Dabeeru C. Rao

Q: What Schools Are Affiliated With Dabeeru C. Rao

Dabeeru C. Rao is affiliated with the following schools: Washington University in St. Louis, Hebrew University of Jerusalem, University of Washington, Université Laval

Dabeeru C. Rao's AcademicInfluence.com Rankings

Dabeeru C. Rao

Biology

#3982

World Rank

#6011

Historical Rank

#1559

USA Rank

Genetics

#362

World Rank

#424

Historical Rank

#158

USA Rank

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Biology

Why Is Dabeeru C. Rao Influential?

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According to Wikipedia, Dabeeru C. Rao is an Indian-American statistical geneticist. He is professor and director of the Division of Biostatistics at Washington University School of Medicine. Born in 1946, Rao was educated at the Indian Statistical Institute, where he received his Ph.D. in 1971. His Ph.D. thesis was entitled A Statistical Study of Tongue Pigmentation in Man, and his doctoral advisor was C. R. Rao. From 1971 to 1979, he was a geneticist in the University of Hawaii's Population Genetics Laboratory, where he worked with Newton Morton. In 1980, he joined the faculty of Washington University School of Medicine as associate professor and founding director of the Division of Biostatistics. He was promoted to full professor there in 1982, and has remained director of the Division of Biostatistics since 1980.

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Dabeeru C. Rao's Published Works

