Haike Reznik‐Wolf
Impact in
- Ophthalmology top 5%
- Glaucoma and retinal disorders
- Nephrology top 10%
Papers in
-
- Sexual Differentiation and Disorders 3
- Mitochondrial Function and Pathology 3
- Genetics 9
- Connective tissue disorders research 4
- Co-authors
- Elon Pras (20 shared papers)Eran Pras (7 shared papers)Dina Marek‐Yagel (5 shared papers)Moshe Frydman (4 shared papers)Yackov Berkun (3 shared papers)Avi Livneh (3 shared papers)Elon Pras (3 shared papers)Shai Padeh (2 shared papers)
- Journals
- European Journal of Medical Genetics (4 papers)European Journal of Human Genetics (2 papers)Human Genetics (2 papers)European Journal of Paediatric Neurology (2 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- IsraelUnited StatesGermany
In The Last Decade
Haike Reznik‐Wolf
37 papers receiving 875 citations
Peers
Comparison fields: 5 of 74
- Ophthalmology 101
- Nephrology 58
- Molecular Biology 554
- Cell Biology 118
- Urology 45
Countries citing papers authored by Haike Reznik‐Wolf
This map shows the geographic impact of Haike Reznik‐Wolf'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 Haike Reznik‐Wolf with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Haike Reznik‐Wolf more than expected).
Fields of papers citing papers by Haike Reznik‐Wolf
This network shows the impact of papers produced by Haike Reznik‐Wolf. 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 Haike Reznik‐Wolf. The network helps show where Haike Reznik‐Wolf may publish in the future.
Co-authors
The 25 scholars most cited alongside Haike Reznik‐Wolf, 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 39 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 152 | |
| 2 | 2012 | 106 | |
| 3 | 2008 | 95 | |
| 4 | Cone-rod dystrophy and a frameshift mutation in the PROM1 gene. | 2009 | 59 |
| 5 | 2006 | 57 | |
| 6 | 2017 | 37 | |
| 7 | 2019 | 32 | |
| 8 | 2012 | 29 | |
| 9 | 2007 | 29 | |
| 10 | 2015 | 27 | |
| 11 | Bloom syndrome and Fanconi's anemia: rate and ethnic origin of mutation carriers in Israel. | 2002 | 24 |
| 12 | 2006 | 23 | |
| 13 | 1996 | 19 | |
| 14 | 2012 | 18 | |
| 15 | 2008 | 16 | |
| 16 | Fundus albipunctatus: novel mutations and phenotypic description of Israeli patients. | 2012 | 14 |
| 17 | 2010 | 13 | |
| 18 | 2020 | 13 | |
| 19 | 2012 | 13 | |
| 20 | 2020 | 11 |
About Haike Reznik‐Wolf
Haike Reznik‐Wolf is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Cell Biology and Pediatrics, Perinatology and Child Health, having authored 39 papers that have together received 888 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (4 papers), Metabolism and Genetic Disorders (4 papers), Connective tissue disorders research (4 papers), Alzheimer's disease research and treatments (3 papers), Sexual Differentiation and Disorders (3 papers), Mitochondrial Function and Pathology (3 papers), Prenatal Screening and Diagnostics (3 papers) and Genetic Neurodegenerative Diseases (3 papers). The work is most often cited by research in Ophthalmology (101 citations), Nephrology (58 citations), Molecular Biology (554 citations), Cell Biology (118 citations) and Urology (45 citations). Haike Reznik‐Wolf has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Elon Pras, Eran Pras, Dina Marek‐Yagel, Moshe Frydman, Yackov Berkun, Avi Livneh, Elon Pras, Shai Padeh, Mordechai Pras and Uri Nir. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Human Genetics, European Journal of Paediatric Neurology 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.