Salia Bamba - Faculté de Médecine et d'Odontostomatologie, USTTB

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论文共 11 篇作者统计合作学者相似作者

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Case Report: Novel Variants Cause Developmental and Epileptic Encephalopathy in Three Unrelated Families from Mali

Salia Bamba, Lala Sidibé,Seybou H Diallo,Lassana Cissé,Kékouta Dembélé,Abdoulaye Yalcouyé,Weizhen Ji, Mohamed Emile Dembélé,Salimata Diarra, Alassane Dit Baneye Maiga,Oumou Traoré,Salimata Diallo, Samuel Ephrata Mefoung,Amadou Touré, Adama Koné,Lauren Jeffries,Cheick O Guinto,Emily K Mis,Kenneth H Fischbeck, Mustafa K Khokha,Saquib A Lakhani,Guida Landouré

Frontiers in genetics (2024): 1412442-1412442

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A Novel De Novo Variant in the RUNX2 Gene Causes Cleidocranial Dysplasia in a Malian Girl

Lassana Cisse,Abdoulaye Yalcouye, Kadidia Oumar Toure, Youlouza Coulibaly,Alassane Baneye Maiga,Salia Bamba,Dramane Diallo,Salimata Diarra,Abdoulaye Tamega,Oumou Traore,Mahamadou Kotioumbe, Moussa Aly Sangare,Hamidou Oumar Ba,Assiatou Simaga, Fatogoma Issa Kone,Oumar Samassekou,Amadou Kone,Cheick Oumar Guinto,Guida Landoure

Clinical Case Reports（2024）

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

Alassane Baneye Maiga, Ibrahim Pamanta,Salia Bamba,Lassana Cissé,Salimata Diarra,Sidi Touré,Abdoulaye Yalcouyé, Seydou Diallo,Salimata Diallo,Fousseyni Kané,Seybou Hassane Diallo,Hamidou Oumar Ba,Cheick Oumar Guinto,Kenneth Fischbeck,Guida Landoure,Idrissa Ahmadou Cissé, HAfrica Consortium

Molecular Genetics & Genomic Medicineno. 11 (2024): n/a-n/a

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A Novel Variant in the GNE Gene in a Malian Patient Presenting with Distal Myopathy

Mahamadou Kotioumbé,Alassane B. Maiga,Salia Bamba,Lassana Cissé,Salimata Diarra,Salimata Diallo,Abdoulaye Yalcouyé,Fousseyni Kané,Seybou H. Diallo,Dramane Coulibaly,Thomas Coulibaly,Kékouta Dembélé,Boubacar Maiga,Cheick O. Guinto,Guida Landouré

NEUROGENETICSno. 4 (2024): 487-492

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Whole Exome Sequencing Reveals Known and Candidate Genes for Hearing Impairment in Mali

Abdoulaye Yalcouyé, Isabelle Schrauwen,Oumou Traoré,Salia Bamba,Elvis Twumasi Aboagye, Anushree Acharya,Thashi Bharadwaj, Rachel Latanich,Kevin Esoh, Cesar A. Fortes-Lima,Carmen de Kock,Mario Jonas, Alassane dit Baneye Maiga, Cheick AK. Cissé, Moussa A. Sangaré,Cheick O. Guinto,Guida Landouré, Suzanne M. Leal, Ambroise Wonkam

Human Genetics and Genomics Advancespp.100391, (2024)

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

Musalula Sinkala,Gaone Retshabile,Phelelani T Mpangase,Salia Bamba, Modibo K Goita, Vicky Nembaware,Samar S M Elsheikh,Jeannine Heckmann,Kevin Esoh,Mogomotsi Matshaba,Clement A Adebamowo,Sally N Adebamowo, Ofon Elvis Amih,Ambroise Wonkam,Michele Ramsay,Nicola Mulder

medRxiv the preprint server for health sciences (2024)

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

Patra Yeetong,Mohamed E. Dembele,Monnat Pongpanich,Lassana Cisse,Chalurmpon Srichomthong,Alassane B. Maiga,Kekouta Dembele,Adjima Assawapitaksakul,Salia Bamba,Abdoulaye Yalcouye,Salimata Diarra, Samuel Ephrata Mefoung, Supphakorn Rakwongkhachon,Oumou Traore,Siraprapa Tongkobpetch,Kenneth H. Fischbeck,William A. Gahl,Cheick O. Guinto,Vorasuk Shotelersuk,Guida Landoure

MOVEMENT DISORDERSno. 1 (2024): 164-172

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Novel Variant in CADM3 Causes Charcot-Marie-Tooth Disease

Abdoulaye Yalcouye,Adriana P. Rebelo,Lassana Cisse,Lynette Rives,Salia Bamba,Joy Cogan,Kevin Esoh,Salimata Diarra, Kimberly M. Ezell,Abdoulaye Tamega,Cheick O. Guinto,Maike F. Dohrn,Rizwan Hamid,Kenneth H. Fischbeck,Stephan Zuchner,Guida Landoure

BRAIN COMMUNICATIONSno. 5 (2023)

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