Richard H Myers
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Computer Science
Richard H Myers's Degrees
- PhD Computer Science Stanford University
- Masters Computer Science University of California, Berkeley
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(Suggest an Edit or Addition)Richard H Myers's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes (1993) (7826)
- Effects of Age, Sex, and Ethnicity on the Association Between Apolipoprotein E Genotype and Alzheimer Disease: A Meta-analysis (1997) (3245)
- Neuropathological Classification of Huntington's Disease (1985) (2504)
- Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium. (1997) (2488)
- Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
- Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease (2014) (1591)
- The genetic defect causing familial Alzheimer's disease maps on chromosome 21. (1987) (1180)
- Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
- Trinucleotide repeat length instability and age of onset in Huntington's disease (1993) (1083)
- Generation of Isogenic Pluripotent Stem Cells Differing Exclusively at Two Early Onset Parkinson Point Mutations (2011) (675)
- CAG repeat number governs the development rate of pathology in Huntington's disease (1997) (623)
- 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 (2000) (620)
- Familial Lipoprotein Disorders in Patients With Premature Coronary Artery Disease (1992) (616)
- 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. (1998) (582)
- Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database (2012) (546)
- Cerebral amyloid angiopathy without and with cerebral hemorrhages: A comparative histological study (1991) (512)
- Apolipoprotein E alleles, dyslipidemia, and coronary heart disease. The Framingham Offspring Study. (1994) (481)
- Genetic Signatures of Exceptional Longevity in Humans (2012) (448)
- Genomewide association study for susceptibility genes contributing to familial Parkinson disease (2009) (446)
- Identification of Genetic Factors that Modify Clinical Onset of Huntington’s Disease (2015) (420)
- Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder (1990) (413)
- Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression (2016) (395)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- Parental history is an independent risk factor for coronary artery disease: the Framingham Study. (1990) (345)
- A Genome-Wide Association Study of Pulmonary Function Measures in the Framingham Heart Study (2009) (344)
- Huntington’s disease genetics (2004) (305)
- HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism. (2005) (296)
- Apolipoprotein E element 4 association with dementia in a population-based study (1996) (296)
- Increased platelet aggregability associated with platelet GPIIIa PlA2 polymorphism: the Framingham Offspring Study. (1999) (274)
- Meta‐analysis of Parkinson's Disease: Identification of a novel locus, RIT2 (2012) (274)
- Familial Aggregation of Stroke: The Framingham Study (1993) (270)
- Genetic associations in age-related hearing thresholds. (1999) (269)
- Kynurenine pathway abnormalities in Parkinson's disease (1992) (266)
- CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion (2012) (263)
- De novo expansion of a (CAG)n repeat in sporadic Huntington's disease (1993) (261)
- Increased rate of suicide among patients with Huntington's disease. (1984) (253)
- Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset. (2009) (250)
- Heritability of left ventricular mass: the Framingham Heart Study. (1997) (240)
- Statement on use of apolipoprotein E testing for Alzheimer disease. American College of Medical Genetics/American Society of Human Genetics Working Group on ApoE and Alzheimer disease. (1995) (238)
- CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset (2019) (236)
- Functional variants in the LRRK2 gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease (2018) (233)
- Apolipoprotein E epsilon4 association with dementia in a population-based study: The Framingham study. (1996) (228)
- Clinical and neuropathologic assessment of severity in Huntington's disease (1988) (226)
- Evidence for a Mendelian gene in a segregation analysis of generalized radiographic osteoarthritis: the Framingham Study. (1998) (219)
- Decreased Neuronal and Increased Oligodendroglial Densities in Huntington's Disease Caudate Nucleus (1991) (219)
