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[article]
Titre : Advancing paternal age and simplex autism Type de document : Texte imprimé et/ou numérique Auteurs : Connor M. PULEO, Auteur ; James SCHMEIDLER, Auteur ; Abraham REICHENBERG, Auteur ; Alexander KOLEVZON, Auteur ; Latha V. SOORYA, Auteur ; Joseph D. BUXBAUM, Auteur Année de publication : 2012 Article en page(s) : p.367-380 Langues : Anglais (eng) Mots-clés : autism spectrum disorder de novo multiplex paternal age sex differences simplex Index. décimale : PER Périodiques Résumé : De novo events appear more common in female and simplex autism spectrum disorder (ASD) cases and may underlie greater ASD risk in older fathers’ offspring. This study examined whether advancing paternal age predicts an increase in simplex (n = 90) versus multiplex ASD cases (n = 587) in 677 participants (340 families). Whether or not controlling for maternal age, results support a significant interaction of linear paternal age and sex of the child on simplex family type. Female ASD cases were significantly more likely to be simplex as paternal age increased, but the increase for males was not significant. Findings suggest that ASD arising from non-familial, de novo events may be far less prominent in males than in females, even if more prevalent in males, due to the substantially larger number of male cases attributable to other, more strongly male-biased risk factors. En ligne : http://dx.doi.org/10.1177/1362361311427154 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=178
in Autism > 16-4 (July 2012) . - p.367-380[article] Advancing paternal age and simplex autism [Texte imprimé et/ou numérique] / Connor M. PULEO, Auteur ; James SCHMEIDLER, Auteur ; Abraham REICHENBERG, Auteur ; Alexander KOLEVZON, Auteur ; Latha V. SOORYA, Auteur ; Joseph D. BUXBAUM, Auteur . - 2012 . - p.367-380.
Langues : Anglais (eng)
in Autism > 16-4 (July 2012) . - p.367-380
Mots-clés : autism spectrum disorder de novo multiplex paternal age sex differences simplex Index. décimale : PER Périodiques Résumé : De novo events appear more common in female and simplex autism spectrum disorder (ASD) cases and may underlie greater ASD risk in older fathers’ offspring. This study examined whether advancing paternal age predicts an increase in simplex (n = 90) versus multiplex ASD cases (n = 587) in 677 participants (340 families). Whether or not controlling for maternal age, results support a significant interaction of linear paternal age and sex of the child on simplex family type. Female ASD cases were significantly more likely to be simplex as paternal age increased, but the increase for males was not significant. Findings suggest that ASD arising from non-familial, de novo events may be far less prominent in males than in females, even if more prevalent in males, due to the substantially larger number of male cases attributable to other, more strongly male-biased risk factors. En ligne : http://dx.doi.org/10.1177/1362361311427154 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=178 Age-related changes of gene expression in the neocortex: Preliminary data on RNA-Seq of the transcriptome in three functionally distinct cortical areas / Oksana Yu NAUMOVA in Development and Psychopathology, 24-4 (November 2012)
[article]
Titre : Age-related changes of gene expression in the neocortex: Preliminary data on RNA-Seq of the transcriptome in three functionally distinct cortical areas Type de document : Texte imprimé et/ou numérique Auteurs : Oksana Yu NAUMOVA, Auteur ; Dean PALEJEV, Auteur ; Natalia V. VLASOVA, Auteur ; Maria LEE, Auteur ; Sergei Yu RYCHKOV, Auteur ; Olga N. BABICH, Auteur ; Flora M. VACCARINO, Auteur ; Elena L. GRIGORENKO, Auteur Année de publication : 2012 Article en page(s) : p.1427-1442 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The study of gene expression (i.e., the study of the transcriptome) in different cells and tissues allows us to understand the molecular mechanisms of their differentiation, development and functioning. In this article, we describe some studies of gene-expression profiling for the purposes of understanding developmental (age-related) changes in the brain using different technologies (e.g., DNA-Microarray) and the new and increasingly popular RNA-Seq. We focus on advancements in studies of gene expression in the human brain, which have provided data on the structure and age-related variability of the transcriptome in the brain. We present data on RNA-Seq of the transcriptome in three distinct areas of the neocortex from different ages: mature and elderly individuals. We report that most age-related transcriptional changes affect cellular signaling systems, and, as a result, the transmission of nerve impulses. In general, the results demonstrate the high potential of RNA-Seq for the study of distinctive features of gene expression among cortical areas and the changes in expression through normal and atypical development of the central nervous system. En ligne : http://dx.doi.org/10.1017/S0954579412000818 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=182
in Development and Psychopathology > 24-4 (November 2012) . - p.1427-1442[article] Age-related changes of gene expression in the neocortex: Preliminary data on RNA-Seq of the transcriptome in three functionally distinct cortical areas [Texte imprimé et/ou numérique] / Oksana Yu NAUMOVA, Auteur ; Dean PALEJEV, Auteur ; Natalia V. VLASOVA, Auteur ; Maria LEE, Auteur ; Sergei Yu RYCHKOV, Auteur ; Olga N. BABICH, Auteur ; Flora M. VACCARINO, Auteur ; Elena L. GRIGORENKO, Auteur . - 2012 . - p.1427-1442.
