Ruti Parvari

4.1k total citations
88 papers, 2.7k citations indexed

About

Ruti Parvari is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Ruti Parvari has authored 88 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 23 papers in Genetics and 16 papers in Rheumatology. Recurrent topics in Ruti Parvari's work include Cardiomyopathy and Myosin Studies (11 papers), Glycogen Storage Diseases and Myoclonus (11 papers) and Congenital heart defects research (9 papers). Ruti Parvari is often cited by papers focused on Cardiomyopathy and Myosin Studies (11 papers), Glycogen Storage Diseases and Myoclonus (11 papers) and Congenital heart defects research (9 papers). Ruti Parvari collaborates with scholars based in Israel, United States and Hungary. Ruti Parvari's co-authors include Shimon Moses, Eli Hershkovitz, Val C. Sheffield, Moshe Phillip, Yael Segev, Jonathan Eli Arbelle, Esther Manor, Vered Chalifa‐Caspi, Rivka Carmi and Aviva Levitas and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Ruti Parvari

87 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ruti Parvari Israel 28 1.2k 831 458 332 306 88 2.7k
Patricia M. Zerfas United States 29 1.6k 1.3× 332 0.4× 296 0.6× 204 0.6× 85 0.3× 62 3.5k
Pnina Fishman Israel 44 1.7k 1.4× 221 0.3× 615 1.3× 293 0.9× 69 0.2× 161 4.9k
Carlos D. Figueroa Chile 29 1.4k 1.1× 310 0.4× 150 0.3× 364 1.1× 67 0.2× 93 4.1k
Nancy E. Cooke United States 42 2.3k 1.9× 1.3k 1.5× 114 0.2× 177 0.5× 160 0.5× 97 5.2k
Ohad S. Birk Israel 33 2.1k 1.7× 1.2k 1.5× 113 0.2× 244 0.7× 195 0.6× 121 3.7k
Miguel Chillón Spain 29 1.6k 1.3× 1.5k 1.8× 108 0.2× 211 0.6× 104 0.3× 80 3.8k
Lincoln R. Potter United States 33 2.2k 1.8× 347 0.4× 155 0.3× 315 0.9× 197 0.6× 75 4.7k
Yvonne Hort Australia 19 1.0k 0.8× 976 1.2× 107 0.2× 493 1.5× 183 0.6× 32 2.4k
Siu Yuen Chan Hong Kong 32 1.4k 1.1× 712 0.9× 166 0.4× 376 1.1× 378 1.2× 99 3.5k
Majed Dasouki United States 29 1.4k 1.2× 691 0.8× 196 0.4× 97 0.3× 33 0.1× 90 2.7k

Countries citing papers authored by Ruti Parvari

Since Specialization
Citations

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

Fields of papers citing papers by Ruti Parvari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruti Parvari

