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Casas JP에 대해
11건.
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Verma A,
Huffman JE,
Rodriguez A,
Conery M,
Liu M,
Ho YL,
Kim Y,
Heise DA,
Guare L,
Panickan VA,
Garcon H,
Linares F
외 59명 — 모두 보기
Costa L,
Goethert I,
Tipton R,
Honerlaw J,
Davies L,
Whitbourne S,
Cohen J,
Posner DC,
Sangar R,
Murray M,
Wang X,
Dochtermann DR,
Devineni P,
Shi Y,
Nandi TN,
Assimes TL,
Brunette CA,
Carroll RJ,
Clifford R,
Duvall S,
Gelernter J,
Hung A,
Iyengar SK,
Joseph J,
Kember R,
Kranzler H,
Kripke CM,
Levey D,
Luoh SW,
Merritt VC,
Overstreet C,
Deak JD,
Grant SFA,
Polimanti R,
Roussos P,
Shakt G,
Sun YV,
Tsao N,
Venkatesh S,
Voloudakis G,
Justice A,
Begoli E,
Ramoni R,
Tourassi G,
Pyarajan S,
Tsao P,
O'Donnell CJ,
Muralidhar S,
Moser J,
Casas JP,
Bick AG,
Zhou W,
Cai T,
Voight BF,
Cho K,
Gaziano JM,
Madduri RK,
Damrauer S,
Liao KP
Science (New York, N.Y.) · 2024 · PMID 39024449 · 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
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Ehret GB,
Munroe PB,
Rice KM,
Bochud M,
Johnson AD,
Chasman DI,
Smith AV,
Tobin MD,
Verwoert GC,
Hwang SJ,
Pihur V,
Vollenweider P
외 336명 — 모두 보기
O'Reilly PF,
Amin N,
Bragg-Gresham JL,
Teumer A,
Glazer NL,
Launer L,
Zhao JH,
Aulchenko Y,
Heath S,
Sõber S,
Parsa A,
Luan J,
Arora P,
Dehghan A,
Zhang F,
Lucas G,
Hicks AA,
Jackson AU,
Peden JF,
Tanaka T,
Wild SH,
Rudan I,
Igl W,
Milaneschi Y,
Parker AN,
Fava C,
Chambers JC,
Fox ER,
Kumari M,
Go MJ,
van der Harst P,
Kao WH,
Sjögren M,
Vinay DG,
Alexander M,
Tabara Y,
Shaw-Hawkins S,
Whincup PH,
Liu Y,
Shi G,
Kuusisto J,
Tayo B,
Seielstad M,
Sim X,
Nguyen KD,
Lehtimäki T,
Matullo G,
Wu Y,
Gaunt TR,
Onland-Moret NC,
Cooper MN,
Platou CG,
Org E,
Org E,
Hardy R,
Dahgam S,
Palmen J,
Vitart V,
Braund PS,
Kuznetsova T,
Kuznetsova T,
Uiterwaal CS,
Adeyemo A,
Palmas W,
Campbell H,
Ludwig B,
Tomaszewski M,
Tzoulaki I,
Palmer ND,
Aspelund T,
Garcia M,
Chang YP,
O'Connell JR,
Steinle NI,
Grobbee DE,
Arking DE,
Kardia SL,
Morrison AC,
Hernandez D,
Najjar S,
McArdle WL,
Hadley D,
Brown MJ,
Connell JM,
Hingorani AD,
Day IN,
Lawlor DA,
Beilby JP,
Lawrence RW,
Clarke R,
Hopewell JC,
Ongen H,
Dreisbach AW,
Li Y,
Young JH,
Bis JC,
Kähönen M,
Viikari J,
Adair LS,
Lee NR,
Chen MH,
Olden M,
Pattaro C,
Bolton JA,
Köttgen A,
Bergmann S,
Mooser V,
Chaturvedi N,
Frayling TM,
Islam M,
Jafar TH,
Erdmann J,
Kulkarni SR,
Bornstein SR,
Grässler J,
Groop L,
Voight BF,
Kettunen J,
Howard P,
Taylor A,
Guarrera S,
Ricceri F,
Emilsson V,
Plump A,
Barroso I,
Khaw KT,
Weder AB,
Hunt SC,
Sun YV,
Bergman RN,
Collins FS,
Bonnycastle LL,
Scott LJ,
