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Journal of Neural Transmission (Vienna, Austria : 1996)
|
December 16, 2019
High-resolution chromosomal microarray analysis for copy-number variations in high-functioning autism reveals large aberration typical for intellectual disability
Anna Maria Werling, Edna Grünblatt, Beatrice Oneda, et al.
BMC Medical Genomics
|
November 29, 2017
High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder
Edna Grünblatt, Beatrice Oneda, Arif B Ekici, et al.
Pharmacogenetics and Genomics
|
December 20, 2012
Contribution of CYP2B6 alleles in explaining extreme (S)-methadone plasma levels: a CYP2B6 gene resequencing study
Maria Dobrinas, Séverine Crettol, Beatrice Oneda, et al.
Journal of Clinical Psychopharmacology
|
July 14, 2009
ABCB1 and cytochrome P450 polymorphisms: clinical pharmacogenetics of clozapine
Eveline Jaquenoud Sirot, Branka Knezevic, Gina Perla Morena, et al.
Journal of Psychopharmacology (Oxford, England)
|
December 15, 2010
Cytochrome P450 and ABCB1 genetics: association with quetiapine and norquetiapine plasma and cerebrospinal fluid concentrations and with clinical response in patients suffering from schizophrenia. A pilot study
Georg Nikisch, Pierre Baumann, Beatrice Oneda, et al.
Molecular Syndromology
|
September 8, 2017
Low-Level Chromosomal Mosaicism in Neurodevelopmental Disorders
Beatrice Oneda, Reza Asadollahi, Silvia Azzarello-Burri, et al.
Molecular Genetics & Genomic Medicine
|
February 14, 2023
The current benefit of genome sequencing compared to exome sequencing in patients with developmental or epileptic encephalopathies
Anna Grether, Ivan Ivanovski, Martina Russo, et al.
Plos One
|
May 30, 2008
Metalloprotease meprin beta in rat kidney: glomerular localization and differential expression in glomerulonephritis
Beatrice Oneda, Nadège Lods, Daniel Lottaz, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2014
A newly recognized 13q12.3 microdeletion syndrome characterized by intellectual disability, microcephaly, and eczema/atopic dermatitis encompassing the HMGB1 and KATNAL1 genes
Deborah Bartholdi, Asbjørg Stray-Pedersen, Silvia Azzarello-Burri, et al.
European Journal of Medical Genetics
|
November 15, 2022
Microdeletions at 19p13.11p12 in five individuals with neurodevelopmental delay
Melissa Rieger, Sébastien Moutton, Sarah Verheyen, et al.
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Search research articles
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Showing results (11-20 of 34) with videos related to
Sort By:
Page
of 4
Journal of Neural Transmission (Vienna, Austria : 1996)
|
December 16, 2019
High-resolution chromosomal microarray analysis for copy-number variations in high-functioning autism reveals large aberration typical for intellectual disability
Anna Maria Werling, Edna Grünblatt, Beatrice Oneda, et al.
BMC Medical Genomics
|
November 29, 2017
High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder
Edna Grünblatt, Beatrice Oneda, Arif B Ekici, et al.
Pharmacogenetics and Genomics
|
December 20, 2012
Contribution of CYP2B6 alleles in explaining extreme (S)-methadone plasma levels: a CYP2B6 gene resequencing study
Maria Dobrinas, Séverine Crettol, Beatrice Oneda, et al.
Journal of Clinical Psychopharmacology
|
July 14, 2009
ABCB1 and cytochrome P450 polymorphisms: clinical pharmacogenetics of clozapine
Eveline Jaquenoud Sirot, Branka Knezevic, Gina Perla Morena, et al.
Journal of Psychopharmacology (Oxford, England)
|
December 15, 2010
Cytochrome P450 and ABCB1 genetics: association with quetiapine and norquetiapine plasma and cerebrospinal fluid concentrations and with clinical response in patients suffering from schizophrenia. A pilot study
Georg Nikisch, Pierre Baumann, Beatrice Oneda, et al.
Molecular Syndromology
|
September 8, 2017
Low-Level Chromosomal Mosaicism in Neurodevelopmental Disorders
Beatrice Oneda, Reza Asadollahi, Silvia Azzarello-Burri, et al.
Molecular Genetics & Genomic Medicine
|
February 14, 2023
The current benefit of genome sequencing compared to exome sequencing in patients with developmental or epileptic encephalopathies
Anna Grether, Ivan Ivanovski, Martina Russo, et al.
Plos One
|
May 30, 2008
Metalloprotease meprin beta in rat kidney: glomerular localization and differential expression in glomerulonephritis
Beatrice Oneda, Nadège Lods, Daniel Lottaz, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2014
A newly recognized 13q12.3 microdeletion syndrome characterized by intellectual disability, microcephaly, and eczema/atopic dermatitis encompassing the HMGB1 and KATNAL1 genes
Deborah Bartholdi, Asbjørg Stray-Pedersen, Silvia Azzarello-Burri, et al.
European Journal of Medical Genetics
|
November 15, 2022
Microdeletions at 19p13.11p12 in five individuals with neurodevelopmental delay
Melissa Rieger, Sébastien Moutton, Sarah Verheyen, et al.
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