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성함이나 학술지명, PMID로 찾아보십시오.
Martin J에 대해
16건.
Genetics of rheumatoid arthritis contributes to biology and drug discovery
Okada Y,
Wu D,
Trynka G,
Raj T,
Terao C,
Ikari K,
Kochi Y,
Ohmura K,
Suzuki A,
Yoshida S,
Graham RR,
Manoharan A
외 83명 — 모두 보기
Ortmann W,
Bhangale T,
Denny JC,
Carroll RJ,
Eyler AE,
Greenberg JD,
Kremer JM,
Pappas DA,
Jiang L,
Yin J,
Ye L,
Su DF,
Yang J,
Xie G,
Keystone E,
Westra HJ,
Esko T,
Metspalu A,
Zhou X,
Gupta N,
Mirel D,
Stahl EA,
Diogo D,
Cui J,
Liao K,
Guo MH,
Myouzen K,
Kawaguchi T,
Coenen MJ,
van Riel PL,
van de Laar MA,
Guchelaar HJ,
Huizinga TW,
Dieudé P,
Mariette X,
Bridges SL Jr,
Zhernakova A,
Toes RE,
Tak PP,
Miceli-Richard C,
Bang SY,
Lee HS,
Martin J,
Gonzalez-Gay MA,
Rodriguez-Rodriguez L,
Rantapää-Dahlqvist S,
Arlestig L,
Choi HK,
Kamatani Y,
Galan P,
Lathrop M,
Eyre S,
Bowes J,
Barton A,
de Vries N,
Moreland LW,
Criswell LA,
Karlson EW,
Taniguchi A,
Yamada R,
Kubo M,
Liu JS,
Bae SC,
Worthington J,
Padyukov L,
Klareskog L,
Gregersen PK,
Raychaudhuri S,
Stranger BE,
De Jager PL,
Franke L,
Visscher PM,
Brown MA,
Yamanaka H,
Mimori T,
Takahashi A,
Xu H,
Behrens TW,
Siminovitch KA,
Momohara S,
Matsuda F,
Yamamoto K,
Plenge RM
RACI consortium · GARNET consortium
Nature · 2014 · PMID 24390342 · open access
페이지 12개+
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
Ishigaki K,
Sakaue S,
Terao C,
Luo Y,
Sonehara K,
Yamaguchi K,
Amariuta T,
Too CL,
Laufer VA,
Scott IC,
Viatte S,
Takahashi M
외 78명 — 모두 보기
Ohmura K,
Murasawa A,
Hashimoto M,
Ito H,
Hammoudeh M,
Emadi SA,
Masri BK,
Halabi H,
Badsha H,
Uthman IW,
Wu X,
Lin L,
Li T,
Plant D,
Barton A,
Orozco G,
Verstappen SMM,
Bowes J,
MacGregor AJ,
Honda S,
Koido M,
Tomizuka K,
Kamatani Y,
Tanaka H,
Tanaka E,
Suzuki A,
Maeda Y,
Yamamoto K,
Miyawaki S,
Xie G,
Zhang J,
Amos CI,
Keystone E,
Wolbink G,
van der Horst-Bruinsma I,
Cui J,
Liao KP,
Carroll RJ,
Lee HS,
Bang SY,
Siminovitch KA,
de Vries N,
Alfredsson L,
Rantapää-Dahlqvist S,
Karlson EW,
Bae SC,
Kimberly RP,
Edberg JC,
Mariette X,
Huizinga T,
Dieudé P,
Schneider M,
Kerick M,
Denny JC,
Matsuda K,
Matsuo K,
Mimori T,
Matsuda F,
Fujio K,
Tanaka Y,
Kumanogoh A,
Traylor M,
Lewis CM,
Eyre S,
Xu H,
Saxena R,
Arayssi T,
Kochi Y,
Ikari K,
Harigai M,
Gregersen PK,
Yamamoto K,
Louis Bridges S Jr,
Padyukov L,
Martin J,
Klareskog L,
Okada Y,
Raychaudhuri S
BioBank Japan Project
Nature genetics · 2022 · PMID 36333501
페이지 12개+
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Demontis D,
Walters RK,
Martin J,
Mattheisen M,
Als TD,
Agerbo E,
Baldursson G,
Belliveau R,
Bybjerg-Grauholm J,
Bækvad-Hansen M,
Cerrato F,
Chambert K
외 69명 — 모두 보기
Churchhouse C,
Dumont A,
Eriksson N,
Gandal M,
Goldstein JI,
Grasby KL,
Grove J,
