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Brain Communications|December 11, 2023
Novel variant in CADM3 causes Charcot-Marie-Tooth diseaseAbdoulaye Yalcouyé, Adriana P Rebelo, Lassana Cissé, et al.Molecular Genetics & Genomic Medicine|November 11, 2024
A Novel Splice Site Variant in COL6A1 Causes Ullrich Congenital Muscular Dystrophy in a Consanguineous Malian FamilyAlassane Baneye Maiga, Ibrahim Pamanta, Salia Bamba, et al.Brain and Behavior|May 5, 2025
Rare Variants Cause Charcot-Marie-Tooth Disease in Malian FamiliesAbdoulaye Yalcouyé, Lassana Cissé, Salimata Diarra, et al.Acta Neurologica Belgica|November 17, 2022
Hereditary spastic paraplegia in Mali: epidemiological and clinical featuresSalimata Diarra, Thomas Coulibaly, Kékouta Dembélé, et al.Clinical Case Reports|June 4, 2021
Friedreich ataxia in a family from Mali, West Africa/Friedreich ataxia in a Malian familyCheick A K Cissé, Lassana Cissé, Hamidou O Ba, et al.Clinical Case Reports|February 28, 2024
A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girlLassana Cissé, Abdoulaye Yalcouyé, Kadidia Oumar Touré, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 23, 2023
Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8Patra Yeetong, Mohamed E Dembélé, Monnat Pongpanich, et al.Frontiers in Genetics|December 3, 2024
Case report: Novel variants cause developmental and epileptic encephalopathy in three unrelated families from MaliSalia Bamba, Lala Sidibé, Seybou H Diallo, et al.Journal of Huntington'S Disease|March 21, 2022
Clinical and Genetic Aspects of Huntington's Disease in the Malian PopulationAbdoulaye Bocoum, Toumany Coulibaly, Madani Ouologuem, et al.Frontiers in Neurology|October 10, 2024
Genetic profile of progressive myoclonic epilepsy in Mali reveals novel findingsLassana Cissé, Salia Bamba, Seybou H Diallo, et al.Pageof 3