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11 matches for
Din L.
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
and 181 more — show all
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) and 1 more consortia
Nature genetics · 2013 · PMID 24076602 · open access
12 pages+
Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia
Law PJ,
Berndt SI,
Speedy HE,
Camp NJ,
Sava GP,
Skibola CF,
Holroyd A,
Joseph V,
Sunter NJ,
Nieters A,
Bea S,
Monnereau A
and 85 more — show all
Martin-Garcia D,
Goldin LR,
Clot G,
Teras LR,
Quintela I,
Birmann BM,
Jayne S,
Cozen W,
Majid A,
Smedby KE,
Lan Q,
Dearden C,
Brooks-Wilson AR,
Hall AG,
Purdue MP,
Mainou-Fowler T,
Vajdic CM,
Jackson GH,
Cocco P,
Marr H,
Zhang Y,
Zheng T,
Giles GG,
Lawrence C,
Call TG,
Liebow M,
Melbye M,
Glimelius B,
Mansouri L,
Glenn M,
Curtin K,
Diver WR,
Link BK,
Conde L,
Bracci PM,
Holly EA,
Jackson RD,
Tinker LF,
Benavente Y,
Boffetta P,
Brennan P,
Maynadie M,
McKay J,
Albanes D,
Weinstein S,
Wang Z,
Caporaso NE,
Morton LM,
Severson RK,
Riboli E,
Vineis P,
Vermeulen RC,
Southey MC,
Milne RL,
Clavel J,
Topka S,
Spinelli JJ,
Kraft P,
Ennas MG,
Summerfield G,
Ferri GM,
Harris RJ,
Miligi L,
Pettitt AR,
North KE,
Allsup DJ,
Fraumeni JF,
Bailey JR,
Offit K,
Pratt G,
Hjalgrim H,
Pepper C,
Chanock SJ,
Fegan C,
Rosenquist R,
de Sanjose S,
Carracedo A,
Dyer MJ,
Catovsky D,
Campo E,
Cerhan JR,
Allan JM,
Rothman N,
Houlston R,
Slager S
Nature communications · 2017 · PMID 28165464 · open access
12 pages+
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
Kiryluk K,
Li Y,
Scolari F,
Sanna-Cherchi S,
Choi M,
Verbitsky M,
Fasel D,
Lata S,
Prakash S,
Shapiro S,
Fischman C,
Snyder HJ
and 80 more — show all
Appel G,
Izzi C,
Viola BF,
Dallera N,
Del Vecchio L,
Barlassina C,
Salvi E,
Bertinetto FE,
Amoroso A,
Savoldi S,
Rocchietti M,
Amore A,
Peruzzi L,
Coppo R,
Salvadori M,
Ravani P,
Magistroni R,
Ghiggeri GM,
Caridi G,
Bodria M,
Lugani F,
Allegri L,
Delsante M,
Maiorana M,
Magnano A,
Frasca G,
Boer E,
Boscutti G,
Ponticelli C,
Mignani R,
Marcantoni C,
Di Landro D,
Santoro D,
Pani A,
Polci R,
Feriozzi S,
Chicca S,
Galliani M,
Gigante M,
Gesualdo L,
Zamboli P,
Battaglia GG,
Garozzo M,
Maixnerová D,
Tesar V,
Eitner F,
Rauen T,
Floege J,
Kovacs T,
Nagy J,
Mucha K,
Pączek L,
Zaniew M,
Mizerska-Wasiak M,
Roszkowska-Blaim M,
Pawlaczyk K,
Gale D,
Barratt J,
Thibaudin L,
Berthoux F,
Canaud G,
Boland A,
Metzger M,
Panzer U,
Suzuki H,
Goto S,
Narita I,
Caliskan Y,
Xie J,
Hou P,
Chen N,
Zhang H,
Wyatt RJ,
Novak J,
Julian BA,
Feehally J,
Stengel B,
Cusi D,
Lifton RP,
Gharavi AG
Nature genetics · 2014 · PMID 25305756 · open access
4 pages
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia
Berndt SI,
Skibola CF,
Joseph V,
