Carol Hardy

Clinical and Molecular Genetic Analysis of 19 Wolfram Syndrome Kindreds Demonstrating a Wide Spectrum of Mutations in WFS1

Carol Hardy, Farhat L. Khanim, Rosarelis Torres et al. · The American Journal of Human Genetics · 1999 · 217 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects

Abdulla Ibrahim, Gail Kirby, Carol Hardy et al. · Clinical Epigenetics · 2014 · 150 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Monogenic diabetes syndromes: Locus-specific databases for Alström, Wolfram, and Thiamine-responsive megaloblastic anemia

Dewi Astuti, Ataf Sabir, Piers Fulton et al. · Human Mutation · 2017 · 71 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology

Louise Tee, Derek Lim, Renuka Dias et al. · Clinical Epigenetics · 2013 · 49 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Analysis of 133 Meioses Places the Genes for Nevoid Basal Cell Carcinoma (Gorlin) Syndrome and Fanconi Anemia Group C in a 2.6-cM Interval and Contributes to the Fine Map of 9q22.3

Peter Farndon, Deborah Morris, Carol Hardy et al. · Genomics · 1994 · 36 citations

Life Sciences, Genetics, Molecular Genetics +13