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Peter K. Rogan | doi.page

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Peter K. Rogan

Directorate-General for Interpretation(BE)

Publications by Year

Research Areas

RNA Research and Splicing, Genomic variations and chromosomal abnormalities, Cancer Genomics and Diagnostics, Genetic Syndromes and Imprinting, BRCA gene mutations in cancer

Most-Cited Works

→ Hepatic CYP2B6 Expression: Gender and Ethnic Differences and Relationship to CYP2B6 Genotype and CAR (Constitutive Androstane Receptor) Expression(2003)400 cited
→ Chromosome Breakage in the Prader-Willi and Angelman Syndromes Involves Recombination between Large, Transcribed Repeats at Proximal and Distal Breakpoints(1999)281 cited
→ Imprinting-Mutation Mechanisms in Prader-Willi Syndrome(1999)276 cited
→ The Frequency of Uniparental Disomy in Prader-Willi Syndrome(1992)260 cited
→ Predicting responses to platin chemotherapy agents with biochemically-inspired machine learning(2019)201 cited
→ Information analysis of human splice site mutations(1998)184 cited

→ Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.(1996)

174 cited

→ Automated splicing mutation analysis by information theory(2005)148 cited

Autosomal dominant zonular cataract with sutural opacities is associated with a splice mutation in the betaA3/A1-crystallin gene.(1998)

→ Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation(1997)141 cited