| Year |
Citation |
Score |
| 2024 |
Nazeen S, Wang X, Zielinski D, Lam I, Hallacli E, Xu P, Ethier E, Strom R, Zanella CA, Nithianandam V, Ritter D, Henderson A, Saurat N, Afroz J, Nutter-Upham A, ... ... Myers RH, et al. 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. PMID 38496508 DOI: 10.1101/2024.03.03.583145 |
0.314 |
|
| 2021 |
Lai D, Alipanahi B, Fontanillas P, Schwantes-An TH, Aasly J, Alcalay RN, Beecham GW, Berg D, Bressman S, Brice A, Brockman K, Clark L, Cookson M, Das S, Van Deerlin V, ... ... Myers RH, et al. Genome-wide association studies of LRRK2 modifiers of Parkinson's disease. Annals of Neurology. PMID 33938021 DOI: 10.1002/ana.26094 |
0.69 |
|
| 2020 |
Raghunathan R, Hogan JD, Labadorf A, Myers RH, Zaia J. A glycomics and proteomics study of aging and Parkinson's disease in human brain. Scientific Reports. 10: 12804. PMID 32733076 DOI: 10.1038/S41598-020-69480-3 |
0.736 |
|
| 2019 |
Ellis N, Tee A, McAllister B, Massey T, McLauchlan D, Stone T, Correia K, Loupe J, Kim KH, Barker D, Hong EP, Chao MJ, Long JD, Lucente D, Vonsattel JPG, ... ... Myers RH, et al. Genetic Risk Underlying Psychiatric and Cognitive Symptoms in Huntington's Disease. Biological Psychiatry. PMID 32087949 DOI: 10.1016/J.Biopsych.2019.12.010 |
0.311 |
|
| 2019 |
Agus F, Crespo D, Myers RH, Labadorf A. The caudate nucleus undergoes dramatic and unique transcriptional changes in human prodromal Huntington's disease brain. Bmc Medical Genomics. 12: 137. PMID 31619230 DOI: 10.1186/S12920-019-0581-9 |
0.72 |
|
| 2019 |
Lee J, Correia K, Loupe J, Kim K, Barker D, Hong EP, Chao MJ, Long JD, Lucente D, Vonsattel JPG, Pinto RM, Elneel KA, Ramos EM, Mysore JS, Gillis T, ... ... Myers RH, et al. CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset Cell. 178. PMID 31398342 DOI: 10.1016/J.Cell.2019.06.036 |
0.379 |
|
| 2018 |
Wyss AB, Sofer T, Lee MK, Terzikhan N, Nguyen JN, Lahousse L, Latourelle JC, Smith AV, Bartz TM, Feitosa MF, Gao W, Ahluwalia TS, Tang W, Oldmeadow C, Duan Q, ... ... Myers RH, et al. Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. Nature Communications. 9: 2976. PMID 30061609 DOI: 10.1038/S41467-018-05369-0 |
0.677 |
|
| 2018 |
Hui KY, Fernandez-Hernandez H, Hu J, Schaffner A, Pankratz N, Hsu NY, Chuang LS, Carmi S, Villaverde N, Li X, Rivas M, Levine AP, Bao X, Labrias PR, Haritunians T, ... ... Myers RH, et al. Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease. Science Translational Medicine. 10. PMID 29321258 DOI: 10.1126/Scitranslmed.Aai7795 |
0.383 |
|
| 2018 |
Khan RR, Altmann A, Napolioni V, Kim Y, Guerreiro R, Bras JT, Carmona S, Pereira M, Santana I, Hardy J, Mead S, Cruchaga C, Fernandez MV, Holstege H, Flier WMVd, ... ... Myers R, et al. P4-240: Stop-Gain Variant In Microglia-Expressed Gene Gmip Is Associated With Early-Onset Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.07.061 |
0.389 |
|
| 2018 |
Bonner D, Nguyen D, Cochran JN, Partridge C, Roberts B, Myers R. P1-171: Mapping Enhancer Regions For Genes Associated With Neurodegenerative Diseases Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.175 |
0.367 |
|
| 2017 |
Labadorf A, Choi SH, Myers RH. Evidence for a Pan-Neurodegenerative Disease Response in Huntington's and Parkinson's Disease Expression Profiles. Frontiers in Molecular Neuroscience. 10: 430. PMID 29375298 DOI: 10.3389/Fnmol.2017.00430 |
0.763 |
|
| 2017 |
Reed ER, Latourelle JC, Bockholt JH, Bregu J, Smock J, Paulsen JS, Myers RH. MicroRNAs in CSF as prodromal biomarkers for Huntington disease in the PREDICT-HD study. Neurology. PMID 29282329 DOI: 10.1212/Wnl.0000000000004844 |
0.647 |
|
| 2017 |
Lee JM, Chao MJ, Harold D, Abu Elneel K, Gillis T, Holmans P, Jones L, Orth M, Myers RH, Kwak S, Wheeler VC, MacDonald ME, Gusella JF. A modifier of Huntington's disease onset at the MLH1 locus. Human Molecular Genetics. 26: 3859-3867. PMID 28934397 DOI: 10.1093/Hmg/Ddx286 |
0.434 |
|
| 2017 |
Chao MJ, Gillis T, Atwal RS, Mysore JS, Arjomand J, Harold D, Holmans P, Jones L, Orth M, Myers RH, Kwak S, Wheeler VC, MacDonald ME, Gusella JF, Lee JM. Haplotype-based stratification of Huntington's disease. European Journal of Human Genetics : Ejhg. PMID 28832564 DOI: 10.1038/Ejhg.2017.125 |
0.416 |
|
| 2017 |
Neueder A, Landles C, Ghosh R, Howland D, Myers RH, Faull RLM, Tabrizi SJ, Bates GP. The pathogenic exon 1 HTT protein is produced by incomplete splicing in Huntington's disease patients. Scientific Reports. 7: 1307. PMID 28465506 DOI: 10.1038/S41598-017-01510-Z |
0.363 |
|
| 2017 |
Choi SH, Labadorf AT, Myers RH, Lunetta KL, Dupuis J, DeStefano AL. Evaluation of logistic regression models and effect of covariates for case-control study in RNA-Seq analysis. Bmc Bioinformatics. 18: 91. PMID 28166718 DOI: 10.1186/S12859-017-1498-Y |
0.687 |
|
| 2016 |
Wake C, Labadorf A, Dumitriu A, Hoss AG, Bregu J, Albrecht KH, DeStefano AL, Myers RH. Novel microRNA discovery using small RNA sequencing in post-mortem human brain. Bmc Genomics. 17: 776. PMID 27716130 DOI: 10.1186/S12864-016-3114-3 |
0.774 |
|
| 2016 |
Trinh J, Gustavsson EK, Vilariño-Güell C, Bortnick S, Latourelle J, McKenzie MB, Tu CS, Nosova E, Khinda J, Milnerwood A, Lesage S, Brice A, Tazir M, Aasly JO, Parkkinen L, ... ... Myers RH, et al. DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study. The Lancet. Neurology. PMID 27692902 DOI: 10.1016/S1474-4422(16)30203-4 |
0.693 |
|
| 2016 |
Nagle MW, Latourelle JC, Labadorf A, Dumitriu A, Hadzi TC, Beach TG, Myers RH. The 4p16.3 Parkinson Disease Risk Locus Is Associated with GAK Expression and Genes Involved with the Synaptic Vesicle Membrane. Plos One. 11: e0160925. PMID 27508417 DOI: 10.1371/Journal.Pone.0160925 |
0.814 |
|
| 2016 |
Nielson CM, Liu CT, Smith AV, Ackert-Bicknell CL, Reppe S, Johanna J, Wassel C, Register TC, Oei L, Alonso Lopez N, Oei EH, Parimi N, Samelson EJ, Nalls MA, Zmuda J, ... ... Myers RH, et al. Novel Genetic Variants are Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SCL1A3 and EPHB2. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 27476799 DOI: 10.1002/Jbmr.2913 |
0.67 |
|
| 2016 |
Labadorf A, Hoss AG, Lagomarsino V, Latourelle JC, Hadzi TC, Bregu J, MacDonald ME, Gusella JF, Chen JF, Akbarian S, Weng Z, Myers RH. Correction: RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression. Plos One. 11: e0160295. PMID 27454300 DOI: 10.1371/journal.pone.0160295 |
0.775 |
|
| 2016 |
Soldner F, Stelzer Y, Shivalila CS, Abraham BJ, Latourelle JC, Barrasa MI, Goldmann J, Myers RH, Young RA, Jaenisch R. Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression. Nature. PMID 27096366 DOI: 10.1038/Nature17939 |
0.721 |
|
| 2016 |
Hoss AG, Labadorf A, Beach TG, Latourelle JC, Myers RH. microRNA Profiles in Parkinson's Disease Prefrontal Cortex. Frontiers in Aging Neuroscience. 8: 36. PMID 26973511 DOI: 10.3389/Fnagi.2016.00036 |
0.807 |
|
| 2016 |
Kilpeläinen TO, Carli JF, Skowronski AA, Sun Q, Kriebel J, Feitosa MF, Hedman ÅK, Drong AW, Hayes JE, Zhao J, Pers TH, Schick U, Grarup N, Kutalik Z, Trompet S, ... ... Myers RH, et al. Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels. Nature Communications. 7: 10494. PMID 26833098 DOI: 10.1038/Ncomms10494 |
0.328 |
|
| 2016 |
Dumitriu A, Golji J, Labadorf AT, Gao B, Beach TG, Myers RH, Longo KA, Latourelle JC. Integrative analyses of proteomics and RNA transcriptomics implicate mitochondrial processes, protein folding pathways and GWAS loci in Parkinson disease. Bmc Medical Genomics. 9: 5. PMID 26793951 DOI: 10.1186/S12920-016-0164-Y |
0.811 |
|
| 2016 |