Number of citations in a given year to any of this author's works

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

Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk (2011) (1928)
Defining the role of common variation in the genomic and biological architecture of adult human height (2014) (1805)
New genetic loci link adipose and insulin biology to body fat distribution (2014) (1227)
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) (785)
Familial aggregation of VO(2max) response to exercise training: results from the HERITAGE Family Study. (1999) (765)
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries (2018) (735)
The effect of sex, age and race on estimating percentage body fat from body mass index: The Heritage Family Study (2002) (625)
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2015) (532)
A unified model for complex segregation analysis. (1983) (466)
Familial resemblance for VO2max in the sedentary state: the HERITAGE family study. (1998) (463)
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure (2011) (424)
Targeting the metabolic syndrome with exercise: evidence from the HERITAGE Family Study. (2003) (412)
Race, visceral adipose tissue, plasma lipids, and lipoprotein lipase activity in men and women: the Health, Risk Factors, Exercise Training, and Genetics (HERITAGE) family study. (2000) (392)
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
Effects of exercise training on glucose homeostasis: the HERITAGE Family Study. (2005) (375)
Genetic covariation between neuroticism and the symptoms of anxiety and depression (1984) (373)
Genomic predictors of the maximal O₂ uptake response to standardized exercise training programs. (2011) (367)
The HERITAGE family study. Aims, design, and measurement protocol. (1995) (358)
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals (2016) (347)
Adverse Metabolic Response to Regular Exercise: Is It a Rare or Common Occurrence? (2012) (329)
Effects of Endurance Exercise Training on Plasma HDL Cholesterol Levels Depend on Levels of Triglycerides: Evidence From Men of the Health, Risk Factors, Exercise Training and Genetics (HERITAGE) Family Study (2001) (325)
NHLBI Family Heart Study: objectives and design. (1996) (305)
Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders (2013) (299)
Acute and chronic effects of exercise on leptin levels in humans. (1997) (291)
Genetic linkage and complex diseases, with special reference to psychiatric disorders (1990) (289)
Admixture mapping for hypertension loci with genome-scan markers (2005) (279)
Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations (2012) (264)
The transmission of schizophrenia under a multifactorial threshold model. (1983) (261)
Genome-Wide Linkage Analysis of Systolic and Diastolic Blood Pressure: The Québec Family Study (2000) (248)
A comparison of sib‐pair linkage tests for disease susceptibility loci (1985) (247)
Age, sex, race, initial fitness, and response to training: the HERITAGE Family Study. (2001) (245)
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk (2016) (242)
Metabolic syndrome and salt sensitivity of blood pressure in non-diabetic people in China: a dietary intervention study (2009) (233)
Effect of exercise training on plasma levels of C-reactive protein in healthy adults: the HERITAGE Family Study. (2005) (224)
Contribution of body fatness and adipose tissue distribution to the age variation in plasma steroid hormone concentrations in men: the HERITAGE Family Study. (2000) (221)
Genomic scan for maximal oxygen uptake and its response to training in the HERITAGE Family Study. (2000) (216)
Construction of human linkage maps: Likelihood calculations for multilocus linkage analysis (1986) (215)
Analysis of family resemblance. II. A linear model for familial correlation. (1974) (211)
Multi-center genetic study of hypertension: The Family Blood Pressure Program (FBPP). (2002) (202)
Role of ghrelin polymorphisms in obesity based on three different studies. (2002) (201)
An epidemiologic approach to gene‐environment interaction (1990) (196)
Influences of genes and shared family environment on adult body mass index assessed in an adoption study by a comprehensive path model. (1995) (194)
Genomewide linkage analysis of quantitative spirometric phenotypes in severe early-onset chronic obstructive pulmonary disease. (2002) (190)
Blood lipid response to 20 weeks of supervised exercise in a large biracial population: the HERITAGE Family Study. (2000) (190)
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study (2011) (185)
Alterations in body weight and composition consequent to 20 wk of endurance training: the HERITAGE Family Study. (1999) (185)
Gender difference in blood pressure responses to dietary sodium intervention in the GenSalt study (2009) (185)
Inherited Causes of Clonal Hematopoiesis in 97,691 TOPMed Whole Genomes (2020) (184)
Familial aggregation of physical activity levels in the Québec Family Study. (2001) (182)
Variants in the CD36 gene associate with the metabolic syndrome and high-density lipoprotein cholesterol. (2008) (181)
NHLBI family blood pressure program: methodology and recruitment in the HyperGEN network. Hypertension genetic epidemiology network. (2000) (176)
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. (2013) (176)
Variability of pulmonary function in alpha-1-antitrypsin deficiency: clinical correlates. (1989) (169)
Resolution of cultural and biological inheritance by path analysis. (1976) (164)
A genome-wide scan for abdominal fat assessed by computed tomography in the Québec Family Study. (2001) (164)
Familial resemblance of plasma lipids, lipoproteins and postheparin lipoprotein and hepatic lipases in the HERITAGE Family Study. (1997) (164)
A genetic study of immunoglobulin E. (1978) (158)
Heart rate and blood pressure changes with endurance training: the HERITAGE Family Study. (2001) (158)
Associations between the leptin receptor gene and adiposity in middle-aged Caucasian males from the HERITAGE family study. (2000) (153)
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits (2017) (149)
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels (2016) (147)
The information contained in multiple sibling pairs (1984) (147)
Fitness alters the associations of BMI and waist circumference with total and abdominal fat. (2004) (145)
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations (2017) (145)
Genetic epidemiology of breast cancer: Segregation analysis of 200 Danish pedigrees (1984) (144)
The collaborative Lipid Research Clinics family study: Biological and cultural determinants of familial resemblance for plasma lipids and lipoproteins (1985) (143)
Testing the association between polymorphic markers and quantitative traits in pedigrees (1987) (143)
Relationship of prevalence of non‐insulin‐dependent diabetes mellitus to Amerindian admixture in the Mexican Americans of San Antonio, Texas (1986) (142)
The Cincinnati Lipid Research Clinic family study: cultural and biological determinants of lipids and lipoprotein concentrations. (1982) (142)
Age, body mass index, race and other determinants of steroid hormone variability: the HERITAGE Family Study. (2001) (142)
Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis (1990) (138)
Angiotensin-converting enzyme ID polymorphism and fitness phenotype in the HERITAGE Family Study. (2000) (138)
Calcium intake is associated with adiposity in Black and White men and White women of the HERITAGE Family Study. (2004) (137)
Resolving genetic models for the transmission of schizophrenia (1985) (133)
A dopamine D2 receptor gene polymorphism and physical activity in two family studies (2003) (132)
Familial resemblance for abdominal visceral fat: the HERITAGE family study (1997) (131)
Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes. (2002) (130)
The power of genetic diversity in genome-wide association studies of lipids (2021) (129)
Melanocortin 4 receptor sequence variations are seldom a cause of human obesity: the Swedish Obese Subjects, the HERITAGE Family Study, and a Memphis cohort. (2002) (128)
Evidence for an association between dehydroepiandrosterone sulfate and nonfatal, premature myocardial infarction in males. (1994) (124)
Variability in the response of HDL cholesterol to exercise training in the HERITAGE Family Study. (2002) (124)
Studies on vitiligo I. Epidemiological profile in Calcutta, India (1985) (124)
Acetylcholinesterase/paraoxonase genotype and expression predict anxiety scores in Health, Risk Factors, Exercise Training, and Genetics study. (2004) (123)
Genome-wide search for genes related to the fat-free body mass in the Québec family study. (2000) (123)
Genome-wide linkage scan for the metabolic syndrome in the HERITAGE Family Study. (2003) (122)
Adaptation to a standardized training program and changes in fitness in a large, heterogeneous population: the HERITAGE Family Study. (2000) (120)
Familial aggregation of abdominal visceral fat level: results from the Quebec family study. (1996) (119)
Methods in Genetic Epidemiology (1983) (118)
Endurance training-induced changes in insulin sensitivity and gene expression. (2005) (118)
Changes in blood lipids consequent to aerobic exercise training related to changes in body fatness and aerobic fitness. (2001) (118)
The effect of nutritional factors on sex hormone levels in male twins (1988) (117)
A meta-analysis of genome-wide linkage scans for hypertension: the National Heart, Lung and Blood Institute Family Blood Pressure Program. (2003) (117)
A more powerful robust sib‐pair test of linkage for quantitative traits (1989) (116)
Genomic scan for genes affecting body composition before and after training in Caucasians from HERITAGE. (2001) (116)
Robust methods for the detection of genetic linkage for quantitative data from pedigrees (1989) (114)
Multiple genes for essential-hypertension susceptibility on chromosome 1q. (2007) (114)
A summary of the effects of antihypertensive medications on measured blood pressure. (2005) (111)
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. (2014) (110)
A genomewide linkage scan for abdominal subcutaneous and visceral fat in black and white families: The HERITAGE Family Study. (2002) (110)
A genetic and environmental analysis of a twin family study of alcohol use, anxiety, and depression (1984) (109)
Familial aggregation of body mass index and subcutaneous fat measures in the longitudinal Québec family study (1999) (109)
Reproducibility of maximal exercise test data in the HERITAGE family study. (1999) (107)
Left ventricular concentric geometry is associated with impaired relaxation in hypertension: the HyperGEN study. (2005) (107)
General purpose model and a computer program for combined segregation and path analysis (SEGPATH): Automatically creating computer programs from symbolic language model specifications (1995) (106)
Genome-wide meta-analyses of smoking behaviors in African Americans (2012) (106)
Association and linkage between an insulin-like growth FACTOR-1 GENE polymorphism and fat free mass in the HERITAGE Family Study (1999) (103)
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium (2017) (102)
Genomewide Linkage Scan of Resting Blood Pressure: HERITAGE Family Study (2002) (102)
Segregation analysis of fat mass and other body composition measures derived from underwater weighing. (1993) (100)
NOS3 Glu298Asp Genotype and Blood Pressure Response to Endurance Training: The HERITAGE Family Study (2000) (100)
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. (2018) (100)
Genome-wide linkage scan for physical activity levels in the Quebec Family study. (2003) (96)
Neuromedin beta: a strong candidate gene linking eating behaviors and susceptibility to obesity. (2004) (95)
Endurance exercise training has a minimal effect on resting heart rate: the HERITAGE Study. (1996) (94)
Changes in ventilatory threshold with exercise training in a sedentary population: the HERITAGE Family Study. (2001) (93)
Genetic and environmental influences on the size and number of cells in the blood (1985) (93)
Cardiovascular risk factors in a French-Canadian population: resolution of genetic and familial environmental effects on blood pressure by using extensive information on environmental correlates. (1989) (93)
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (93)
Muscle-specific creatine kinase gene polymorphism and VO2max in the HERITAGE Family Study. (1997) (91)
Path analysis under generalized assortative mating. I. Theory. (1979) (91)
Associations between cardiorespiratory responses to exercise and the C34T AMPD1 gene polymorphism in the HERITAGE Family Study. (2003) (90)
Familial aggregation of submaximal aerobic performance in the HERITAGE Family study. (2001) (90)
A polymorphism in the human agouti-related protein is associated with late-onset obesity. (2002) (90)
Heritability of HR and BP response to exercise training in the HERITAGE Family Study. (2002) (88)
Analysis of the distribution of erythrocyte sodium lithium countertransport in a sample representative of the general population (1986) (88)
CAT scans, PET scans, and genomic scans (1998) (87)
Genetic analysis of idiopathic hemochromatosis using both qualitative (disease status) and quantitative (serum iron) information. (1985) (87)
Prediction of physical activity and physical work capacity (PWC150) in young adulthood from childhood and adolescence with consideration of parental measures (2001) (87)
Combining extremely concordant sibpairs with extremely discordant sibpairs provides a cost effective way to linkage analysis of quantitative trait loci (1996) (85)
Heritability of Blood Pressure Responses to Dietary Sodium and Potassium Intake in a Chinese Population (2007) (85)
Associations of candidate loci angiotensinogen and angiotensin-converting enzyme with severe hypertension: The NHLBI Family Heart Study. (1997) (85)
Possible Locus on Chromosome 18q Influencing Postural Systolic Blood Pressure Changes (2000) (85)
Major gene for abdominal visceral fat area in the Québec Family Study. (1996) (84)
Analysis of family resemblance. V. Height and weight in northeastern Brazil. (1975) (83)
AGT M235T and ACE ID polymorphisms and exercise blood pressure in the HERITAGE Family Study. (2000) (83)
Multiple regression analysis of twin data obtained from selected samples (1986) (82)
A genome-wide linkage scan for dietary energy and nutrient intakes: the Health, Risk Factors, Exercise Training, and Genetics (HERITAGE) Family Study. (2004) (81)
Competing targets of microRNA-608 affect anxiety and hypertension (2014) (80)
Relationship of changes in maximal and submaximal aerobic fitness to changes in cardiovascular disease and non-insulin-dependent diabetes mellitus risk factors with endurance training: the HERITAGE Family Study. (2001) (79)
Improvements in glucose homeostasis in response to regular exercise are influenced by the PPARG Pro12Ala variant: results from the HERITAGE Family Study (2010) (79)
Lifestyle factors in monozygotic and dizygotic twins (1988) (79)
Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease (2017) (78)
Polymorphisms in the Nonmuscle Myosin Heavy Chain 9 Gene (MYH9) Are Associated with Albuminuria in Hypertensive African Americans: The HyperGEN Study (2009) (78)
Smoking and Genetic Risk Variation Across Populations of European, Asian, and African American Ancestry—A Meta‐Analysis of Chromosome 15q25 (2012) (77)
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. (2019) (77)
Genetic variation at the apolipoprotein gene loci contribute to response of plasma lipids to dietary change (1990) (77)
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits. (2019) (77)
