Richard H. Myers
Richard H. Myers
Professor Emeritus, Boston University School of Medicine
Verified email at
Cited by
Cited by
Heart disease and stroke statistics 2005 update
American Heart Association
http://www. americanheart. org/statistics/, 2005
Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease: a meta-analysis
LA Farrer, LA Cupples, JL Haines, B Hyman, WA Kukull, R Mayeux, ...
Jama 278 (16), 1349-1356, 1997
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
EK Speliotes, CJ Willer, SI Berndt, KL Monda, G Thorleifsson, AU Jackson, ...
Nature genetics 42 (11), 937-948, 2010
Effectiveness of Covid-19 vaccines against the B. 1.617. 2 (Delta) variant
J Lopez Bernal, N Andrews, C Gower, E Gallagher, R Simmons, ...
New England Journal of Medicine 385 (7), 585-594, 2021
Neuropathological classification of Huntington's disease
JP Vonsattel, RH Myers, TJ Stevens, RJ Ferrante, ED Bird, ...
Journal of Neuropathology & Experimental Neurology 44 (6), 559-577, 1985
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
ME MacDonald, CM Ambrose, MP Duyao, RH Myers, C Lin, L Srinidhi, ...
Cell 72 (6), 971-983, 1993
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
Nature genetics 46 (9), 989-993, 2014
The genetic defect causing familial Alzheimer's disease maps on chromosome 21
PH St George-Hyslop, RE Tanzi, RJ Polinsky, JL Haines, L Nee, ...
Science 235 (4791), 885-890, 1987
Trinucleotide repeat length instability and age of onset in Huntington's disease
MP Duyao, CM Ambrose, RH Myers, A Novelletto, F Persichetti, M Frontali, ...
Nature genetics 4 (4), 387-392, 1993
Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations
F Soldner, J Laganière, AW Cheng, D Hockemeyer, Q Gao, R Alagappan, ...
Cell 146 (2), 318-331, 2011
Familial lipoprotein disorders in patients with premature coronary artery disease.
JJ Genest Jr, SS Martin-Munley, JR McNamara, JM Ordovas, J Jenner, ...
Circulation 85 (6), 2025-2033, 1992
CAG repeat number governs the development rate of pathology in Huntington's disease
JB Penney Jr, JP Vonsattel, ME Macdonald, JF Gusella, RH Myers
Annals of Neurology: Official Journal of the American Neurological …, 1997
Evidence for association and genetic linkage of the angiotensin-converting enzyme locus with hypertension and blood pressure in men but not women in the Framingham Heart Study
CJ O’Donnell, K Lindpaintner, MG Larson, VS Rao, JM Ordovas, ...
Circulation 97 (18), 1766-1772, 1998
Evidence for a gene influencing blood pressure on chromosome 17: genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the Framingham Heart Study
D Levy, AL DeStefano, MG Larson, CJ O’Donnell, RP Lifton, H Gavras, ...
Hypertension 36 (4), 477-483, 2000
Cerebral amyloid angiopathy without and with cerebral hemorrhages: a comparative histological study
JPG Vonsattel, RH Myers, E Tessa Hedley‐Whyte, AH Ropper, ED Bird, ...
Annals of Neurology: Official Journal of the American Neurological …, 1991
Apolipoprotein E alleles, dyslipidemia, and coronary heart disease: the Framingham Offspring Study
PWF Wilson, RH Myers, MG Larson, JM Ordovas, PA Wolf, EJ Schaefer
Jama 272 (21), 1666-1671, 1994
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database
CM Lill, JT Roehr, MB McQueen, FK Kavvoura, S Bagade, BMM Schjeide, ...
PLoS genetics 8 (3), e1002548, 2012
Genetic signatures of exceptional longevity in humans
P Sebastiani, N Solovieff, AT DeWan, KM Walsh, A Puca, SW Hartley, ...
PloS one 7 (1), e29848, 2012
Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression
F Soldner, Y Stelzer, CS Shivalila, BJ Abraham, JC Latourelle, MI Barrasa, ...
Nature 533 (7601), 95-99, 2016
Genomewide association study for susceptibility genes contributing to familial Parkinson disease
N Pankratz, JB Wilk, JC Latourelle, AL DeStefano, C Halter, EW Pugh, ...
Human genetics 124, 593-605, 2009
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