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Auteur Latha V. SOORYA
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Documents disponibles écrits par cet auteur (17)
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[article]
Titre : Advancing paternal age and simplex autism Type de document : texte imprimé 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] / 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
Titre : Behavioral and Psychosocial Interventions for Individuals with ASD Type de document : texte imprimé Auteurs : Latha V. SOORYA, Auteur ; Laura A. CARPENTER, Auteur ; Zachary WARREN, Auteur Année de publication : 2013 Importance : p.69-84 Langues : Anglais (eng) Index. décimale : SCI-D SCI-D - Neurosciences Résumé : This chapter provides a current overview of behavioral and psychosocial treatments for individuals with ASD. The approaches include empirically based methods as well as popular interventions designed to address core and associated symptoms. The chapter includes reviews of major comprehensive treatment programs and educational programs designed for young children with ASD, as well as targeted treatments to improve core deficits. Interventions designed to reduce problem behaviors, and alternative treatments commonly used in ASD are also addressed. Finally, trends and directions for future behavioral and psychosocial treatment research including a focus on implementation in community settings and designing treatments for older individuals with ASD are discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=189 Behavioral and Psychosocial Interventions for Individuals with ASD [texte imprimé] / Latha V. SOORYA, Auteur ; Laura A. CARPENTER, Auteur ; Zachary WARREN, Auteur . - 2013 . - p.69-84.
Langues : Anglais (eng)
Index. décimale : SCI-D SCI-D - Neurosciences Résumé : This chapter provides a current overview of behavioral and psychosocial treatments for individuals with ASD. The approaches include empirically based methods as well as popular interventions designed to address core and associated symptoms. The chapter includes reviews of major comprehensive treatment programs and educational programs designed for young children with ASD, as well as targeted treatments to improve core deficits. Interventions designed to reduce problem behaviors, and alternative treatments commonly used in ASD are also addressed. Finally, trends and directions for future behavioral and psychosocial treatment research including a focus on implementation in community settings and designing treatments for older individuals with ASD are discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=189 Exemplaires(0)
Disponibilité aucun exemplaire Brief Report: Sensory Reactivity in Children with Phelan–McDermid Syndrome / A.M. MIESES in Journal of Autism and Developmental Disorders, 46-7 (July 2016)
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[article]
Titre : Brief Report: Sensory Reactivity in Children with Phelan–McDermid Syndrome Type de document : texte imprimé Auteurs : A.M. MIESES, Auteur ; Teresa TAVASSOLI, Auteur ; Erin LI, Auteur ; Latha SOORYA, Auteur ; Stacey LURIE, Auteur ; A. Ting WANG, Auteur ; Paige M. SIPER, Auteur ; Alexander KOLEVZON, Auteur Article en page(s) : p.2508-2513 Langues : Anglais (eng) Mots-clés : Phelan–McDermid syndrome 22q13 deletion syndrome Autism Autism spectrum disorder Sensory reactivity Sensory profile Index. décimale : PER Périodiques Résumé : Phelan–McDermid syndrome (PMS), a monogenic form of autism spectrum disorder (ASD), results from deletion or mutation of the SHANK3 gene. Atypical sensory reactivity is now included in the diagnostic criteria for ASD. Examining the sensory phenotype in monogenic forms of ASD, such as PMS, may help identify underlying mechanisms of sensory reactivity. Using the Short Sensory Profile, the current study compared sensory reactivity in 24 children with PMS to 61 children with idiopathic ASD (iASD). Results suggest that children with PMS show more low energy/weak symptoms and less sensory sensitivity as compared to children with iASD. This study is the first to demonstrate differences in sensory reactivity between children with PMS and iASD, helping to refine the PMS phenotype. En ligne : http://dx.doi.org/10.1007/s10803-016-2754-0 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=290
in Journal of Autism and Developmental Disorders > 46-7 (July 2016) . - p.2508-2513[article] Brief Report: Sensory Reactivity in Children with Phelan–McDermid Syndrome [texte imprimé] / A.M. MIESES, Auteur ; Teresa TAVASSOLI, Auteur ; Erin LI, Auteur ; Latha SOORYA, Auteur ; Stacey LURIE, Auteur ; A. Ting WANG, Auteur ; Paige M. SIPER, Auteur ; Alexander KOLEVZON, Auteur . - p.2508-2513.