- Genetic and Environmental Contributions to Platelet Aggregation: The Framingham Heart Study (2001) (218)
- Absence of association or genetic linkage between the angiotensin-converting-enzyme gene and left ventricular mass. (1996) (213)
- Factors associated with slow progression in Huntington's disease. (1991) (213)
- Juvenile onset Huntington's disease--clinical and research perspectives. (2001) (208)
- Morphometric analysis of the prefrontal cortex in Huntington's disease (1991) (204)
- Gametic but not somatic instability of CAG repeat length in Huntington's disease. (1993) (201)
- Environmental, medical, and family history risk factors for Parkinson's disease: a New England-based case control study. (1999) (192)
- Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum. (1995) (191)
- Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. (2012) (187)
- Coronary risk associated with age and sex of parental heart disease in the Framingham Study. (1989) (185)
- A Genome-Wide Scan for Loci Linked to Plasma Levels of Glucose and HbA1c in a Community-Based Sample of Caucasian Pedigrees: The Framingham Offspring Study (2002) (176)
- Predictive testing for Huntington's disease with use of a linked DNA marker. (1988) (175)
- Reduced penetrance of the Huntington's disease mutation. (1997) (170)
- The Huntington's disease candidate region exhibits many different haplotypes (1992) (165)
- Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease (2003) (161)
- Quantitative neuropathological changes in presymptomatic Huntington's disease (2001) (159)
- Laboratory Guidelines for Huntington Disease Genetic Testing (1998) (158)
- The BsmI Vitamin D Receptor Restriction Fragment Length Polymorphism (bb) Influences the Effect of Calcium Intake on Bone Mineral Density (1997) (157)
- A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study. (2003) (155)
- Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study (2013) (155)
- A clinical genetic study of Parkinson's disease (1994) (153)
- Attitudes toward presymptomatic testing in Huntington disease. (1987) (152)
- Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels (2016) (147)
- Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study. (2002) (146)
- The pathogenic exon 1 HTT protein is produced by incomplete splicing in Huntington’s disease patients (2017) (145)
- Directional dominance on stature and cognition in diverse human populations (2015) (144)
- Assessment of genetic risk for alzheimer's disease among first‐degree relatives (1989) (144)
- Absence of duplication of chromosome 21 genes in familial and sporadic Alzheimer's disease. (1987) (139)
- Genome Screen for Quantitative Trait Loci Contributing to Normal Variation in Bone Mineral Density: The Framingham Study (2002) (138)
- RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression (2015) (137)
- Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study. (2006) (133)
- Factors associated with HD CAG repeat instability in Huntington disease (2007) (132)
- Parkinson-associated risk variant in enhancer element produces subtle effect on target gene expression (2016) (132)
- Homozygote for Huntington disease. (1989) (128)
- Late onset of Huntington's disease. (1985) (124)
- Human-Specific Histone Methylation Signatures at Transcription Start Sites in Prefrontal Neurons (2012) (123)
- microRNA Profiles in Parkinson's Disease Prefrontal Cortex (2016) (119)
- Genomewide association study for onset age in Parkinson disease (2009) (116)
- miR-10b-5p expression in Huntington’s disease brain relates to age of onset and the extent of striatal involvement (2015) (114)
- The Relationship Between CAG Repeat Length and Age of Onset Differs for Huntington's Disease Patients with Juvenile Onset or Adult Onset (2007) (113)
- Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham study. (2000) (112)
- Segregation analysis of pulmonary function among families in the Framingham Study. (1998) (109)
- Haplotypes and gene expression implicate the MAPT region for Parkinson disease (2008) (108)
- Evidence for major genes influencing pulmonary function in the NHLBI Family Heart Study (2000) (107)
- The Etiopathogenesis of Parkinson Disease and Suggestions for Future Research. Part II (2007) (106)
