Søgeresultater - Zsofia Nemoda

Birth weight discordance, gene expression, and DNA methylation: A scoping review of epigenetic twin studies. af Dany Laure Wadji, Zsofia Nemoda, Chantal Martin-Soelch, Linda Booij, Chantal Wicky

Få fuldtekst

Polymorphism in the serotonin receptor 2a (HTR2A) gene as possible predisposal factor for aggressive traits. af Zsofia Banlaki, Zsuzsanna Elek, Tibor Nanasi, Anna Szekely, Zsofia Nemoda, Maria Sasvari-Szekely, Zsolt Ronai

Få fuldtekst

Emotion dysregulation and impulsivity as overlapping symptoms in adult Attention-Deficit/Hyperactivity Disorder and Borderline Personality Disorder: severity profiles and associati... af Eszter Kenézlői, Lívia Balogh, Szilvia Somogyi, Evelyn E. Lévay, Zsuzsa Halmai, Zsófia Nemoda, Zsolt S. Unoka, János M. Réthelyi

Få fuldtekst

Psychometric properties of the Hungarian childhood trauma questionnaire short form and its validity in patients with adult attention-deficit hyperactivity disorder or borderline pe... af Eszter Kenézlői, Eszter Csernela, Zsófia Nemoda, Krisztina Lakatos, Boldizsár Czéh, Zsolt Szabolcs Unoka, Mária Simon, János M. Réthelyi

Få fuldtekst

Differential Genetic Effect of the Norepinephrine Transporter Promoter Polymorphisms on Attention Problems in Clinical and Non-clinical Samples af Zsofia Nemoda, Nora Angyal, Zsanett Tarnok, Emma Birkas, Emma Birkas, Emese Bognar, Maria Sasvari-Szekely, Judit Gervai, Krisztina Lakatos

Få fuldtekst

Haloperidol, Olanzapine, and Risperidone Induce Morphological Changes in an In Vitro Model of Human Hippocampal Neurogenesis af Bálint Jezsó, Sára Kálmán, Kiara Gitta Farkas, Edit Hathy, Katalin Vincze, Dzsenifer Kovács-Schoblocher, Julianna Lilienberg, Csongor Tordai, Zsófia Nemoda, László Homolya, Ágota Apáti, János M. Réthelyi

Få fuldtekst

Investigation of de novo mutations in a schizophrenia case-parent trio by induced pluripotent stem cell-based in vitro disease modeling: convergence of schizophrenia- and autism-re... af Edit Hathy, Eszter Szabó, Nóra Varga, Zsuzsa Erdei, Csongor Tordai, Boróka Czehlár, Máté Baradits, Bálint Jezsó, Júlia Koller, László Nagy, Mária Judit Molnár, László Homolya, Zsófia Nemoda, Ágota Apáti, János M. Réthelyi

Få fuldtekst

Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome af Pritesh Jain, Tyne Miller-Fleming, Apostolia Topaloudi, Dongmei Yu, Petros Drineas, Marianthi Georgitsi, Zhiyu Yang, Renata Rizzo, Kirsten R. Müller-Vahl, Zeynep Tumer, Nanette Mol Debes, Andreas Hartmann, Christel Depienne, Yulia Worbe, Pablo Mir, Danielle C. Cath, Dorret I. Boomsma, Veit Roessner, Tomasz Wolanczyk, Piotr Janik, Natalia Szejko, Cezary Zekanowski, Csaba Barta, Zsofia Nemoda, Zsanett Tarnok, Joseph D. Buxbaum, Dorothy Grice, Jeffrey Glennon, Hreinn Stefansson, Bastian Hengerer, Noa Benaroya-Milshtein, Francesco Cardona, Tammy Hedderly, Isobel Heyman, Chaim Huyser, Astrid Morer, Norbert Mueller, Alexander Munchau, Kerstin J. Plessen, Cesare Porcelli, Susanne Walitza, Anette Schrag, Davide Martino, The Psychiatric Genomics Consortium Tourette Syndrome Working Group (PGC-TS), The EMTICS collaborative group, Andrea Dietrich, The TS-EUROTRAIN Network, Carol A. Mathews, Jeremiah M. Scharf, Pieter J. Hoekstra, Lea K. Davis, Peristera Paschou

Få fuldtekst