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Mohammed M Alfayyadh

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Genes|July 29, 2025
Gene-Based Burden Testing of Rare Variants in Hemiplegic Migraine: A Computational Approach to Uncover the Genetic Architecture of a Rare Brain DisorderMohammed M Alfayyadh, Neven Maksemous, Heidi G Sutherland, et al.
Genes|April 27, 2024
Unravelling the Genetic Landscape of Hemiplegic Migraine: Exploring Innovative Strategies and Emerging ApproachesMohammed M Alfayyadh, Neven Maksemous, Heidi G Sutherland, et al.
Computers in Biology and Medicine|April 25, 2026
Machine learning-based prediction of Familial Hemiplegic Migraine risk from genetic variantsMohammed M Alfayyadh, Neven Maksemous, Heidi G Sutherland, et al.
Clinical Genetics|October 12, 2024
PathVar: A Customisable NGS Variant Calling Algorithm Implicates Novel Candidate Genes and Pathways in Hemiplegic MigraineMohammed M Alfayyadh, Neven Maksemous, Heidi G Sutherland, et al.
Genomics|April 8, 2026
Identification of case-specific copy number variants reveals novel genetic insights into familial hemiplegic migraine pathogenesisMohammed M Alfayyadh, Thais Zielke, Neven Maksemous, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Genes|July 29, 2025
Gene-Based Burden Testing of Rare Variants in Hemiplegic Migraine: A Computational Approach to Uncover the Genetic Architecture of a Rare Brain DisorderMohammed M Alfayyadh, Neven Maksemous, Heidi G Sutherland, et al.
Genes|April 27, 2024
Unravelling the Genetic Landscape of Hemiplegic Migraine: Exploring Innovative Strategies and Emerging ApproachesMohammed M Alfayyadh, Neven Maksemous, Heidi G Sutherland, et al.
Computers in Biology and Medicine|April 25, 2026
Machine learning-based prediction of Familial Hemiplegic Migraine risk from genetic variantsMohammed M Alfayyadh, Neven Maksemous, Heidi G Sutherland, et al.
Clinical Genetics|October 12, 2024
PathVar: A Customisable NGS Variant Calling Algorithm Implicates Novel Candidate Genes and Pathways in Hemiplegic MigraineMohammed M Alfayyadh, Neven Maksemous, Heidi G Sutherland, et al.
Genomics|April 8, 2026
Identification of case-specific copy number variants reveals novel genetic insights into familial hemiplegic migraine pathogenesisMohammed M Alfayyadh, Thais Zielke, Neven Maksemous, et al.
Pageof 1