Search Results - "neurogenetics"

Structural architecture and brain network efficiency link polygenic scores to intelligence by Genç, Erhan (Author) , Metzen, Dorothea (Author) , Fraenz, Christoph (Author) , Schlüter, Caroline (Author) , Voelkle, Manuel C. (Author) , Arning, Larissa (Author) , Streit, Fabian (Author) , Nguyen, Huu Phuc (Author) , Güntürkün, Onur (Author) , Ocklenburg, Sebastian (Author) , Kumsta, Robert (Author) ,

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PSEN1/SLC20A2 double mutation causes early-onset Alzheimer’s disease and primary familial brain calcification co-morbidity by Hebestreit, Sophie (Author) , Schwahn, Janine (Author) , Sandikci, Vesile (Author) , Maros, Máté E. (Author) , Valkadinov, Ivan (Author) , Yılmaz, Rüstem (Author) , Eckrich, Lukas (Author) , Loghmani, Seyed Babak (Author) , Lesch, Hendrik (Author) , Conrad, Julian (Author) , Wenz, Holger (Author) , Ebert, Anne (Author) , Brenner, David (Author) , Weishaupt, Jochen H. (Author) ,

Subjects: “…Neurogenetics…”

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Frequency of C9orf72 and SOD1 mutations in 302 sporadic ALS patients from three German ALS centers by Yılmaz, Rüstem (Author) , Grehl, Torsten (Author) , Eckrich, Lukas (Author) , Marschalkowski, Ines (Author) , Weishaupt, Kanchi (Author) , Valkadinov, Ivan (Author) , Simic, Melita (Author) , Brenner, David (Author) , Andersen, Peter M. (Author) , Wolf, Joachim (Author) , Weishaupt, Jochen H. (Author) ,

Subjects: “…neurogenetics…”

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Quantitative longitudinal natural history of eight gangliosidoses: conceptual framework and baseline data of the German 8-in-1 disease registry : a cross-sectional analysis by Ries, Markus (Author) , Mendoza, Grecia (Author) , Arash-Kaps, Laila (Author) , Amraoui, Yasmina (Author) , Quack, Folker (Author) , Hardt, Brigitte (Author) , Diederich, Stefan (Author) , Beck, Michael (Author) , Mengel, Eugen (Author) ,

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Quantitative longitudinal natural history of 8 gangliosidoses: conceptual framework and baseline data of the German 8-in-1 disease registry : a cross-sectional analysis by Ries, Markus (Author) , Mendoza, Grecia (Author) , Arash-Kaps, Laila (Author) , Amraoui, Yasmina (Author) , Quack, Folker (Author) , Hardt, Brigitte (Author) , Diederich, Stefan (Author) , Beck, Michael (Author) , Mengel, Eugen (Author) ,

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FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees by Brenner, David (Author) , Müller, Kathrin (Author) , Lattante, Serena (Author) , Yılmaz, Rüstem (Author) , Knehr, Antje (Author) , Freischmidt, Axel (Author) , Ludolph, Albert C. (Author) , Andersen, Peter M. (Author) , Weishaupt, Jochen H. (Author) ,

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Quantitative retrospective natural history modeling for orphan drug development by Garbade, Sven (Author) , Zielonka, Matthias (Author) , Komatzsuzaki, Shoko (Author) , Kölker, Stefan (Author) , Hoffmann, Georg F. (Author) , Hinderhofer, Katrin (Author) , Mountford, William K. (Author) , Mengel, Eugen (Author) , Sláma, Tomáš (Author) , Mechler, Konstantin (Author) , Ries, Markus (Author) ,

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Reply to: Comparing VUS and AUS parallels and differences in neurogenetics and neuroimmunology by Balint, Bettina (Author) , Bhatia, Kailash P. (Author) , Dalmau, Josep (Author) ,

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KCNN2 mutation in autosomal-dominant tremulous myoclonus-dystonia by Balint, Bettina (Author) , Guerreiro, R. (Author) , Carmona, S. (Author) , Dehghani, N. (Author) , Latorre, Anna (Author) , Cordivari, C. (Author) , Bhatia, K. P. (Author) , Bras, J. (Author) ,

