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성함이나 학술지명, PMID로 찾아보십시오.
Schreiber S에 대해
41건, 그중 20건 표시.
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer
Houlston RS,
Webb E,
Broderick P,
Pittman AM,
Di Bernardo MC,
Lubbe S,
Chandler I,
Vijayakrishnan J,
Sullivan K,
Penegar S,
Carvajal-Carmona L,
Howarth K
외 38명 — 모두 보기
Jaeger E,
Spain SL,
Walther A,
Barclay E,
Martin L,
Gorman M,
Domingo E,
Teixeira AS,
Kerr D,
Cazier JB,
Niittymäki I,
Tuupanen S,
Karhu A,
Aaltonen LA,
Tomlinson IP,
Farrington SM,
Tenesa A,
Prendergast JG,
Barnetson RA,
Cetnarskyj R,
Porteous ME,
Pharoah PD,
Koessler T,
Hampe J,
Buch S,
Schafmayer C,
Tepel J,
Schreiber S,
Völzke H,
Chang-Claude J,
Hoffmeister M,
Brenner H,
Zanke BW,
Montpetit A,
Hudson TJ,
Gallinger S,
Campbell H,
Dunlop MG
COGENT Study · Colorectal Cancer Association Study Consortium 외 컨소시엄 1곳
Nature genetics · 2008 · PMID 19011631
페이지 3개
Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways
Nair RP,
Duffin KC,
Helms C,
Ding J,
Stuart PE,
Goldgar D,
Gudjonsson JE,
Li Y,
Tejasvi T,
Feng BJ,
Ruether A,
Schreiber S
외 18명 — 모두 보기
Weichenthal M,
Gladman D,
Rahman P,
Schrodi SJ,
Prahalad S,
Guthery SL,
Fischer J,
Liao W,
Kwok PY,
Menter A,
Lathrop GM,
Wise CA,
Begovich AB,
Voorhees JJ,
Elder JT,
Krueger GG,
Bowcock AM,
Abecasis GR
Collaborative Association Study of Psoriasis
Nature genetics · 2009 · PMID 19169254 · open access
페이지 3개
Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL)
Franke A,
Balschun T,
Sina C,
Ellinghaus D,
Ellinghaus D,
Häsler R,
Mayr G,
Albrecht M,
Wittig M,
Buchert E,
Nikolaus S,
Gieger C
외 16명 — 모두 보기
Wichmann HE,
Sventoraityte J,
Kupcinskas L,
Onnie CM,
Gazouli M,
Anagnou NP,
Strachan D,
McArdle WL,
Mathew CG,
Rutgeerts P,
Vermeire S,
Vatn MH,
Krawczak M,
Rosenstiel P,
Karlsen TH,
Schreiber S
IBSEN study group
Nature genetics · 2010 · PMID 20228798
페이지 3개
Genome-wide meta-analysis identifies new susceptibility loci for migraine
Anttila V,
Winsvold BS,
Gormley P,
Kurth T,
Bettella F,
McMahon G,
Kallela M,
Malik R,
de Vries B,
Terwindt G,
Medland SE,
Todt U
외 85명 — 모두 보기
McArdle WL,
Quaye L,
Koiranen M,
Ikram MA,
Lehtimäki T,
Stam AH,
Ligthart L,
Wedenoja J,
Dunham I,
Neale BM,
Palta P,
Hamalainen E,
Schürks M,
Rose LM,
Buring JE,
Ridker PM,
Steinberg S,
Stefansson H,
Jakobsson F,
Lawlor DA,
Evans DM,
Ring SM,
Färkkilä M,
Artto V,
Kaunisto MA,
Freilinger T,
Schoenen J,
Frants RR,
Pelzer N,
Weller CM,
Zielman R,
Heath AC,
Madden PAF,
Montgomery GW,
Martin NG,
Borck G,
Göbel H,
Heinze A,
Heinze-Kuhn K,
Williams FMK,
Hartikainen AL,
Pouta A,
van den Ende J,
Uitterlinden AG,
Hofman A,
Amin N,
Hottenga JJ,
Vink JM,
Heikkilä K,
Alexander M,
Muller-Myhsok B,
Schreiber S,
Meitinger T,
Wichmann HE,
Aromaa A,