Langues : Anglais (eng)
in Development and Psychopathology > 24-4 (November 2012) . - p.1427-1442
Index. décimale : PER Périodiques Résumé : The study of gene expression (i.e., the study of the transcriptome) in different cells and tissues allows us to understand the molecular mechanisms of their differentiation, development and functioning. In this article, we describe some studies of gene-expression profiling for the purposes of understanding developmental (age-related) changes in the brain using different technologies (e.g., DNA-Microarray) and the new and increasingly popular RNA-Seq. We focus on advancements in studies of gene expression in the human brain, which have provided data on the structure and age-related variability of the transcriptome in the brain. We present data on RNA-Seq of the transcriptome in three distinct areas of the neocortex from different ages: mature and elderly individuals. We report that most age-related transcriptional changes affect cellular signaling systems, and, as a result, the transmission of nerve impulses. In general, the results demonstrate the high potential of RNA-Seq for the study of distinctive features of gene expression among cortical areas and the changes in expression through normal and atypical development of the central nervous system. En ligne : http://dx.doi.org/10.1017/S0954579412000818 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=182 Allelic Variation Within the Putative Autism Spectrum Disorder Risk Gene Homeobox A1 and Cerebellar Maturation in Typically Developing Children and Adolescents / Armin RAZNAHAN in Autism Research, 5-2 (April 2012)
[article]
Titre : Allelic Variation Within the Putative Autism Spectrum Disorder Risk Gene Homeobox A1 and Cerebellar Maturation in Typically Developing Children and Adolescents Type de document : Texte imprimé et/ou numérique Auteurs : Armin RAZNAHAN, Auteur ; Yohan LEE, Auteur ; Catherine VAITUZIS, Auteur ; Lan TRAN, Auteur ; Susan MACKIE, Auteur ; Henning TIEMEIER, Auteur ; Liv S. CLASEN, Auteur ; Francois LALONDE, Auteur ; Deanna GREENSTEIN, Auteur ; Ron PIERSON, Auteur ; Jay N. GIEDD, Auteur Année de publication : 2012 Article en page(s) : p.93-100 Langues : Anglais (eng) Mots-clés : autism HOXA1 cerebellum gene brain MRI Index. décimale : PER Périodiques Résumé : Homeobox A1 (HOXA1) has been proposed as a candidate gene for autism spectrum disorder (ASD) as it regulates embryological patterning of hind-brain structures implicated in autism neurobiology. In line with this notion, a nonsynonymous single nucleotide polymorphism within a highly conserved domain of HOXA1—A218G (rs10951154)—has been linked to both ASD risk, and cross-sectional differences in superior posterior lobar cerebellar anatomy in late adulthood. Despite evidence for early onset and developmentally dynamic cerebellar involvement in ASD, little is known of the relationship between A218G genotype and maturation of the cerebellum over early development. We addressed this issue using 296 longitudinally acquired structural magnetic resonance imaging brain scans from 116 healthy individuals between 5 and 23 years of age. Mixed models were used to compare the relationship between age and semi-automated measures of cerebellar volume in A-homozygotes (AA) and carriers of the G allele (Gcar). Total cerebellar volume increased between ages of 5 and 23 years in both groups. However, this was accelerated in the Gcar relative to the AA group (Genotype-by-age interaction term, P = 0.03), and driven by genotype-dependent differences in the rate of bilateral superior posterior lobar volume change with age (P = 0.002). Resultantly, although superior posterior lobar volume did not differ significantly between genotype groups at age 5 (P = 0.9), by age 23 it was 12% greater in Gcar than AA (P = 0.002). Our results suggest that common genetic variation within this putative ASD risk gene has the capacity to modify the development of cerebellar systems implicated in ASD neurobiology. En ligne : http://dx.doi.org/10.1002/aur.238 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=155
in Autism Research > 5-2 (April 2012) . - p.93-100[article] Allelic Variation Within the Putative Autism Spectrum Disorder Risk Gene Homeobox A1 and Cerebellar Maturation in Typically Developing Children and Adolescents [Texte imprimé et/ou numérique] / Armin RAZNAHAN, Auteur ; Yohan LEE, Auteur ; Catherine VAITUZIS, Auteur ; Lan TRAN, Auteur ; Susan MACKIE, Auteur ; Henning TIEMEIER, Auteur ; Liv S. CLASEN, Auteur ; Francois LALONDE, Auteur ; Deanna GREENSTEIN, Auteur ; Ron PIERSON, Auteur ; Jay N. GIEDD, Auteur . - 2012 . - p.93-100.
