Scott H. Coppel

Statistics

Publications

Citations

336

H-Index

Active since

2012

Affiliations

Massachusetts General Hospital(Current)

Center for Human Genetics

Scott H. Coppel is an author at Massachusetts General Hospital specializing in life sciences, neurodegenerative disorders, and neurodegenerative diseases.

Publications per year

2012–2013

Publications

Human iPSC models of neuronal ceroid lipofuscinosis capture distinct effects of TPP1 and CLN3 mutations on the endocytic pathway

Xenia Lojewski, John F. Staropoli, Sunita Biswas-Legrand et al. · Human Molecular Genetics · 2013 · 140 citations · Full text

Life Sciences, Cell Biology, Neuroscience +17

A Homozygous Mutation in KCTD7 Links Neuronal Ceroid Lipofuscinosis to the Ubiquitin-Proteasome System

John F. Staropoli, Amel Karaa, Elaine T. Lim et al. · The American Journal of Human Genetics · 2012 · 114 citations · Full text

Life Sciences, Molecular Biology, Neuroscience +14

Mutations in the Gene DNAJC5 Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families

Milen Velinov, Natalia Dolzhanskaya, Michael Gonzalez et al. · PLoS ONE · 2012 · 82 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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