Jacqueline Woolf

Congenital erythropoietic porphyria: a single-observer clinical study of 29 cases

Ruwani Katugampola, Michael N. Badminton, A.Y. Finlay et al. · British Journal of Dermatology · 2012 · 95 citations

Medicine, Dermatology, Pediatrics +12

Diagnostic Strategies for Autosomal Dominant Acute Porphyrias: Retrospective Analysis of 467 Unrelated Patients Referred for Mutational Analysis of the HMBS, CPOX, or PPOX Gene

Sharon D. Whatley, Nicola Mason, Jacqueline Woolf et al. · Clinical Chemistry · 2009 · 87 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A management algorithm for congenital erythropoietic porphyria derived from a study of 29 cases

R. P. Katugampola, A. Anstey, A.Y. Finlay et al. · British Journal of Dermatology · 2012 · 82 citations

Medicine, Hematology, Pediatrics +17

Characterization of Mutations in the CPO Gene in British Patients Demonstrates Absence of Genotype-Phenotype Correlation and Identifies Relationship between Hereditary Coproporphyria and Harderoporphyria

J. Lamoril, Hervé Puy, Sharon D. Whatley et al. · The American Journal of Human Genetics · 2001 · 71 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6

Detection of latent variegate porphyria by fluorescence emission spectroscopy of plasma

Calista Long, Stuart J. Smyth, Jacqueline Woolf et al. · British Journal of Dermatology · 1993 · 68 citations

Life Sciences, Genetics, Pathology +10