Fernando Kok
Impact in
- Neurology top 1%
- Amyotrophic Lateral Sclerosis Research
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Papers in
- Genetics 71
- Genetics and Neurodevelopmental Disorders 34
- Genomics and Rare Diseases 25
- Genomic variations and chromosomal abnormalities 22
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- Metabolism and Genetic Disorders 25
- Co-authors
- Agnes Lumi Nishimura (2 shared papers)Susan Middleton (1 shared paper)Paul Skehel (1 shared paper)Duilio Cascio (1 shared paper)João Ricardo Mendes de Oliveira (1 shared paper)Helga Cristina Almeida da Silva (1 shared paper)Jeanette Webb (1 shared paper)Antônio Richieri‐Costa (1 shared paper)
- Journals
- The American Journal of Human Genetics (12 papers)Clinical Genetics (9 papers)Brain (8 papers)Neurology Genetics (6 papers)Brain and Development (6 papers)
- Partner nations
- BrazilUnited StatesUnited Kingdom
In The Last Decade
Fernando Kok
209 papers receiving 6.0k citations
Fernando Kok's Hit Papers
Peers
Comparison fields: 5 of 129
- Neurology 1.0k
- Clinical Biochemistry 452
- Genetics 629
- Neurology 465
- Genetics 1.5k
Countries citing papers authored by Fernando Kok
This map shows the geographic impact of Fernando Kok'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 Fernando Kok with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fernando Kok more than expected).
Fields of papers citing papers by Fernando Kok
This network shows the impact of papers produced by Fernando Kok. 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 Fernando Kok. The network helps show where Fernando Kok may publish in the future.
Co-authors
The 25 scholars most cited alongside Fernando Kok, 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 224 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A Mutation in the Vesicle-Trafficking Protein VAPB Causes Late-Onset Spinal Muscular Atrophy and Amyotrophic Lateral Sclerosis Hit paper breakdown → | 2004 | 831 |
| 2 | 2019 | 190 | |
| 3 | 2010 | 184 | |
| 4 | 2007 | 142 | |
| 5 | 2006 | 141 | |
| 6 | 2002 | 124 | |
| 7 | 2018 | 123 | |
| 8 | 2021 | 119 | |
| 9 | Altered expression of ALDP in X-linked adrenoleukodystrophy. | 1995 | 114 |
| 10 | 2007 | 113 | |
| 11 | 2018 | 102 | |
| 12 | 2014 | 97 | |
| 13 | 2015 | 96 | |
| 14 | 2006 | 94 | |
| 15 | 2004 | 93 | |
| 16 | 2004 | 93 | |
| 17 | 1995 | 91 | |
| 18 | 2008 | 79 | |
| 19 | 2006 | 78 | |
| 20 | 2017 | 76 |
About Fernando Kok
Fernando Kok is a scholar working on Genetics, Clinical Biochemistry, Molecular Biology, Cellular and Molecular Neuroscience and Genetics, having authored 224 papers that have together received 6.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (34 papers), Metabolism and Genetic Disorders (25 papers), Genomics and Rare Diseases (25 papers), Genomic variations and chromosomal abnormalities (22 papers), Mitochondrial Function and Pathology (19 papers), Genetic Neurodegenerative Diseases (17 papers), RNA regulation and disease (17 papers) and Hereditary Neurological Disorders (15 papers). The work is most often cited by research in Neurology (1.0k citations), Clinical Biochemistry (452 citations), Genetics (629 citations), Neurology (465 citations) and Genetics (1.5k citations). Fernando Kok has collaborated with scholars based in Brazil, United States and United Kingdom. Frequent co-authors include Agnes Lumi Nishimura, Susan Middleton, Paul Skehel, Duilio Cascio, João Ricardo Mendes de Oliveira, Helga Cristina Almeida da Silva, Jeanette Webb, Antônio Richieri‐Costa, Mayana Zatz and Miguel Mitne‐Neto. Their work appears in journals such as The American Journal of Human Genetics, Clinical Genetics, Brain, Neurology Genetics and Brain and Development.
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.