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성함이나 학술지명, PMID로 찾아보십시오.
Lieb W에 대해
39건, 그중 19건 표시.
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Kathiresan S,
Voight BF,
Purcell S,
Musunuru K,
Ardissino D,
Mannucci PM,
Anand S,
Engert JC,
Samani NJ,
Schunkert H,
Erdmann J,
Reilly MP
외 174명 — 모두 보기
Rader DJ,
Morgan T,
Spertus JA,
Stoll M,
Girelli D,
McKeown PP,
Patterson CC,
Siscovick DS,
O'Donnell CJ,
Elosua R,
Peltonen L,
Salomaa V,
Schwartz SM,
Melander O,
Altshuler D,
Ardissino D,
Merlini PA,
Berzuini C,
Bernardinelli L,
Peyvandi F,
Tubaro M,
Celli P,
Ferrario M,
Fetiveau R,
Marziliano N,
Casari G,
Galli M,
Ribichini F,
Rossi M,
Bernardi F,
Zonzin P,
Piazza A,
Mannucci PM,
Schwartz SM,
Siscovick DS,
Yee J,
Friedlander Y,
Elosua R,
Marrugat J,
Lucas G,
Subirana I,
Sala J,
Ramos R,
Kathiresan S,
Meigs JB,
Williams G,
Nathan DM,
MacRae CA,
O'Donnell CJ,
Salomaa V,
Havulinna AS,
Peltonen L,
Melander O,
Berglund G,
Voight BF,
Kathiresan S,
Hirschhorn JN,
Asselta R,
Duga S,
Spreafico M,
Musunuru K,
Daly MJ,
Purcell S,
Voight BF,
Purcell S,
Nemesh J,
Korn JM,
McCarroll SA,
Schwartz SM,
Yee J,
Kathiresan S,
Lucas G,
Subirana I,
Elosua R,
Surti A,
Guiducci C,
Gianniny L,
Mirel D,
Parkin M,
Burtt N,
Gabriel SB,
Samani NJ,
Thompson JR,
Braund PS,
Wright BJ,
Balmforth AJ,
Ball SG,
Hall A,
Schunkert H,
Erdmann J,
Linsel-Nitschke P,
Lieb W,
Ziegler A,
König I,
Hengstenberg C,
Fischer M,
Stark K,
Grosshennig A,
Preuss M,
Wichmann HE,
Schreiber S,
Schunkert H,
Samani NJ,
Erdmann J,
Ouwehand W,
Hengstenberg C,
Deloukas P,
Scholz M,
Cambien F,
Reilly MP,
Li M,
Chen Z,
Wilensky R,
Matthai W,
Qasim A,
Hakonarson HH,
Devaney J,
Burnett MS,
Pichard AD,
Kent KM,
Satler L,
Lindsay JM,
Waksman R,
Knouff CW,
Waterworth DM,
Walker MC,
Mooser V,
Epstein SE,
Rader DJ,
Scheffold T,
Berger K,
Stoll M,
Huge A,
Girelli D,
Martinelli N,
Olivieri O,
Corrocher R,
Morgan T,
Spertus JA,
McKeown P,
Patterson CC,
Schunkert H,
Erdmann E,
Linsel-Nitschke P,
Lieb W,
Ziegler A,
König IR,
Hengstenberg C,
Fischer M,
Stark K,
Grosshennig A,
Preuss M,
Wichmann HE,
Schreiber S,
Hólm H,
Thorleifsson G,
Thorsteinsdottir U,
Stefansson K,
Engert JC,
Do R,
Xie C,
Anand S,
Kathiresan S,
Ardissino D,
Mannucci PM,
Siscovick D,
O'Donnell CJ,
Samani NJ,
Melander O,
Elosua R,
Peltonen L,
Salomaa V,
Schwartz SM,
Altshuler D
Myocardial Infarction Genetics Consortium · Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19198609
페이지 4개
Genome-wide association study in essential tremor identifies three new loci
Müller SH,
Girard SL,
Hopfner F,
Merner ND,
Bourassa CV,
Lorenz D,
Clark LN,
Tittmann L,
Soto-Ortolaza AI,
Klebe S,
Hallett M,
Schneider SA
외 37명 — 모두 보기
Hodgkinson CA,
Lieb W,
Wszolek ZK,
Pendziwiat M,
Lorenzo-Betancor O,
Poewe W,
Ortega-Cubero S,