Eriksson JG,
Traynor B,
Trabzuni D,
Rossin E,
Lage K,
Jacobs SBR,
Jacobs SBR,
Gibbs JR,
Birney E,
Kaprio J,
Penninx BW,
Boomsma DI,
van Duijn C,
van Duijn C,
Raitakari O,
Jarvelin MR,
Zwart JA,
Cherkas L,
Strachan DP,
Kubisch C,
Ferrari MD,
van den Maagdenberg AMJM,
Dichgans M,
Wessman M,
Smith GD,
Stefansson K,
Daly MJ,
Nyholt DR,
Chasman D,
Palotie A
North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
페이지 3개
Genetic determinants of circulating sphingolipid concentrations in European populations
Hicks AA,
Pramstaller PP,
Johansson A,
Vitart V,
Rudan I,
Ugocsai P,
Aulchenko Y,
Franklin CS,
Liebisch G,
Erdmann J,
Jonasson I,
Zorkoltseva IV
외 34명 — 모두 보기
Pattaro C,
Hayward C,
Isaacs A,
Hengstenberg C,
Campbell S,
Gnewuch C,
Janssens AC,
Kirichenko AV,
König IR,
Marroni F,
Polasek O,
Demirkan A,
Kolcic I,
Schwienbacher C,
Igl W,
Biloglav Z,
Witteman JC,
Pichler I,
Zaboli G,
Axenovich TI,
Peters A,
Schreiber S,
Wichmann HE,
Schunkert H,
Hastie N,
Oostra BA,
Wild SH,
Meitinger T,
Gyllensten U,
van Duijn CM,
Wilson JF,
Wright A,
Schmitz G,
Campbell H
PLoS genetics · 2009 · PMID 19798445 · open access
페이지 2개
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate
Mangold E,
Ludwig KU,
Birnbaum S,
Baluardo C,
Ferrian M,
Herms S,
Reutter H,
de Assis NA,
Chawa TA,
Mattheisen M,
Steffens M,
Barth S
외 26명 — 모두 보기
Kluck N,
Paul A,
Becker J,
Lauster C,
Schmidt G,
Braumann B,
Scheer M,
Reich RH,
Hemprich A,
Pötzsch S,
Blaumeiser B,
Moebus S,
Krawczak M,
Schreiber S,
Meitinger T,
Wichmann HE,
Steegers-Theunissen RP,
Kramer FJ,
Cichon S,
Propping P,
Wienker TF,
Knapp M,
Rubini M,
Mossey PA,
Hoffmann P,
Nöthen MM
Nature genetics · 2010 · PMID 20023658
페이지 2개
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder
Cichon S,
Mühleisen TW,
Degenhardt FA,
Mattheisen M,
Miró X,
Strohmaier J,
Steffens M,
Meesters C,
Herms S,
Weingarten M,
Priebe L,
Haenisch B
외 64명 — 모두 보기
Alexander M,
Vollmer J,
Breuer R,
Schmäl C,
Tessmann P,
Moebus S,
Wichmann HE,
Schreiber S,
Müller-Myhsok B,
Lucae S,
Jamain S,
Leboyer M,
Bellivier F,
Etain B,
Henry C,
Kahn JP,
Heath S,
Hamshere M,
O'Donovan MC,
Owen MJ,
Craddock N,
Schwarz M,
Vedder H,
Kammerer-Ciernioch J,
Reif A,
Sasse J,
Bauer M,
Hautzinger M,
Wright A,
Mitchell PB,
Schofield PR,
Montgomery GW,
Medland SE,
Gordon SD,
Martin NG,
Gustafsson O,
Andreassen O,
Djurovic S,
Sigurdsson E,
Steinberg S,
Stefansson H,
Stefansson K,
Kapur-Pojskic L,
Oruc L,
Rivas F,
Mayoral F,
Chuchalin A,
Babadjanova G,
Tiganov AS,
Pantelejeva G,
Abramova LI,
Grigoroiu-Serbanescu M,
Diaconu CC,
Czerski PM,
Hauser J,
Zimmer A,
Lathrop M,
Schulze TG,
Wienker TF,
Schumacher J,
Maier W,
Propping P,
Rietschel M,
Nöthen MM
Bipolar Disorder Genome Study (BiGS) Consortium