Gudmundsson OO,
Hansen CS,
Hauberg ME,
Hollegaard MV,
Howrigan DP,
Huang H,
Maller JB,
Martin AR,
Martin NG,
Moran J,
Pallesen J,
Palmer DS,
Pedersen CB,
Pedersen MG,
Poterba T,
Poulsen JB,
Ripke S,
Robinson EB,
Satterstrom FK,
Stefansson H,
Stevens C,
Turley P,
Walters GB,
Won H,
Wright MJ,
Andreassen OA,
Asherson P,
Burton CL,
Boomsma DI,
Cormand B,
Dalsgaard S,
Franke B,
Gelernter J,
Geschwind D,
Hakonarson H,
Haavik J,
Kranzler HR,
Kuntsi J,
Langley K,
Lesch KP,
Middeldorp C,
Reif A,
Rohde LA,
Roussos P,
Schachar R,
Sklar P,
Sonuga-Barke EJS,
Sullivan PF,
Thapar A,
Tung JY,
Waldman ID,
Medland SE,
Stefansson K,
Nordentoft M,
Hougaard DM,
Werge T,
Mors O,
Mortensen PB,
Daly MJ,
Faraone SV,
Børglum AD,
Neale BM
ADHD Working Group of the Psychiatric Genomics Consortium (PGC) · Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium 외 컨소시엄 1곳
Nature genetics · 2019 · PMID 30478444
페이지 8개
Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes
van der Laan CM,
Ip HF,
Schipper M,
Hottenga JJ,
St Pourcain B,
Zayats T,
Pool R,
Krapohl EML,
Brikell I,
Soler Artigas M,
Cabana-Domínguez J,
Llonga N
외 117명 — 모두 보기
Nolte IM,
Bolhuis K,
Palviainen T,
Zafarmand H,
Gordon S,
Aliev F,
Burt SA,
Wang CA,
Saunders G,
Karhunen V,
Adkins DE,
Border R,
Peterson RE,
Prinz JA,
Thiering E,
Vilor-Tejedor N,
Ahluwalia TS,
Allegrini A,
Rimfeld K,
Chen Q,
Lu Y,
Martin J,
Bosch R,
Ramos-Quiroga JA,
Neumann A,
Ensink J,
Grasby KL,
Morosoli JJ,
Tong X,
Marrington S,
Scott JG,
Shabalin AA,
Corley R,
Evans LM,
Sugden K,
Alemany S,
Sass L,
Vinding R,
Ehli EA,
Hagenbeek FA,
Derks EM,
Larsson H,
Snieder H,
Cecil C,
Whipp AM,
Korhonen T,
Vuoksimaa E,
Rose RJ,
Uitterlinden AG,
Haavik J,
Harris JR,
Helgeland Ø,
Johansson S,
Knudsen GPS,
Njolstad PR,
Lu Q,
Rodriguez A,
Henders AK,
Mamun A,
Najman JM,
Brown S,
Hopfer C,
Krauter K,
Reynolds CA,
Smolen A,
Stallings M,
Wadsworth S,
Wall TL,
Eaves L,
Silberg JL,
Miller A,
Havdahl A,
Llop S,
Lopez-Espinosa MJ,
Bønnelykke K,
Sunyer J,
Arseneault L,
Standl M,
Heinrich J,
Boden J,
Pearson J,
Horwood J,
Kennedy M,
Poulton R,
Maes HH,
Hewitt J,
Copeland WE,
Middeldorp CM,
Williams GM,
Wray N,
Järvelin MR,
McGue M,
Iacono W,
Caspi A,
Moffitt TE,
Whitehouse AJO,
Pennell CE,
Klump KL,
Jiang C,
Dick DM,
Reichborn-Kjennerud T,
Martin NG,
Medland SE,
Vrijkotte T,
Kaprio J,
Tiemeier H,
Davey Smith G,
Hartman CA,
Oldehinkel AJ,
Casas M,
Ribasés M,
Lichtenstein P,
Lundström S,
Plomin R,
Bartels M,
Nivard MG,
Boomsma DI
Nature genetics · 2025 · PMID 40962958
페이지 8개
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation
Pereyra F,
Jia X,
McLaren PJ,
Telenti A,
de Bakker PI,
Walker BD,
Ripke S,
Brumme CJ,
Pulit SL,
Carrington M,
Kadie CM,
Carlson JM
외 326명 — 모두 보기
Heckerman D,
Graham RR,
Plenge RM,
Deeks SG,
