Published in Ann Hum Genet on September 01, 2006
Genome-wide association analysis identifies multiple loci related to resting heart rate. Hum Mol Genet (2010) 1.67
Beta-1-adrenoceptor genetic variants and ethnicity independently affect response to beta-blockade. Pharmacogenet Genomics (2008) 1.04
Heritability and linkage study on heart rates in a Mongolian population. Exp Mol Med (2008) 0.82
β-1 and β-2 adrenergic receptor polymorphism and association with cardiovascular response to orthostatic screening. Auton Neurosci (2011) 0.77
AGT M235T genotype/anxiety interaction and gender in the HyperGEN study. PLoS One (2010) 0.77
Human heart rate: heritability of resting and stress values in twin pairs, and influence of genetic variation in the adrenergic pathway at a microribonucleic acid (microrna) motif in the 3'-UTR of cytochrome b561 [corrected]. J Am Coll Cardiol (2013) 0.76
Pharmacogenetic Associations of β1-Adrenergic Receptor Polymorphisms With Cardiovascular Outcomes in the SPS3 Trial (Secondary Prevention of Small Subcortical Strokes). Stroke (2017) 0.75
Clustering heart rate dynamics is associated with β-adrenergic receptor polymorphisms: analysis by information-based similarity index. PLoS One (2011) 0.75
ADRB1 variants in atrial fibrillation: small steps and giant leaps toward personalized therapy in cardiovascular disease. J Am Coll Cardiol (2012) 0.75
Race contributes to beta-blocker efficacy in pediatric patients with arrhythmias. Pediatr Cardiol (2013) 0.75
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 (2000) 8.84
Neuropathological classification of Huntington's disease. J Neuropathol Exp Neurol (1985) 7.93
Molecular basis of human hypertension: role of angiotensinogen. Cell (1992) 6.07
Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations. Circulation (1996) 4.62
Inverse association of dietary fat with development of ischemic stroke in men. JAMA (1998) 4.20
CAG repeat number governs the development rate of pathology in Huntington's disease. Ann Neurol (1997) 4.01
Bone mass and the risk of breast cancer among postmenopausal women. N Engl J Med (1997) 3.96
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. Circulation (1998) 3.89
Predictive testing for Huntington's disease with use of a linked DNA marker. N Engl J Med (1988) 3.82
The APOL1 gene and allograft survival after kidney transplantation. Am J Transplant (2011) 3.69
Primary and subsequent coronary risk appraisal: new results from the Framingham study. Am Heart J (2000) 3.61
The genetic defect causing familial Alzheimer's disease maps on chromosome 21. Science (1987) 3.59
Recent trends in acute coronary heart disease--mortality, morbidity, medical care, and risk factors. The Minnesota Heart Survey Investigators. N Engl J Med (1996) 3.32
Race-specific HIV-1 disease-modifying effects associated with CCR5 haplotypes. Proc Natl Acad Sci U S A (1999) 3.21
NHLBI Family Heart Study: objectives and design. Am J Epidemiol (1996) 3.21
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology (2012) 3.12
The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis. Cell (1993) 2.99
Glycosylated hemoglobins and long-term blood glucose control in diabetes mellitus. J Clin Endocrinol Metab (1977) 2.84
Problem drinking and medication adherence among persons with HIV infection. J Gen Intern Med (2001) 2.81
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature (1990) 2.80
Genome-wide linkage analysis of systolic and diastolic blood pressure: the Québec Family Study. Circulation (2000) 2.75
Comparison of glycated albumin and hemoglobin A(1c) levels in diabetic subjects on hemodialysis. Kidney Int (2008) 2.74
Cerebral amyloid angiopathy without and with cerebral hemorrhages: a comparative histological study. Ann Neurol (1991) 2.70
The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer. Gastroenterology (2001) 2.68
Effects of indomethacin in premature infants with patent ductus arteriosus: results of a national collaborative study. J Pediatr (1983) 2.65
Total serum bilirubin and risk of cardiovascular disease in the Framingham offspring study. Am J Cardiol (2001) 2.57
Genetic and environmental contributions to platelet aggregation: the Framingham heart study. Circulation (2001) 2.54
Protective effect of fruits and vegetables on development of stroke in men. JAMA (1995) 2.50
Marked longevity of human lung parenchymal elastic fibers deduced from prevalence of D-aspartate and nuclear weapons-related radiocarbon. J Clin Invest (1991) 2.49
Absence of association or genetic linkage between the angiotensin-converting-enzyme gene and left ventricular mass. N Engl J Med (1996) 2.49
Rate of functional decline in Huntington's disease. Huntington Study Group. Neurology (2000) 2.49
Identification of a mutation in the gene causing hyperkalemic periodic paralysis. Cell (1991) 2.48
Evidence for a Mendelian gene in a segregation analysis of generalized radiographic osteoarthritis: the Framingham Study. Arthritis Rheum (1998) 2.45
Acute-phase inflammatory response to periodontal disease in the US population. J Dent Res (2000) 2.38
Cardiac tumors in infancy. Am J Cardiol (1968) 2.37
Increased rate of suicide among patients with Huntington's disease. J Neurol Neurosurg Psychiatry (1984) 2.31
A comparison of positive family history definitions for defining risk of future disease. J Chronic Dis (1986) 2.30
NHLBI family blood pressure program: methodology and recruitment in the HyperGEN network. Hypertension genetic epidemiology network. Ann Epidemiol (2000) 2.28
Television viewing and change in body fat from preschool to early adolescence: The Framingham Children's Study. Int J Obes Relat Metab Disord (2003) 2.26