Camp NJ,
Nieters A,
Wang Z,
Cozen W,
Monnereau A,
Wang SS,
Kelly RS,
Lan Q,
Teras LR
and 118 more — show all
Chatterjee N,
Chung CC,
Yeager M,
Brooks-Wilson AR,
Hartge P,
Purdue MP,
Birmann BM,
Armstrong BK,
Cocco P,
Zhang Y,
Severi G,
Zeleniuch-Jacquotte A,
Lawrence C,
Burdette L,
Yuenger J,
Hutchinson A,
Jacobs KB,
Call TG,
Shanafelt TD,
Novak AJ,
Kay NE,
Liebow M,
Wang AH,
Smedby KE,
Adami HO,
Melbye M,
Glimelius B,
Chang ET,
Glenn M,
Curtin K,
Cannon-Albright LA,
Jones B,
Diver WR,
Link BK,
Weiner GJ,
Conde L,
Bracci PM,
Riby J,
Holly EA,
Smith MT,
Jackson RD,
Tinker LF,
Benavente Y,
Becker N,
Boffetta P,
Brennan P,
Foretova L,
Maynadie M,
McKay J,
Staines A,
Rabe KG,
Achenbach SJ,
Vachon CM,
Goldin LR,
Strom SS,
Lanasa MC,
Spector LG,
Leis JF,
Cunningham JM,
Weinberg JB,
Morrison VA,
Caporaso NE,
Norman AD,
Linet MS,
De Roos AJ,
Morton LM,
Severson RK,
Riboli E,
Vineis P,
Kaaks R,
Trichopoulos D,
Masala G,
Weiderpass E,
Chirlaque MD,
Vermeulen RC,
Travis RC,
Giles GG,
Albanes D,
Virtamo J,
Weinstein S,
Clavel J,
Zheng T,
Holford TR,
Offit K,
Zelenetz A,
Klein RJ,
Spinelli JJ,
Bertrand KA,
Laden F,
Giovannucci E,
Kraft P,
Kricker A,
Turner J,
Vajdic CM,
Ennas MG,
Ferri GM,
Miligi L,
Liang L,
Sampson J,
Crouch S,
Park JH,
North KE,
Cox A,
Snowden JA,
Wright J,
Carracedo A,
Lopez-Otin C,
Bea S,
Salaverria I,
Martin-Garcia D,
Campo E,
Fraumeni JF Jr,
de Sanjose S,
Hjalgrim H,
Cerhan JR,
Chanock SJ,
Rothman N,
Slager SL
Nature genetics · 2013 · PMID 23770605 · open access
3 pages
Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32
Conde L,
Halperin E,
Akers NK,
Brown KM,
Smedby KE,
Rothman N,
Nieters A,
Slager SL,
Brooks-Wilson A,
Agana L,
Riby J,
Liu J
and 59 more — show all
Adami HO,
Darabi H,
Hjalgrim H,
Low HQ,
Humphreys K,
Melbye M,
Chang ET,
Glimelius B,
Cozen W,
Davis S,
Hartge P,
Morton LM,
Schenk M,
Wang SS,
Armstrong B,
Kricker A,
Milliken S,
Purdue MP,
Vajdic CM,
Boyle P,
Lan Q,
Zahm SH,
Zhang Y,
Zheng T,
Becker N,
Benavente Y,
Boffetta P,
Brennan P,
Butterbach K,
Cocco P,
Foretova L,
Maynadié M,
de Sanjosé S,
Staines A,
Spinelli JJ,
Achenbach SJ,
Call TG,
Camp NJ,
Glenn M,
Caporaso NE,
Cerhan JR,
Cunningham JM,
Goldin LR,
Hanson CA,
Kay NE,
Lanasa MC,
Leis JF,
Marti GE,
Rabe KG,
Rassenti LZ,
Spector LG,
Strom SS,
Vachon CM,
Weinberg JB,
Holly EA,
Chanock S,
Smith MT,
Bracci PM,
Skibola CF
Nature genetics · 2010 · PMID 20639881 · open access
2 pages
Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia
Berndt SI,
Camp NJ,
Skibola CF,
Vijai J,
Wang Z,
Gu J,
Nieters A,
Kelly RS,
Smedby KE,
Monnereau A,
Cozen W,
Cox A
and 115 more — show all
Wang SS,
Lan Q,
Teras LR,
Machado M,
Yeager M,
Brooks-Wilson AR,
Hartge P,
Purdue MP,
Birmann BM,
Vajdic CM,
