A. A. J. Pannett

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome

John D. Carpten, Christiane M. Robbins, Andrea Villablanca et al. · Nature Genetics · 2002 · 742 citations

Parathyroid Hormone, Parathyroid Disease, Pathology +2

Characterization of Mutations in Patients with Multiple Endocrine Neoplasia Type 1

J. H. Duncan Bassett, S. A. Forbes, A. A. J. Pannett et al. · The American Journal of Human Genetics · 1998 · 440 citations · Full text

Tumor Biology, Endocrine Oncology, Somatic Variant +7

Localization of Familial Benign Hypercalcemia, Oklahoma Variant (FBHOk), to Chromosome 19q13

Sarah E. Lloyd, A. A. J. Pannett, Peter Dixon et al. · The American Journal of Human Genetics · 1999 · 136 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7

MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMDMO)

Ann Kennedy, Masaki Inada, Stephen M. Krane et al. · Journal of Clinical Investigation · 2005 · 115 citations · Full text

Genetics, Genetic Epidemiology, Pathology +17

Somatic Mutations in MEN Type 1 Tumors, Consistent with the Knudson “Two-Hit” Hypothesis

A. A. J. Pannett, Rajesh V. Thakker · The Journal of Clinical Endocrinology & Metabolism · 2001 · 97 citations · Full text