Richard H. Myers, PhD
Affiliations: | Neurology & Medicine | Boston University, Boston, MA, United States |
Area:
http://www.researchprofiles.collexis.com/jad/expert.asp?u_id=145Website:
http://www.bumc.bu.edu/neurology/clinicalfaculty/myers/Google:
"Richard Myers"Bio:
http://snp.bumc.bu.edu/
http://www.bumc.bu.edu/genetics/genetics-people/faculty/myers/
http://www.linkedin.com/profile/view?id=74561086&authType=name&authToken=5xAm&pvs=pp&pohelp=&trk=ndir_viewmore
Mean distance: 21373.2
Cross-listing: Alzheimer's Tree
Parents
Sign in to add mentor| Arthur Falek, PhD | grad student | 1976-1980 | Emory University School of Medicine | |
| (Chief, Human and Behavioral Genetics Laboratory) | ||||
Children
Sign in to add trainee| Jemma B. Wilk | grad student | 1998-2002 | Boston University School of Public Health and School of Medicine |
| Jian-Liang Li | grad student | 2001-2006 | Boston University |
| Jason M. Laramie | grad student | 2003-2008 | Boston University |
| Jeanne C. Latourelle | grad student | 2004-2009 | Boston University School of Public Health and School of Medicine (Epi Tree) |
| Alexandra Dumitriu | grad student | 2007-2012 | Boston University |
| Michael W. Nagle | grad student | 2011-2014 | Boston University |
| Andrew G. Hoss | grad student | 2012-2015 | Boston University |
| Adam T. Labadorf | grad student | 2013-2016 | Boston University |
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Publications
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| Nazeen S, Wang X, Zielinski D, et al. (2024) Deep sequencing of proteotoxicity modifier genes uncovers a Presenilin-2/beta-amyloid-actin genetic risk module shared among alpha-synucleinopathies. Biorxiv : the Preprint Server For Biology |
| Lai D, Alipanahi B, Fontanillas P, et al. (2021) Genome-wide association studies of LRRK2 modifiers of Parkinson's disease. Annals of Neurology |
| Raghunathan R, Hogan JD, Labadorf A, et al. (2020) A glycomics and proteomics study of aging and Parkinson's disease in human brain. Scientific Reports. 10: 12804 |
| Ellis N, Tee A, McAllister B, et al. (2019) Genetic Risk Underlying Psychiatric and Cognitive Symptoms in Huntington's Disease. Biological Psychiatry |
| Agus F, Crespo D, Myers RH, et al. (2019) The caudate nucleus undergoes dramatic and unique transcriptional changes in human prodromal Huntington's disease brain. Bmc Medical Genomics. 12: 137 |
| Lee J, Correia K, Loupe J, et al. (2019) CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset Cell. 178 |
| Wyss AB, Sofer T, Lee MK, et al. (2018) Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. Nature Communications. 9: 2976 |
| Hui KY, Fernandez-Hernandez H, Hu J, et al. (2018) Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease. Science Translational Medicine. 10 |
| Khan RR, Altmann A, Napolioni V, et al. (2018) P4-240: Stop-Gain Variant In Microglia-Expressed Gene Gmip Is Associated With Early-Onset Alzheimer'S Disease Alzheimers & Dementia. 14 |
| Bonner D, Nguyen D, Cochran JN, et al. (2018) P1-171: Mapping Enhancer Regions For Genes Associated With Neurodegenerative Diseases Alzheimers & Dementia. 14 |