Year |
Citation |
Score |
2015 |
Zukosky K, Meilleur K, Traynor BJ, Dastgir J, Medne L, Devoto M, Collins J, Rooney J, Zou Y, Yang ML, Gibbs JR, Meier M, Stetefeld J, Finkel RS, Schessl J, et al. Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family. Jama Neurology. 72: 689-98. PMID 25938801 DOI: 10.1001/Jamaneurol.2015.37 |
0.302 |
|
2013 |
Landouré G, Mochel F, Meilleur K, Ly M, Sangaré M, Bocoum N, Bagayoko K, Coulibaly T, Sarr AM, Bâ HO, Coulibaly S, Guinto CO, Touré M, Traoré M, Fischbeck KH. Novel mutation in the ATM gene in a Malian family with ataxia telangiectasia. Journal of Neurology. 260: 324-6. PMID 23142947 DOI: 10.1007/s00415-012-6738-5 |
0.311 |
|
2011 |
Meilleur KG, Coulibaly S, Traoré M, Landouré G, La Pean A, Sangaré M, Mochel F, Traoré S, Fischbeck KH, Han HR. Genetic testing and counseling for hereditary neurological diseases in Mali. Journal of Community Genetics. 2: 33-42. PMID 22109722 DOI: 10.1007/S12687-011-0038-0 |
0.412 |
|
2011 |
Traoré M, Coulibaly T, Meilleur KG, La Pean A, Sangaré M, Landouré G, Mochel F, Karambé M, Guinto CO, Fischbeck KH. Clinical and genetic analysis of spinocerebellar ataxia in Mali. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 18: 1269-71. PMID 21418439 DOI: 10.1111/J.1468-1331.2011.03376.X |
0.396 |
|
2010 |
Meilleur KG, Traoré M, Sangaré M, Britton A, Landouré G, Coulibaly S, Niaré B, Mochel F, La Pean A, Rafferty I, Watts C, Shriner D, Littleton-Kearney MT, Blackstone C, Singleton A, et al. Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19. Neurogenetics. 11: 313-8. PMID 20039086 DOI: 10.1007/S10048-009-0230-0 |
0.445 |
|
2009 |
Traoré M, Landouré G, Motley W, Sangaré M, Meilleur K, Coulibaly S, Traoré S, Niaré B, Mochel F, La Pean A, Vortmeyer A, Mani H, Fischbeck KH. Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora disease. Neurogenetics. 10: 319-23. PMID 19322595 DOI: 10.1007/S10048-009-0190-4 |
0.33 |
|
2009 |
Meilleur KG, Littleton-Kearney MT. Interventions to improve patient education regarding multifactorial genetic conditions: a systematic review. American Journal of Medical Genetics. Part A. 149: 819-30. PMID 19291763 DOI: 10.1002/Ajmg.A.32723 |
0.447 |
|
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