Gianniny L,
Crawford G,
Sullivan J,
Gonzalez E,
Davies L,
Camargo A,
Moore JM,
Beattie N,
Gupta S,
Crenshaw A,
Burtt NP,
Guiducci C,
Gupta N,
Gao X,
Qi Y,
Yuki Y,
Piechocka-Trocha A,
Cutrell E,
Rosenberg R,
Moss KL,
Lemay P,
O'Leary J,
Schaefer T,
Verma P,
Toth I,
Block B,
Baker B,
Rothchild A,
Lian J,
Proudfoot J,
Alvino DM,
Vine S,
Addo MM,
Allen TM,
Altfeld M,
Henn MR,
Le Gall S,
Streeck H,
Haas DW,
Kuritzkes DR,
Robbins GK,
Shafer RW,
Gulick RM,
Shikuma CM,
Haubrich R,
Riddler S,
Sax PE,
Daar ES,
Ribaudo HJ,
Agan B,
Agarwal S,
Ahern RL,
Allen BL,
Altidor S,
Altschuler EL,
Ambardar S,
Anastos K,
Anderson B,
Anderson V,
Andrady U,
Antoniskis D,
Bangsberg D,
Barbaro D,
Barrie W,
Bartczak J,
Barton S,
Basden P,
Basgoz N,
Bazner S,
Bellos NC,
Benson AM,
Berger J,
Bernard NF,
Bernard AM,
Birch C,
Bodner SJ,
Bolan RK,
Boudreaux ET,
Bradley M,
Braun JF,
Brndjar JE,
Brown SJ,
Brown K,
Brown ST,
Burack J,
Bush LM,
Cafaro V,
Campbell O,
Campbell J,
Carlson RH,
Carmichael JK,
Casey KK,
Cavacuiti C,
Celestin G,
Chambers ST,
Chez N,
Chirch LM,
Cimoch PJ,
Cohen D,
Cohn LE,
Conway B,
Cooper DA,
Cornelson B,
Cox DT,
Cristofano MV,
Cuchural G Jr,
Czartoski JL,
Dahman JM,
Daly JS,
Davis BT,
Davis K,
Davod SM,
DeJesus E,
Dietz CA,
Dunham E,
Dunn ME,
Ellerin TB,
Eron JJ,
Fangman JJ,
Farel CE,
Ferlazzo H,
Fidler S,
Fleenor-Ford A,
Frankel R,
Freedberg KA,
French NK,
Fuchs JD,
Fuller JD,
Gaberman J,
Gallant JE,
Gandhi RT,
Garcia E,
Garmon D,
Gathe JC Jr,
Gaultier CR,
Gebre W,
Gilman FD,
Gilson I,
Goepfert PA,
Gottlieb MS,
Goulston C,
Groger RK,
Gurley TD,
Haber S,
Hardwicke R,
Hardy WD,
Harrigan PR,
Hawkins TN,
Heath S,
Hecht FM,
Henry WK,
Hladek M,
Hoffman RP,
Horton JM,
Hsu RK,
Huhn GD,
Hunt P,
Hupert MJ,
Illeman ML,
Jaeger H,
Jellinger RM,
John M,
Johnson JA,
Johnson KL,
Johnson H,
Johnson K,
Joly J,
Jordan WC,
Kauffman CA,
Khanlou H,
Killian RK,
Kim AY,
Kim DD,
Kinder CA,
Kirchner JT,
Kogelman L,
Kojic EM,
Korthuis PT,
Kurisu W,
Kwon DS,
LaMar M,
Lampiris H,
Lanzafame M,
Lederman MM,
Lee DM,
Lee JM,
Lee MJ,
Lee ET,
Lemoine J,
Levy JA,
Llibre JM,
Liguori MA,
Little SJ,
Liu AY,
Lopez AJ,
Loutfy MR,
Loy D,
Mohammed DY,
Man A,
Mansour MK,
Marconi VC,
Markowitz M,
Marques R,
Martin JN,
Martin HL Jr,
Mayer KH,
McElrath MJ,
McGhee TA,
McGovern BH,
McGowan K,
McIntyre D,
Mcleod GX,
Menezes P,
Mesa G,
Metroka CE,
Meyer-Olson D,
Miller AO,
Montgomery K,
Mounzer KC,
Nagami EH,
Nagin I,
Nahass RG,
Nelson MO,
Nielsen C,
Norene DL,
O'Connor DH,
Ojikutu BO,
Okulicz J,
Oladehin OO,
Oldfield EC 3rd,
Olender SA,
Ostrowski M,
Owen WF Jr,
Pae E,
Parsonnet J,
Pavlatos AM,
Perlmutter AM,
Pierce MN,
Pincus JM,
Pisani L,
Price LJ,
Proia L,
Prokesch RC,
Pujet HC,
Ramgopal M,
Rathod A,
Rausch M,
Ravishankar J,
Rhame FS,
Richards CS,