Influence of genotype-dependent effects of covariates on the outcome of segregation analysis of the body mass index. (1993) (76)
Leptin and leptin receptor gene polymorphisms and changes in glucose homeostasis in response to regular exercise in nondiabetic individuals: the HERITAGE family study. (2004) (76)
Variability of pulmonary function in alpha-1-antitrypsin deficiency: residual family resemblance beyond the effect of the Pi locus. (1990) (76)
Cardiac output and stroke volume changes with endurance training: the HERITAGE Family Study. (2001) (75)
A genome-wide affected sibpair linkage analysis of hypertension: the HyperGEN network. (2003) (75)
Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3. (2004) (75)
Familial clustering of insulin and abdominal visceral fat: the HERITAGE Family Study. (1998) (75)
Early onset periodontitis: A comparison and evaluation of two proposed modes of inheritance (1987) (74)
Familial resemblance in fatness and fat distribution (2000) (73)
Alterations in resting metabolic rate as a consequence of 20 wk of endurance training: the HERITAGE Family Study. (1998) (73)
The effects of exercise on the lipoprotein subclass profile: A meta-analysis of 10 interventions. (2015) (72)
An exploratory investigation of genetic linkage with body composition and fatness phenotypes: the Québec Family Study. (1994) (72)
Familial resemblance in eating behaviors in men and women from the Quebec Family Study. (2005) (72)
Equivalence of the mixed and regressive models for genetic analysis. I. Continuous traits (1989) (71)
The Future of Path Analysis, Segregation Analysis, and Combined Models for Genetic Dissection of Complex Traits (1999) (71)
Positional identification of variants of Adamts16 linked to inherited hypertension (2009) (70)
Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program (2008) (70)
Familial aggregation of exercise heart rate and blood pressure in response to 20 weeks of endurance training: the HERITAGE family study. (2003) (69)
Familial Aggregation of Blood Lipid Response to Exercise Training in the Health, Risk Factors, Exercise Training, and Genetics (HERITAGE) Family Study (2002) (69)
Cardiovascular risk factors in a french canadian population: Resolution of genetic and familial environmental effects on blood pressure using twins, adoptees, and extensive information on environmental correlates (1989) (69)
Outline of genetic epidemiology. (1983) (69)
The genetics of obesity and the metabolic syndrome. (2010) (69)
Associations of autozygosity with a broad range of human phenotypes (2019) (68)
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2021) (68)
Fitness, fatness, and estimated coronary heart disease risk: the HERITAGE Family Study. (2001) (68)
Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2017) (68)
Gender difference in diastolic function in hypertension (the HyperGEN study). (2002) (68)
Familial aggregation of resting blood pressure and heart rate in a sedentary population: the HERITAGE Family Study. Health, Risk Factors, Exercise Training, and Genetics. (1999) (67)
Quantitative trait loci for maximal exercise capacity phenotypes and their responses to training in the HERITAGE Family Study. (2004) (67)
Genome-Wide Association Study Meta-Analysis Reveals Transethnic Replication of Mean Arterial and Pulse Pressure Loci (2013) (67)
Linkage between a muscle-specific CK gene marker and VO2max in the HERITAGE Family Study. (1999) (66)
Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat (2015) (66)
Heritability estimate for refractive errors—a population‐based sample of adult twins (1988) (65)
A saturated map of common genetic variants associated with human height (2022) (65)
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (65)
Segregation and linkage analysis of nine Utah breast cancer pedigrees (1988) (65)
Segregation analysis of hereditary nonpolyposis colorectal cancer (1986) (64)
Genome-wide linkage scans for fasting glucose, insulin, and insulin resistance in the National Heart, Lung, and Blood Institute Family Blood Pressure Program: evidence of linkages to chromosome 7q36 and 19q13 from meta-analysis. (2005) (64)
Reproducibility of anthropometric and body composition measurements: the HERITAGE Family Study (1997) (64)
Reproducibility of cardiovascular, respiratory, and metabolic responses to submaximal exercise: the HERITAGE Family Study. (1998) (63)
Genome-Wide Association Study Identifies 8 Novel Loci Associated With Blood Pressure Responses to Interventions in Han Chinese (2013) (63)
A family study of the variability of pulmonary function in alpha 1-antitrypsin deficiency. Quantitative phenotypes. (1990) (63)
Genetic Effect on Blood Pressure Is Modulated by Age: The Hypertension Genetic Epidemiology Network Study (2009) (63)
Adropin: An endocrine link between the biological clock and cholesterol homeostasis (2017) (62)
Ethnicity and human genetic linkage maps. (2005) (62)
Phenotypic effects of apolipoprotein structural variation on lipid profiles: II. Apolipoprotein A‐IV and quantitative lipid measures in the healthy women study (1989) (62)
Associations between candidate loci angiotensin-converting enzyme and angiotensinogen with coronary heart disease and myocardial infarction: the NHLBI Family Heart Study. (1997) (62)
Familial resemblance of 7-year changes in body mass and adiposity. (2002) (61)
Association of inappropriate left ventricular mass with systolic and diastolic dysfunction: the HyperGEN study. (2004) (61)
The resolution of genotype × environment interaction in segregation analysis of nuclear families (1984) (61)
Effect of Endothelin 1 Genotype on Blood Pressure Is Dependent on Physical Activity or Fitness Levels (2007) (61)
Genetics of the Lp lipoprotein in Japanese‐Americans (1985) (60)
Path analysis under generalized assortative mating. II. American I.Q. (1982) (60)
Genetic etiology of gastric carcinoma: I. Chronic atrophic gastritis (1986) (60)
Uncoupling protein 3 gene is associated with body composition changes with training in HERITAGE study. (2002) (60)
Familial resemblance for body composition measures: the HERITAGE Family Study. (1997) (60)
Cross-trait familial resemblance for body fat and blood pressure: familial correlations in the Québec Family Study. (1994) (60)
Family resemblance for blood pressure. (1983) (59)
The HERITAGE Family Study: quality assurance and quality control. (1996) (59)
Mining gold dust under the genome wide significance level: a two‐stage approach to analysis of GWAS (2011) (59)
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape (2016) (59)
Association of apolipoprotein E polymorphism with blood lipids and maximal oxygen uptake in the sedentary state and after exercise training in the HERITAGE family study. (2004) (59)
Segregation analysis of serum uric acid in the NHLBI Family Heart Study (2000) (58)
Variability of human linkage data. (1978) (58)
Common Variants in Epithelial Sodium Channel Genes Contribute to Salt Sensitivity of Blood Pressure: The GenSalt Study (2011) (58)
Estimation of myriad haplotype frequencies (1985) (58)
Twin concordance for a binary trait: III. A bivariate analysis of hay fever and asthma (1990) (57)
NHLBI Family Heart Study (1996) (57)
Is adiposity at normal body weight relevant for cardiovascular disease risk? (2002) (56)
Phenomapping for the Identification of Hypertensive Patients with the Myocardial Substrate for Heart Failure with Preserved Ejection Fraction (2017) (56)
Heart rate versus %VO2max: age, sex, race, initial fitness, and training response--HERITAGE. (2003) (56)
Family study of α1‐antitrypsin deficiency: Effects of cigarette smoking, measured genotype, and their interaction on pulmonary function and biochemical traits (1992) (56)
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference (2016) (56)
Genetic variation at the lipoprotein lipase locus and plasma lipoprotein and insulin levels in the Québec Family Study. (2001) (56)
Segregation analysis of juvenile myoclonic epilepsy (1994) (56)
Evaluation of path analysis through computer simulation: Effect of incorrectly assuming independent distribution of familial correlations (1984) (55)
Estimating familial effects on age at onset and liability to schizophrenia. I. Results of a large sample family study (1990) (55)
Cleft lip with or without cleft palate: Reanalysis of a three‐generation family study from England (1986) (55)
Studies on vitiligo. II. Familial aggregation and genetics (1985) (55)
Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium (2018) (54)
The Alpha2-Adrenergic Receptor Gene and Body Fat Content and Distribution: The HERITAGE Family Study (2002) (54)
FTO Genotype Is Associated With Exercise Training–induced Changes in Body Composition (2010) (54)
Twin study of genetic and environmental effects on lipid levels (1988) (54)
Familial aggregation of amount and distribution of subcutaneous fat and their responses to exercise training in the HERITAGE family study. (2000) (54)
Genome-wide linkage scans for prediabetes phenotypes in response to 20 weeks of endurance exercise training in non-diabetic whites and blacks: the HERITAGE Family Study (2005) (53)
Major locus inheritance of apolipoprotein B in Utah pedigrees (1987) (53)
G protein β3 polymorphism and hemodynamic and body composition phenotypes in the HERITAGE Family Study (2002) (53)
Genomic Scan for Exercise Blood Pressure in the Health, Risk Factors, Exercise Training and Genetics (HERITAGE) Family Study (2001) (53)
Robust inference for variance components models in families ascertained through probands: I. Conditioning on proband's phenotype (1987) (53)
Measured maximal heart rates compared to commonly used age‐based prediction equations in the heritage family study (2013) (53)
Statistical modeling and analysis in human genetics. (1978) (53)
Meta‐analysis methodology for combining non‐parametric sibpair linkage results: Genetic homogeneity and identical markers (1998) (53)
Genetic variants in the renin–angiotensin–aldosterone system and salt sensitivity of blood pressure (2010) (52)
An investigation of the effects of lipid-lowering medications: genome-wide linkage analysis of lipids in the HyperGEN study (2007) (52)
Two ethnic-specific polymorphisms in the human Agouti-related protein gene are associated with macronutrient intake. (2005) (52)
19 Classification methods for confronting heterogeneity (2001) (52)
A time‐dependent logistic hazard function for modeling variable age of onset in analysis of familial diseases (1990) (52)
Familial risk of obesity and central adipose tissue distribution in the general Canadian population. (1999) (52)
Plasma post-heparin lipase activities in the HERITAGE Family Study: the reproducibility, gender differences, and associations with lipoprotein levels. HEalth, RIsk factors, exercise Training and GEnetics. (1999) (51)
Tree‐based recursive partitioning methods for subdividing sibpairs into relatively more homogeneous subgroups (2001) (51)
Between Candidate Genes and Whole Genomes: Time for Alternative Approaches in Blood Pressure Genetics (2012) (51)
Search for faster methods of fitting the regressive models to quantitative traits (1990) (51)
An evaluation of the metabolic syndrome in a large multi-ethnic study: the Family Blood Pressure Program (2005) (50)
Familial aggregation of QT‐interval variability in a general population: results from the NHLBI Family Heart Study (2001) (50)
Familial resemblance for glucose and insulin metabolism indices derived from an intravenous glucose tolerance test in Blacks and Whites of the HERITAGE Family Study (2001) (50)
Commingling analysis of generalized body mass and composition measures: the Québec Family Study. (1991) (50)
An evaluation of the metabolic syndrome in the HyperGEN study (2005) (50)
Familial risk of overweight and obesity in the Canadian population using the WHO/NIH criteria. (2000) (50)
On the role of vitamin D binding globulin in glucose homeostasis: Results from the San Luis Valley diabetes study (1989) (49)
The genetic epidemiology of leprosy in a Brazilian population. (1995) (49)
Demonstration of a common major gene with pleiotropic effects on immunoglobulin E levels and allergy (1985) (49)
Familial aggregation of lipids and lipoproteins in families ascertained through random and nonrandom probands in the Iowa Lipid Research Clinics family study. (1991) (49)
Peroxisome proliferator-activated receptor-δ polymorphisms are associated with physical performance and plasma lipids: the HERITAGE Family Study (2007) (49)
Race differences in the response of postheparin plasma lipoprotein lipase and hepatic lipase activities to endurance exercise training in men: results from the HERITAGE Family Study. (2001) (49)
Linkage and segregation analyses of apolipoproteins A1 and B, and lipoprotein cholesterol levels in a large pedigree with excess coronary heart disease: The Bogalusa heart study (1987) (49)
A genome-wide linkage scan for steroids and SHBG levels in black and white families: the HERITAGE Family Study. (2002) (49)
Three Ontologies to Define Phenotype Measurement Data (2012) (49)
Effect of regular exercise on homocysteine concentrations: the HERITAGE Family Study (2006) (48)
Heritability of submaximal exercise heart rate response to exercise training is accounted for by nine SNPs. (2012) (48)
A quantitative trait locus on 7q31 for the changes in plasma insulin in response to exercise training: the HERITAGE Family Study. (2003) (48)
Assessing the effect of multiple linkage tests in complex diseases (1990) (48)
Multiancestry Study of Gene–Lifestyle Interactions for Cardiovascular Traits in 610 475 Individuals From 124 Cohorts: Design and Rationale (2017) (48)
Familial aggregation of stroke volume and cardiac output during submaximal exercise: the HERITAGE Family Study. (2000) (48)
Familial resemblance for free androgens and androgen glucuronides in sedentary black and white individuals: the HERITAGE Family Study. Health, Risk Factors, Exercise Training and Genetics. (2001) (48)
Genetic epidemiology of coronary heart disease. Past, present, and future. (1984) (48)
Inheritance of human platelet thermolabile phenol sulfotransferase (TL PST) activity (1988) (47)
Gene-smoking interactions identify several novel blood pressure loci in the Framingham Heart Study. (2015) (47)
Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration (2019) (47)
Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: The HyperGEN Study (2009) (47)
Adiponectin polymorphisms, adiposity and insulin metabolism: HERITAGE family study and Oulu diabetic study (2005) (47)
Evidence of LPL gene-exercise interaction for body fat and LPL activity: the HERITAGE Family Study. (2001) (46)
Evidence for a Major Quantitative Trait Locus on Chromosome 17q21 Affecting Low-Density Lipoprotein Peak Particle Diameter (2003) (46)
An Empirical Comparison of Meta‐analysis and Mega‐analysis of Individual Participant Data for Identifying Gene‐Environment Interactions (2014) (46)
An overview of the genetic dissection of complex traits. (2008) (46)
Effects of β2-Adrenergic Receptor Gene Variants on Adiposity: The HERITAGE Family Study (2003) (46)
Linkage detection tests under heterogeneity (1989) (46)
Segregation analysis of abdominal visceral fat: the HERITAGE Family Study. (1997) (46)
Sib‐pair linkage tests for disease susceptibility loci: Common tests vs. the asymptotically most powerful test (1990) (46)
A maximum likelihood map of chromosome 1. (1979) (46)
A chi‐square test to distinguish allelic association from other causes of phenotypic association between two loci (1985) (45)
Major gene influence on the propensity to store fat in trunk versus extremity depots: evidence from the Québec Family Study. (1995) (45)
Three mitochondrial DNA restriction polymorphisms in elite endurance athletes and sedentary controls. (1998) (45)