Bates GP, Osborne GF, Ali N, Benjamin AC, Papadopoulou AS, Howland D, Tabrizi SJ, Faull RL, Myers RH, Landles C, Neueder A. B4 Detection of the aberrantly spliced exon 1 – intron 1 htt mRNA in HD patient post mortem brain tissue and fibroblast lines Journal of Neurology, Neurosurgery & Psychiatry. 87: A10.2-A10. DOI: 10.1136/Jnnp-2016-314597.35 |
0.309 |
|
| 2015 |
Labadorf A, Hoss AG, Lagomarsino V, Latourelle JC, Hadzi TC, Bregu J, MacDonald ME, Gusella JF, Chen JF, Akbarian S, Weng Z, Myers RH. RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression. Plos One. 10: e0143563. PMID 26636579 DOI: 10.1371/Journal.Pone.0143563 |
0.793 |
|
| 2015 |
Dong X, Tsuji J, Labadorf A, Roussos P, Chen JF, Myers RH, Akbarian S, Weng Z. The Role of H3K4me3 in Transcriptional Regulation Is Altered in Huntington's Disease. Plos One. 10: e0144398. PMID 26636336 DOI: 10.1371/Journal.Pone.0144398 |
0.719 |
|
| 2015 |
Hoss AG, Lagomarsino VN, Frank S, Hadzi TC, Myers RH, Latourelle JC. Study of plasma-derived miRNAs mimic differences in Huntington's disease brain. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 26573701 DOI: 10.1002/Mds.26457 |
0.784 |
|
| 2015 |
Labadorf AT, Myers RH. Evidence of Extensive Alternative Splicing in Post Mortem Human Brain HTT Transcription by mRNA Sequencing. Plos One. 10: e0141298. PMID 26496077 DOI: 10.1371/Journal.Pone.0141298 |
0.714 |
|
| 2015 |
Correia K, Harold D, Kim KH, Holmans P, Jones L, Orth M, Myers RH, Kwak S, Wheeler VC, MacDonald ME, Gusella JF, Lee JM. The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease. Journal of Huntington's Disease. 4: 279-84. PMID 26444025 DOI: 10.3233/Jhd-150169 |
0.365 |
|
| 2015 |
Lee JM, Kim KH, Shin A, Chao MJ, Abu Elneel K, Gillis T, Mysore JS, Kaye JA, Zahed H, Kratter IH, Daub AC, Finkbeiner S, Li H, Roach JC, Goodman N, ... ... Myers RH, et al. Sequence-Level Analysis of the Major European Huntington Disease Haplotype. American Journal of Human Genetics. 97: 435-44. PMID 26320893 DOI: 10.1016/J.Ajhg.2015.07.017 |
0.419 |
|
| 2015 |
Joshi PK, Esko T, Mattsson H, Eklund N, Gandin I, Nutile T, Jackson AU, Schurmann C, Smith AV, Zhang W, Okada Y, Stančáková A, Faul JD, Zhao W, Bartz TM, ... ... Myers RH, et al. Directional dominance on stature and cognition in diverse human populations. Nature. 523: 459-62. PMID 26131930 DOI: 10.1038/Nature14618 |
0.322 |
|
| 2015 |
Hoss AG, Labadorf A, Latourelle JC, Kartha VK, Hadzi TC, Gusella JF, MacDonald ME, Chen JF, Akbarian S, Weng Z, Vonsattel JP, Myers RH. miR-10b-5p expression in Huntington's disease brain relates to age of onset and the extent of striatal involvement. Bmc Medical Genomics. 8: 10. PMID 25889241 DOI: 10.1186/S12920-015-0083-3 |
0.774 |
|
| 2015 |
Bai G, Cheung I, Shulha HP, Coelho JE, Li P, Dong X, Jakovcevski M, Wang Y, Grigorenko A, Jiang Y, Hoss A, Patel K, Zheng M, Rogaev E, Myers RH, et al. Epigenetic dysregulation of hairy and enhancer of split 4 (HES4) is associated with striatal degeneration in postmortem Huntington brains. Human Molecular Genetics. 24: 1441-56. PMID 25480889 DOI: 10.1093/Hmg/Ddu561 |
0.787 |
|
| 2015 |
DiMucci D, Ivison R, Jenkins D, Dumitriu A, Labadorf A, Wake C, Benson G, Myers RH. Identifying allele specific expression in Parkinson's disease brain tissue F1000research. 4. DOI: 10.7490/F1000Research.1110302.1 |
0.799 |
|
| 2015 |
Lee JM, Wheeler VC, Chao MJ, Vonsattel JPG, Pinto RM, Lucente D, Abu-Elneel K, Ramos EM, Mysore JS, Gillis T, MacDonald ME, Gusella JF, Harold D, Stone TC, Escott-Price V, ... ... Myers RH, et al. Identification of Genetic Factors that Modify Clinical Onset of Huntington's Disease Cell. 162: 516-526. DOI: 10.1016/J.Cell.2015.07.003 |
0.402 |
|
| 2014 |
Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, DeStefano AL, Kara E, Bras J, Sharma M, Schulte C, Keller MF, Arepalli S, Letson C, Edsall C, ... ... Myers RH, et al. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nature Genetics. 46: 989-93. PMID 25064009 DOI: 10.1038/Ng.3043 |
0.414 |
|
| 2014 |
Hoss AG, Kartha VK, Dong X, Latourelle JC, Dumitriu A, Hadzi TC, Macdonald ME, Gusella JF, Akbarian S, Chen JF, Weng Z, Myers RH. MicroRNAs located in the Hox gene clusters are implicated in huntington's disease pathogenesis. Plos Genetics. 10: e1004188. PMID 24586208 DOI: 10.1371/Journal.Pgen.1004188 |
0.776 |
|
| 2014 |
Hendricks AE, Dupuis J, Logue MW, Myers RH, Lunetta KL. Correction for multiple testing in a gene region. European Journal of Human Genetics : Ejhg. 22: 414-8. PMID 23838599 DOI: 10.1038/Ejhg.2013.144 |
0.339 |
|
| 2014 |
Jones L, Gusella J, MacDonald M, Wheeler V, Lee J, Myers R, Latourelle J, Harold D, Holmans P, Orth M, Kwak S. A03 Genetic Modifiers Affecting The Age At Motor Onset In Huntington’s Disease Journal of Neurology, Neurosurgery, and Psychiatry. 85. DOI: 10.1136/Jnnp-2014-309032.3 |
0.707 |
|
| 2013 |
Pichler I, Del Greco M F, Gögele M, Lill CM, Bertram L, Do CB, Eriksson N, Foroud T, Myers RH, Nalls M, Keller MF, Benyamin B, et al. Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study. Plos Medicine. 10: e1001462. PMID 23750121 DOI: 10.1371/Journal.Pmed.1001462 |
0.38 |
|
| 2013 |
Ramos EM, Latourelle JC, Gillis T, Mysore JS, Squitieri F, Di Pardo A, Di Donato S, Gellera C, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Gomez-Tortosa E, Ayuso C, ... ... Myers RH, et al. Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset. Neurogenetics. 14: 173-9. PMID 23644918 DOI: 10.1007/S10048-013-0364-Y |
0.696 |
|
| 2013 |
Dumitriu A, Myers RH, McKee A, Seshadri S, Destefano A. P1-067: RNA-sequencing evaluation of fresh frozen and formaldehyde-fixed prefrontal cortex brain tissue for the study of Alzheimer's disease Alzheimer's & Dementia. 9: P177-P177. DOI: 10.1016/J.Jalz.2013.05.288 |
0.618 |
|
| 2012 |
Shulha HP, Crisci JL, Reshetov D, Tushir JS, Cheung I, Bharadwaj R, Chou HJ, Houston IB, Peter CJ, Mitchell AC, Yao WD, Myers RH, Chen JF, Preuss TM, Rogaev EI, et al. Human-specific histone methylation signatures at transcription start sites in prefrontal neurons. Plos Biology. 10: e1001427. PMID 23185133 DOI: 10.1371/Journal.Pbio.1001427 |
0.336 |
|
| 2012 |
Latourelle JC, Dumitriu A, Hadzi TC, Beach TG, Myers RH. Evaluation of Parkinson disease risk variants as expression-QTLs. Plos One. 7: e46199. PMID 23071545 DOI: 10.1371/Journal.Pone.0046199 |
0.811 |
|
| 2012 |
Hadzi TC, Hendricks AE, Latourelle JC, Lunetta KL, Cupples LA, Gillis T, Mysore JS, Gusella JF, MacDonald ME, Myers RH, Vonsattel JP. Assessment of cortical and striatal involvement in 523 Huntington disease brains. Neurology. 79: 1708-15. PMID 23035064 DOI: 10.1212/Wnl.0B013E31826E9A5D |
0.65 |
|
| 2012 |
Wilk JB, Shrine NR, Loehr LR, Zhao JH, Manichaikul A, Lopez LM, Smith AV, Heckbert SR, Smolonska J, Tang W, Loth DW, Curjuric I, Hui J, Cho MH, Latourelle JC, ... ... Myers RH, et al. Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. American Journal of Respiratory and Critical Care Medicine. 186: 622-32. PMID 22837378 DOI: 10.1164/Rccm.201202-0366Oc |
0.785 |
|
| 2012 |
Ramos EM, Latourelle JC, Lee JH, Gillis T, Mysore JS, Squitieri F, Di Pardo A, Di Donato S, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Gomez-Tortosa E, Ayuso C, ... ... Myers RH, et al. Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset. Human Genetics. 131: 1833-40. PMID 22825315 DOI: 10.1007/S00439-012-1205-Z |
0.697 |
|
| 2012 |
