Abdoulaye Yalcouyé

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 18 papers. Top paper: “AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia”.

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

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

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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

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0.269DataRank · unranked

5 citations

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

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0.104DataRank · unranked

1 citations

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

Friedreich ataxia in a family from Mali, West Africa

(2021)10.22541/au.161414432.28217723/v1

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0DataRank · unranked

0 citations

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

Current profile of Charcot‐Marie‐Tooth disease in Africa: A systematic review

Journal of the Peripheral Nervous System(2022)10.1111/jns.12489

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0DataRank · unranked

22 citations

Kevin Esoh, Guida Landouré, Ambroise Wonkam, Abdoulaye Yalcouyé

The Implementation of Laboratory Information Management System in Multi-Site Genetics Study in Africa: The Challenges and Up-Scaling Opportunities

Journal of Molecular Pathology(2022)10.3390/jmp3040022

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0DataRank · unranked

11 citations

Chandre Oosterwyk, Dominique Anderson, Samuel Mawuli Adadey, Khuthala Mnika, Noluthando Manyisa +13 more

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

Movement Disorders(2023)10.1002/mds.29654

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0DataRank · unranked

24 citations

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

Human genetics and genomics as a unifying factor for harmony and progress in Africa: a report from the 12th African Society of Human Genetics meeting in Bamako, Mali

Pan African Medical Journal(2024)10.11604/pamj.2024.49.19.41189

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0DataRank · unranked

1 citations

Abdoulaye Yalcouyé, Djénéba Dabitao, Oumar Samassékou, Victoria Nembaware, Fousseyni Kané +10 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

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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

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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

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0DataRank · unranked

1 citations

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

Parasite-resistant variants in African genomes: implications for global genetic medicine

Trends in Parasitology(2025)10.1016/j.pt.2025.05.007

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0DataRank · unranked

2 citations

Abdoulaye Yalcouyé, Ambroise Wonkam, Kevin Esoh

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

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0DataRank · unranked

2 citations

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

Exome sequencing revealed a novel homozygous variant in TRMT61 A in a multiplex family with atypical Cornelia de Lange Syndrome from Rwanda

BMC Medical Genomics(2025)10.1186/s12920-025-02153-0

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0DataRank · unranked

1 citations

Abdoulaye Yalcouyé, Elvis Twumasi Aboagye, Lettilia Xhakaza, Kalinka Popel, Norbert Dukuze +7 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

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0DataRank · unranked

12 citations

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

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0DataRank · unranked

0 citations

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

Hearing loss and brain disorders: A review of multiple pathologies

Open Medicine(2021)10.1515/med-2021-0402

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0DataRank · unranked

16 citations

Kili James, Abdoulaye Yalcouyé, Ambroise Wonkam, Oluwafemi Gabriel Oluwole

Etiologies of Childhood Hearing Impairment in Schools for the Deaf in Mali

Frontiers in Pediatrics(2021)10.3389/fped.2021.726776

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0DataRank · unranked

11 citations

Oumou Traoré, Abdoulaye Taméga, Alassane Baneye Maīga, Fousseyni Kané, Oluwafemi G. Oluwole +7 more