Murat Bastepe

7.1k total citations
104 papers, 4.6k citations indexed

About

Murat Bastepe is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Murat Bastepe has authored 104 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Molecular Biology, 67 papers in Genetics and 18 papers in Nephrology. Recurrent topics in Murat Bastepe's work include Genetic Syndromes and Imprinting (63 papers), Genomics and Rare Diseases (45 papers) and Congenital heart defects research (20 papers). Murat Bastepe is often cited by papers focused on Genetic Syndromes and Imprinting (63 papers), Genomics and Rare Diseases (45 papers) and Congenital heart defects research (20 papers). Murat Bastepe collaborates with scholars based in United States, Türkiye and Canada. Murat Bastepe's co-authors include Harald Jüppner, Harald Jüppner, Serap Turan, Agnès Linglart, Leopold F. Fröhlich, Hilal Abu-Zahra, Andrew Lane, Lee S. Weinstein, Barrie Ashby and Robert Gensure and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Murat Bastepe

100 papers receiving 4.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Murat Bastepe United States 36 2.9k 2.9k 1.0k 544 486 104 4.6k
Anna Spada Italy 46 1.4k 0.5× 2.6k 0.9× 390 0.4× 337 0.6× 600 1.2× 172 7.0k
Harald Jüppner United States 28 2.4k 0.8× 3.5k 1.2× 2.1k 2.1× 408 0.8× 1.6k 3.4× 65 6.4k
Takanori Muto Japan 13 1.3k 0.5× 1.8k 0.6× 2.5k 2.4× 337 0.6× 594 1.2× 16 4.1k
Anita Farhi United States 12 1.1k 0.4× 2.3k 0.8× 299 0.3× 162 0.3× 369 0.8× 14 3.5k
Steven Mumm United States 35 1.2k 0.4× 2.2k 0.8× 276 0.3× 1.3k 2.4× 1.1k 2.2× 126 5.2k
Toshio Mochizuki Japan 27 2.3k 0.8× 2.2k 0.8× 761 0.7× 122 0.2× 83 0.2× 109 4.1k
M. Andrew Nesbit United Kingdom 27 720 0.3× 1.6k 0.6× 830 0.8× 122 0.2× 368 0.8× 87 2.9k
Maja Di Rocco Italy 34 860 0.3× 1.5k 0.5× 163 0.2× 778 1.4× 305 0.6× 147 3.6k
Sami A. Sanjad Lebanon 16 704 0.2× 2.6k 0.9× 662 0.6× 97 0.2× 106 0.2× 46 3.8k
Marjo Kestilä Finland 23 1.2k 0.4× 2.7k 0.9× 2.6k 2.6× 92 0.2× 155 0.3× 48 4.8k

Countries citing papers authored by Murat Bastepe

Since Specialization
Citations

This map shows the geographic impact of Murat Bastepe's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Murat Bastepe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Murat Bastepe more than expected).

Fields of papers citing papers by Murat Bastepe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Murat Bastepe. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Murat Bastepe. The network helps show where Murat Bastepe may publish in the future.