- Influence of Apolipoprotein E, Smoking, and Alcohol Intake on Carotid Atherosclerosis: National Heart, Lung, and Blood Institute Family Heart Study (2002) (104)
- Linkage analysis of a composite factor for the multiple metabolic syndrome: the National Heart, Lung, and Blood Institute Family Heart Study. (2003) (103)
- 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. (2004) (103)
- The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study (2008) (102)
- Normal and Expanded Huntington’s Disease Gene Alleles Produce Distinguishable Proteins Due to Translation Across the CAG Repeat (1995) (102)
- Transmission and age‐at‐onset patterns in familial Alzheimer's disease (1990) (100)
- 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 (2000) (98)
- Factors related to onset age of Huntington disease. (1982) (98)
- Neocortical Dendritic Pathology in Human Partial Epilepsy: A Quantitative Golgi Study (1994) (97)
- Association of plasma bilirubin with coronary heart disease and segregation of bilirubin as a major gene trait: the NHLBI family heart study. (2001) (95)
- MicroRNAs Located in the Hox Gene Clusters Are Implicated in Huntington's Disease Pathogenesis (2014) (94)
- Genome scan for quantity of hand osteoarthritis: the Framingham Study. (2002) (94)
- MATERNAL TRANSMISSION IN HUNTINGTON'S DISEASE (1983) (93)
- Integrative analyses of proteomics and RNA transcriptomics implicate mitochondrial processes, protein folding pathways and GWAS loci in Parkinson disease (2015) (91)
- Segregation analysis reveals evidence of a major gene for Alzheimer disease. (1991) (91)
- Genetic loci influencing lung function: a genome-wide scan in the Framingham Study. (2002) (91)
- PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study. (2002) (91)
- Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in mice. (2006) (90)
- Genomewide linkage analysis to presbycusis in the Framingham Heart Study. (2003) (87)
- Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16 (2004) (84)
- Huntington's disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains (1994) (84)
- Genome-wide significance for a modifier of age at neurological onset in Huntington's Disease at 6q23-24: the HD MAPS study (2006) (83)
- Family patterns of coronary heart disease mortality: the Framingham Longevity Study. (1992) (83)
- Parental age at child's birth and son's risk of prostate cancer. The Framingham Study. (1999) (82)
- Evidence of presymptomatic cognitive decline in Huntington's disease. (1992) (80)
- Copy Number Variation in Familial Parkinson Disease (2011) (78)
- Genome-Wide Linkage Analysis of Lipids in the Hypertension Genetic Epidemiology Network (HyperGEN) Blood Pressure Study (2001) (77)
- BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study (2005) (76)
- The Etiopathogenesis of Parkinson Disease and Suggestions for Future Research. Part I (2007) (75)
- Genome Scan for Quantitative Trait Loci Linked to High-Density Lipoprotein Cholesterol: The NHLBI Family Heart Study (2001) (74)
- Genetic variability of adult body mass index: a longitudinal assessment in framingham families. (2002) (73)
- Leptin Is Associated With Blood Pressure and Hypertension in Women From the National Heart, Lung, and Blood Institute Family Heart Study (2009) (73)
- Conserved Higher-Order Chromatin Regulates NMDA Receptor Gene Expression and Cognition (2014) (73)
- Gene Expression Profiles in Parkinson Disease Prefrontal Cortex Implicate FOXO1 and Genes under Its Transcriptional Regulation (2012) (72)
- Heritability of longitudinal change in lung function. The Framingham study. (2001) (72)
- Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function (2018) (71)
- A modifier of Huntington's disease onset at the MLH1 locus (2017) (71)
- Familial Alzheimer's disease: Progress and problems (1989) (70)
- Generation of Isogenic Pluripotent Stem Cells Differing Exclusively at Two Early Onset Parkinson Point Mutations (2011) (70)
- Understanding the decision to take the predictive test for Huntington disease. (1991) (70)
- Longitudinal and age trends of metabolic syndrome and its risk factors: The Family Heart Study (2006) (69)
- 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. (2002) (69)
- Inverse relationship between age at onset of Huntington disease and paternal age suggests involvement of genetic imprinting. (1992) (69)
- DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study (2016) (65)