American journal of human genetics · 2011 · PMID 21353194
페이지 2개
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age
Deelen J,
Beekman M,
Uh HW,
Broer L,
Ayers KL,
Tan Q,
Kamatani Y,
Bennet AM,
Tamm R,
Trompet S,
Guðbjartsson DF,
Flachsbart F
외 75명 — 모두 보기
Rose G,
Viktorin A,
Fischer K,
Nygaard M,
Cordell HJ,
Crocco P,
van den Akker EB,
Böhringer S,
Helmer Q,
Nelson CP,
Saunders GI,
Alver M,
Andersen-Ranberg K,
Breen ME,
van der Breggen R,
Caliebe A,
Capri M,
Cevenini E,
Collerton JC,
Dato S,
Davies K,
Ford I,
Gampe J,
Garagnani P,
de Geus EJ,
Harrow J,
van Heemst D,
Heijmans BT,
Heinsen FA,
Hottenga JJ,
Hofman A,
Jeune B,
Jonsson PV,
Lathrop M,
Lechner D,
Martin-Ruiz C,
Mcnerlan SE,
Mihailov E,
Montesanto A,
Mooijaart SP,
Murphy A,
Nohr EA,
Paternoster L,
Postmus I,
Rivadeneira F,
Ross OA,
Salvioli S,
Sattar N,
Schreiber S,
Stefánsson H,
Stott DJ,
Tiemeier H,
Uitterlinden AG,
Westendorp RG,
Willemsen G,
Samani NJ,
Galan P,
Sørensen TI,
Boomsma DI,
Jukema JW,
Rea IM,
Passarino G,
de Craen AJ,
Christensen K,
Nebel A,
Stefánsson K,
Metspalu A,
Magnusson P,
Blanché H,
Christiansen L,
Kirkwood TB,
van Duijn CM,
Franceschi C,
Houwing-Duistermaat JJ,
Slagboom PE
Human molecular genetics · 2014 · PMID 24688116 · open access
페이지 2개
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis
Buch S,
Stickel F,
Trépo E,
Way M,
Herrmann A,
Nischalke HD,
Brosch M,
Rosendahl J,
Berg T,
Ridinger M,
Rietschel M,
McQuillin A
외 36명 — 모두 보기
Frank J,
Kiefer F,
Schreiber S,
Lieb W,
Soyka M,
Semmo N,
Aigner E,
Datz C,
Schmelz R,
Brückner S,
Zeissig S,
Stephan AM,
Wodarz N,
Devière J,
Clumeck N,
Sarrazin C,
Lammert F,
Gustot T,
Deltenre P,
Völzke H,
Lerch MM,
Mayerle J,
Eyer F,
Schafmayer C,
Cichon S,
Nöthen MM,
Nothnagel M,
Ellinghaus D,
Huse K,
Franke A,
Zopf S,
Hellerbrand C,
Moreno C,
Franchimont D,
Morgan MY,
Hampe J
Nature genetics · 2015 · PMID 26482880
페이지 2개
Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci
Ellinghaus E,
Ellinghaus D,
Krusche P,
Greiner A,
Schreiber C,
Nikolaus S,
Gieger C,
Strauch K,
Lieb W,
Rosenstiel P,
Frings N,
Fiebig A
외 2명 — 모두 보기
Scientific reports · 2017 · PMID 28374850 · open access
페이지 2개
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia
Hillmer AM,
Hanneken S,
Ritzmann S,
Becker T,
Freudenberg J,
Brockschmidt FF,
Flaquer A,
Freudenberg-Hua Y,
Jamra RA,
Metzen C,
Heyn U,
Schweiger N
외 13명 — 모두 보기
Betz RC,
Blaumeiser B,
Hampe J,
Schreiber S,
Schulze TG,
Hennies HC,
Schumacher J,
Propping P,
Ruzicka T,
Cichon S,
Wienker TF,
Kruse R,
Nothen MM
American journal of human genetics · 2005 · PMID 15902657
페이지 1개
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
Tenesa A,
Farrington SM,
Prendergast JG,
Porteous ME,
Walker M,
Haq N,
Barnetson RA,
Theodoratou E,
Cetnarskyj R,
