G. Barnes

发表

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

Manish S. Shah, A. Poustka, D. Church, 1993, Cell.

Trinucleotide repeat length instability and age of onset in Huntington's disease

J. Penney, S. Folstein, A. Falek, 1993, Nature Genetics.

Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4.

J. Gusella, G. Barnes, M. Altherr, 1992, Molecular and cellular probes.

Huntington's disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains

M. MacDonald, J. Gusella, J. Vonsattel, 1994, Neurobiology of Disease.

A novel G protein-coupled receptor kinase gene cloned from 4p16.3.

D. Church, M. MacDonald, C. Ambrose, 1992, Human molecular genetics.

Targeted inactivation of the mouse Huntington's disease gene homolog Hdh.

A. Joyner, J. Gusella, J. Vonsattel, 1996, Cold Spring Harbor symposia on quantitative biology.

De novo expansion of a (CAG)n repeat in sporadic Huntington's disease

J. Gusella, W. Koroshetz, J. Vonsattel, 1993, Nature genetics.

Exon trapping and sequence-based methods of gene finding in transcript mapping of human 4p 16.3

D. Church, M. MacDonald, H. Lehrach, 1997, Somatic Cell Genetics.

The Huntington's disease candidate region exhibits many different haplotypes

Hans Lehrach, Francis S. Collins, James F. Gusella, 1992, Nature Genetics.

Reduced penetrance of the Huntington's disease mutation.

M. MacDonald, J. Gusella, R. Myers, 1997, Human molecular genetics.

Sequence-tagged sites (STSs) spanning 4p16.3 and the Huntington disease candidate region.

F. Collins, M. MacDonald, J. Gusella, 1992, Genomics.

Inactivation of the mouse Huntington's disease gene homolog Hdh.

A. Joyner, J. Gusella, J. Vonsattel, 1995, Science.

Huntingtin interacts with a family of WW domain proteins.

M. MacDonald, J. Gusella, G. Barnes, 1998, Human molecular genetics.

Normal and Expanded Huntington’s Disease Gene Alleles Produce Distinguishable Proteins Due to Translation Across the CAG Repeat

M. MacDonald, J. Gusella, J. Vonsattel, 1995, Molecular medicine.

Gametic but not somatic instability of CAG repeat length in Huntington's disease.

M. MacDonald, J. Penney, C. Ambrose, 1993, Journal of medical genetics.

A recombination event that redefines the Huntington disease region.

F. Collins, M. MacDonald, R. Snell, 1992, American journal of human genetics.

Fine-scale mapping of a locus for severe bipolar mood disorder on chromosome 18p11.3 in the Costa Rican population

J. Molina, S. Lewitzky, S. Jawahar, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Fine mapping of a locus for severe bipolar mood disorder in the Costa Rican population using linkage disequilibrium methods.

Reus, N. Freimer, S. Barondes, 1997 .

Structure and expression of the Huntington's disease gene: Evidence against simple inactivation due to an expanded CAG repeat

R. Durbin, D. Church, M. MacDonald, 1994, Somatic cell and molecular genetics.

Mouse Huntington's disease gene homolog (Hdh)

M. MacDonald, J. Gusella, C. Ambrose, 1994, Somatic cell and molecular genetics.

Cloning of the α–adducin gene from the Huntington's disease candidate region of chromosome 4 by exon amplification

D. Church, D. Housman, R. Snell, 1992, Nature Genetics.

Differential Expression of Normal and Mutant Huntington's Disease Gene Alleles

James F. Gusella, Marcy E. MacDonald, M. MacDonald, 1996, Neurobiology of Disease.

A dinucleotide repeat polymorphism at the D4S127 locus.

J. Gusella, G. Barnes, M. Macdonald, 1992, Human molecular genetics.

A gene from chromosome 4p16.3 with similarity to a superfamily of transporter proteins.

D. Church, M. MacDonald, D. Housman, 1993, Human molecular genetics.