Richman DD,
Rodes B,
Rodriguez M,
Rose RC 3rd,
Rosenberg ES,
Rosenthal D,
Ross PE,
Rubin DS,
Rumbaugh E,
Saenz L,
Salvaggio MR,
Sanchez WC,
Sanjana VM,
Santiago S,
Schmidt W,
Schuitemaker H,
Sestak PM,
Shalit P,
Shay W,
Shirvani VN,
Silebi VI,
Sizemore JM Jr,
Skolnik PR,
Sokol-Anderson M,
Sosman JM,
Stabile P,
Stapleton JT,
Starrett S,
Stein F,
Stellbrink HJ,
Sterman FL,
Stone VE,
Stone DR,
Tambussi G,
Taplitz RA,
Tedaldi EM,
Telenti A,
Theisen W,
Torres R,
Tosiello L,
Tremblay C,
Tribble MA,
Trinh PD,
Tsao A,
Ueda P,
Vaccaro A,
Valadas E,
Vanig TJ,
Vecino I,
Vega VM,
Veikley W,
Wade BH,
Walworth C,
Wanidworanun C,
Ward DJ,
Warner DA,
Weber RD,
Webster D,
Weis S,
Wheeler DA,
White DJ,
Wilkins E,
Winston A,
Wlodaver CG,
van't Wout A,
Wright DP,
Yang OO,
Yurdin DL,
Zabukovic BW,
Zachary KC,
Zeeman B,
Zhao M
International HIV Controllers Study
Science (New York, N.Y.) · 2010 · PMID 21051598
페이지 6개
Genome-wide meta-analysis reveals shared new <i>loci</i> in systemic seropositive rheumatic diseases
Acosta-Herrera M,
Kerick M,
González-Serna D,
Wijmenga C,
Franke A,
Gregersen PK,
Padyukov L,
Worthington J,
Vyse TJ,
Alarcón-Riquelme ME,
Mayes MD,
Martin J
Myositis Genetics Consortium · Scleroderma Genetics Consortium
Annals of the rheumatic diseases · 2019 · PMID 30573655
페이지 6개
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis
Eyre S,
Bowes J,
Diogo D,
Lee A,
Barton A,
Martin P,
Zhernakova A,
Stahl E,
Viatte S,
McAllister K,
Amos CI,
Padyukov L
외 32명 — 모두 보기
Toes RE,
Huizinga TW,
Wijmenga C,
Trynka G,
Franke L,
Westra HJ,
Alfredsson L,
Hu X,
Sandor C,
de Bakker PI,
Davila S,
Khor CC,
Heng KK,
Andrews R,
Edkins S,
Hunt SE,
Langford C,
Symmons D,
Concannon P,
Onengut-Gumuscu S,
Rich SS,
Deloukas P,
Gonzalez-Gay MA,
Rodriguez-Rodriguez L,
Ärlsetig L,
Martin J,
Rantapää-Dahlqvist S,
Plenge RM,
Raychaudhuri S,
Klareskog L,
Gregersen PK,
Worthington J
Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate · Wellcome Trust Case Control Consortium
Nature genetics · 2012 · PMID 23143596 · open access
페이지 4개
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci
Cortes A,
Hadler J,
Pointon JP,
Robinson PC,
Karaderi T,
Leo P,
Cremin K,
Pryce K,
Harris J,
Lee S,
Joo KB,
Shim SC
외 53명 — 모두 보기
Weisman M,
Ward M,
Zhou X,
Garchon HJ,
Chiocchia G,
Nossent J,
Lie BA,
Førre Ø,
Tuomilehto J,
Laiho K,
Jiang L,
Liu Y,
Wu X,
Bradbury LA,
Elewaut D,
Burgos-Vargas R,
Stebbings S,
Appleton L,
Farrah C,
Lau J,
Kenna TJ,
Haroon N,
Ferreira MA,
Yang J,
Mulero J,
Fernandez-Sueiro JL,
Gonzalez-Gay MA,
Lopez-Larrea C,
Deloukas P,
Donnelly P,
Bowness P,
Gafney K,
Gaston H,
Gladman DD,
Rahman P,
Maksymowych WP,
Xu H,
Crusius JB,
van der Horst-Bruinsma IE,
Chou CT,
Valle-Oñate R,
Romero-Sánchez C,
Hansen IM,
Pimentel-Santos FM,