Seppi K,
Rajput A,
Hussl A,
Rajput AH,
Berg D,
Dion PA,
Wurster I,
Shulman JM,
Srulijes K,
Haubenberger D,
Pastor P,
Vilariño-Güell C,
Postuma RB,
Bernard G,
Ladwig KH,
Dupré N,
Jankovic J,
Strauch K,
Panisset M,
Winkelmann J,
Testa CM,
Reischl E,
Zeuner KE,
Ross OA,
Arzberger T,
Chouinard S,
Deuschl G,
Louis ED,
Kuhlenbäumer G,
Rouleau GA
Brain : a journal of neurology · 2016 · PMID 27797806 · open access
페이지 4개
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
Zheng T,
Ellinghaus D,
Juzenas S,
Cossais F,
Burmeister G,
Mayr G,
Jørgensen IF,
Teder-Laving M,
Skogholt AH,
Chen S,
Strege PR,
Ito G
외 73명 — 모두 보기
Banasik K,
Becker T,
Bokelmann F,
Brunak S,
Buch S,
Clausnitzer H,
Datz C,
Degenhardt F,
Doniec M,
Erikstrup C,
Esko T,
Forster M,
Frey N,
Fritsche LG,
Gabrielsen ME,
Gräßle T,
Gsur A,
Gross J,
Hampe J,
Hendricks A,
Hinz S,
Hveem K,
Jongen J,
Junker R,
Karlsen TH,
Hemmrich-Stanisak G,
Kruis W,
Kupcinskas J,
Laubert T,
Rosenstiel PC,
Röcken C,
Laudes M,
Leendertz FH,
Lieb W,
Limperger V,
Margetis N,
Mätz-Rensing K,
Németh CG,
Ness-Jensen E,
Nowak-Göttl U,
Pandit A,
Pedersen OB,
Peleikis HG,
Peuker K,
Rodriguez CL,
Rühlemann MC,
Schniewind B,
Schulzky M,
Skieceviciene J,
Tepel J,
Thomas L,
Uellendahl-Werth F,
Ullum H,
Vogel I,
Volzke H,
von Fersen L,
von Schönfels W,
Vanderwerff B,
Wilking J,
Wittig M,
Zeissig S,
Zobel M,
Zawistowski M,
Vacic V,
Sazonova O,
Noblin ES,
Farrugia G,
Beyder A,
Wedel T,
Kahlke V,
Schafmayer C,
D'Amato M,
Franke A
DBDS Consortium · 23andMe Research Team
Gut · 2021 · PMID 33888516 · open access
페이지 4개
Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus
Kunz M,
König IR,
Schillert A,
Kruppa J,
Ziegler A,
Grallert H,
Müller-Nurasyid M,
Lieb W,
Franke A,
Ranki A,
Panelius J,
Koskenmies S
외 14명 — 모두 보기
Hasan T,
Kere J,
Rönn AC,
Simon JC,
Schmidt E,
Wenzel J,
Tüting T,
Landsberg J,
Zeller T,
Blankenberg S,
Gläser R,
Patsinakidis N,
Kuhn A,
Ibrahim SM
Experimental dermatology · 2015 · PMID 25827949
페이지 3개
Meta-analysis identifies seven susceptibility loci involved in the atopic march
Marenholz I,
Esparza-Gordillo J,
Rüschendorf F,
Bauerfeind A,
Strachan DP,
Spycher BD,
Baurecht H,
Margaritte-Jeannin P,
Sääf A,
Kerkhof M,
Ege M,
Baltic S
외 61명 — 모두 보기
Matheson MC,
Li J,
Michel S,
Ang WQ,
McArdle W,
Arnold A,
Homuth G,
Demenais F,
Bouzigon E,
Söderhäll C,
Pershagen G,
de Jongste JC,
Postma DS,
Braun-Fahrländer C,
Horak E,
Ogorodova LM,
Puzyrev VP,
Bragina EY,
Hudson TJ,
Morin C,
Duffy DL,
Marks GB,
Robertson CF,
Montgomery GW,
Musk B,
Thompson PJ,
Martin NG,
James A,
Sleiman P,
Toskala E,
Rodriguez E,
Fölster-Holst R,
Franke A,
Lieb W,
Gieger C,
Heinzmann A,
Rietschel E,
Keil T,
Cichon S,
Nöthen MM,
Pennell CE,
Sly PD,
Schmidt CO,
Matanovic A,
Schneider V,
Heinig M,
