Russell G. Snell - Researcher Profile

Publications

4 shown

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

Marcy E. MacDonald , Christine Ambrose , Mabel P. Duyao +55 more

1993 Cell 8288 citations

Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

J. David Brook , Mila E. McCurrach , H G Harley +21 more

1992 Cell 2750 citations

A recombination event that redefines the Huntington disease region.

Russell G. Snell , Leslie M. Thompson , Dan Tagle +7 more

We report both a recombination event that places the Huntington disease gene proximal to the marker D4S98 and an extended linkage-disequilibrium study that uses this marker and ...

1992 PubMed 19 citations

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

Stacy Taylor , Russell G. Snell , Alan Buckler +15 more

1992 Nature Genetics 39 citations

Frequent Co-Authors

Researcher Info

h-index: 4
Publications: 4
Citations: 11,096
Institution: University of Wales

External Links

ORCID Profile Google Scholar

Identifiers

ORCID: 0000-0002-8166-4014

Impact Metrics

h-index 4

h-index: Number of publications with at least h citations each.