Inman RD,
Videm V,
Martin J,
Breban M,
Reveille JD,
Evans DM,
Kim TH,
Wordsworth BP,
Brown MA
International Genetics of Ankylosing Spondylitis Consortium (IGAS) · Australo-Anglo-American Spondyloarthritis Consortium (TASC) 외 컨소시엄 4곳
Nature genetics · 2013 · PMID 23749187
페이지 4개
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Demontis D,
Walters GB,
Athanasiadis G,
Walters R,
Therrien K,
Nielsen TT,
Farajzadeh L,
Voloudakis G,
Bendl J,
Zeng B,
Zhang W,
Grove J
외 35명 — 모두 보기
Als TD,
Duan J,
Satterstrom FK,
Bybjerg-Grauholm J,
Bækved-Hansen M,
Gudmundsson OO,
Magnusson SH,
Baldursson G,
Davidsdottir K,
Haraldsdottir GS,
Agerbo E,
Hoffman GE,
Dalsgaard S,
Martin J,
Ribasés M,
Boomsma DI,
Soler Artigas M,
Roth Mota N,
Howrigan D,
Medland SE,
Zayats T,
Rajagopal VM,
Nordentoft M,
Mors O,
Hougaard DM,
Mortensen PB,
Daly MJ,
Faraone SV,
Stefansson H,
Roussos P,
Franke B,
Werge T,
Neale BM,
Stefansson K,
Børglum AD
ADHD Working Group of the Psychiatric Genomics Consortium · iPSYCH-Broad Consortium
Nature genetics · 2023 · PMID 36702997
페이지 4개
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus
Radstake TR,
Gorlova O,
Rueda B,
Martin JE,
Alizadeh BZ,
Palomino-Morales R,
Coenen MJ,
Vonk MC,
Voskuyl AE,
Schuerwegh AJ,
Broen JC,
van Riel PL
외 51명 — 모두 보기
van 't Slot R,
Italiaander A,
Ophoff RA,
Riemekasten G,
Hunzelmann N,
Simeon CP,
Ortego-Centeno N,
González-Gay MA,
González-Escribano MF,
Airo P,
van Laar J,
Herrick A,
Worthington J,
Hesselstrand R,
Smith V,
de Keyser F,
Houssiau F,
Chee MM,
Madhok R,
Shiels P,
Westhovens R,
Kreuter A,
Kiener H,
de Baere E,
Witte T,
Padykov L,
Klareskog L,
Beretta L,
Scorza R,
Lie BA,
Hoffmann-Vold AM,
Carreira P,
Varga J,
Hinchcliff M,
Gregersen PK,
Lee AT,
Ying J,
Han Y,
Weng SF,
Amos CI,
Wigley FM,
Hummers L,
Nelson JL,
Agarwal SK,
Assassi S,
Gourh P,
Tan FK,
Koeleman BP,
Arnett FC,
Martin J,
Mayes MD
Spanish Scleroderma Group
Nature genetics · 2010 · PMID 20383147
페이지 3개
High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci
Kim K,
Bang SY,
Lee HS,
Cho SK,
Choi CB,
Sung YK,
Kim TH,
Jun JB,
Yoo DH,
Kang YM,
Kim SK,
Suh CH
외 30명 — 모두 보기
Shim SC,
Lee SS,
Lee J,
Chung WT,
Choe JY,
Shin HD,
Lee JY,
Han BG,
Nath SK,
Eyre S,
Bowes J,
Pappas DA,
Kremer JM,
Gonzalez-Gay MA,
Rodriguez-Rodriguez L,
Ärlestig L,
Okada Y,
Diogo D,
Liao KP,
Karlson EW,
Raychaudhuri S,
Rantapää-Dahlqvist S,
Martin J,
Klareskog L,
Padyukov L,
Gregersen PK,
Worthington J,
Greenberg JD,
Plenge RM,
Bae SC
Annals of the rheumatic diseases · 2015 · PMID 24532676
페이지 3개
GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
López-Isac E,
Acosta-Herrera M,
Kerick M,
Assassi S,
Satpathy AT,
Granja J,
Mumbach MR,
Beretta L,
Simeón CP,
Carreira P,
Ortego-Centeno N,
Castellvi I
외 30명 — 모두 보기
