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 · 514 citations · Full text

Developmental Biology, Bone Morphogenic Protein, Genetics +9

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 · 479 citations · Full text

Slc34a3 Mutations, Urology, Molecular Physiology +10

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 · 256 citations · Full text

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 · 249 citations

Developmental Biology, Region Causes Loss, Genetic Disorder +8

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 · 203 citations · Full text

Developmental Biology, Natural Sciences, Genetics +9