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성함이나 학술지명, PMID로 찾아보십시오.
Wichmann HE에 대해
92건, 그중 20건 표시.
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
Wnt signaling and Dupuytren's disease
Dolmans GH,
Werker PM,
Hennies HC,
Furniss D,
Festen EA,
Franke L,
Becker K,
van der Vlies P,
Wolffenbuttel BH,
Tinschert S,
Toliat MR,
Nothnagel M
외 7명 — 모두 보기
Dutch Dupuytren Study Group · German Dupuytren Study Group 외 컨소시엄 2곳
The New England journal of medicine · 2011 · PMID 21732829
페이지 2개
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1
Winkelmann J,
Czamara D,
Schormair B,
Knauf F,
Schulte EC,
Trenkwalder C,
Dauvilliers Y,
Polo O,
Högl B,
Berger K,
Fuhs A,
Gross N
외 45명 — 모두 보기
Stiasny-Kolster K,
Oertel W,
Bachmann CG,
Paulus W,
Xiong L,
Montplaisir J,
Rouleau GA,
Fietze I,
Vávrová J,
Kemlink D,
Sonka K,
Nevsimalova S,
Lin SC,
Wszolek Z,
Vilariño-Güell C,
Farrer MJ,
Gschliesser V,
Frauscher B,
Falkenstetter T,
Poewe W,
Allen RP,
Earley CJ,
Ondo WG,
Le WD,
Spieler D,
Kaffe M,
Zimprich A,
Kettunen J,
Perola M,
Silander K,
Cournu-Rebeix I,
Francavilla M,
Fontenille C,
Fontaine B,
Vodicka P,
Prokisch H,
Lichtner P,
Peppard P,
Faraco J,
Mignot E,
Gieger C,
Illig T,
Wichmann HE,
Müller-Myhsok B,
Meitinger T
PLoS genetics · 2011 · PMID 21779176 · open access
페이지 2개
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque
Bis JC,
Kavousi M,
Franceschini N,
Isaacs A,
Abecasis GR,
Schminke U,
Post WS,
Smith AV,
Cupples LA,
Markus HS,
Schmidt R,
Huffman JE
외 81명 — 모두 보기
Lehtimäki T,
Baumert J,
Münzel T,
Heckbert SR,
Dehghan A,
North K,
Oostra B,
Bevan S,
Stoegerer EM,
Hayward C,
Raitakari O,
Meisinger C,
Schillert A,
Sanna S,
Völzke H,
Cheng YC,
Thorsson B,
Fox CS,
Rice K,
Rivadeneira F,
Nambi V,
Halperin E,
Petrovic KE,
Peltonen L,
Wichmann HE,
Schnabel RB,
Dörr M,
Parsa A,
Aspelund T,
Demissie S,
Kathiresan S,
Reilly MP,
Taylor K,
Uitterlinden A,
Couper DJ,
Sitzer M,
Kähönen M,
Illig T,
Wild PS,
Orru M,
Lüdemann J,
Shuldiner AR,
Eiriksdottir G,
White CC,
Rotter JI,
Hofman A,
Seissler J,
Zeller T,
Usala G,
Ernst F,
Launer LJ,
D'Agostino RB Sr,
O'Leary DH,
Ballantyne C,
Thiery J,
Ziegler A,
Lakatta EG,
Chilukoti RK,
Harris TB,
Wolf PA,
Psaty BM,
Polak JF,
Li X,
Rathmann W,
Uda M,
Boerwinkle E,
Klopp N,
Schmidt H,
Wilson JF,
Viikari J,
Koenig W,
Blankenberg S,
Newman AB,
Witteman J,
Heiss G,
Duijn Cv,
Scuteri A,
Homuth G,
Mitchell BD,
Gudnason V,
O'Donnell CJ
CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21909108 · open access
페이지 2개
A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation
Coviello AD,
Haring R,
Wellons M,
Vaidya D,
Lehtimäki T,
Keildson S,
Lunetta KL,
He C,
Fornage M,
Lagou V,
Mangino M,
Onland-Moret NC
외 87명 — 모두 보기
Chen B,
Eriksson J,
Garcia M,
Liu YM,
Koster A,
Lohman K,
Lyytikäinen LP,
Petersen AK,
Prescott J,
Stolk L,
Vandenput L,
Wood AR,
Zhuang WV,
Ruokonen A,
Hartikainen AL,
Pouta A,
Bandinelli S,
Biffar R,
Brabant G,
Cox DG,
Chen Y,
Cummings S,
Ferrucci L,
Gunter MJ,
Hankinson SE,
Martikainen H,