School-based cardiovascular health promotion: the child and adolescent trial for cardiovascular health (CATCH). J Sch Health (1990) 2.23
Relation between dietary linolenic acid and coronary artery disease in the National Heart, Lung, and Blood Institute Family Heart Study. Am J Clin Nutr (2001) 2.22
Influence of parents' physical activity levels on activity levels of young children. J Pediatr (1991) 2.22
Adiponectin as a novel determinant of bone mineral density and visceral fat. Bone (2003) 2.17
Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study. Neurology (2008) 2.16
Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease. Am J Med Genet A (2003) 2.15
Usefulness of cardiovascular family history data for population-based preventive medicine and medical research (the Health Family Tree Study and the NHLBI Family Heart Study). Am J Cardiol (2001) 2.14
Utah pedigree studies: design and preliminary data for premature male CHD deaths. Prog Clin Biol Res (1979) 2.11
Familial resemblance for VO2max in the sedentary state: the HERITAGE family study. Med Sci Sports Exerc (1998) 2.11
Clinical investigation in Duchenne dystrophy: 2. Determination of the "power" of therapeutic trials based on the natural history. Muscle Nerve (1983) 1.99
A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians. Diabetes (1999) 1.99
Improved survival of stroke patients during the 1980s. The Minnesota Stroke Survey. Stroke (1995) 1.99
Leptin and incident type 2 diabetes: risk or protection? Diabetologia (2006) 1.95
Genetic associations in age-related hearing thresholds. Arch Otolaryngol Head Neck Surg (1999) 1.94
Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham study. Hum Mol Genet (2000) 1.94
Higher serum bilirubin is associated with decreased risk for early familial coronary artery disease. Arterioscler Thromb Vasc Biol (1996) 1.94
Factors related to onset age of Huntington disease. Am J Hum Genet (1982) 1.93
Epidemiologic study of 203 sibling pairs with Parkinson's disease: the GenePD study. Neurology (2002) 1.90
Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics. Am J Cardiol (1993) 1.87
The tracking of nutrient intake in young children: the Framingham Children's Study. Am J Public Health (1995) 1.87
Factors associated with HD CAG repeat instability in Huntington disease. J Med Genet (2007) 1.86
Parent-child relationships in nutrient intake: the Framingham Children's Study. Am J Clin Nutr (1992) 1.85
Variants in intron 13 of the ELMO1 gene are associated with diabetic nephropathy in African Americans. Ann Hum Genet (2009) 1.85
BMI and waist circumference as predictors of lifetime colon cancer risk in Framingham Study adults. Int J Obes Relat Metab Disord (2004) 1.85
Familial lipoprotein disorders in patients with premature coronary artery disease. Circulation (1992) 1.84
Inverse relationship between microsatellite instability and K-ras and p53 gene alterations in colon cancer. Am J Pathol (2001) 1.79
Weight loss in early stage of Huntington's disease. Neurology (2002) 1.79
Parental age at child's birth and son's risk of prostate cancer. The Framingham Study. Am J Epidemiol (1999) 1.77
Worldwide ethnic distribution of the G protein beta3 subunit 825T allele and its association with obesity in Caucasian, Chinese, and Black African individuals. J Am Soc Nephrol (1999) 1.76
Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita. Neuron (1992) 1.75
Attitudes toward presymptomatic testing in Huntington disease. Am J Med Genet (1987) 1.75
The feasibility of using rural health workers to determine cause of death in remote regions of Cameroon, West Africa. Ethn Dis (2001) 1.73
A genome scan for loci linked to quantitative insulin traits in persons without diabetes: the Framingham Offspring Study. Diabetologia (2003) 1.72
Familial resemblance of plasma lipids, lipoproteins and postheparin lipoprotein and hepatic lipases in the HERITAGE Family Study. Arterioscler Thromb Vasc Biol (1997) 1.71
Apolipoprotein E alleles, dyslipidemia, and coronary heart disease. The Framingham Offspring Study. JAMA (1994) 1.71
Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort. Genes Immun (2011) 1.70
Influence of leisure time physical activity and television watching on atherosclerosis risk factors in the NHLBI Family Heart Study. Atherosclerosis (2000) 1.70
Huntington disease: no evidence for locus heterogeneity. Genomics (1989) 1.70
Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains. J Clin Endocrinol Metab (1996) 1.69
Familial aggregation of coronary artery calcium in families with type 2 diabetes. Diabetes (2001) 1.69
Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum. Hum Mol Genet (1995) 1.67
Coronary risk associated with age and sex of parental heart disease in the Framingham Study. Am J Cardiol (1989) 1.65
Maternal transmission in Huntington's disease. Lancet (1983) 1.64
Heritability of left ventricular mass: the Framingham Heart Study. Hypertension (1997) 1.63
Factors encouraging cohort maintenance in a longitudinal study. J Clin Epidemiol (1991) 1.61
Genetic associations in diabetic nephropathy: a meta-analysis. Diabetologia (2010) 1.60
Evidence for the GluR6 gene associated with younger onset age of Huntington's disease. Neurology (1999) 1.60
Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy. Diabetes (1997) 1.60
Heritability of longitudinal change in lung function. The Framingham study. Am J Respir Crit Care Med (2001) 1.60
Variants in the 5q31 cytokine gene cluster are associated with psoriasis. Genes Immun (2007) 1.59
Genome screen for quantitative trait loci contributing to normal variation in bone mineral density: the Framingham Study. J Bone Miner Res (2002) 1.58