Genetics and Genomics of Neurobehavioral Disorders
19%
off

Genetics and Genomics of Neurobehavioral Disorders

Edited by 

Free delivery worldwide

Available. Dispatched from the UK in 4 business days
When will my order arrive?

Description

A clear and comprehensive account of how genetic abnormalities, neurobiology, and neuropsychology work together to manifest cognitive-behavioral dysfunction. The authors review the current status of research in autosomal disorders that produce cognitive-behavioral dysfunction and syndromal and nonsyndromal disorders that produce mental retardation. Comprehensive and up-to-date, Genetics and Genomics of Neurobehavioral Disorders integrates the molecular, genomic, neuropsychological, and neurobehavioral factors that produce learning disabilities and mental retardation into a coherent framework for the understanding and assessment of neurobehavioral disorders.
show more

Product details

  • Hardback | 428 pages
  • 157 x 242.8 x 25.7mm | 825.55g
  • Totowa, NJ, United States
  • English
  • 2003 ed.
  • 27 Illustrations, black and white; X, 428 p. 27 illus.
  • 158829045X
  • 9781588290458

Back cover copy

In recent years, significant gains have been made in the cloning and identification of numerous genes that produce neurobehavioral disorders, as well as in the ability of neuropsychological tests to accurately assess and evaluate cognitive deficits and behavioral dysfunction. In Genetics and Genomics of Neurobehavioral Disorders, a panel of leading researchers draws on this new knowledge to provide a clear and comprehensive account of how genetic abnormalities, neurobiology, and neuropsychology work together to manifest cognitive-behavioral dysfunction. The authors review the current status of research in autosomal disorders that produce such dysfunctions, examining both microdeletion disorders (Prader-Willi syndrome/Angelman syndrome, deletion 22q11, and Williams syndrome) and syndromes arising from microdeletions and sequence variants, among them neurofibromatosis (NF1 and NF2), tuberous sclerosis (TSC1 and TSC2), and myotonic dystrophy. X-linked disorders producing mental retardation in syndromal disorders (ATRX, Rett, and fragile X) and nonsyndromal disorders (FRAXE and MRX) are also discussed. An insightful introduction surveys the history of neurobehavioral disorders, the establishment of relationships between genetic and cognitive impairment, the relationship between neurobiology and behavior, recent advances in neurogenomics, and the use of animal models for complex human disorders and cognitive impairment.
Comprehensive and up-to-date, Genetics and Genomics of Neurobehavioral Disorders integrates the molecular, genomic, neuropsychological, and neurobehavioral factors that produce learning disabilities and mental retardation into a coherent framework for the understanding and assessment of neurobehavioral disorders.
show more

Table of contents

Part I. Introduction and Overview

The Genetics and Genomics of Neurobehavioral Disorders: Historical Introduction and Overview
Gene S. Fisch

Neuroanatomical Considerations Specific to the Study of Neurogenetics
Albert M. Galaburda and J. Eric Schmitt

Modeling Cognitive Disorders: From Genes to Therapies
Rui M. Costa, Ype Elgersma, and Alcino J. Silva

What Can the Study of Behavioral Phenotypes Teach Us About the Pathway from Genes to Behavior?
Jonathan Flint

Part II. Autosomal Disorders and Neurobehavioral Dysfunction

The Central Nervous System in Neurofibromatosis Type 1
Nancy Ratner and Kathryn North

Prader-Willi and Angelman Syndromes: Cognitive and Behavioral Phenotypes
Elisabeth M. Dykens and Suzanne B. Cassidy

Tuberous Sclerosis
Julian R. Sampson and Julia C. Lewis

Behavioral Phenotype in Velo-Cardio-Facial Syndrome
Kieran C. Murphy

Williams-Beuren Syndrome
Monica Bayes and Luis A. Perez Jurado

Behavioral Phenotype in Myotonic Dystrophy (Steinert's Disease)
Jean Steyaert

Part III. X-Linked Nonsyndromal Disorders and Neurobehavioral Dysfunction

Genetics of X-Linked Mental Retardation
Jamel Chelly and Ben C. J. Hamel

Nonsyndromal Mental Retardation Associated with the FRAXE Fragile Site and the FMR2 Gene
Jozef Gecz and Gene S. Fisch

Part IV. X-Linked Syndromal Disorders and Neurobehavioral Dysfunction

ATR-X Syndrome
Takahito Wada and Richard J. Gibbons

The Fragile X Syndrome and the Fragile X Mutation
Mark C. Hirst and Gene S. Fisch

Rett Syndrome: Clinical-Molecular Correlates
Alan K. Percy, Joanna Dragich, and N. Carolyn Schanen

Index
show more

Review quote

"this book brings together research from neuroscience, genetics, and psychology in a concise and unique way. This type of synthesis is sorely needed as we struggle to understand the complexities of human brain function and dysfunction. It is a valuable contribution to these fields as is, and it is exciting to speculate what future editions will contain. "-Doody's Health Sciences Book Review Journal



"...Gene Fisch has edited a remarkable volume...I highly recommend this book for clinicians, researchers, and students interested in neurodevelopmental disorders." - Human Genetics



"...a comprehensive and highly accessible review of this enormously interesting body of work...a highly readable and thought-provoking volume." - J. AM. ACAD. CHILD ADOLESC. PSYCHIATRY



"...a useful update on behavioral phenotypes for which the neurobiological substrates are beginning to reveal their secrets." - Association for Child Psychology



"...a useful update on behavioral phenotypes for which the neurobiological substrates are beginning to reveal their secrets." - Journal of Child Psychology and Psychiatry
show more