Langues : Anglais (eng)
in Autism Research > 5-2 (April 2012) . - p.93-100
Mots-clés : autism HOXA1 cerebellum gene brain MRI Index. décimale : PER Périodiques Résumé : Homeobox A1 (HOXA1) has been proposed as a candidate gene for autism spectrum disorder (ASD) as it regulates embryological patterning of hind-brain structures implicated in autism neurobiology. In line with this notion, a nonsynonymous single nucleotide polymorphism within a highly conserved domain of HOXA1—A218G (rs10951154)—has been linked to both ASD risk, and cross-sectional differences in superior posterior lobar cerebellar anatomy in late adulthood. Despite evidence for early onset and developmentally dynamic cerebellar involvement in ASD, little is known of the relationship between A218G genotype and maturation of the cerebellum over early development. We addressed this issue using 296 longitudinally acquired structural magnetic resonance imaging brain scans from 116 healthy individuals between 5 and 23 years of age. Mixed models were used to compare the relationship between age and semi-automated measures of cerebellar volume in A-homozygotes (AA) and carriers of the G allele (Gcar). Total cerebellar volume increased between ages of 5 and 23 years in both groups. However, this was accelerated in the Gcar relative to the AA group (Genotype-by-age interaction term, P = 0.03), and driven by genotype-dependent differences in the rate of bilateral superior posterior lobar volume change with age (P = 0.002). Resultantly, although superior posterior lobar volume did not differ significantly between genotype groups at age 5 (P = 0.9), by age 23 it was 12% greater in Gcar than AA (P = 0.002). Our results suggest that common genetic variation within this putative ASD risk gene has the capacity to modify the development of cerebellar systems implicated in ASD neurobiology. En ligne : http://dx.doi.org/10.1002/aur.238 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=155 An A-Z of Genetic Factors in Autism / Kenneth J. AITKEN
Titre : An A-Z of Genetic Factors in Autism : A Handbook for Professionals Type de document : Texte imprimé et/ou numérique Auteurs : Kenneth J. AITKEN, Auteur Editeur : Londres [Angleterre] : Jessica Kingsley Publishers Année de publication : 2010 Importance : 542 p. Format : 19,2cm x 26cm x 4cm ISBN/ISSN/EAN : 978-1-84310-976-1 Note générale : Bibliogr., Index Langues : Anglais (eng) Index. décimale : SCI-B SCI-B - Génétique Résumé : Our understanding of the biological bases to the autistic spectrum disorders (ASDs) is advancing rapidly. Over 80 genetic conditions have now been reported in people who have also been diagnosed with ASDs. Many of these conditions have specific implications for the presenting phenotype and for treatment, management, and intervention. If the basis to the presenting behavioural phenotype is not identified, this can result in a sub-optimal level of care, complications, or even permanent damage.
Kenneth J. Aitken shows that the notion of a single condition known as 'autism' is no longer tenable, and challenges current trends in the diagnosis and management of these behaviours as a homogenous group by drawing on recent research into brain function, genetics, epidemiology and neurology. This volume explains the biology and genetics of ASD, and provides clinicians and researchers with a comprehensive summary of each genetic factor including the research that links it to ASD, diagnosis and treatment issues, and related animal models, as well as detailing relevant professional organisations and avenues for further research.
An A-Z of Genetic Factors in Autism is an essential resource for a wide range of researchers, clinical professionals and students interested in autism spectrum disorders, including clinical and educational psychologists, dieticians, psychiatrists, and neurologists. [Résumé d'Auteur/Editeur]Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=266 An A-Z of Genetic Factors in Autism : A Handbook for Professionals [Texte imprimé et/ou numérique] / Kenneth J. AITKEN, Auteur . - Londres [Angleterre] : Jessica Kingsley Publishers, 2010 . - 542 p. ; 19,2cm x 26cm x 4cm.
ISBN : 978-1-84310-976-1
Bibliogr., Index
Langues : Anglais (eng)
Index. décimale : SCI-B SCI-B - Génétique Résumé : Our understanding of the biological bases to the autistic spectrum disorders (ASDs) is advancing rapidly. Over 80 genetic conditions have now been reported in people who have also been diagnosed with ASDs. Many of these conditions have specific implications for the presenting phenotype and for treatment, management, and intervention. If the basis to the presenting behavioural phenotype is not identified, this can result in a sub-optimal level of care, complications, or even permanent damage.
Kenneth J. Aitken shows that the notion of a single condition known as 'autism' is no longer tenable, and challenges current trends in the diagnosis and management of these behaviours as a homogenous group by drawing on recent research into brain function, genetics, epidemiology and neurology. This volume explains the biology and genetics of ASD, and provides clinicians and researchers with a comprehensive summary of each genetic factor including the research that links it to ASD, diagnosis and treatment issues, and related animal models, as well as detailing relevant professional organisations and avenues for further research.