Associations between angiotensinogen gene variants and left ventricular mass and function in the HyperGEN study. (2002) (45)
A defense of path analysis in genetic epidemiology. (1983) (45)
Complete hydatidiform mole in Hawaii: An epidemiological study (1984) (45)
Post-heparin lipolytic enzyme activities, sex hormones and sex hormone-binding globulin (SHBG) in men and women: The HERITAGE Family Study. (2003) (45)
Genetics of total serum IgE levels: A regressive model approach to segregation analysis (1991) (44)
A method to detect excess risk of disease in structured data: Cancer in relatives of retinoblastoma patients (1984) (44)
Genome-wide linkage scan reveals multiple susceptibility loci influencing lipid and lipoprotein levels in the Québec Family Studys⃞s⃞ The online version of this article (available at http://www.jlr.org) contains one additional table. Published, JLR Papers in Press, December 16, 2003. DOI 10.1194/jl (2004) (44)
Familial resemblance in ventilatory threshold: the HERITAGE Family Study. (2001) (43)
Familial resemblance for resting blood pressure with particular reference to racial differences: preliminary analyses from the HERITAGE Family Study. (1998) (43)
Novel findings and future directions on the genetics of hypertension (2012) (43)
The Na+-K+-ATPase α2 gene and trainability of cardiorespiratory endurance: The HERITAGE Family Study (2000) (43)
Genetic variants in the apelin system and blood pressure responses to dietary sodium interventions: a family-based association study (2010) (43)
Familial correlations in the Québec family study: cross-trait familial resemblance for body fat with plasma glucose and insulin (1996) (42)
Robust inference for variance components models in families ascertained through probands: II. Analysis of spirometric measures (1987) (42)
Relationship of epithelial ovarian cancer to other malignancies within families (1988) (42)
The detection of major loci by segregation and linkage analysis: A simulation study (1984) (42)
Causal analysis of academic performance (1977) (42)
Commingling analysis of regional fat distribution measures: the Québec family study. (1992) (42)
A new model for the resolution of cultural and biological inheritance in the presence of temporal trends: Application to systolic blood pressure (1985) (42)
Optimum designs for next‐generation sequencing to discover rare variants for common complex disease (2011) (42)
Lifestyle and blood pressure levels in male twins in Utah (1988) (42)
Evidence for at least two major loci influencing human fatness. (1998) (42)
Classification methods for confronting heterogeneity. (2001) (42)
Sex differences in the relationships of abdominal fat to cardiovascular disease risk among normal-weight white subjects (2004) (42)
Body fat, resting and exercise blood pressure and the angiotensinogen M235T polymorphism: the heritage family study. (1999) (41)
FAMILIAL AGGREGATION OF CARDIOVASCULAR RESPONSE TO SUBMAXIMAL EXERCISE IN THE HERITAGE FAMILY STUDY (2001) (41)
Biological and cultural sources of familial resemblance in plasma lipids: A comparison between North America and Israel—the lipid research clinics program (1988) (41)
Possible linkage of a breast cancer‐susceptibility locus to the ABO locus: Sensitivity of LOD scores to a single new recombinant observation (1984) (41)
Increased risk for gestational diabetes mellitus associated with insulin receptor and insulin‐like growth factor II restriction fragment length polymorphisms (1989) (41)
Estimation of individual genetic and environmental factor scores (1990) (41)
Phenylthiocarbamide taste sensitivity revisited: Complete sorting test supports residual family resemblance (1989) (41)
Linkage and association studies of the lipoprotein lipase gene with postheparin plasma lipase activities, body fat, and plasma lipid and lipoprotein concentrations: the HERITAGE Family Study. (2000) (41)
Mixed-model segregation analysis of schizophrenia in the lindelius Swedish pedigrees (1990) (41)
Two Major QTLs and Several Others Relate to Factors of Metabolic Syndrome in the Family Blood Pressure Program (2005) (40)
Combining least absolute shrinkage and selection operator (LASSO) and principal-components analysis for detection of gene-gene interactions in genome-wide association studies (2009) (40)
Segregation analyses of stuttering (1984) (40)
Association of genetic variants in the apelin-APJ system and ACE2 with blood pressure responses to potassium supplementation: the GenSalt study. (2010) (40)
Heritability of clinical chemistries in an older twin cohort: The NHLBI Twin Study (1987) (40)
Linkage analysis assuming a single‐locus mode of inheritance for traits determined by two loci: Inferring mode of inheritance and estimating penetrance (1990) (40)
Path analysis of family resemblance with temporal trends: applications to height, weight, and Quetelet index in northeastern Brazil. (1985) (40)
Body composition and fat distribution influence systemic hemodynamics in the absence of obesity: the HyperGEN Study. (2005) (39)
Genome-wide linkage scan for exercise stroke volume and cardiac output in the HERITAGE Family Study. (2002) (39)
Performance of Genotype Imputations Using Data from the 1000 Genomes Project (2011) (39)
Stability of adiposity phenotypes from childhood and adolescence into young adulthood with contribution of parental measures. (2001) (39)
The Cincinnati Myocardial Infarction and Hormone Family Study: family resemblance for dehydroepiandrosterone sulfate in control and myocardial infarction families. (1993) (39)
Aortic valve sclerosis is associated with preclinical cardiovascular disease in hypertensive adults: the Hypertension Genetic Epidemiology Network study (2005) (39)
Power of the linkage test for a heterogeneous disorder due to two independent inherited causes: A simulation study (1990) (39)
Reproducibility of resting blood pressure and heart rate measurements. The HERITAGE Family Study. (2000) (39)
Further evidence of a quantitative trait locus on chromosome 18 influencing postural change in systolic blood pressure: the Hypertension Genetic Epidemiology Network (HyperGEN) Study. (2005) (39)
Familial clustering of abdominal visceral fat and total fat mass: the Québec Family Study. (1996) (38)
Genetic dissection of complex traits: an overview. (2001) (38)
Linkage disequilibrium between DNA markers at the low‐density lipoprotein receptor gene (1990) (38)
Random effects model for meta‐analysis of multiple quantitative sibpair linkage studies (1996) (38)
Menopause, estrogen, and training effects on exercise hemodynamics: the HERITAGE study. (2002) (38)
Maximum-likelihood estimation of familial correlations from multivariate quantitative data on pedigrees: a general method and examples. (1987) (38)
Familial aggregation of V ˙ O 2max response to exercise training: results from the HERITAGE Family Study (1999) (38)
Commingling and segregation analysis of blood pressure in a French-Canadian population. (1990) (38)
Glucose tolerance and ancestral genetic admixture in six semitraditional pacific populations (1984) (38)
An updated meta-analysis of genome scans for hypertension and blood pressure in the NHLBI Family Blood Pressure Program (FBPP). (2006) (38)
Colchester revisited: a genetic study of mental defect. (1977) (37)
Genetics of Hypertension and Cardiovascular Disease and Their Interconnected Pathways: Lessons from Large Studies (2011) (37)
Novel genetic variants contributing to left ventricular hypertrophy: the HyperGEN study (2009) (37)
Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2016) (37)
Familial resemblance for muscle phenotypes in the HERITAGE Family Study. (2003) (37)
The hormone-sensitive lipase gene and body composition: the HERITAGE Family Study (2002) (37)
Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9 (2013) (37)
Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans (2016) (37)
Availability of schizophrenic patients and their families for genetic linkage studies: Findings from the Maryland epidemiology sample (1989) (36)
Familial resemblance of bone mass in adult women (1986) (36)
Evidence for linkage between Wilson disease and esterase D in three kindreds: Detection of linkage for an autosomal recessive disorder by the family study method (1986) (36)
A genetic analysis of clubfoot in Hawaii (1987) (36)
Commingling in the distributions of immunoglobulin levels. (1989) (36)
Segregation analysis of body mass index in an unselected French-Canadian sample: the Québec Family Study. (1993) (35)
Segregation analysis of plasminogen activator inhibitor-1 and fibrinogen levels in the NHLBI family heart study. (1998) (35)
Immunoglobulin E revisited. (1980) (35)
Hepatic lipase gene variant -514C>T is associated with lipoprotein and insulin sensitivity response to regular exercise: the HERITAGE Family Study. (2005) (35)
Congenital anomalies in American Indians of British Columbia (1986) (35)
Role of gene expression microarray analysis in finding complex disease genes (2002) (34)
A genetic study of sex hormone--binding globulin measured before and after a 20-week endurance exercise training program: the HERITAGE Family Study. (2000) (34)
A variance components/major locus likelihood approximation on quantitative data (1991) (34)
G protein beta 3 polymorphism and hemodynamic and body composition phenotypes in the HERITAGE Family Study. (2002) (34)
Endogenous sex hormone levels and breast cancer risk (1987) (34)
Genetic association mapping under founder heterogeneity via weighted haplotype similarity analysis in candidate genes (2004) (34)
Multifactorial analysis of family data ascertained through truncation: a comparative evaluation of two methods of statistical inference. (1988) (34)
Family History of Coronary Heart Disease and Hemostatic Variables in Middle-Aged Adults (1997) (34)
The distribution of debrisoquine metabolic phenotypes and implications for the suggested association with lung cancer risk (1989) (34)
On the asymmetry of biological frequency distributions (1990) (34)
Extensions to sib‐pair linkage tests applicable to disorders characterized by delayed onset (1990) (33)
Trade‐off between false positives and false negatives in the linkage analysis of complex traits (1997) (33)
CREB1 Is a Strong Genetic Predictor of the Variation in Exercise Heart Rate Response to Regular Exercise: The HERITAGE Family Study (2010) (32)
Segregation analysis of serum uric acid in the NHLBI Family Heart Study. (2000) (32)
Blood pressure stress reactivity and left ventricular mass in a random community sample of African-American and caucasian men and women. (2006) (32)
Plasma cholesterol variation in the national heart, lung and blood institute twin study (1987) (32)
The agouti-related protein and body fatness in humans (2003) (32)
Familial aggregation in chronic obstructive pulmonary disease: Use of the loglinear model to analyze intermediate environmental and genetic risk factors (1985) (32)
Compendium of genome-wide scans of lipid-related phenotypes: adding a new genome-wide search of apolipoprotein levels. (2004) (32)
Familial clustering of multiple measures of adiposity and fat distribution in the Québec Family Study: a trivariate analysis of percent body fat, body mass index, and trunk-to-extremity skinfold ratio. (1995) (32)
A linkage strategy for detection of human quantitative-trait loci. I. Generalized relative risk ratios and power of sib pairs with extreme trait values. (1997) (32)
Familial resemblance of adiposity-related parameters: Results from a health check-up population in Taiwan (2002) (31)
NOS 3 Glu 298 Asp Genotype and Blood Pressure Response to Endurance Training The HERITAGE Family Study (2000) (31)
Race and sex similarities in exercise-induced changes in blood lipids and fatness. (2004) (31)
Cross-trait familial resemblance for body fat and blood lipids: familial correlations in the Quebec Family Study. (1997) (31)
A major simplification in the preliminary ordering of linked loci (1988) (31)
The alpha 2-adrenergic receptor gene and body fat content and distribution: the HERITAGE Family Study. (2002) (31)
Population sequencing data reveal a compendium of mutational processes in human germline (2020) (31)
Familial resemblance for physique: heritabilities for somatotype components. (2000) (31)
A Review of the Genetics of Hypertension with a Focus on Gene-Environment Interactions (2017) (31)
Genome-Wide Linkage Mapping for Valve Calcification Susceptibility Loci in Hypertensive Sibships: The Hypertension Genetic Epidemiology Network Study (2007) (30)
Quantitative Trait Locus on 15q for a Metabolic Syndrome Variable Derived from Factor Analysis (2007) (30)
Spousal resemblance and risk of 7-year increases in obesity and central adiposity in the Canadian population. (1999) (30)
Genomic scan of glucose and insulin metabolism phenotypes: the HERITAGE Family Study. (2003) (30)
Huntington disease: Estimation of heterozygote status using linked genetic markers (1984) (30)
A whole genome scan for pulse pressure/stroke volume ratio in African Americans: the HyperGEN study. (2007) (30)
A linkage strategy for detection of human quantitative-trait loci. II. Optimization of study designs based on extreme sib pairs and generalized relative risk ratios. (1997) (29)
A genetic and epidemiologic study of periodontal disease in Hawaii. II. Genetic and environmental influence. (1977) (29)
Genetic regulation of plasma and red blood cell magnesium concentrations in man. I. Univariate and bivariate path analyses. (1982) (29)
Familial factors associated with malignant gliomas (1990) (29)
Association between polymorphic blood markers and risk factors for cardiovascular disease in a large pedigree (1987) (29)
The TNF-α G-308A polymorphism is associated with C-reactive protein levels: The HERITAGE Family Study (2006) (29)
CETP genotypes and HDL-cholesterol phenotypes in the HERITAGE Family Study. (2007) (28)
Assessing familial aggregation of congenital cardiovascular malformations in case‐control studies (1988) (28)
Haplotype Association Analysis of AGT Variants with Hypertension-Related Traits: The HyperGEN Study (2005) (28)
KIF5B gene sequence variation and response of cardiac stroke volume to regular exercise. (2009) (28)
Pleiotropic QTL on chromosome 19q13 for triglycerides and adiposity: the HERITAGE Family Study. (2006) (28)
Meta-analysis of genome-wide scans for blood pressure in African American and Nigerian samples. The National Heart, Lung, and Blood Institute GeneLink Project. (2006) (28)
A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. (2019) (28)
Genome-wide linkage scan reveals multiple susceptibility loci inﬂuencing lipid and lipoprotein levels in the Québec Family Study (2004) (27)
Variants in CXADR and F2RL1 are associated with blood pressure and obesity in African-Americans in regions identified through admixture mapping (2012) (27)
Path analysis of family resemblance in the presence of gene-environment interaction. (1974) (27)
Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study. (2016) (27)
Using Tree‐Based Recursive Partitioning Methods to Group Haplotypes for Increased Power in Association Studies (2005) (27)
Human parotid proline‐rich proteins: Correlation of genetic polymorphisms to dental caries (1986) (27)
The analysis of Schizophrenia family data (1986) (27)
Segregation analysis of body mass index in a large sample selected for obesity: the Swedish Obese Subjects study. (1999) (27)
A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction (2016) (27)
Sex differences in affective disorder: Genetic transmission (1987) (27)
PCSK9 variation and association with blood pressure in African Americans: preliminary findings from the HyperGEN and REGARDS studies (2015) (27)