Lee JH, Lee JM, Ramos EM, Gillis T, Mysore JS, Kishikawa S, Hadzi T, Hendricks AE, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Squitieri F, Gellera C, ... ... Myers RH, et al. TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease. Biochemical and Biophysical Research Communications. 424: 404-8. PMID 22771793 DOI: 10.1016/J.Bbrc.2012.06.120 |
0.41 |
|
| 2012 |
Dumitriu A, Latourelle JC, Hadzi TC, Pankratz N, Garza D, Miller JP, Vance JM, Foroud T, Beach TG, Myers RH. Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation. Plos Genetics. 8: e1002794. PMID 22761592 DOI: 10.1371/Journal.Pgen.1002794 |
0.823 |
|
| 2012 |
Dumitriu A, Moser C, Hadzi TC, Williamson SL, Pacheco CD, Hendricks AE, Latourelle JC, Wilk JB, Destefano AL, Myers RH. Postmortem Interval Influences α-Synuclein Expression in Parkinson Disease Brain. Parkinson's Disease. 2012: 614212. PMID 22530163 DOI: 10.1155/2012/614212 |
0.818 |
|
| 2012 |
Pankratz N, Beecham GW, DeStefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, ... ... Myers RH, et al. Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. Annals of Neurology. 71: 370-84. PMID 22451204 DOI: 10.1002/Ana.22687 |
0.731 |
|
| 2012 |
Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide BM, Schjeide LM, Meissner E, Zauft U, Allen NC, Liu T, Schilling M, Anderson KJ, Beecham G, Berg D, ... ... Myers RH, et al. Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. Plos Genetics. 8: e1002548. PMID 22438815 DOI: 10.1371/Journal.Pgen.1002548 |
0.735 |
|
| 2012 |
Lee JM, Gillis T, Mysore JS, Ramos EM, Myers RH, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Squitieri F, Griguoli A, Di Donato S, Gomez-Tortosa E, Ayuso C, et al. Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. American Journal of Human Genetics. 90: 434-44. PMID 22387017 DOI: 10.1016/J.Ajhg.2012.01.005 |
0.422 |
|
| 2012 |
Lee JM, Ramos EM, Lee JH, Gillis T, Mysore JS, Hayden MR, Warby SC, Morrison P, Nance M, Ross CA, Margolis RL, Squitieri F, Orobello S, Di Donato S, Gomez-Tortosa E, ... ... Myers RH, et al. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology. 78: 690-5. PMID 22323755 DOI: 10.1212/Wnl.0B013E318249F683 |
0.342 |
|
| 2012 |
Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, et al. Genetic signatures of exceptional longevity in humans. Plos One. 7: e29848. PMID 22279548 DOI: 10.1371/Journal.Pone.0029848 |
0.654 |
|
| 2012 |
Sebastiani P, Solovieff N, DeWan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, et al. Example of 9 clusters of genetic risk profiles in centenarians of the discovery set and 3 similar clusters in replication sets 1 and 2. Plos One. DOI: 10.1371/Journal.Pone.0029848.G008 |
0.583 |
|
| 2011 |
Pankratz N, Dumitriu A, Hetrick KN, Sun M, Latourelle JC, Wilk JB, Halter C, Doheny KF, Gusella JF, Nichols WC, Myers RH, Foroud T, DeStefano AL. Copy number variation in familial Parkinson disease. Plos One. 6: e20988. PMID 21829596 DOI: 10.1371/Journal.Pone.0020988 |
0.824 |
|
| 2011 |
Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Retraction. Science (New York, N.Y.). 333: 404. PMID 21778381 DOI: 10.1126/science.333.6041.404-a |
0.502 |
|
| 2011 |
Soldner F, Laganière J, Cheng AW, Hockemeyer D, Gao Q, Alagappan R, Khurana V, Golbe LI, Myers RH, Lindquist S, Zhang L, Guschin D, Fong LK, Vu BJ, Meng X, et al. Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations. Cell. 146: 318-31. PMID 21757228 DOI: 10.1016/J.Cell.2011.06.019 |
0.335 |
|
| 2011 |
Latourelle JC, Hendricks AE, Pankratz N, Wilk JB, Halter C, Nichols WC, Gusella JF, Destefano AL, Myers RH, Foroud T. Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 26: 2039-44. PMID 21661047 DOI: 10.1002/Mds.23781 |
0.799 |
|
| 2011 |
Dumitriu A, Pacheco CD, Wilk JB, Strathearn KE, Latourelle JC, Goldwurm S, Pezzoli G, Rochet JC, Lindquist S, Myers RH. Cyclin-G-associated kinase modifies α-synuclein expression levels and toxicity in Parkinson's disease: results from the GenePD Study. Human Molecular Genetics. 20: 1478-87. PMID 21258085 DOI: 10.1093/Hmg/Ddr026 |
0.828 |
|
| 2010 |
Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, Lango Allen H, Lindgren CM, Luan J, Mägi R, Randall JC, Vedantam S, Winkler TW, Qi L, Workalemahu T, ... ... Myers RH, et al. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nature Genetics. 42: 937-48. PMID 20935630 DOI: 10.1038/Ng.686 |
0.341 |
|
| 2010 |
Latourelle JC, Dybdahl M, Destefano AL, Myers RH, Lash TL. Estrogen-related and other disease diagnoses preceding Parkinson's disease. Clinical Epidemiology. 2: 153-70. PMID 20865113 DOI: 10.2147/Clep.S9621 |
0.769 |
|
| 2010 |
Lanoue AC, Dumitriu A, Myers RH, Soghomonian JJ. Decreased glutamic acid decarboxylase mRNA expression in prefrontal cortex in Parkinson's disease. Experimental Neurology. 226: 207-17. PMID 20832408 DOI: 10.1016/J.Expneurol.2010.09.001 |
0.687 |
|
| 2010 |
Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Genetic signatures of exceptional longevity in humans. Science (New York, N.Y.). 2010. PMID 20595579 DOI: 10.1126/Science.1190532 |
0.662 |
|
| 2010 |
Latourelle JC, Dybdahl M, Destefano AL, Myers RH, Lash TL. Risk of Parkinson's disease after tamoxifen treatment. Bmc Neurology. 10: 23. PMID 20385012 DOI: 10.1186/1471-2377-10-23 |
0.738 |
|
| 2009 |
Latourelle JC, Pankratz N, Dumitriu A, Wilk JB, Goldwurm S, Pezzoli G, Mariani CB, DeStefano AL, Halter C, Gusella JF, Nichols WC, Myers RH, Foroud T. Genomewide association study for onset age in Parkinson disease. Bmc Medical Genetics. 10: 98. PMID 19772629 DOI: 10.1186/1471-2350-10-98 |
0.84 |
|
| 2009 |
Feitosa MF, North KE, Myers RH, Pankow JS, Borecki IB. Evidence for three novel QTLs for adiposity on chromosome 2 with epistatic interactions: the NHLBI Family Heart Study. Obesity (Silver Spring, Md.). 17: 2190-5. PMID 19521348 DOI: 10.1038/Oby.2009.181 |
0.307 |
|
| 2009 |
Hendricks AE, Latourelle JC, Lunetta KL, Cupples LA, Wheeler V, MacDonald ME, Gusella JF, Myers RH. Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27-35 CAG). American Journal of Medical Genetics. Part A. 149: 1375-81. PMID 19507258 DOI: 10.1002/Ajmg.A.32901 |
0.67 |
|
| 2009 |
Swami M, Hendricks AE, Gillis T, Massood T, Mysore J, Myers RH, Wheeler VC. Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset. Human Molecular Genetics. 18: 3039-47. PMID 19465745 DOI: 10.1093/Hmg/Ddp242 |
0.379 |
|
| 2009 |
Laramie JM, Wilk JB, Williamson SL, Nagle MW, Latourelle JC, Tobin JE, Province MA, Borecki IB, Myers RH. Multiple genes influence BMI on chromosome 7q31-34: the NHLBI Family Heart Study. Obesity (Silver Spring, Md.). 17: 2182-9. PMID 19461589 DOI: 10.1038/Oby.2009.141 |
0.801 |
|
| 2009 |
Wilk JB, Chen TH, Gottlieb DJ, Walter RE, Nagle MW, Brandler BJ, Myers RH, Borecki IB, Silverman EK, Weiss ST, O'Connor GT. A genome-wide association study of pulmonary function measures in the Framingham Heart Study. Plos Genetics. 5: e1000429. PMID 19300500 DOI: 10.1371/Journal.Pgen.1000429 |
0.809 |
|
| 2009 |
Franceschini N, North KE, Arnett D, Pankow JS, Chung JH, Baird L, Leppert MF, Eckfeldt JH, Boerwinkle E, Gu CC, Lewis CE, Myers RH, Turner ST, Weder A, Kao WH, et al. The association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study. American Journal of Hypertension. 22: 552-8. PMID 19265784 DOI: 10.1038/Ajh.2009.41 |
0.349 |
|
| 2009 |
Wu J, Pankow JS, Tracy RP, North KE, Myers RH, Feitosa ME, Province MA, Borecki IB. A QTL on 12q influencing an inflammation marker and obesity in white women: the NHLBI Family Heart Study. Obesity (Silver Spring, Md.). 17: 525-31. PMID 19238141 DOI: 10.1038/Oby.2008.556 |
0.307 |
|
| 2009 |