Cartwright N,
Semple C,
Clark AJ
외 45명 — 모두 보기
Reid FJ,
Smith LA,
Kavoussanakis K,
Koessler T,
Pharoah PD,
Buch S,
Schafmayer C,
Tepel J,
Schreiber S,
Völzke H,
Schmidt CO,
Hampe J,
Chang-Claude J,
Hoffmeister M,
Brenner H,
Wilkening S,
Canzian F,
Capella G,
Moreno V,
Deary IJ,
Starr JM,
Tomlinson IP,
Kemp Z,
Howarth K,
Carvajal-Carmona L,
Webb E,
Broderick P,
Vijayakrishnan J,
Houlston RS,
Rennert G,
Ballinger D,
Rozek L,
Gruber SB,
Matsuda K,
Kidokoro T,
Nakamura Y,
Zanke BW,
Greenwood CM,
Rangrej J,
Kustra R,
Montpetit A,
Hudson TJ,
Gallinger S,
Campbell H,
Dunlop MG
Nature genetics · 2008 · PMID 18372901
페이지 1개
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
Tomlinson IP,
Webb E,
Carvajal-Carmona L,
Broderick P,
Howarth K,
Pittman AM,
Spain S,
Lubbe S,
Walther A,
Sullivan K,
Jaeger E,
Fielding S
외 63명 — 모두 보기
Rowan A,
Vijayakrishnan J,
Domingo E,
Chandler I,
Kemp Z,
Qureshi M,
Farrington SM,
Tenesa A,
Prendergast JG,
Barnetson RA,
Penegar S,
Barclay E,
Wood W,
Martin L,
Gorman M,
Thomas H,
Peto J,
Bishop DT,
Gray R,
Maher ER,
Lucassen A,
Kerr D,
Evans DG,
Schafmayer C,
Buch S,
Völzke H,
Hampe J,
Schreiber S,
John U,
Koessler T,
Pharoah P,
van Wezel T,
Morreau H,
Wijnen JT,
Hopper JL,
Southey MC,
Giles GG,
Severi G,
Castellví-Bel S,
Ruiz-Ponte C,
Carracedo A,
Castells A,
Försti A,
Hemminki K,
Vodicka P,
Naccarati A,
Lipton L,
Ho JW,
Cheng KK,
Sham PC,
Luk J,
Agúndez JA,
Ladero JM,
de la Hoya M,
Caldés T,
Niittymäki I,
Tuupanen S,
Karhu A,
Aaltonen L,
Cazier JB,
Campbell H,
Dunlop MG,
Houlston RS
CORGI Consortium · EPICOLON Consortium
Nature genetics · 2008 · PMID 18372905
페이지 1개
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Simón-Sánchez J,
Schulte C,
Bras JM,
Sharma M,
Gibbs JR,
Berg D,
Paisan-Ruiz C,
Lichtner P,
Scholz SW,
Hernandez DG,
Krüger R,
Federoff M
외 35명 — 모두 보기
Klein C,
Goate A,
Perlmutter J,
Bonin M,
Nalls MA,
Illig T,
Gieger C,
Houlden H,
Steffens M,
Okun MS,
Racette BA,
Cookson MR,
Foote KD,
Fernandez HH,
Traynor BJ,
Schreiber S,
Arepalli S,
Zonozi R,
Gwinn K,
van der Brug M,
Lopez G,
Chanock SJ,
Schatzkin A,
Park Y,
Hollenbeck A,
Gao J,
Huang X,
Wood NW,
Lorenz D,
Deuschl G,
Chen H,
Riess O,
Hardy JA,
Singleton AB,
Gasser T
Nature genetics · 2009 · PMID 19915575 · open access
페이지 1개
Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2
Ellinghaus E,
Ellinghaus D,
Stuart PE,
Nair RP,
Debrus S,
Raelson JV,
Belouchi M,
Fournier H,
Reinhard C,
Ding J,
Li Y,
Tejasvi T
외 21명 — 모두 보기
Gudjonsson J,
Stoll SW,
Voorhees JJ,
Lambert S,
Weidinger S,
Eberlein B,
Kunz M,
Rahman P,
Gladman DD,
Gieger C,
Wichmann HE,
Karlsen TH,
Mayr G,
Albrecht M,
Kabelitz D,
Mrowietz U,
Abecasis GR,
Elder JT,
Schreiber S,
Weichenthal M,
Franke A
Nature genetics · 2010 · PMID 20953188