Cocco P,
Zhang Y,
Giles GG,
Zeleniuch-Jacquotte A,
Lawrence C,
Montalvan R,
Burdett L,
Hutchinson A,
Ye Y,
Call TG,
Shanafelt TD,
Novak AJ,
Kay NE,
Liebow M,
Cunningham JM,
Allmer C,
Hjalgrim H,
Adami HO,
Melbye M,
Glimelius B,
Chang ET,
Glenn M,
Curtin K,
Cannon-Albright LA,
Diver WR,
Link BK,
Weiner GJ,
Conde L,
Bracci PM,
Riby J,
Arnett DK,
Zhi D,
Leach JM,
Holly EA,
Jackson RD,
Tinker LF,
Benavente Y,
Sala N,
Casabonne D,
Becker N,
Boffetta P,
Brennan P,
Foretova L,
Maynadie M,
McKay J,
Staines A,
Chaffee KG,
Achenbach SJ,
Vachon CM,
Goldin LR,
Strom SS,
Leis JF,
Weinberg JB,
Caporaso NE,
Norman AD,
De Roos AJ,
Morton LM,
Severson RK,
Riboli E,
Vineis P,
Kaaks R,
Masala G,
Weiderpass E,
Chirlaque MD,
Vermeulen RCH,
Travis RC,
Southey MC,
Milne RL,
Albanes D,
Virtamo J,
Weinstein S,
Clavel J,
Zheng T,
Holford TR,
Villano DJ,
Maria A,
Spinelli JJ,
Gascoyne RD,
Connors JM,
Bertrand KA,
Giovannucci E,
Kraft P,
Kricker A,
Turner J,
Ennas MG,
Ferri GM,
Miligi L,
Liang L,
Ma B,
Huang J,
Huang J,
Crouch S,
Park JH,
Chatterjee N,
North KE,
Snowden JA,
Wright J,
Fraumeni JF,
Offit K,
Wu X,
de Sanjose S,
Cerhan JR,
Chanock SJ,
Rothman N,
Slager SL
Nature communications · 2016 · PMID 26956414 · open access
2 pages
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma
Landi MT,
Chatterjee N,
Yu K,
Goldin LR,
Goldstein AM,
Rotunno M,
Mirabello L,
Jacobs K,
Wheeler W,
Yeager M,
Bergen AW,
Li Q
and 56 more — show all
Consonni D,
Pesatori AC,
Wacholder S,
Thun M,
Diver R,
Oken M,
Virtamo J,
Albanes D,
Wang Z,
Burdette L,
Doheny KF,
Pugh EW,
Laurie C,
Brennan P,
Hung R,
Gaborieau V,
McKay JD,
Lathrop M,
McLaughlin J,
Wang Y,
Tsao MS,
Spitz MR,
Wang Y,
Krokan H,
Vatten L,
Skorpen F,
Arnesen E,
Benhamou S,
Bouchard C,
Metspalu A,
Metsapalu A,
Vooder T,
Nelis M,
Välk K,
Field JK,
Chen C,
Goodman G,
Sulem P,
Thorleifsson G,
Rafnar T,
Eisen T,
Sauter W,
Rosenberger A,
Bickeböller H,
Risch A,
Chang-Claude J,
Wichmann HE,
Stefansson K,
Houlston R,
Amos CI,
Fraumeni JF Jr,
Savage SA,
Bertazzi PA,
Tucker MA,
Chanock S,
Caporaso NE
American journal of human genetics · 2009 · PMID 19836008
1 page
Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL
Slager SL,
Rabe KG,
Achenbach SJ,
Vachon CM,
Goldin LR,
Strom SS,
Lanasa MC,
Spector LG,
Rassenti LZ,
Leis JF,
Camp NJ,
Glenn M
and 10 more — show all
Blood · 2011 · PMID 21131588
1 page
ABCC5, a gene that influences the anterior chamber depth, is associated with primary angle closure glaucoma
Nongpiur ME,
Khor CC,
Jia H,
Cornes BK,
Chen LJ,
Qiao C,
Nair KS,
Cheng CY,
Xu L,
George R,
Tan D,
Abu-Amero K
and 61 more — show all
Perera SA,
Ozaki M,
Mizoguchi T,
Kurimoto Y,
Low S,
Tajudin LS,
Ho CL,
Tham CC,
Soto I,
Chew PT,
Wong HT,
Shantha B,
Kuroda M,