Ma D, Feitosa MF, Wilk JB, Laramie JM, Yu K, Leiendecker-Foster C, Myers RH, Province MA, Borecki IB. Leptin is associated with blood pressure and hypertension in women from the National Heart, Lung, and Blood Institute Family Heart Study. Hypertension. 53: 473-9. PMID 19204185 DOI: 10.1161/Hypertensionaha.108.118133 |
0.756 |
|
| 2009 |
Feitosa MF, Myers RH, Pankow JS, Province MA, Borecki IB. LIPC variants in the promoter and intron 1 modify HDL-C levels in a sex-specific fashion. Atherosclerosis. 204: 171-7. PMID 19101670 DOI: 10.1016/J.Atherosclerosis.2008.09.007 |
0.351 |
|
| 2009 |
Shi G, Gu CC, Kraja AT, Arnett DK, Myers RH, Pankow JS, Hunt SC, Rao DC. Genetic effect on blood pressure is modulated by age: the Hypertension Genetic Epidemiology Network Study. Hypertension. 53: 35-41. PMID 19029486 DOI: 10.1161/Hypertensionaha.108.120071 |
0.341 |
|
| 2009 |
Pankratz N, Wilk JB, Latourelle JC, DeStefano AL, Halter C, Pugh EW, Doheny KF, Gusella JF, Nichols WC, Foroud T, Myers RH. Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Human Genetics. 124: 593-605. PMID 18985386 DOI: 10.1007/S00439-008-0582-9 |
0.815 |
|
| 2008 |
Latourelle JC, Sun M, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts RL, Guttman M, Racette BA, Perlmutter JS, Ahmed A, Shill HA, ... ... Myers RH, et al. The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study. Bmc Medicine. 6: 32. PMID 18986508 DOI: 10.1186/1741-7015-6-32 |
0.803 |
|
| 2008 |
McNicoll CF, Latourelle JC, MacDonald ME, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts RL, Guttman M, Racette BA, Perlmutter JS, Ahmed A, ... ... Myers RH, et al. Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study. Movement Disorders : Official Journal of the Movement Disorder Society. 23: 1596-601. PMID 18649400 DOI: 10.1002/Mds.22186 |
0.733 |
|
| 2008 |
DeStefano AL, Latourelle J, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts R, Guttman M, Racette BA, Perlmutter JS, Marlor L, Shill HA, ... ... Myers RH, et al. Replication of association between ELAVL4 and Parkinson disease: the GenePD study. Human Genetics. 124: 95-9. PMID 18587682 DOI: 10.1007/S00439-008-0526-4 |
0.825 |
|
| 2008 |
Tobin JE, Latourelle JC, Lew MF, Klein C, Suchowersky O, Shill HA, Golbe LI, Mark MH, Growdon JH, Wooten GF, Racette BA, Perlmutter JS, Watts R, Guttman M, Baker KB, ... ... Myers RH, et al. Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study. Neurology. 71: 28-34. PMID 18509094 DOI: 10.1212/01.Wnl.0000304051.01650.23 |
0.823 |
|
| 2008 |
Laramie JM, Wilk JB, Williamson SL, Nagle MW, Latourelle JC, Tobin JE, Province MA, Borecki IB, Myers RH. Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; the NHLBI Family Heart Study. Bmc Medical Genetics. 9: 46. PMID 18498660 DOI: 10.1186/1471-2350-9-46 |
0.791 |
|
| 2008 |
Wilk JB, Laramie JM, Latourelle JC, Williamson S, Nagle MW, Tobin JE, Foster CL, Eckfeldt JH, Province MA, Borecki IB, Myers RH. NYD-SP18 is associated with obesity in the NHLBI Family Heart Study. International Journal of Obesity (2005). 32: 930-5. PMID 18317470 DOI: 10.1038/Ijo.2008.23 |
0.785 |
|
| 2008 |
Zhang Q, Lewis CE, Wagenknecht LE, Myers RH, Pankow JS, Hunt SC, North KE, Hixson JE, Jeffrey Carr J, Shimmin LC, Borecki I, Province MA. Genome-wide admixture mapping for coronary artery calcification in African Americans: the NHLBI Family Heart Study. Genetic Epidemiology. 32: 264-72. PMID 18200599 DOI: 10.1002/Gepi.20301 |
0.328 |
|
| 2008 |
Bielinski SJ, Pankow JS, Foster CL, Miller MB, Hopkins PN, Eckfeldt JH, Hixson J, Liu Y, Register T, Myers RH, Arnett DK. Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19: the NHLBI Family Heart Study follow-up examination. Atherosclerosis. 199: 172-8. PMID 18045607 DOI: 10.1016/J.Atherosclerosis.2007.10.006 |
0.398 |
|
| 2007 |
Bielinski SJ, Pankow JS, Miller MB, Hopkins PN, Eckfeldt JH, Hixson J, Liu Y, Register T, Myers RH, Arnett DK. Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3: the NHLBI family heart study follow-up examination. Genes and Immunity. 8: 684-90. PMID 17917677 DOI: 10.1038/Sj.Gene.6364434 |
0.352 |
|
| 2007 |
Dupré N, Rivière JB, Myers RH, Provencher P, Pourcher E, Emond F, Rouleau GA. LRRK2 is not a significant cause of Parkinson's disease in French-Canadians. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 34: 333-5. PMID 17803032 DOI: 10.1017/S0317167100006776 |
0.448 |
|
| 2007 |
Wheeler VC, Persichetti F, McNeil SM, Mysore JS, Mysore SS, MacDonald ME, Myers RH, Gusella JF, Wexler NS. Factors associated with HD CAG repeat instability in Huntington disease. Journal of Medical Genetics. 44: 695-701. PMID 17660463 DOI: 10.1136/Jmg.2007.050930 |
0.319 |
|
| 2007 |
Laramie JM, Wilk JB, DeStefano AL, Myers RH. HaploBuild: an algorithm to construct non-contiguous associated haplotypes in family based genetic studies. Bioinformatics (Oxford, England). 23: 2190-2. PMID 17586827 DOI: 10.1093/Bioinformatics/Btm316 |
0.783 |
|
| 2007 |
Litvan I, Chesselet MF, Gasser T, Di Monte DA, Parker D, Hagg T, Hardy J, Jenner P, Myers RH, Price D, Hallett M, Langston WJ, Lang AE, Halliday G, Rocca W, et al. The etiopathogenesis of Parkinson disease and suggestions for future research. Part II. Journal of Neuropathology and Experimental Neurology. 66: 329-36. PMID 17483689 DOI: 10.1097/Nen.0B013E318053716A |
0.389 |
|
| 2007 |
Tobin JE, Cui J, Wilk JB, Latourelle JC, Laramie JM, McKee AC, Guttman M, Karamohamed S, DeStefano AL, Myers RH. Sepiapterin reductase expression is increased in Parkinson's disease brain tissue. Brain Research. 1139: 42-7. PMID 17270157 DOI: 10.1016/J.Brainres.2007.01.001 |
0.828 |
|
| 2007 |
Greenwood TA, Libiger O, Kardia S, Hanis C, Morrison AC, Gu CC, Rice T, Miller M, Turner ST, Myers RH, Grove J, Hsiao CF, Weder AB, Schork NJ. Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure Program. Genetic Epidemiology. 31: 195-210. PMID 17266112 DOI: 10.1002/Gepi.20202 |
0.369 |
|
| 2007 |
North KE, Franceschini N, Borecki IB, Gu CC, Heiss G, Province MA, Arnett DK, Lewis CE, Miller MB, Myers RH, Hunt SC, Freedman BI. Genotype-by-sex interaction on fasting insulin concentration: the HyperGEN study. Diabetes. 56: 137-42. PMID 17192475 DOI: 10.2337/Db06-0624 |
0.306 |
|
| 2007 |
Andresen JM, Gayán J, Djoussé L, Roberts S, Brocklebank D, Cherny SS, Cardon LR, Gusella JF, MacDonald ME, Myers RH, Housman DE, Wexler NS. The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset. Annals of Human Genetics. 71: 295-301. PMID 17181545 DOI: 10.1111/J.1469-1809.2006.00335.X |
0.334 |
|
| 2007 |
Feitosa MF, Province MA, Heiss G, Arnett DK, Myers RH, Pankow JS, Hopkins PN, Borecki IB. Evidence of QTL on 15q21 for high-density lipoprotein cholesterol: the National Heart, Lung, and Blood Institute Family Heart Study (NHLBI FHS). Atherosclerosis. 190: 232-7. PMID 16529751 DOI: 10.1016/J.Atherosclerosis.2006.02.006 |
0.309 |
|
| 2006 |
Wilk JB, Tobin JE, Suchowersky O, Shill HA, Klein C, Wooten GF, Lew MF, Mark MH, Guttman M, Watts RL, Singer C, Growdon JH, Latourelle JC, Saint-Hilaire MH, DeStefano AL, ... ... Myers RH, et al. Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age: the GenePD Study. Neurology. 67: 2206-10. PMID 17190945 DOI: 10.1212/01.Wnl.0000249149.22407.D1 |
0.801 |
|
| 2006 |
Kishikawa S, Li JL, Gillis T, Hakky MM, Warby S, Hayden M, MacDonald ME, Myers RH, Gusella JF. Brain-derived neurotrophic factor does not influence age at neurologic onset of Huntington's disease. Neurobiology of Disease. 24: 280-5. PMID 16962786 DOI: 10.1016/J.Nbd.2006.07.008 |
0.557 |
|
| 2006 |
