Orit Reish
Impact in
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
-
- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
Papers in
- Genetics 30
- Genomic variations and chromosomal abnormalities 11
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Genetic Syndromes and Imprinting 5
- Neurogenetic and Muscular Disorders Research 5
- Co-authors
- Arie Herman (11 shared papers)Susan A. Berry (4 shared papers)Ron Maymon (9 shared papers)Aliza Amiel (11 shared papers)Zvi Vaknin (6 shared papers)Eli Heyman (5 shared papers)Moshe Fejgin (9 shared papers)Heather Etchevers (1 shared paper)
- Journals
- Prenatal Diagnosis (8 papers)Genetics in Medicine (5 papers)Chromosome Research (4 papers)Fetal Diagnosis and Therapy (3 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- IsraelUnited StatesUnited Kingdom
In The Last Decade
Orit Reish
72 papers receiving 1.8k citations
Orit Reish's Hit Papers
Peers
Comparison fields: 5 of 111
- Clinical Biochemistry 165
- Pediatrics, Perinatology and Child Health 425
- Genetics 516
- Molecular Biology 880
- Cancer Research 146
Countries citing papers authored by Orit Reish
This map shows the geographic impact of Orit Reish'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 Orit Reish with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Orit Reish more than expected).
Fields of papers citing papers by Orit Reish
This network shows the impact of papers produced by Orit Reish. 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 Orit Reish. The network helps show where Orit Reish may publish in the future.
Co-authors
The 25 scholars most cited alongside Orit Reish, 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 72 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations Hit paper breakdown → | 2009 | 294 |
| 2 | 2009 | 135 | |
| 3 | 2007 | 119 | |
| 4 | 2009 | 68 | |
| 5 | Cone-rod dystrophy and a frameshift mutation in the PROM1 gene. | 2009 | 59 |
| 6 | Tyrosinase inhibition due to interaction of homocyst(e)ine with copper: the mechanism for reversible hypopigmentation in homocystinuria due to cystathionine beta-synthase deficiency. | 1995 | 52 |
| 7 | 1993 | 47 | |
| 8 | 2002 | 45 | |
| 9 | 2006 | 43 | |
| 10 | 2013 | 41 | |
| 11 | 1995 | 41 | |
| 12 | 1995 | 41 | |
| 13 | 2001 | 39 | |
| 14 | 2006 | 36 | |
| 15 | 2009 | 35 | |
| 16 | 2009 | 34 | |
| 17 | 2018 | 33 | |
| 18 | Prenatal diagnosis for detecting congenital malformations: acceptance among Israeli Arab women. | 2000 | 31 |
| 19 | 2002 | 31 | |
| 20 | 1997 | 28 |
About Orit Reish
Orit Reish is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Public Health, Environmental and Occupational Health, having authored 72 papers that have together received 1.8k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (22 papers), Genomic variations and chromosomal abnormalities (11 papers), Metabolism and Genetic Disorders (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Genetic Syndromes and Imprinting (5 papers), Chromosomal and Genetic Variations (5 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Parvovirus B19 Infection Studies (5 papers). The work is most often cited by research in Clinical Biochemistry (165 citations), Pediatrics, Perinatology and Child Health (425 citations), Genetics (516 citations), Molecular Biology (880 citations) and Cancer Research (146 citations). Orit Reish has collaborated with scholars based in Israel, United States and United Kingdom. Frequent co-authors include Arie Herman, Susan A. Berry, Ron Maymon, Aliza Amiel, Zvi Vaknin, Eli Heyman, Moshe Fejgin, Heather Etchevers, Barbara Sedgwick and Giles S.H. Yeo. Their work appears in journals such as Prenatal Diagnosis, Genetics in Medicine, Chromosome Research, Fetal Diagnosis and Therapy and The American Journal of Human Genetics.
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.