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American Journal of Medical Genetics. Part A|May 16, 2019
Hereditary spastic paraplegia type 35 in a family from MaliGuida Landouré, Kékouta Dembélé, Lassana Cissé, et al.
Molecular Genetics & Genomic Medicine|June 8, 2019
A novel mutation in the GARS gene in a Malian family with Charcot-Marie-Tooth diseaseAbdoulaye Yalcouyé, Seybou H Diallo, Thomas Coulibaly, et al.
Molecular Genetics & Genomic Medicine|June 14, 2022
A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian familyAbdoulaye Yalcouyé, Oumou Traoré, Salimata Diarra, et al.
Nature Reviews. Neurology|May 23, 2025
Advancing neurogenetics in Africa: past achievements, current developments and shaping the futureGuida Landouré, Abdoulaye Yalcouyé, Salimata Diarra, et al.
Annales Medico-Psychologiques|May 21, 2020
Neuropsychiatric and socio-cultural aspects in a Malian family with spinocerebellar ataxiaSouleymane P Coulibaly, Souleymane Coulibaly, Hammadoun A Sango, et al.
Neurogenetics|August 1, 2024
A novel variant in the GNE gene in a Malian patient presenting with distal myopathyMahamadou Kotioumbé, Alassane B Maiga, Salia Bamba, et al.
Annals of Clinical and Translational Neurology|April 7, 2017
A novel mutation in KIF5A in a Malian family with spastic paraplegia and sensory lossCheick O Guinto, Salimata Diarra, Salimata Diallo, et al.
Research Square|March 18, 2024
A novel variant in the GNE gene in a Malian patient presenting with distal myopathyMahamadou Kotioumbe, Alassane B Maiga, Salia Bamba, et al.
Medicine|August 5, 2025
Unusual catecholaminergic polymorphic ventricular tachycardia and bradycardia caused by a novel triadin variant in 2 siblings from a Malian familyMamadou Diakité, Oumar Samassékou, Koudoussou O Sanni, et al.
Neurogenetics|March 11, 2025
A novel variant in ARSA causes a rare phenotype of infantile metachromatic leukodystrophy in a Malian familyAlassane Baneye Maiga, Abdoulaye Arama, Abdoulaye Yalcouyé, et al.
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