Bella Davidov

1.1k total citations
17 papers, 422 citations indexed

About

Bella Davidov is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery. According to data from OpenAlex, Bella Davidov has authored 17 papers receiving a total of 422 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Pediatrics, Perinatology and Child Health, 6 papers in Genetics and 4 papers in Surgery. Recurrent topics in Bella Davidov's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Bella Davidov is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Bella Davidov collaborates with scholars based in Israel, United States and France. Bella Davidov's co-authors include Mordechai Shohat, Ellen Taub, Lina Basel‐Vanagaite, Nurit Magal, Valerie Drasinover, Gabrielle J. Halpern, Hagit Toledano‐Alhadef, Mordechai Shohat, Lisa G. Shaffer and Liron Gershovitz and has published in prestigious journals such as The American Journal of Human Genetics, European Journal of Human Genetics and International Journal of Biometeorology.

In The Last Decade

Bella Davidov

15 papers receiving 395 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bella Davidov Israel 11 270 141 112 111 35 17 422
Matthew F. Hunter Australia 13 273 1.0× 49 0.3× 225 2.0× 105 0.9× 21 0.6× 35 478
Karen Fieggen South Africa 13 125 0.5× 70 0.5× 146 1.3× 26 0.2× 26 0.7× 42 390
Antonia Paula Marques‐de‐Faria Brazil 15 391 1.4× 75 0.5× 383 3.4× 65 0.6× 41 1.2× 51 617
Jean‐Pierre Frijns Belgium 17 328 1.2× 138 1.0× 300 2.7× 114 1.0× 45 1.3× 23 670
Aude Charollais France 9 137 0.5× 144 1.0× 170 1.5× 31 0.3× 18 0.5× 19 428
Teresa Sadeghin United States 13 369 1.4× 107 0.8× 245 2.2× 73 0.7× 48 1.4× 33 462
Srinivasan Muthuswamy India 9 95 0.4× 80 0.6× 140 1.3× 31 0.3× 42 1.2× 29 391
Kaushal Sharma India 14 88 0.3× 66 0.5× 150 1.3× 6 0.1× 32 0.9× 50 613
Christalena Sofocleous Greece 14 261 1.0× 81 0.6× 218 1.9× 67 0.6× 26 0.7× 45 459
Nance We United States 12 185 0.7× 115 0.8× 205 1.8× 13 0.1× 42 1.2× 38 498

Countries citing papers authored by Bella Davidov

Since Specialization
Citations

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

Fields of papers citing papers by Bella Davidov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bella Davidov

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

All Works

17 of 17 papers shown
1.
Brownstein, Zippora, Yoel Hirsch, Hagar Mor‐Shaked, et al.. (2025). A multicenter study reveals a novel pathogenic splice-site founder variant in OTOF. Human Genomics. 19(1). 112–112.
2.
Bardin, Ron, et al.. (2024). Agenesis of the Ductus Venosus and Its Association With Genetic Abnormalities. Prenatal Diagnosis. 44(13). 1585–1592. 1 indexed citations
3.
Davidov, Bella, et al.. (2022). Pathogenic variant‐based preconception carrier screening in the Israeli Jewish population. Clinical Genetics. 101(5-6). 517–529. 5 indexed citations
4.
Bardin, Ron, Eran Ashwal‏, Bella Davidov, et al.. (2015). Nonvisualization of the Fetal Gallbladder: Can Levels of γ-Glutamyl Transpeptidase in Amniotic Fluid Predict Fetal Prognosisγ. Fetal Diagnosis and Therapy. 39(1). 50–55. 18 indexed citations
5.
Reinstein, Eyal, Pola Smirin‐Yosef, Irina Lagovsky, et al.. (2015). A founder mutation in ADAMTSL4 causes early-onset bilateral ectopia lentis among Jews of Bukharian origin. Molecular Genetics and Metabolism. 117(1). 38–41. 11 indexed citations
6.
Behar, Doron M., Nurit Magal, Elon Pras, et al.. (2014). Founder mutation for Huntington disease in Caucasus Jews. Clinical Genetics. 87(2). 167–172. 5 indexed citations
7.
Behar, Doron M., Bella Davidov, Zippora Brownstein, et al.. (2013). The Many Faces of Sensorineural Hearing Loss: One Founder and Two Novel Mutations Affecting One Family of Mixed Jewish Ancestry. Genetic Testing and Molecular Biomarkers. 18(2). 123–126. 7 indexed citations
8.
Brownstein, Zippora, Amal Abu Rayyan, Serena Sirigu, et al.. (2013). Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing. European Journal of Human Genetics. 22(6). 768–775. 35 indexed citations
9.
Maya, Idit, Bella Davidov, Liron Gershovitz, et al.. (2010). Diagnostic utility of array‐based comparative genomic hybridization (aCGH) in a prenatal setting. Prenatal Diagnosis. 30(12-13). 1131–1137. 61 indexed citations
10.
Davidov, Bella, et al.. (2008). Escroto agudo como presentación de apendicitis aguda. Presentación de un caso y revisión de la literatura. Revista Mexicana de Urología. 68(1). 64–66.
11.
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
12.
Basel‐Vanagaite, Lina, et al.. (2006). Amniotic trisomy 11 mosaicism—is it a benign finding?. Prenatal Diagnosis. 26(9). 778–781. 18 indexed citations
13.
Stoupel, E, Z. Appelman, Ziva Ben‐Neriah, et al.. (2005). Chromosome aberration and environmental physical activity: Down syndrome and solar and cosmic ray activity, Israel, 1990–2000. International Journal of Biometeorology. 50(1). 1–5. 20 indexed citations
14.
Shohat, Mordechai, Z. Appelman, Ziva Ben‐Neriah, et al.. (2003). Prenatal diagnosis of Down syndrome: Ten year experience in the Israeli population. American Journal of Medical Genetics Part A. 122A(3). 215–222. 24 indexed citations
15.
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
16.
Shohat, Mordechai, Bella Davidov, Gad Barkai, et al.. (1995). Amniocentesis rate and the detection of down syndrome and other chromosomal anomalies in Israel. Prenatal Diagnosis. 15(10). 967–970. 12 indexed citations
17.
Davidov, Bella, Boleslaw Goldman, Galia Barkai, et al.. (1994). Prenatal testing for Down syndrome in the Jewish and non-Jewish populations in Israel.. PubMed. 30(8). 629–33. 15 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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