Joan H.M. Knoll

Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia

Stefan Mundlos, F Otto, C Mundlos et al. · Cell · 1997 · 1.5K citations · Full text

Dentistry, Genetics, Molecular Genetics +7

Inhibition of telomerase limits the growth of human cancer cells

William C. Hahn, Sheila A. Stewart, Mary W. Brooks et al. · Nature Medicine · 1999 · 1K citations

Medicine, Cell Biology, Oncology +12

Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome

Robert D. Nicholls, Joan H.M. Knoll, Merlin G. Butler et al. · Nature · 1989 · 887 citations

Life Sciences, Genetics, Molecular Genetics +11

Angelman syndrome 2005: Updated consensus for diagnostic criteria

Charles A. Williams, Arthur L. Beaudet, Jill Clayton‐Smith et al. · American Journal of Medical Genetics Part A · 2006 · 646 citations

Medicine, Neurology, Psychiatry +12

Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

Joan H.M. Knoll, Robert D. Nicholls, R.E. Magenis et al. · American Journal of Medical Genetics · 1989 · 583 citations

Life Sciences, Genetics, Molecular Genetics +17