An A-Z of Genetic Factors in Autism is an essential resource for a wide range of researchers, clinical professionals and students interested in autism spectrum disorders, including clinical and educational psychologists, dieticians, psychiatrists, and neurologists. [Résumé d'Auteur/Editeur]Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=266 Exemplaires (1)
Code-barres Cote Support Localisation Section Disponibilité DOC0003395 SCI-B AIT Livre Centre d'Information et de Documentation du CRA Rhône-Alpes SCI - Disciplines Scientifiques Disponible Les abonnés qui ont emprunté ce document ont également emprunté :
Les écrits de Martha Harris et d'Esther Bick HARRIS WILLIAMS, Meg Histoire de l’empathie BOUVAREL, Alain Sequences: 4-Step HARRISON, Vanessa J'identifie l'intrus 1 AUTISME ET APPRENTISSAGES Decisions ColorCards Qu'est-ce que l'autisme ? GEORGIEFF, Nicolas Analysis of Three Coding Region Polymorphisms in Autism: Evidence for an Association with the Serotonin Transporter / Nurit YIRMIYA
Titre : Analysis of Three Coding Region Polymorphisms in Autism: Evidence for an Association with the Serotonin Transporter Type de document : Texte imprimé et/ou numérique Auteurs : Nurit YIRMIYA, Auteur ; Tammy PILOWSKY, Auteur ; Lubov NEMANOV, Auteur ; Shoshana ARBELLE, Auteur ; Temira FEINSILVER, Auteur ; Iris FRIED, Auteur ; Richard P. EBSTEIN, Auteur Année de publication : 2001 Importance : p.91-101 Langues : Anglais (eng) Index. décimale : APP-D APP-D - Interventions Educatives - Généralités Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=100 Analysis of Three Coding Region Polymorphisms in Autism: Evidence for an Association with the Serotonin Transporter [Texte imprimé et/ou numérique] / Nurit YIRMIYA, Auteur ; Tammy PILOWSKY, Auteur ; Lubov NEMANOV, Auteur ; Shoshana ARBELLE, Auteur ; Temira FEINSILVER, Auteur ; Iris FRIED, Auteur ; Richard P. EBSTEIN, Auteur . - 2001 . - p.91-101.
Langues : Anglais (eng)
Index. décimale : APP-D APP-D - Interventions Educatives - Généralités Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=100 Exemplaires
Code-barres Cote Support Localisation Section Disponibilité aucun exemplaire Annual Research Review: Impact of advances in genetics in understanding developmental psychopathology / Anjene M. ADDINGTON in Journal of Child Psychology and Psychiatry, 53-5 (May 2012)
PermalinkAnxiety Disorders and Phobias / Thompson E. III DAVIS
PermalinkL'apport de la génétique à la compréhension des origines de l'autisme / Sylvain BRIAULT
PermalinkL'apport de la génétique à la compréhension des origines de l'autisme / Sylvain BRIAULT
PermalinkApproche neuropsychologique du syndrome de Down / Annick COMBLAIN
PermalinkApproche neuropsychologique du syndrome de Williams. Introduction générale et aspects langagiers / Steve MAJERUS
PermalinkAspects neurobiologiques et génétiques / Diane PURPER-OUAKIL
PermalinkAssessment and Treatment in Autism Spectrum Disorders: A Focus on Genetics and Psychiatry / Merlin G. BUTLER in Autism Research and Treatment, (March 2012)
PermalinkAssociation of a functional variant of the nitric oxide synthase 1 gene with personality, anxiety, and depressiveness / Triin KURRIKOFF in Development and Psychopathology, 24-4 (November 2012)
PermalinkAssociation of GTF2i in the Williams-Beuren Syndrome Critical Region with Autism Spectrum Disorders / Patrick MALENFANT in Journal of Autism and Developmental Disorders, 42-7 (July 2012)
PermalinkAttentes des familles en difficulté / Marie-Odile RETHORE
PermalinkAutism and its Medical Management / Michael G. CHEZ
PermalinkAutism and Joint Attention / Peter C. MUNDY
PermalinkAutism and Other Neurodevelopmental Disorders / Robin L. HANSEN
PermalinkAutism and Pervasive Developmental Disorders / Fred R. VOLKMAR
PermalinkAutism and Pervasive Developmental Disorders / Fred R. VOLKMAR
PermalinkAutism and tuberous sclerosis complex / Susan L. SMALLEY
PermalinkAutism / Andrew W. ZIMMERMAN
PermalinkAutism: familial aggregation and genetic implications / S. E. FOLSTEIN
PermalinkAutism in Genetic Intellectual Disability : Insights into Idiopathic Autism / Walter E. KAUFMANN
PermalinkAutism : neuropathology, alterations of the GABAergic system, and animal models / Christoph SCHMITZ
PermalinkAutism Spectrum Disorder: Neuromodulation, Neurofeedback, and Sensory Integration Approaches to Research and Treatment / Estate M. SOKHADZE
