Mark F. Bennett

2.7k total citations
27 papers, 401 citations indexed

About

Mark F. Bennett is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Mark F. Bennett has authored 27 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 13 papers in Genetics and 7 papers in Psychiatry and Mental health. Recurrent topics in Mark F. Bennett's work include Genetics and Neurodevelopmental Disorders (10 papers), Epilepsy research and treatment (7 papers) and Genomics and Rare Diseases (6 papers). Mark F. Bennett is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Epilepsy research and treatment (7 papers) and Genomics and Rare Diseases (6 papers). Mark F. Bennett collaborates with scholars based in Australia, United States and Canada. Mark F. Bennett's co-authors include Melanie Bahlo, Samuel F. Berkovic, Ingrid E. Scheffer, Karen Oliver, Rick M. Tankard, Paul J. Lockhart, Martin B. Delatycki, Bronwyn E. Grinton, A. Melatos and P. D. Lasky and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Astrophysical Journal and Neurology.

In The Last Decade

Mark F. Bennett

22 papers receiving 400 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark F. Bennett Australia 10 200 182 142 52 42 27 401
Su-Chin Ho Singapore 13 228 1.1× 62 0.3× 130 0.9× 8 0.2× 63 1.5× 16 730
Lucia Abela Switzerland 13 259 1.3× 83 0.5× 43 0.3× 40 0.8× 32 0.8× 22 438
Shruti Bagla United States 11 262 1.3× 46 0.3× 83 0.6× 77 1.5× 15 0.4× 19 449
Flip Mulder Netherlands 11 279 1.4× 285 1.6× 23 0.2× 72 1.4× 13 0.3× 13 581
Deborah L. Renaud United States 11 233 1.2× 79 0.4× 51 0.4× 29 0.6× 180 4.3× 41 470
Katsuhito Yasuno United States 12 274 1.4× 146 0.8× 100 0.7× 2 0.0× 134 3.2× 17 538
Elisa Rahikkala Finland 9 163 0.8× 81 0.4× 37 0.3× 17 0.3× 19 0.5× 38 269
Takehiko Inui Japan 13 194 1.0× 116 0.6× 46 0.3× 126 2.4× 35 0.8× 48 459
A Bellan-Koch Germany 7 269 1.3× 120 0.7× 125 0.9× 111 2.1× 14 0.3× 7 408
Kodai Kume Japan 11 166 0.8× 22 0.1× 103 0.7× 16 0.3× 98 2.3× 34 347

Countries citing papers authored by Mark F. Bennett

Since Specialization
Citations

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

Fields of papers citing papers by Mark F. Bennett

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark F. Bennett. 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 Mark F. Bennett. The network helps show where Mark F. Bennett may publish in the future.

