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The Genetic Architecture of Selection at the Human Dopamine Receptor D4 ( DRD4) Gene Locus

American journal of human genetics, 2004-05, Vol.74 (5), p.931-944

2004

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Evidence for multiple loci from a genome scan of autism kindreds

Molecular psychiatry, 2006-11, Vol.11 (11), p.1049-1060

2006

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Evidence for multiple loci from a genome scan of autism kindreds

Molecular psychiatry, 2006-11, Vol.11 (11), p.1049-1060

2006

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High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder

Molecular psychiatry, 2003-05, Vol.8 (5), p.536-545

2003

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A new βA1-crystallin splice junction mutation in autosomal dominant cataract

Investigative ophthalmology & visual science, 2000-10, Vol.41 (11), p.3278-3285

2000

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Sequence variants of the DRD4 gene in autism: Further evidence that rare DRD4 7R haplotypes are ADHD specific

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2005-07, Vol.136B (1), p.33-35

2005

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Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease

Nature genetics, 1992-09, Vol.2 (1), p.37-41

1992

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Evidence of Positive Selection Acting at the Human Dopamine Receptor D4 Gene Locus

Proceedings of the National Academy of Sciences - PNAS, 2002-01, Vol.99 (1), p.309-314

2002

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Co-occurrence of celiac disease and other autoimmune diseases in celiacs and their first-degree relatives

Journal of autoimmunity, 2008-09, Vol.31 (2), p.160-165

2008

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A genetic linkage map of the rat derived from recombinant inbred strains

Mammalian genome, 1996-02, Vol.7 (2), p.117-127

1996

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Evidence for genetic linkage of autism to chromosomes 7 and 4

Molecular psychiatry, 2006-11, Vol.11 (11), p.979-979

2006

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Molecular genetic delineation of a deletion of chromosome 13q12→q13 in a patient with autism and auditory processing deficits

Cytogenetic and genome research, 2002-01, Vol.98 (4), p.233-239

2002

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Language and other regression: Assessment and timing

Journal of autism and developmental disorders, 2003-12, Vol.33 (6), p.607-616

2003

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Bipolar disorder: Evidence for a major locus

American journal of medical genetics, 1995-10, Vol.60 (5), p.370-376

1995

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Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR

Cytogenetic and genome research, 2001-01, Vol.94 (1-2), p.15-22

2001

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A Genome Survey Indicates a Possible Susceptibility Locus for Bipolar Disorder on Chromosome 22

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (2), p.585-590

2001

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Dopamine genes and ADHD

Neuroscience and biobehavioral reviews, 2000, Vol.24 (1), p.21-25

2000

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Novel Single-Base Deletional Mutation in Major Intrinsic Protein ( MIP) in Autosomal Dominant Cataract

American journal of ophthalmology, 2006-04, Vol.141 (4), p.761-761.e4

2006

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Attention Deficit/Hyperactivity Disorder Children with a 7-Repeat Allele of the Dopamine Receptor D4 Gene Have Extreme Behavior but Normal Performance on Critical Neuropsychological Tests of Attention

Proceedings of the National Academy of Sciences - PNAS, 2000-04, Vol.97 (9), p.4754-4759

2000

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Preliminary Implementation of New Data Mining Techniques for the Analysis of Simulation Data from Genetic Analysis Workshop 12: Problem 2

Genetic epidemiology, 2001, Vol.21 (S1), p.S390-S395

2001

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Dopamine receptor D4 (DRD4) gene in Han Chinese children with attention-deficit/hyperactivity disorder (ADHD): Increased prevalence of the 2-repeat allele

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2005-02, Vol.133B (1), p.54-56

2005

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Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa

American journal of human genetics, 1996-02, Vol.58 (2), p.347-355

1996

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Mapping of a gene determining tuberous sclerosis to human chromosome 11q1411q23

Genomics (San Diego, Calif.), 1990, Vol.6 (1), p.105-114

1990

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Estimating Recombination Fraction Separately for Males and Females: A Counterintuitive Result

Human heredity, 1998-01, Vol.48 (1), p.42-48

1998

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Presence of Large Deletions in Kindreds with Autism

American journal of human genetics, 2002-07, Vol.71 (1), p.100-115

2002

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The Genetic Architecture of Selection at the Human Dopamine Receptor D4 ( DRD4) Gene Locus

Evidence for multiple loci from a genome scan of autism kindreds

Evidence for multiple loci from a genome scan of autism kindreds

High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder

A new βA1-crystallin splice junction mutation in autosomal dominant cataract

Sequence variants of the DRD4 gene in autism: Further evidence that rare DRD4 7R haplotypes are ADHD specific

Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease

Evidence of Positive Selection Acting at the Human Dopamine Receptor D4 Gene Locus

Co-occurrence of celiac disease and other autoimmune diseases in celiacs and their first-degree relatives

A genetic linkage map of the rat derived from recombinant inbred strains

Evidence for genetic linkage of autism to chromosomes 7 and 4

Molecular genetic delineation of a deletion of chromosome 13q12→q13 in a patient with autism and auditory processing deficits

Language and other regression: Assessment and timing

Bipolar disorder: Evidence for a major locus

Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR

A Genome Survey Indicates a Possible Susceptibility Locus for Bipolar Disorder on Chromosome 22

Dopamine genes and ADHD

Novel Single-Base Deletional Mutation in Major Intrinsic Protein ( MIP) in Autosomal Dominant Cataract

Attention Deficit/Hyperactivity Disorder Children with a 7-Repeat Allele of the Dopamine Receptor D4 Gene Have Extreme Behavior but Normal Performance on Critical Neuropsychological Tests of Attention

Preliminary Implementation of New Data Mining Techniques for the Analysis of Simulation Data from Genetic Analysis Workshop 12: Problem 2

Dopamine receptor D4 (DRD4) gene in Han Chinese children with attention-deficit/hyperactivity disorder (ADHD): Increased prevalence of the 2-repeat allele

Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa

Mapping of a gene determining tuberous sclerosis to human chromosome 11q1411q23

Estimating Recombination Fraction Separately for Males and Females: A Counterintuitive Result

Presence of Large Deletions in Kindreds with Autism

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