PermalinkAutism spectrum disorders in Hispanics and non-Hispanics / Virginia CHAIDEZ in Autism, 16-4 (July 2012)
PermalinkAutism Spectrum Disorders Through the Life Span / Digby TANTAM
PermalinkAutism, Stress and Chromosome 7 Genes / Michael SHAPIRA
PermalinkAutism: Where Genetics Meets the Immune System / Antonio M. PERSICO in Autism Research and Treatment, (July 2012)
PermalinkL'autisme / Carole TARDIF
PermalinkL' autisme. 100 questions-réponses / Laurence ROBEL
PermalinkAutisme et autres troubles envahissants du développement : État des connaissances hors mécanismes physiopathologiques, psychopathologiques et recherche fondamentale / HAUTE AUTORITÉ DE SANTÉ - HAS
PermalinkAutisme, discours croisés / Delia STEINMANN
PermalinkL'autisme: de l'enfance à l'âge adulte / Catherine BARTHELEMY
PermalinkL'autisme : de l'enfance à l'âge adulte / Catherine BARTHELEMY
PermalinkAutisme : état des lieux et horizons / Bernard GOLSE
PermalinkAutisme : une fatalité génétique ? / Marie-Christine DEPREAUX
PermalinkAutisme, le gène introuvable / Bertrand JORDAN
PermalinkAutisme, le gène introuvable. « de la science au business ». Bertrand Jordan / Sophie BIETTE in Bulletin Scientifique de l'arapi (Le), 29 (Juillet 2012)
PermalinkAutisme et génétique, une relation avérée mais complexe... / Bertrand JORDAN in Science et pseudo-sciences, 300 (Avril-Juin 2012)
PermalinkL'autisme infantile / Pierre FERRARI
PermalinkAutisme infantile / Marion LEBOYER
PermalinkAutisme, mieux comprendre / Alain BOUVAREL
PermalinkAutismes / Bruno GEPNER
PermalinkAutour de l'autisme / Michel GERMAIN
PermalinkLes bases biologiques de l'autisme / Francisco NOYA
PermalinkLes bases génétiques et environnementales du comportement social / Nadine FORGET-DUBOIS
PermalinkBases génétiques de la physiopathologie / Laurence ROBEL
PermalinkBases neurobiologiques de l’autisme / Caroline KARSENTY
PermalinkBrief Report: Peculiar Evolution of Autistic Behaviors in Two Unrelated Children with Brachidactyly-Mental Retardation Syndrome / Luigi MAZZONE in Journal of Autism and Developmental Disorders, 42-10 (October 2012)
PermalinkBringing a developmental perspective to anxiety genetics / Lauren M. MCGRATH in Development and Psychopathology, 24-4 (November 2012)
PermalinkCan Prenatal Factors Cause ASC? / Mina HAH
PermalinkCandidate susceptibility genes for autism / Irina N. BESPALOVA
PermalinkLes causes des troubles d’acquisition du langage écrit / Alain CONTENT in Approche Neuropsychologique des Apprentissages chez l'Enfant - A.N.A.E., 116 (Février 2012)
PermalinkCerveau et comportement / Bryan KOLB
PermalinkChildhood adversity and DNA methylation of genes involved in the hypothalamus–pituitary–adrenal axis and immune system: Whole-genome and candidate-gene associations / Johanna BICK in Development and Psychopathology, 24-4 (November 2012)
PermalinkChromosome 15 and autism / Edwin H. Jr COOK
PermalinkChromosome 7 / Beth ROSEN-SHEIDLEY
PermalinkClinique des troubles de l'apprentissage / Christophe-Loïc GERARD
PermalinkCognition sociale et neuropsychologie / Philippe ALLAIN
PermalinkComparison of Siblings of Individuals with Autism and Siblings of Individuals with Other Diagnoses: An Empirical Summary / Nurit YIRMIYA
PermalinkComprehensive Education-Based Mental Health Services for Students Diagnosed on the Autism Spectrum / Raymond W. DUCHARME
PermalinkComprendre et prévenir la déficience intellectuelle / Evelyne PANNETIER
PermalinkConfluence of genes, environment, development, and behavior in a post Genome-Wide Association Study world / Scott I. VRIEZE in Development and Psychopathology, 24-4 (November 2012)
PermalinkControverses sur l'autisme et témoignages / Denys RIBAS
PermalinkA la découverte de l'autisme / Dominique YVON
PermalinkA la découverte de l'autisme / Dominique YVON
PermalinkLa déficience intellectuelle / Jean-François MARTIN
PermalinkLa déficience intellectuelle face aux progrès des neurosciences / Roland BROCA
PermalinkDéficiences intellectuelles et intégration sociale / Michèle CARLIER
PermalinkDéficit de l'attention-hyperactivité chez l'adulte / Nader PERROUD
PermalinkDefining behavioural phenotypes: exploring phenotype/genotype interrelationships / Gregory O'BRIEN
PermalinkDevelopmental genetics and psychopathology: Some new feathers for a fine old hat / Wendy JOHNSON in Development and Psychopathology, 24-4 (November 2012)
