Elaine Kendall

A novel X–linked gene, DDP, shows mutations in families with deafness (DFN–1), dystonia, mental deficiency and blindness

Melanie May, Lisbeth Tranebjærg, Elaine Kendall et al. · Nature Genetics · 1996 · 269 citations

Neurodevelopmental Disorders, Genetic Diseases, Developmental Biology +13

Pelizaeus-Merzbacher Disease: Identification of Xq22 Proteolipid-Protein Duplications and Characterization of Breakpoints by Interphase FISH

Karen Woodward, Elaine Kendall, David Vetrie et al. · The American Journal of Human Genetics · 1998 · 145 citations · Full text

Biology, Xq22 Proteolipid-protein Duplications, Medicine +10

Human major histocompatibility complex contains a new cluster of genes between the HLA-D and complement C4 loci

Elaine Kendall, Carole A. Sargent, R. Duncan Campbell · Nucleic Acids Research · 1990 · 83 citations · Full text

Characterization of DRP2, a novel human dystrophin homologue

Roland G. Roberts, Tom C. Freeman, Elaine Kendall et al. · Nature Genetics · 1996 · 73 citations

Protein Function, Molecular Biology, Degenerative Disease +4

The Human Family of Deafness/Dystonia Peptide (DDP) Related Mitochondrial Import Proteins

Elaine Kendall, Tom C. Freeman, Roland G. Roberts et al. · Genomics · 1999 · 59 citations

Mitochondrial Myopathy, Neurodegenerative Diseases, Mitochondrial Function +9