페이지 1개
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia
Ellinghaus E,
Stanulla M,
Richter G,
Ellinghaus D,
te Kronnie G,
Cario G,
Cazzaniga G,
Horstmann M,
Panzer Grümayer R,
Cavé H,
Trka J,
Cinek O
외 15명 — 모두 보기
Teigler-Schlegel A,
ElSharawy A,
Häsler R,
Nebel A,
Meissner B,
Bartram T,
Lescai F,
Franceschi C,
Giordan M,
Nürnberg P,
Heinzow B,
Zimmermann M,
Schreiber S,
Schrappe M,
Franke A
Leukemia · 2012 · PMID 22076464 · open access
페이지 1개
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
Voight BF,
Peloso GM,
Orho-Melander M,
Frikke-Schmidt R,
Barbalic M,
Jensen MK,
Hindy G,
Hólm H,
Ding EL,
Johnson T,
Schunkert H,
Samani NJ
외 114명 — 모두 보기
Clarke R,
Hopewell JC,
Thompson JF,
Li M,
Thorleifsson G,
Newton-Cheh C,
Musunuru K,
Pirruccello JP,
Saleheen D,
Chen L,
Stewart A,
Schillert A,
Thorsteinsdottir U,
Thorgeirsson G,
Anand S,
Engert JC,
Morgan T,
Spertus J,
Stoll M,
Berger K,
Martinelli N,
Girelli D,
McKeown PP,
Patterson CC,
Epstein SE,
Devaney J,
Burnett MS,
Mooser V,
Ripatti S,
Surakka I,
Nieminen MS,
Sinisalo J,
Lokki ML,
Perola M,
Havulinna A,
de Faire U,
Gigante B,
Ingelsson E,
Zeller T,
Wild P,
de Bakker PI,
Klungel OH,
Maitland-van der Zee AH,
Peters BJ,
de Boer A,
Grobbee DE,
Kamphuisen PW,
Deneer VH,
Elbers CC,
Onland-Moret NC,
Hofker MH,
Wijmenga C,
Verschuren WM,
Boer JM,
van der Schouw YT,
Rasheed A,
Frossard P,
Demissie S,
Willer C,
Do R,
Ordovas JM,
Abecasis GR,
Boehnke M,
Mohlke KL,
Daly MJ,
Guiducci C,
Burtt NP,
Surti A,
Gonzalez E,
Purcell S,
Gabriel S,
Marrugat J,
Peden J,
Erdmann J,
Diemert P,
Willenborg C,
König IR,
Fischer M,
Hengstenberg C,
Ziegler A,
Buysschaert I,
Lambrechts D,
Van de Werf F,
Fox KA,
El Mokhtari NE,
Rubin D,
Schrezenmeir J,
Schreiber S,
Schäfer A,
Danesh J,
Blankenberg S,
Roberts R,
McPherson R,
Watkins H,
Hall AS,
Overvad K,
Rimm E,
Boerwinkle E,
Tybjaerg-Hansen A,
Cupples LA,
Reilly MP,
Melander O,
Mannucci PM,
Ardissino D,
Siscovick D,
Elosua R,
Stefansson K,
O'Donnell CJ,
Salomaa V,
Rader DJ,
Peltonen L,
Schwartz SM,
Altshuler D,
Kathiresan S
Lancet (London, England) · 2012 · PMID 22607825 · open access
페이지 1개
Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4
Ellinghaus D,
Folseraas T,
Holm K,
Ellinghaus E,
Melum E,
Balschun T,
Laerdahl JK,
Shiryaev A,
Gotthardt DN,
Weismüller TJ,
Schramm C,
Wittig M
외 25명 — 모두 보기
Bergquist A,
Björnsson E,
Marschall HU,
Vatn M,
Teufel A,
Rust C,
Gieger C,
Wichmann HE,
Runz H,
Sterneck M,
Rupp C,
Braun F,
Weersma RK,
Wijmenga C,
Ponsioen CY,
Mathew CG,
Rutgeerts P,
Vermeire S,
Schrumpf E,
Hov JR,
Manns MP,
Boberg KM,
Schreiber S,
Franke A,
Karlsen TH
Hepatology (Baltimore, Md.) · 2013 · PMID 22821403
페이지 1개
FTO genotype is associated with phenotypic variability of body mass index
