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Détail de l'auteur
Auteur Y. KAWASAKI |
Documents disponibles écrits par cet auteur (3)



Correction to: Review of Cognitive Characteristics of Autism Spectrum Disorder Using Performance on Six Subtests on Four Versions of the Wechsler Intelligence Scale for Children / M. TAKAYANAGI in Journal of Autism and Developmental Disorders, 52-1 (January 2022)
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[article]
Titre : Correction to: Review of Cognitive Characteristics of Autism Spectrum Disorder Using Performance on Six Subtests on Four Versions of the Wechsler Intelligence Scale for Children Type de document : Texte imprimé et/ou numérique Auteurs : M. TAKAYANAGI, Auteur ; Y. KAWASAKI, Auteur ; M. SHINOMIYA, Auteur ; H. HIROSHI, Auteur ; S. OKADA, Auteur ; T. INO, Auteur ; K. SAKAI, Auteur ; K. MURAKAMI, Auteur ; R. ISHIDA, Auteur ; K. MIZUNO, Auteur ; S. I. NIWA, Auteur Article en page(s) : p.254 Langues : Anglais (eng) Index. décimale : PER Périodiques En ligne : http://dx.doi.org/10.1007/s10803-021-05020-w Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=454
in Journal of Autism and Developmental Disorders > 52-1 (January 2022) . - p.254[article] Correction to: Review of Cognitive Characteristics of Autism Spectrum Disorder Using Performance on Six Subtests on Four Versions of the Wechsler Intelligence Scale for Children [Texte imprimé et/ou numérique] / M. TAKAYANAGI, Auteur ; Y. KAWASAKI, Auteur ; M. SHINOMIYA, Auteur ; H. HIROSHI, Auteur ; S. OKADA, Auteur ; T. INO, Auteur ; K. SAKAI, Auteur ; K. MURAKAMI, Auteur ; R. ISHIDA, Auteur ; K. MIZUNO, Auteur ; S. I. NIWA, Auteur . - p.254.
Langues : Anglais (eng)
in Journal of Autism and Developmental Disorders > 52-1 (January 2022) . - p.254
Index. décimale : PER Périodiques En ligne : http://dx.doi.org/10.1007/s10803-021-05020-w Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=454 Genetic Analysis of UGT1A1 Polymorphisms Using Preserved Dried Umbilical Cord for Assessing the Potential of Neonatal Jaundice as a Risk Factor for Autism Spectrum Disorder in Children / T. HORINOUCHI in Journal of Autism and Developmental Disorders, 52-2 (February 2022)
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Titre : Genetic Analysis of UGT1A1 Polymorphisms Using Preserved Dried Umbilical Cord for Assessing the Potential of Neonatal Jaundice as a Risk Factor for Autism Spectrum Disorder in Children Type de document : Texte imprimé et/ou numérique Auteurs : T. HORINOUCHI, Auteur ; K. MAEYAMA, Auteur ; M. NAGAI, Auteur ; M. MIZOBUCHI, Auteur ; Y. TAKAGI, Auteur ; Y. OKADA, Auteur ; T. KATO, Auteur ; M. NISHIMURA, Auteur ; Y. KAWASAKI, Auteur ; M. YOSHIOKA, Auteur ; S. TAKADA, Auteur ; H. MATSUMOTO, Auteur ; Y. NAKAMACHI, Auteur ; J. SAEGUSA, Auteur ; S. FUKUSHIMA, Auteur ; K. FUJIOKA, Auteur ; K. TOMIOKA, Auteur ; H. NAGASE, Auteur ; K. NOZU, Auteur ; K. IIJIMA, Auteur ; N. NISHIMURA, Auteur Article en page(s) : p.483-489 Langues : Anglais (eng) Mots-clés : Autism Spectrum Disorder/diagnosis/genetics Child Female Glucuronosyltransferase/genetics Humans Infant, Newborn Jaundice, Neonatal/complications Polymorphism, Genetic Pregnancy Risk Factors Umbilical Cord Autism spectrum disorder Dried umbilical cord Neonatal jaundice Polymorphism Ugt1a1 Index. décimale : PER Périodiques Résumé : Neonatal jaundice has been suggested as a perinatal risk factor for autism spectrum disorder (ASD). We examined UGT1A1 polymorphisms to assess the potential of neonatal jaundice as a risk factor for ASD in children by using DNA extracted from preserved umbilical cord. In total, 79 children with ASD were genotyped for UGT1A1*28 (c.