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Current Genomics|May 5, 2009
The GNAS Locus: Quintessential Complex Gene Encoding Gsalpha, XLalphas, and other Imprinted TranscriptsMurat BastepeAdvances in Experimental Medicine and Biology|April 1, 2008
The GNAS locus and pseudohypoparathyroidismMurat BastepeThe Journal of Clinical Endocrinology and Metabolism|October 23, 2012
De novo STX16 deletions: an infrequent cause of pseudohypoparathyroidism type Ib that should be excluded in sporadic casesSerap Turan, Jaakko Ignatius, Jukka S Moilanen, et al.Proceedings of the National Academy of Sciences of the United States of America|April 13, 2012
Loss of XLαs (extra-large αs) imprinting results in early postnatal hypoglycemia and lethality in a mouse model of pseudohypoparathyroidism IbEduardo Fernández-Rebollo, Akira Maeda, Monica Reyes, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 26, 2010
Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutationOuti Mäkitie, Renata C Pereira, Ilkka Kaitila, et al.Reviews in Endocrine & Metabolic Disorders|March 28, 2008
Inherited hypophosphatemic disorders in children and the evolving mechanisms of phosphate regulationMurat Bastepe, Harald JüppnerCurrent Protocols in Human Genetics|October 7, 2015
Huntington Disease: Molecular Diagnostics ApproachMurat Bastepe, Winnie XinJournal of Pediatric Endocrinology & Metabolism : JPEM|June 23, 2006
Different mutations within or upstream of the GNAS locus cause distinct forms of pseudohypoparathyroidismHarald Jüppner, Murat BastepeHormone Research|February 16, 2005
GNAS locus and pseudohypoparathyroidismMurat Bastepe, Harald JüppnerJournal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 19, 2025
Imprinting and skeletal disorders: lessons from pseudohypoparathyroidism and related disordersYorihiro Iwasaki, Murat BastepePageof 23