Stringham HM,
Peltonen L,
Perola M,
Vartiainen E,
Brand SM,
Staessen JA,
Wang TJ,
Burton PR,
Soler Artigas M,
Dong Y,
Snieder H,
Wang X,
Zhu H,
Lohman KK,
Rudock ME,
Heckbert SR,
Smith NL,
Wiggins KL,
Doumatey A,
Shriner D,
Veldre G,
Viigimaa M,
Kinra S,
Prabhakaran D,
Tripathy V,
Langefeld CD,
Rosengren A,
Thelle DS,
Corsi AM,
Singleton A,
Forrester T,
Hilton G,
McKenzie CA,
Salako T,
Iwai N,
Kita Y,
Ogihara T,
Ohkubo T,
Okamura T,
Ueshima H,
Umemura S,
Eyheramendy S,
Meitinger T,
Wichmann HE,
Cho YS,
Kim HL,
Lee JY,
Scott J,
Sehmi JS,
Zhang W,
Hedblad B,
Nilsson P,
Smith GD,
Wong A,
Narisu N,
Stančáková A,
Raffel LJ,
Yao J,
Kathiresan S,
O'Donnell CJ,
Schwartz SM,
Ikram MA,
Longstreth WT Jr,
Mosley TH,
Seshadri S,
Shrine NR,
Wain LV,
Morken MA,
Swift AJ,
Laitinen J,
Prokopenko I,
Zitting P,
Cooper JA,
Humphries SE,
Danesh J,
Rasheed A,
Goel A,
Hamsten A,
Watkins H,
Bakker SJ,
van Gilst WH,
Janipalli CS,
Mani KR,
Yajnik CS,
Hofman A,
Mattace-Raso FU,
Oostra BA,
Demirkan A,
Isaacs A,
Rivadeneira F,
Lakatta EG,
Orru M,
Scuteri A,
Ala-Korpela M,
Kangas AJ,
Lyytikäinen LP,
Soininen P,
Tukiainen T,
Würtz P,
Ong RT,
Dörr M,
Kroemer HK,
Völker U,
Völzke H,
Galan P,
Hercberg S,
Lathrop M,
Zelenika D,
Deloukas P,
Mangino M,
Spector TD,
Zhai G,
Meschia JF,
Nalls MA,
Sharma P,
Terzic J,
Kumar MV,
Denniff M,
Zukowska-Szczechowska E,
Wagenknecht LE,
Fowkes FG,
Charchar FJ,
Schwarz PE,
Hayward C,
Guo X,
Rotimi C,
Bots ML,
Brand E,
Samani NJ,
Polasek O,
Talmud PJ,
Nyberg F,
Kuh D,
Laan M,
Hveem K,
Palmer LJ,
van der Schouw YT,
Casas JP,
Mohlke KL,
Vineis P,
Raitakari O,
Ganesh SK,
Wong TY,
Tai ES,
Cooper RS,
Laakso M,
Rao DC,
Harris TB,
Morris RW,
Dominiczak AF,
Kivimaki M,
Marmot MG,
Miki T,
Saleheen D,
Chandak GR,
Coresh J,
Navis G,
Salomaa V,
Han BG,
Zhu X,
Kooner JS,
Melander O,
Ridker PM,
Bandinelli S,
Gyllensten UB,
Wright AF,
Wilson JF,
Ferrucci L,
Farrall M,
Tuomilehto J,
Pramstaller PP,
Elosua R,
Soranzo N,
Sijbrands EJ,
Altshuler D,
Loos RJ,
Shuldiner AR,
Gieger C,
Meneton P,
Uitterlinden AG,
Wareham NJ,
Gudnason V,
Rotter JI,
Rettig R,
Uda M,
Strachan DP,
Witteman JC,
Hartikainen AL,
Beckmann JS,
Boerwinkle E,
Vasan RS,
Boehnke M,
Larson MG,
Järvelin MR,
Psaty BM,
Abecasis GR,
Chakravarti A,
Elliott P,
van Duijn CM,
Newton-Cheh C,
Levy D,
Caulfield MJ,
Johnson T
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium 외 컨소시엄 4곳
Nature · 2011 · PMID 21909115 · open access
페이지 5개
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
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
Franceschini N,
Giambartolomei C,
de Vries PS,
Finan C,
Bis JC,
Huntley RP,
Lovering RC,
Tajuddin SM,
