Einat Granot‐Hershkovitz
Impact in
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- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
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- Birth, Development, and Health
- Prenatal Screening and Diagnostics
Papers in
- Genetics 10
- Genetic Associations and Epidemiology 7
- Genomic variations and chromosomal abnormalities 3
- BRCA gene mutations in cancer 2
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- Birth, Development, and Health 4
- Co-authors
- Elad Lerer (1 shared paper)Shai Carmi (2 shared papers)Shlomit Levi (1 shared paper)Maya Yaari (1 shared paper)Richard P. Ebstein (1 shared paper)Tamar Sofer (10 shared papers)Nurit Yirmiya (1 shared paper)Sagiv Shifman (1 shared paper)
- Journals
- Alzheimer s & Dementia (3 papers)Human Genetics and Genomics Advances (2 papers)European Journal of Human Genetics (2 papers)Scientific Reports (1 paper)Alzheimer s Research & Therapy (1 paper)
- Partner nations
- United StatesIsraelChina
In The Last Decade
Einat Granot‐Hershkovitz
17 papers receiving 212 citations
Peers
Comparison fields: 5 of 49
- Genetics 93
- Pediatrics, Perinatology and Child Health 65
- Obstetrics and Gynecology 17
- Reproductive Medicine 18
- Psychiatry and Mental health 26
Countries citing papers authored by Einat Granot‐Hershkovitz
This map shows the geographic impact of Einat Granot‐Hershkovitz'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 Einat Granot‐Hershkovitz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Einat Granot‐Hershkovitz more than expected).
Fields of papers citing papers by Einat Granot‐Hershkovitz
This network shows the impact of papers produced by Einat Granot‐Hershkovitz. 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 Einat Granot‐Hershkovitz. The network helps show where Einat Granot‐Hershkovitz may publish in the future.
Co-authors
The 25 scholars most cited alongside Einat Granot‐Hershkovitz, 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 | 2011 | 43 | |
| 2 | 2021 | 40 | |
| 3 | 2020 | 31 | |
| 4 | 2013 | 22 | |
| 5 | 2022 | 18 | |
| 6 | 2015 | 13 | |
| 7 | 2023 | 8 | |
| 8 | 2022 | 8 | |
| 9 | 2018 | 7 | |
| 10 | 2022 | 6 | |
| 11 | 2011 | 5 | |
| 12 | 2022 | 4 | |
| 13 | 2020 | 4 | |
| 14 | 2023 | 2 | |
| 15 | 2020 | 2 | |
| 16 | 2023 | 1 | |
| 17 | 2024 | 1 | |
| 18 | 2013 | 0 |
About Einat Granot‐Hershkovitz
Einat Granot‐Hershkovitz is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Public Health, Environmental and Occupational Health and Psychiatry and Mental health, having authored 18 papers that have together received 215 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (7 papers), Birth, Development, and Health (4 papers), Dementia and Cognitive Impairment Research (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Alzheimer's disease research and treatments (2 papers), Obesity, Physical Activity, Diet (2 papers), BRCA gene mutations in cancer (2 papers) and Metabolomics and Mass Spectrometry Studies (2 papers). The work is most often cited by research in Genetics (93 citations), Pediatrics, Perinatology and Child Health (65 citations), Obstetrics and Gynecology (17 citations), Reproductive Medicine (18 citations) and Psychiatry and Mental health (26 citations). Einat Granot‐Hershkovitz has collaborated with scholars based in United States, Israel and China. Frequent co-authors include Elad Lerer, Shai Carmi, Shlomit Levi, Maya Yaari, Richard P. Ebstein, Tamar Sofer, Nurit Yirmiya, Sagiv Shifman, Eyal Ben‐David and Hector M. González. Their work appears in journals such as Alzheimer s & Dementia, Human Genetics and Genomics Advances, European Journal of Human Genetics, Scientific Reports and Alzheimer s Research & Therapy.
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.