Zeng W, Gillis T, Hakky M, Djoussé L, Myers RH, MacDonald ME, Gusella JF. Genetic analysis of the GRIK2 modifier effect in Huntington's disease. Bmc Neuroscience. 7: 62. PMID 16959037 DOI: 10.1186/1471-2202-7-62 |
0.414 |
|
| 2006 |
Li JL, Hayden MR, Warby SC, Durr A, Morrison PJ, Nance M, Ross CA, Margolis RL, Rosenblatt A, Squitieri F, Frati L, Gómez-Tortosa E, García CA, Suchowersky O, Klimek ML, ... ... Myers RH, et al. Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: the HD MAPS study. Bmc Medical Genetics. 7: 71. PMID 16914060 DOI: 10.1186/1471-2350-7-71 |
0.564 |
|
| 2006 |
Wilk JB, Myers RH, Pankow JS, Hunt SC, Leppert MF, Freedman BI, Province MA, Ellison RC. Adrenergic receptor polymorphisms associated with resting heart rate: the HyperGEN Study. Annals of Human Genetics. 70: 566-73. PMID 16907703 DOI: 10.1111/J.1469-1809.2005.00258.X |
0.614 |
|
| 2006 |
Avery CL, Freedman BI, Kraja AT, Borecki IB, Miller MB, Pankow JS, Arnett D, Lewis CE, Myers RH, Hunt SC, North KE. Genotype-by-sex interaction in the aetiology of type 2 diabetes mellitus: support for sex-specific quantitative trait loci in Hypertension Genetic Epidemiology Network participants. Diabetologia. 49: 2329-36. PMID 16906437 DOI: 10.1007/S00125-006-0375-4 |
0.323 |
|
| 2006 |
Sun M, Latourelle JC, Wooten GF, Lew MF, Klein C, Shill HA, Golbe LI, Mark MH, Racette BA, Perlmutter JS, Parsian A, Guttman M, Nicholson G, Xu G, Wilk JB, ... ... Myers RH, et al. Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study. Archives of Neurology. 63: 826-32. PMID 16769863 DOI: 10.1001/Archneur.63.6.826 |
0.779 |
|
| 2006 |
Lloret A, Dragileva E, Teed A, Espinola J, Fossale E, Gillis T, Lopez E, Myers RH, MacDonald ME, Wheeler VC. Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in mice. Human Molecular Genetics. 15: 2015-24. PMID 16687439 DOI: 10.1093/Hmg/Ddl125 |
0.341 |
|
| 2006 |
Myers RH. Considerations for genomewide association studies in Parkinson disease. American Journal of Human Genetics. 78: 1081-2. PMID 16685659 DOI: 10.1086/504730 |
0.496 |
|
| 2006 |
Laramie JM, Wilk JB, Hunt SC, Ellison RC, Chakravarti A, Boerwinkle E, Myers RH. Evidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program. Bmc Medical Genetics. 7: 17. PMID 16509988 DOI: 10.1186/1471-2350-7-17 |
0.774 |
|
| 2006 |
An P, Freedman BI, Rich SS, Mandel SA, Arnett DK, Myers RH, Chen YD, Hunt SC, Rao DC. Quantitative trait loci on chromosome 8q24 for pancreatic beta-cell function and 7q11 for insulin sensitivity in obese nondiabetic white and black families: evidence from genome-wide linkage scans in the NHLBI Hypertension Genetic Epidemiology Network (HyperGEN) study. Diabetes. 55: 551-8. PMID 16443794 DOI: 10.2337/Diabetes.55.02.06.Db05-0714 |
0.304 |
|
| 2005 |
Karamohamed S, Latourelle JC, Racette BA, Perlmutter JS, Wooten GF, Lew M, Klein C, Shill H, Golbe LI, Mark MH, Guttman M, Nicholson G, Wilk JB, Saint-Hilaire M, DeStefano AL, ... ... Myers RH, et al. BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study. Neurology. 65: 1823-5. PMID 16344533 DOI: 10.1212/01.Wnl.0000187075.81589.Fd |
0.809 |
|
| 2005 |
Seong IS, Ivanova E, Lee JM, Choo YS, Fossale E, Anderson M, Gusella JF, Laramie JM, Myers RH, Lesort M, MacDonald ME. HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism. Human Molecular Genetics. 14: 2871-80. PMID 16115812 DOI: 10.1093/Hmg/Ddi319 |
0.679 |
|
| 2005 |
Yu K, Zhang S, Borecki I, Kraja A, Xiong C, Myers R, Province M. A haplotype similarity based transmission/disequilibrium test under founder heterogeneity Annals of Human Genetics. 69: 455-467. PMID 15996173 DOI: 10.1046/J.1529-8817.2005.00168.X |
0.356 |
|
| 2005 |
Karamohamed S, Golbe LI, Mark MH, Lazzarini AM, Suchowersky O, Labelle N, Guttman M, Currie LJ, Wooten GF, Stacy M, Saint-Hilaire M, Feldman RG, Liu J, Shoemaker CM, Wilk JB, ... ... Myers RH, et al. Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study. Movement Disorders : Official Journal of the Movement Disorder Society. 20: 1188-91. PMID 15966003 DOI: 10.1002/Mds.20515 |
0.812 |
|
| 2005 |
Friedman JH, Trieschmann ME, Myers RH, Fernandez HH. Monozygotic twins discordant for Huntington disease after 7 years. Archives of Neurology. 62: 995-7. PMID 15956172 DOI: 10.1001/Archneur.62.6.995 |
0.335 |
|
| 2004 |
Myers RH. Huntington's disease genetics. Neurorx : the Journal of the American Society For Experimental Neurotherapeutics. 1: 255-62. PMID 15717026 DOI: 10.1602/Neurorx.1.2.255 |
0.382 |
|
| 2004 |
Wilk JB, Djousse L, Arnett DK, Hunt SC, Province MA, Heiss G, Myers RH. Genome-wide linkage analyses for age at diagnosis of hypertension and early-onset hypertension in the HyperGEN study. American Journal of Hypertension. 17: 839-44. PMID 15363829 DOI: 10.1016/J.Amjhyper.2004.06.003 |
0.626 |
|
| 2004 |
Jiang Y, Wilk JB, Borecki I, Williamson S, DeStefano AL, Xu G, Liu J, Ellison RC, Province M, Myers RH. Common variants in the 5' region of the leptin gene are associated with body mass index in men from the National Heart, Lung, and Blood Institute Family Heart Study. American Journal of Human Genetics. 75: 220-30. PMID 15197684 DOI: 10.1086/422699 |
0.672 |
|
| 2004 |
Djoussé L, Knowlton B, Hayden MR, Almqvist EW, Brinkman RR, Ross CA, Margolis RL, Rosenblatt A, Durr A, Dode C, Morrison PJ, Novelletto A, Frontali M, Trent RJ, McCusker E, ... ... Myers RH, et al. Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. Neurogenetics. 5: 109-14. PMID 15029481 DOI: 10.1007/S10048-004-0175-2 |
0.411 |
|
| 2004 |
Herrera VL, Didishvili T, Lopez LV, Myers RH, Ruiz-Opazo N. Genome-wide scan identifies novel QTLs for cholesterol and LDL levels in F2[Dahl RxS]-intercross rats. Circulation Research. 94: 446-52. PMID 14739155 DOI: 10.1161/01.Res.0000117770.03168.E7 |
0.331 |
|
| 2003 |
Karamohamed S, DeStefano AL, Wilk JB, Shoemaker CM, Golbe LI, Mark MH, Lazzarini AM, Suchowersky O, Labelle N, Guttman M, Currie LJ, Wooten GF, Stacy M, Saint-Hilaire M, Feldman RG, ... ... Myers RH, et al. A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD study. Neurology. 61: 1557-61. PMID 14663042 DOI: 10.1212/01.Wnl.0000095966.99430.F4 |
0.717 |
|
| 2003 |
Tang W, Miller MB, Rich SS, North KE, Pankow JS, Borecki IB, Myers RH, Hopkins PN, Leppert M, Arnett DK. Linkage analysis of a composite factor for the multiple metabolic syndrome: the National Heart, Lung, and Blood Institute Family Heart Study. Diabetes. 52: 2840-7. PMID 14578304 DOI: 10.2337/Diabetes.52.11.2840 |
0.343 |
|
| 2003 |
Mukhopadhyay N, Finegold DN, Larson MG, Cupples LA, Myers RH, Weeks DE. A genome-wide scan for loci affecting normal adult height in the Framingham Heart Study. Human Heredity. 55: 191-201. PMID 14566097 DOI: 10.1159/000073203 |
0.349 |
|
| 2003 |
Gagnon DR, Glickman ME, Myers RH, Cupples LA. The analysis of survival data with a non-susceptible fraction and dual censoring mechanisms. Statistics in Medicine. 22: 3249-62. PMID 14518026 DOI: 10.1002/Sim.1568 |
0.361 |
|
| 2003 |
Wilk JB, DeStefano AL, Joost O, Myers RH, Cupples LA, Slater K, Atwood LD, Heard-Costa NL, Herbert A, O'Connor GT, Gottlieb DJ. Linkage and association with pulmonary function measures on chromosome 6q27 in the Framingham Heart Study. Human Molecular Genetics. 12: 2745-51. PMID 12966033 DOI: 10.1093/Hmg/Ddg311 |
0.659 |
|
| 2003 |
Li JL, Hayden MR, Almqvist EW, Brinkman RR, Durr A, Dodé C, Morrison PJ, Suchowersky O, Ross CA, Margolis RL, Rosenblatt A, Gómez-Tortosa E, Cabrero DM, Novelletto A, Frontali M, ... ... Myers RH, et al. A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study. American Journal of Human Genetics. 73: 682-7. PMID 12900792 DOI: 10.1086/378133 |