Hofman A,
Homuth G,
Illig T,
Jansson JO,
Johnson AD,
Karasik D,
Karlsson M,
Kettunen J,
Kiel DP,
Kraft P,
Liu J,
Ljunggren Ö,
Lorentzon M,
Maggio M,
Markus MR,
Mellström D,
Miljkovic I,
Mirel D,
Nelson S,
Morin Papunen L,
Peeters PH,
Prokopenko I,
Raffel L,
Reincke M,
Reiner AP,
Rexrode K,
Rivadeneira F,
Schwartz SM,
Siscovick D,
Soranzo N,
Stöckl D,
Tworoger S,
Uitterlinden AG,
van Gils CH,
Vasan RS,
Wichmann HE,
Zhai G,
Bhasin S,
Bidlingmaier M,
Chanock SJ,
De Vivo I,
Harris TB,
Hunter DJ,
Kähönen M,
Liu S,
Ouyang P,
Spector TD,
van der Schouw YT,
Viikari J,
Wallaschofski H,
McCarthy MI,
Frayling TM,
Murray A,
Franks S,
Järvelin MR,
de Jong FH,
Raitakari O,
Teumer A,
Ohlsson C,
Murabito JM,
Perry JR
PLoS genetics · 2012 · PMID 22829776 · open access
페이지 2개
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
Steffens M,
Leu C,
Ruppert AK,
Zara F,
Striano P,
Robbiano A,
Capovilla G,
Tinuper P,
Gambardella A,
Bianchi A,
La Neve A,
Crichiutti G
외 78명 — 모두 보기
de Kovel CG,
Kasteleijn-Nolst Trenité D,
de Haan GJ,
Lindhout D,
Gaus V,
Schmitz B,
Janz D,
Weber YG,
Becker F,
Lerche H,
Steinhoff BJ,
Kleefuß-Lie AA,
Kunz WS,
Surges R,
Elger CE,
Muhle H,
von Spiczak S,
Ostertag P,
Helbig I,
Stephani U,
Møller RS,
Hjalgrim H,
Dibbens LM,
Bellows S,
Oliver K,
Mullen S,
Scheffer IE,
Berkovic SF,
Everett KV,
Gardiner MR,
Marini C,
Guerrini R,
Lehesjoki AE,
Siren A,
Guipponi M,
Malafosse A,
Thomas P,
Nabbout R,
Baulac S,
Leguern E,
Guerrero R,
Serratosa JM,
Reif PS,
Rosenow F,
Mörzinger M,
Feucht M,
Zimprich F,
Kapser C,
Schankin CJ,
Suls A,
Smets K,
De Jonghe P,
Jordanova A,
Caglayan H,
Yapici Z,
Yalcin DA,
Baykan B,
Bebek N,
Ozbek U,
Gieger C,
Wichmann HE,
Balschun T,
Ellinghaus D,
Franke A,
Meesters C,
Becker T,
Wienker TF,
Hempelmann A,
Schulz H,
Rüschendorf F,
Leber M,
Pauck SM,
Trucks H,
Toliat MR,
Nürnberg P,
Avanzini G,
Koeleman BP,
Sander T
EPICURE Consortium · EMINet Consortium
Human molecular genetics · 2012 · PMID 22949513
페이지 2개
Genetic studies of body mass index yield new insights for obesity biology
Locke AE,
Kahali B,
Berndt SI,
Justice AE,
Pers TH,
Day FR,
Powell C,
Vedantam S,
Buchkovich ML,
Yang J,
Croteau-Chonka DC,
Esko T
외 470명 — 모두 보기
Fall T,
Ferreira T,
Gustafsson S,
Kutalik Z,
Luan J,
Mägi R,
Randall JC,
Winkler TW,
Wood AR,
Workalemahu T,
Faul JD,
Smith JA,
Zhao JH,
Zhao W,
Chen J,
Fehrmann R,
Hedman ÅK,
Karjalainen J,
Schmidt EM,
Absher D,
Amin N,
Anderson D,
Beekman M,
Bolton JL,
Bragg-Gresham JL,
Buyske S,
Demirkan A,
Deng G,
Ehret GB,
Feenstra B,
Feitosa MF,
Fischer K,
Goel A,
Gong J,
Jackson AU,
Kanoni S,
Kleber ME,
Kristiansson K,
Lim U,
Lotay V,
Mangino M,
Leach IM,
Medina-Gomez C,
Medland SE,
Nalls MA,
Palmer CD,
Pasko D,
Pechlivanis S,
Peters MJ,
Prokopenko I,
Shungin D,
Stančáková A,
Strawbridge RJ,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van Setten J,
Van Vliet-Ostaptchouk JV,
Wang Z,
Yengo L,
Zhang W,
Isaacs A,
Albrecht E,
Ärnlöv J,
Arscott GM,
Attwood AP,
Bandinelli S,
Barrett A,
Bas IN,
