Manoj P. Menezes
- Molecular Biology
- Cellular and Molecular Neuroscience top 5%
- Neurology top 5%
- Genetics top 5%
- Genetics
- Co-authors
- Joshua BurnsRobert OuvrierRichard WebsterKayla CornettMichelle A. FarrarAmy D. SmanMonique M. RyanKathryn N. North
- Topics
- Hereditary Neurological Disorders (18 papers)Neurogenetic and Muscular Disorders Research (15 papers)Genetic Neurodegenerative Diseases (11 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Manoj P. Menezes
48 papers receiving 919 citations
Peers
Comparison fields: 5 of 94
- Molecular Biology 353
- Cellular and Molecular Neuroscience 329
- Neurology 195
- Genetics 164
- Genetics 122
Countries citing papers authored by Manoj P. Menezes
This map shows the geographic impact of Manoj P. Menezes'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 Manoj P. Menezes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Manoj P. Menezes more than expected).
Fields of papers citing papers by Manoj P. Menezes
This network shows the impact of papers produced by Manoj P. Menezes. 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 Manoj P. Menezes. The network helps show where Manoj P. Menezes may publish in the future.
Co-authorship network of co-authors of Manoj P. Menezes
This figure shows the co-authorship network connecting the top 25 collaborators of Manoj P. Menezes. A scholar is included among the top collaborators of Manoj P. Menezes based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Manoj P. Menezes. Manoj P. Menezes is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 3 | |
| 2 | 0 | |
| 3 | 3 | |
| 4 | 2 | |
| 5 | 0 | |
| 6 | 3 | |
| 7 | 10 | |
| 8 | 3 | |
| 9 | 14 | |
| 10 | 15 | |
| 11 | 20 | |
| 12 | 9 | |
| 13 | 50 | |
| 14 | 3 | |
| 15 | Eye movement disorders are an early manifestation of CACNA1A mutations in children | 2 |
| 16 | 27 | |
| 17 | 7 | |
| 18 | 15 | |
| 19 | 34 | |
| 20 | 95 |
About Manoj P. Menezes
Manoj P. Menezes is a scholar working on Genetics, Cellular and Molecular Neuroscience and Clinical Biochemistry, having authored 52 papers that have together received 933 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (18 papers), Neurogenetic and Muscular Disorders Research (15 papers) and Genetic Neurodegenerative Diseases (11 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (329 citations), Genetics (164 citations) and Clinical Biochemistry (100 citations). Manoj P. Menezes has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Joshua Burns, Robert Ouvrier, Richard Webster, Kayla Cornett, Michelle A. Farrar, Amy D. Sman, Monique M. Ryan, Kathryn N. North, Elizabeth Wojciechowski and Christopher Troedson. Their work appears in journals such as Neurology, Annals of Neurology and European Heart Journal.
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.