PermalinkDevelopmental psychopathology: The role of structural variation in the genome / Michael GILL in Development and Psychopathology, 24-4 (November 2012)
PermalinkLe développement de la parole chez l'enfant âgé de 6 à 11 ans / Jean-Marc COLLETTA
PermalinkDéveloppement social et émotionnel chez l'enfant et l'adolescent / Jean-Pascal LEMELIN
PermalinkLe diagnostic génétique dans l'autisme / Caroline DEMILLY
PermalinkDiagnostic Yield of Chromosomal Microarray Analysis in an Autism Primary Care Practice: Which Guidelines to Implement? / Susan G. MCGREW in Journal of Autism and Developmental Disorders, 42-8 (August 2012)
PermalinkDifferential Diagnosis / Marie NEBEL-SCHWALM
PermalinkDosage effects of X and Y chromosomes on language and social functioning in children with supernumerary sex chromosome aneuploidies: implications for idiopathic language impairment and autism spectrum disorders / Nancy RAITANO LEE in Journal of Child Psychology and Psychiatry, 53-10 (October 2012)
PermalinkLa dyslexie développementale : apports récents de la génétique et de la neuro-imagerie / Yves CHAIX ; Maria TRABANINO ; Margot J. TAYLOR ; Jean-François DEMONET
PermalinkDes enfants du spectre autistique et l'émotion / Marie-Rose DEBOT-SEVRIN
PermalinkENGRAILED2 and Cerebellar Development in the Pathogenesis of Autism Spectrum Disorders / Ian T. ROSSMAN
PermalinkEpigenetic Dysregulation of 15q11-13 GABAA Receptor Genes in Autism / Amber HOGART
PermalinkL'épigénétique chez l'enfant / Boris CHAUMETTE
PermalinkÉtat actuel sur les recherches biologiques dans l’autisme / Sylvie TORDJMAN
PermalinkEtiology: essential autism / Mark E. REBER
PermalinkEtiology: syndromic autism / Mark E. REBER
PermalinkL’Etre, l’Espace et le Temps: les travaux de D. Meltzer sur l’autisme (1975) / Jean BÉGOIN
PermalinkEvidence for Environmental Susceptibility in Autism : What We Need to Know About Gene × Environment Interactions / Isaac N. PESSAH
PermalinkEvidence of novel fine-scale structural variation at autism spectrum disorder candidate loci / Dale HEDGES in Molecular Autism, (April 2012)
PermalinkEvocative gene–parenting correlations and academic performance at first grade: An exploratory study / Cathi B. PROPPER in Development and Psychopathology, 24-4 (November 2012)
PermalinkL'exploration de l'autisme / Gilbert LELORD
PermalinkExternalizing problems, attention regulation, and household chaos: A longitudinal behavioral genetic study / Zhe WANG in Development and Psychopathology, 24-3 (August 2012)
PermalinkFacteurs génétiques impliqués dans l'autisme / Philip GORWOOD
PermalinkFaire face à l'anxiété et aux troubles anxieux / Michel BOURIN
PermalinkLes fondements génétiques et psychophysiologiques de l'agression / Ginette DIONNE
PermalinkLa fratrie confrontée aux inégalités de la génétique / Martine FRISCHMANN
PermalinkFuture directions / Jessica BRIAN
PermalinkGABRB3 gene deficient mice : a potential model of autism spectrum disorder / Timothy M. DELOREY
PermalinkGene × Environment interaction and resilience: Effects of child maltreatment and serotonin, corticotropin releasing hormone, dopamine, and oxytocin genes / Dante CICCHETTI in Development and Psychopathology, 24-2 (May 2012)
PermalinkGene–environment interaction in teacher-rated internalizing and externalizing problem behavior in 7- to 12-year-old twins / Diane J. LAMB in Journal of Child Psychology and Psychiatry, 53-8 (August 2012)
PermalinkGene expression in autism / Jonathan PEVSNER
PermalinkDes gènes, des synapses, des autismes / Thomas BOURGERON
PermalinkGenetic and neurocognitive contributions to the development of psychopathy / Essi VIDING in Development and Psychopathology, 24-3 (August 2012)
PermalinkGenetic epidemiology of autism spectrum disorders / Peter SZATMARI
PermalinkGenetic Heavy Metal Toxicity / Tara CHAPMAN
PermalinkLa génétique / Thierry BIENVENU
PermalinkLa génétique / Steve JONES
PermalinkLa génétique de l'autisme / Richard DELORME in Cerveau & Psycho, 51 (Mai-Juin 2012)
PermalinkGénétique et autisme / Arnold MUNNICH
PermalinkGénétique et autisme: du codage DSM au décodage ADN? / Ariane GIACOBINO
PermalinkGénétique de la déficience intellectuelle / Laurence COLLEAUX
PermalinkGénétique de la dyslexie développementale / Franck RAMUS
PermalinkGénétique médicale / Marc JEANPIERRE
