Bella Davidov
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Sensory Systems top 10%
- Hearing, Cochlea, Tinnitus, Genetics
Papers in
-
- Prenatal Screening and Diagnostics 5
- Genetics 6
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- Connective tissue disorders research 1
- Co-authors
- Mordechai Shohat (8 shared papers)Ellen Taub (3 shared papers)Lina Basel‐Vanagaite (4 shared papers)Nurit Magal (5 shared papers)Valerie Drasinover (3 shared papers)Gabrielle J. Halpern (2 shared papers)Hagit Toledano‐Alhadef (1 shared paper)Mordechai Shohat (2 shared papers)
- Journals
- Prenatal Diagnosis (4 papers)European Journal of Human Genetics (2 papers)Clinical Genetics (2 papers)The American Journal of Human Genetics (1 paper)Human Genomics (1 paper)
- Partner nations
- IsraelUnited StatesMexico
In The Last Decade
Bella Davidov
15 papers receiving 395 citations
Peers
Comparison fields: 5 of 60
- Genetics 270
- Sensory Systems 35
- Pediatrics, Perinatology and Child Health 141
- Cognitive Neuroscience 111
- Otorhinolaryngology 13
Countries citing papers authored by Bella Davidov
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
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-authors
The 25 scholars most cited alongside Bella Davidov, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 159 | |
| 2 | 2010 | 61 | |
| 3 | 2013 | 35 | |
| 4 | 2006 | 31 | |
| 5 | 2003 | 24 | |
| 6 | 2005 | 20 | |
| 7 | 2015 | 18 | |
| 8 | 2006 | 18 | |
| 9 | Prenatal testing for Down syndrome in the Jewish and non-Jewish populations in Israel. | 1994 | 15 |
| 10 | 1995 | 12 | |
| 11 | 2015 | 11 | |
| 12 | 2013 | 7 | |
| 13 | 2022 | 5 | |
| 14 | 2014 | 5 | |
| 15 | 2024 | 1 | |
| 16 | Escroto agudo como presentación de apendicitis aguda. Presentación de un caso y revisión de la literatura | 2008 | 0 |
| 17 | 2025 | 0 |
About Bella Davidov
Bella Davidov is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Surgery, Molecular Biology and Pulmonary and Respiratory Medicine, having authored 17 papers that have together received 422 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (3 papers), Autism Spectrum Disorder Research (2 papers), Congenital Anomalies and Fetal Surgery (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers), Intestinal Malrotation and Obstruction Disorders (1 paper) and Connective tissue disorders research (1 paper). The work is most often cited by research in Genetics (270 citations), Sensory Systems (35 citations), Pediatrics, Perinatology and Child Health (141 citations), Cognitive Neuroscience (111 citations) and Otorhinolaryngology (13 citations). Bella Davidov has collaborated with scholars based in Israel, United States and Mexico. Frequent co-authors include Mordechai Shohat, Ellen Taub, Lina Basel‐Vanagaite, Nurit Magal, Valerie Drasinover, Gabrielle J. Halpern, Hagit Toledano‐Alhadef, Mordechai Shohat, Liron Gershovitz and Idit Maya. Their work appears in journals such as Prenatal Diagnosis, European Journal of Human Genetics, Clinical Genetics, The American Journal of Human Genetics and Human Genomics.
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.