Murat Bastepe

DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis

Bettina Lorenz‐Depiereux, Murat Bastepe, Anna Benet‐Pagès et al. · Nature Genetics · 2006 · 526 citations · Full text

Medicine, Genetics, Molecular Genetics +17

SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaPi-IIc in Maintaining Phosphate Homeostasis

Clemens Bergwitz, Nicole M. Roslin, Martin Tieder et al. · The American Journal of Human Genetics · 2006 · 488 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS

Murat Bastepe, Leopold F. Fröhlich, Geoffrey N. Hendy et al. · Journal of Clinical Investigation · 2003 · 259 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib

Murat Bastepe, Leopold F. Fröhlich, Agnès Linglart et al. · Nature Genetics · 2004 · 252 citations

Life Sciences, Genetics, Molecular Genetics +16

A Novel STX16 Deletion in Autosomal Dominant Pseudohypoparathyroidism Type Ib Redefines the Boundaries of a cis-Acting Imprinting Control Element of GNAS

Agnès Linglart, Robert Gensure, Robert C. Olney et al. · The American Journal of Human Genetics · 2005 · 204 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13