Neven Maksemous

556 total citations
28 papers, 362 citations indexed

About

Neven Maksemous is a scholar working on Molecular Biology, Psychiatry and Mental health and Neurology. According to data from OpenAlex, Neven Maksemous has authored 28 papers receiving a total of 362 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Psychiatry and Mental health and 8 papers in Neurology. Recurrent topics in Neven Maksemous's work include Migraine and Headache Studies (8 papers), Neurological diseases and metabolism (7 papers) and Cerebrovascular and genetic disorders (7 papers). Neven Maksemous is often cited by papers focused on Migraine and Headache Studies (8 papers), Neurological diseases and metabolism (7 papers) and Cerebrovascular and genetic disorders (7 papers). Neven Maksemous collaborates with scholars based in Australia, United Kingdom and France. Neven Maksemous's co-authors include Lyn R. Griffiths, Robert A. Smith, Larisa M. Haupt, Heidi G. Sutherland, Cassie L. Albury, Miles C. Benton, Rod A. Lea, Robert L. Smith, Manoj P. Menezes and Esther Tantsis and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Frontiers in Immunology.

In The Last Decade

Neven Maksemous

24 papers receiving 355 citations

Peers

Countries citing papers authored by Neven Maksemous

Since Specialization

Citations

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

Fields of papers citing papers by Neven Maksemous

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Neven Maksemous

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Gene-Based Burden Testing of Rare Variants in Hemiplegic Migraine: A Computational Approach to Uncover the Genetic Architecture of a Rare Brain Disorder 2025 ·Genes ·Majid Al-Fayyadh, Neven Maksemous, Heidi G. Sutherland, Rod A. Lea, Lyn R. Griffiths	0
2	PathVar: A Customisable NGS Variant Calling Algorithm Implicates Novel Candidate Genes and Pathways in Hemiplegic Migraine 2024 ·Clinical Genetics ·(unknown), Neven Maksemous, Heidi G. Sutherland, Rod A. Lea, Lyn R. Griffiths	2
3	Targeted exonic sequencing identifies novel variants in a cerebral small vessel disease cohort 2024 ·Clinica Chimica Acta ·(unknown), Neven Maksemous, Robert A. Smith, Heidi G. Sutherland, Larisa M. Haupt, Lyn R. Griffiths	1
4	Unravelling the Genetic Landscape of Hemiplegic Migraine: Exploring Innovative Strategies and Emerging Approaches 2024 ·Genes ·(unknown), Neven Maksemous, Heidi G. Sutherland, Rod A. Lea, Lyn R. Griffiths	3
5	Exonic mutations in cell–cell adhesion may contribute to CADASIL-related CSVD pathology 2023 ·Human Genetics ·(unknown), Rod A. Lea, Neven Maksemous, Robert A. Smith, Heidi G. Sutherland, Larisa M. Haupt, Lyn R. Griffiths	0
6	Whole Exome Sequencing of Hemiplegic Migraine Patients Shows an Increased Burden of Missense Variants in CACNA1H and CACNA1I Genes 2023 ·Molecular Neurobiology ·Neven Maksemous, Aster V. E. Harder, (unknown), Lisanne S. Vijfhuizen, Heidi G. Sutherland, Nadine Pelzer, Irene de Boer, Gisela M. Terwindt, Rod A. Lea, Arn M. J. M. van den Maagdenberg, Lyn R. Griffiths	10
7	Investigating a Genetic Link Between Alzheimer’s Disease and CADASIL-Related Cerebral Small Vessel Disease 2022 ·Molecular Neurobiology ·(unknown), Rod A. Lea, Neven Maksemous, Robert A. Smith, Heidi G. Sutherland, Larisa M. Haupt, Lyn R. Griffiths	4
