CARLIER Michele
Onglets principaux
Equipe(s) de recherche
Fonctions
Voir le pdf pour le résumé de carrière et la liste des publications. Voir aussi Research Gate M. Carlier
See pdf for information - see also Research Gate M. Carlier
Domaines de recherche
Génétique et comportement - Behavior Genetics
Handicap intellectuel associé à des maladies génétiques -
Stéréotype social et trisomie 21 - Social stereotype and Down syndrome
Jumeaux (comparaison sociale, différences entre fille et garçons, cognition, personnalité) - Twins - social comparison, gender differences, cognition, personality)
Latéralité manuelle - Handedeness
Autisme - Autism
Modèle murin (trisomie 21, autisme) - Murine model (Down syndrome, autism)
Créativité - Creativity
Enseignements
Documents
Articles
http://api.archives-ouvertes.fr/search/?&fq=authLastNameFirstName_s:%28%22Carlier+Mich%C3%A8le%22+OR+%22Carlier+M.%22+OR+%22Carlier+Michele%22%29&fl=title_s,en_title_s,docid,label_s,en_label_s,docType_s,authIdHal_s,halId_s,structId_i,uri_s,keyword_s,en_keyword_s,authLastNameFirstName_s,journalTitle_s,abstract_s,en_abstract_s,producedDate_tdate,producedDateY_i,language_s,fileMain_s&sort=producedDate_tdate+desc
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Construct Validity and Cross Validity of a Test Battery Modeling Autism Spectrum Disorder (ASD) in MiceBehavior Genetics2019
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Postnatal Tshz3 Deletion Drives Altered Corticostriatal Function and Autism Spectrum Disorder–like BehaviorBiological Psychiatry2019
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Théories implicites à l’égard des personnes porteuses de trisomie 2.2018
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Relationships Between Self-Injurious Behaviors, Pain Reactivity, and β-Endorphin in Children and Adolescents With AutismJournal of Clinical Psychiatry2018
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Social Comparison Orientation in Monozygotic and Dizygotic TwinsTwin Research and Human Genetics2017
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Implicit theories concerning the intelligence of individuals with Down syndromePLoS ONE2017
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Differential Brain, Cognitive and Motor Profiles Associated with Partial Trisomy. Modeling Down Syndrome in MiceBehavior Genetics2017
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Manual performance as predictor of literacy acquisition : A study from kindergarten to Grade 1Cognitive Development2017
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TSHZ3 deletion causes an autism syndrome and defects in cortical projection neuronsNature Genetics2016
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Localisation et dynamiques de concentration des productions animales en Europe : état des lieux et facteurs explicatifs2015
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Vascular calcification: from pathophysiology to biomarkersClinica Chimica Acta2015
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Misleading face-based judgment of cognitive level in intellectual disability: The case of trisomy 21 (Down syndrome)Research in Developmental Disabilities2014
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Explaining sex differences in 3-D Mental Rotation Tasks (MRT) using dizygotic twins: From hormonal to cultural factors (negative stereotypes about women and spatial skills)Behavior Genetics2013
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Wide genome transcriptional analysis of the hippocampus in segmental models of trisomy 21 (Down syndrome) presenting learning impairment and atypical brain morphometryBehavior Genetics2013
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Social comparison orientation: A new perspective in the study of co-twin relationshipsBehavior Genetics2013
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Facial phenotype linked to one genetic disease and wrong face-based judgement on behavioral phenotype (intelligence). The emblematic case of the trisomy 21Behavior Genetics2013
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Presence of autism, hyperserotonemia, and severe expressive language impairment in Williams-Beuren syndrome.Molecular Autism2013
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Stéréotype social de la trisomie 21 et variables individuelles2013
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The five factor model of personality and intelligence: A twin study on the relationship between the two constructsPersonality and Individual Differences2012
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Perception de l'espace d'action chez les patients hémiplégiques2012
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Tracking Subtle Stereotypes of Children with Trisomy 21: From Facial-Feature-Based to Implicit StereotypingPLoS ONE2012
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Autistic Disorder in Patients with Williams-Beuren Syndrome: A Reconsideration of the Williams-Beuren Syndrome PhenotypePLoS ONE2012
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Good use and misuse of ``genetic determinismJournal of Physiology - Paris2011
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Laterality Preference and Cognition: Cross-Syndrome Comparison of Patients with Trisomy 21 (Down), del7q11.23 (Williams-Beuren) and del22q11.2 (DiGeorge or Velo-Cardio-Facial) SyndromesBehavior Genetics2011
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Modulation of Brain b-Endorphin Concentration by the Specific Part of the Y Chromosome in MicePLoS ONE2011
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Amélioration des enquêtes transfusionnelles concernant les infections transmises par transfusion (IBTT): Données 2008 - 20092010
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Specific grasp characteristics of children with trisomy 21Developmental Psychobiology2010
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Laterality and cognition: lesson from individuals with microdeletion 22q11 (DiGeorge syndrome-velocardiofacial syndrome)Behavior Genetics2010
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Genes contributing to brain and cognitive impairment of mouse models for trisomy 21 (Down syndrome)Behavior Genetics2010
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Brain Pathways Mediating the Pro-Aggressive Effect of the Steroid Sulfatase (Sts) GeneBehavior Genetics2010