Decreased fasting and oral glucose stimulated C-peptide in nondiabetic subjects with sequence variants in the sulfonylurea receptor 1 gene. (2001) (26)
Etiological heterogeneity in Hodgkin's disease: HLA linked and unlinked determinants of susceptibility independent of histological concordance (1986) (26)
Bivariate survival models for analysis of genetic and environmental effects in twins (1990) (26)
Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans (2016) (26)
Relationship between body mass index, cigarette smoking, and plasma sex steroids in normal male twins (1989) (26)
Causes of death in huntington disease as reported on death certificates (1986) (26)
Longitudinal trends in the association of metabolic syndrome with 550 k single-nucleotide polymorphisms in the Framingham Heart Study (2009) (26)
Estimation of genetic model parameters: Variables correlated with a quantitative phenotype exhibiting major locus inheritance (1989) (26)
Total body fat and abdominal visceral fat response to exercise training in the HERITAGE Family Study: evidence for major locus but no multifactorial effects. (1999) (25)
Resolution of genetic and cultural inheritance in twin families by path analysis: application to HDL-cholesterol. (1985) (25)
Complex segregation analysis of blood pressure and heart rate measured before and after a 20-week endurance exercise training program: the HERITAGE Family Study. (2000) (25)
Quantitative trait loci for metabolic syndrome in the Hypertension Genetic Epidemiology Network study. (2005) (25)
Relation of insulin to left ventricular geometry and function in African American and white hypertensive adults: the HyperGEN study. (2002) (25)
The genetic susceptibility to insulin‐dependent diabetes mellitus: Combined segregation and linkage analysis (1985) (25)
An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP) (2007) (25)
Peroxisome proliferator-activated receptor-delta polymorphisms are associated with physical performance and plasma lipids: the HERITAGE Family Study. (2007) (25)
Associations of aortic and mitral regurgitation with body composition and myocardial energy expenditure in adults with hypertension: the Hypertension Genetic Epidemiology Network study. (2003) (25)
Protein tyrosine phosphatase 1B variant associated with fat distribution and insulin metabolism. (2005) (25)
A family study of panic disorder (1987) (25)
Test of genetic heterogeneity of cleft lip with or without cleft palate as related to race and severity (1989) (25)
An application of a model for a genotype‐dependent relationship between a concomitant (age) and a quantitative trait(LDL cholesterol)in pedigree data (1984) (24)
Functional dimorphism of two hAgRP promoter SNPs in linkage disequilibrium (2004) (24)
Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose (2020) (24)
Heterogeneity in the familial aggregation of fasting serum uric acid level in five North American populations: the Lipid Research Clinics Family Study. (1990) (24)
Two‐disease locus model: Sib pair method using information on both HLA and Gm (1986) (24)
An approach to the multivariate analysis of high‐density‐lipoprotein cholesterol in a large kindred: The Bogalusa Heart Study (1986) (24)
The inheritance of pyloric stenosis explained by a multifactorial threshold model with sex dimorphism for liability (1986) (24)
Testing causal hypotheses in multivariate linkage analysis of quantitative traits: General formulation and application to sibpair data (1998) (24)
A major gene for primary hypoalphalipoproteinemia. (1986) (24)
The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis (2018) (24)
The Cincinnati Lipid Research Clinic family study. Bivariate path analyses of lipoprotein concentrations. (1983) (23)
Blood pressure responses to acute stress and left ventricular mass (The Hypertension Genetic Epidemiology Network Study). (2002) (23)
TGF-β1 gene-race interactions for resting and exercise blood pressure in the HERITAGE family study (2001) (23)
Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes (2019) (23)
The Family Risk Score for coronary heart disease: associations with lipids, lipoproteins, and body habitus in a middle-aged bi-racial cohort: The ARIC study. (2000) (23)
Titin is a candidate gene for stroke volume response to endurance training: the HERITAGE Family Study. (2003) (23)
Linkage and Association of the Sodium Potassium-Adenosine Triphosphatase α2 and β1 Genes with Respiratory Quotient and Resting Metabolic Rate in the Québec Family Study (1999) (23)
A Genetic study of hypoalphalipoproteinemia (1984) (23)
Genetic variants in the renin–angiotensin–aldosterone system and blood pressure responses to potassium intake (2011) (23)
Effects of beta2-adrenergic receptor gene variants on adiposity: the HERITAGE Family Study. (2003) (22)
A Monte Carlo evaluation of three statistical methods used in path analysis (1987) (22)
Variants in the CD 36 gene associate with the metabolic syndrome and high-density lipoprotein cholesterol (2008) (22)
Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians (2017) (22)
Blood Pressure Genetic Risk Score Predicts Blood Pressure Responses to Dietary Sodium and Potassium: The GenSalt Study (Genetic Epidemiology Network of Salt Sensitivity) (2017) (22)
Heritability of LDL peak particle diameter in the Quebec Family Study (2003) (22)
Genome-wide linkage scan for submaximal exercise heart rate in the HERITAGE family study. (2007) (22)
Phenotypic effects of apolipoprotein structural variation on lipid profiles. I. APO H and quantitative lipid measures in the healthy women study (1989) (22)
Nonrandom segregation: Uniformly most powerful test and related considerations (1987) (22)
Variations in the four and a half LIM domains 1 gene (FHL1) are associated with fasting insulin and insulin sensitivity responses to regular exercise (2007) (22)
Possible heterogeneity in the segregation pattern of breast cancer in families with bilateral breast cancer (1988) (22)
Resequencing Epithelial Sodium Channel Genes Identifies Rare Variants Associated With Blood Pressure Salt-Sensitivity: The GenSalt Study (2018) (22)
The TNF-alpha G-308A polymorphism is associated with C-reactive protein levels: the HERITAGE Family Study. (2006) (21)
Genetic pleiotropy for resting metabolic rate with fat-free mass and fat mass: the Québec Family Study. (1996) (21)
The Na(+)-K(+)-ATPase alpha2 gene and trainability of cardiorespiratory endurance: the HERITAGE family study. (2000) (21)
A genetic study of cortisol measured before and after endurance training: the HERITAGE Family Study. (2002) (21)
Trade-off between sibship size and sampling scheme for detecting quantitative trait loci. (1997) (21)
Heterogeneity in the biological and cultural determinants of high-density lipoprotein cholesterol in five North American populations: the Lipid Research Clinics Family Study. (1989) (21)
Major gene effects on exercise ventilatory threshold: the HERITAGE Family Study. (2002) (21)
Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2020) (21)
Efficient methods for computing linkage likelihoods of recessive diseases in inbred pedigrees (1991) (21)
Estimating familial effects on age at onset and liability to schizophrenia. II. Adjustment for censored data (1990) (21)
Testing for developmental changes in gene expression on resemblance for quantitative traits in kinships of twins: Application to height, weight, and blood pressure (1986) (21)
TGF-beta(1) gene-race interactions for resting and exercise blood pressure in the HERITAGE Family Study. (2001) (21)
Functional identification of the promoter of SLC4A5, a gene associated with cardiovascular and metabolic phenotypes in the HERITAGE Family Study (2009) (21)
Epidemiology and medical statistics (2008) (21)
Large deviations in the distribution of rare genes. (1973) (21)
Genetic epidemiology of differences in low‐density lipoprotein (LDL) cholesterol concentration: Possible involvement of variation at the apolipoprotein B gene locus in LDL kinetics (1990) (21)
Inheritance of the waist-to-hip ratio in the National Heart, Lung, and Blood Institute Family Heart Study. (2000) (21)
Genetic dissection of complex traits (2001) (21)
An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene‐Lifestyle Interactions Working Group (2016) (21)
Heritability of blood pressure in 7‐ to 12‐year‐old Chinese twins, with special reference to body size effects (1990) (20)
The Trp64Arg polymorphism of the β3-adrenergic receptor gene is not associated with training-induced changes in body composition: The HERITAGE Family Study (2001) (20)
Using survival methods to estimate age‐at‐onset distributions for genetic diseases with an application to Huntington disease (1989) (20)
Genome screening using extremely discordant and extremely concordant sib pairs (1997) (20)
Cincinnati myocardial infarction and hormone family study: family resemblance for testosterone in random and MI families. (1993) (20)
Whole-exome Sequencing and an iPSC-Derived Cardiomyocyte Model Provides a Powerful Platform for Gene Discovery in Left Ventricular Hypertrophy (2012) (20)
Prevalence and associations of apolipoprotein A‐I linked DNA polymorphisms: Results from a population study (1986) (20)
Familial aggregation of subcutaneous fat patterning: Principal components of skinfolds in the Québec family study (1996) (20)
Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program. (2010) (20)
Phenotypic effects of apolipoprotein structural variation on lipid profiles. IV. Apolipoprotein polymorphisms in a small group of black women from the Healthy Women Study (1989) (20)
Age and prevalence of sickle‐cell trait in a large ambulatory population (1987) (20)
Effect of maternal and infant covariates on sibship correlation in birth weight (1988) (20)
Mentored Training to Increase Diversity among Faculty in the Biomedical Sciences: The NHLBI Summer Institute Programs to Increase Diversity (SIPID) and the Programs to Increase Diversity among Individuals Engaged in Health-related Research (PRIDE). (2017) (19)
Repeated‐measures model for the investigation of temporal trends using longitudinal family studies: Application to systolic blood pressure (1989) (19)
Commingling and segregation analyses: Comparison of results from a simulation study of a quantitative trait (1990) (19)
Familial resemblance for coronary heart disease risk: the HERITAGE Family Study. (2000) (19)
Effects of household sharing on high density lipoprotein and its subfractions (1985) (19)
Linkage and association of the sodium potassium-adenosine triphosphatase alpha2 and beta1 genes with respiratory quotient and resting metabolic rate in the Québec Family Study. (1999) (19)
A Gene-Based Analysis of Variants in the Serum/Glucocorticoid Regulated Kinase (SGK) Genes with Blood Pressure Responses to Sodium Intake: The GenSalt Study (2014) (19)
Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study (2011) (19)
Ignoring temporal trends in genetic effects substantially reduces power of quantitative trait linkage analysis (2008) (19)
Familial aggregation of cancer in Laredo, Texas: A generally low‐risk Mexican‐American population (1986) (19)
Interactions of genetic variants with physical activity are associated with blood pressure in Chinese: the GenSalt study. (2011) (19)
Fine mapping of a QTL on chromosome 13 for submaximal exercise capacity training response: the HERITAGE Family Study (2012) (19)
Race differences in the pattern of familial aggregation for dehydroepiandrosterone sulfate and its responsiveness to training in the HERITAGE Family Study. (2001) (19)
Criteria for onset critically influence the estimation of familial risk in Alzheimer's disease (1989) (19)
Major gene effect on body mass index: the role of energy intake and energy expenditure. (2000) (19)
Genome-wide scans for heritability of fasting serum insulin and glucose concentrations in hypertensive families (2005) (19)
Genome-wide linkage scans for loci affecting total cholesterol, HDL-C, and triglycerides: the Family Blood Pressure Program (2006) (19)
Evidence of major genes for exercise heart rate and blood pressure at baseline and in response to 20 weeks of endurance training: the HERITAGE family study. (2003) (19)
Associations of epithelial sodium channel genes with blood pressure changes and hypertension incidence: the GenSalt study. (2014) (18)
Evidence for a dominant gene mechanism underlying coeliac disease in the West of Ireland (1991) (18)
Using factor scores to detect G × E Interactive Origin of “pure” genetic or environmental factors obtained in genetic covariance structure analysis (1990) (18)
Evidence of major genes for plasma HDL, LDL cholesterol and triglyceride levels at baseline and in response to 20 weeks of endurance training: the HERITAGE Family Study. (2005) (18)
Genetic and environmental determinants of periodontal disease. (1979) (18)
Multivariate analysis of lipoprotein cholesterol fractions. (1987) (18)
73 THE ROLE OF THE KALLIKREIN-KININ SYSTEM GENES IN THE SALT-SENSITIVITY OF BLOOD PRESSURE: THE GENSALT STUDY (2012) (18)
A family study of panic disorder: Reanalysis using a regressive logistic model that incorporates a sibship environment (1990) (18)
Human epithelial Na+ channel missense variants identified in the GenSalt study alter channel activity. (2016) (18)
Tests of linkage and heterogeneity in Mendelian diseases using identity by descent scores (1987) (18)
Reduction of physical assignments to a standard lod table: Chromosome 1 (1981) (18)
HLA antigens and acute rheumatic fever: Evidence for a recessive susceptibility gene linked to HLA (1985) (18)
False‐positive reporting of Down syndrome on Ohio and New York birth certificates (1985) (17)
Testing for familial aggregation of a dichotomous trait (1986) (17)
Genetic analysis of human breast cancer: Implications for family study designs (1988) (17)
Meta‐analysis of genetic linkage to quantitative trait loci with study‐specific covariates: A mixed‐effects model (1999) (17)
Blood pressure response to potassium supplementation is associated with genetic variation in endothelin 1 and interactions with E selectin in rural Chinese (2010) (17)
Genomic Predictors of Maximal Oxygen Uptake 4 Response to Standardized Exercise Training Programs (2010) (17)
Segregation analysis of apolipoproteins A-1 and B-100 measured before and after an exercise training program: the HERITAGE Family Study. (2000) (17)
Evidence of QTLs on chromosomes 13q and 14q for triglycerides before and after 20 weeks of exercise training: the HERITAGE Family Study. (2005) (17)
A major gene for resting metabolic rate unassociated with body composition: results from the Québec Family Study. (1996) (17)
Analysis of family resemblance for immunoglobulin M, G and A levels. (1981) (17)
The Cincinnati lipid research clinic family study: Analysis of commingling and family resemblance for fasting blood glucose (1984) (17)
Some effects of selection strategies on linkage analysis (1988) (17)
Variants on chromosome 6p22.3 associated with blood pressure in the HyperGEN study: follow-up of FBPP quantitative trait loci. (2011) (17)
Major gene polymorphism for human erythrocyte (RBC) thiol methyltransferase (TMT) (1989) (17)
Titin is a candidate gene for stroke volume response to endurance training: the HERITAGE Family Study (2003) (17)
Nonrandom sampling in genetic epidemiology: Maximum likelihood methods for multifactorial analysis of quantitative data ascertained through truncation (1987) (17)
Genetic regulation of plasma and red blood cell magnesium concentration in man. II. Segregation analysis. (1983) (17)
Assessment of the interaction of heritability of volume load and left ventricular mass: the HyperGEN offspring study (2007) (16)