Bellis C,
Bennett AJ,
Berne C,
Blagieva R,
Blüher M,
Böhringer S,
Bonnycastle LL,
Böttcher Y,
Boyd HA,
Bruinenberg M,
Caspersen IH,
Chen YI,
Clarke R,
Daw EW,
de Craen AJM,
Delgado G,
Dimitriou M,
Doney ASF,
Eklund N,
Estrada K,
Eury E,
Folkersen L,
Fraser RM,
Garcia ME,
Geller F,
Giedraitis V,
Gigante B,
Go AS,
Golay A,
Goodall AH,
Gordon SD,
Gorski M,
Grabe HJ,
Grallert H,
Grammer TB,
Gräßler J,
Grönberg H,
Groves CJ,
Gusto G,
Haessler J,
Hall P,
Haller T,
Hallmans G,
Hartman CA,
Hassinen M,
Hayward C,
Heard-Costa NL,
Helmer Q,
Hengstenberg C,
Holmen O,
Hottenga JJ,
James AL,
Jeff JM,
Johansson Å,
Jolley J,
Juliusdottir T,
Kinnunen L,
Koenig W,
Koskenvuo M,
Kratzer W,
Laitinen J,
Lamina C,
Leander K,
Lee NR,
Lichtner P,
Lind L,
Lindström J,
Lo KS,
Lobbens S,
Lorbeer R,
Lu Y,
Mach F,
Magnusson PKE,
Mahajan A,
McArdle WL,
McLachlan S,
Menni C,
Merger S,
Mihailov E,
Milani L,
Moayyeri A,
Monda KL,
Morken MA,
Mulas A,
Müller G,
Müller-Nurasyid M,
Musk AW,
Nagaraja R,
Nöthen MM,
Nolte IM,
Pilz S,
Rayner NW,
Renstrom F,
Rettig R,
Ried JS,
Ripke S,
Robertson NR,
Rose LM,
Sanna S,
Scharnagl H,
Scholtens S,
Schumacher FR,
Scott WR,
Seufferlein T,
Shi J,
Smith AV,
Smolonska J,
Stanton AV,
Steinthorsdottir V,
Stirrups K,
Stringham HM,
Sundström J,
Swertz MA,
Swift AJ,
Syvänen AC,
Tan ST,
Tayo BO,
Thorand B,
Thorleifsson G,
Tyrer JP,
Uh HW,
Vandenput L,
Verhulst FC,
Vermeulen SH,
Verweij N,
Vonk JM,
Waite LL,
Warren HR,
Waterworth D,
Weedon MN,
Wilkens LR,
Willenborg C,
Wilsgaard T,
Wojczynski MK,
Wong A,
Wright AF,
Zhang Q,
Brennan EP,
Choi M,
Dastani Z,
Drong AW,
Eriksson P,
Franco-Cereceda A,
Gådin JR,
Gharavi AG,
Goddard ME,
Handsaker RE,
Huang J,
Karpe F,
Kathiresan S,
Keildson S,
Kiryluk K,
Kubo M,
Lee JY,
Liang L,
Lifton RP,
Ma B,
McCarroll SA,
McKnight AJ,
Min JL,
Moffatt MF,
Montgomery GW,
Murabito JM,
Nicholson G,
Nyholt DR,
Okada Y,
Perry JRB,
Dorajoo R,
Reinmaa E,
Salem RM,
Sandholm N,
Scott RA,
Stolk L,
Takahashi A,
Tanaka T,
van 't Hooft FM,
Vinkhuyzen AAE,
Westra HJ,
Zheng W,
Zondervan KT,
Heath AC,
Arveiler D,
Bakker SJL,
Beilby J,
Bergman RN,
Blangero J,
Bovet P,
Campbell H,
Caulfield MJ,
Cesana G,
Chakravarti A,
Chasman DI,
Chines PS,
Collins FS,
Crawford DC,
Cupples LA,
Cusi D,
Danesh J,
de Faire U,
den Ruijter HM,
Dominiczak AF,
Erbel R,
Erdmann J,
Eriksson JG,
Farrall M,
Felix SB,
Ferrannini E,
Ferrières J,
Ford I,
Forouhi NG,
Forrester T,
Franco OH,
Gansevoort RT,
Gejman PV,
Gieger C,
Gottesman O,
Gudnason V,
Gyllensten U,
Hall AS,
Harris TB,
Hattersley AT,
Hicks AA,
Hindorff LA,
Hingorani AD,
Hofman A,
Homuth G,
Hovingh GK,
Humphries SE,
Hunt SC,
Hyppönen E,
Illig T,
Jacobs KB,
Jarvelin MR,
Jöckel KH,
Johansen B,
Jousilahti P,
Jukema JW,
Jula AM,
Kaprio J,
Kastelein JJP,
Keinanen-Kiukaanniemi SM,
Kiemeney LA,
Knekt P,
Kooner JS,
Kooperberg C,
Kovacs P,
Kraja AT,
Kumari M,
Kuusisto J,
Lakka TA,
Langenberg C,
Marchand LL,
Lehtimäki T,
Lyssenko V,
Männistö S,
Marette A,
Matise TC,
McKenzie CA,
McKnight B,
Moll FL,