8	Investigation of Mitochondrial Related Variants in a Cerebral Small Vessel Disease Cohort 2022 ·Molecular Neurobiology ·(unknown), Nicholas R. Harvey, Neven Maksemous, Robert A. Smith, Heidi G. Sutherland, Larisa M. Haupt, Lyn R. Griffiths	6
9	The MinION as a cost-effective technology for diagnostic screening of the SCN1A gene in epilepsy patients 2021 ·Epilepsy Research ·(unknown), Rod A. Lea, Neven Maksemous, David Eccles, Robert A. Smith, (unknown), (unknown), (unknown), Chi‐Bao Bui, Larisa M. Haupt, Rodney J. Scott, Lyn R. Griffiths	3
10	Exploring Neuronal Vulnerability to Head Trauma Using a Whole Exome Approach 2020 ·Journal of Neurotrauma ·(unknown), Heidi G. Sutherland, Neven Maksemous, Robert L. Smith, Larisa M. Haupt, Lyn R. Griffiths	8
11	Tiered analysis of whole-exome sequencing for epilepsy diagnosis 2020 ·Molecular Genetics and Genomics ·(unknown), Bridget H. Maher, Cassie L. Albury, Shani Stuart, Heidi G. Sutherland, Neven Maksemous, Miles C. Benton, Robert A. Smith, Larisa M. Haupt, Lyn R. Griffiths	15
12	Investigating diagnostic sequencing techniques for CADASIL diagnosis 2020 ·Human Genomics ·(unknown), Neven Maksemous, Robert A. Smith, Heidi G. Sutherland, Larisa M. Haupt, Lyn R. Griffiths	11
13	Variant Call Format–Diagnostic Annotation and Reporting Tool 2019 ·Journal of Molecular Diagnostics ·Miles C. Benton, Robert A. Smith, Larisa M. Haupt, Heidi G. Sutherland, (unknown), Cassie L. Albury, Neven Maksemous, Rod A. Lea, Lyn R. Griffiths	8
14	Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes 2018 ·Frontiers in Genetics ·(unknown), Cassie L. Albury, Neven Maksemous, Miles C. Benton, Heidi G. Sutherland, Robert A. Smith, Larisa M. Haupt, Lyn R. Griffiths	92
15	Exome Sequencing Diagnoses X-Linked Moesin-Associated Immunodeficiency in a Primary Immunodeficiency Case 2018 ·Frontiers in Immunology ·(unknown), (unknown), Cassie L. Albury, Neven Maksemous, (unknown), Robert A. Smith, Miles C. Benton, David Eccles, Rod A. Lea, Heidi G. Sutherland, Larisa M. Haupt, Lyn R. Griffiths	23
16	Next generation sequencing identifies novel CACNA1A gene mutations in Episodic Ataxia type 2 2016 ·QUT ePrints (Queensland University of Technology) ·Neven Maksemous, (unknown), Robert A. Smith, Lyn R. Griffiths	0
17	Eye movement disorders are an early manifestation of CACNA1A mutations in children 2016 ·Esther Tantsis, Deepak Gill, Lyn R. Griffiths, Sachin Gupta, John A. Lawson, Neven Maksemous, Robert Ouvrier, Florence Riant, Robert L. Smith, Christopher Troedson, Richard Webster, Manoj P. Menezes	2
18	Targeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patients 2016 ·Human Genomics ·Neven Maksemous, Robert A. Smith, Larisa M. Haupt, Lyn R. Griffiths	20
19	Eye movement disorders are an early manifestation of CACNA1A mutations in children 2016 ·Developmental Medicine & Child Neurology ·Esther Tantsis, Deepak Gill, Lyn R. Griffiths, Sachin Gupta, John A. Lawson, Neven Maksemous, Robert Ouvrier, Florence Riant, Robert L. Smith, Christopher Troedson, Richard Webster, Manoj P. Menezes	51
20	Two novel mutations and a previously unreported intronic polymorphism in the NOTCH3 gene 2012 ·Mutation research. Fundamental and molecular mechanisms of mutagenesis ·(unknown), Neven Maksemous, Robert A. Smith, Shruti Menon, Gail Davies, Lyn R. Griffiths	13

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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