Salia Bamba

Also affiliated with Yale University, Université des Sciences, des Techniques et des Technologies de Bamako

NeuroscienceMedicineBiochemistry, Genetics and Molecular Biology

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 9 papers. Top paper: “Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8”.

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

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

0DataRank · unranked

5 citations

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

Whole-exome sequencing reveals known and candidate genes for hearing impairment in Mali

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100391

N/A

0DataRank · unranked

1 citations

Isabelle Schrauwen, Oumou Traoré, Salia Bamba, Elvis Twumasi Aboagye, Anushree Acharya +14 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

Mapping Epigenetic Gene Variant Dynamics: Comparative Analysis of Frequency, Functional Impact and Trait Associations in African and European Populations

medRxiv(2024)10.1101/2024.08.11.24311816

N/A

0DataRank · unranked

0 citations

Gaone Retshabile, Phelelani Thokozani Mpangase, Salia Bamba, Modibo K. Goita, Victoria Nembaware +11 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

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