Ashraf U. Mannan
Impact in
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- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Neurology top 10%
- Neurological diseases and metabolism
Papers in
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- Epigenetics and DNA Methylation 3
- Ubiquitin and proteasome pathways 2
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- Hereditary Neurological Disorders 8
- Co-authors
- Wolfgang Engel (5 shared papers)Simone M. Sauter (3 shared papers)Jürgen Neesen (3 shared papers)Moneef Shoukier (2 shared papers)Walter Paulus (1 shared paper)Karim Nayernia (3 shared papers)D. V. Krishna Pantakani (2 shared papers)Chiranjeevi Bodda (3 shared papers)
In The Last Decade
Ashraf U. Mannan
32 papers receiving 650 citations
Peers
Comparison fields: 5 of 69
- Cellular and Molecular Neuroscience 246
- Neurology 100
- Cell Biology 140
- Genetics 75
- Developmental Neuroscience 20
Countries citing papers authored by Ashraf U. Mannan
This map shows the geographic impact of Ashraf U. Mannan'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 Ashraf U. Mannan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ashraf U. Mannan more than expected).
Fields of papers citing papers by Ashraf U. Mannan
This network shows the impact of papers produced by Ashraf U. Mannan. 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 Ashraf U. Mannan. The network helps show where Ashraf U. Mannan may publish in the future.
Co-authors
The 25 scholars most cited alongside Ashraf U. Mannan, 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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 110 | |
| 2 | 2008 | 68 | |
| 3 | 2008 | 54 | |
| 4 | 2006 | 45 | |
| 5 | 2004 | 35 | |
| 6 | 2013 | 33 | |
| 7 | 2010 | 31 | |
| 8 | 2020 | 26 | |
| 9 | 2018 | 26 | |
| 10 | 2014 | 23 | |
| 11 | 2014 | 22 | |
| 12 | 2003 | 21 | |
| 13 | 2008 | 20 | |
| 14 | Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort. | 2016 | 19 |
| 15 | 2019 | 19 | |
| 16 | 2011 | 18 | |
| 17 | 2019 | 14 | |
| 18 | 2003 | 12 | |
| 19 | 2020 | 10 | |
| 20 | 2019 | 10 |
About Ashraf U. Mannan
Ashraf U. Mannan is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Cell Biology and Neurology, having authored 32 papers that have together received 652 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (8 papers), Neurological diseases and metabolism (4 papers), Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Epigenetics and DNA Methylation (3 papers), Botulinum Toxin and Related Neurological Disorders (3 papers), Ubiquitin and proteasome pathways (2 papers) and Microtubule and mitosis dynamics (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (246 citations), Neurology (100 citations), Cell Biology (140 citations), Genetics (75 citations) and Developmental Neuroscience (20 citations). Ashraf U. Mannan has collaborated with scholars based in India, Germany and Canada. Frequent co-authors include Wolfgang Engel, Simone M. Sauter, Jürgen Neesen, Moneef Shoukier, Walter Paulus, Karim Nayernia, D. V. Krishna Pantakani, Chiranjeevi Bodda, Ibrahim M. Adham and P. Byrne. Their work appears in journals such as American Journal Of Pathology, The American Journal of Human Genetics, Neurogenetics, PLoS ONE and Epilepsy Research.
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.