Morris AD,
Morris AP,
Murray JC,
Nelis M,
Ohlsson C,
Oldehinkel AJ,
Ong KK,
Madden PAF,
Pasterkamp G,
Peden JF,
Peters A,
Postma DS,
Pramstaller PP,
Price JF,
Qi L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Ridker PM,
Rioux JD,
Ritchie MD,
Rudan I,
Salomaa V,
Samani NJ,
Saramies J,
Sarzynski MA,
Schunkert H,
Schwarz PEH,
Sever P,
Shuldiner AR,
Sinisalo J,
Stolk RP,
Strauch K,
Tönjes A,
Trégouët DA,
Tremblay A,
Tremoli E,
Virtamo J,
Vohl MC,
Völker U,
Waeber G,
Willemsen G,
Witteman JC,
Zillikens MC,
Adair LS,
Amouyel P,
Asselbergs FW,
Assimes TL,
Bochud M,
Boehm BO,
Boerwinkle E,
Bornstein SR,
Bottinger EP,
Bouchard C,
Cauchi S,
Chambers JC,
Chanock SJ,
Cooper RS,
de Bakker PIW,
Dedoussis G,
Ferrucci L,
Franks PW,
Froguel P,
Groop LC,
Haiman CA,
Hamsten A,
Hui J,
Hunter DJ,
Hveem K,
Kaplan RC,
Kivimaki M,
Kuh D,
Laakso M,
Liu Y,
Martin NG,
März W,
Melbye M,
Metspalu A,
Moebus S,
Munroe PB,
Njølstad I,
Oostra BA,
Palmer CNA,
Pedersen NL,
Perola M,
Pérusse L,
Peters U,
Power C,
Quertermous T,
Rauramaa R,
Rivadeneira F,
Saaristo TE,
Saleheen D,
Sattar N,
Schadt EE,
Schlessinger D,
Slagboom PE,
Snieder H,
Spector TD,
Thorsteinsdottir U,
Stumvoll M,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
van der Harst P,
Walker M,
Wallaschofski H,
Wareham NJ,
Watkins H,
Weir DR,
Wichmann HE,
Wilson JF,
Zanen P,
Borecki IB,
Deloukas P,
Fox CS,
Heid IM,
O'Connell JR,
Strachan DP,
Stefansson K,
van Duijn CM,
Abecasis GR,
Franke L,
Frayling TM,
McCarthy MI,
Visscher PM,
Scherag A,
Willer CJ,
Boehnke M,
Mohlke KL,
Lindgren CM,
Beckmann JS,
Barroso I,
North KE,
Ingelsson E,
Hirschhorn JN,
Loos RJF,
Speliotes EK
LifeLines Cohort Study · ADIPOGen Consortium 외 컨소시엄 12곳
Nature · 2015 · PMID 25673413
페이지 2개
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome
Schormair B,
Kemlink D,
Roeske D,
Eckstein G,
Xiong L,
Lichtner P,
Ripke S,
Trenkwalder C,
Zimprich A,
Stiasny-Kolster K,
Oertel W,
Bachmann CG
외 20명 — 모두 보기
Paulus W,
Högl B,
Frauscher B,
Gschliesser V,
Poewe W,
Peglau I,
Vodicka P,
Vávrová J,
Sonka K,
Nevsimalova S,
Montplaisir J,
Turecki G,
Rouleau G,
Gieger C,
Illig T,
Wichmann HE,
Holsboer F,
Müller-Myhsok B,
Meitinger T,
Winkelmann J
Nature genetics · 2008 · PMID 18660810
페이지 1개
Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus
Weidinger S,
Gieger C,
Rodriguez E,
Baurecht H,
Mempel M,
Klopp N,
Gohlke H,
Wagenpfeil S,
Ollert M,
Ring J,
Behrendt H,
Heinrich J
외 20명 — 모두 보기
Novak N,
Bieber T,
Krämer U,
Berdel D,
von Berg A,
Bauer CP,
Herbarth O,
Koletzko S,
Prokisch H,
Mehta D,
Mehta D,
Meitinger T,
Depner M,
von Mutius E,
Liang L,
Moffatt M,
Cookson W,
Kabesch M,
Wichmann HE,
Illig T
PLoS genetics · 2008 · PMID 18846228 · open access
페이지 1개
Variants in MTNR1B influence fasting glucose levels
Prokopenko I,
Langenberg C,
Florez JC,
Saxena R,
Soranzo N,
Thorleifsson G,
Loos RJ,
Manning AK,
Jackson AU,
Aulchenko Y,
Potter SC,
Erdos MR
외 96명 — 모두 보기
Sanna S,
Hottenga JJ,
Wheeler E,
Kaakinen M,
Lyssenko V,
Chen WM,
Ahmadi K,
