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Effects of single genetic variants and polygenic obesity risk scores on disordered eating in adolescents - The HUNT study Sardahaee, Farzaneh Saeedzadeh; Holmen, Turid Lingaas; Micali, Nadia; Kvaløy, Kirsti 2017
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The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism Klebe, Stephan; Golmard, Jean-Louis; Nalls, Michael A; Saad, Mohamad; ... Corvol, Jean-Christophe 2013
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Preliminary structure and predictive value of attenuated negative symptoms in 22q11.2 deletion syndrome Schneider, Maude; Van der Linden, Martial; Glaser, Bronwyn; Rizzi, Eleonora; ... Eliez, Stéphan 2012
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Hippocampal volume reduction in chromosome 22q11.2 deletion syndrome (22q11.2DS): a longitudinal study of morphometry and symptomatology Flahault, Astrid; Schaer, Marie; Ottet, Marie-Christine; Debbané, Martin; Eliez, Stéphan 2012
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Catechol-O-methyltransferase Val158Met polymorphism moderates anterior cingulate volume in posttraumatic stress disorder Schulz-Heik, R Jay; Schaer, Marie; Eliez, Stéphan; Hallmayer, Joachim F; ... Woodward, Steven H 2011
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Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome Gothelf, Doron; Hoeft, Fumiko; Hinard, Christine; Hallmayer, J. F.; ... Reiss, A. L. 2007