Faisal Fecto
Impact in
Papers in
- Neurology 13
- Amyotrophic Lateral Sclerosis Research 11
- Parkinson's Disease Mechanisms and Treatments 5
- Neurological diseases and metabolism 4
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- Ion Channels and Receptors 2
- Co-authors
- Teepu Siddique (16 shared papers)Han‐Xiang Deng (9 shared papers)Nailah Siddique (3 shared papers)Yong Shi (4 shared papers)Kaouther Ajroud (3 shared papers)Senda Ajroud‐Driss (3 shared papers)Marco Martina (3 shared papers)Enrico Mugnaini (2 shared papers)
- Journals
- Neurology (4 papers)Neurogenetics (2 papers)Annals of Neurology (2 papers)The Lancet Neurology (1 paper)Nature Genetics (1 paper)
- Partner nations
- United StatesPakistanCzechia
In The Last Decade
Faisal Fecto
20 papers receiving 2.7k citations
Faisal Fecto's Hit Papers
Peers
Comparison fields: 5 of 82
- Neurology 1.8k
- Genetics 871
- Neurology 496
- Sensory Systems 190
- Cellular and Molecular Neuroscience 430
Countries citing papers authored by Faisal Fecto
This map shows the geographic impact of Faisal Fecto'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 Faisal Fecto with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Faisal Fecto more than expected).
Fields of papers citing papers by Faisal Fecto
This network shows the impact of papers produced by Faisal Fecto. 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 Faisal Fecto. The network helps show where Faisal Fecto may publish in the future.
Co-authors
The 25 scholars most cited alongside Faisal Fecto, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia Hit paper breakdown → | 2011 | 997 |
| 2 | SQSTM1 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis Hit paper breakdown → | 2011 | 559 |
| 3 | 2010 | 293 | |
| 4 | 2009 | 222 | |
| 5 | 2010 | 171 | |
| 6 | 2014 | 89 | |
| 7 | 2011 | 69 | |
| 8 | 2011 | 65 | |
| 9 | 2014 | 63 | |
| 10 | 2005 | 61 | |
| 11 | 2011 | 48 | |
| 12 | 2011 | 45 | |
| 13 | 2014 | 28 | |
| 14 | Signaling mechanisms mediated by G-protein coupled receptors in human platelets. | 2004 | 13 |
| 15 | 2009 | 13 | |
| 16 | 2010 | 13 | |
| 17 | 2011 | 7 | |
| 18 | 2010 | 3 | |
| 19 | 2011 | 3 | |
| 20 | Patterns of tuberculosis in the central nervous system | 2004 | 2 |
About Faisal Fecto
Faisal Fecto is a scholar working on Neurology, Neurology, Sensory Systems, Cellular and Molecular Neuroscience and Genetics, having authored 22 papers that have together received 2.8k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (11 papers), Parkinson's Disease Mechanisms and Treatments (5 papers), Neurological diseases and metabolism (4 papers), Neurogenetic and Muscular Disorders Research (2 papers), Genetic Neurodegenerative Diseases (2 papers), Hereditary Neurological Disorders (2 papers), Alzheimer's disease research and treatments (2 papers) and Ion Channels and Receptors (2 papers). The work is most often cited by research in Neurology (1.8k citations), Genetics (871 citations), Neurology (496 citations), Sensory Systems (190 citations) and Cellular and Molecular Neuroscience (430 citations). Faisal Fecto has collaborated with scholars based in United States, Pakistan and Czechia. Frequent co-authors include Teepu Siddique, Han‐Xiang Deng, Nailah Siddique, Yong Shi, Kaouther Ajroud, Senda Ajroud‐Driss, Marco Martina, Enrico Mugnaini, Eileen H. Bigio and Hong Xiang Zhai. Their work appears in journals such as Neurology, Neurogenetics, Annals of Neurology, The Lancet Neurology and Nature 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.