Barbara M. Ross

Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions

Konstantin Petrukhin, Svetiana Lutsenko, Barbara M. Ross et al. · Human Molecular Genetics · 1994 · 355 citations

Iron Metabolism, Genetics, Wilson Disease Gene +16

Identification and Analysis of Mutations in the Wilson Disease Gene (ATP7B): Population Frequencies, Genotype-Phenotype Correlation, and Functional Analyses

Anjali B. Shah, Hong Tao Zhang, Barbara M. Ross et al. · The American Journal of Human Genetics · 1997 · 353 citations · Full text

Association of Glucocerebrosidase Mutations With Dementia With Lewy Bodies

Lorraine N. Clark, Lykourgos A. Kartsaklis, Rebecca Gilbert et al. · Archives of Neurology · 2009 · 198 citations · Full text

TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosa

Poulabi Banerjee, Patrick W. Kleyn, James A. Knowles et al. · Nature Genetics · 1998 · 158 citations

Biology, Mendelian Disorder, Genetic Disorder +7

Frequency of Known Mutations in Early-Onset Parkinson Disease

Roy N. Alcalay, Elise Caccappolo, Helen Mejia‐Santana et al. · Archives of Neurology · 2010 · 145 citations · Full text