Hübner N,
Holt PG,
Lau S,
Kabesch M,
Weidinger S,
Hakonarson H,
Ferreira MAR,
Laprise C,
Freidin MB,
Genuneit J,
Koppelman GH,
Melén E,
Dizier MH,
Henderson AJ,
Lee YA
Nature communications · 2015 · PMID 26542096 · open access
페이지 3개
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Schmit SL,
Edlund CK,
Schumacher FR,
Gong J,
Harrison TA,
Huyghe JR,
Qu C,
Melas M,
Van Den Berg DJ,
Wang H,
Tring S,
Plummer SJ
외 171명 — 모두 보기
Albanes D,
Alonso MH,
Amos CI,
Anton K,
Aragaki AK,
Arndt V,
Barry EL,
Berndt SI,
Bezieau S,
Bien S,
Bloomer A,
Boehm J,
Boutron-Ruault MC,
Brenner H,
Brezina S,
Buchanan DD,
Butterbach K,
Caan BJ,
Campbell PT,
Carlson CS,
Castelao JE,
Chan AT,
Chang-Claude J,
Chanock SJ,
Cheng I,
Cheng YW,
Chin LS,
Church JM,
Church T,
Coetzee GA,
Cotterchio M,
Cruz Correa M,
Curtis KR,
Duggan D,
Easton DF,
English D,
Feskens EJM,
Fischer R,
FitzGerald LM,
Fortini BK,
Fritsche LG,
Fuchs CS,
Gago-Dominguez M,
Gala M,
Gallinger SJ,
Gauderman WJ,
Giles GG,
Giovannucci EL,
Gogarten SM,
Gonzalez-Villalpando C,
Gonzalez-Villalpando EM,
Grady WM,
Greenson JK,
Gsur A,
Gunter M,
Haiman CA,
Hampe J,
Harlid S,
Harju JF,
Hayes RB,
Hofer P,
Hoffmeister M,
Hopper JL,
Huang SC,
Huerta JM,
Hudson TJ,
Hunter DJ,
Idos GE,
Iwasaki M,
Jackson RD,
Jacobs EJ,
Jee SH,
Jenkins MA,
Jia WH,
Jiao S,
Joshi AD,
Kolonel LN,
Kono S,
Kooperberg C,
Krogh V,
Kuehn T,
Küry S,
LaCroix A,
Laurie CA,
Lejbkowicz F,
Lemire M,
Lenz HJ,
Levine D,
Li CI,
Li L,
Lieb W,
Lin Y,
Lindor NM,
Liu YR,
Loupakis F,
Lu Y,
Luh F,
Ma J,
Mancao C,
Manion FJ,
Markowitz SD,
Martin V,
Matsuda K,
Matsuo K,
McDonnell KJ,
McNeil CE,
Milne R,
Molina AJ,
Mukherjee B,
Murphy N,
Newcomb PA,
Offit K,
Omichessan H,
Palli D,
Cotoré JPP,
Pérez-Mayoral J,
Pharoah PD,
Potter JD,
Qu C,
Raskin L,
Rennert G,
Rennert HS,
Riggs BM,
Schafmayer C,
Schoen RE,
Sellers TA,
Seminara D,
Severi G,
Shi W,
Shibata D,
Shu XO,
Siegel EM,
Slattery ML,
Southey M,
Stadler ZK,
Stern MC,
Stintzing S,
Taverna D,
Thibodeau SN,
Thomas DC,
Trichopoulou A,
Tsugane S,
Ulrich CM,
van Duijnhoven FJB,
van Guelpan B,
Vijai J,
Virtamo J,
Weinstein SJ,
White E,
Win AK,
Wolk A,
Woods M,
Wu AH,
Wu K,
Xiang YB,
Yen Y,
Zanke BW,
Zeng YX,
Zhang B,
Zubair N,
Kweon SS,
Figueiredo JC,
Zheng W,
Marchand LL,
Lindblom A,
Moreno V,
Peters U,
Casey G,
Hsu L,
Conti DV,
Gruber SB
Journal of the National Cancer Institute · 2019 · PMID 29917119
페이지 3개
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
van Rheenen W,
van der Spek RAA,
Bakker MK,
van Vugt JJFA,
Hop PJ,
Zwamborn RAJ,
de Klein N,
Westra HJ,
Bakker OB,
Deelen P,
Shireby G,
Hannon E
외 180명 — 모두 보기
Moisse M,
Baird D,
Restuadi R,
Dolzhenko E,
Dekker AM,
Gawor K,
Westeneng HJ,
Tazelaar GHP,
van Eijk KR,
Kooyman M,
Byrne RP,
Doherty M,
Heverin M,
Al Khleifat A,
