Katherine G. Meilleur, Ph.D. - Publications

2009 Johns Hopkins University, Baltimore, MD 
Nursing, Genetics, Neuroscience Biology

9 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Meilleur KG, Jain MS, Hynan LS, Shieh CY, Kim E, Waite M, McGuire M, Fiorini C, Glanzman AM, Main M, Rose K, Duong T, Bendixen R, Linton MM, Arveson IC, et al. Results of a two-year pilot study of clinical outcome measures in collagen VI- and laminin alpha2-related congenital muscular dystrophies. Neuromuscular Disorders : Nmd. 25: 43-54. PMID 25307854 DOI: 10.1016/j.nmd.2014.09.010  1
2014 Vuillerot C, Meilleur KG, Jain M, Waite M, Wu T, Linton M, Datsgir J, Donkervoort S, Leach ME, Rutkowski A, Rippert P, Payan C, Iwaz J, Hamroun D, Bérard C, et al. English cross-cultural translation and validation of the neuromuscular score: a system for motor function classification in patients with neuromuscular diseases. Archives of Physical Medicine and Rehabilitation. 95: 2064-2070.e1. PMID 24862765 DOI: 10.1016/j.apmr.2014.05.003  1
2014 Meilleur KG, Zukosky K, Medne L, Fequiere P, Powell-Hamilton N, Winder TL, Alsaman A, El-Hattab AW, Dastgir J, Hu Y, Donkervoort S, Golden JA, Eagle R, Finkel R, Scavina M, et al. Clinical, pathologic, and mutational spectrum of dystroglycanopathy caused by LARGE mutations. Journal of Neuropathology and Experimental Neurology. 73: 425-41. PMID 24709677 DOI: 10.1097/NEN.0000000000000065  1
2014 Sangaré M, Hendrickson B, Sango HA, Chen K, Nofziger J, Amara A, Dutra A, Schindler AB, Guindo A, Traoré M, Harmison G, Pak E, Yaro FN, Bricceno K, Grunseich C, ... ... Meilleur KG, et al. Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa. Annals of Neurology. 75: 525-32. PMID 24515897 DOI: 10.1002/ana.24114  1
2013 Landouré G, Zhu PP, Lourenço CM, Johnson JO, Toro C, Bricceno KV, Rinaldi C, Meilleur KG, Sangaré M, Diallo O, Pierson TM, Ishiura H, Tsuji S, Hein N, Fink JK, et al. Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12. Human Mutation. 34: 1357-60. PMID 23857908 DOI: 10.1002/humu.22378  1
2012 Adeyemo A, Bentley AR, Meilleur KG, Doumatey AP, Chen G, Zhou J, Shriner D, Huang H, Herbert A, Gerry NP, Christman MF, Rotimi CN. Transferability and fine mapping of genome-wide associated loci for lipids in African Americans. Bmc Medical Genetics. 13: 88. PMID 22994408 DOI: 10.1186/1471-2350-13-88  1
2010 Meilleur KG, Doumatey A, Huang H, Charles B, Chen G, Zhou J, Shriner D, Adeyemo A, Rotimi C. Circulating adiponectin is associated with obesity and serum lipids in West Africans. The Journal of Clinical Endocrinology and Metabolism. 95: 3517-21. PMID 20382687 DOI: 10.1210/jc.2009-2765  1
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  1
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  1
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