Neurobiology of Psychiatric Disorders: New Perspectives on Mental Illness Associated with High Penetrance Genetic Variants
New Perspectives on Mental Illness Associated with High Penetrance Genetic Variants
- 1st Edition - January 1, 2027
- Latest edition
- Editor: Noboru Hiroi
- Language: English
"The Neurobiology of Psychiatric Disorders" provides a conceptually innovative framework to understand psychiatric disorders including autism spectrum disorders, schizophrenia,… Read more
Description
Description
"The Neurobiology of Psychiatric Disorders" provides a conceptually innovative framework to understand psychiatric disorders including autism spectrum disorders, schizophrenia, intellectual disability, bipolar disorder, and ADHD. This book will allow readers to learn diverse mechanistic bases of psychiatric disorders causally associated with genetic variants. Because rare genetic variants have unprecedentedly high levels of penetrance for psychiatric disorders, this book provides reliable genetic links and their mechanistic substrates, thereby providing the starting points of precision medicine.
Key features
Key features
- Explores diverse mechanistic bases of psychiatric disorders causally associated with genetic variants
- Offers a multidisciplinary approach, allowing the reader to incorporate precision medicine
- Introduces innovative framework to understand psychiatric disorders including autism spectrum disorders, schizophrenia and more
Readership
Readership
Researchers in neuroscience, neurobiology, psychiatrists interested in potential genetic foundations of psychiatric disorders
Table of contents
Table of contents
1. Rare and ultra-rare genetic variants associated with psychiatric disorders
2. 3q29: Psychiatric disorder-related phenotypes in a mouse model of recurrent 3q29 deletion
3. 7q11.23 deletion (Williams syndrome)
4. GTF2I: Unveiling the Multifaceted Role in Williams Syndrome - Insights into Brain Development, Myelination, and Social Behavior
5. Genetics of 15q11-q13 duplication syndrome and its mouse models
6. The 16p11.2 syndromes, common and specific impacts of genetic dosage in mammals
7. The impact of gene copy number on psychiatric disorders and its usefulness for gene discovery
8. A genomic window for cognitive and social dimensions of Intellectual disability, ASD, and schizophrenia
9. Molecular Analysis of Glutamatergic Neurons and Microglia Derived from Induced Pluripotent Stem Cells Containing PPM1D Mutations Associated with Jansen de Vries Syndrome.
10. Pitt-Hopkins syndrome: TCF4: A transcriptional regulator of neural cell type composition, circuit maturation, and myelination.
11. SCN2A: Cell-specific functions in developing epilepsy and ASD.
12. Molecular and clinical implications at the intersection of Schaaf-Yang syndrome and Prader-Willi syndrome.
13. Rett/MECP2: Roles in postnatal brain development through maintaining chromatin integrity, neuronal function, and circuitry balance.
14. Post-embryonic stem cells as the origin of Tbx1-dependent social and cognitive dysfunctions of developmental neuropsychiatric disorders
15. Dysmyelination and ASD
16. High-confidence autism risk gene product POGZ regulates neurodevelopment and social behavior.
17. Mechanistic Insights into FoxP1 and Neurodevelopmental Disorders: Cellular, molecular, and genomic perspectives
18. The neurodevelopmental spectrum of CHD2-related brain disorders
19. Smith-Magenis Syndrome: emerging roles in the regulation of transcription and synaptic function 20. Physiopathological roles in brain development and social/cognitive functions
21. Pten: Interneuron-based therapeutic approach
22. A neuron-specific gene in controlling forebrain development and autism-linked phenotypes
23. Fragile X: Genetic perspective of Fragile X syndrome therapeutics
24. Synaptic dysfunctions of Phelan-McDermid syndrome
2. 3q29: Psychiatric disorder-related phenotypes in a mouse model of recurrent 3q29 deletion
3. 7q11.23 deletion (Williams syndrome)
4. GTF2I: Unveiling the Multifaceted Role in Williams Syndrome - Insights into Brain Development, Myelination, and Social Behavior
5. Genetics of 15q11-q13 duplication syndrome and its mouse models
6. The 16p11.2 syndromes, common and specific impacts of genetic dosage in mammals
7. The impact of gene copy number on psychiatric disorders and its usefulness for gene discovery
8. A genomic window for cognitive and social dimensions of Intellectual disability, ASD, and schizophrenia
9. Molecular Analysis of Glutamatergic Neurons and Microglia Derived from Induced Pluripotent Stem Cells Containing PPM1D Mutations Associated with Jansen de Vries Syndrome.
10. Pitt-Hopkins syndrome: TCF4: A transcriptional regulator of neural cell type composition, circuit maturation, and myelination.
11. SCN2A: Cell-specific functions in developing epilepsy and ASD.
12. Molecular and clinical implications at the intersection of Schaaf-Yang syndrome and Prader-Willi syndrome.
13. Rett/MECP2: Roles in postnatal brain development through maintaining chromatin integrity, neuronal function, and circuitry balance.
14. Post-embryonic stem cells as the origin of Tbx1-dependent social and cognitive dysfunctions of developmental neuropsychiatric disorders
15. Dysmyelination and ASD
16. High-confidence autism risk gene product POGZ regulates neurodevelopment and social behavior.
17. Mechanistic Insights into FoxP1 and Neurodevelopmental Disorders: Cellular, molecular, and genomic perspectives
18. The neurodevelopmental spectrum of CHD2-related brain disorders
19. Smith-Magenis Syndrome: emerging roles in the regulation of transcription and synaptic function 20. Physiopathological roles in brain development and social/cognitive functions
21. Pten: Interneuron-based therapeutic approach
22. A neuron-specific gene in controlling forebrain development and autism-linked phenotypes
23. Fragile X: Genetic perspective of Fragile X syndrome therapeutics
24. Synaptic dysfunctions of Phelan-McDermid syndrome
Product details
Product details
- Edition: 1
- Latest edition
- Published: January 1, 2027
- Language: English
About the editor
About the editor
NH
Noboru Hiroi
Dr. Noburo Hiroi is a researcher interested in improving our understanding of the fundamental causes of developmental neuropsychiatric disorders such as autism, schizophrenia, and intellectual disabilities. His approach is interdisciplinary and his expertise includes cell biology, genetics, anatomy, mouse behavior, and developmental neuropsychology.
Affiliations and expertise
The University of Texas at San Antonio, USA