-41-40dup), UGT1A1*6 (c.211 G?>?A), and UGT1A1*27 (c.686 C?>?A). The allele frequency of UGT1A1*6 (OR?=?1.34, p?=?0.26) and UGT1A1*28 (OR?=?0.80, p?=?0.54) and the prevalence of UGT1A1*28/*6 diplotypes did not differ significantly from those in the control population. No UGT1A1*27 allele was detected in the subjects. ASD symptom assessment scores were not associated with UGT1A1*28/*6/*27 genotypes or UGT1A1*28/*6 diplotypes. These results suggest that neonatal jaundice is not significantly associated with ASD. En ligne : http://dx.doi.org/10.1007/s10803-021-04941-w Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=455
in Journal of Autism and Developmental Disorders > 52-2 (February 2022) . - p.483-489[article] Genetic Analysis of UGT1A1 Polymorphisms Using Preserved Dried Umbilical Cord for Assessing the Potential of Neonatal Jaundice as a Risk Factor for Autism Spectrum Disorder in Children [Texte imprimé et/ou numérique] / T. HORINOUCHI, Auteur ; K. MAEYAMA, Auteur ; M. NAGAI, Auteur ; M. MIZOBUCHI, Auteur ; Y. TAKAGI, Auteur ; Y. OKADA, Auteur ; T. KATO, Auteur ; M. NISHIMURA, Auteur ; Y. KAWASAKI, Auteur ; M. YOSHIOKA, Auteur ; S. TAKADA, Auteur ; H. MATSUMOTO, Auteur ; Y. NAKAMACHI, Auteur ; J. SAEGUSA, Auteur ; S. FUKUSHIMA, Auteur ; K. FUJIOKA, Auteur ; K. TOMIOKA, Auteur ; H. NAGASE, Auteur ; K. NOZU, Auteur ; K. IIJIMA, Auteur ; N. NISHIMURA, Auteur . - p.483-489.
Langues : Anglais (eng)
in Journal of Autism and Developmental Disorders > 52-2 (February 2022) . - p.483-489
Mots-clés : Autism Spectrum Disorder/diagnosis/genetics Child Female Glucuronosyltransferase/genetics Humans Infant, Newborn Jaundice, Neonatal/complications Polymorphism, Genetic Pregnancy Risk Factors Umbilical Cord Autism spectrum disorder Dried umbilical cord Neonatal jaundice Polymorphism Ugt1a1 Index. décimale : PER Périodiques Résumé : Neonatal jaundice has been suggested as a perinatal risk factor for autism spectrum disorder (ASD). We examined UGT1A1 polymorphisms to assess the potential of neonatal jaundice as a risk factor for ASD in children by using DNA extracted from preserved umbilical cord. In total, 79 children with ASD were genotyped for UGT1A1*28 (c.-41-40dup), UGT1A1*6 (c.211 G?>?A), and UGT1A1*27 (c.686 C?>?A). The allele frequency of UGT1A1*6 (OR?=?1.34, p?=?0.26) and UGT1A1*28 (OR?=?0.80, p?=?0.54) and the prevalence of UGT1A1*28/*6 diplotypes did not differ significantly from those in the control population. No UGT1A1*27 allele was detected in the subjects. ASD symptom assessment scores were not associated with UGT1A1*28/*6/*27 genotypes or UGT1A1*28/*6 diplotypes. These results suggest that neonatal jaundice is not significantly associated with ASD. En ligne : http://dx.doi.org/10.1007/s10803-021-04941-w Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=455 Review of Cognitive Characteristics of Autism Spectrum Disorder Using Performance on Six Subtests on Four Versions of the Wechsler Intelligence Scale for Children / M. TAKAYANAGI in Journal of Autism and Developmental Disorders, 52-1 (January 2022)
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[article]
