Lista de obras - Jean Steyaert - Dominio Público Uruguay

A complex Xp11.22 deletion in a patient with syndromic autism: Exploration ofFAM120Cas a positional candidate gene for autism

article

A distinct neurocognitive phenotype in female fragile-X premutation carriers assessed with visual attention tasks

artículo científico publicado en 2003

A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy ⬇️

artículo científico publicado el 1 de septiembre de 1997

An 8.9 year old girl with autism and Gorlin syndrome ⬇️

artículo científico publicado el 28 de diciembre de 2010

Association of CDH11 with non-syndromic ASD.

artículo científico publicado en 2014

Behavioral phenotype in childhood type of dystrophia myotonica

scientific article published on 01 December 2000

Brief report: Reduced grouping interference in children with ASD: evidence from a Multiple Object Tracking Task

artículo científico publicado en 2014

CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior.

artículo científico publicado en 2003

Child psychiatric diagnoses in a population of Dutch schoolchildren aged 6 to 8 years

artículo científico publicado en 2001

Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.

artículo científico publicado en 2004

Controlled visuomotor preparation deficits in attention-deficit/hyperactivity disorder.

artículo científico publicado en 2005

DISC1 duplication in two brothers with autism and mild mental retardation.

artículo científico publicado en 2009

Disturbed interplay between mid- and high-level vision in ASD? Evidence from a contour identification task with everyday objects.

artículo científico publicado en 2014

Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiency.

artículo científico publicado en 2006

Factors affecting the relation between parental education as well as occupation and problem behaviour in Dutch 5- to 6-year-old children

artículo científico publicado en 2001

Fast Periodic Visual Stimulation EEG Reveals Reduced Neural Sensitivity to Fearful Faces in Children with Autism

scientific article published on 01 November 2019

Human plasma glycome in attention-deficit hyperactivity disorder and autism spectrum disorders

artículo científico publicado en 2010

Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism.

artículo científico publicado en 2007

Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion

article

Is there a common neuroanatomical substrate of language deficit between autism spectrum disorder and specific language impairment?

artículo científico publicado en 2011

Low- and high-level controlled processing in executive motor control tasks in 5-6-year-old children at risk of ADHD.

artículo científico publicado en 2003

Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene

artículo científico publicado en 1996

Narrowing the critical deletion region for autism spectrum disorders on 16p11.2.

artículo científico publicado en 2011

New findings in the behavioral profile of young FraX females

artículo científico publicado en 1996

No differences in emotion recognition strategies in children with autism spectrum disorder: evidence from hybrid faces

artículo científico publicado en 2014

Position effect leading to haploinsufficiency in a mosaic ring chromosome 14 in a boy with autism

artículo científico publicado en 2008

Psychiatric genetics: the case of single gene disorders.

artículo científico publicado en 2002

Quantitative autism traits in first degree relatives: evidence for the broader autism phenotype in fathers, but not in mothers and siblings ⬇️

artículo científico publicado el 26 de septiembre de 2011

SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles.

artículo científico publicado en 2010

The XYY syndrome: a follow-up study on 38 boys

artículo científico publicado el 1 de enero de 2003

The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism.

artículo científico publicado en 2003

Underconnectivity of the superior temporal sulcus predicts emotion recognition deficits in autism

artículo científico publicado en 2013

Young children with language difficulties: a dimensional approach to subgrouping.

artículo científico publicado en 2013

Lista de obras de Jean Steyaert

A complex Xp11.22 deletion in a patient with syndromic autism: Exploration ofFAM120Cas a positional candidate gene for autism

A distinct neurocognitive phenotype in female fragile-X premutation carriers assessed with visual attention tasks

A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy ⬇️

An 8.9 year old girl with autism and Gorlin syndrome ⬇️

Association of CDH11 with non-syndromic ASD.

Behavioral phenotype in childhood type of dystrophia myotonica

Brief report: Reduced grouping interference in children with ASD: evidence from a Multiple Object Tracking Task

CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior.

Child psychiatric diagnoses in a population of Dutch schoolchildren aged 6 to 8 years

Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.

Controlled visuomotor preparation deficits in attention-deficit/hyperactivity disorder.

DISC1 duplication in two brothers with autism and mild mental retardation.

Disturbed interplay between mid- and high-level vision in ASD? Evidence from a contour identification task with everyday objects.

Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiency.

Factors affecting the relation between parental education as well as occupation and problem behaviour in Dutch 5- to 6-year-old children

Fast Periodic Visual Stimulation EEG Reveals Reduced Neural Sensitivity to Fearful Faces in Children with Autism

Human plasma glycome in attention-deficit hyperactivity disorder and autism spectrum disorders

Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism.

Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion

Is there a common neuroanatomical substrate of language deficit between autism spectrum disorder and specific language impairment?

Low- and high-level controlled processing in executive motor control tasks in 5-6-year-old children at risk of ADHD.

Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene

Narrowing the critical deletion region for autism spectrum disorders on 16p11.2.

New findings in the behavioral profile of young FraX females

No differences in emotion recognition strategies in children with autism spectrum disorder: evidence from hybrid faces

Position effect leading to haploinsufficiency in a mosaic ring chromosome 14 in a boy with autism

Psychiatric genetics: the case of single gene disorders.

Quantitative autism traits in first degree relatives: evidence for the broader autism phenotype in fathers, but not in mothers and siblings ⬇️

SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles.

The XYY syndrome: a follow-up study on 38 boys

The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism.

Underconnectivity of the superior temporal sulcus predicts emotion recognition deficits in autism

Young children with language difficulties: a dimensional approach to subgrouping.