Harvard Catalyst Profiles

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Murat Bastepe, Ph.D., M.D.

Co-Author

This page shows the publications co-authored by Murat Bastepe and Harald Jueppner.
Connection Strength

3.172
  1. Bastepe M, Jüppner H. GNAS locus and pseudohypoparathyroidism. Horm Res. 2005; 63(2):65-74.
    View in: PubMed
    Score: 0.331
  2. Bastepe M, Fröhlich LF, Linglart A, Abu-Zahra HS, Tojo K, Ward LM, Jüppner H. Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib. Nat Genet. 2005 Jan; 37(1):25-7.
    View in: PubMed
    Score: 0.327
  3. Bastepe M, Fröhlich LF, Hendy GN, Indridason OS, Josse RG, Koshiyama H, Körkkö J, Nakamoto JM, Rosenbloom AL, Slyper AH, Sugimoto T, Tsatsoulis A, Crawford JD, Jüppner H. Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS. J Clin Invest. 2003 Oct; 112(8):1255-63.
    View in: PubMed
    Score: 0.301
  4. Bastepe M, Jüppner H. Editorial: Pseudohypoparathyroidism and mechanisms of resistance toward multiple hormones: molecular evidence to clinical presentation. J Clin Endocrinol Metab. 2003 Sep; 88(9):4055-8.
    View in: PubMed
    Score: 0.299
  5. Bastepe M, Gunes Y, Perez-Villamil B, Hunzelman J, Weinstein LS, Jüppner H. Receptor-mediated adenylyl cyclase activation through XLalpha(s), the extra-large variant of the stimulatory G protein alpha-subunit. Mol Endocrinol. 2002 Aug; 16(8):1912-9.
    View in: PubMed
    Score: 0.278
  6. Bastepe M, Pincus JE, Sugimoto T, Tojo K, Kanatani M, Azuma Y, Kruse K, Rosenbloom AL, Koshiyama H, Jüppner H. Positional dissociation between the genetic mutation responsible for pseudohypoparathyroidism type Ib and the associated methylation defect at exon A/B: evidence for a long-range regulatory element within the imprinted GNAS1 locus. Hum Mol Genet. 2001 Jun 01; 10(12):1231-41.
    View in: PubMed
    Score: 0.256
  7. Bastepe M, Lane AH, Jüppner H. Paternal uniparental isodisomy of chromosome 20q--and the resulting changes in GNAS1 methylation--as a plausible cause of pseudohypoparathyroidism. Am J Hum Genet. 2001 May; 68(5):1283-9.
    View in: PubMed
    Score: 0.254
  8. Bastepe M, Jüppner H. Pseudohypoparathyroidism. New insights into an old disease. Endocrinol Metab Clin North Am. 2000 Sep; 29(3):569-89.
    View in: PubMed
    Score: 0.243
  9. Bastepe M, Jüppner H. Identification and characterization of two new, highly polymorphic loci adjacent to GNAS1 on chromosome 20q13.3. Mol Cell Probes. 2000 Aug; 14(4):261-4.
    View in: PubMed
    Score: 0.242
  10. Bastepe M, Pincus JE, Jüppner H. Two frequent tetra-nucleotide repeat polymorphisms between VAPB and STX16 on chromosome 20q13. Mol Cell Probes. 1999 Dec; 13(6):449-51.
    View in: PubMed
    Score: 0.231
  11. Fröhlich LF, Gensure RC, Schipani E, Jüppner H, Bastepe M. Haplotype frequencies and linkage disequilibrium analysis of four frequent polymorphisms at the PTH/PTH-related peptide receptor gene locus. Mol Cell Probes. 2004 Oct; 18(5):353-7.
    View in: PubMed
    Score: 0.081
  12. Bastepe M, Weinstein LS, Ogata N, Kawaguchi H, Jüppner H, Kronenberg HM, Chung UI. Stimulatory G protein directly regulates hypertrophic differentiation of growth plate cartilage in vivo. Proc Natl Acad Sci U S A. 2004 Oct 12; 101(41):14794-9.
    View in: PubMed
    Score: 0.081
  13. Bastepe M, Raas-Rothschild A, Silver J, Weissman I, Wientroub S, Jüppner H, Gillis D. A form of Jansen's metaphyseal chondrodysplasia with limited metabolic and skeletal abnormalities is caused by a novel activating parathyroid hormone (PTH)/PTH-related peptide receptor mutation. J Clin Endocrinol Metab. 2004 Jul; 89(7):3595-600.
    View in: PubMed
    Score: 0.079
  14. Gensure RC, Ponugoti B, Gunes Y, Papasani MR, Lanske B, Bastepe M, Rubin DA, Jüppner H. Identification and characterization of two parathyroid hormone-like molecules in zebrafish. Endocrinology. 2004 Apr; 145(4):1634-9.
    View in: PubMed
    Score: 0.076
  15. Jüppner H, Schipani E, Bastepe M, Cole DE, Lawson ML, Mannstadt M, Hendy GN, Plotkin H, Koshiyama H, Koh T, Crawford JD, Olsen BR, Vikkula M. The gene responsible for pseudohypoparathyroidism type Ib is paternally imprinted and maps in four unrelated kindreds to chromosome 20q13.3. Proc Natl Acad Sci U S A. 1998 Sep 29; 95(20):11798-803.
    View in: PubMed
    Score: 0.053
  16. Mahmud FH, Linglart A, Bastepe M, Jüppner H, Lteif AN. Molecular diagnosis of pseudohypoparathyroidism type Ib in a family with presumed paroxysmal dyskinesia. Pediatrics. 2005 Feb; 115(2):e242-4.
    View in: PubMed
    Score: 0.021
  17. Laspa E, Bastepe M, Jüppner H, Tsatsoulis A. Phenotypic and molecular genetic aspects of pseudohypoparathyroidism type Ib in a Greek kindred: evidence for enhanced uric acid excretion due to parathyroid hormone resistance. J Clin Endocrinol Metab. 2004 Dec; 89(12):5942-7.
    View in: PubMed
    Score: 0.020
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.