Titre : Review of Cognitive Characteristics of Autism Spectrum Disorder Using Performance on Six Subtests on Four Versions of the Wechsler Intelligence Scale for Children Type de document : Texte imprimé et/ou numérique Auteurs : M. TAKAYANAGI, Auteur ; Y. KAWASAKI, Auteur ; M. SHINOMIYA, Auteur ; H. HIROSHI, Auteur ; S. OKADA, Auteur ; T. INO, Auteur ; K. SAKAI, Auteur ; K. MURAKAMI, Auteur ; R. ISHIDA, Auteur ; K. MIZUNO, Auteur ; S. I. NIWA, Auteur Article en page(s) : p.240-253 Langues : Anglais (eng) Mots-clés : Aptitude Autism Spectrum Disorder/diagnosis Child Cognition Humans Prevalence Wechsler Scales Autism spectrum disorder (ASD) Cognitive function Intelligence ability Systematic review Index. décimale : PER Périodiques Résumé : This study was a systematic review of research using the Wechsler Intelligence Scale for Children (WISC) with Autism Spectrum Disorder (ASD) to examine cognitive characteristics of children with ASD beyond the impact of revisions based on WISC and diagnostic criteria changes. The classic "islets of ability" was found in individuals with full-scale IQs?100. The "right-descending profiles" were observed among high IQ score individuals. High levels on the Block Design and low Coding levels were consistently found regardless of the variation in intellectual functioning or diagnosis. This review identified patterns of cognitive characteristics in ASD individuals using empirical data that researchers may have previously been aware of, based on their experiences, owing to the increased prevalence of ASD. En ligne : http://dx.doi.org/10.1007/s10803-021-04932-x Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=454
in Journal of Autism and Developmental Disorders > 52-1 (January 2022) . - p.240-253[article] Review of Cognitive Characteristics of Autism Spectrum Disorder Using Performance on Six Subtests on Four Versions of the Wechsler Intelligence Scale for Children [Texte imprimé et/ou numérique] / M. TAKAYANAGI, Auteur ; Y. KAWASAKI, Auteur ; M. SHINOMIYA, Auteur ; H. HIROSHI, Auteur ; S. OKADA, Auteur ; T. INO, Auteur ; K. SAKAI, Auteur ; K. MURAKAMI, Auteur ; R. ISHIDA, Auteur ; K. MIZUNO, Auteur ; S. I. NIWA, Auteur . - p.240-253.
Langues : Anglais (eng)
in Journal of Autism and Developmental Disorders > 52-1 (January 2022) . - p.240-253
Mots-clés : Aptitude Autism Spectrum Disorder/diagnosis Child Cognition Humans Prevalence Wechsler Scales Autism spectrum disorder (ASD) Cognitive function Intelligence ability Systematic review Index. décimale : PER Périodiques Résumé : This study was a systematic review of research using the Wechsler Intelligence Scale for Children (WISC) with Autism Spectrum Disorder (ASD) to examine cognitive characteristics of children with ASD beyond the impact of revisions based on WISC and diagnostic criteria changes. The classic "islets of ability" was found in individuals with full-scale IQs?100. The "right-descending profiles" were observed among high IQ score individuals. High levels on the Block Design and low Coding levels were consistently found regardless of the variation in intellectual functioning or diagnosis. This review identified patterns of cognitive characteristics in ASD individuals using empirical data that researchers may have previously been aware of, based on their experiences, owing to the increased prevalence of ASD. En ligne : http://dx.doi.org/10.1007/s10803-021-04932-x Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=454