Orest Hurko
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Papers in
-
- Mitochondrial Function and Pathology 12
- ATP Synthase and ATPases Research 9
- Muscle Physiology and Disorders 5
- Genetics 18
- Connective tissue disorders research 11
- Co-authors
- Giuseppe Attardi (4 shared papers)Anne Chomyn (3 shared papers)Andrea Martinuzzi (2 shared papers)Menelas N. Pangalos (3 shared papers)Makoto Yoneda (2 shared papers)Lee E. Schechter (1 shared paper)Donald R. Johns (4 shared papers)Ikuya Nonaka (1 shared paper)
- Journals
- Neurology (4 papers)Annals of Neurology (4 papers)Proceedings of the National Academy of Sciences (3 papers)Parkinsonism & Related Disorders (2 papers)Genomics (2 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Orest Hurko
71 papers receiving 3.3k citations
Peers
Comparison fields: 5 of 117
- Clinical Biochemistry 611
- Cellular and Molecular Neuroscience 503
- Molecular Biology 1.9k
- Genetics 248
- Neurology 186
Countries citing papers authored by Orest Hurko
This map shows the geographic impact of Orest Hurko'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 Orest Hurko with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Orest Hurko more than expected).
Fields of papers citing papers by Orest Hurko
This network shows the impact of papers produced by Orest Hurko. 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 Orest Hurko. The network helps show where Orest Hurko may publish in the future.
Co-authors
The 25 scholars most cited alongside Orest Hurko, 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 75 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 428 | |
| 2 | 2007 | 272 | |
| 3 | 1992 | 245 | |
| 4 | 2008 | 213 | |
| 5 | Family study and segregation analysis of Tourette syndrome: evidence for a mixed model of inheritance. | 1996 | 170 |
| 6 | 1996 | 150 | |
| 7 | 1987 | 121 | |
| 8 | 1996 | 100 | |
| 9 | 1999 | 98 | |
| 10 | 1990 | 83 | |
| 11 | 1998 | 82 | |
| 12 | 1999 | 82 | |
| 13 | 1978 | 79 | |
| 14 | 2005 | 76 | |
| 15 | 1989 | 74 | |
| 16 | Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophy. | 1994 | 73 |
| 17 | 1994 | 72 | |
| 18 | 2009 | 72 | |
| 19 | 1990 | 64 | |
| 20 | Reversibility of white matter changes and dementia after treatment of dural fistulas. | 1995 | 57 |
About Orest Hurko
Orest Hurko is a scholar working on Molecular Biology, Genetics, Neurology, Cellular and Molecular Neuroscience and Clinical Biochemistry, having authored 75 papers that have together received 3.5k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (12 papers), Connective tissue disorders research (11 papers), Metabolism and Genetic Disorders (10 papers), ATP Synthase and ATPases Research (9 papers), Computational Drug Discovery Methods (7 papers), Muscle Physiology and Disorders (5 papers), Neurosurgical Procedures and Complications (4 papers) and Neurological diseases and metabolism (4 papers). The work is most often cited by research in Clinical Biochemistry (611 citations), Cellular and Molecular Neuroscience (503 citations), Molecular Biology (1.9k citations), Genetics (248 citations) and Neurology (186 citations). Orest Hurko has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Giuseppe Attardi, Anne Chomyn, Andrea Martinuzzi, Menelas N. Pangalos, Makoto Yoneda, Lee E. Schechter, Donald R. Johns, Ikuya Nonaka, C. Angelini and Andrea Daga. Their work appears in journals such as Neurology, Annals of Neurology, Proceedings of the National Academy of Sciences, Parkinsonism & Related Disorders and Genomics.
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.