Langues : Anglais (eng)
in Journal of Autism and Developmental Disorders > 46-7 (July 2016) . - p.2508-2513
Mots-clés : Phelan–McDermid syndrome 22q13 deletion syndrome Autism Autism spectrum disorder Sensory reactivity Sensory profile Index. décimale : PER Périodiques Résumé : Phelan–McDermid syndrome (PMS), a monogenic form of autism spectrum disorder (ASD), results from deletion or mutation of the SHANK3 gene. Atypical sensory reactivity is now included in the diagnostic criteria for ASD. Examining the sensory phenotype in monogenic forms of ASD, such as PMS, may help identify underlying mechanisms of sensory reactivity. Using the Short Sensory Profile, the current study compared sensory reactivity in 24 children with PMS to 61 children with idiopathic ASD (iASD). Results suggest that children with PMS show more low energy/weak symptoms and less sensory sensitivity as compared to children with iASD. This study is the first to demonstrate differences in sensory reactivity between children with PMS and iASD, helping to refine the PMS phenotype. En ligne : http://dx.doi.org/10.1007/s10803-016-2754-0 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=290 Brief Report: The Autism Mental Status Examination: Development of a Brief Autism-Focused Exam / David GRODBERG in Journal of Autism and Developmental Disorders, 42-3 (March 2012)
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[article]
Titre : Brief Report: The Autism Mental Status Examination: Development of a Brief Autism-Focused Exam Type de document : texte imprimé Auteurs : David GRODBERG, Auteur ; Paige M. WEINGER, Auteur ; Alexander KOLEVZON, Auteur ; Latha V. SOORYA, Auteur ; Joseph D. BUXBAUM, Auteur Année de publication : 2012 Article en page(s) : p.455-459 Langues : Anglais (eng) Mots-clés : Autism spectrum disorder Mental status examination Autism Diagnostic Observation Schedule Autism Mental Status Examination Index. décimale : PER Périodiques Résumé : The Autism Mental Status Examination (AMSE) described here is an eight-item observational assessment that prompts the observation and recording of signs and symptoms of autism spectrum disorders (ASD). The AMSE is intended to take place seamlessly in the context of a clinical exam and produces a total score. Subjects were independently administered the AMSE and the Autism Diagnostic Observation Schedule (ADOS). The ADOS was used to estimate the most effective criterion cut-off on the AMSE. A score of five or greater produced excellent sensitivity and good specificity in a high-risk sample. Internal consistency was acceptable and inter-rater reliability was good to excellent. Preliminary findings indicate excellent classification accuracy and suggest that the AMSE provides a rapid and reliable observational assessment in a high-risk population. En ligne : http://dx.doi.org/10.1007/s10803-011-1255-4 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=152
in Journal of Autism and Developmental Disorders > 42-3 (March 2012) . - p.455-459[article] Brief Report: The Autism Mental Status Examination: Development of a Brief Autism-Focused Exam [texte imprimé] / David GRODBERG, Auteur ; Paige M. WEINGER, Auteur ; Alexander KOLEVZON, Auteur ; Latha V. SOORYA, Auteur ; Joseph D. BUXBAUM, Auteur . - 2012 . - p.455-459.
Langues : Anglais (eng)
in Journal of Autism and Developmental Disorders > 42-3 (March 2012) . - p.455-459
Mots-clés : Autism spectrum disorder Mental status examination Autism Diagnostic Observation Schedule Autism Mental Status Examination Index. décimale : PER Périodiques Résumé : The Autism Mental Status Examination (AMSE) described here is an eight-item observational assessment that prompts the observation and recording of signs and symptoms of autism spectrum disorders (ASD). The AMSE is intended to take place seamlessly in the context of a clinical exam and produces a total score. Subjects were independently administered the AMSE and the Autism Diagnostic Observation Schedule (ADOS). The ADOS was used to estimate the most effective criterion cut-off on the AMSE. A score of five or greater produced excellent sensitivity and good specificity in a high-risk sample. Internal consistency was acceptable and inter-rater reliability was good to excellent. Preliminary findings indicate excellent classification accuracy and suggest that the AMSE provides a rapid and reliable observational assessment in a high-risk population. En ligne : http://dx.doi.org/10.1007/s10803-011-1255-4 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=152 Effects of age and symptomatology on cortical thickness in autism spectrum disorders / Krissy DOYLE-THOMAS in Research in Autism Spectrum Disorders, 7-1 (January 2013)
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[article]
