Nurit Magal

2.5k total citations
51 papers, 1.7k citations indexed

About

Nurit Magal is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Nurit Magal has authored 51 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 15 papers in Genetics and 14 papers in Surgery. Recurrent topics in Nurit Magal's work include Genetic Neurodegenerative Diseases (7 papers), Inflammasome and immune disorders (6 papers) and Genomics and Rare Diseases (5 papers). Nurit Magal is often cited by papers focused on Genetic Neurodegenerative Diseases (7 papers), Inflammasome and immune disorders (6 papers) and Genomics and Rare Diseases (5 papers). Nurit Magal collaborates with scholars based in Israel, United States and Türkiye. Nurit Magal's co-authors include Mordechai Shohat, Lina Basel‐Vanagaite, Gabrielle J. Halpern, Mordechai Shohat, Valerie Drasinover, Ellen Taub, Yehuda L. Danon, Metsada Pasmanik‐Chor, Nathan Fischel‐Ghodsian and Bella Davidov and has published in prestigious journals such as Circulation, Journal of Clinical Investigation and Neurology.

In The Last Decade

Nurit Magal

51 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nurit Magal Israel 21 962 439 294 223 179 51 1.7k
Hammadi Ayadi Tunisia 29 1.3k 1.3× 673 1.5× 298 1.0× 164 0.7× 129 0.7× 137 2.6k
Bruno Leheup France 29 1.1k 1.2× 758 1.7× 238 0.8× 239 1.1× 78 0.4× 97 2.2k
David Geneviève France 24 1.3k 1.4× 1.1k 2.5× 175 0.6× 285 1.3× 233 1.3× 80 2.3k
Mordechai Shohat Israel 26 1.7k 1.7× 540 1.2× 129 0.4× 139 0.6× 154 0.9× 83 2.9k
Maha S. Zaki Egypt 27 1.2k 1.2× 679 1.5× 175 0.6× 158 0.7× 326 1.8× 147 2.4k
Maria Hoeltzenbein Germany 23 899 0.9× 794 1.8× 722 2.5× 272 1.2× 92 0.5× 54 2.8k
Ituro Inoue Japan 35 1.5k 1.6× 637 1.5× 475 1.6× 486 2.2× 151 0.8× 101 3.6k
Kazuhiro Nishii Japan 29 965 1.0× 414 0.9× 537 1.8× 120 0.5× 56 0.3× 105 2.6k
Bruce E. Hayward United Kingdom 27 1.7k 1.8× 1.3k 3.0× 151 0.5× 277 1.2× 142 0.8× 54 2.9k
Dvorah Abeliovich Israel 31 1.5k 1.5× 1.4k 3.1× 163 0.6× 340 1.5× 98 0.5× 98 3.0k

Countries citing papers authored by Nurit Magal

Since Specialization
Citations

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

Fields of papers citing papers by Nurit Magal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nurit Magal

