Cargando…

Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?

BACKGROUND: Autism spectrum disorders (ASD) and epilepsy frequently occur together. Prevalence rates are variable, and have been attributed to age, gender, comorbidity, subtype of pervasive developmental disorder (PDD) and risk factors. Recent studies have suggested disparate clinical and genetic se...

Descripción completa

Detalles Bibliográficos
Autores principales:	Amiet, Claire, Gourfinkel-An, Isabelle, Laurent, Claudine, Bodeau, Nicolas, Génin, Bérengère, Leguern, Eric, Tordjman, Sylvie, Cohen, David
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2013
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176303/ https://www.ncbi.nlm.nih.gov/pubmed/24289166 http://dx.doi.org/10.1186/2040-2392-4-47

Ejemplares similares

Genetics of inherited human epilepsies
por: Gourfinkel-An, Isabelle, et al.
Publicado: (2001)

A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism
por: Carayol, Jérôme, et al.
Publicado: (2014)

Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism
por: Couarch, Philippe, et al.
Publicado: (2011)

Are There Cultural Differences in Parental Interest in Early Diagnosis and Genetic Risk Assessment for Autism Spectrum Disorder?
por: Amiet, Claire, et al.
Publicado: (2014)

Genome-wide linkage in Utah autism pedigrees
por: Allen-Brady, K, et al.
Publicado: (2009)

Autism Spectrum and Other Neurodevelopmental Disorders in Children of Immigrants: A Brief Review of Current Evidence and Implications for Clinical Practice
por: Schmengler, Heiko, et al.
Publicado: (2021)

Methods for detecting gene × gene interaction in multiplex extended pedigrees
por: Brock, Guy N, et al.
Publicado: (2005)

Subgrouping siblings of people with autism: Identifying the broader autism phenotype
por: Ruzich, Emily, et al.
Publicado: (2015)

Multiplex gene and phenotype network to characterize shared genetic pathways of epilepsy and autism
por: Peng, Jacqueline, et al.
Publicado: (2021)

Aripiprazole for treating irritability in children & adolescents with autism: a systematic review
por: Ghanizadeh, Ahmad, et al.
Publicado: (2015)

Subgrouping the Autism “Spectrum": Reflections on DSM-5
por: Lai, Meng-Chuan, et al.
Publicado: (2013)

Presence of autism, hyperserotonemia, and severe expressive language impairment in Williams-Beuren syndrome
por: Tordjman, Sylvie, et al.
Publicado: (2013)

Premigration social adversity and autism spectrum disorder
por: Augereau, Natacha, et al.
Publicado: (2020)

A molecular genetic study of autism and related phenotypes in extended pedigrees
por: Piven, Joseph, et al.
Publicado: (2013)

A Multidimensional Approach to the Study of Emotion Recognition in Autism Spectrum Disorders
por: Xavier, Jean, et al.
Publicado: (2015)

A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson’s disease with dementia
por: Fanciulli, Alessandra, et al.
Publicado: (2022)

Does Pet Arrival Trigger Prosocial Behaviors in Individuals with Autism?
por: Grandgeorge, Marine, et al.
Publicado: (2012)

A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees
por: Woodbury-Smith, Marc, et al.
Publicado: (2018)

Environmental Factors Influence Language Development in Children with Autism Spectrum Disorders
por: Grandgeorge, Marine, et al.
Publicado: (2009)

Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees
por: Coon, Hilary, et al.
Publicado: (2010)

Mutational interactions define novel cancer subgroups
por: Kuipers, Jack, et al.
Publicado: (2018)

The Autism Phenome Project: Toward Identifying Clinically Meaningful Subgroups of Autism
por: Nordahl, Christine Wu, et al.
Publicado: (2022)

Mutations and Deletions in PCDH19 Account for Various Familial or Isolated Epilepsies in Females
por: Depienne, Christel, et al.
Publicado: (2011)

Is There Evidence for Aetiologically Distinct Subgroups of Idiopathic Congenital Talipes Equinovarus? A Case-Only Study and Pedigree Analysis
por: Cardy, Amanda H., et al.
Publicado: (2011)

Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders
por: Nava, Caroline, et al.
Publicado: (2015)

Melatonin: From Pharmacokinetics to Clinical Use in Autism Spectrum Disorder
por: Lalanne, Sébastien, et al.
Publicado: (2021)

Prevalence of Clinically and Empirically Defined Talents and Strengths in Autism
por: Meilleur, Andrée-Anne S., et al.
Publicado: (2014)

Functionally and medically defined subgroups of nursing home populations
por: Manton, Kenneth G., et al.
Publicado: (1990)

Molecular subtyping for clinically defined breast cancer subgroups
por: Zhao, Xi, et al.
Publicado: (2015)

Natural IgG Anti-F (ab’)(2) Autoantibody Activity in Children with Autism
por: Tordjman, Sylvie, et al.
Publicado: (2023)

Parasites and Their Pedigree
Publicado: (1884)

Comparative analysis of the autism-related variants between different autistic children in a family pedigree
por: Shen, Luxi, et al.
Publicado: (2021)

Germline mosaicism of a missense variant in KCNC2 in a multiplex family with autism and epilepsy characterized by long‐read sequencing
por: Mehinovic, Elvisa, et al.
Publicado: (2022)

Advances in the Research of Melatonin in Autism Spectrum Disorders: Literature Review and New Perspectives
por: Tordjman, Sylvie, et al.
Publicado: (2013)

Defining the broader, medium and narrow autism phenotype among parents using the Autism Spectrum Quotient (AQ)
por: Wheelwright, Sally, et al.
Publicado: (2010)

TTTCA Repeat Expansion of SAMD12 in a New Benign Adult Familial Myoclonic Epilepsy Pedigree
por: Liu, Chaorong, et al.
Publicado: (2020)

AKT Pathway Genes Define 5 Prognostic Subgroups in Glioblastoma
por: Joy, Anna, et al.
Publicado: (2014)

Integrative Analysis Defines Distinct Prognostic Subgroups of Intrahepatic Cholangiocarcinoma
por: Goeppert, Benjamin, et al.
Publicado: (2019)

Whole-genome sequencing in an autism multiplex family
por: Shi, Lingling, et al.
Publicado: (2013)

A Developmental and Sequenced One-to-One Educational Intervention for Autism Spectrum Disorder: A Randomized Single-Blind Controlled Trial
por: Tanet, Antoine, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_0eqrr48r33ablmum7pljgfa1ld