0.56 |
|
| 2003 |
Djoussé L, Knowlton B, Hayden M, Almqvist EW, Brinkman R, Ross C, Margolis R, Rosenblatt A, Durr A, Dode C, Morrison PJ, Novelletto A, Frontali M, Trent RJ, McCusker E, ... ... Myers RH, et al. Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease. American Journal of Medical Genetics. Part A. 119: 279-82. PMID 12784292 DOI: 10.1002/Ajmg.A.20190 |
0.366 |
|
| 2003 |
Wu X, Cooper RS, Boerwinkle E, Turner ST, Hunt S, Myers R, Olshen RA, Curb D, Zhu X, Kan D, Luke A. Combined analysis of genomewide scans for adult height: results from the NHLBI Family Blood Pressure Program. European Journal of Human Genetics : Ejhg. 11: 271-4. PMID 12673281 DOI: 10.1038/Sj.Ejhg.5200952 |
0.326 |
|
| 2003 |
Wilk JB, DeStefano AL, Arnett DK, Rich SS, Djousse L, Crapo RO, Leppert MF, Province MA, Cupples LA, Gottlieb DJ, Myers RH. A genome-wide scan of pulmonary function measures in the National Heart, Lung, and Blood Institute Family Heart Study. American Journal of Respiratory and Critical Care Medicine. 167: 1528-33. PMID 12637344 DOI: 10.1164/Rccm.200207-755Oc |
0.637 |
|
| 2003 |
DeStefano AL, Gates GA, Heard-Costa N, Myers RH, Baldwin CT. Genomewide linkage analysis to presbycusis in the Framingham Heart Study. Archives of Otolaryngology--Head & Neck Surgery. 129: 285-9. PMID 12622536 DOI: 10.1001/Archotol.129.3.285 |
0.373 |
|
| 2002 |
Van Laer L, DeStefano AL, Myers RH, Flothmann K, Thys S, Fransen E, Gates GA, Van Camp G, Baldwin CT. Is DFNA5 a susceptibility gene for age-related hearing impairment? European Journal of Human Genetics : Ejhg. 10: 883-6. PMID 12461698 DOI: 10.1038/Sj.Ejhg.5200878 |
0.346 |
|
| 2002 |
Djoussé L, Knowlton B, Cupples LA, Marder K, Shoulson I, Myers RH. Weight loss in early stage of Huntington's disease. Neurology. 59: 1325-30. PMID 12427878 DOI: 10.1212/01.Wnl.0000031791.10922.Cf |
0.343 |
|
| 2002 |
Karasik D, Myers RH, Hannan MT, Gagnon D, McLean RR, Cupples LA, Kiel DP. Mapping of quantitative ultrasound of the calcaneus bone to chromosome 1 by genome-wide linkage analysis. Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of the Usa. 13: 796-802. PMID 12378368 DOI: 10.1007/S001980200110 |
0.354 |
|
| 2002 |
Coon H, Eckfeldt JH, Leppert MF, Myers RH, Arnett DK, Heiss G, Province MA, Hunt SC. A genome-wide screen reveals evidence for a locus on chromosome 11 influencing variation in LDL cholesterol in the NHLBI Family Heart Study. Human Genetics. 111: 263-9. PMID 12215839 DOI: 10.1007/S00439-002-0773-8 |
0.335 |
|
| 2002 |
Karasik D, Myers RH, Cupples LA, Hannan MT, Gagnon DR, Herbert A, Kiel DP. Genome screen for quantitative trait loci contributing to normal variation in bone mineral density: the Framingham Study. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 17: 1718-27. PMID 12211443 DOI: 10.1359/Jbmr.2002.17.9.1718 |
0.326 |
|
| 2002 |
Wilk JB, Myers RH, Zhang Y, Lewis CE, Atwood L, Hopkins PN, Ellison RC. Evidence for a gene influencing heart rate on chromosome 4 among hypertensives. Human Genetics. 111: 207-13. PMID 12189495 DOI: 10.1007/S00439-002-0780-9 |
0.65 |
|
| 2002 |
Maher NE, Currie LJ, Lazzarini AM, Wilk JB, Taylor CA, Saint-Hilaire MH, Feldman RG, Golbe LI, Wooten GF, Myers RH. Segregation analysis of Parkinson disease revealing evidence for a major causative gene. American Journal of Medical Genetics. 109: 191-7. PMID 11977177 DOI: 10.1002/Ajmg.10335 |
0.711 |
|
| 2002 |
DeStefano AL, Lew MF, Golbe LI, Mark MH, Lazzarini AM, Guttman M, Montgomery E, Waters CH, Singer C, Watts RL, Currie LJ, Wooten GF, Maher NE, Wilk JB, Sullivan KM, ... ... Myers RH, et al. PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study. American Journal of Human Genetics. 70: 1089-95. PMID 11920285 DOI: 10.1086/339814 |
0.711 |
|
| 2002 |
Joost O, Wilk JB, Cupples LA, Harmon M, Shearman AM, Baldwin CT, O'Connor GT, Myers RH, Gottlieb DJ. Genetic loci influencing lung function: a genome-wide scan in the Framingham Study. American Journal of Respiratory and Critical Care Medicine. 165: 795-9. PMID 11897646 DOI: 10.1164/Ajrccm.165.6.2102057 |
0.639 |
|
| 2002 |
Meigs JB, Panhuysen CI, Myers RH, Wilson PW, Cupples LA. A genome-wide scan for loci linked to plasma levels of glucose and HbA(1c) in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study. Diabetes. 51: 833-40. PMID 11872688 DOI: 10.2337/Diabetes.51.3.833 |
0.317 |
|
| 2002 |
Maher NE, Golbe LI, Lazzarini AM, Mark MH, Currie LJ, Wooten GF, Saint-Hilaire M, Wilk JB, Volcjak J, Maher JE, Feldman RG, Guttman M, Lew M, Waters CH, Schuman S, ... ... Myers RH, et al. Epidemiologic study of 203 sibling pairs with Parkinson's disease: the GenePD study. Neurology. 58: 79-84. PMID 11781409 DOI: 10.1212/Wnl.58.1.79 |
0.693 |
|
| 2002 |
Feitosa MF, Borecki IB, Rich SS, Arnett DK, Sholinsky P, Myers RH, Leppert M, Province MA. Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study. American Journal of Human Genetics. 70: 72-82. PMID 11713718 DOI: 10.1086/338144 |
0.366 |
|
| 2001 |
Heard-Costa NL, Demissie S, DeStefano AL, Knowlton BA, Maher NE, Myers RH, Volcjak JS, Wilk JB, Cupples LA. Influence of marker heterozygosity and genetic heterogeneity on fine mapping. Genetic Epidemiology. 21: S467-72. PMID 11793720 DOI: 10.1002/Gepi.2001.21.S1.S467 |
0.632 |
|
| 2001 |
Wilk JB, Volcjak JS, Myers RH, Maher NE, Knowlton BA, Heard-Costa NL, Demissie S, Cupples LA, DeStefano AL. Family-based association tests for qualitative and quantitative traits using single-nucleotide polymorphism and microsatellite data. Genetic Epidemiology. 21: S364-9. PMID 11793700 DOI: 10.1002/Gepi.2001.21.S1.S364 |
0.667 |
|
| 2001 |
Coon H, Leppert MF, Eckfeldt JH, Oberman A, Myers RH, Peacock JM, Province MA, Hopkins PN, Heiss G. Genome-wide linkage analysis of lipids in the Hypertension Genetic Epidemiology Network (HyperGEN) Blood Pressure Study. Arteriosclerosis, Thrombosis, and Vascular Biology. 21: 1969-76. PMID 11742872 DOI: 10.1161/Hq1201.100228 |
0.32 |
|
| 2001 |
Gottlieb DJ, Wilk JB, Harmon M, Evans JC, Joost O, Levy D, O'Connor GT, Myers RH. Heritability of longitudinal change in lung function. The Framingham study. American Journal of Respiratory and Critical Care Medicine. 164: 1655-9. PMID 11719305 DOI: 10.1164/Ajrccm.164.9.2010122 |
0.606 |
|
| 2001 |
Peacock JM, Arnett DK, Atwood LD, Myers RH, Coon H, Rich SS, Province MA, Heiss G. Genome scan for quantitative trait loci linked to high-density lipoprotein cholesterol: The NHLBI Family Heart Study. Arteriosclerosis, Thrombosis, and Vascular Biology. 21: 1823-8. PMID 11701472 DOI: 10.1161/Hq1101.097804 |
0.333 |
|
| 2001 |
DeStefano AL, Golbe LI, Mark MH, Lazzarini AM, Maher NE, Saint-Hilaire M, Feldman RG, Guttman M, Watts RL, Suchowersky O, Lafontaine AL, Labelle N, Lew MF, Waters CH, Growdon JH, ... ... Myers RH, et al. Genome-wide scan for Parkinson's disease: the GenePD Study. Neurology. 57: 1124-6. PMID 11571351 DOI: 10.1212/Wnl.57.6.1124 |
0.428 |
|
| 2001 |
Nance MA, Myers RH. Juvenile onset Huntington's disease--clinical and research perspectives. Mental Retardation and Developmental Disabilities Research Reviews. 7: 153-7. PMID 11553930 DOI: 10.1002/Mrdd.1022 |
0.36 |
|
| 2001 |
Glorioso N, Filigheddu F, Troffa C, Soro A, Parpaglia PP, Tsikoudakis A, Myers RH, Herrera VL, Ruiz-Opazo N. Interaction of alpha(1)-Na,K-ATPase and Na,K,2Cl-cotransporter genes in human essential hypertension. Hypertension. 38: 204-9. PMID 11509477 DOI: 10.1161/01.Hyp.38.2.204 |
0.338 |
|
| 2001 |
