Roger E. Stevenson

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

Heather C. Mefford, Andrew J. Sharp, Carl Baker et al. · New England Journal of Medicine · 2008 · 811 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

<i>AGTR2</i> Mutations in X-Linked Mental Retardation

Virginie Vervoort, Michael A. Beachem, Penny S. Edwards et al. · Science · 2002 · 719 citations

Natural Sciences, Physics, Biophotonics +16

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

Andrew J. Sharp, Heather C. Mefford, Kelly Li et al. · Nature Genetics · 2008 · 591 citations

Medicine, Genetics, Pediatrics +14

X–linked spastic paraplegia (SPG1), MASA syndrome and X–linked hydrocephalus result from mutations in the L1 gene

Monique Jouet, André Rosenthal, Giles Armstrong et al. · Nature Genetics · 1994 · 420 citations

Life Sciences, Molecular Genetics, Neurology +8

Autism and maternally derived aberrations of chromosome 15q

Richard J. Schroer, Mary C. Phelan, Ron C. Michaelis et al. · American Journal of Medical Genetics · 1998 · 372 citations

Life Sciences, Genetics, Molecular Genetics +15