,
Parodi L,
Bae HJ,
Chauhan G,
Chong MR,
Tomppo L,
Akinyemi R,
Roshchupkin GV,
Habib N,
Jee YH,
Thomassen JQ,
Abedi V,
Cárcel-Márquez J,
Nygaard M,
Leonard HL,
Yang C,
Yonova-Doing E,
Knol MJ,
Lewis AJ,
Judy RL,
Ago T,
Amouyel P,
Armstrong ND,
Bakker MK,
Bartz TM,
Bennett DA,
Bis JC,
Bordes C,
Børte S,
Cain A,
Ridker PM,
Cho K,
Chen Z,
Cruchaga C,
Cole JW,
de Jager PL,
de Cid R,
Endres M,
Ferreira LE,
Geerlings MI,
Gasca NC,
Gudnason V,
Hata J,
He J,
Heath AK,
Ho YL,
Havulinna AS,
Hopewell JC,
Hyacinth HI,
Inouye M,
Jacob MA,
Jeon CE,
Jern C,
Kamouchi M,
Keene KL,
Kitazono T,
Kittner SJ,
Konuma T,
Kumar A,
Lacaze P,
Launer LJ,
Lee KJ,
Lepik K,
Li J,
Li L,
Manichaikul A,
Markus HS,
Marston NA,
Meitinger T,
Mitchell BD,
Montellano FA,
Morisaki T,
Mosley TH,
Nalls MA,
Nordestgaard BG,
O'Donnell MJ,
Okada Y,
Onland-Moret NC,
Ovbiagele B,
Peters A,
Psaty BM,
Rich SS,
Rosand J,
Sabatine MS,
Sacco RL,
Saleheen D,
Sandset EC,
Salomaa V,
Sargurupremraj M,
Sasaki M,
Satizabal CL,
Schmidt CO,
Shimizu A,
Smith NL,
Sloane KL,
Sutoh Y,
Sun YV,
Tanno K,
Tiedt S,
Tatlisumak T,
Torres-Aguila NP,
Tiwari HK,
Trégouët DA,
Trompet S,
Tuladhar AM,
Tybjærg-Hansen A,
van Vugt M,
Vibo R,
Verma SS,
Wiggins KL,
Wennberg P,
Woo D,
Wilson PWF,
Xu H,
Yang Q,
Yoon K,
Millwood IY,
Gieger C,
Ninomiya T,
Grabe HJ,
Jukema JW,
Rissanen IL,
Strbian D,
Kim YJ,
Chen PH,
Mayerhofer E,
Howson JMM,
Irvin MR,
Adams H,
Wassertheil-Smoller S,
Christensen K,
Ikram MA,
Rundek T,
Worrall BB,
Lathrop GM,
Riaz M,
Simonsick EM,
Kõrv J,
França PHC,
Zand R,
Prasad K,
Frikke-Schmidt R,
de Leeuw FE,
Liman T,
Haeusler KG,
Ruigrok YM,
Heuschmann PU,
Longstreth WT,
Jung KJ,
Bastarache L,
Paré G,
Damrauer SM,
Chasman DI,
Rotter JI,
Anderson CD,
Zwart JA,
Niiranen TJ,
Fornage M,
Liaw YP,
Seshadri S,
Fernández-Cadenas I,
Walters RG,
Ruff CT,
Owolabi MO,
Huffman JE,
Milani L,
Kamatani Y,
Dichgans M,
Debette S
COMPASS Consortium · INVENT Consortium 외 컨소시엄 13곳
Nature · 2022 · PMID 36180795 · open access
페이지 5개
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways
Cordell HJ,
Han Y,
Mells GF,
Li Y,
Hirschfield GM,
Greene CS,
Xie G,
Juran BD,
Zhu D,
Qian DC,
Floyd JA,
Morley KI
외 11명 — 모두 보기
Prati D,
Lleo A,
Cusi D,
Gershwin ME,
Anderson CA,
Lazaridis KN,
Invernizzi P,
Seldin MF,
Sandford RN,
Amos CI,
Siminovitch KA
Canadian-US PBC Consortium · Italian PBC Genetics Study Group 외 컨소시엄 1곳
Nature communications · 2015 · PMID 26394269 · open access
페이지 3개
