Претрага

Резултати

Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease [2008]

Monti, Jan; Fischer, Judith; Paskas, Svetlana ; Heinig, Matthias; Schulz, Herbert; Goesele, Claudia; Heuser, Arnd; Fischer, Robert; Schmidt, Cosima; Schirdewan, Alexander;

Gross, Volkmar; Hummel, Oliver; Maatz, Henrike; Patone, Giannino; Saar, Kathrin; Vingron, Martin; Weldon, Steven M.; Lindpaintner, Klaus; Hammock, Bruce D.; Rohde, Klaus; Dietz, Rainer; Cook, Stuart A.; Schunck, Wolf-Hagen; Luft, Friedrich C.; Hubner, Norbert;

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach (✓) [2011]

Giardine, Belinda; Borg, Joseph; Higgs, Douglas R; Peterson, Kenneth R; Philipsen, Sjaak; Maglott, Donna; Singleton, Belinda K; Anstee, David J; Basak, A Nazli; Clark, Barnaby;

Costa, Flavia C; Faustino, Paula; Fedosyuk, Halyna; Felice, Alex E; Francina, Alain; Galanello, Renzo; Gallivan, Monica V E; Georgitsi, Marianthi; Gibbons, Richard J; Giordano, Piero C; Harteveld, Cornelis L; Hoyer, James D; Jarvis, Martin; Joly, Philippe; Kanavakis, Emmanuel; Kollia, Panagoula; Menzel, Stephan; Miller, Webb; Moradkhani, Kamran; Old, John; Papachatzopoulou, Adamantia; Papadakis, Manoussos N; Papadopoulos, Petros; Pavlović, Sonja ; Perseu, Lucia; Radmilović Milena ; Riemer, Cathy; Satta, Stefania; Schrijver, Iris; Stojiljković, Maja ; Thein, Swee Lay; Traeger-Synodinos, Jan; Tully, Ray; Wada, Takahito; Waye, John S; Wiemann, Claudia; Zukić, Branka ; Chui, David H K; Wajcman, Henri; Hardison, Ross C; Patrinos, George P;

Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease [2014]

Flanagan, Sarah E; ...; Milenkovic, Tatjana; ...; (broj, koautora 23)

Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome [2016]

Braun, Daniela A; ...; Bogdanovic, Radovan M; ...; (broj, koautora 27)

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (✓) [2018]

Pardiñas, Antonio F.; Holmans, Peter; Pocklington, Andrew J.; Escott-Price, Valentina; Ripke, Stephan; Carrera, Noa; Legge, Sophie E.; Bishop, Sophie; Cameron, Darren; Hamshere, Marian L.;

Han, Jun; Hubbard, Leon; Lynham, Amy; Mantripragada, Kiran; Rees, Elliott; MacCabe, James H.; McCarroll, Steven A.; Baune, Bernhard T.; Breen, Gerome; Byrne, Enda M.; Dannlowski, Udo; Eley, Thalia C.; Hayward, Caroline; Martin, Nicholas G.; McIntosh, Andrew M.; Plomin, Robert; Porteous, David J.; Wray, Naomi R.; Caballero, Armando; Geschwind, Daniel H.; Huckins, Laura M.; Ruderfer, Douglas M.; Santiago, Enrique; Sklar, Pamela; Stahl, Eli A.; Won, Hyejung; Agerbo, Esben; Als, Thomas D.; Andreassen, Ole A.; Bækvad-Hansen, Marie; Mortensen, Preben Bo; Pedersen, Carsten Bøcker; Børglum, Anders D.; Bybjerg-Grauholm, Jonas; Đurović, Srđan; Durmishi, Naser; Pedersen, Marianne Giørtz; Golimbet, Vera; Grove, Jakob; Hougaard, David M.; Mattheisen, Manuel; Molden, Espen; Mors, Ole; Nordentoft, Merete; Pejović-Milovančević, Milica ; Sigurdsson, Engilbert; Silagadze, Teimuraz; Hansen, Christine Søholm; Stefansson, Kari; Stefansson, Hreinn; Steinberg, Stacy; Tosato, Sarah; Werge, Thomas; Collier, David A.; Rujescu, Dan; Kirov, George; Owen, Michael J.; O’Donovan, Michael C.; Walters, James T. R.;

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes [2016]

McKay JD; Hung RJ; Han Y; Zong X; Carreras-Torres R; Christiani DC; Caporaso NE; Johansson M; Xiao X; Li Y;

Byun J; Dunning A; Pooley KA; Qian DC; Ji X; Liu G; Timofeeva MN; Bojesen SE; Wu X; Le Marchand L; Albanes D; Bickeböller H; Aldrich MC; Bush WS; Tardon A; Rennert G; Teare MD; Field JK; Kiemeney LA; Lazarus P; Haugen A; Lam S; Schabath MB; Andrew AS; Shen H; Hong YC; Yuan JM; Bertazzi PA; Pesatori AC; Ye Y; Diao N; Su L; Zhang R; Brhane Y; Leighl N; Johansen JS; Mellemgaard A; Saliba W; Haiman CA; Wilkens LR; Fernandez-Somoano A; Fernandez-Tardon G; van der Heijden HFM; Kim JH; Dai J; Hu Z; Davies MPA; Marcus MW; Brunnström H; Manjer J; Melander O; Muller DC; Overvad K; Trichopoulou A; Tumino R; Doherty JA; Barnett MP; Chen C; Goodman GE; Cox A; Taylor F; Woll P; Brüske I; Wichmann HE; Manz J; Muley TR; Risch A; Rosenberger A; Grankvist K; Johansson M; Shepherd FA; Tsao MS; Arnold SM; Haura EB; Bolca C; Holcatova I; Janout V; Kontić, Milica ; Lissowska J; Mukeria A; Ognjanovic S; Orlowski TM; Scelo G; Swiatko;

Deletion of Crhr2 reveals an anxiolytic role for corticotropin-releasing hormone receptor-2 (✓) [2000]

Kishimoto, Toshimitsu; Radulovic, Jelena ; Radulovic, Marko ; Lin, Chijen R.; Schrick, Christina; Hooshmand, Farideh; Hermanson, Ola; Rosenfeld, Michael G.; Spiess, Joachim

Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia [2012]

Zimoń, Magdalena; Baets, Jonathan; Almeida-Souza, Leonardo; De, Vriendt Els; Nikodinovic, Jelena; Parman, Yesim; Battaloǧlu, Esra; Matur, Zeliha; Guergueltcheva, Velina; Tournev, Ivailo;

Auer-Grumbach, Michaela; De, Rijk Peter; Petersen, Britt-Sabina; Müller, Thomas; Fransen, Erik; Van, Damme Philip; Löscher, Wolfgang N; Barišić, Nina; Mitrovic, Zoran; Previtali, Stefano C; Topaloǧlu, Haluk; Bernert, Günther; Beleza-Meireles, Ana; Todorovic, Slobodanka; Savić Pavićević, Dušanka ; Ishpekova, Boryana; Lechner, Silvia; Peeters, Kristien; Ooms, Tinne; Hahn, Angelika F; Züchner, Stephan; Timmerman, Vincent; Van, Dijck Patrick; Milić Rašić, Vedrana ; Janecke, Andreas R; De, Jonghe Peter; Jordanova, Albena;

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021) [2022]

van, Rheenen Wouter; ...; Stevic, Zorica D; ...; (broj, koautora 281)

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology [2021]

Van, Rheenen Wouter; ...; Stevic, Zorica D; ...; (broj, koautora 281)