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Neurogenetic approaches to stress and fear in humans as pathophysiological mechanisms for posttraumatic stress disorder by Nees, Frauke (Author) , Witt, Stephanie (Author) , Flor, Herta (Author) ,

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SERAC1 deficiency causes complicated HSP: evidence from a novel splice mutation in a large family by Röben, Benjamin (Author) , Langhans, Claus-Dieter (Author) ,

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Epigenome-wide DNA methylation analysis in siblings and monozygotic twins discordant for sporadic Parkinson’s disease revealed different epigenetic patterns in peripheral blood mon... by Kaut, Oliver (Author) , Rietschel, Marcella (Author) ,

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• Verlag, Volltext

Common variation in the GTF2I gene a promising neurogenetic mechanism for affiliative drive and social anxiety by Schweiger, Janina (Author) , Meyer-Lindenberg, Andreas (Author) ,

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Orphan drug development in rare neurogenetic disorders by Mechler, Konstantin (Author)

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Neurogenetic evidence in the courtroom a randomised controlled trial with German judges by Fuß, Johannes (Author) , Dreßing, Harald (Author) , Briken, Peer (Author) ,

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Neuroscience of aggression

Table of Contents: “…Neurogenetics of Aggressive Behavior - Studies in RodentsNeurogenetics of Aggressive Behavior - Studies in Primates -- Glucocorticoids and Escalated Aggressive Behavior.- Models of Female Aggression - Prefrontal Cortex.- Nitric Oxide, Serotonin and Aggression -- Hypothalamus and Aggressive Behavior -- Vasopressin-Serotonin Interactions in Aggressive Behavior -- Dopamine-oxytocin: Attachment and Conflict -- Stress and violence.- Gene-environment interactions and violence.- MAO-A and genetic risk for violence -- The development of violent behavior in humans -- Schizophrenia and violence.- Psychopathy -- Violent and callous behavior in children -- Aggression in Children and Adolescents- Alcohol and Aggression.…”

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Impaired rRNA synthesis triggers homeostatic responses in hippocampal neurons by Kiryk, Anna (Author) , Kreiner, Grzegorz (Author) , Sowodniok, Katharina (Author) , Rodriguez-Parkitna, Jan (Author) , Sönmez, Aynur (Author) , Górkiewicz, Tomasz (Author) , Bierhoff, Holger (Author) , Wawrzyniak, Marcin (Author) , Janusz, Artur K. (Author) , Liss, Birgit (Author) , Konopka, Witold (Author) , Schütz, Günther (Author) , Kaczmarek, L. (Author) , Parlato, Rosanna (Author) ,

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• Verlag, lizenzpflichtig, Volltext

A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genes

Hippocampal function in healthy carriers of the CLU Alzheimer's disease risk variant by Erk, Susanne (Author) , Meyer-Lindenberg, Andreas (Author) , Boberfeld, Carola Opitz von (Author) , Esslinger, Christine (Author) , Schnell, Knut (Author) , Kirsch, Peter (Author) , Mattheisen, Manuel (Author) , Mühleisen, Thomas W. (Author) , Cichon, Sven (Author) , Witt, Stephanie H. (Author) , Rietschel, Marcella (Author) , Nöthen, Markus M. (Author) , Walter, Henrik (Author) ,

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• Verlag, lizenzpflichtig, Volltext

Brain function in carriers of a genome-wide supported bipolar disorder variant by Erk, Susanne (Author) , Meyer-Lindenberg, Andreas (Author) , Schnell, Knut (Author) , Opitz von Boberfeld, Carola (Author) , Esslinger, Christine (Author) , Kirsch, Peter (Author) , Grimm, Oliver (Author) , Arnold, Claudia (Author) , Haller, Leila (Author) , Witt, Stephanie (Author) , Cichon, Sven (Author) , Nöthen, Markus M. (Author) , Rietschel, Marcella (Author) , Walter, Henrik (Author) ,

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