Ann Singleton
Affiliations: | Educational Leadership | Union University, Jackson, TN, United States |
Area:
Reading Education, Secondary EducationGoogle:
"Ann Singleton"Children
Sign in to add traineeDeborah W. Joy | grad student | 2004 | Union University |
Eric Cohu | grad student | 2005 | Union University |
Norma S. Gerrell | grad student | 2005 | Union University |
Mary C. Alsup | grad student | 2007 | Union University |
Angela Holloway | grad student | 2007 | Union University |
Teresa J. Tritt | grad student | 2007 | Union University |
Sherlyn W. Haley | grad student | 2009 | Union University |
Kelli B. Deere | grad student | 2010 | Union University |
Christopher G. Nye | grad student | 2011 | Union University |
Mary C. Gatlin | grad student | 2012 | Union University |
LaJuana M. Hamer | grad student | 2012 | Union University |
Michele Webb | grad student | 2013 | Union University |
Kymberly M. Kelley | grad student | 2014 | Union University |
Lillian Tubbs | grad student | 2014 | Union University |
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Publications
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Orme T, Hernandez D, Ross OA, et al. (2020) Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies. Acta Neuropathologica Communications. 8: 5 |
Blauwendraat C, Reed X, Krohn L, et al. (2019) Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia. Brain : a Journal of Neurology |
Blauwendraat C, Nalls MA, Singleton AB. (2019) The genetic architecture of Parkinson's disease. The Lancet. Neurology |
Jansen IE, Gibbs JR, Nalls MA, et al. (2017) Establishing the role of rare coding variants in known Parkinson's disease risk loci. Neurobiology of Aging |
Hernandez DG, Reed X, Singleton AB. (2016) Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance. Journal of Neurochemistry |
Federoff M, Schottlaender LV, Houlden H, et al. (2015) Multiple system atrophy: the application of genetics in understanding etiology. Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society. 25: 19-36 |
Bras J, Guerreiro R, Darwent L, et al. (2014) Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies. Human Molecular Genetics. 23: 6139-46 |
Hernandez DG, Nalls MA, Ylikotila P, et al. (2012) Genome wide assessment of young onset Parkinson's disease from Finland. Plos One. 7: e41859 |
Houlden H, Singleton AB. (2012) The genetics and neuropathology of Parkinson's disease. Acta Neuropathologica. 124: 325-38 |
Simón-Sánchez J, Kilarski LL, Nalls MA, et al. (2012) Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease. Plos One. 7: e28787 |