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Richard H. Myers
Richard H. Myers
Professor Emeritus, Boston University School of Medicine
Bestätigte E-Mail-Adresse bei bu.edu
Titel
Zitiert von
Zitiert von
Jahr
Heart disease and stroke statistics 2005 update
American Heart Association
http://www. americanheart. org/statistics/, 2005
8560*2005
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
73251993
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
53371997
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
35172010
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
30601985
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
19912014
Effectiveness of Covid-19 vaccines against the B. 1.617. 2 (Delta) variant
JL Bernal, N Andrews, C Gower, E Gallagher, R Simmons, S Thelwall, ...
The New England journal of medicine, 2021
19252021
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
16301987
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
13671993
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
9262011
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
9251992
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
7541998
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
7401997
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
7342000
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
6571991
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
6431994
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
6122012
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
5852012
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
5412016
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
5292009
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