Fernando Kok
Impact in
Papers in
-
- RNA regulation and disease 13
- Mitochondrial Function and Pathology 12
- Genetics 57
- Genetics and Neurodevelopmental Disorders 24
- Genomic variations and chromosomal abnormalities 16
- Genomics and Rare Diseases 12
- Genetic Syndromes and Imprinting 12
- Co-authors
- Agnes L. Nishimura (2 shared papers)Miguel Mitne‐Neto (2 shared papers)Paul Skehel (1 shared paper)Helga Cristina Almeida da Silva (1 shared paper)Duilio Cascio (1 shared paper)Jeanette Webb (1 shared paper)João Ricardo Mendes de Oliveira (1 shared paper)Susan Middleton (1 shared paper)
- Journals
- Clinical Genetics (7 papers)Neurology Genetics (6 papers)Neurology (5 papers)Brain and Development (5 papers)European Journal of Human Genetics (4 papers)
- Partner nations
- BrazilUnited StatesUnited Kingdom
In The Last Decade
Fernando Kok
167 papers receiving 4.0k citations
Fernando Kok's Hit Papers
Peers
Comparison fields: 5 of 113
- Neurology 792
- Genetics 489
- Clinical Biochemistry 295
- Neurology 326
- Genetics 1.0k
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 179 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 | 811 |
| 2 | 2007 | 140 | |
| 3 | 2006 | 132 | |
| 4 | 2002 | 120 | |
| 5 | Altered expression of ALDP in X-linked adrenoleukodystrophy. | 1995 | 113 |
| 6 | 1995 | 91 | |
| 7 | 2014 | 91 | |
| 8 | 2004 | 90 | |
| 9 | 2004 | 89 | |
| 10 | 2006 | 89 | |
| 11 | 2006 | 79 | |
| 12 | 2008 | 76 | |
| 13 | 2001 | 61 | |
| 14 | 2005 | 57 | |
| 15 | 2004 | 56 | |
| 16 | 2005 | 55 | |
| 17 | 1992 | 50 | |
| 18 | 2003 | 50 | |
| 19 | 2006 | 48 | |
| 20 | 2000 | 48 |
About Fernando Kok
Fernando Kok is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Clinical Biochemistry and Neurology, having authored 179 papers that have together received 4.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (24 papers), Metabolism and Genetic Disorders (20 papers), Genomic variations and chromosomal abnormalities (16 papers), Genetic Neurodegenerative Diseases (14 papers), RNA regulation and disease (13 papers), Genomics and Rare Diseases (12 papers), Genetic Syndromes and Imprinting (12 papers) and Mitochondrial Function and Pathology (12 papers). The work is most often cited by research in Neurology (792 citations), Genetics (489 citations), Clinical Biochemistry (295 citations), Neurology (326 citations) and Genetics (1.0k citations). Fernando Kok has collaborated with scholars based in Brazil, United States and United Kingdom. Frequent co-authors include Agnes L. Nishimura, Miguel Mitne‐Neto, Paul Skehel, Helga Cristina Almeida da Silva, Duilio Cascio, Jeanette Webb, João Ricardo Mendes de Oliveira, Susan Middleton, Antônio Richieri‐Costa and Mayana Zatz. Their work appears in journals such as Clinical Genetics, Neurology Genetics, Neurology, Brain and Development and European 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.