Iacoangeli A,
Shatunov A,
Ticozzi N,
Cooper-Knock J,
Smith BN,
Gromicho M,
Chandran S,
Pal S,
Morrison KE,
Shaw PJ,
Hardy J,
Orrell RW,
Sendtner M,
Meyer T,
Başak N,
van der Kooi AJ,
Ratti A,
Fogh I,
Gellera C,
Lauria G,
Corti S,
Cereda C,
Sproviero D,
D'Alfonso S,
Sorarù G,
Siciliano G,
Filosto M,
Padovani A,
Chiò A,
Calvo A,
Moglia C,
Brunetti M,
Canosa A,
Grassano M,
Beghi E,
Pupillo E,
Logroscino G,
Nefussy B,
Osmanovic A,
Nordin A,
Lerner Y,
Zabari M,
Gotkine M,
Baloh RH,
Bell S,
Vourc'h P,
Corcia P,
Couratier P,
Millecamps S,
Meininger V,
Salachas F,
Mora Pardina JS,
Assialioui A,
Rojas-García R,
Dion PA,
Ross JP,
Ludolph AC,
Weishaupt JH,
Brenner D,
Freischmidt A,
Bensimon G,
Brice A,
Durr A,
Payan CAM,
Saker-Delye S,
Wood NW,
Topp S,
Rademakers R,
Tittmann L,
Lieb W,
Franke A,
Ripke S,
Braun A,
Kraft J,
Whiteman DC,
Olsen CM,
Uitterlinden AG,
Hofman A,
Rietschel M,
Cichon S,
Nöthen MM,
Amouyel P,
Traynor BJ,
Singleton AB,
Mitne Neto M,
Cauchi RJ,
Ophoff RA,
Wiedau-Pazos M,
Lomen-Hoerth C,
van Deerlin VM,
Grosskreutz J,
Roediger A,
Gaur N,
Jörk A,
Barthel T,
Theele E,
Ilse B,
Stubendorff B,
Witte OW,
Steinbach R,
Hübner CA,
Graff C,
Brylev L,
Fominykh V,
Demeshonok V,
Ataulina A,
Rogelj B,
Koritnik B,
Zidar J,
Ravnik-Glavač M,
Glavač D,
Stević Z,
Drory V,
Povedano M,
Blair IP,
Kiernan MC,
Benyamin B,
Henderson RD,
Furlong S,
Mathers S,
McCombe PA,
Needham M,
Ngo ST,
Nicholson GA,
Pamphlett R,
Rowe DB,
Steyn FJ,
Williams KL,
Mather KA,
Sachdev PS,
Henders AK,
Wallace L,
de Carvalho M,
Pinto S,
Petri S,
Weber M,
Rouleau GA,
Silani V,
Curtis CJ,
Breen G,
Glass JD,
Brown RH Jr,
Landers JE,
Shaw CE,
Andersen PM,
Groen EJN,
van Es MA,
Pasterkamp RJ,
Fan D,
Garton FC,
McRae AF,
Davey Smith G,
Gaunt TR,
Eberle MA,
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Hardiman O,
Kenna KP,
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Tsai E,
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Veldink JH
SLALOM Consortium · PARALS Consortium 외 컨소시엄 2곳
Nature genetics · 2021 · PMID 34873335 · open access
페이지 3개
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Kato N,
Loh M,
Takeuchi F,
Verweij N,
Wang X,
Zhang W,
Kelly TN,
Saleheen D,
Lehne B,
Leach IM,
Drong AW,
Abbott J
외 233명 — 모두 보기
Wahl S,
Tan ST,
Scott WR,
Campanella G,
Chadeau-Hyam M,
Afzal U,
Ahluwalia TS,
Bonder MJ,
Chen P,
Dehghan A,
Edwards TL,
Esko T,
Go MJ,
Harris SE,
Hartiala J,
Kasela S,
Kasturiratne A,
Khor CC,
Kleber ME,
Li H,
Yu Mok Z,
Nakatochi M,
Sapari NS,
Saxena R,
Stewart AFR,
Stolk L,
Tabara Y,
Teh AL,
Wu Y,
Wu JY,
Zhang Y,
Aits I,
Da Silva Couto Alves A,
Das S,
Dorajoo R,
Hopewell JC,
Kim YK,
Koivula RW,
Luan J,
Lyytikäinen LP,
Nguyen QN,
Pereira MA,
Postmus I,
Raitakari OT,
Scannell Bryan M,
Scott RA,
Sorice R,
Tragante V,