QTLs of factors of the metabolic syndrome and echocardiographic phenotypes: the hypertension genetic epidemiology network study (2008) (16)
Causal analysis of family resemblance. (1979) (16)
Path Analysis of Quantitative Inheritance (1980) (16)
Characterization of LD structures and the utility of HapMap in genetic association studies. (2008) (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)
Combined segregation and linkage analysis of genetic hemochromatosis using affection status, serum iron, and HLA. (1990) (16)
Angiogenin gene-race interaction for resting and exercise BP phenotypes: the HERITAGE Family Study. (2001) (16)
Genetic epidemiology of the Mitsuda reaction in leprosy. (1996) (16)
Familial resemblance of plasma apolipoprotein B: The Nancy study (1990) (16)
Trends in metabolic syndrome and gene networks in human and rodent models. (2008) (16)
Path analysis under generalized marital resemblance: Evaluation of the assumptions underlying the mixed homogamy model by the Monte Carlo method (1989) (16)
Familial risk ratios for high and low physical fitness levels in the Canadian population. (2000) (16)
Aggregation of colon cancer in family data (1984) (16)
Genetic epidemiology of myotonic dystrophy (1987) (16)
No linkage of the lipoprotein lipase locus to hypertension in Caucasians. (1999) (16)
A genetic study of red blood cell zinc concentration in man. (1983) (16)
Efficient computation of patterned covariance matrix mixed models in quantitative segregation analysis (1991) (16)
Pleiotropic QTL on Chromosome 12q23–q24 Influences Triglyceride and High-Density Lipoprotein Cholesterol Levels: The HERITAGE Family Study (2006) (16)
Factor relationships of metabolic syndrome and echocardiographic phenotypes in the HyperGEN study (2008) (16)
Determinants of blood pressure in Japanese-American families (1980) (16)
Linkage of left ventricular early diastolic peak filling velocity to chromosome 5 in hypertensive African Americans: the HyperGEN echocardiography study. (2002) (16)
Gene-education interactions identify novel blood pressure loci in the Framingham Heart Study. (2014) (16)
Interactions among the glucocorticoid receptor, lipoprotein lipase, and adrenergic receptor genes and plasma insulin and lipid levels in the Quebec Family Study. (2001) (15)
AGT M 235 T and ACE ID polymorphisms and exercise blood pressure in the HERITAGE Family Study (2000) (15)
Genome-Wide Linkage and Positional Candidate Gene Study of Blood Pressure Response to Dietary Potassium Intervention: The Genetic Epidemiology Network of Salt Sensitivity Study (2010) (15)
Interactions among the β2- and β3- adrenergic receptor genes and total body fat and abdominal fat level in the HERITAGE Family Study (2003) (15)
An update on genome-wide association studies of hypertension (2015) (15)
Polymorphisms of ACE2 are associated with blood pressure response to cold pressor test: the GenSalt study. (2012) (15)
Genotype Imputation for African Americans Using Data From HapMap Phase II Versus 1000 Genomes Projects (2012) (15)
Linkage Analysis of Alpha 1-Antitrypsin Deficiency: Lessons for Complex Diseases (2001) (15)
Statistical analysis of outcomes from repeated pregnancies: Effects of HLA sharing on fetal loss rates (1991) (15)
Robustness of path analysis of family resemblance against deviations from multivariate normality. (1987) (14)
Genetics, response to exercise, and risk factors: the HERITAGE Family Study. (1997) (14)
Familial Resemblance for Hostility: The National Heart, Lung, and Blood Institute Family Heart Study (2000) (14)
Heterogeneity in multifactorial inheritance of plasma lipids and lipoproteins in ethnically diverse families in Jerusalem (1986) (14)
Complex segregation analysis of low levels of plasma high‐density lipoprotein cholesterol in a sample of nuclear families in Jerusalem (1986) (14)
Serum ferritin as a marker of affection for genetic hemochromatosis. (1990) (14)
Genome-wide linkage and positional association analyses identify associations of novel AFF3 and NTM genes with triglycerides: the GenSalt study. (2015) (14)
An expected decrease in the incidence of autosomal recessive disease due to decreasing consanguineous marriages (1988) (14)
Alcohol effects on the percentage of beta waves in the electroencephalograms of twins (1988) (14)
Sex-linked determinants for IgM? (1990) (14)
The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program (2006) (14)
Quantitative trait locus on chromosome 20q13 for plasma levels of C-reactive protein in healthy whites: the HERITAGE Family Study. (2006) (14)
Heterogeneity between populations for multifactorial inheritance of plasma lipids. (1983) (14)
Development and Evaluation of Two Abbreviated Questionnaires for Mentoring and Research Self-Efficacy. (2017) (14)
Environmental index in genetic epidemiology: an investigation of its role, adequacy, and limitations. (1990) (14)
Efficiency of lod scores for representing multiple locus linkage data (1985) (14)
Familial predisposition for otitis media in Apache Indians at Canyon Day, Arizona (1987) (14)
Absence of linkage between VO2max and its response to training with markers spanning chromosome 22. (1997) (14)
Tracking of familial resemblance for resting blood pressure over time in the Québec Family Study. (2000) (14)
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data (2019) (14)
Common Genetic and Environmental Effects on Lipid Phenotypes: The HERITAGE Family Study (2005) (14)
Scaling submaximal exercise cardiac output and stroke volume: the HERITAGE Family Study. (2006) (13)
Detection of a major gene effect for LDL peak particle diameter and association with apolipoprotein H gene haplotype. (2005) (13)
Genome-wide Linkage Scans for Fasting Glucose , Insulin , and Insulin Resistance in the National Heart , Lung , and Blood Institute Family Blood Pressure Program Evidence of Linkages to Chromosome 7 q 36 and 19 q 13 From Meta-Analysis (2005) (13)
Familiality of triglyceride and LPL response to exercise training: the HERITAGE study. (2000) (13)
Genetic epidemiology of Menkes disease (1986) (13)
Genomic and transcriptomic predictors of triglyceride response to regular exercise (2015) (13)
Familial aggregation in the presence of temporal trends. (1988) (13)
Effects of selective return on estimates of heritability for body mass index in the national heart, lung, and blood institute twin study (1991) (13)
A Quantitative Trait Locus on 7 q 31 for the Changes in Plasma Insulin in Response to Exercise Training The HERITAGE Family Study (2003) (13)
Enhancing the Careers of Under-Represented Junior Faculty in Biomedical Research: The Summer Institute Program to Increase Diversity (SIPID). (2014) (13)
Family resemblance for fasting blood glucose in a population of Japanese Americans (1983) (13)
Accuracy of prediction equations to estimate submaximal VO2 during cycle ergometry: the HERITAGE Family Study. (1998) (13)
Associations of NADPH Oxidase Related Genes with Blood Pressure Changes and Incident Hypertension: The GenSalt Study (2018) (12)
Familial resemblance for plasma leptin: sample homogeneity across adiposity and ethnic groups. (2002) (12)
Biochemical intermediates in α1‐antitrypsin deficiency: Residual family resemblance for total α1‐antitrypsin, oxidized α1‐antitrypsin, and immunoglobulin E after adjustment for the effect of the Pi locus (1990) (12)
Detection of the inbreeding coefficient from ABO blood-group data. (1972) (12)
Segregation of genetic hemochromatosis indexed by latent capacity of transferrin. (1989) (12)
Cultural and biological inheritance of plasma lipids. (1983) (12)
A linkage analysis of the Gm locus and multiple sclerosis (1985) (12)
Variants for HDL-C, LDL-C, and Triglycerides Identified from Admixture Mapping and Fine-Mapping Analysis in African American Families (2015) (12)
Description of a large pedigree with an adverse lipoprotein cholesterol phenotype: The Bogalusa Heart Study (1986) (12)
Segregation analysis of quantitative traits in nuclear families: Comparison of three program packages (1989) (12)
Genotyping errors and their impact on genetic analysis. (2008) (12)
Familial aggregation of lipids and lipoproteins in families ascertained through random and nonrandom probands in the Stanford Lipid Research Clinics Family Study. (1991) (12)
Complex segregation analysis of diabetes mellitus. (1979) (12)
Genetic variants in the renin–angiotensin system and blood pressure reactions to the cold pressor test (2010) (12)
The role of SNP-loop diuretic interactions in hypertension across ethnic groups in HyperGEN (2013) (12)
Genetic epidemiology of coeliac disease (1984) (12)
Population and family studies of cleft lip and palate. (1980) (12)
Identification of a pleiotropic locus on chromosome 7q for a composite left ventricular wall thickness factor and body mass index: the HyperGEN Study (2009) (12)
The Trp64Arg polymorphism of the beta3-adrenergic receptor gene is not associated with training-induced changes in body composition: The HERITAGE Family Study. (2001) (11)
Agreement of Blood Pressure Measurements Between Random-Zero and Standard Mercury Sphygmomanometers (2008) (11)
Resequencing Study Identifies Rare Renin–Angiotensin–Aldosterone System Variants Associated With Blood Pressure Salt-Sensitivity: The GenSalt Study (2017) (11)
Influence of Smoking Status and Intensity on Discovery of Blood Pressure Loci Through Gene‐Smoking Interactions (2015) (11)
Genetic and environmental causes of variation in renal tubular handling of sodium and potassium: A twin study (1985) (11)
Genetic hemochromatosis: distribution analysis of six laboratory measures of iron metabolism. (1989) (11)
Associations of Variants in the CACNA1A and CACNA1C Genes With Longitudinal Blood Pressure Changes and Hypertension Incidence: The GenSalt Study. (2016) (11)
Left Ventricular Systolic Dysfunction in a Biracial Sample of Hypertensive Adults (2001) (11)
Blood pressure and other cardiovascular disease risk factors in black adults with sickle cell trait or glucose‐6‐phosphate dehydrogenase deficiency (1990) (11)
Influence of fat-free mass on detection of appropriateness of left ventricular mass: the HyperGEN Study (2003) (10)
Linkage analysis incorporating gene-age interactions identifies seven novel lipid loci: the Family Blood Pressure Program. (2014) (10)
A test of nonrandom segregation (1984) (10)
Principal components analysis of morphological measures in the Québec family study: Familial correlations (1997) (10)
Enriching rare variants using family-specific linkage information (2011) (10)
Commingling and segregation analysis of blood pressure in consanguineous and nonconsanguineous families from Andhra Pradesh, India (1992) (10)
A genetic study of hyper-alpha-lipoproteinemia. (1983) (10)
Some biological and social factors of risk associated with the birth of pre‐term infants (1988) (10)
Cross‐trait familial resemblance for resting blood pressure and body composition and fat distribution: The HERITAGE family study (2000) (10)
Multipoint linkage analysis of spinocerebellar ataxia and markers on chromosome 6 (1986) (10)
Resolution of cultural and biological inheritance by path analysis: Corrigenda and reply to Goldberger letter. (1978) (10)
The role of path analysis in coronary heart disease research. (1984) (10)
Correlation between blood pressure responses to dietary sodium and potassium intervention in a Chinese population. (2009) (10)
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. (2021) (10)
Maternal history of hypertension and blood pressure response to potassium intake: the GenSalt Study. (2012) (10)
Familial hypoalphalipoproteinemia. (1986) (10)
Blood pressure responses to dietary sodium and potassium interventions and the cold pressor test: the GenSalt replication study in rural North China. (2014) (10)
Possible linkages (lod score over 1.5) and a tentative map of the Jk-Km linkage group. (1978) (10)
Effects of regular endurance exercise on GlycA: Combined analysis of 14 exercise interventions. (2018) (10)
Genetic etiology of gastric carcinoma: II. Segregation analysis of gastric pH, nitrate, and nitrite (1987) (10)
Family Resemblance for Plasma Lipids and Lipoprotein Concentrations in Blacks: Cincinnati Lipid Research Clinic Family Study (1984) (10)
Genome-wide Linkage and Regional Association Study of Obesity-related Phenotypes: The GenSalt study (2013) (10)
Goodness‐of‐fit tests for locus order in three‐point mapping (1987) (10)
The impact of altered fitness on the risk of illness in relatives (1989) (10)
Associations of epithelial sodium channel genes with blood pressure: the GenSalt study (2014) (10)
Unitary personality source traits analyzed for heritability. (1981) (9)
Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure (2021) (9)
The impact of energy intake and energy expenditure of activity on the familial transmission of adiposity in an indian population (1993) (9)
Linkage analysis of Von Recklinghausen neurofibromatosis: Chromosomes 4 and 19 (1986) (9)
A Perspective on Promoting Diversity in the Biomedical Research Workforce: The National Heart, Lung, and Blood Institute's PRIDE Program. (2016) (9)
Estimating the age‐at‐onset function using life‐table methods (1988) (9)
Variation in Genes that Regulate Blood Pressure Are Associated with Glomerular Filtration Rate in Chinese (2014) (9)
The Role of Rare Variants in Systolic Blood Pressure: Analysis of ExomeChip Data in HyperGEN African Americans (2015) (9)
Efficient gene-environment interaction tests for large biobank-scale sequencing studies (2020) (9)
The cincinnati lipid research clinic family study: Familial determinants of plasma uric acid (2004) (9)
Obesity-insulin targeted genes in the 3p26-25 region in human studies and LG/J and SM/J mice. (2012) (9)
A resolution of the ascertainment sampling problem: IV. Continuous phenotypes (1988) (9)
Genetic and nongenetic determinants of blood pressure in a Southern Brazilian sample (1991) (9)
Genome-Wide Linkage Analysis of Systolic and Diastolic Blood Pressure (2000) (9)
Designing an optimum genetic association study using dense SNP markers and family-based sample. (2003) (9)
Body composition and fat distribution influence systemic hemodynamics in the absence of obesity: the HyperGEN Study 1–3 (2005) (9)
Research Education and Mentoring Program in Cardiovascular Diseases for Under-Represented Junior Faculty From NHLBI SIPID/PRIDE. (2019) (9)
Characterization of autosomal copy-number variation in African Americans: the HyperGEN Study (2011) (9)
Effect of exercise training on in vitro LDL oxidation and free radical-induced hemolysis: the HERITAGE Family Study. (2007) (9)
GENOMIC SCAN FOR EXERCISE STROKE VOLUME AND CARDIAC OUTPUT IN THE HERITAGE FAMILY STUDY (2001) (9)
Sex-specific effects of ACE I/D and AGT-M235T on pulse pressure: the HyperGEN Study (2007) (9)
Determinants of plasma uric acid (1979) (9)
Association between blood pressure responses to the cold pressor test and dietary sodium intervention in a Chinese population. (2008) (9)
Apolipoprotein AI- and AI:AII-containing lipoproteins in white men and women of the HERITAGE Family study: Associations with metabolic risk profile variables. (2003) (9)
A genetic study of immunoglobulin E and atopic disease based on families ascertained through asthmatic children. (1990) (9)
On the properties of maximum likelihood estimators of familial correlations under variable sibship size. (1988) (9)
Major gene effect on subcutaneous fat distribution in a sedentary population and its response to exercise training: The HERITAGE Family Study (2000) (9)
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci (2020) (9)
A twin study of intelligence in Russia (1975) (8)
Competing targets of microRNA-608 affect anxiety and hypertension (2014) (8)