Osman EA,
Tang G,
Fan S,
Meng H,
Wang H,
Feng B,
Yong VH,
Ting SM,
Li Y,
Wang YX,
Li Z,
Lavanya R,
Wu RY,
Zheng YF,
Su DH,
Loon SC,
Yong VK,
Allingham RR,
Hauser MA,
Soumittra N,
Ramprasad VL,
Waseem N,
Yaakub A,
Chia KS,
Kumaramanickavel G,
Wong TT,
How AC,
Chau TN,
Simmons CP,
Bei JX,
Zeng YX,
Bhattacharya SS,
Zhang M,
Tan DT,
Teo YY,
Al-Obeidan SA,
Hon DN,
Tai ES,
Saw SM,
Foster PJ,
Vijaya L,
Jonas JB,
Wong TY,
John SW,
Pang CP,
Vithana EN,
Wang N,
Aung T
PLoS genetics · 2014 · PMID 24603532 · open access
1 page
Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia
McMaster ML,
Berndt SI,
Zhang J,
Slager SL,
Li SA,
Vajdic CM,
Smedby KE,
Yan H,
Birmann BM,
Brown EE,
Smith A,
Kleinstern G
and 69 more — show all
Fansler MM,
Mayr C,
Zhu B,
Chung CC,
Park JH,
Burdette L,
Hicks BD,
Hutchinson A,
Teras LR,
Adami HO,
Bracci PM,
McKay J,
Monnereau A,
Link BK,
Vermeulen RCH,
Ansell SM,
Maria A,
Diver WR,
Melbye M,
Ojesina AI,
Kraft P,
Boffetta P,
Clavel J,
Giovannucci E,
Besson CM,
Canzian F,
Travis RC,
Vineis P,
Weiderpass E,
Montalvan R,
Wang Z,
Yeager M,
Becker N,
Benavente Y,
Brennan P,
Foretova L,
Maynadie M,
Nieters A,
de Sanjose S,
Staines A,
Conde L,
Riby J,
Glimelius B,
Hjalgrim H,
Pradhan N,
Feldman AL,
Novak AJ,
Lawrence C,
Bassig BA,
Lan Q,
Zheng T,
North KE,
Tinker LF,
Cozen W,
Severson RK,
Hofmann JN,
Zhang Y,
Jackson RD,
Morton LM,
Purdue MP,
Chatterjee N,
Offit K,
Cerhan JR,
Chanock SJ,
Rothman N,
Vijai J,
Goldin LR,
Skibola CF,
Caporaso NE
Nature communications · 2018 · PMID 30305637 · open access
1 page
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes
Din L,
Sheikh M,
Kosaraju N,
Smedby KE,
Bernatsky S,
Berndt SI,
Skibola CF,
Nieters A,
Wang S,
McKay JD,
Cocco P,
Maynadié M
and 80 more — show all
Foretová L,
Staines A,
Mack TM,
de Sanjosé S,
Vyse TJ,
Padyukov L,
Monnereau A,
Arslan AA,
Moore A,
Brooks-Wilson AR,
Novak AJ,
Glimelius B,
Birmann BM,
Link BK,
Stewart C,
Vajdic CM,
Haioun C,
Magnani C,
Conti DV,
Cox DG,
Casabonne D,
Albanes D,
Kane E,
Roman E,
Muzi G,
Salles G,
Giles GG,
Adami HO,
Ghesquières H,
De Vivo I,
Clavel J,
Cerhan JR,
Spinelli JJ,
Hofmann J,
Vijai J,
Curtin K,
Costenbader KH,
Onel K,
Offit K,
Teras LR,
Morton L,
Conde L,
Miligi L,
Melbye M,
Ennas MG,
Liebow M,
Purdue MP,
Glenn M,
Southey MC,
Din M,
Rothman N,
Camp NJ,
Wong Doo N,
Becker N,
Pradhan N,
Bracci PM,
Boffetta P,
Vineis P,
Brennan P,
Kraft P,
Lan Q,
Severson RK,
Vermeulen RCH,
Milne RL,
Kaaks R,
Travis RC,
Weinstein SJ,
Chanock SJ,
Ansell SM,
Slager SL,
Zheng T,
Zhang Y,
Benavente Y,
Taub Z,
Madireddy L,
Gourraud PA,
Oksenberg JR,
Cozen W,
Hjalgrim H,
Khankhanian P
Genetic epidemiology · 2019 · PMID 31407831
1 page
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