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M Rietschel

Showing results (81-90 of 207) with videos related to

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Psychoneuroendocrinology|November 25, 2018
Stress reactivity in preschool-aged children: Evaluation of a social stress paradigm and investigation of the impact of prenatal maternal stressT S Send, S Bardtke, M Gilles, et al.
Molecular Psychiatry|June 4, 2014
Identification of increased genetic risk scores for schizophrenia in treatment-resistant patientsJ Frank, M Lang, S H Witt, et al.
Acta Psychiatrica Scandinavica|November 28, 2001
Familial occurrence of tardive dyskinesiaD J Müller, T G Schulze, M Knapp, et al.
American Journal of Medical Genetics|July 18, 2000
Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controlsM Rietschel, A Schorr, M Albus, et al.
Neuroscience Letters|July 25, 2000
Decreased frontal lobe ratio of N-acetyl aspartate to choline in familial schizophrenia: a proton magnetic resonance spectroscopy studyW Block, T A Bayer, R Tepest, et al.
Human Genetics|May 1, 1996
Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: identification of two naturally occurring receptor variants and association analysis in schizophreniaJ Erdmann, D Shimron-Abarbanell, M Rietschel, et al.
American Journal of Medical Genetics|July 26, 1996
Systematic screening for mutations in the 5'-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorderS Cichon, M M Nöthen, G Stöber, et al.
American Journal of Medical Genetics|April 9, 1996
Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophreniaD Shimron-Abarbanell, H Harms, J Erdmann, et al.
Translational Psychiatry|July 25, 2013
Functional impact of a recently identified quantitative trait locus for hippocampal volume with genome-wide supportS Erk, A Meyer-Lindenberg, P Schmierer, et al.
American Journal of Human Genetics|April 16, 1998
A gene for universal congenital alopecia maps to chromosome 8p21-22M M Nöthen, S Cichon, I R Vogt, et al.
Pageof 21

Showing results (81-90 of 207) with videos related to

Sort By:
Pageof 21
Psychoneuroendocrinology|November 25, 2018
Stress reactivity in preschool-aged children: Evaluation of a social stress paradigm and investigation of the impact of prenatal maternal stressT S Send, S Bardtke, M Gilles, et al.
Molecular Psychiatry|June 4, 2014
Identification of increased genetic risk scores for schizophrenia in treatment-resistant patientsJ Frank, M Lang, S H Witt, et al.
Acta Psychiatrica Scandinavica|November 28, 2001
Familial occurrence of tardive dyskinesiaD J Müller, T G Schulze, M Knapp, et al.
American Journal of Medical Genetics|July 18, 2000
Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controlsM Rietschel, A Schorr, M Albus, et al.
Neuroscience Letters|July 25, 2000
Decreased frontal lobe ratio of N-acetyl aspartate to choline in familial schizophrenia: a proton magnetic resonance spectroscopy studyW Block, T A Bayer, R Tepest, et al.
Human Genetics|May 1, 1996
Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: identification of two naturally occurring receptor variants and association analysis in schizophreniaJ Erdmann, D Shimron-Abarbanell, M Rietschel, et al.
American Journal of Medical Genetics|July 26, 1996
Systematic screening for mutations in the 5'-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorderS Cichon, M M Nöthen, G Stöber, et al.
American Journal of Medical Genetics|April 9, 1996
Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophreniaD Shimron-Abarbanell, H Harms, J Erdmann, et al.
Translational Psychiatry|July 25, 2013
Functional impact of a recently identified quantitative trait locus for hippocampal volume with genome-wide supportS Erk, A Meyer-Lindenberg, P Schmierer, et al.
American Journal of Human Genetics|April 16, 1998
A gene for universal congenital alopecia maps to chromosome 8p21-22M M Nöthen, S Cichon, I R Vogt, et al.
Pageof 21