Murat Bastepe
Brigham and Women's Hospital(US)Massachusetts General Hospital(US)
Publications by Year
Research Areas
Genetic Syndromes and Imprinting, Genomics and Rare Diseases, Congenital heart defects research, Parathyroid Disorders and Treatments, Epigenetics and DNA Methylation
Most-Cited Works
- → DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis(2006)521 cited
- → 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(2006)482 cited
- → Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement(2018)329 cited
- → Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS(2003)259 cited
- → Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib(2004)251 cited
- → The GNAS Locus and Pseudohypoparathyroidism(2008)223 cited