Naama Orenstein

1.2k total citations
31 papers, 311 citations indexed

About

Naama Orenstein is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Naama Orenstein has authored 31 papers receiving a total of 311 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Surgery. Recurrent topics in Naama Orenstein's work include Genomics and Rare Diseases (8 papers), Genetic factors in colorectal cancer (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Naama Orenstein is often cited by papers focused on Genomics and Rare Diseases (8 papers), Genetic factors in colorectal cancer (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Naama Orenstein collaborates with scholars based in Israel, United States and Slovakia. Naama Orenstein's co-authors include Lina Basel‐Vanagaite, Nurit Magal, Lily Bazak, Monika Weisz Hubshman, Noa Ruhrman‐Shahar, Raanan Shamir, Gabriel Lidzbarsky, Yael Mozer‐Glassberg, Orith Waisbourd‐Zinman and Osnat Konen and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of Neurology and Gene.

In The Last Decade

Naama Orenstein

29 papers receiving 308 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Naama Orenstein Israel 10 123 103 50 33 31 31 311
Erwin Lankes Germany 11 74 0.6× 158 1.5× 30 0.6× 36 1.1× 32 1.0× 20 342
Ken Saida Japan 10 92 0.7× 114 1.1× 18 0.4× 13 0.4× 18 0.6× 37 275
Güven Toksoy Türkiye 12 116 0.9× 185 1.8× 25 0.5× 9 0.3× 57 1.8× 51 353
Khalid Ibrahim Qatar 13 44 0.4× 156 1.5× 18 0.4× 20 0.6× 40 1.3× 27 395
Kalpana Gowrishankar India 10 94 0.8× 172 1.7× 15 0.3× 21 0.6× 10 0.3× 23 305
Geneviève Beaurain France 8 64 0.5× 93 0.9× 44 0.9× 26 0.8× 15 0.5× 9 349
Onur Baykara Türkiye 13 53 0.4× 149 1.4× 57 1.1× 10 0.3× 28 0.9× 28 348
Kathleen Brown United States 8 40 0.3× 76 0.7× 10 0.2× 20 0.6× 94 3.0× 11 462
Yoonhyuk Jang South Korea 10 26 0.2× 63 0.6× 103 2.1× 24 0.7× 23 0.7× 30 288
Birsen Karaman Türkiye 12 157 1.3× 180 1.7× 15 0.3× 7 0.2× 57 1.8× 58 345