This figure shows the co-authorship network connecting the top 25 collaborators of Ruti Parvari. A scholar is included among the top collaborators of Ruti Parvari 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 Ruti Parvari. Ruti Parvari 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.
Etzion, Sharon, et al.. (2024). Plekhm2 acts as an autophagy modulator in murine heart and cardiofibroblasts. Scientific Reports. 14(1). 14949–14949.
2.
Kleiman, Sandra E., Atif Zeadna, Eliahu Levitas, et al.. (2021). Pathogenic variations in Germ Cell Nuclear Acidic Peptidase (GCNA) are associated with human male infertility. European Journal of Human Genetics. 29(12). 1781–1788. 11 indexed citations
3.
4.
Levitas, Aviva, Emad Muhammad, Yuan Zhang, et al.. (2020). A Novel Recessive Mutation in SPEG Causes Early Onset Dilated Cardiomyopathy. PLoS Genetics. 16(9). e1009000–e1009000. 21 indexed citations
5.
Loewenthal, Neta, Alon Haim, Ruti Parvari, & Eli Hershkovitz. (2015). Phosphoglucomutase‐1 deficiency: Intrafamilial clinical variability and common secondary adrenal insufficiency. American Journal of Medical Genetics Part A. 167(12). 3139–3143. 21 indexed citations
6.
Muhammad, Emad, Aviva Levitas, Alex Braiman, et al.. (2015). PLEKHM2mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction. Human Molecular Genetics. 24(25). 7227–7240. 58 indexed citations
7.
Feinstein, Yael, Baruch Yerushalmi, Neta Loewenthal, et al.. (2014). Natural History and Clinical Manifestations of Hyponatremia and Hyperchlorhidrosis due to Carbonic Anhydrase XII Deficiency. Hormone Research in Paediatrics. 81(5). 336–342. 11 indexed citations
8.
Shorer, Zamir, et al.. (2013). A Novel Mutation in SCN9A in a Child With Congenital Insensitivity to Pain. Pediatric Neurology. 50(1). 73–76. 17 indexed citations
9.
Mazor, M., Soliman Alkrinawi, Vered Chalifa‐Caspi, et al.. (2011). Primary Ciliary Dyskinesia Caused by Homozygous Mutation in DNAL1, Encoding Dynein Light Chain 1. The American Journal of Human Genetics. 88(5). 599–607. 88 indexed citations
10.
Levitas, Aviva, Emad Muhammad, Ann Saada, et al.. (2010). Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase. European Journal of Human Genetics. 18(10). 1160–1165. 89 indexed citations
11.
Hershkovitz, Eli, Dani Bercovich, Vered Chalifa‐Caspi, et al.. (2010). Autosomal-Recessive Hypophosphatemic Rickets Is Associated with an Inactivation Mutation in the ENPP1 Gene. The American Journal of Human Genetics. 86(2). 273–278. 205 indexed citations
12.
Melamed, Isaac, Jaime Levy, Ruti Parvari, & Erwin W. Gelfand. (2004). A Novel Lymphocyte Signaling Defect: trk A Mutation in the Syndrome of Congenital Insensitivity to Pain and Anhidrosis (CIPA). Journal of Clinical Immunology. 24(4). 441–448. 29 indexed citations
13.
Díaz, George A., Bruce D. Gelb, Marios Kambouris, et al.. (2002). Mutation of a tubulin folding gene, TCFE, causes the autosomal recessive Kenny-Caffey syndrome. Journal of Investigative Medicine. 50(2). 161. 1 indexed citations
14.
Bar‐On, Elhanan, et al.. (2002). Congenital insensitivity to pain: Orthopaedic manifestations. Journal of Bone and Joint Surgery - British Volume. 84(2). 252–257. 70 indexed citations
15.
Miura, Yoshitaka, Eli Hershkovitz, Akemi Inagaki, et al.. (2000). A Novel Mutation Causing Complete Thyroxine-Binding Globulin Deficiency (TBG-CD-Negev) among the Bedouins in Southern Israel. The Journal of Clinical Endocrinology & Metabolism. 85(10). 3687–3689. 15 indexed citations
16.
Hershkovitz, Eli, et al.. (2000). Prenatal diagnosis of hypoparathyroidism retardation and dysmorphism (HRD) syndrome. Prenatal Diagnosis. 20(6). 475–477. 2 indexed citations
17.
Parvari, Ruti, Ke-Jian Lei, László Szönyi, et al.. (1998). Two new mutations in the glucose-6-phosphatase gene cause glycogen storage disease in Hungarian patients.. PubMed. 5(4). 191–5. 13 indexed citations
18.
Parvari, Ruti, Eli Hershkovitz, Adam B. Kanis, et al.. (1998). Homozygosity and Linkage-Disequilibrium Mapping of the Syndrome of Congenital Hypoparathyroidism, Growth and Mental Retardation, and Dysmorphism to a 1-cM Interval on Chromosome 1q42-43. The American Journal of Human Genetics. 63(1). 163–169. 45 indexed citations
19.
Annabi, Borhane, Brian C. Mansfield, Hisayuki Hiraiwa, et al.. (1998). The Gene for Glycogen-Storage Disease Type 1b Maps to Chromosome 11q23. The American Journal of Human Genetics. 62(2). 400–405. 91 indexed citations
20.
Parvari, Ruti, Eli Hershkovitz, Rivka Carmi, & Shimon Moses. (1996). PRENATAL DIAGNOSIS OF GLYCOGEN STORAGE DISEASE TYPE 1a BY SINGLE STRANDED CONFORMATION POLYMORPHISM (SSCP). Prenatal Diagnosis. 16(9). 862–865. 14 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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