Idit Maya
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Papers in
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- Prenatal Screening and Diagnostics 32
- Fetal and Pediatric Neurological Disorders 8
- Genetics 17
- Genomic variations and chromosomal abnormalities 13
- Genomics and Rare Diseases 7
- BRCA gene mutations in cancer 2
- Connective tissue disorders research 2
- Congenital Ear and Nasal Anomalies 2
- Co-authors
- Lena Sagi‐Dain (37 shared papers)Lina Basel‐Vanagaite (15 shared papers)Sarit Kahana (22 shared papers)Mordechai Shohat (11 shared papers)Amihood Singer (20 shared papers)Tamar Tenne (10 shared papers)Josepha Yeshaya (6 shared papers)Shiri Yacobson (9 shared papers)
- Journals
- Genetics in Medicine (4 papers)Journal of Perinatal Medicine (4 papers)Ultrasound in Obstetrics and Gynecology (4 papers)American Journal of Obstetrics and Gynecology (3 papers)Obstetrics and Gynecology (3 papers)
- Partner nations
- IsraelUnited StatesGermany
In The Last Decade
Idit Maya
53 papers receiving 883 citations
Peers
Comparison fields: 5 of 65
- Pediatrics, Perinatology and Child Health 425
- Genetics 274
- Molecular Biology 219
- Epidemiology 86
- Cell Biology 45
Countries citing papers authored by Idit Maya
This map shows the geographic impact of Idit Maya'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 Idit Maya with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Idit Maya more than expected).
Fields of papers citing papers by Idit Maya
This network shows the impact of papers produced by Idit Maya. 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 Idit Maya. The network helps show where Idit Maya may publish in the future.
Co-authors
The 25 scholars most cited alongside Idit Maya, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 61 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 120 | |
| 2 | 2010 | 62 | |
| 3 | 2009 | 60 | |
| 4 | 2019 | 54 | |
| 5 | 2017 | 48 | |
| 6 | 2017 | 46 | |
| 7 | 2014 | 41 | |
| 8 | 2016 | 37 | |
| 9 | 2018 | 30 | |
| 10 | 2015 | 29 | |
| 11 | 2014 | 28 | |
| 12 | 2013 | 23 | |
| 13 | Chromosomal Microarray Analysis (CMA) a Clinical Diagnostic Tool in the Prenatal and Postnatal Settings. | 2015 | 23 |
| 14 | 2018 | 21 | |
| 15 | 2020 | 19 | |
| 16 | 2021 | 16 | |
| 17 | 2018 | 16 | |
| 18 | 2017 | 15 | |
| 19 | 2020 | 15 | |
| 20 | 2019 | 14 |
About Idit Maya
Idit Maya is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Epidemiology and Genetics, having authored 61 papers that have together received 931 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (32 papers), Genomic variations and chromosomal abnormalities (13 papers), Fetal and Pediatric Neurological Disorders (8 papers), Genomics and Rare Diseases (7 papers), BRCA gene mutations in cancer (2 papers), Renal and related cancers (2 papers), Connective tissue disorders research (2 papers) and Congenital Ear and Nasal Anomalies (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (425 citations), Genetics (274 citations), Molecular Biology (219 citations), Epidemiology (86 citations) and Cell Biology (45 citations). Idit Maya has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Lena Sagi‐Dain, Lina Basel‐Vanagaite, Sarit Kahana, Mordechai Shohat, Amihood Singer, Tamar Tenne, Josepha Yeshaya, Shiri Yacobson, Lina Basel‐Salmon and J. M. M. van Lith. Their work appears in journals such as Genetics in Medicine, Journal of Perinatal Medicine, Ultrasound in Obstetrics and Gynecology, American Journal of Obstetrics and Gynecology and Obstetrics and Gynecology.
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.