This figure shows the co-authorship network connecting the top 25 collaborators of Nurit Magal. A scholar is included among the top collaborators of Nurit Magal 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 Nurit Magal. Nurit Magal 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.
Ruhrman‐Shahar, Noa, Nurit Assia Batzir, Gabriel Lidzbarsky, et al.. (2021). A nonsense variant in the second exon of the canonical transcript of NSD1 does not cause Sotos syndrome. American Journal of Medical Genetics Part A. 188(1). 369–372. 1 indexed citations
2.
Sukenik‐Halevy, Rivka, Noa Ruhrman‐Shahar, Naama Orenstein, et al.. (2021). The diagnostic efficacy of exome data analysis using fixed neurodevelopmental gene lists: Implications for prenatal setting. Prenatal Diagnosis. 41(6). 701–707. 4 indexed citations
3.
Reinstein, Eyal, Valerie Drasinover, Rachel Lotan, et al.. (2017). Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type. Clinical Genetics. 93(1). 160–163. 8 indexed citations
4.
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
5.
Behar, Doron M., Lina Basel‐Vanagaite, Fabian Glaser, et al.. (2013). Identification of a novel mutation in the PNLIP gene in two brothers with congenital pancreatic lipase deficiency. Journal of Lipid Research. 55(2). 307–312. 24 indexed citations
6.
Sukenik‐Halevy, Rivka, et al.. (2010). Large-Scale Population Carrier Screening for Spinal Muscular Atrophy in Israel—Effect of Ethnicity on the False-Negative Rate. Genetic Testing and Molecular Biomarkers. 14(3). 319–324. 6 indexed citations
7.
Basel‐Vanagaite, Lina, Ellen Taub, Valerie Drasinover, et al.. (2008). Genetic Carrier Screening for Spinal Muscular Atrophy and Spinal Muscular Atrophy with Respiratory Distress 1 in an Isolated Population in Israel. Genetic Testing. 12(1). 53–56. 22 indexed citations
8.
Lavi, Shahar, Nurit Magal, Gabrielle J. Halpern, et al.. (2008). Identification of the gene causing long QT syndrome in an Israeli family.. PubMed. 10(11). 809–11. 2 indexed citations
9.
Avrahami, Limor, Saskia M. Maas, Metsada Pasmanik‐Chor, et al.. (2008). Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype. Clinical Genetics. 74(1). 47–53. 40 indexed citations
10.
Basel‐Vanagaite, Lina, Ellen Taub, Gabrielle J. Halpern, et al.. (2006). Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in Israel. European Journal of Human Genetics. 15(2). 250–253. 31 indexed citations
11.
Mager, Aviv, Alexander Battler, Yochai Birnbaum, Nurit Magal, & Mordechai Shohat. (2002). Plasma homocysteine, methylenetetrahydrofolate reductase genotypes, and age at onset of symptoms of myocardial ischemia. The American Journal of Cardiology. 89(8). 919–923. 18 indexed citations
12.
Toledano‐Alhadef, Hagit, Lina Basel‐Vanagaite, Nurit Magal, et al.. (2001). Fragile-X Carrier Screening and the Prevalence of Premutation and Full-Mutation Carriers in Israel. The American Journal of Human Genetics. 69(2). 351–360. 159 indexed citations
13.
Magal, Nurit, et al.. (2001). Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qter. American Journal of Medical Genetics. 104(2). 152–156. 11 indexed citations
14.
Drasinover, Valerie, Nurit Magal, Ellen Taub, et al.. (2000). Increased transmission of intermediate alleles of theFMR1 gene compared with normal alleles among female heterozygotes. American Journal of Medical Genetics. 93(2). 155–157. 14 indexed citations
15.
Stoffman, Nava, Nurit Magal, Tamy Shohat, et al.. (2000). Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups. European Journal of Human Genetics. 8(4). 307–310. 112 indexed citations
16.
Shohat, Mordechai, Nurit Magal, Tami Shohat, et al.. (1999). Phenotype–genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis. European Journal of Human Genetics. 7(3). 287–292. 167 indexed citations
17.
Shohat, M, Rachel Lotan, Nurit Magal, et al.. (1998). Amyloidosis in Familial Mediterranean Fever Is Associated with a Specific Ancestral Haplotype in the MEFV Locus. Molecular Genetics and Metabolism. 65(3). 197–202. 6 indexed citations
18.
Shohat, Mordechai, Rona Lotan, Nurit Magal, et al.. (1997). A Gene for Arthrogryposis Multiplex Congenita Neuropathic Type Is Linked to D5S394 on Chromosome 5qter. The American Journal of Human Genetics. 61(5). 1139–1143. 18 indexed citations
19.
20.
Appelman, Z., Moshe Manor, Nurit Magal, et al.. (1994). Prenatal diagnosis of twin zygosity by DNA ‘fingerprint’ analysis. Prenatal Diagnosis. 14(4). 307–309. 7 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Hammadi Ayadi Breakdown of academic impact, for papers by Bruno Leheup Breakdown of academic impact, for papers by David Geneviève Breakdown of academic impact, for papers by Mordechai Shohat Breakdown of academic impact, for papers by Maha S. Zaki Breakdown of academic impact, for papers by Maria Hoeltzenbein Breakdown of academic impact, for papers by Ituro Inoue Breakdown of academic impact, for papers by Kazuhiro Nishii Breakdown of academic impact, for papers by Bruce E. Hayward Breakdown of academic impact, for papers by Dvorah Abeliovich
Rankless by CCL
2026