Disruption of a Novel Gene (IMMP2L) by a Breakpoint in 7q31 Associated with Tourette Syndrome

Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer

1992 • 1,413 citations

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

2000 • 867 citations

An international perspective on Tourette syndrome: selected findings from 3500 individuals in 22 countries

2000 • 810 citations

A decrease of reelin expression as a putative vulnerability factor in schizophrenia

1998 • 757 citations

Online Mendelian Inheritance in Man 'OMIM'.

2007 • 306 citations

A Mitochondrial Protease with Two Catalytic Subunits of Nonoverlapping Specificities

1993 • 263 citations

Signal peptidases in prokaryotes and eukaryotes - a new protease family

1992 • 212 citations

The SPCH1 Region on Human 7q31: Genomic Characterization of the Critical Interval and Localization of Translocations Associated with Speech and Language Disorder

2000 • 206 citations

Mitochondrial respiratory chain disorders II: neurodegenerative disorders and nuclear gene defects

2000 • 202 citations

The prevalence of Gilles de la Tourette syndrome in children and adolescents with autism: a large scale study

1999 • 179 citations

Identification of a Novel Gene on Chromosome 7q31 That Is Interrupted by a Translocation Breakpoint in an Autistic Individual

2000 • 121 citations

Annotation: Gilles de la Tourette Syndrome—An Update

1994 • 115 citations

Significant Linkage for Tourette Syndrome in a Large French Canadian Family

2000 • 108 citations

Mitochondrial involvement in schizophrenia and other functional psychoses

1996 • 104 citations

Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3.

1996 • 92 citations

Autosomal Dominant Gene Transmission in a Large Kindred with Gilles de la Tourette Syndrome

1992 • 82 citations

A Prospective Longitudinal Study of Gilles de la Tourette's Syndrome

1994 • 80 citations

Recent developments in the molecular genetics of mitochondrial disorders

1998 • 79 citations

Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31

2000 • 72 citations

Candidate region for Gilles de la Tourette syndrome at 7q31

2001 • 46 citations

Candidate region for Gilles de la Tourette syndrome at 7q31

2001 • 40 citations

Cloning and expression of a novel gene for a protein with leucine-rich repeats in the developing mouse nervous system

1996 • 35 citations

Current Status of Genetic Studies of Gilles de la Tourette Syndrome

1998 • 31 citations

Isolation of Site-Specific Insert Probes from Chimeric YACs

1997 • 23 citations

Cloning, sequencing and localization to chromosome 11 of a cDNA encoding a human opioid-binding cell adhesion molecule (OBCAM)

1995 • 20 citations

Chromosome 7q22-q31 duplication: Report of a new case and review

2000 • 9 citations