- Epigenetic dysregulation of hairy and enhancer of split 4 (HES4) is associated with striatal degeneration in postmortem Huntington brains. (2015) (63)
- Genetic Effect on Blood Pressure Is Modulated by Age: The Hypertension Genetic Epidemiology Network Study (2009) (63)
- Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. (2012) (62)
- A genome scan for loci linked to quantitative insulin traits in persons without diabetes: the Framingham Offspring Study (2003) (61)
- Mapping of Quantitative Ultrasound of the Calcaneus Bone to Chromosome 1 by Genome-Wide Linkage Analysis (2002) (61)
- The normal Huntington disease (HD) allele, or a closely linked gene, influences age at onset of HD. (1993) (60)
- Cyclin-G-associated kinase modifies α-synuclein expression levels and toxicity in Parkinson's disease: results from the GenePD Study. (2011) (60)
- A haplotype at the PARK3 locus influences onset age for Parkinson’s disease (2003) (58)
- Segregation analysis of serum uric acid in the NHLBI Family Heart Study (2000) (58)
- Epidemiologic study of 203 sibling pairs with Parkinson’s disease (2002) (57)
- Transmission and age-at-onset patterns in familial Alzheimer??s disease: evidence for heterogeneity (1991) (56)
- Evidence of cortical metabolic dysfunction in early Huntington's disease by single‐photon‐emission computed tomography (1996) (56)
- Monozygotic twins discordant for Huntington disease after 7 years. (2005) (55)
- A genome-wide scan of pulmonary function measures in the National Heart, Lung, and Blood Institute Family Heart Study. (2003) (55)
- Hybrid ape offspring of a mating of gibbon and siamang. (1979) (55)
- Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials. (2016) (54)
- BMC Medicine (2006) (53)
- MicroRNAs in CSF as prodromal biomarkers for Huntington disease in the PREDICT-HD study (2017) (51)
- Genome-wide scan for Parkinson's disease: the GenePD Study. (2001) (51)
- An evaluation of the metabolic syndrome in the HyperGEN study (2005) (50)
- 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) (2009) (50)
- Assessment of cortical and striatal involvement in 523 Huntington disease brains (2012) (49)
- Huntington disease: no evidence for locus heterogeneity. (1989) (49)
- Genetic signatures of exceptional longevity in humans. (2010) (49)
- Potential impact of a predictive test on the gene frequency of Huntington disease. (1984) (48)
- Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis (2007) (48)
- Genome-wide scan for Parkinson's disease (2001) (47)
- β-glucocerebrosidase gene locus as a link for Gaucher's disease and familial hypo-α-lipoproteinaemia (1998) (47)
- A Genome-Wide Scan for Loci Linked to Plasma Levels of Glucose and HbA 1 c in a Community-Based Sample of Caucasian Pedigrees The Framingham Offspring Study (2002) (45)
- Maternal factors in onset of Huntington disease. (1985) (45)
- Alzheimer's Disease, Down's Syndrome, and Aging: The Genetic Approach (1982) (44)
- Huntington's disease in monozygotic twins reared apart. (1983) (44)
- Combined analysis of genomewide scans for adult height: results from the NHLBI Family Blood Pressure Program (2003) (44)
- Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2 (2016) (43)
- State of the art review: Molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis (2003) (43)
- The Role of H3K4me3 in Transcriptional Regulation Is Altered in Huntington’s Disease (2015) (43)
- Decreased glutamic acid decarboxylase mRNA expression in prefrontal cortex in Parkinson's disease (2010) (42)
- Replication of association between ELAVL4 and Parkinson disease: the GenePD study (2008) (41)
- Lewis blood group phenotype as an independent risk factor for coronary heart disease (the NHLBI Family Heart Study). (1999) (41)
- Multiple sclerosis sibling pairs (1990) (41)
- Linkage and association with pulmonary function measures on chromosome 6q27 in the Framingham Heart Study. (2003) (40)
- Absence of linkage or association for osteoarthritis with the vitamin D receptor/type II collagen locus: the Framingham Osteoarthritis Study. (2002) (40)
- Genome-wide linkage analyses for age at diagnosis of hypertension and early-onset hypertension in the HyperGEN study. (2004) (40)
- Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age (2006) (39)
