Zvi Borochowitz
Impact in
- Genetics top 2%
- Connective tissue disorders research
- Craniofacial Disorders and Treatments
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Nutrition and Dietetics top 2%
- Magnesium in Health and Disease
Papers in
- Genetics 34
- Connective tissue disorders research 10
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 7
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- Congenital heart defects research 5
- RNA regulation and disease 4
- Bone Metabolism and Diseases 3
- Co-authors
- Rivka Carmi (1 shared paper)Gretel Beck (1 shared paper)Μαρία Τσολιά (1 shared paper)Richard Englehardt (1 shared paper)Melanie Barbara Boettger (1 shared paper)Hanna Shalev (1 shared paper)Roxanne Y. Walder (1 shared paper)Daniel Landau (1 shared paper)
- Journals
- Clinical Genetics (5 papers)The American Journal of Human Genetics (5 papers)Nature Genetics (3 papers)European Journal of Pediatrics (2 papers)Prenatal Diagnosis (2 papers)
- Partner nations
- IsraelUnited StatesGermany
In The Last Decade
Zvi Borochowitz
66 papers receiving 2.1k citations
Peers
Comparison fields: 5 of 110
- Genetics 816
- Nutrition and Dietetics 363
- Sensory Systems 109
- Nephrology 123
- Rheumatology 204
Countries citing papers authored by Zvi Borochowitz
This map shows the geographic impact of Zvi Borochowitz'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 Zvi Borochowitz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Zvi Borochowitz more than expected).
Fields of papers citing papers by Zvi Borochowitz
This network shows the impact of papers produced by Zvi Borochowitz. 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 Zvi Borochowitz. The network helps show where Zvi Borochowitz may publish in the future.
Co-authors
The 25 scholars most cited alongside Zvi Borochowitz, 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 67 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 408 | |
| 2 | 2001 | 183 | |
| 3 | 2008 | 177 | |
| 4 | 1998 | 161 | |
| 5 | 2009 | 85 | |
| 6 | 2008 | 84 | |
| 7 | 2019 | 71 | |
| 8 | 1981 | 64 | |
| 9 | 1998 | 64 | |
| 10 | 2009 | 61 | |
| 11 | Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype. | 1997 | 55 |
| 12 | 2012 | 41 | |
| 13 | 1992 | 39 | |
| 14 | 1985 | 38 | |
| 15 | 1997 | 35 | |
| 16 | 2012 | 29 | |
| 17 | 2005 | 28 | |
| 18 | 2006 | 28 | |
| 19 | 1994 | 27 | |
| 20 | 1986 | 27 |
About Zvi Borochowitz
Zvi Borochowitz is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Rheumatology and Endocrinology, Diabetes and Metabolism, having authored 67 papers that have together received 2.2k indexed citations. Recurring topics across this work include Connective tissue disorders research (10 papers), Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Prenatal Screening and Diagnostics (6 papers), Congenital heart defects research (5 papers), RNA regulation and disease (4 papers), Bone Metabolism and Diseases (3 papers) and Genetic Neurodegenerative Diseases (3 papers). The work is most often cited by research in Genetics (816 citations), Nutrition and Dietetics (363 citations), Sensory Systems (109 citations), Nephrology (123 citations) and Rheumatology (204 citations). Zvi Borochowitz has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Rivka Carmi, Gretel Beck, Μαρία Τσολιά, Richard Englehardt, Melanie Barbara Boettger, Hanna Shalev, Roxanne Y. Walder, Daniel Landau, Peter Meyer and Val C. Sheffield. Their work appears in journals such as Clinical Genetics, The American Journal of Human Genetics, Nature Genetics, European Journal of Pediatrics and Prenatal Diagnosis.
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.