Countries citing papers authored by Naama Orenstein

Since Specialization
Citations

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

Fields of papers citing papers by Naama Orenstein

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Naama Orenstein

This figure shows the co-authorship network connecting the top 25 collaborators of Naama Orenstein. A scholar is included among the top collaborators of Naama Orenstein 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 Naama Orenstein. Naama Orenstein 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.
Batzir, Nurit Assia, Julián Nevado, Jair Tenorio, et al.. (2025). N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder. European Journal of Human Genetics. 34(3). 314–323.
2.
3.
Orenstein, Naama, Lily Bazak, Gabriel Lidzbarsky, et al.. (2024). High frequency of MEFV disease-causing variants in children with very-early-onset inflammatory bowel disease. Pediatric Research. 97(1). 268–272. 2 indexed citations
4.
Landau, Yuval E., et al.. (2023). A novel SLC25A13 gene splice site variant causes Citrin deficiency in an infant. Gene. 874. 147483–147483. 3 indexed citations
5.
Cohen, Hadar, Naama Orenstein, Gabriel Lidzbarsky, et al.. (2023). Discovery of a Novel Missense Variant in NLRP3 Causing Atypical Cryopyrin‐Associated Periodic Syndromes With Hearing Loss as the Primary Presentation, Responsive to Anti–Interleukin‐1 Therapy. Arthritis & Rheumatology. 76(3). 444–454. 7 indexed citations
6.
Basel‐Salmon, Lina, Noa Ruhrman‐Shahar, Naama Orenstein, et al.. (2023). Clinically actionable incidental and secondary parental genomic findings after proband exome sequencing: Yield and dilemmas. SHILAP Revista de lepidopterología. 1(1). 100813–100813. 1 indexed citations
7.
Orenstein, Naama, Lina Basel‐Salmon, Irina Lagovsky, et al.. (2023). Severe early-onset Wilson disease caused by a common pathogenic variant in the Bukharan Jewish population in Israel. Gene. 887. 147728–147728. 1 indexed citations
8.
Lehtokari, Vilma‐Lotta, Mark R. Davis, K. Kiiski, et al.. (2023). A recurrent ACTA1 amino acid change in mosaic form causes milder asymmetric myopathy. Neuromuscular Disorders. 34. 32–40. 6 indexed citations
9.
Zerem, Ayelet, Liat Ben‐Sira, Z. Leibovitz, et al.. (2021). White matter abnormalities and iron deposition in prenatal mucolipidosis IV- fetal imaging and pathology. Metabolic Brain Disease. 36(7). 2155–2167. 8 indexed citations
10.
Schob, Claudia, Maja Hempel, Dana Šafka Brožková, et al.. (2021). Dominant KPNA3 Mutations Cause Infantile‐Onset Hereditary Spastic Paraplegia. Annals of Neurology. 90(5). 738–750. 6 indexed citations
11.
Fellner, Avi, Noa Ruhrman‐Shahar, Naama Orenstein, et al.. (2021). The role of phenotype-based search approaches using public online databases in diagnostics of Mendelian disorders. Genetics in Medicine. 23(6). 1095–1100. 4 indexed citations
12.
Ehrenberg, Miriam, et al.. (2021). Genetic causes of nystagmus, foveal hypoplasia and subnormal visual acuity- other than albinism. Ophthalmic Genetics. 42(3). 243–251. 5 indexed citations
13.
Basel‐Vanagaite, Lina, Noa Ruhrman‐Shahar, Naama Orenstein, et al.. (2020). When phenotype does not match genotype: importance of “real-time” refining of phenotypic information for exome data interpretation. Genetics in Medicine. 23(1). 215–221. 14 indexed citations
14.
Aharoni, Sharon, Yoram Nevo, Naama Orenstein, et al.. (2020). Impact of a national population-based carrier-screening program on spinal muscular atrophy births. Neuromuscular Disorders. 30(12). 970–974. 17 indexed citations
15.
Basel‐Vanagaite, Lina, Naama Orenstein, Noa Ruhrman‐Shahar, et al.. (2018). Improved diagnostics by exome sequencing following raw data reevaluation by clinical geneticists involved in the medical care of the individuals tested. Genetics in Medicine. 21(6). 1443–1451. 55 indexed citations
16.
Mei‐Zahav, Meir, Patrick Stafler, Hanoch Senderowitz, et al.. (2018). The Q359K/T360K mutation causes cystic fibrosis in Georgian Jews. Journal of Cystic Fibrosis. 17(5). e41–e45. 4 indexed citations
17.
Orenstein, Naama, Hadassa Goldberg‐Stern, Rachel Straussberg, et al.. (2017). A de novo GABRA2 missense mutation in severe early-onset epileptic encephalopathy with a choreiform movement disorder. European Journal of Paediatric Neurology. 22(3). 516–524. 23 indexed citations
18.
Orenstein, Naama, et al.. (2017). Is the Bishop-score significant in predicting the success of labor induction in multiparous women?. Journal of Perinatology. 37(5). 480–483. 10 indexed citations
19.
Aharoni, Sharon, Menachem Sadeh, Yehuda Shapira, et al.. (2016). Congenital myasthenic syndrome in Israel: Genetic and clinical characterization. Neuromuscular Disorders. 27(2). 136–140. 26 indexed citations
20.
Orenstein, Naama, Karin Weiss, Stephanie N. Oprescu, et al.. (2016). Bi‐allelic IARS mutations in a child with intra‐uterine growth retardation, neonatal cholestasis, and mild developmental delay. Clinical Genetics. 91(6). 913–917. 19 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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