Co-authorship network of co-authors of Murat Bastepe

This figure shows the co-authorship network connecting the top 25 collaborators of Murat Bastepe. A scholar is included among the top collaborators of Murat Bastepe based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Murat Bastepe. Murat Bastepe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Reyes, Monica, Barbara Gales, Agnès Linglart, et al.. (2025). Bidirectional disruption of GNAS transcripts causes broad methylation defects in pseudohypoparathyroidism type 1B. Proceedings of the National Academy of Sciences. 122(16). e2423271122–e2423271122. 2 indexed citations
2.
Reyes, Monica, et al.. (2025). A biallelically active embryonic enhancer dictates GNAS imprinting through allele-specific conformations. Nature Communications. 16(1). 1377–1377. 1 indexed citations
3.
4.
Reyes, Monica, et al.. (2023). The long-range interaction between two GNAS imprinting control regions delineates pseudohypoparathyroidism type 1B pathogenesis. Journal of Clinical Investigation. 133(8). 10 indexed citations
5.
Zhou, Wen, Eva S. Liu, Sherri‐Ann M. Burnett‐Bowie, et al.. (2023). 1,25-Dihydroxyvitamin D3 regulates furin-mediated FGF23 cleavage. JCI Insight. 8(17). 9 indexed citations
6.
Wentworth, Kelly L., et al.. (2016). A Novel T55A Variant of GsαAssociated with Impaired cAMP Production, Bone Fragility, and Osteolysis. Case Reports in Endocrinology. 2016. 1–6. 4 indexed citations
7.
Turan, Serap, Susanne Thiele, Zeynep Atay, et al.. (2014). Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS. Bone. 71. 53–57. 23 indexed citations
8.
9.
Lecumberri, Beatriz, Eduardo Fernández‐Rebollo, Lucia Sentchordi, et al.. (2009). Coexistence of two different pseudohypoparathyroidism subtypes (Ia and Ib) in the same kindred with independent Gsα coding mutations and GNAS imprinting defects. Journal of Medical Genetics. 47(4). 276–280. 32 indexed citations
10.
Bastepe, Murat & Harald Jüppner. (2008). Inherited hypophosphatemic disorders in children and the evolving mechanisms of phosphate regulation. Reviews in Endocrine and Metabolic Disorders. 9(2). 171–180. 48 indexed citations
11.
Bastepe, Murat, Bettina Lorenz‐Depiereux, Michella Ghassibe‐Sabbagh, et al.. (2006). An autosomal recessive hypophosphatemic disorder caused by homozygous mutations in dentin matrix protein 1 (DMP1).. Journal of Bone and Mineral Research. 21.
12.
Bergwitz, Clemens, Nicole M. Roslin, Martin Tieder, et al.. (2006). 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. The American Journal of Human Genetics. 78(2). 179–192. 324 indexed citations
13.
Jüppner, Harald, Agnès Linglart, Leopold F. Fröhlich, & Murat Bastepe. (2006). Autosomal‐Dominant Pseudohypoparathyroidism Type Ib is Caused by Different Microdeletions Within or Upstream of the GNAS Locus. Annals of the New York Academy of Sciences. 1068(1). 250–255. 17 indexed citations
14.
Gensure, Robert, Outi Mäkitie, Steven R. DePalma, et al.. (2005). A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders. Journal of Clinical Investigation. 115(5). 1250–1257. 101 indexed citations
15.
Bastepe, Murat, et al.. (2002). Receptor-Mediated Adenylyl Cyclase Activation Through XLαs, the Extra-Large Variant of the Stimulatory G Protein α-Subunit. Molecular Endocrinology. 16(8). 1912–1919. 103 indexed citations
16.
D’Souza-Li, Lilia Freire Rodrigues, Bing Yang, Lucie Canaff, et al.. (2002). Identification and Functional Characterization of Novel Calcium-Sensing Receptor Mutations in Familial Hypocalciuric Hypercalcemia and Autosomal Dominant Hypocalcemia. The Journal of Clinical Endocrinology & Metabolism. 87(3). 1309–1318. 79 indexed citations
17.
18.
Bastepe, Murat & Harald Jüppner. (2000). Identification and characterization of two new, highly polymorphic loci adjacent to GNAS1 on chromosome 20q13.3. Molecular and Cellular Probes. 14(4). 261–264. 7 indexed citations
19.
Bastepe, Murat & Harald Jüppner. (2000). PSEUDOHYPOPARATHYROIDISM. Endocrinology and Metabolism Clinics of North America. 29(3). 569–589. 34 indexed citations
20.
Bastepe, Murat & Barrie Ashby. (1997). The Long Cytoplasmic Carboxyl Terminus of the Prostaglandin E2 Receptor EP4 Subtype Is Essential for Agonist-Induced Desensitization. Molecular Pharmacology. 51(2). 343–349. 45 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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