Concepedia

C. Pollitt

CP

Statistics

Publications

10

Citations

1.4K

H-Index

10

Active since

1998

Affiliations

Newcastle University(Current)

Inserm

Johannes Gutenberg University Mainz

Hammersmith Hospital

Institut de Myologie

C. Pollitt is an author at Newcastle University specializing in medicine, molecular genetics, and muscular dystrophy.

Publications per year

1998–2001

10

Publications

10

Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene

Gisèle Bonne, Eugenio Mercuri, Antoine Muchir et al. · Annals of Neurology · 2000 · 491 citations

, , +14

Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B

Michael Oldridge, Ana María Fortuna, Monika Maringa et al. · Nature Genetics · 2000 · 232 citations

, , +10

Calpainopathy—A Survey of Mutations and Polymorphisms

Carinne Roudaut, Amets Sáenz, Robert Pogue et al. · The American Journal of Human Genetics · 1999 · 206 citations · Full text

, , +12

Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)

Louise V.B. Anderson, Ruth M Harrison, Robert Pogue et al. · Neuromuscular Disorders · 2000 · 164 citations · Full text

, , +13

The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach

C. Pollitt, L.V.B. Anderson, Robert Pogue et al. · Neuromuscular Disorders · 2001 · 95 citations · Full text

, , +2

1–5 of 10