Search Results - "DELONG, G. R"
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Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism
Published in American journal of human genetics (01-09-2005)“…Autism is a common neurodevelopmental disorder with a significant genetic component. Existing research suggests that multiple genes contribute to autism and…”
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Analysis of the RELN gene as a genetic risk factor for autism
Published in Molecular psychiatry (01-06-2005)“…Several genome-wide screens have indicated the presence of an autism susceptibility locus within the distal long arm of chromosome 7 (7q). Mapping at 7q22…”
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Fine Mapping of Autistic Disorder to Chromosome 15q11-q13 by Use of Phenotypic Subtypes
Published in American journal of human genetics (01-03-2003)“…Autistic disorder (AutD) is a complex genetic disease. Available evidence suggests that several genes contribute to the underlying genetic risk for the…”
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Autism : New data suggest a new hypothesis
Published in Neurology (23-03-1999)Get full text
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Genetic Studies of Autistic Disorder and Chromosome 7
Published in Genomics (San Diego, Calif.) (01-11-1999)“…Genome-wide scans have suggested that a locus on 7q is involved in the etiology of autistic disorder (AD). We have identified an AD family in which three sibs…”
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Analysis of linkage disequilibrium in γ-aminobutyric acid receptor subunit genes in autistic disorder
Published in American journal of medical genetics (07-02-2000)“…Autistic disorder (AD) is a neurodevelopmental disorder characterized by abnormalities in behavior, communication, and social interactions and functioning…”
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Timing of vulnerability of the brain to iodine deficiency in endemic cretinism
Published in The New England journal of medicine (29-12-1994)“…Background: Endemic cretinism, caused by severe iodine deficiency during pregnancy, is the world's most common preventable cause of mental retardation. It can…”
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An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder
Published in Annals of human genetics (01-05-2006)“…Gene-gene interactions are likely involved in many complex genetic disorders and new statistical approaches for detecting such interactions are needed. We…”
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The clinical syndrome of early-life bilateral hippocampal sclerosis
Published in Annals of neurology (01-07-1997)“…Four infants had bilateral hippocampal sclerosis by magnetic resonance scans, including oblique coronal fast spin echo images of the temporal lobes;…”
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Autism, amnesia, hippocampus, and learning
Published in Neuroscience and biobehavioral reviews (1992)“…Autism is held to be the result of the failure of a central cognitive processor which is necessary for flexible multidimensional association of sensorial…”
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Genetic studies in autistic disorder and chromosome 15
Published in Neurogenetics (01-03-2000)“…Autistic disorder (AD) is a developmental disorder affecting social interactions, communication, and behavior. AD is a disease of complex genetic architecture…”
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Ordered-subset analysis of savant skills in autism for 15q11-q13
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05-05-2005)“…Autism is a complex disorder characterized by genetic and phenotypic heterogeneity. Analysis of phenotypically homogeneous subtypes has been used to both…”
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Effect on infant mortality of iodination of irrigation water in a severely iodine-deficient area of China
Published in The Lancet (British edition) (13-09-1997)“…Hotien county in Xinjiang province, China, is an area of severe iodine deficiency and has a high infantmortality rate. We investigated whether iodine…”
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Iodination of irrigation water as a method of supplying iodine to a severely iodine-deficient population in Xinjiang, China
Published in The Lancet (British edition) (09-07-1994)“…Severe iodine deficiency still occurs in many countries, and causes cretinism and mental impairment. In southern Xinjiang province, China, after usual methods…”
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Effects of nutrition on brain development in humans
Published in The American journal of clinical nutrition (01-02-1993)“…Brain development in humans is remarkably resistant to permanent damage from protein-energy malnutrition. However, specific nutrients have crucial roles…”
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Magnetic resonance imaging evidence of hippocampal sclerosis in progression: a case report
Published in Epilepsia (Copenhagen) (01-11-1994)“…A 32-month-old child presented in status epilepticus (SE) involving the left side of the body. Fast spin-echo magnetic resonance imaging (FSE-MRI) with…”
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No association between the APOE gene and autism
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (15-02-2004)“…Autism is a neurodevelopmental disorder characterized by stereotypic and repetitive behavior and interests, together with social and communicative…”
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Correlation of family history with specific autistic subgroups: Asperger's syndrome and bipolar affective disease
Published in Journal of autism and developmental disorders (01-12-1988)“…The etiology of infantile autism is not known. To assess the possible role of familial psychopathology, we investigated a group of autistic subjects subgrouped…”
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An Analysis Paradigm for Investigating Multi‐locus Effects in Complex Disease: Examination of Three GABAA Receptor Subunit Genes on 15q11‐q13 as Risk Factors for Autistic Disorder
Published in Annals of human genetics (01-05-2006)“…Summary Gene‐gene interactions are likely involved in many complex genetic disorders and new statistical approaches for detecting such interactions are needed…”
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Three Children With a Syndrome of Obesity and Overgrowth, Atypical Psychosis, and Seizures: A Problem in Neuropsychopharmacology
Published in Journal of child neurology (01-08-2000)“…Three children presented with a complex syndrome of atypical psychotic and extremely immature behavior, obesity and overgrowth, borderline retardation, and…”
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