Search Results - "DELONG, G. R"

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    Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism by Ma, D.Q., Whitehead, P.L., Menold, M.M., Martin, E.R., Ashley-Koch, A.E., Mei, H., Ritchie, M.D., DeLong, G.R., Abramson, R.K., Wright, H.H., Cuccaro, M.L., Hussman, J.P., Gilbert, J.R., Pericak-Vance, M.A.

    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 by SKAAR, D. A, SHAO, Y, ASHLEY-KOCH, A. E, CUCCARO, M. L, FOLSTEIN, S. E, GILBERT, J. R, PERICAK-VANCE, M. A, HAINES, J. L, STENGER, J. E, JAWORSKI, J, MARTIN, E. R, DELONG, G. R, MOORE, J. H, MCCAULEY, J. L, SUTCLIFFE, J. S

    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 by Shao, Yujun, Cuccaro, M.L., Hauser, E.R., Raiford, K.L., Menold, M.M., Wolpert, C.M., Ravan, S.A., Elston, L., Decena, K., Donnelly, S.L., Abramson, R.K., Wright, H.H., DeLong, G.R., Gilbert, J.R., Pericak-Vance, M.A.

    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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    Genetic Studies of Autistic Disorder and Chromosome 7 by Ashley-Koch, A., Wolpert, C.M., Menold, M.M., Zaeem, L., Basu, S., Donnelly, S.L., Ravan, S.A., Powell, C.M., Qumsiyeh, M.B., Aylsworth, A.S., Vance, J.M., Gilbert, J.R., Wright, H.H., Abramson, R.K., DeLong, G.R., Cuccaro, M.L., Pericak-Vance, M.A.

    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 by Martin, E.R., Menold, M.M., Wolpert, C.M., Bass, M.P., Donnelly, S.L., Ravan, S.A., Zimmerman, A., Gilbert, J.R., Vance, J.M., Maddox, L.O., Wright, H.H., Abramson, R.K., DeLong, G.R., Cuccaro, M.L., Pericak-Vance, M.A.

    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 by Cao, X.Y. (Xinjiang Anti-Epidemic and Health Station, Urumchi, China.), Jiang, X.M, Dou, Z.H, Rakeman, M.A, Zhang, M.L, O'Donnell, K, Ma, T, Amette, K, DeLong, N, DeLong, G.R

    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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    The clinical syndrome of early-life bilateral hippocampal sclerosis by DeLong, G R, Heinz, E R

    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 by DeLong, G R

    “…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 by BASS, M. P, MENOLD, M. M, GILBERT, J. R, CUCCARO, M. L, DELONG, G. R, PERICAK-VANCE, M. A, WOLPERT, C. M, DONNELLY, S. L, RAVAN, S. A, HAUSER, E. R, MADDOX, L. O, VANCE, J. M, ABRAMSON, R. K, WRIGHT, H. H

    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 by Ma, D.Q., Jaworski, J., Menold, M.M., Donnelly, S., Abramson, R.K., Wright, H.H., Delong, G.R., Gilbert, J.R., Pericak-Vance, M.A., Cuccaro, Michael L.

    “…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 by DeLong, G R, Leslie, P W, Wang, S H, Jiang, X M, Zhang, M L, Rakeman, M, Jiang, J Y, Ma, T, Cao, X Y

    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 by Cao, X Y, Jiang, X M, Kareem, A, Dou, Z H, Abdul Rakeman, M, Zhang, M L, Ma, T, O'Donnell, K, DeLong, N, DeLong, G R

    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 by DeLong, GR

    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 by Nohria, V, Lee, N, Tien, R D, Heinz, E R, Smith, J S, DeLong, G R, Skeen, M B, Resnick, T J, Crain, B, Lewis, D V

    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 by Raiford, K.L., Shao, Y., Allen, I.C., Martin, E.R., Menold, M.M., Wright, H.H., Abramson, R.K., Worley, G., DeLong, G.R., Vance, J.M., Cuccaro, M.L., Gilbert, J.R., Pericak-Vance, M.A.

    “…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 by DELONG, G. R, DWYER, J. T

    “…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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    Three Children With a Syndrome of Obesity and Overgrowth, Atypical Psychosis, and Seizures: A Problem in Neuropsychopharmacology by Jobe, Anna, Lewis, Darrell, Wainwright, Mark, DeLong, G. Robert

    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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