Beckmann JS,
Bergman RN,
Bochud M,
Bonnycastle LL,
Buchanan TA,
Cao A,
Cervino A,
Coin L,
Collins FS,
Crisponi L,
de Geus EJ,
Dehghan A,
Deloukas P,
Doney AS,
Elliott P,
Freimer N,
Gateva V,
Herder C,
Hofman A,
Hughes TE,
Hunt S,
Illig T,
Inouye M,
Isomaa B,
Johnson T,
Kong A,
Krestyaninova M,
Kuusisto J,
Laakso M,
Lim N,
Lindblad U,
Lindgren CM,
McCann OT,
Mohlke KL,
Morris AD,
Naitza S,
Orrù M,
Palmer CN,
Pouta A,
Randall J,
Rathmann W,
Saramies J,
Scheet P,
Scott LJ,
Scuteri A,
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페이지 1개
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
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외 133명 — 모두 보기
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Wellcome Trust Case Control Consortium · Genetic Investigation of ANthropometric Traits Consortium
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페이지 1개
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
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외 44명 — 모두 보기
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페이지 1개
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma
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외 56명 — 모두 보기
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페이지 1개
Common variants in KCNN3 are associated with lone atrial fibrillation
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외 50명 — 모두 보기
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페이지 1개
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
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외 82명 — 모두 보기
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Nature genetics · 2010 · PMID 20418888
페이지 1개
Common genetic variants associate with serum phosphorus concentration
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외 27명 — 모두 보기
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Journal of the American Society of Nephrology : JASN · 2010 · PMID 20558539
페이지 1개
Genome-wide association analysis identifies multiple loci related to resting heart rate
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외 62명 — 모두 보기
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Human molecular genetics · 2010 · PMID 20639392
페이지 1개
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis
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외 18명 — 모두 보기
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Nature genetics · 2010 · PMID 20953186 · open access
페이지 1개
Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2
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외 21명 — 모두 보기
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Nature genetics · 2010 · PMID 20953188
페이지 1개
Genome-wide association analysis identifies three psoriasis susceptibility loci
Stuart PE,
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외 12명 — 모두 보기
Ike R,
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Nature genetics · 2010 · PMID 20953189 · open access
페이지 1개
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