- Interaction of α1-Na,K-ATPase and Na,K,2Cl-Cotransporter Genes in Human Essential Hypertension (2001) (39)
- Correction for multiple testing in a gene region (2013) (39)
- Incomplete dominance of type III hyperlipoproteinemia is associated with the rare apolipoprotein E2 (Arg136-->Ser) variant in multigenerational pedigree studies. (1996) (38)
- Meta-analysis of genetic association with diagnosed Alzheimer’s disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing (2018) (36)
- Segregation analysis of Parkinson disease revealing evidence for a major causative gene. (2002) (36)
- Long-term impact of Huntington disease linkage testing. (1997) (35)
- Correction: Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study (2013) (34)
- Evaluation of Parkinson Disease Risk Variants as Expression-QTLs (2012) (33)
- Estimation of morbid risk and age at onset with missing information. (1991) (33)
- Genetic background of Lewis negative blood group phenotype and its association with atherosclerotic disease in the NHLBI Family Heart Study (2000) (33)
- Considerations for genomewide association studies in Parkinson disease. (2006) (33)
- Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset (2012) (32)
- Segregation analysis of serum uric acid in the NHLBI Family Heart Study. (2000) (32)
- A genome-wide screen reveals evidence for a locus on chromosome 11 influencing variation in LDL cholesterol in the NHLBI Family Heart Study (2002) (31)
- Adrenergic Receptor Polymorphisms Associated with Resting Heart Rate: The HyperGEN Study (2005) (31)
- Increased Platelet Aggregability Associated With Platelet GPIIIa PlA2 Polymorphism : The Framingham Offspring Study (1999) (31)
- Study of plasma‐derived miRNAs mimic differences in Huntington's disease brain (2015) (31)
- Adhesive bonding of wood and other structural materials (1984) (31)
- Apolipoprotein E polymorphism modifies the alcohol-HDL association observed in the National Heart, Lung, and Blood Institute Family Heart Study. (2004) (30)
- Is DFNA5 a susceptibility gene for age-related hearing impairment? (2002) (30)
- Effects of similarities in lifestyle habits on familial aggregation of high density lipoprotein and low density lipoprotein cholesterol: the NHLBI Family Heart Study. (1999) (30)
- A glycomics and proteomics study of aging and Parkinson’s disease in human brain (2020) (30)
- Brain-derived neurotrophic factor does not influence age at neurologic onset of Huntington’s disease (2006) (30)
- Evidence for a Pan-Neurodegenerative Disease Response in Huntington's and Parkinson's Disease Expression Profiles (2018) (30)
- Sepiapterin reductase expression is increased in Parkinson's disease brain tissue (2007) (30)
- Novel microRNA discovery using small RNA sequencing in post-mortem human brain (2016) (28)
- The caudate nucleus undergoes dramatic and unique transcriptional changes in human prodromal Huntington’s disease brain (2019) (28)
- Risk of Parkinson's disease after tamoxifen treatment (2010) (28)
- A Genome-Wide Scan for Loci Affecting Normal Adult Height in the Framingham Heart Study (2003) (27)
- The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease. (2015) (27)
- Considerations in using linkage analysis as a presymptomatic test for Huntington's disease. (1987) (25)
- Quantitative trait loci for metabolic syndrome in the Hypertension Genetic Epidemiology Network study. (2005) (25)
- Change in attitudes toward presymptomatic testing in Huntington disease. (1986) (25)
- Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; The NHLBI Family Heart Study (2008) (24)
- Interaction of alpha(1)-Na,K-ATPase and Na,K,2Cl-cotransporter genes in human essential hypertension. (2001) (24)
- Genetic analysis of the GRIK2 modifier effect in Huntington's disease (2006) (24)
- Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3: the NHLBI Family Heart Study follow-up examination (2007) (24)
- Evidence for a gene influencing heart rate on chromosome 4 among hypertensives (2002) (24)
- Sequence-Level Analysis of the Major European Huntington Disease Haplotype. (2015) (22)
- Beta-glucocerebrosidase gene locus as a link for Gaucher's disease and familial hypo-alpha-lipoproteinaemia. (1998) (21)
- TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease. (2012) (20)
- Using survival methods to estimate age‐at‐onset distributions for genetic diseases with an application to Huntington disease (1989) (20)
