Salimata Diarra

Centre National de la Recherche Scientifique

Also affiliated with National Institutes of Health, Yale University, National Institute of Neurological Disorders and Stroke, Université des Sciences, des Techniques et des Technologies de Bamako, Institut de Recherche pour le Développement, Université Paris 1 Panthéon-Sorbonne

NeuroscienceBiochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 11 papers. Top paper: “High-depth African genomes inform human migration and health”.

High-depth African genomes inform human migration and health

Nature(2020)10.1038/s41586-020-2859-7

N/A

0.889DataRank · unranked

374 citations

Shaun Aron, Laura R. Botigué, Dhriti Sengupta, Gerrit Botha, Taoufik Bensellak +62 more

AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia

Neurobiology of Disease(2024)10.1016/j.nbd.2024.106537

N/A

0.273DataRank · unranked

5 citations

Saikat Ghosh, Lassana Cissé, Thomas Coulibaly, Abdoulaye Yalcouyé, George G. Harmison +20 more

GJB1 variants in Charcot‐Marie‐Tooth disease X‐linked type 1 in Mali

Journal of the Peripheral Nervous System(2022)10.1111/jns.12486

N/A

0.269DataRank · unranked

5 citations

Seybou Hassane Diallo, Lassana Cissé, Mamadou Karembé, Salimata Diallo, Thomas Coulibaly +8 more

Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8

Movement Disorders(2023)10.1002/mds.29654

N/A

0DataRank · unranked

24 citations

Mohamed E. Dembélé, Monnat Pongpanich, Lassana Cissé, Chalurmpon Srichomthong, Alassane Baneye Maīga +15 more

A novel variant in the spatacsin gene causing SPG11 in a Malian family

Journal of the Neurological Sciences(2020)10.1016/j.jns.2020.116675

N/A

0DataRank · unranked

12 citations

Kékouta Dembélé, Salimata Diarra, Lassana Cissé, Oumar Samassékou, A Bocoum +5 more

A Novel Splice Site Variant in COL6A1 Causes Ullrich Congenital Muscular Dystrophy in a Consanguineous Malian Family

Molecular Genetics & Genomic Medicine(2024)10.1002/mgg3.70032

N/A

0DataRank · unranked

2 citations

I.S. Pamanta, Salia Bamba, Lassana Cissé, Salimata Diarra, Sidi Touré +11 more

Genetic profile of progressive myoclonic epilepsy in Mali reveals novel findings

Frontiers in Neurology(2024)10.3389/fneur.2024.1455467

N/A

0DataRank · unranked

1 citations

Salia Bamba, Seybou Hassane Diallo, Weizhen Ji, M Dembélé, Abdoulaye Yalcouyé +18 more

A novel variant in the GNE gene in a Malian patient presenting with distal myopathy

Research Square(2024)10.21203/rs.3.rs-4004982/v1

N/A

0DataRank · unranked

1 citations

Alassane Baneye Maīga, Salia Bamba, Lassana Cissé, Salimata Diarra, Salimata Diallo +10 more

A novel variant in ARSA causes a rare phenotype of infantile metachromatic leukodystrophy in a Malian family

Neurogenetics(2025)10.1007/s10048-025-00814-x

N/A

0DataRank · unranked

2 citations

Abdoulaye Arama, Abdoulaye Yalcouyé, Mohamed Albakaye, Ji Weizhen, Salia Bamba +10 more

Friedreich ataxia in a family from Mali, West Africa

(2021)10.22541/au.161414432.28217723/v1

N/A

0DataRank · unranked

0 citations

Lassana Cissé, Hamidou O Bah, Oumar Samassékou, Assiatou Simaga, Abdoulaye Taméga +12 more

Trio exome analysis is a valuable tool for genetic diagnosis of epilepsy in Mali

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103449

N/A

0DataRank · unranked

0 citations

Lauren Jeffries, Salimata Diarra, Karamoko Nimaga, Amadou Touré, Modibo K. Goita +28 more