Hunt SC, Kronenberg F, Eckfeldt JH, Hopkins PN, Myers RH, Heiss G. Association of plasma bilirubin with coronary heart disease and segregation of bilirubin as a major gene trait: the NHLBI family heart study. Atherosclerosis. 154: 747-54. PMID 11257278 DOI: 10.1016/S0021-9150(00)00420-2 |
0.334 |
|
| 2001 |
Gómez-Tortosa E, MacDonald ME, Friend JC, Taylor SA, Weiler LJ, Cupples LA, Srinidhi J, Gusella JF, Bird ED, Vonsattel JP, Myers RH. Quantitative neuropathological changes in presymptomatic Huntington's disease. Annals of Neurology. 49: 29-34. PMID 11198293 DOI: 10.1002/1531-8249(200101)49:1<29::Aid-Ana7>3.0.Co;2-B |
0.373 |
|
| 2000 |
Zee RY, Myers RH, Hannan MT, Wilson PW, Ordovas JM, Schaefer EJ, Lindpaintner K, Kiel DP. Absence of linkage for bone mineral density to chromosome 12q12-14 in the region of the vitamin D receptor gene. Calcified Tissue International. 67: 434-9. PMID 11289690 DOI: 10.1007/S002230001175 |
0.33 |
|
| 2000 |
Levy D, DeStefano AL, Larson MG, O'Donnell CJ, Lifton RP, Gavras H, Cupples LA, Myers RH. 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. Hypertension. 36: 477-83. PMID 11040222 DOI: 10.1161/01.Hyp.36.4.477 |
0.351 |
|
| 2000 |
Coon H, Myers RH, Borecki IB, Arnett DK, Hunt SC, Province MA, Djousse L, Leppert MF. Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart Study. Arteriosclerosis, Thrombosis, and Vascular Biology. 20: 2275-80. PMID 11031215 DOI: 10.1161/01.Atv.20.10.2275 |
0.358 |
|
| 2000 |
Salomaa V, Pankow J, Heiss G, Cakir B, Eckfeldt JH, Ellison RC, Myers RH, Hiller KM, Brantley KR, Morris TL, Weston BW. Genetic background of Lewis negative blood group phenotype and its association with atherosclerotic disease in the NHLBI family heart study. Journal of Internal Medicine. 247: 689-98. PMID 10886491 DOI: 10.1046/J.1365-2796.2000.00682.X |
0.335 |
|
| 2000 |
Wilk JB, Djousse L, Arnett DK, Rich SS, Province MA, Hunt SC, Crapo RO, Higgins M, Myers RH. Evidence for major genes influencing pulmonary function in the NHLBI family heart study. Genetic Epidemiology. 19: 81-94. PMID 10861898 DOI: 10.1002/1098-2272(200007)19:1<81::Aid-Gepi6>3.0.Co;2-8 |
0.643 |
|
| 2000 |
Shearman AM, Ordovas JM, Cupples LA, Schaefer EJ, Harmon MD, Shao Y, Keen JD, DeStefano AL, Joost O, Wilson PW, Housman DE, Myers RH. Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham study. Human Molecular Genetics. 9: 1315-20. PMID 10814713 DOI: 10.1093/Hmg/9.9.1315 |
0.307 |
|
| 2000 |
Wilk JB, Djousse L, Borecki I, Atwood LD, Hunt SC, Rich SS, Eckfeldt JH, Arnett DK, Rao DC, Myers RH. Segregation analysis of serum uric acid in the NHLBI Family Heart Study. Human Genetics. 106: 355-9. PMID 10798367 DOI: 10.1007/S004390051050 |
0.628 |
|
| 1999 |
Coon H, Leppert MF, Kronenberg F, Province MA, Myers RH, Arnett DK, Eckfeldt JH, Heiss G, Williams RR, Hunt SC. Evidence for a major gene accounting for mild elevation in LDL cholesterol: the NHLBI Family Heart Study. Annals of Human Genetics. 63: 401-12. PMID 10735582 DOI: 10.1046/J.1469-1809.1999.6350401.X |
0.316 |
|
| 1999 |
Wilk JB, Premkumar S, Nicolaou M, Myers RH, Maher NE, Harmon MD, Farrer LA, DeStefano AL, Cupples LA, Couropmitree NN. Stratification techniques to explore genotype environment interactions. Genetic Epidemiology. 17: S761-6. PMID 10597527 DOI: 10.1002/Gepi.13701707125 |
0.65 |
|
| 1999 |
Taylor CA, Saint-Hilaire MH, Cupples LA, Thomas CA, Burchard AE, Feldman RG, Myers RH. Environmental, medical, and family history risk factors for Parkinson's disease: a New England-based case control study. American Journal of Medical Genetics. 88: 742-9. PMID 10581500 DOI: 10.1002/(Sici)1096-8628(19991215)88:6<742::Aid-Ajmg29>3.0.Co;2-# |
0.428 |
|
| 1999 |
MacDonald ME, Vonsattel JP, Shrinidhi J, Couropmitree NN, Cupples LA, Bird ED, Gusella JF, Myers RH. Evidence for the GluR6 gene associated with younger onset age of Huntington's disease. Neurology. 53: 1330-2. PMID 10522893 DOI: 10.1212/Wnl.53.6.1330 |
0.42 |
|
| 1999 |
Joost O, Taylor CA, Thomas CA, Cupples LA, Saint-Hilaire MH, Feldman RG, Baldwin CT, Myers RH. Absence of effect of seven functional mutations in the CYP2D6 gene in Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 14: 590-5. PMID 10435495 DOI: 10.1002/1531-8257(199907)14:4<590::AID-MDS1007>3.0.CO;2-2 |
0.33 |
|
| 1999 |
Karluk D, Myers RH, DiFiglia M, Gusella JF, MacDonald ME, Penney JB, Young AB, Hobbs W, Lenzi S, Srinidhi S, Hedley-Whyte ET, Vonsattel J. NONAGENARIANS WITH HUNTINGTON DISEASE (HD) HAVE LOW CAG REPEATS Journal of Neuropathology and Experimental Neurology. 58: 549. DOI: 10.1097/00005072-199905000-00170 |
0.31 |
|
| 1998 |
Arnett DK, Borecki IB, Ludwig EH, Pankow JS, Myers R, Evans G, Folsom AR, Heiss G, Higgins M. Angiotensinogen and angiotensin converting enzyme genotypes and carotid atherosclerosis: the atherosclerosis risk in communities and the NHLBI family heart studies. Atherosclerosis. 138: 111-6. PMID 9678776 DOI: 10.1016/S0021-9150(98)00009-4 |
0.329 |
|
| 1998 |
Pocovi M, Cenarro A, Civeira F, Torralba MA, Perez-Calvo JI, Mozas P, Giraldo P, Giralt M, Myers RH, Cupples LA, Ordovas JM. Beta-glucocerebrosidase gene locus as a link for Gaucher's disease and familial hypo-alpha-lipoproteinaemia. Lancet. 351: 1919-23. PMID 9654259 DOI: 10.1016/S0140-6736(97)09490-7 |
0.311 |
|
| 1998 |
Givelber RJ, Couropmitree NN, Gottlieb DJ, Evans JC, Levy D, Myers RH, O'Connor GT. Segregation analysis of pulmonary function among families in the Framingham Study. American Journal of Respiratory and Critical Care Medicine. 157: 1445-51. PMID 9603122 DOI: 10.1164/Ajrccm.157.5.9704021 |
0.313 |
|
| 1998 |
Jenkins BG, Rosas HD, Chen YC, Makabe T, Myers R, MacDonald M, Rosen BR, Beal MF, Koroshetz WJ. 1H NMR spectroscopy studies of Huntington's disease: correlations with CAG repeat numbers. Neurology. 50: 1357-65. PMID 9595987 DOI: 10.1212/Wnl.50.5.1357 |
0.335 |
|
| 1997 |
DeStefano AL, Cupples LA, Myers RH, Farrer LA. Detecting linkage for a complex disease using simulated extended pedigrees. Genetic Epidemiology. 14: 981-6. PMID 9433611 DOI: 10.1002/(Sici)1098-2272(1997)14:6<981::Aid-Gepi70>3.0.Co;2-G |
0.351 |
|
| 1997 |
Aaltonen J, Horelli-Kuitunen N, Fan J, Björses P, Perheentupa J, Myers R, Palotie A, Peltonen L. High-Resolution Physical and Transcriptional Mapping of the Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Locus on Chromosome 21q22.3 by FISH Genome Research. 7: 820-829. PMID 9267805 DOI: 10.1101/Gr.7.8.820 |
0.334 |
|
| 1997 |
McNeil SM, Novelletto A, Srinidhi J, Barnes G, Kornbluth I, Altherr MR, Wasmuth JJ, Gusella JF, MacDonald ME, Myers RH. Reduced penetrance of the Huntington's disease mutation. Human Molecular Genetics. 6: 775-9. PMID 9158152 DOI: 10.1093/Hmg/6.5.775 |
0.341 |
|
| 1997 |
Penney JB, Vonsattel JP, MacDonald ME, Gusella JF, Myers RH. CAG repeat number governs the development rate of pathology in Huntington's disease. Annals of Neurology. 41: 689-92. PMID 9153534 DOI: 10.1002/Ana.410410521 |
0.356 |
|
| 1996 |
Gusella JF, McNeil S, Persichetti F, Srinidhi J, Novelletto A, Bird E, Faber P, Vonsattel JP, Myers RH, MacDonald ME. Huntington's disease. Cold Spring Harbor Symposia On Quantitative Biology. 61: 615-26. PMID 9246488 DOI: 10.1055/S-2008-1063867 |
0.305 |
|
| 1995 |
Leeflang EP, Zhang L, Tavaré S, Hubert R, Srinidhi J, MacDonald ME, Myers RH, de Young M, Wexler NS, Gusella JF. Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum. Human Molecular Genetics. 4: 1519-26. PMID 8541834 DOI: 10.1093/Hmg/4.9.1519 |
0.318 |
|
| 1995 |