- Genetic Risk Underlying Psychiatric and Cognitive Symptoms in Huntington’s Disease (2019) (20)
- 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 (2006) (19)
- Genotype-by-Sex Interaction on Fasting Insulin Concentration (2007) (18)
- Smoking influences the association between apolipoprotein E and lipids: The national heart, lung, and blood institute family heart study (2000) (18)
- Evidence of Extensive Alternative Splicing in Post Mortem Human Brain HTT Transcription by mRNA Sequencing (2015) (18)
- Multiple Genes Influence BMI on Chromosome 7q31–34: The NHLBI Family Heart Study (2009) (18)
- Evaluation of logistic regression models and effect of covariates for case–control study in RNA-Seq analysis (2017) (18)
- Haplotype-based stratification of Huntington's disease (2017) (18)
- Estimation of fertility and fitness in Huntington disease in New England. (1989) (18)
- Linkage analysis of diabetes status among hypertensive families: the Hypertension Genetic Epidemiology Network study. (2004) (17)
- Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19: the NHLBI Family Heart Study follow-up examination. (2008) (17)
- The 4p16.3 Parkinson Disease Risk Locus Is Associated with GAK Expression and Genes Involved with the Synaptic Vesicle Membrane (2016) (17)
- HaploBuild: an algorithm to construct non-contiguous associated haplotypes in family based genetic studies (2007) (16)
- Genome-Wide Scan Identifies Novel QTLs for Cholesterol and LDL Levels in F2[Dahl R×S]-Intercross Rats (2004) (16)
- LIPC variants in the promoter and intron 1 modify HDL-C levels in a sex-specific fashion. (2009) (16)
- 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. (2006) (16)
- 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 (2005) (16)
- Phenotypic variation in 2 Huntington's disease families with linkage to chromosome 4 (1989) (15)
- Absence of effect of seven functional mutations in the cyp2d6 gene in Parkinson's disease (1999) (15)
- Absence of Linkage for Bone Mineral Density to Chromosome 12q12-14 in the Region of the Vitamin D Receptor Gene (2000) (15)
- Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease (2021) (15)
- Quantification of muscle tremor of Huntington's disease patients and their offspring in an early detection study. (1979) (15)
- Segregation analysis for high density lipoprotein in the berkeley data (1993) (14)
- Huntington's disease. (1982) (13)
- Postmortem Interval Influences α-Synuclein Expression in Parkinson Disease Brain (2012) (13)
- A Haplotype Similarity Based Transmission/Disequilibrium Test under Founder Heterogeneity (2005) (13)
- Smokeless Tobacco Use and the Risk of Parkinson's Disease Mortality (2005) (11)
- Genome‐wide admixture mapping for coronary artery calcification in African Americans: the NHLBI Family Heart Study (2008) (11)
- A QTL on 12q Influencing an Inflammation Marker and Obesity in White Women: The NHLBI Family Heart Study (2009) (11)
- 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 (2006) (11)
- Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington’s disease motor onset (2013) (11)
- Insulin and hypertension in the NHLBI Family Heart Study: a sibpair approach to a controversial issue. (2000) (11)
- Learned aversions to intracerebral carbachol (1977) (10)
- Evidence for a major gene accounting for mild elevation in LDL cholesterol: The NHLBI Family Heart Study (1999) (10)
- Attitudes toward marriage and childbearing of individuals at risk for Huntington's disease. (1984) (9)
- LRRK2 is not a Significant Cause of Parkinson's Disease in French-Canadians (2007) (8)
- NYD-SP18 is associated with obesity in the NHLBI Family Heart Study (2008) (8)
- Genomewide linkage study of modifiers of LRRK2‐related Parkinson's disease (2011) (8)
- The Role of H 3 K 4 me 3 in Transcriptional Regulation Is Altered in Huntington ' s Disease Authors (2017) (7)
- Dysfunction of X-linked inhibitor of apoptosis protein (XIAP) triggers neuropathological processes via altered p53 activity in Huntington’s disease (2021) (7)
- Estrogen-related and other disease diagnoses preceding Parkinson’s disease (2010) (7)
- Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: The GenePD study (2008) (7)
- False-negative results with levodopa for early detection of Huntington's disease. (1982) (7)
