Orit Topaz

1.3k total citations
8 papers, 901 citations indexed

About

Orit Topaz is a scholar working on Nephrology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Orit Topaz has authored 8 papers receiving a total of 901 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Nephrology, 4 papers in Pulmonary and Respiratory Medicine and 4 papers in Genetics. Recurrent topics in Orit Topaz's work include Parathyroid Disorders and Treatments (7 papers), Medical Imaging and Pathology Studies (4 papers) and Genetic Syndromes and Imprinting (3 papers). Orit Topaz is often cited by papers focused on Parathyroid Disorders and Treatments (7 papers), Medical Imaging and Pathology Studies (4 papers) and Genetic Syndromes and Imprinting (3 papers). Orit Topaz collaborates with scholars based in Israel, United States and Germany. Orit Topaz's co-authors include Eli Sprecher, Richard N. Bergman, Gabriele Richard, Margarita Indelman, Doron M. Behar, Ilana Chefetz, S. Raimer, Daniel L. Shurman, Paulina Ratajczak and Ziad Khamaysi and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Journal of Investigative Dermatology.

In The Last Decade

Orit Topaz

8 papers receiving 882 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Orit Topaz Israel	7	481	361	353	213	206	8	901
Bettina Lorenz Germany	8	220 0.5×	294 0.8×	413 1.2×	51 0.2×	49 0.2×	12	703
Dominic J. Ciavatta United States	14	52 0.1×	139 0.4×	526 1.5×	76 0.4×	249 1.2×	23	963
Ruth Belostotsky Israel	14	73 0.2×	63 0.2×	517 1.5×	33 0.2×	395 1.9×	23	811
Dirk Kieback Germany	13	27 0.1×	367 1.0×	393 1.1×	24 0.1×	74 0.4×	24	877
David G. Winkler United States	13	27 0.1×	82 0.2×	612 1.7×	73 0.3×	24 0.1×	14	855
Selene Colon United States	13	165 0.3×	25 0.1×	165 0.5×	37 0.2×	96 0.5×	19	516
Anh T. Nguyen United States	10	25 0.1×	116 0.3×	1.1k 3.1×	23 0.1×	51 0.2×	11	1.3k
Nadia Alhashmi Oman	9	15 0.0×	214 0.6×	247 0.7×	233 1.1×	33 0.2×	15	678
Marieke Levitus Netherlands	10	55 0.1×	307 0.9×	973 2.8×	11 0.1×	53 0.3×	12	1.1k
Natasa Zamurovic Switzerland	9	32 0.1×	60 0.2×	365 1.0×	66 0.3×	19 0.1×	16	546

Countries citing papers authored by Orit Topaz

Since Specialization

Citations

This map shows the geographic impact of Orit Topaz'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 Orit Topaz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Orit Topaz more than expected).

Fields of papers citing papers by Orit Topaz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Orit Topaz. 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 Orit Topaz. The network helps show where Orit Topaz may publish in the future.

Co-authorship network of co-authors of Orit Topaz

This figure shows the co-authorship network connecting the top 25 collaborators of Orit Topaz. A scholar is included among the top collaborators of Orit Topaz 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 Orit Topaz. Orit Topaz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

Chefetz, Ilana, Karl Skorecki, Noam Adir, et al.. (2007). Normophosphatemic Familial Tumoral Calcinosis Is Caused by Deleterious Mutations in SAMD9, Encoding a TNF-α Responsive Protein. Journal of Investigative Dermatology. 128(6). 1423–1429. 57 indexed citations

Topaz, Orit, Margarita Indelman, Ilana Chefetz, et al.. (2006). A Deleterious Mutation in SAMD9 Causes Normophosphatemic Familial Tumoral Calcinosis. The American Journal of Human Genetics. 79(4). 759–764. 96 indexed citations

Topaz, Orit, Richard N. Bergman, Ulla Mandel, et al.. (2005). Absence of Intraepidermal Glycosyltransferase ppGalNac-T3 Expression in Familial Tumoral Calcinosis. American Journal of Dermatopathology. 27(3). 211–215. 19 indexed citations

Sprecher, Eli, Akemi Ishida‐Yamamoto, Debora Rapaport, et al.. (2005). A Mutation in SNAP29, Coding for a SNARE Protein Involved in Intracellular Trafficking, Causes a Novel Neurocutaneous Syndrome Characterized by Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma. The American Journal of Human Genetics. 77(2). 242–251. 131 indexed citations

Chefetz, Ilana, Raoul Heller, Assimina Galli‐Τsinopoulou, et al.. (2005). A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcification. Human Genetics. 118(2). 261–266. 89 indexed citations

Frishberg, Yaacov, Orit Topaz, Richard N. Bergman, et al.. (2005). Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders. Journal of Molecular Medicine. 83(3). 240–240. 1 indexed citations

Topaz, Orit, Daniel L. Shurman, Richard N. Bergman, et al.. (2004). Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis. Nature Genetics. 36(6). 579–581. 424 indexed citations

Frishberg, Yaacov, Orit Topaz, Richard N. Bergman, et al.. (2004). Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders. Journal of Molecular Medicine. 83(1). 33–38. 84 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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