Bossini-Castillo L,
Carmona FD,
Orozco G,
Hunzelmann N,
Distler JHW,
Franke A,
Lunardi C,
Moroncini G,
Gabrielli A,
de Vries-Bouwstra J,
Wijmenga C,
Koeleman BPC,
Nordin A,
Padyukov L,
Hoffmann-Vold AM,
Lie B,
Proudman S,
Stevens W,
Nikpour M,
Vyse T,
Herrick AL,
Worthington J,
Denton CP,
Allanore Y,
Brown MA,
Radstake TRDJ,
Fonseca C,
Chang HY,
Mayes MD,
Martin J
European Scleroderma Group† · Australian Scleroderma Interest Group (ASIG)
Nature communications · 2019 · PMID 31672989 · open access
페이지 3개
Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency
Bronson PG,
Chang D,
Bhangale T,
Seldin MF,
Ortmann W,
Ferreira RC,
Urcelay E,
Pereira LF,
Martin J,
Plebani A,
Lougaris V,
Friman V
외 7명 — 모두 보기
Nature genetics · 2016 · PMID 27723758 · open access
페이지 2개
A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder
Martin J,
Walters RK,
Demontis D,
Mattheisen M,
Lee SH,
Robinson E,
Brikell I,
Ghirardi L,
Larsson H,
Lichtenstein P,
Eriksson N,
Werge T
외 13명 — 모두 보기
Mortensen PB,
Pedersen MG,
Mors O,
Nordentoft M,
Hougaard DM,
Bybjerg-Grauholm J,
Wray NR,
Franke B,
Faraone SV,
O'Donovan MC,
Thapar A,
Børglum AD,
Neale BM
23andMe Research Team · Psychiatric Genomics Consortium: ADHD Subgroup 외 컨소시엄 1곳
Biological psychiatry · 2018 · PMID 29325848 · open access
페이지 1개
Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease
Ortiz Fernández L,
Coit P,
Yilmaz V,
Yentür SP,
Alibaz-Oner F,
Aksu K,
Erken E,
Düzgün N,
Keser G,
Cefle A,
Yazici A,
Ergen A
외 25명 — 모두 보기
Alpsoy E,
Salvarani C,
Casali B,
Kısacık B,
Kötter I,
Henes J,
Çınar M,
Schaefer A,
Nohutcu RM,
Zhernakova A,
Wijmenga C,
Takeuchi F,
Harihara S,
Kaburaki T,
Messedi M,
Song YW,
Kaşifoğlu T,
Carmona FD,
Guthridge JM,
James JA,
Martin J,
González Escribano MF,
Saruhan-Direskeneli G,
Direskeneli H,
Sawalha AH
Arthritis & rheumatology (Hoboken, N.J.) · 2021 · PMID 33393726
페이지 1개
Risk loci involved in giant cell arteritis susceptibility: a genome-wide association study
Borrego-Yaniz G,
Ortiz-Fernández L,
Madrid-Paredes A,
Kerick M,
Hernández-Rodríguez J,
Mackie SL,
Vaglio A,
Castañeda S,
Solans R,
Mestre-Torres J,
Khalidi N,
Langford CA
외 39명 — 모두 보기
Ytterberg S,
Beretta L,
Govoni M,
Emmi G,
Cimmino MA,
Witte T,
Neumann T,
Holle J,
Schönau V,
Pugnet G,
Papo T,
Haroche J,
Mahr A,
Mouthon L,
Molberg Ø,
Diamantopoulos AP,
Voskuyl A,
Daikeler T,
Berger CT,
Molloy ES,
Blockmans D,
van Sleen Y,
Iles M,
Sorensen L,
Luqmani R,
Reynolds G,
Bukhari M,
Bhagat S,
Ortego-Centeno N,
Brouwer E,
Lamprecht P,
Klapa S,
Salvarani C,
Merkel PA,
Cid MC,
González-Gay MA,
Morgan AW,
Martin J,
Márquez A
Spanish GCA Group · UK GCA Consortium 외 컨소시엄 1곳
The Lancet. Rheumatology · 2024 · PMID 38734017 · open access
페이지 1개
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