- Morphometric analysis of prefrontal cortex in Huntingtonʼs disease (HD): 256 (1990) (7)
- Evidence of QTL on 15q21 for high-density lipoprotein cholesterol: the National Heart, Lung, and Blood Institute Family Heart Study (NHLBI FHS). (2007) (7)
- Family‐Based Association Tests for Qualitative and Quantitative Traits Using Single‐Nucleotide Polymorphism and Microsatellite Data (2001) (6)
- Genome-wide scan for Parkinson’s disease:: The Gene PD Study (2001) (6)
- Evidence for a major gene accounting for mild elevation in LDL cholesterol: the NHLBI Family Heart Study. (1999) (6)
- Huntington’s Disease: Neuropathological Grading (1987) (6)
- Huntington's disease: genetics, chemical pathology, and management. (1985) (5)
- Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure Program (2007) (5)
- Multiethnic meta-analysis identifies new loci for pulmonary function (2017) (5)
- Search for the familial Alzheimer's disease gene. (1987) (5)
- Correction: RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression (2016) (5)
- Evidence for Three Novel QTLs for Adiposity on Chromosome 2 With Epistatic Interactions: The NHLBI Family Heart Study (2009) (5)
- Molecular genetics of familial Alzheimer's disease. (1989) (4)
- Segregation analysis of total nevus density and estimation of lifetime risk and average onset age of melanoma. (1992) (4)
- Feasibility of Huntington disease trials in the disease prodrome (2014) (4)
- Molecular Genetic Strategies in Familial Alzheimer’s Disease: Theoretical and Practical Considerations (1988) (4)
- 729-4 Left Ventricular Hypertrophy and the Deletion-Insertion Polymorphism of the Angiotensin Converting Enzyme Gene (1995) (3)
- Effects of Age and Ethnicity on the Link Between APOE ∊4 and Alzheimer Disease—Reply (1998) (3)
- Influence of Apolipoprotein E, Smoking, and Alcohol Intake on Carotid Atherosclerosis Study (2002) (3)
- Genetic and Environmental Contributions to Platelet Aggregation The Framingham Heart Study Clinical Investigation and Reports (2001) (3)
- Characteristics of a Gibbon-Siamang hybrid ape (1980) (3)
- The analysis of survival data with a non‐susceptible fraction and dual censoring mechanisms (2003) (3)
- Discrepancy resolved (1993) (3)
- [Huntington disease: 7 cases with relatively preserved neostriatal islets]. (1992) (3)
- Genome-Wide Association Studies Identify CHRNA5/3 and HTR4 in the Development of Airflow Obstruction (2012) (2)
- Genetic overlap between psychiatric disorders and neuropsychiatric symptoms in HD (2019) (2)
- Correction (2020) (2)
- Polymorphisms near EXOC 4 and LRGUK on chromosome 7 q 32 are associated with Type 2 Diabetes and fasting glucose ; The NHLBI Family Heart Study (2019) (2)
- No evidence of linkage between the very-low-density lipoprotein receptor gene and fasting serum insulin or homeostasis model assessment insulin resistance index: the National Heart, Lung, and Blood Institute Family Heart Study. (2000) (2)
- Linkage of the cholesterol 7α-hydroxylase gene and low-density lipoprotein cholesterol conditional on apolipoprotein E association: The National Heart, Lung, and Blood Institute Family Heart Study (2005) (2)
- Linkage of the cholesterol 7alpha-hydroxylase gene and low-density lipoprotein cholesterol conditional on apolipoprotein E association: the National Heart, Lung, and Blood Institute Family Heart Study. (2005) (2)
- Comparative Huntington and Parkinson Disease mRNA Analysis Reveals Common Inflammatory Processes (2017) (1)
- Influence of Marker Heterozygosity and Genetic Heterogeneity on Fine Mapping (2001) (1)
- 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. (2009) (1)
- Considerations inusinglinkage analysis as a presymptomatic testforHuntington's disease (1988) (1)
- miR-10b-5p expression in Huntington’s disease brain relates to age of onset and the extent of striatal involvement (2015) (1)
- 901-81 Association of a Molecular Variant of the Angiotensinogen Gene and Hypertension (1995) (1)
- NONAGENARIANS WITH HUNTINGTON DISEASE (HD) HAVE LOW CAG REPEATS (1999) (1)
- Genotype-by-Sex Interaction on Fasting Insulin Levels: The Hypergen Study (2006) (1)
- ALZHEIMER DISEASE DOES NOT PROTECT THE NEOSTRIATUM IN COMBINED CASES OF HUNTINGTON (HD) AND ALZHEIMER DISEASE (AD) (1997) (1)
- University of Groningen Genome-wide association studies identify CHRNA 5 / 3 and HTR 4 in the development of airflow obstruction (2017) (1)