Winkler TW,
Graff M,
Kavousi M,
Dale C
외 146명 — 모두 보기
Smith AV,
Hofer E,
van Leeuwen EM,
Nolte IM,
Lu L,
Scholz M,
Sargurupremraj M,
Pitkänen N,
Franzén O,
Joshi PK,
Noordam R,
Marioni RE,
Hwang SJ,
Musani SK,
Schminke U,
Palmas W,
Isaacs A,
Correa A,
Zonderman AB,
Hofman A,
Teumer A,
Cox AJ,
Uitterlinden AG,
Wong A,
Smit AJ,
Newman AB,
Britton A,
Ruusalepp A,
Sennblad B,
Hedblad B,
Pasaniuc B,
Penninx BW,
Langefeld CD,
Wassel CL,
Tzourio C,
Fava C,
Baldassarre D,
O'Leary DH,
Teupser D,
Kuh D,
Tremoli E,
Mannarino E,
Grossi E,
Boerwinkle E,
Schadt EE,
Ingelsson E,
Veglia F,
Rivadeneira F,
Beutner F,
Chauhan G,
Heiss G,
Snieder H,
Campbell H,
Völzke H,
Markus HS,
Deary IJ,
Jukema JW,
de Graaf J,
Price J,
Pott J,
Hopewell JC,
Liang J,
Thiery J,
Engmann J,
Gertow K,
Rice K,
Taylor KD,
Dhana K,
Kiemeney LALM,
Lind L,
Raffield LM,
Launer LJ,
Holdt LM,
Dörr M,
Dichgans M,
Traylor M,
Sitzer M,
Kumari M,
Kivimaki M,
Nalls MA,
Melander O,
Raitakari O,
Franco OH,
Rueda-Ochoa OL,
Roussos P,
Whincup PH,
Amouyel P,
Giral P,
Anugu P,
Wong Q,
Malik R,
Rauramaa R,
Burkhardt R,
Hardy R,
Schmidt R,
de Mutsert R,
Morris RW,
Strawbridge RJ,
Wannamethee SG,
Hägg S,
Shah S,
McLachlan S,
Trompet S,
Seshadri S,
Kurl S,
Heckbert SR,
Ring S,
Harris TB,
Lehtimäki T,
Galesloot TE,
Shah T,
de Faire U,
Plagnol V,
Rosamond WD,
Post W,
Zhu X,
Zhang X,
Guo X,
Saba Y,
Dehghan A,
Seldenrijk A,
Morrison AC,
Hamsten A,
Psaty BM,
van Duijn CM,
Lawlor DA,
Mook-Kanamori DO,
Bowden DW,
Schmidt H,
Wilson JF,
Wilson JG,
Rotter JI,
Wardlaw JM,
Deanfield J,
Halcox J,
Lyytikäinen LP,
Loeffler M,
Evans MK,
Debette S,
Humphries SE,
Völker U,
Gudnason V,
Hingorani AD,
Björkegren JLM,
Casas JP,
O'Donnell CJ
MEGASTROKE Consortium
Nature communications · 2018 · PMID 30510157 · open access
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
Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure
Rasooly D,
Peloso GM,
Pereira AC,
Dashti H,
Giambartolomei C,
Wheeler E,
Aung N,
Ferolito BR,
Pietzner M,
Farber-Eger EH,
Wells QS,
Kosik NM
외 22명 — 모두 보기
Gaziano L,
Posner DC,
Bento AP,
Hui Q,
Liu C,
Aragam K,
Wang Z,
Charest B,
Huffman JE,
Wilson PWF,
Phillips LS,
Whittaker J,
Munroe PB,
Petersen SE,
Cho K,
Leach AR,
Magariños MP,
Gaziano JM,
Langenberg C,
Sun YV,
Joseph J,
Casas JP
VA Million Veteran Program
Nature communications · 2023 · PMID 37429843 · 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
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women
Steinthorsdottir V,
McGinnis R,
Williams NO,
Stefansdottir L,
Thorleifsson G,
Shooter S,
Fadista J,
Sigurdsson JK,
Auro KM,
Berezina G,
Borges MC,
Bumpstead S
외 63명 — 모두 보기
