Collette K. Hand

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

Collette K. Hand, Hitoshi Osuga, Yoshiko Yanagisawa et al. · Nature Genetics · 2001 · 675 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Genetics +7

A Novel Locus for Familial Amyotrophic Lateral Sclerosis, on Chromosome 18q

Collette K. Hand, Jawad Khoris, François Salachas et al. · The American Journal of Human Genetics · 2002 · 138 citations · Full text

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Neurological Disorder +8

Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family

Collette K. Hand, Véronique Mayeux‐Portas, Jawad Khoris et al. · Annals of Neurology · 2001 · 81 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, D96n Sod1 Mutations +13

Spectrum of SPG4 Mutations in a Large Collection of North American Families With Hereditary Spastic Paraplegia

Inge A. Meijer, Collette K. Hand, Patrick Cossette et al. · Archives of Neurology · 2002 · 77 citations

Novel RPGR mutations with distinct retinitis pigmentosa phenotypes in French-Canadian families

Robert K. Koenekoop, Magali Loyer, Collette K. Hand et al. · American Journal of Ophthalmology · 2003 · 74 citations

Mendelian Disorder, Genetic Disorder, Medicine +11