Traglia M,
White J,
Yamamoto K,
Zhang Y,
Adair LS,
Ahmed A,
Akiyama K,
Asif R,
Aung T,
Barroso I,
Bjonnes A,
Braun TR,
Cai H,
Chang LC,
Chen CH,
Cheng CY,
Chong YS,
Collins R,
Courtney R,
Davies G,
Delgado G,
Do LD,
Doevendans PA,
Gansevoort RT,
Gao YT,
Grammer TB,
Grarup N,
Grewal J,
Gu D,
Wander GS,
Hartikainen AL,
Hazen SL,
He J,
Heng CK,
Hixson JE,
Hofman A,
Hsu C,
Huang W,
Husemoen LLN,
Hwang JY,
Ichihara S,
Igase M,
Isono M,
Justesen JM,
Katsuya T,
Kibriya MG,
Kim YJ,
Kishimoto M,
Koh WP,
Kohara K,
Kumari M,
Kwek K,
Lee NR,
Lee J,
Liao J,
Lieb W,
Liewald DCM,
Matsubara T,
Matsushita Y,
Meitinger T,
Mihailov E,
Milani L,
Mills R,
Mononen N,
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Nabika T,
Nakashima E,
Ng HK,
Nikus K,
Nutile T,
Ohkubo T,
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Parish S,
Paternoster L,
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Pham ST,
Pinidiyapathirage MJ,
Rahman M,
Rakugi H,
Rolandsson O,
Ann Rozario M,
Ruggiero D,
Sala CF,
Sarju R,
Shimokawa K,
Snieder H,
Sparsø T,
Spiering W,
Starr JM,
Stott DJ,
Stram DO,
Sugiyama T,
Szymczak S,
Tang WHW,
Tong L,
Trompet S,
Turjanmaa V,
Ueshima H,
Uitterlinden AG,
Umemura S,
Vaarasmaki M,
van Dam RM,
van Gilst WH,
van Veldhuisen DJ,
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Wang Y,
Wang A,
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Wong TY,
Xiang YB,
Yamaguchi S,
Ye X,
Young RD,
Young TL,
Yuan JM,
Zhou X,
Asselbergs FW,
Ciullo M,
Clarke R,
Deloukas P,
Franke A,
Franks PW,
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Friedlander Y,
Gross MD,
Guo Z,
Hansen T,
Jarvelin MR,
Jørgensen T,
Jukema JW,
Kähönen M,
Kajio H,
Kivimaki M,
Lee JY,
Lehtimäki T,
Linneberg A,
Miki T,
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Samani NJ,
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Takayanagi R,
Toniolo D,
Ahsan H,
Allayee H,
Chen YT,
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Franco OH,
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Holbrook JD,
Isaacs A,
Kim BJ,
Lin X,
Liu J,
März W,
Metspalu A,
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Sanghera DK,
Shu XO,
van Meurs JBJ,
Vithana E,
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Wijmenga C,
Wolffenbuttel BHW,
Yokota M,
Zheng W,
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Zhu D,
Vineis P,
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Kleinjans JCS,
McCarthy MI,
Soong R,
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Teo YY,
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Chambers JC
BIOS-consortium · CARDIo GRAMplusCD 외 컨소시엄 2곳
Nature genetics · 2015 · PMID 26390057
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,
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