PermalinkGénétique pédiatrique pratique : Du symptôme au syndrôme / Marion GÉRARD
PermalinkGénétique des troubles du développement du jeune enfant / Bérénice DORAY
PermalinkGenomic sciences for developmentalists: The current state of affairs / Elena L. GRIGORENKO in Development and Psychopathology, 24-4 (November 2012)
PermalinkGenomic structural variation in psychiatric disorders / James J. H. RUCKER in Development and Psychopathology, 24-4 (November 2012)
PermalinkGut and Psychology Syndrome / Natasha CAMPBELL-MCBRIDE
PermalinkHandbook of Interdisciplinary Treatments for Autism Spectrum Disorder / Robert D. RIESKE
PermalinkHandicap et fratrie / SESSAD LES MARMOTS
PermalinkHaploinsufficiency of CMIP in a Girl With Autism Spectrum Disorder and Developmental Delay due to a De Novo Deletion on Chromosome 16q23.2 / Nathalie VAN DER AA in Autism Research, 5-4 (August 2012)
PermalinkIdentification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder / Kumiko YANAGI in Autism Research and Treatment, (May 2012)
PermalinkImmune function genes CD99L2, JARID2 and TPO show association with autism spectrum disorder / Paula S. RAMOS in Molecular Autism, (June 2012)
PermalinkL’incidence des nouvelles connaissances génétiques et les nouveaux dialogues / François VITTECOQ
PermalinkIntégrer l’hétérogénéité clinique et génétique dans l’autisme / Michael L. CUCCARO
PermalinkInteraction between Genetic Vulnerability and Neurosteroids in Purkinje cells as a Possible Neurobiological Mechanism in Autism Spectrum Disorders / Flavio KELLER
PermalinkInteraction of dopamine transporter (DAT1) genotype and maltreatment for ADHD: a latent class analysis / James J. LI in Journal of Child Psychology and Psychiatry, 53-9 (September 2012)
PermalinkInteractions gènes-environnement dans la pathogénie / Marcello D’AMELIO
PermalinkInterparental conflict, parent psychopathology, hostile parenting, and child antisocial behavior: Examining the role of maternal versus paternal influences using a novel genetically sensitive research design / Gordon T. HAROLD in Development and Psychopathology, 24-4 (November 2012)
PermalinkIntroduction / Mary COLEMAN
PermalinkIs Autism a Common Personality Trait? / John N. CONSTANTINO
PermalinkIs Autism a Member of a Family of Diseases Resulting from Genetic/Cultural Mismatches? Implications for Treatment and Prevention / Staci D. BILBO in Autism Research and Treatment, (April 2012)
PermalinkLettre à des parents à bout de souffle / Eve NICOLAS
PermalinkLexical decision as an endophenotype for reading comprehension: An exploration of an association / Adam J. NAPLES in Development and Psychopathology, 24-4 (November 2012)
PermalinkLiens entre gènes, cerveau, cognition et comportement social: L’apport du syndrome de Williams / Andreia SANTOS
PermalinkLinking behaviour, brain, and genes in two different genetic syndromes / Ursula BELLUGI
PermalinkLinking prenatal maternal adversity to developmental outcomes in infants: The role of epigenetic pathways / Catherine MONK in Development and Psychopathology, 24-4 (November 2012)
PermalinkLoci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci / Lea K. DAVIS in Molecular Autism, (May 2012)
PermalinkLPHN3 and attention-deficit/hyperactivity disorder: interaction with maternal stress during pregnancy / Zia CHOUDHRY in Journal of Child Psychology and Psychiatry, 53-8 (August 2012)
PermalinkMale Gender Bias in Autism and Pediatric Autoimmunity / Kevin G. BECKER in Autism Research, 5-2 (April 2012)
PermalinkMédecine et santé de l'adolescent / Priscille GERARDIN
PermalinkMedical Issues / Fred R. VOLKMAR
PermalinkMedical needs of the autistic adolescent / Joanna S. DALLDORF
PermalinkMendel, le chromosome X et le garçon autiste / Claude MORAINE
PermalinkMéthodologies génétiques et protéines synaptiques dans l’autisme infantile / Stéphane JAMAIN
PermalinkMon combat pour les enfants autistes / Bernard GOLSE
PermalinkNeurobiological implications of sex differences in autism / Catherine LORD
PermalinkNeurobiologie du développement du système nerveux central et autisme / Christian ANDRES
PermalinkNeurobiology and Genetics of Autism: A Developmental Perspective / Kathleen KOENIG
PermalinkNeurobiology, diagnosis and treatment in autism / Daria RIVA
