A Major Locus for Autosomal Recessive Retinitis Pigmentosa on 6q, Determined by Homozygosity Mapping of Chromosomal Regions That Contain Gamma-Aminobutyric Acid–Receptor Clusters

Glutamate neurotoxicity and diseases of the nervous system

1988 • 7,257 citations

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1996 • 2,983 citations

Excitatory Amino Acids as a Final Common Pathway for Neurologic Disorders

1994 • 2,668 citations

Epilepsy and Exacerbation of Brain Injury in Mice Lacking the Glutamate Transporter GLT-1

1997 • 1,715 citations

Current Protocols in Human Genetics

2001 • 1,023 citations

A gene map of the human genome.

1996 • 986 citations

Homozygosity Mapping: A Way to Map Human Recessive Traits with the DNA of Inbred Children

1987 • 875 citations

A Gene Map of the Human Genome

1996 • 737 citations

Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy

1997 • 645 citations

Recessive mutations in the gene encoding the β–subunit of rod phosphodiesterase in patients with retinitis pigmentosa

1993 • 573 citations

GABA receptor mechanisms in the central nervous system

1991 • 555 citations

Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene

1997 • 448 citations

Cloning of the gamma-aminobutyric acid (GABA) rho 1 cDNA: a GABA receptor subunit highly expressed in the retina.

1991 • 426 citations

A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

1992 • 417 citations

Mutation of the gene encoding cellular retinaldehyde–binding protein in autosomal recessive retinitis pigmentosa

1997 • 323 citations

Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa.

1995 • 270 citations

Molecular genetics of retinitis pigmentosa

1995 • 255 citations

Autosomal recessive retinitis pigmentosa caused by mutations in the α subunit of rod cGMP phosphodiesterase

1995 • 244 citations

GABAc receptors

1995 • 243 citations

Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping.

1995 • 226 citations

Gamma-aminobutyric acidA receptor structure and function.

1992 • 208 citations

Identification of a putative γ-aminobutyric acid (GABA) receptor subunit rho2 cDNA and colocalization of the genes encoding rho2 (GABRR2) and rho1 (GABRR1) to human chromosome 6q14–q21 and mouse chromosome 4

1992 • 190 citations

North Carolina macular dystrophy is assigned to chromosome 6

1992 • 173 citations

The connections between horizontal cells and photoreceptors in the retina of the cat: Electron microscopy of Golgi preparations

1974 • 172 citations

Clinical Features of a Stargardt-Like Dominant Progressive Macular Dystrophy With Genetic Linkage to Chromosome 6q

1994 • 169 citations

Assignment of a Gene for Autosomal Recessive Retinitis Pigmentosa (RP12) to Chromosome 1q31-q32.1 in an Inbred and Genetically Heterogeneous Disease Population

1994 • 118 citations

GABAC receptors in the vertebrate retina

1996 • 115 citations

The architecture of functional neural circuits in the vertebrate retina. The Proctor Lecture.

1994 • 87 citations

Human chromosomal localization of genes encoding the gamma 1 and gamma 2 subunits of the gamma-aminobutyric acid receptor indicates that members of this gene family are often clustered in the genome.

1992 • 81 citations

Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p

1994 • 77 citations

Support for the equivalent light hypothesis for RP

1995 • 71 citations

Localization of a gene for oculodentodigital syndrome to human chromosome 6q22-q24

1997 • 68 citations

Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q

1995 • 64 citations

A New Locus for Autosomal Recessive Retinitis Pigmentosa (RP19) Maps to 1p13–1p21

1997 • 60 citations

Homozygosity mapping of the gene for Chediak-Higashi syndrome to chromosome 1q42-q44 in a segment of conserved synteny that includes the mouse beige locus (bg).

1996 • 57 citations

A locus for Fanconi anemia on 16q determined by homozygosity mapping.

1996 • 34 citations

Inherited Retinal Diseases: A Diagnostic Guide

1992 • 22 citations

Quantitative aspects of synaptic ribbon formation in the outer plexiform layer of the developing cat retina

1989 • 14 citations

Inherited Retinal Diseases: A Diagnostic Guide

1990 • 8 citations

Deleted Work

1955 • 0 citations