Adel Misk

621 total citations
6 papers, 324 citations indexed

About

Adel Misk is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Adel Misk has authored 6 papers receiving a total of 324 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Cellular and Molecular Neuroscience, 2 papers in Molecular Biology and 2 papers in Cognitive Neuroscience. Recurrent topics in Adel Misk's work include Neuroscience and Neuropharmacology Research (2 papers), Glycogen Storage Diseases and Myoclonus (1 paper) and Neural dynamics and brain function (1 paper). Adel Misk is often cited by papers focused on Neuroscience and Neuropharmacology Research (2 papers), Glycogen Storage Diseases and Myoclonus (1 paper) and Neural dynamics and brain function (1 paper). Adel Misk collaborates with scholars based in Australia, United States and Israel. Adel Misk's co-authors include Alejandro Cohen, Dominik Zumsteg, Alon Friedman, Ilan Shelef, Oren Tomkins‐Netzer, Mohammad M. Herzallah, Ahmed A. Moustafa, Catherine E. Myers, Mark A. Gluck and Giovanni Stévanin and has published in prestigious journals such as Neurology, Human Molecular Genetics and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Adel Misk

6 papers receiving 316 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Adel Misk Australia 6 118 95 76 75 66 6 324
Elżbieta Pasennik Poland 12 101 0.9× 103 1.1× 36 0.5× 176 2.3× 43 0.7× 21 397
Pierre Labauge France 11 193 1.6× 172 1.8× 69 0.9× 52 0.7× 148 2.2× 31 499
Lorenzo De Santi Italy 12 69 0.6× 79 0.8× 72 0.9× 39 0.5× 99 1.5× 16 325
Mar O’Callaghan Spain 12 273 2.3× 52 0.5× 42 0.6× 27 0.4× 80 1.2× 26 489
Jiangwei Ding China 10 108 0.9× 32 0.3× 75 1.0× 49 0.7× 77 1.2× 31 335
Carmen Muñoz‐Ballester United States 9 123 1.0× 90 0.9× 31 0.4× 181 2.4× 86 1.3× 10 395
Yoshio Morimatsu Japan 11 69 0.6× 114 1.2× 77 1.0× 59 0.8× 76 1.2× 33 336
Anne Koy Germany 14 114 1.0× 299 3.1× 115 1.5× 27 0.4× 105 1.6× 40 535
Sarah Al–Bachari United Kingdom 9 77 0.7× 182 1.9× 110 1.4× 120 1.6× 110 1.7× 14 468
Niranjanan Nirmalananthan United Kingdom 11 293 2.5× 177 1.9× 29 0.4× 49 0.7× 159 2.4× 23 537

Countries citing papers authored by Adel Misk

Since Specialization
Citations

This map shows the geographic impact of Adel Misk'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 Adel Misk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Adel Misk more than expected).

Fields of papers citing papers by Adel Misk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Adel Misk. 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 Adel Misk. The network helps show where Adel Misk may publish in the future.

Co-authorship network of co-authors of Adel Misk

This figure shows the co-authorship network connecting the top 25 collaborators of Adel Misk. A scholar is included among the top collaborators of Adel Misk 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 Adel Misk. Adel Misk is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

6 of 6 papers shown
2.
Damiano, John A., Zaid Afawi, Melanie Bahlo, et al.. (2015). Mutation of the nuclear lamin geneLMNB2in progressive myoclonus epilepsy with early ataxia. Human Molecular Genetics. 24(16). 4483–4490. 35 indexed citations
3.
Lossos, Alexander, Giovanni Stévanin, Marion Gaussen, et al.. (2015). Fe/S protein assembly gene IBA57 mutation causes hereditary spastic paraplegia. Neurology. 84(7). 659–667. 56 indexed citations
4.
Herzallah, Mohammad M., et al.. (2010). Depression Impairs Learning Whereas Anticholinergics Impair Transfer Generalization in Parkinson Patients Tested on Dopaminergic Medications. Cognitive and Behavioral Neurology. 23(2). 98–105. 19 indexed citations
5.
Tomkins‐Netzer, Oren, Ilan Shelef, Adel Misk, et al.. (2007). Blood-brain barrier disruption in post-traumatic epilepsy. Journal of Neurology Neurosurgery & Psychiatry. 79(7). 774–777. 184 indexed citations
6.
Afawi, Zaid, Amos D. Korczyn, Adel Misk, et al.. (2007). Founder Effect with Variable Age at Onset in Arab Families with Lafora Disease and EPM2A Mutation. Epilepsia. 48(5). 1011–1014. 17 indexed citations

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.

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