Genetic correlation of blood pressure responses to dietary sodium and potassium intervention and cold pressor test in chinese population (2011) (8)
Familial aggregation of seven-year changes in blood pressure in Canada. (2001) (8)
A statistical test for detection of ancestral genetic contributions to disease occurrence in finite populations (1984) (8)
Familial resemblance for immunoglobulin levels (1994) (8)
Linkage information and bias in the presence of interference (1988) (8)
Linkage analysis of complex traits using affected sibpairs: Effects of single‐locus approximations on estimates of the required sample size (1997) (8)
Efficient gene–environment interaction tests for large biobank‐scale sequencing studies (2020) (8)
Genome-wide scan to identify quantitative trait loci for baseline resting heart rate and its response to endurance exercise training: the HERITAGE Family Study. (2006) (8)
Associations of Renin-Angiotensin-Aldosterone System Genes With Blood Pressure Changes and Hypertension Incidence. (2015) (8)
Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes (2020) (8)
Cytogenetic studies of couples with repeated spontaneous abortions of known karyotype (1988) (8)
Association of Duffy blood group with schizophrenia in Chinese (1990) (8)
Biological and cultural determinants of immunoglobulin levels in a Brazilian population with Chagas' disease (2004) (8)
Segregation analysis of dopamine‐beta‐hydroxylase (DBH) and catechol‐o‐methyltransferase (COMT): Identification of major locus and polygenic components (1985) (8)
Tree-Based Models for Fiting Stratified Linear Regression Models (2002) (8)
Family resemblance for glucose tolerance in a Melanesian population, the Tolai. (1989) (8)
Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations (2018) (8)
A mitochondrial DNA D-loop polymorphism and obesity in three cohorts of women (1999) (8)
Estimation of segregation and ascertainment probabilities by discarding the single probands (1987) (8)
An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels (2018) (7)
Interaction of genetics and epidemiology in the literature (1986) (7)
Race, height, and blood pressure in Northeastern Brazil. (1983) (7)
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices (2021) (7)
The collaborative lipid research clinics program family study: Detection of major genes influencing lipid levels by examination of heterogeneity of familial variances (1984) (7)
%Heart Rate Reserve Is Better Related to %VO2max Than to %VO2 reserve: The HERITAGE Family Study (2004) (7)
Genome-Wide Gene–Potassium Interaction Analyses on Blood Pressure: The GenSalt Study (Genetic Epidemiology Network of Salt Sensitivity) (2017) (7)
Patha analysis of aptitude, personality, and achievement scores in Brazilian twins (1976) (7)
Biochemical intermediates in alpha 1-antitrypsin deficiency: residual family resemblance for total alpha 1-antitrypsin, oxidized alpha 1-antitrypsin, and immunoglobulin E after adjustment for the effect of the Pi locus. (1990) (7)
Family history of cancer related to cholesterol level in young adults (1986) (7)
Genome-wide linkage and positional association study of blood pressure response to dietary sodium intervention: the GenSalt Study. (2012) (7)
Genome-wide linkage scan to detect loci influencing levels of dehydroepiandrosterones in the HERITAGE Family Study. (2001) (7)
Nonrandom sampling in human genetics: Skewness and kurtosis (1987) (7)
Evidence of pleiotropic loci for fasting insulin, total fat mass, and abdominal visceral fat in a sedentary population: the HERITAGE family study. (2000) (7)
Body mass index modulates blood pressure heritability: the Family Blood Pressure Program. (2014) (7)
The HERITAGE Family Study: A Review of the Effects of Exercise Training on Cardiometabolic Health, with Insights into Molecular Transducers (2022) (7)
Modeling the age‐of‐onset function in segregation analysis: A causal scheme for leprosy (1989) (7)
Population differences in the pattern of familial aggregation for sex hormone‐binding globulin and its response to exercise training: The HERITAGE family study (2001) (7)
Subclinical, hemodynamic, and echocardiographic abnormalities of high pulse pressure in hypertensive and non-hypertensive adults. (2012) (7)
Associations of Endothelial System Genes With Blood Pressure Changes and Hypertension Incidence: The GenSalt Study. (2015) (6)
PT224 Genome-wide association study identifies eight novel loci associated with blood pressure responses to interventions in Han Chinese (2014) (6)
Genetic epidemiology of duchenne muscular dystrophy in Japan: Classical segregation analysis (1987) (6)
The Clinical Lipid Research Clinic Family Study: familial determinants of plasma uric acid. (1982) (6)
Essential statistical methods for medical statistics : a derivative of Handbook of Statistics : epidemiology and medical statistics, vol. 27 (2011) (6)
Regular exercise and patterns of response across multiple cardiometabolic traits: the HERITAGE family study (2021) (6)
Single nucleotide polymorphism-single nucleotide polymorphism interactions among inflammation genes in the genetic architecture of blood pressure in the Framingham Heart Study. (2015) (6)
Application of collapsing methods for continuous traits to the Genetic Analysis Workshop 17 exome sequence data (2011) (6)
Predicting intrauterine growth reterdation in sibships while considering maternal and infant covariates (1989) (6)
Heterogeneity in the familial aggregation of fasting plasma glucose in five North American populations: the Lipid Research Clinics Family Study. (1990) (6)
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids (2021) (6)
Reproducibility of the HERITAGE Family Study intervention protocol: drift over time. (1997) (6)
A genetic study of dehydroepiandrosterone sulfate measured before and after a 20-week endurance exercise training program: the HERITAGE Family Study. (2000) (6)
Familial risk of high blood pressure in the Canadian population (2001) (6)
Model‐based linkage analysis with imprinting for quantitative traits: ignoring imprinting effects can severely jeopardize detection of linkage (2008) (6)
Familial aggregation of lipids and lipoproteins in families ascertained through random and nonrandom probands in the Minnesota Lipid Research Clinic Family Study. (1991) (6)
Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group‐specific loci: Use of restriction fragment length polymorphisms extends exclusion region (1986) (6)
Assessing Genetic and Cultural Heritabilities (1994) (6)
Comparison of two methods for analysis of gene–environment interactions in longitudinal family data: the Framingham heart study (2014) (6)
Cancer and autoimmune disease in families with common variable immune deficiency (1986) (6)
Association of mitral annular calcification and aortic valve sclerosis with left ventricular geometry and function in hypertensive adults: the hypertension genetic epidemiology network (HyperGEN) study (2004) (6)
A genome scan for linkage with aortic root diameter in hypertensive African Americans and whites in the Hypertension Genetic Epidemiology Network (HyperGEN) study. (2005) (5)
Likely linkage: Inv with Jk (1977) (5)
Partial normalization of components of metabolic syndrome does not influence prevalent echocardiographic abnormalities: the HyperGEN study. (2013) (5)
On the detection of excess disease risk in family data (1987) (5)
Erratum: Familial resemblance for muscle phenotypes: The HERITAGE family study (Medicine and Science in Sports and Exercise (2003) 35 (1360-1366)) (2005) (5)
No evidence for linkage between an insulin‐dependent diabetes mellitus‐susceptibility locus and immunoglobulin loci KM or GM (1984) (5)
Inferring a major gene for quantitative traits by using segregation analysis with tests on transmission probabilities: how often do we miss? (1995) (5)
Familial determinants of blood pressure in Northeastern Brazil (1980) (5)
Properties of alternative estimators of familial correlations under variable sibship size. (1995) (5)
Genetics and Schizophrenia — Current State of Negotiations (1987) (5)
Genome-Wide Gene–Sodium Interaction Analyses on Blood PressureNovelty and Significance (2016) (5)
Genome-wide scans for heritability of fasting serum insulin and glucose concentrations in hypertensive families (2005) (5)
Genome-Wide Linkage and Regional Association Study of Blood Pressure Response to the Cold Pressor Test in Han Chinese: The Genetic Epidemiology Network of Salt Sensitivity Study (2014) (5)
Inferences on the inheritance of congenital anomalies from temporal and spatial patterns of occurrence (1989) (5)
Whole genome sequence analysis of the simulated systolic blood pressure in Genetic Analysis Workshop 18 family data: long-term average and collapsing methods (2014) (5)
Gene-lifestyle interactions in the genomics of human complex traits (2022) (5)
Polymorphisms in the GNB3 and ADD1 genes and blood pressure in a Chinese population (2010) (5)
Commingling analysis of blood pressure in the Tecumseh community health study (1990) (5)
The Cincinnati Lipid Research Clinic Family Study: commingling in the distributions of lipids and lipoprotein concentrations. (1983) (5)
Complex segregation analysis for a three‐allele locus: Experience from an analysis of acid phosphatase activity (1989) (4)
Genetic analysis combining path analysis with regressive models: The beta path model of polygenic and familial environmental transmission (1994) (4)
Race differences in reproducibilities: The HERITAGE family study (1997) (4)
Pharmacogenomics of heart failure - focus on drug disposition and action (2010) (4)
Commingling and complex segregation analysis of fasting plasma glucose in the Lipid Research Clinics family study. (1992) (4)
Residual family resemblance for PTC taste sensitivity (1977) (4)
Percent transferrin saturation in segregating hemochromatosis. (1990) (4)
Methods in Genetic Epidemiology (Contributions to Epidemiology and Biostatistics). (1985) (4)
Genetic epidemiology of bilateral breast cancer: A linkage analysis using the affected‐pedigree‐member method (1990) (4)
Lack of pleiotropic genetic effects between adiposity and sex hormone-binding globulin concentrations before and after 20 weeks of exercise training: the HERITAGE family study. (2003) (4)
The generalized Wright's model and population structure with special reference to the ABO blood group system. (1974) (4)
Associations of the Serum/Glucocorticoid Regulated Kinase Genes With BP Changes and Hypertension Incidence: The Gensalt Study (2017) (4)
Path Analysis in Genetics (2005) (4)
HLA and down syndrome (DS): Parents at the origin of the nondisjunction share no more HLA‐A and ‐B antigens with their DS child than controls (1988) (4)
Association between genetic variants of the ADD1 and GNB3 genes and blood pressure response to the cold pressor test in a Chinese Han population: the GenSalt Study (2012) (4)
Path Analysis in Genetic Epidemiology (2006) (4)
Genetic analysis combining path analysis with regressive models: the TAU model of multifactorial transmission. (1994) (4)
FAMILIAL RESEMBLANCE FOR SEVEN YEAR CHANGES IN MUSCULOSKELETAL FITNESS (2001) (4)
Estimation of linkage disequilibrium from conditional haplotype data: Application to β‐globin gene cluster in American blacks (1986) (4)
Effect of Regular Aerobic Exercise on Plasma Homocysteine Concentrations: The HERITAGE Family Study (2004) (3)
Variants on Chromosome 6 p 22 . 3 Associated With Blood Pressure in the HyperGEN Study : Follow-Up of FBPP Quantitative Trait Loci (2011) (3)
Evaluation of ACSM Guidelines on Prescribing Exercise Intensity for ???Quite Unfit???: The HERITAGE Family Study (2004) (3)
Heritability in the personality control system: Ego strength (C), super ego strength (G) and the self sentiment (Q3); by the MAVA Model, Q-Data, and maximum likelihood analyses (1985) (3)
Commingling and segregation analysis of serum uric acid in five North American populations: the Lipid Research Clinics family study (1992) (3)
Note on linkage analysis when the mode of transmission is unknown (1990) (3)
Studies on an isolated West Indies population: IV. Genetic study of hearing loss (1986) (3)
Smoking and Genetic Risk Variation Across Populations of European, Asian, and African American Ancestry—A Meta‐Analysis of Chromosome 15q25 (2012) (3)
Heterogeneity among populations for familial aggregation of blood pressure (1991) (3)
Three Approaches to Modeling Gene‐Environment Interactions in Longitudinal Family Data: Gene‐Smoking Interactions in Blood Pressure (2016) (3)
Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure (2020) (3)
Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures. (2020) (3)
Characteristics of a linkage heterogeneity test. (1978) (3)
3 Statistical considerations in applications of path analysis in genetic epidemiology (1991) (3)
Abstract 1194: Lp-PLA2 is Weakly to Modestly Correlated with Insulin, Visceral Fat, and Lipids and Lipoproteins, but is Uncorrelated with C-Reactive Protein (hsCRP) and Blood Pressure: The HERITAGE Family Study (2006) (3)
A commingling analysis of obesity in the Tecumseh community health study (1991) (3)
On the measurement of susceptibility to genetic factors (1989) (3)
Pedigree discriminant analysis of two French Canadian Tay‐Sachs families (1987) (3)
Evidence of a major locus for lipoprotein lipase (LPL) activity in addition to a pleiotropic locus for both LPL and fasting insulin: results from the HERITAGE Family Study. (1999) (3)
Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31 (2018) (3)
Interactions among the beta2- and beta3- adrenergic receptor genes and total body fat and abdominal fat level in the HERITAGE Family Study. (2003) (3)
The recurrence risks for isolated cases with incompletely penetrant X‐linked conditions (1986) (3)
A general autosomal/X‐linked model (1984) (3)
The information content of phase‐known matings for ordering genetic loci (3)
The role of smoothing techniques in the interpretation of results from genomic scans using sib‐pair data (1997) (3)
Simulation of Huntington's disease onset (1989) (3)
Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals (2022) (3)
Endurance Exercise TVaining Reduces Lp-PLA2 in Young White Adults: The HERITAGE Family Study (2007) (2)
Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (2)
Considerations on study designs using the extreme sibpairs methods under multilocus oligogenic models. (2002) (2)
CARDIORESPIRATORY RESPONSES TO EXERCISE AND THE C34T AMPD1 GENE POLYMORPHISM IN THE HERITAGE FAMILY STUDY (2003) (2)
Abstract 1654: Prevalence and Correlates of Aortic Root Dilatation in Normotensive and Hypertensive Adults: The Family Blood Pressure Program (2009) (2)
Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension (2022) (2)
Erratum: Genomic scan for maximal oxygen uptake and its response to training in the HERITAGE Family Study (Journal of Applied Physiology (February 2000) 88 (551-559)) (2004) (2)
Heritabilities, by the multiple abstract variance analysis (MAVA) model and objective test measures, of personality traits U.I.23, capacity to mobilize, U.I.24, anxiety, U.I.26, narcistic ego and U.I.28, asthenia, by maximum-likelihood methods (1982) (2)
Classification of rheumatoid arthritis: The importance of including data from the siblings (1987) (2)
Coagulation factor XIII: Genetic linkage studies with F13B (1987) (2)
Familial aggregation of lipids and lipoproteins in families identified through random and nonrandom probands in the Oklahoma Lipid Research Clinic Family Study (1991) (2)
Genetic epidemiology of coronary heart disease, past, present, and future. Proceedings of a workshop held in St. Louis, Missouri, August 10-12,1983. (1984) (2)