Titre : Effects of age and symptomatology on cortical thickness in autism spectrum disorders Type de document : texte imprimé Auteurs : Krissy DOYLE-THOMAS, Auteur ; Emma G. DUERDEN, Auteur ; Margot J. TAYLOR, Auteur ; Jason P. LERCH, Auteur ; Latha V. SOORYA, Auteur ; A. Ting WANG, Auteur ; Jin FAN, Auteur ; Eric HOLLANDER, Auteur ; Evdokia ANAGNOSTOU, Auteur Année de publication : 2013 Article en page(s) : p.141-50 Langues : Anglais (eng) Mots-clés : Autism spectrum disorders Structural MRI Cortical thickness Social impairment Developmental changes Index. décimale : PER Périodiques Résumé : Several brain regions show structural and functional abnormalities in individuals with autism spectrum disorders (ASD), but the developmental trajectory of abnormalities in these structures and how they may relate to social and communicative impairments are still unclear. We assessed the effects of age on cortical thickness in individuals with ASD, between the ages of 7 and 39 years in comparison to typically developing controls. Additionally, we examined differences in cortical thickness in relation to symptomatology in the ASD group, and their association with age. Analyses were conducted using a general linear model, controlling for sex. Social and communication scores from the Autism Diagnostic Interview-Revised (ADI-R) were correlated with the thickness of regions implicated in those functions. Controls showed widespread cortical thinning relative to the ASD group. Within regions-of-interest, increased thickness in the rostral anterior cingulate cortex was associated with poorer social scores. Additionally, a significant interaction between age and social impairment was found in the orbitofrontal cortex, with more impaired younger children having decreased thickness in this region. These results suggest that differential neurodevelopmental trajectories are present in individuals with ASD and some differences are associated with diagnostic behaviours. En ligne : http://dx.doi.org/10.1016/j.rasd.2012.08.004 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=179
in Research in Autism Spectrum Disorders > 7-1 (January 2013) . - p.141-50[article] Effects of age and symptomatology on cortical thickness in autism spectrum disorders [texte imprimé] / Krissy DOYLE-THOMAS, Auteur ; Emma G. DUERDEN, Auteur ; Margot J. TAYLOR, Auteur ; Jason P. LERCH, Auteur ; Latha V. SOORYA, Auteur ; A. Ting WANG, Auteur ; Jin FAN, Auteur ; Eric HOLLANDER, Auteur ; Evdokia ANAGNOSTOU, Auteur . - 2013 . - p.141-50.
Langues : Anglais (eng)
in Research in Autism Spectrum Disorders > 7-1 (January 2013) . - p.141-50
Mots-clés : Autism spectrum disorders Structural MRI Cortical thickness Social impairment Developmental changes Index. décimale : PER Périodiques Résumé : Several brain regions show structural and functional abnormalities in individuals with autism spectrum disorders (ASD), but the developmental trajectory of abnormalities in these structures and how they may relate to social and communicative impairments are still unclear. We assessed the effects of age on cortical thickness in individuals with ASD, between the ages of 7 and 39 years in comparison to typically developing controls. Additionally, we examined differences in cortical thickness in relation to symptomatology in the ASD group, and their association with age. Analyses were conducted using a general linear model, controlling for sex. Social and communication scores from the Autism Diagnostic Interview-Revised (ADI-R) were correlated with the thickness of regions implicated in those functions. Controls showed widespread cortical thinning relative to the ASD group. Within regions-of-interest, increased thickness in the rostral anterior cingulate cortex was associated with poorer social scores. Additionally, a significant interaction between age and social impairment was found in the orbitofrontal cortex, with more impaired younger children having decreased thickness in this region. These results suggest that differential neurodevelopmental trajectories are present in individuals with ASD and some differences are associated with diagnostic behaviours. En ligne : http://dx.doi.org/10.1016/j.rasd.2012.08.004 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=179 Erratum: A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome / Alexander KOLEVZON in Molecular Autism, (June 2015)
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PermalinkErratum to: Neural selectivity for communicative auditory signals in Phelan-McDermid syndrome / A. Ting WANG in Journal of Neurodevelopmental Disorders, 8-1 (December 2016)
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PermalinkExamining a stepped-care telehealth program for parents of young children with autism: a proof-of-concept trial / Allison L. WAINER in Molecular Autism, 12 (2021)
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PermalinkIntranasal oxytocin versus placebo in the treatment of adults with autism spectrum disorders: a randomized controlled trial / Evdokia ANAGNOSTOU in Molecular Autism, (December 2012)
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PermalinkMetabolic mapping of deep brain structures and associations with symptomatology in autism spectrum disorders / Krissy DOYLE-THOMAS in Research in Autism Spectrum Disorders, 8-1 (January 2014)
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PermalinkNeural selectivity for communicative auditory signals in Phelan-McDermid syndrome / A. Ting WANG in Journal of Neurodevelopmental Disorders, 8-1 (December 2016)
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PermalinkParent-reported measure of repetitive behavior in Phelan-McDermid syndrome / Siddharth SRIVASTAVA in Journal of Neurodevelopmental Disorders, 13 (2021)
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PermalinkA pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome / Alexander KOLEVZON in Molecular Autism, (December 2014)
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PermalinkProspective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency / Latha V. SOORYA in Molecular Autism, (June 2013)
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PermalinkPsychometric Study of the Social Responsiveness Scale in Phelan-McDermid Syndrome / Kellie GERGOUDIS in Autism Research, 13-8 (August 2020)
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