L. Lazarou

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

Russell G. Snell, John MacMillan, Jeremy P. Cheadle et al. · Nature Genetics · 1993 · 713 citations

Genetic Analysis, Phenotypic Variation, Genetic Disorder +8

Early onset seizures and Rett-like features associated with mutations in CDKL5

Julie Evans, Hayley Archer, James Colley et al. · European Journal of Human Genetics · 2005 · 173 citations · Full text

Early Onset Seizures, Rett-like Features, Genetic Disorder +7

Molecular analysis and clinical correlations of the Huntington's disease mutation

J. MacMillan, Russell G. Snell, Audrey Tyler et al. · The Lancet · 1993 · 95 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

Linkage disequilibrium in Huntington's disease: an improved localisation for the gene.

Russell G. Snell, L. Lazarou, S Youngman et al. · Journal of Medical Genetics · 1989 · 78 citations · Full text

Familial phenotype differences in PKD1

Nick Hateboer, L. Lazarou, Andrew J Williams et al. · Kidney International · 1999 · 66 citations · Full text

Genetic Disorder, Genetics, Genetic Epidemiology +6