- Estimation of familial risk in Alzheimer's disease (1990) (1)
- Reply to Tzourio et al. (1992) (1)
- 750-5 Apolipoprotein E Alleles, Dyslipidemia, and Coronary Heart Disease: The Framingham Offspring Study (1995) (1)
- Stratification techniques to explore genotype environment interactions (1999) (1)
- Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function (2018) (1)
- Interaction of a1-Na,K-ATPase and Na,K,2Cl-Cotransporter Genes in Human Essential Hypertension (2001) (1)
- RNA-sequencing of human post-mortem hypothalamus and nucleus accumbens identifies expression profiles associated with obesity (2022) (0)
- Comparative Huntington and Parkinson Disease (2017) (0)
- The Role of Neurofilament Genes in Familial Alzheimer's Disease (1987) (0)
- Contents Vol. 55, 2003 (2003) (0)
- Supporting Online Material for Genetic Signatures of Exceptional Longevity in Humans (2010) (0)
- Linkage map of anonymous loci near the CF gene. (1989) (0)
- Title Sequence-Level Analysis of the Major European Huntington Disease Haplotype Permalink (0)
- Nitric Oxide Synthase and Causes Hypertension and Vascular Dysfunction Loss of Collectrin, an Angiotensin-Converting Enzyme 2 Homolog, Uncouples Endothelial (2015) (0)
- Reply to Krawczak and Bockel. (1992) (0)
- Evaluation of logistic regression models and effect of covariates for case–control study in RNA-Seq analysis (2017) (0)
- RNA-sequencing evaluation of fresh frozen and formaldehyde-fixed prefrontal cortex brain tissue for the study of Alzheimer's disease (2013) (0)
- Homozygote forHuntington Disease (1989) (0)
- Interaction of &agr;1-Na,K-ATPase and Na,K,2Cl-Cotransporter Genes in Human Essential Hypertension (2001) (0)
- Prediction in the Onset and Detection of Huntington's Disease (2021) (0)
- The caudate nucleus undergoes dramatic and unique transcriptional changes in human prodromal Huntington’s disease brain (2019) (0)
- B4 Detection of the aberrantly spliced exon 1 – intron 1 htt mRNA in HD patient post mortem brain tissue and fibroblast lines (2016) (0)
- Neuropsychological functioning in juvenile/adolescent onset Huntington's disease: A case series (1997) (0)
- Novel microRNA discovery using small RNA sequencing in post-mortem human brain (2016) (0)
- EFFECTS OF AGE AND ETHNICITY ON THE LINK BETWEEN APOE EPSILON 4 AND ALZHEIMER DISEASE. AUTHORS' REPLY (1998) (0)
- STOP-GAIN VARIANT IN MICROGLIA-EXPRESSED GENE GMIP IS ASSOCIATED WITH EARLY-ONSET ALZHEIMER’S DISEASE (2018) (0)
- Huntington’s disease genetics (2004) (0)
- Example of 9 clusters of genetic risk profiles in centenarians of the discovery set and 3 similar clusters in replication sets 1 and 2. (2012) (0)
- Reply (1990) (0)
- Contributors and Participants (1982) (0)
- Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset (2012) (0)
- Subject Index Vol. 55, 2003 (2003) (0)
- Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington’s disease motor onset (2013) (0)
- The pathogenic exon 1 HTT protein is produced by incomplete splicing in Huntington’s disease patients (2017) (0)
- Detecting linkage for a complex disease using simulated extended pedigrees (1997) (0)
- Increased rateofsuicide among patients with Huntington's disease (1984) (0)
- The Chromosome Connection (1980) (0)
- Reply (1998) (0)
- Clinical phenotype of chromosome 14q24 associated FAD in the Italian-American (Feldman FAD Family) pedigree (1994) (0)
- Large-scale exome sequencing in ALS identifies new risk genes and pathways (S34.005) (2015) (0)
- Oligodendroglial proliferation in presymptomatic Huntington`s disease (1994) (0)
- Identifying allele specific expression in Parkinson's disease brain tissue (2015) (0)
- Authors' response to commentaries (1989) (0)
- Integrative analyses of proteomics and RNA transcriptomics implicate mitochondrial processes, protein folding pathways and GWAS loci in Parkinson disease (2015) (0)
- Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease (2018) (0)
- CORTICAL PATHOLOGY IN HUNTINGTONʼS DISEASE: MORPHOMETRIC AND OBSERVATIONAL STUDY (1993) (0)
- Greater Cardiac Hypertrophy in Hypertensive Rats (2016) (0)
- HD Repeat Determines the Rate of Neuropathological Change (2008) (0)
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What Schools Are Affiliated With Richard H Myers?
Richard H Myers is affiliated with the following schools:
