Simple repeat DNA is not replicated simply

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

1993 • 7,941 citations

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

1991 • 2,763 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

1992 • 2,719 citations

Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

1993 • 2,711 citations

A second-generation linkage map of the human genome

1992 • 1,721 citations

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1

1993 • 1,596 citations

Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)

1994 • 1,122 citations

Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair

1993 • 1,076 citations

Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n

1991 • 903 citations

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

1994 • 721 citations

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation

1993 • 522 citations

Complex gene conversion events in germline mutation at human minisatellites

1994 • 491 citations

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I

1993 • 473 citations

Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer

1993 • 434 citations

Instability of short tandem repeats (microsatellites) in human cancers

1994 • 413 citations

Two cytoplasmic candidates for immunophilin action are revealed by affinity for a new cyclophilin: One in the presence and one in the absence of CsA

1991 • 399 citations

Dynamic mutations: A new class of mutations causing human disease

1992 • 315 citations

Polygenic control of autoimmune diabetes in nonobese diabetic mice

1993 • 298 citations

An Association between the Risk of Cancer and Mutations in the HRAS1 Minisatellite Locus

1993 • 290 citations

Direct detection of novel expanded trinucleotide repeats in the human genome

1993 • 275 citations

Origin of the expansion mutation in myotonic dystrophy

1993 • 213 citations

Evidence of founder chromosomes in fragile X syndrome

1992 • 187 citations

The Huntington's disease candidate region exhibits many different haplotypes

1992 • 157 citations

Heritable unstable DNA sequences

1992 • 120 citations

Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker.

1991 • 93 citations

Mutations and polymorphisms in the prion protein gene

1993 • 53 citations

Retreat of the triplet repeat?

1993 • 29 citations