Wilson PW, Myers RH, Larson MG, Ordovas JM, Wolf PA, Schaefer EJ. 750-5 Apolipoprotein E Alleles, Dyslipidemia, and Coronary Heart Disease: The Framingham Offspring Study Journal of the American College of Cardiology. 25: 196A. DOI: 10.1016/0735-1097(95)92270-F |
0.306 |
|
| 1995 |
Levy D, Lindpaintner K, Larson MG, Ramachandran VS, Myers RH, Pfeffer MA, Ordovas JM, Schaefer EJ, Wilson PW. 729-4 Left Ventricular Hypertrophy and the Deletion-Insertion Polymorphism of the Angiotensin Converting Enzyme Gene Journal of the American College of Cardiology. 25: 136A. DOI: 10.1016/0735-1097(95)92019-2 |
0.335 |
|
| 1995 |
Ramachandran VS, Levy D, Larson MG, Ordovas JM, Schaefer EJ, Myers RH, Lindpaintner K, Wilson PW. 901-81 Association of a Molecular Variant of the Angiotensinogen Gene and Hypertension Journal of the American College of Cardiology. 25: 24A. DOI: 10.1016/0735-1097(95)91558-F |
0.37 |
|
| 1994 |
Persichetti F, Srinidhi J, Kanaley L, Ge P, Myers RH, D'Arrigo K, Barnes GT, MacDonald ME, Vonsattel JP, Gusella JF. Huntington's disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains. Neurobiology of Disease. 1: 159-66. PMID 9173995 DOI: 10.1006/Nbdi.1994.0019 |
0.368 |
|
| 1994 |
Lazzarini AM, Myers RH, Zimmerman TR, Mark MH, Golbe LI, Sage JI, Johnson WG, Duvoisin RC. A clinical genetic study of Parkinson's disease: evidence for dominant transmission. Neurology. 44: 499-506. PMID 8145922 DOI: 10.1212/Wnl.44.3_Part_1.499 |
0.429 |
|
| 1993 |
MacDonald ME, Ambrose CM, Duyao MP, Myers RH, Lin C, Srinidhi L, Barnes G, Taylor SA, James M, Groot N, MacFarlane H, Jenkins B, Anderson MA, Wexler NS, Gusella JF, et al. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes Cell. 72: 971-983. PMID 8458085 DOI: 10.1016/0092-8674(93)90585-E |
0.407 |
|
| 1993 |
Duyao M, Ambrose C, Myers R, Novelletto A, Persichetti F, Frontali M, Folstein S, Ross C, Franz M, Abbott M, Gray J, Conneally P, Young A, Penney J, Hollingsworth Z, et al. Trinucleotide repeat length instability and age of onset in Huntington's disease Nature Genetics. 4: 387-392. PMID 8401587 DOI: 10.1038/Ng0893-387 |
0.371 |
|
| 1992 |
Ogawa T, Matson WR, Beal MF, Myers RH, Bird ED, Milbury P, Saso S. Kynurenine pathway abnormalities in Parkinson's disease. Neurology. 42: 1702-6. PMID 1513457 DOI: 10.1212/Wnl.42.9.1702 |
0.387 |
|
| 1992 |
Diamond R, White RF, Myers RH, Mastromauro C, Koroshetz WJ, Butters N, Rothstein DM, Moss MB, Vasterling J. Evidence of presymptomatic cognitive decline in Huntington's disease. Journal of Clinical and Experimental Neuropsychology. 14: 961-75. PMID 1452640 DOI: 10.1080/01688639208402547 |
0.323 |
|
| 1992 |
MacDonald ME, Novelletto A, Lin C, Tagle D, Barnes G, Bates G, Taylor S, Allitto B, Altherr M, Myers R. The Huntington's disease candidate region exhibits many different haplotypes. Nature Genetics. 1: 99-103. PMID 1302016 DOI: 10.1038/Ng0592-99 |
0.387 |
|
| 1990 |
St George-Hyslop PH, Haines JL, Farrer LA, Polinsky R, Van Broeckhoven C, Goate A, McLachlan DR, Orr H, Bruni AC, Sorbi S, Rainero I, Foncin JF, Pollen D, Cantu JM, Tupler R, ... ... Myers RH, et al. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature. 347: 194-7. PMID 2395471 DOI: 10.1038/347194A0 |
0.383 |
|
| 1990 |
Farrer LA, Myers RH, Cupples LA, St George-Hyslop PH, Bird TD, Rossor MN, Mullan MJ, Polinsky R, Nee L, Heston L. Transmission and age-at-onset patterns in familial Alzheimer's disease: evidence for heterogeneity. Neurology. 40: 395-403. PMID 2314579 DOI: 10.1097/00002093-199100510-00015 |
0.326 |
|
| 1989 |
Farrer LA, O'Sullivan DM, Cupples LA, Growdon JH, Myers RH. Assessment of genetic risk for Alzheimer's disease among first-degree relatives. Annals of Neurology. 25: 485-93. PMID 2774490 DOI: 10.1002/Ana.410250511 |
0.333 |
|
| 1989 |
St George-Hyslop PH, Tanzi RE, Haines JL, Polinsky RJ, Farrer L, Myers RH, Gusella JF. Molecular genetics of familial Alzheimer's disease. European Neurology. 29: 25-7. PMID 2693103 DOI: 10.1159/000116477 |
0.385 |
|
| 1989 |
St George-Hyslop PH, Myers RH, Haines JL, Farrer LA, Tanzi RE, Abe K, James MF, Conneally PM, Polinsky RJ, Gusella JF. Familial Alzheimer's disease: progress and problems. Neurobiology of Aging. 10: 417-25. PMID 2682321 DOI: 10.1016/0197-4580(89)90082-1 |
0.303 |
|
| 1989 |
St George-Hyslop PH, Haines JL, Polinsky RJ, Tanzi RE, Farrer L, Myers RH, Gusella JF. Molecular genetics of familial Alzheimer's disease. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 16: 465-7. PMID 2680005 DOI: 10.1017/S0317167100029772 |
0.351 |
|
| 1989 |
Conneally PM, Haines JL, Tanzi RE, Wexler NS, Penchaszadeh GK, Harper PS, Folstein SE, Cassiman JJ, Myers RH, Young AB. Huntington disease: no evidence for locus heterogeneity. Genomics. 5: 304-8. PMID 2571579 DOI: 10.1016/0888-7543(89)90062-1 |
0.333 |
|
| 1989 |
Sax DS, Bird ED, Gusella JF, Myers RH. Phenotypic variation in 2 Huntington's disease families with linkage to chromosome 4. Neurology. 39: 1332-6. PMID 2529452 DOI: 10.1212/Wnl.39.10.1332 |
0.407 |
|
| 1989 |
Mastromauro CA, Meissen GJ, Cupples LA, Kiely DK, Berkman B, Myers RH. Estimation of fertility and fitness in Huntington disease in New England. American Journal of Medical Genetics. 33: 248-54. PMID 2527461 DOI: 10.1002/Ajmg.1320330222 |
0.303 |
|
| 1989 |
Cupples LA, Terrin NC, Myers RH, D'Agostino RB. Using survival methods to estimate age-at-onset distributions for genetic diseases with an application to Huntington disease. Genetic Epidemiology. 6: 361-71. PMID 2524419 DOI: 10.1002/Gepi.1370060206 |
0.321 |
|
| 1988 |
Myers RH, Vonsattel JP, Stevens TJ, Cupples LA, Richardson EP, Martin JB, Bird ED. Clinical and neuropathologic assessment of severity in Huntington's disease. Neurology. 38: 341-7. PMID 2964565 DOI: 10.1212/Wnl.38.3.341 |
0.35 |
|
| 1988 |
Farrer LA, Myers RH, Cupples LA, Conneally PM. Considerations in using linkage analysis as a presymptomatic test for Huntington's disease. Journal of Medical Genetics. 25: 577-88. PMID 2903248 DOI: 10.1136/Jmg.25.9.577 |
0.323 |
|
| 1988 |
Meissen GJ, Myers RH, Mastromauro CA, Koroshetz WJ, Klinger KW, Farrer LA, Watkins PA, Gusella JF, Bird ED, Martin JB. Predictive testing for Huntington's disease with use of a linked DNA marker. The New England Journal of Medicine. 318: 535-42. PMID 2893260 DOI: 10.1056/Nejm198803033180903 |
0.341 |
|
| 1987 |
St George-Hyslop PH, Tanzi RE, Polinsky RJ, Neve RL, Pollen D, Drachman D, Growdon J, Cupples LA, Nee L, Myers RH. Absence of duplication of chromosome 21 genes in familial and sporadic Alzheimer's disease. Science (New York, N.Y.). 238: 664-6. PMID 2890206 DOI: 10.1126/Science.2890206 |
0.322 |
|
| 1987 |
St George-Hyslop PH, Tanzi RE, Polinsky RJ, Haines JL, Nee L, Watkins PC, Myers RH, Feldman RG, Pollen D, Drachman D. The genetic defect causing familial Alzheimer's disease maps on chromosome 21. Science (New York, N.Y.). 235: 885-90. PMID 2880399 DOI: 10.1126/Science.2880399 |
0.361 |
|
| 1985 |
Myers RH, Sax DS, Schoenfeld M, Bird ED, Wolf PA, Vonsattel JP, White RF, Martin JB. Late onset of Huntington's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 48: 530-4. PMID 3159849 DOI: 10.1136/Jnnp.48.6.530 |
0.334 |
|
| 1983 |
Sudarsky L, Myers RH, Walshe TM. Huntington's disease in monozygotic twins reared apart. Journal of Medical Genetics. 20: 408-11. PMID 6228662 DOI: 10.1136/Jmg.20.6.408 |
0.346 |
|
| 1982 |
Sinex FM, Myers RH. Alzheimer's disease, Down's syndrome, and aging: the genetic approach. Annals of the New York Academy of Sciences. 396: 3-13. PMID 6217775 DOI: 10.1111/J.1749-6632.1982.Tb26839.X |
0.305 |
|
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