Co-authorship network of co-authors of Mark F. Bennett

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

All Works

20 of 20 papers shown
1.
Gambardella, Antonio, Yu‐Chi Liu, Mark F. Bennett, et al.. (2025). PAK3 pathogenic variant associated with sleep‐related hypermotor epilepsy in a family with parental mosaicism. Epilepsia Open. 10(2). 593–601.
2.
Chiu, Annie Ting Gee, Mark F. Bennett, Amy Schneider, et al.. (2025). Pathogenic Variants in RNU2‐2 , a Non‐coding Spliceosomal RNA , Cause a Distinctive Developmental and Epileptic Encephalopathy. Annals of Neurology. 99(1). 51–58. 1 indexed citations
3.
Valles‐Ibáñez, Guillem de, et al.. (2024). SCN8A self‐limited infantile epilepsy: Does epilepsy resolve?. Epilepsia. 65(8). e156–e162.
4.
Silveira, Isabel & Mark F. Bennett. (2023). Pentanucleotide repeat‐related disorders: Genetics and bioinformatic discovery and detection. Epilepsia. 64(S1). S22–S30.
5.
Hildebrand, Michael S., Guillem de Valles‐Ibáñez, Zimeng Ye, et al.. (2023). Leveraging multiple approaches for the detection of pathogenic deep intronic variants in developmental and epileptic encephalopathies: A case report. Epilepsia Open. 9(2). 758–764. 1 indexed citations
6.
Bennett, Mark F., Ilka Immisch, Jeremy L. Freeman, et al.. (2023). Mosaic variants detectable in blood extend the clinicogenetic spectrum of GLI3-related hypothalamic hamartoma. SHILAP Revista de lepidopterología. 1(1). 100810–100810. 2 indexed citations
7.
Oliver, Karen, Ingrid E. Scheffer, Mark F. Bennett, et al.. (2023). Genes4Epilepsy: An epilepsy gene resource. Epilepsia. 64(5). 1368–1375. 60 indexed citations
8.
Brown, Natasha J., M. De Silva, Mark F. Bennett, et al.. (2023). Improving genetic diagnostic yield in a large cohort of children with rare vascular anomalies or PIK3CA-related overgrowth spectrum. Genetics in Medicine Open. 2. 100837–100837.
9.
Rafehi, Haloom, Mark F. Bennett, & Melanie Bahlo. (2023). Detection and discovery of repeat expansions in ataxia enabled by next-generation sequencing: present and future. Emerging Topics in Life Sciences. 7(3). 349–359. 4 indexed citations
10.
Schimmel, Mareike, Susanna Schubert, Johannes R. Lemke, et al.. (2022). Bi-allelic SMO variants in hypothalamic hamartoma: a recessive cause of Pallister-Hall syndrome. European Journal of Human Genetics. 30(3). 384–388. 6 indexed citations
11.
Grinton, Bronwyn E., Liam G. Fearnley, Ingrid E. Scheffer, et al.. (2022). A founder event causing a dominant childhood epilepsy survives 800 years through weak selective pressure. The American Journal of Human Genetics. 109(11). 2080–2087. 3 indexed citations
12.
Ye, Zimeng, Mark F. Bennett, Andrew Neal, et al.. (2022). Somatic Mosaic Pathogenic Variant Gradient Detected in Trace Brain Tissue From Stereo-EEG Depth Electrodes. Neurology. 99(23). 1036–1041. 20 indexed citations
13.
Fearnley, Liam G., Mark F. Bennett, & Melanie Bahlo. (2022). Detection of repeat expansions in large next generation DNA and RNA sequencing data without alignment. Scientific Reports. 12(1). 13124–13124. 9 indexed citations
14.
Bagnall, Richard D., Mark F. Bennett, A. Marie Phillips, et al.. (2021). Loss‐of‐function variants in Kv11.1 cardiac channels as a biomarker for SUDEP. Annals of Clinical and Translational Neurology. 8(7). 1422–1432. 9 indexed citations
15.
Myers, Kenneth A., Mark F. Bennett, Bronwyn E. Grinton, et al.. (2021). Contribution of rare genetic variants to drug response in absence epilepsy. Epilepsy Research. 170. 106537–106537. 7 indexed citations
16.
Myers, Kenneth A., Mark F. Bennett, Michael S. Hildebrand, et al.. (2020). Transcriptome analysis of a ring chromosome 20 patient cohort. Epilepsia. 62(1). e22–e28. 3 indexed citations
17.
Bennett, Mark F., Karen Oliver, Brigid M. Regan, et al.. (2020). Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian families. European Journal of Human Genetics. 28(7). 973–978. 22 indexed citations
18.
Dolzhenko, Egor, Mark F. Bennett, Phillip A. Richmond, et al.. (2020). ExpansionHunter Denovo: a computational method for locating known and novel repeat expansions in short-read sequencing data. Genome biology. 21(1). 102–102. 95 indexed citations
19.
Yeetong, Patra, Chaipat Chunharas, Monnat Pongpanich, et al.. (2020). Founder effect of the TTTCA repeat insertions in SAMD12 causing BAFME1. European Journal of Human Genetics. 29(2). 343–348. 14 indexed citations
20.
Tankard, Rick M., et al.. (2018). Detecting Expansions of Tandem Repeats in Cohorts Sequenced with Short-Read Sequencing Data. The American Journal of Human Genetics. 103(6). 858–873. 68 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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