Preliminary evidence for a cognitive phenotype in Barth syndrome

Manual for The Child Behavior Checklist/4-18 and 1991 Profile

1991 • 10,188 citations

Manual for the Child: Behavior Checklist and Revised Child Behavior Profile

1983 • 4,225 citations

Rapid ‘automatized’ naming (R.A.N.): Dyslexia differentiated from other learning disabilities

1976 • 1,412 citations

Woodcock-Johnson Psycho-Educational Battery-Revised

1990 • 1,187 citations

Conners' rating scales-revised : technical manual

1997 • 1,027 citations

A novel X-linked gene, G4.5. is responsible for Barth syndrome

1996 • 733 citations

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1983 • 662 citations

A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases.

1994 • 296 citations

Neuropsychology of Early-treated Phenylketonuria: Specific Executive Function Deficits

1990 • 279 citations

X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria

1991 • 270 citations

Test of Early Mathematics Ability-3

2021 • 263 citations

The X-Linked Gene G4.5 Is Responsible for Different Infantile Dilated Cardiomyopathies

1997 • 229 citations

Neuropsychology of Early-Treated Phenylketonuria: Specific Executive Function Deficits

1990 • 175 citations

The Psychoeducational Characteristics of Children with Turner Syndrome

1993 • 169 citations

X‐linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)

1999 • 168 citations

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28.

1991 • 144 citations

Early Developmental Trajectories of Males With Fragile X Syndrome

1998 • 140 citations

Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome

1997 • 134 citations

Contribution of the FMR1 gene mutation to human intellectual dysfunction

1995 • 133 citations

Barth syndrome: Clinical features and confirmation of gene localisation to distal Xq28

1993 • 117 citations

Molecular‐neurobehavioral associations in females with the fragile X full mutation

1994 • 113 citations

Specific arithmetic calculation deficits in children with turner syndrome

1994 • 101 citations

Barth syndrome: Clinical observations and genetic linkage studies

1994 • 100 citations

Genetic analysis of the G4.5 gene in families with suspected Barth syndrome

1999 • 83 citations

Frontal lobe function and executive skills in children with turner's syndrome

1996 • 76 citations

X Chromosome Inactivation in Carriers of Barth Syndrome

1998 • 74 citations

Multiple syndromes of 3-methylglutaconic aciduria

1993 • 63 citations

X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.

1995 • 58 citations

Dilated cardiomyopathy with neutropenia, short stature, and abnormal carnitine metabolism

1988 • 44 citations

The Influence of Extended‐Year Schooling on Growth of Achievement and Perceived Competence in Early Elementary School

1998 • 35 citations

Developmental test of visual perception : Examiner's manual

1993 • 34 citations

Molecular-Clinical Correlations in Children and Adults With Fragile X Syndrome

1993 • 27 citations