Julie D. Sharp

The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8

Susanna Ranta, Yonghui Zhang, Barbara Ross et al. · Nature Genetics · 1999 · 318 citations

Neuronal Ceroid Lipofuscinoses, Molecular Neuroscience, Ependyma +7

The Gene Mutated in Variant Late-Infantile Neuronal Ceroid Lipofuscinosis (CLN6) and in nclf Mutant Mice Encodes a Novel Predicted Transmembrane Protein

Ruth B. Wheeler, Julie D. Sharp, Roger A. Schultz et al. · The American Journal of Human Genetics · 2002 · 201 citations · Full text

Molecular Neuroscience, Developmental Biology, Ependyma +6

Association study of a dopamine transporter polymorphism and attention deficit hyperactivity disorder in UK and Turkish samples

Sarah Curran, Jonathan Mill, Lindsey Kent et al. · Molecular Psychiatry · 2001 · 161 citations · Full text

CLN6, which is associated with a lysosomal storage disease, is an endoplasmic reticulum protein

Sara Mole, Grégoire Michaux, Sandra Codlin et al. · Experimental Cell Research · 2004 · 115 citations

Endoplasmic Reticulum Protein, Natural Sciences, Endocytic Pathway +9

Defined chromosomal assignment of CLN5 demonstrates that at least four genetic loci are involved in the pathogenesis of human ceroid lipofuscinoses.

Minna Savukoski, Marjo Kestilä, Rhys Williams et al. · PubMed · 1994 · 108 citations