Bybjerg-Grauholm J,
Colgiu I,
Dolby VA,
Dudbridge F,
Engel SM,
Franklin CS,
Frigge ML,
Frisbaek Y,
Geirsson RT,
Geller F,
Gretarsdottir S,
Gudbjartsson DF,
Harmon Q,
Hougaard DM,
Hegay T,
Helgadottir A,
Hjartardottir S,
Jääskeläinen T,
Johannsdottir H,
Jonsdottir I,
Juliusdottir T,
Kalsheker N,
Kasimov A,
Kemp JP,
Kivinen K,
Klungsøyr K,
Lee WK,
Melbye M,
Miedzybrodska Z,
Moffett A,
Najmutdinova D,
Nishanova F,
Olafsdottir T,
Perola M,
Pipkin FB,
Poston L,
Prescott G,
Saevarsdottir S,
Salimbayeva D,
Scaife PJ,
Skotte L,
Staines-Urias E,
Stefansson OA,
Sørensen KM,
Thomsen LCV,
Tragante V,
Trogstad L,
Simpson NAB,
Aripova T,
Casas JP,
Dominiczak AF,
Walker JJ,
Thorsteinsdottir U,
Iversen AC,
Feenstra B,
Lawlor DA,
Boyd HA,
Magnus P,
Laivuori H,
Zakhidova N,
Svyatova G,
Stefansson K,
Morgan L
FINNPEC Consortium · GOPEC Consortium
Nature communications · 2020 · PMID 33239696 · open access
페이지 1개
Genome-wide association study of circulating interleukin 6 levels identifies novel loci
Ahluwalia TS,
Prins BP,
Abdollahi M,
Armstrong NJ,
Aslibekyan S,
Bain L,
Jefferis B,
Baumert J,
Beekman M,
Ben-Shlomo Y,
Bis JC,
Mitchell BD
외 114명 — 모두 보기
de Geus E,
Delgado GE,
Marek D,
Eriksson J,
Kajantie E,
Kanoni S,
Kemp JP,
Lu C,
Marioni RE,
McLachlan S,
Milaneschi Y,
Nolte IM,
Petrelis AM,
Porcu E,
Sabater-Lleal M,
Naderi E,
Seppälä I,
Shah T,
Singhal G,
Standl M,
Teumer A,
Thalamuthu A,
Thiering E,
Trompet S,
Ballantyne CM,
Benjamin EJ,
Casas JP,
Toben C,
Dedoussis G,
Deelen J,
Durda P,
Engmann J,
Feitosa MF,
Grallert H,
Hammarstedt A,
Harris SE,
Homuth G,
Hottenga JJ,
Jalkanen S,
Jamshidi Y,
Jawahar MC,
Jess T,
Kivimaki M,
Kleber ME,
Lahti J,
Liu Y,
Marques-Vidal P,
Mellström D,
Mooijaart SP,
Müller-Nurasyid M,
Penninx B,
Revez JA,
Rossing P,
Räikkönen K,
Sattar N,
Scharnagl H,
Sennblad B,
Silveira A,
Pourcain BS,
Timpson NJ,
Trollor J,
van Dongen J,
Van Heemst D,
Visvikis-Siest S,
Vollenweider P,
Völker U,
Waldenberger M,
Willemsen G,
Zabaneh D,
Morris RW,
Arnett DK,
Baune BT,
Boomsma DI,
Chang YC,
Deary IJ,
Deloukas P,
Eriksson JG,
Evans DM,
Ferreira MA,
Gaunt T,
Gudnason V,
Hamsten A,
Heinrich J,
Hingorani A,
Humphries SE,
Jukema JW,
Koenig W,
Kumari M,
Kutalik Z,
Lawlor DA,
Lehtimäki T,
März W,
Mather KA,
Naitza S,
Nauck M,
Ohlsson C,
Price JF,
Raitakari O,
Rice K,
Sachdev PS,
Slagboom E,
Sørensen TIA,
Spector T,
Stacey D,
Stathopoulou MG,
Tanaka T,
Wannamethee SG,
Whincup P,
Rotter JI,
Dehghan A,
Boerwinkle E,
Psaty BM,
Snieder H,
Alizadeh BZ
CHARGE Inflammation Working Group
Human molecular genetics · 2021 · PMID 33517400 · open access
페이지 1개
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