PermalinkNeurobiology meets genomic science: The promise of human-induced pluripotent stem cells / Hanna E. STEVENS in Development and Psychopathology, 24-4 (November 2012)
PermalinkNeurocognitive phenotypes of dyslexia / Giovanna ZARDINI
PermalinkNeurodevelopmental Disorders: Cognitive/Behavioural Phenotypes / Daria RIVA
PermalinkNeuronal and Synaptic Dysfunction in Autism Spectrum Disorder and Intellectual Disability / Carlo SALA
PermalinkNeuropathology of autism / Gerry A. STEFANATOS
PermalinkNeuroscience of Schizophrenia / Christine PESOLD
PermalinkL’organisation soi / autrui dans le développement psychologique humain / Kenneth J. AITKEN in Psychiatrie de l'Enfant (La), 46-2 (2003)
PermalinkLes origines développementales des problèmes de comportement perturbateur et leurs conséquences en matière de prévention / Richard E. TREMBLAY
PermalinkOverview of biomedical issues in autism / Robert-Jay REICHLER
PermalinkLes pathologies souvent associées à l'autisme (comorbidités) / Linnea HJALMARSSON
PermalinkLes pathologies souvent associées à l'autisme (comorbidités) / Linnea HJALMARSSON
PermalinkPerspectives génétiques et génomiques en psychiatrie / Christelle DE MEES
PermalinkPour une approche intégrative des désordres de la constellation autistique / Bruno GEPNER
PermalinkLa précocité intellectuelle / Jean-Claude GRUBAR
PermalinkPrenatal and Postnatal Epigenetic Programming: Implications for GI, Immune, and Neuronal Function in Autism / Mostafa WALY in Autism Research and Treatment, (May 2012)
PermalinkPrévention du retard mental. Tome 2 / Yvon L'ABBE
PermalinkPsychiatrie de l'enfant / Anne DANION-GRILLIAT
PermalinkLa psychobiologie développementale du stress / Sarah A. STELLERN
PermalinkPsychobiologie des émotions / Robert DANTZER
PermalinkPsychobiology of Personality Disorders / Brian KNUTSON
PermalinkPsychologie du handicap / Nathalie NADER-GROSBOIS
PermalinkPsychologie du handicap / Nathalie NADER-GROSBOIS
PermalinkPsychometric Study of the Aberrant Behavior Checklist in Fragile X Syndrome and Implications for Targeted Treatment / Stephanie M. SANSONE in Journal of Autism and Developmental Disorders, 42-7 (July 2012)
PermalinkPsychopathologie / Michel DELBROUCK
PermalinkQuelles vérités annoncer aux parents et à quels moments? / Paul MESSERSCHMITT
PermalinkQuelles vérités annoncer aux parents et à quels moments? / Arnold MUNNICH
PermalinkEn quoi la création artistique peut-elle être considérée comme la résolution d'un problème ? / Catherine THOMAS-ANTERION
PermalinkRapport annuel RHEOP 2007 - Enfants avec déficience sévère - génération 1998 - Observatoire périnatal données 2006 / RHEOP - REGISTRE DES HANDICAPS DE L'ENFANT ET OBSERVATOIRE PÉRINATAL
PermalinkRapport annuel RHEOP 2008 - Enfants avec déficience sévère - génération 1999 - Observatoire périnatal données 2007 / RHEOP - REGISTRE DES HANDICAPS DE L'ENFANT ET OBSERVATOIRE PÉRINATAL
PermalinkReconfiguration contemporaine de l’autisme: enjeux cliniques / François ANSERMET
PermalinkResearching the Autism Spectrum / Ilona ROTH
PermalinkResilience and measured gene–environment interactions / Julia KIM-COHEN in Development and Psychopathology, 24-4 (November 2012)
PermalinkRett disorder / Alison KERR
PermalinkRett syndrome : a Rosetta stone for understanding the molecular pathogenesis of autism / Janine M. LASALLE
PermalinkSerotonin in autism / George M. ANDERSON
PermalinkShared chromosomal susceptibility regions between autism and other mental disorders / Yvon C. CHAGNON
PermalinkShared genetic influences on ADHD symptoms and very low-frequency EEG activity: a twin study / Charlotte TYE in Journal of Child Psychology and Psychiatry, 53-6 (June 2012)
PermalinkSingle Nucleotide Polymorphisms Predict Symptom Severity of Autism Spectrum Disorder / Yun JIAO in Journal of Autism and Developmental Disorders, 42-6 (June 2012)
PermalinkSociophysiology and Evolutionary Aspects of Psychiatry / Russell GARDNER
PermalinkSortir de l'autisme / Jacqueline BERGER
PermalinkSortir de l'autisme / Jacqueline BERGER
PermalinkStimuler le cerveau de l'enfant / Christel DEMEY
PermalinkLe syndrome de l'enfant téflon / Daniel KEMP
PermalinkSyndromes génétiques et phénotypes comportementaux / Diane MORIN
PermalinkTDA/H : Trouble Déficit de l'Attention / Hyperactivité / François BANGE
PermalinkTDA/H : Trouble Déficit de l'Attention / Hyperactivité / François BANGE
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