Brian Harding

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

A common molecular basis for three inherited kidney stone diseases

Sarah E. Lloyd, Simon H. S. Pearce, Simon E. Fisher et al. · Nature · 1996 · 717 citations · Full text

Urology, Genetic Disorder, Common Molecular Basis +10

GATA3 haplo-insufficiency causes human HDR syndrome

Hilde Van Esch, Peter Groenen, M. Andrew Nesbit et al. · Nature · 2000 · 645 citations

Autoimmune Disease, Genetic Disorder, Genetics +5

Drug resistance in epilepsy: expression of drug resistance proteins in common causes of refractory epilepsy

Sanjay M. Sisodiya, W-R Lin, Brian Harding et al. · Brain · 2002 · 477 citations · Full text

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