Leslie J. Sheffield

A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy

Brunella Franco, Germana Meroni, Giancarlo Parenti et al. · Cell · 1995 · 316 citations · Full text

Developmental Biology, Chondrodysplasia Punctata, Genetic Disorder +10

Familial temporal lobe epilepsy: A common disorder identified in twins

Samuel F. Berkovic, Anne M. McIntosh, R. Anne Howell et al. · Annals of Neurology · 1996 · 225 citations

Neuropsychiatric symptomatology predicts seizure recurrence in newly treated patients

Slavé Petrovski, Cassandra Szoeke, Nigel C. Jones et al. · Neurology · 2010 · 213 citations

Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study

Gianpiero L. Cavalleri, Michael E. Weale, Kevin V. Shianna et al. · The Lancet Neurology · 2007 · 187 citations

Genetic Disorder, Genetics, Psychiatric Genetics +10

An Ultrasound Renal Cyst Prevalence Survey: Specificity Data for Inherited Renal Cystic Diseases

David Ravine, Robert N. Gibson, John Donlan et al. · American Journal of Kidney Diseases · 1993 · 166 citations

Urology, Renal Pathology, Pediatrics +5