Genome-wide association meta-analysis identifies new endometriosis risk loci
Nyholt DR,
Low SK,
Anderson CA,
Painter JN,
Uno S,
Morris AP,
MacGregor S,
Gordon SD,
Henders AK,
Martin NG,
Attia J,
Holliday EG
외 11명 — 모두 보기
McEvoy M,
Scott RJ,
Kennedy SH,
Treloar SA,
Missmer SA,
Adachi S,
Tanaka K,
Nakamura Y,
Zondervan KT,
Zembutsu H,
Montgomery GW
Nature genetics · 2012 · PMID 23104006 · open access
페이지 2개
Genetic variation at 16q24.2 is associated with small vessel stroke
Traylor M,
Malik R,
Nalls MA,
Cotlarciuc I,
Radmanesh F,
Thorleifsson G,
Hanscombe KB,
Langefeld C,
Saleheen D,
Rost NS,
Yet I,
Spector TD
외 55명 — 모두 보기
Bell JT,
Hannon E,
Mill J,
Chauhan G,
Debette S,
Bis JC,
Longstreth WT Jr,
Ikram MA,
Launer LJ,
Seshadri S,
Hamilton-Bruce MA,
Jimenez-Conde J,
Cole JW,
Schmidt R,
Słowik A,
Lemmens R,
Lindgren A,
Melander O,
Grewal RP,
Sacco RL,
Rundek T,
Rexrode K,
Arnett DK,
Johnson JA,
Benavente OR,
Wasssertheil-Smoller S,
Lee JM,
Pulit SL,
Wong Q,
Rich SS,
de Bakker PI,
McArdle PF,
Woo D,
Anderson CD,
Xu H,
Heitsch L,
Fornage M,
Jern C,
Stefansson K,
Thorsteinsdottir U,
Gretarsdottir S,
Lewis CM,
Sharma P,
Sudlow CL,
Rothwell PM,
Boncoraglio GB,
Thijs V,
Levi C,
Meschia JF,
Rosand J,
Kittner SJ,
Mitchell BD,
Dichgans M,
Worrall BB,
Markus HS
METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
Annals of neurology · 2017 · PMID 27997041 · open access
페이지 1개
Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease
Lee JC,
Biasci D,
Roberts R,
Gearry RB,
Mansfield JC,
Ahmad T,
Prescott NJ,
Satsangi J,
Wilson DC,
Jostins L,
Anderson CA,
Traherne JA
외 3명 — 모두 보기
UK IBD Genetics Consortium
Nature genetics · 2017 · PMID 28067912
페이지 1개
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies
Traylor M,
Persyn E,
Tomppo L,
Klasson S,
Abedi V,
Bakker MK,
Torres N,
Li L,
Bell S,
Rutten-Jacobs L,
Tozer DJ,
Griessenauer CJ
외 29명 — 모두 보기
Zhang Y,
Pedersen A,
Sharma P,
Jimenez-Conde J,
Rundek T,
Grewal RP,
Lindgren A,
Meschia JF,
Salomaa V,
Havulinna A,
Kourkoulis C,
Crawford K,
Marini S,
Mitchell BD,
Kittner SJ,
Rosand J,
Dichgans M,
Jern C,
Strbian D,
Fernandez-Cadenas I,
Zand R,
Ruigrok Y,
Rost N,
Lemmens R,
Rothwell PM,
Anderson CD,
Wardlaw J,
Lewis CM,
Markus HS
Helsinki Stroke, Study Dutch Parelsnoer Institute-Cerebrovascular Accident (CVA) Study Group · National Institute of Neurological Disorders and Stroke (NINDS) Stroke Genetics Network 외 컨소시엄 2곳
The Lancet. Neurology · 2021 · PMID 33773637 · 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.