Yang J,
Loos RJ,
Powell JE,
Medland SE,
Speliotes EK,
Chasman DI,
Rose LM,
Thorleifsson G,
Steinthorsdottir V,
Mägi R,
Waite L,
Smith AV
외 160명 — 모두 보기
Yerges-Armstrong LM,
Monda KL,
Hadley D,
Mahajan A,
Li G,
Kapur K,
Vitart V,
Huffman JE,
Wang SR,
Palmer C,
Esko T,
Fischer K,
Zhao JH,
Demirkan A,
Isaacs A,
Feitosa MF,
Luan J,
Heard-Costa NL,
White C,
Jackson AU,
Preuss M,
Ziegler A,
Eriksson J,
Kutalik Z,
Frau F,
Nolte IM,
Van Vliet-Ostaptchouk JV,
Hottenga JJ,
Jacobs KB,
Verweij N,
Goel A,
Medina-Gomez C,
Estrada K,
Bragg-Gresham JL,
Sanna S,
Sidore C,
Tyrer J,
Teumer A,
Prokopenko I,
Mangino M,
Lindgren CM,
Assimes TL,
Shuldiner AR,
Hui J,
Beilby JP,
McArdle WL,
Hall P,
Haritunians T,
Zgaga L,
Kolcic I,
Polasek O,
Zemunik T,
Oostra BA,
Junttila MJ,
Grönberg H,
Schreiber S,
Peters A,
Hicks AA,
Stephens J,
Foad NS,
Laitinen J,
Pouta A,
Kaakinen M,
Willemsen G,
Vink JM,
Wild SH,
Navis G,
Asselbergs FW,
Homuth G,
John U,
Iribarren C,
Harris T,
Launer L,
Gudnason V,
O'Connell JR,
Boerwinkle E,
Cadby G,
Palmer LJ,
James AL,
Musk AW,
Ingelsson E,
Psaty BM,
Beckmann JS,
Waeber G,
Vollenweider P,
Hayward C,
Wright AF,
Rudan I,
Groop LC,
Metspalu A,
Khaw KT,
van Duijn CM,
Borecki IB,
Province MA,
Wareham NJ,
Tardif JC,
Huikuri HV,
Cupples LA,
Atwood LD,
Fox CS,
Boehnke M,
Collins FS,
Mohlke KL,
Erdmann J,
Schunkert H,
Hengstenberg C,
Stark K,
Lorentzon M,
Ohlsson C,
Cusi D,
Staessen JA,
Van der Klauw MM,
Pramstaller PP,
Kathiresan S,
Jolley JD,
Ripatti S,
Jarvelin MR,
de Geus EJ,
Boomsma DI,
Penninx B,
Wilson JF,
Campbell H,
Chanock SJ,
van der Harst P,
Hamsten A,
Watkins H,
Hofman A,
Witteman JC,
Zillikens MC,
Uitterlinden AG,
Rivadeneira F,
Zillikens MC,
Kiemeney LA,
Vermeulen SH,
Abecasis GR,
Schlessinger D,
Schipf S,
Stumvoll M,
Tönjes A,
Spector TD,
North KE,
Lettre G,
McCarthy MI,
Berndt SI,
Heath AC,
Madden PA,
Nyholt DR,
Montgomery GW,
Martin NG,
McKnight B,
Strachan DP,
Hill WG,
Snieder H,
Ridker PM,
Thorsteinsdottir U,
Stefansson K,
Frayling TM,
Hirschhorn JN,
Goddard ME,
Visscher PM
Nature · 2012 · PMID 22982992
페이지 1개
Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk
Fischer A,
Ellinghaus D,
Nutsua M,
Hofmann S,
Montgomery CG,
Iannuzzi MC,
Rybicki BA,
Petrek M,
Mrazek F,
Pabst S,
Grohé C,
Grunewald J
외 23명 — 모두 보기
Ronninger M,
Eklund A,
Padyukov L,
Mihailovic-Vucinic V,
Jovanovic D,
Sterclova M,
Homolka J,
Nöthen MM,
Herms S,
Gieger C,
Strauch K,
Winkelmann J,
Boehm BO,
Brand S,
Büning C,
Schürmann M,
Ellinghaus E,
Baurecht H,
Lieb W,
Nebel A,
Müller-Quernheim J,
Franke A,
Schreiber S
GenPhenReSa Consortium
American journal of respiratory and critical care medicine · 2015 · PMID 26051272
페이지 1개
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