TGF- b 1 gene-race interactions for resting and exercise blood pressure in the HERITAGE Family Study (2001) (2)
Metabolic Syndrome and Salt-Sensitivity of Blood Pressure among Persons without Diabetes (2010) (2)
Hereditary genius: a centennial problem in resolution of cultural and biological inheritance. (1980) (2)
Construction of conditional lod tables from multiple‐locus linkage data (1985) (2)
Nonrandom sampling in genetic epidemiology: An implementation of the Hanis‐Chakraborty method for multifactorial analysis (1989) (2)
Circulatory disease mortality and diabetes incidence in 27 families with Friedreich ataxia (1988) (2)
Large-scale multivariate multi-ancestry Interaction analyses point towards different genetic mechanisms by population and exposure (2019) (2)
A genome-wide linkage scan for dietary energy and nutrient intakes: the Health, Risk Factors, Exercise Training, and Genetics (2004) (1)
Monomorphism and heterozygosity (1975) (1)
REPRODUCIBILITY OF RESTING BLOOD PRESSURE AND HEART RATE: THE HERITAGE FAMILY STUDY (1999) (1)
Abstract P263: Resequencing Study Identifies Renin-Angiotensin-Aldosterone System Genes and Novel Low Frequency Variants Associated with Blood Pressure Salt-sensitivity (2016) (1)
Genetic variants in the ADD1 and GNB3 genes and blood pressure response to potassium supplementation (2010) (1)
Genome-Wide Meta-analysis of Variant-by-Diuretic Interactions as Modulators of Lipid Traits in Persons of European and African Ancestry (2019) (1)
1142-179 Body fat distribution influences cardiac output in normotensive and hypertensive overweight individuals: The hyperGEN study (2004) (1)
Genome-Wide Association Study Identifies Eight Novel Loci Associated with Blood Pressure Responses to Interventions in Han Chinese Running title : He et al . ; Novel loci for BP responses (2013) (1)
Structure of ischemic heart disease risk factors in the North Khanty population of Western Siberia (1990) (1)
Multi-omics insights into the biological mechanisms underlying gene-by-lifestyle interactions with smoking and alcohol consumption detected by genome-wide trans-ancestry meta-analysis (2021) (1)
Genetics of Complex Traits with Particular Attention to Fat Patterning (2001) (1)
Concentric remodeling more than increased ventricular mass is associated with impaired relaxation (2003) (1)
A Conversation With Professor Newton Ennis Morton (2013) (1)
ACCURACY OF THE KARVONEN FORMULA IN A LARGE HETEROGENEOUS POPULATION: THE HERITAGE FAMILY STUDY (2001) (1)
A review of recent genetic epidemiological studies of blood pressure (2000) (1)
Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile (2019) (1)
Multi-omics insights into the biological mechanisms underlying statistical gene-by-lifestyle interactions with smoking and alcohol consumption (2022) (1)
Abstract P253: Genomewide Gene-potassium Interaction Analyses on Blood Pressure: The GenSalt Study (2016) (1)
Heritability of some personality source traits : evidence from MAVA design, maximum likelihood analysis, and the OA battery. (1981) (1)
Familial resemblance on the thurstone activity scale, systolic blood pressure, and total cholesterol among first degree relatives of subjects with and without coronary heart disease (1985) (1)
Cincinnati Lipid Research Clinic. (1984) (1)
Statistical Analysis of Nonrectangular Family Data (1993) (1)
The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions (2019) (1)
Adducin 1 (alpha) Gly460Trp variant is associated with left ventricular geometry in Caucasians and African Americans: The HyperGEN Study. (2010) (1)
ASSOCIATION AND LINKAGE STUDIES BETWEEN THE IGF-1 GENE AND BODY COMPOSITION: THE HERITAGE FAMILY STUDY (1998) (1)
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (1)
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (1)
Detection of inbreeding and efficiency of mating bioassay. (1974) (1)
Further tests of nonrandom segregation with special reference to linkage (1987) (1)
Log‐linear model analysis of allelic associations (1986) (1)
Pleiotropic relationships between cortisol levels and adiposity: The HERITAGE Family Study. (2002) (1)
Abstract 11954: Phenomapping: Hierarchical Cluster Analysis of Phenotypic Data for Novel Classification of Hypertension (2013) (1)
CLASSIFICATION OF RESPONDERS AND NON-RESPONDERS TO STANDARDIZED TRAINING: THE HERITAGE FAMILY STUDY (1999) (1)
ABSENCE OF LINKAGE BETWEEN THE TRAINING RESPONSE OF VO2 MAX AND CHROMOSOME 22 MARKERS 1301 (1997) (0)
highlighted topics The Na 1 -K 1 -ATPase a 2 gene and trainability of cardiorespiratory endurance: the HERITAGE Family Study (1999) (0)
Quantitative trait locus on chromosome 20 q 13 for plasma levels of C-reactive protein in healthy whites : the HERITAGE Family Study (2006) (0)
Link between systolic and diastolic dysfunction in hypertensive subjects with inappropriate left ventricular hypertrophy: the hyperGEN study (2002) (0)
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2021) (0)
Abstract P530: Pleiotropic Effects on Blood Pressure Traits Using Genome-wide Analysis of Gene-alcohol Interactions (2017) (0)
BP phenotypes: the HERITAGE Family Study Angiogenin gene-race interaction for resting and exercise (2013) (0)
Whole exome analyses to examine the impact of rare variants on left ventricular traits in African American participants from the HyperGEN and GENOA studies. (2017) (0)
Abstract P185: Novel Loci for Blood Pressure Using Gene-alcohol Interactions and 1000g Imputed Data (2016) (0)
Deriving stratified effects from joint models investigating gene-environment interactions (2020) (0)
Genomics of model organisms (2009) (0)
Lifestyle Risk Score: handling missingness of individual lifestyle components in meta-analysis of gene-by-lifestyle interactions (2021) (0)
Abstract P236: The Heritability of Submaximal Exercise Heart Rate Response to Regular Exercise is Accounted for by Nine SNPs (2012) (0)
AGT M235 amd ACE ID polymorphisms for exercise blood pressure: The HERITAGE Family Study (2000) (0)
training: results from the HERITAGE Family Study response to exercise (2014) (0)
Genomics of model organisms (2009) (0)
Effect of Endurance Exercise Training on Serum Adiponectin Concentration: the HERITAGE Family Study (2006) (0)
Aggregate blood pressure responses to serial dietary sodium and potassium intervention: defining responses using independent component analysis (2015) (0)
Fine mapping of a QTL on chromosome 13 for submaximal exercise capacity training response: the HERITAGE Family Study (2011) (0)
Xbal ERYTHROPOIETIN GENE POLYMORPHISM AND AEROBIC RESPONSE TO TRAINING IN THE HERITAGE STUDY 1105 (1996) (0)
Abstract MP15: Single And Joint Associations Of Genetic Variants In The Serum/glucocorticoid Regulated Kinase (sgk) Genes With Blood Pressure Responses To Sodium Intake: The Gensalt Study (2014) (0)
ENDURANCE TRAINING AND PERCEIVED EXERTION (RPE) 1217 (1997) (0)
Abstract 36: Changes in HDL Particle Traits in Response to Regular Exercise: Results from the HERITAGE Family Study (2014) (0)
Segregation ofGenetic Hemochromatosis Indexed by (1989) (0)
Locus on Chromosome 2q37 Is Associated With Hemodynamic Training Responses: The Heritage Family Study: 2929 (2010) (0)
Exclusion Criteria for Case and Control Probands in the Cincinnati Family Study of Endogenous Hormones and Myocardial Infarction (2005) (0)
REPRODUCIBILITY OF PLASMA SUBSTRATE LEVELS DURING EXERCISE: THE HERITAGE FAMILY STUDY (1998) (0)
EFFECTS OF EXERCISE TRAINING ON PLASMA TOTAL HOMOCYSTEINE AND GLUTATHIONE LEVELS: THE HERITAGE FAMILY STUDY (1998) (0)
Gender Specific Changes In Substrate Utilization Following 20 Weeks Of Aerobic Training: Heritage (2005) (0)
Effect of endurance exercise training on plasma HDL cholesterol levels depend on the levels of triglycerides. Evidence from men of the Health, Risk Factors, Exercise Trainijng and ˝enetics (HERITAGE) Family Study (2001) (0)
OS 06-04 CHANGES IN GENE EXPRESSION PATHWAYS PREDICT DELAYED SODIUM EXCRETION DURING SALINE INFUSION. (2016) (0)
CREATINE KINASE B-SUBUNIT GENE POLYMORPHISM ASSOCIATION WITH VO2MAX: THE HERITAGE FAMILY STUDY (2001) (0)
Aggregate blood pressure responses to serial dietary sodium and potassium intervention: defining responses using independent component analysis (2015) (0)
983 MATERNAL HISTORY OF HYPERTENSION PREDICTS BLOOD PRESSURE RESPONSE TO POTASSIUM INTAKE: THE GENSALT STUDY (2012) (0)
STATISTICAL MODELING AND ANAL YSIS IN HUMAN GENETICS (1978) (0)
Subject Index Vol. 22, 1978 (1978) (0)
endurance training: the HERITAGE Family Study Titin is a candidate gene for stroke volume response to (2015) (0)
Energy Expenditure during Exercise Training and Changes in Body Composition: 1000 (2008) (0)
The most recent and extensive genome-wide human genetic linkage maps (2005) (0)
Changes in Glucose Metabolism Induced by Exercise Training in a Large Biracial Sedentary Population: The HERITAGE Family Study (2002) (0)
Gender differences in plasma Lp A-I and Ip A-I:A-I levels in the heritage family study (2000) (0)
PATH ANALYSIS IN GENETIC EPIDEMIOLOGY: THEORY AND APPLICATIONS (1993) (0)
BODY FAT VERSUS DIETARY FAT IN A BI-RACIAL POPULATION OF MEN AND WOMEN: THE HERITAGE FAMILY STUDY (1998) (0)
Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits (2020) (0)
RELATION OF CARDIOVASCULAR STRESS REACTIVITY TO LEFT VENTRICULAR MASS AND RELATIVE WALL THICKNESS IN HYPERTENSIVES: EFFECTS OF RACE AND GENDER (1999) (0)
Abstract P234: Genetic Variants of the Kallikrein-kinin System Associated with the Salt Sensitivity of Blood Pressure: The GenSalt Study (2012) (0)
KCNA4 Gene SNP and OV2max Response to Endurance Training: The HERITAGE Family Study (2004) (0)
GENETICS AND RESPONSE TO EXERCISE: THE HERITAGE FAMILY STUDY864 (1997) (0)
Abstract MP78: Effects of Regular Endurance Exercise on GlycA: Results Across Four Exercise Training Studies (2016) (0)
Abstract MP60: Investigation of Blood Pressure Genetic Loci in African Americans using the Metabochip (2013) (0)
TRANSFORMING GROWTH FACTOR B1 GENE POLYMORPHISM AND BLOOD PRESSURE RESPONSE TO ACUTE EXERCISE IN THE HERITAGE FAMILY STUDY (1999) (0)
BLOOD LIPID RESPONSES TO EXERCISE IN BLACKS VS WHITES: THE HERITAGE FAMILY STUDY (1998) (0)
OR-10: Prevalence and correlates of aortic valve sclerosis in hypertensive adults: The hypergen study (2003) (0)
THE EFFECT OF EXERCISE TRAINING ON HEART RATE VARIABILITY AND STROKE VOLUME: THE HERITAGE FAMILY STUDY (1998) (0)
Abstract P213: Regular Exercise Improves the Lipoprotein Subclass Profile: Meta-Analysis of 10 Exercise Training Intervention Groups (2015) (0)
HERITAGE Family Study phenotypes and their responses to training in the Quantitative trait loci for maximal exercise capacity (2013) (0)
and LPL activity: the HERITAGE Family Study Evidence of LPL gene-exercise interaction for body fat (2015) (0)
BamHI POLYMORPHISM IN MITOCHONDRIAL DNA (mtDNA) AND AEROBIC PERFORMANCE IN THE HERITAGE STUDY 1104 (1996) (0)
Novel Measures to Evaluate the Cardiorespiratory Response to Exercise Training Without a Follow-up Exercise Test: 2126 (2011) (0)
GENDER DIFFERENCES IN PRE- TO POST-TRAINING CHANGES IN VENTILATORY THRESHOLD: THE HERITAGE FAMILY STUDY (1999) (0)
P-485: Genetic determinants of exercise blood pressure and heart rate in response to 20-week endurance exercise training in whites and blacks: The HERITAGE family study (2001) (0)
Abstract MP037: Blood Pressure Genetic Risk Score Predicts Blood Pressure Responses to Dietary Sodium and Potassium Interventions: The GenSalt Study (2017) (0)
LINKAGE BETWEEN A MUSCLE-SPECIFIC CREATINE KINASE GENE POLYMORPHISM AND VO2MAX TRAINABILITY IN THE HERITAGE FAMILY STUDY (1998) (0)
Relations of ethnicity and vascular parameters to left ventricular structure in hypertensive adults (2003) (0)
A Unified ModelforComplexSegregation Analysis (1983) (0)
Effect of Endurance Exercise Training on Serum Adiponectin Concentration: the HERITAGE Family Study 7 3:15 AM – 3:30 AM (2006) (0)
Human Nutrition and Metabolism Calcium Intake Is Associated with Adiposity in Black and White Men and White Women of the HERITAGE Family Study 1 , 2 (2004) (0)
ESTROGEN REPLACEMENT AND EXERCISE EFFECTS ON VISCERAL FAT IN POSTMENOPAUSAL WOMEN - THE HERITAGE FAMILY STUDY (2003) (0)
Endurance training alleviates PRKCQ genotype-related metabolic abnormalities: the HERITAGE Family Study (2007) (0)
Newton E. Morton (1929-2018). (2018) (0)
RESPONSE OF SKELETAL MUSCLE ENZYME ACTIVITIES TO ENDURANCE TRAINING: VARIATION WITHIN AND BETWEEN FAMILIES.: 543 (1995) (0)
Lifestyle Risk Score for aggregating multiple lifestyle factors: Handling missingness of individual lifestyle components in meta-analysis of gene-by-lifestyle interactions (2020) (0)
A Defense ofPathAnalysis inGenetic Epidemiology (1983) (0)
Abstract 54: Genome-Wide Association Analysis of Gene-Sodium Interactions on Blood Pressure Phenotypes: The GenSalt Study (2015) (0)
A molecular signature linked to calcium signalling is predictive of exercise training-induced changes in insulin sensitivity (2016) (0)
P-515: ATPIII-defined metabolic syndrome is associated with prevalence of LV hypertrophy in white, but not in African American, treated hypertensives: The hypergen study (2003) (0)
9.26 Diagnosis of Metabolic Syndrome Based on History of Exposure or Present Abnormalities: Evidence of Necessity of a Better Definition (2008) (0)
Compendium of genome-wide scans of lipid-related phenotypes Published, JLR Papers in Press, September 17, 2004. DOI 10.1194/jlr.R400008-JLR200 (2004) (0)
The s100alpha gene and cardiorespiratory trainability in the heritage family study (2000) (0)
ANGIOTENSIN-CONVERTING ENZYME (ACE) I/D POLYMORPHISM AND TRAINABILITY OF FITNESS PHENOTYPES: THE HERITAGE FAMILY STUDY (1999) (0)
On Haldane’s exact test for random mating (1974) (0)
LINKAGE AND ASSOCIATION STUDIES OF THE LIPOPROTEIN LIPASE SER447TER MUTATION: THE HERITAGE FAMILY STUDY (1998) (0)
Major Gene and Environmental Determinants of High-Density Lipoprotein Cholesterol (1987) (0)
ACE I/D POLYMORPHISM AND SKELETAL MUSCLE CHARACTERISTICS IN THE QUEBEC AND HERITAGE FAMILY STUDIES (2003) (0)
Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos (2017) (0)
Meeting Summary Genetic Epidemiology of Coronary Heart Disease Past, Present, and Future (2005) (0)
THE EFFECT OF EXERCISE ON PERCEIVED EXERTION, BP AND HR AT THE VENTILATORY THRESHOLD. THE HERITAGE FAMILY STUDY. (1999) (0)
KCNJ11 AND KCNQ1 GENES INTERACTION IN VO2MAX: THE HERITAGE FAMILY STUDY (2003) (0)
Genetics of Obesity: Etiologic Heterogeneity and Temporal Trends (2020) (0)
AGenetic andEpidemiologic Study ofPeriodontal Disease inHawali. II.Genetic andEnvironmental Influence (1977) (0)
training: results from the HERITAGE Family Study (2014) (0)
Abstract P159: Genetic Variants of the Angiotensinogen Gene Predict Hypertension Incidence among Chinese Han Population: The GenSalt Study (2013) (0)
A Quantitative Trait Locus For Maximal Exercise Heart Rate On Chromosome 10p13: The Heritage Family Study (2005) (0)
Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify MYRIP, TRAPPC11, and SLC27A6 of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry Population (2021) (0)
Abstract 12987: A Combined Analysis of the Transcriptional Response of iPS-cell Derived Human Cardiomyocytes and GWAS for Left Ventricular Hypertrophy Reveals Common Biology in Both African American and Caucasians (2011) (0)
UTILITY OF THE MINNESOTA EATING PATTERN ASSESSMENT TOOL IN TRACKING DIETARY LIPID INTAKE DURING EXERCISE TRAINING 1665 (1997) (0)
INVESTIGATION OF THE FAMILIAL RESEMBLANCE BETWEEN BODY FAT AND BLOOD LIPIDS 33 (1997) (0)
RACE SIMILARITIES IN THE MULTIVARIATE ASSOCIATIONS BETWEEN EXERCISE-INDUCED CHANGES IN BLOOD LIPIDS AND BODY FATNESS (2003) (0)
THE LEPR GENE AND BODY FAT AND LEPTIN RESPONSES TO ENDURANCE TRAINING IN THE HERITAGE FAMILY STUDY. (1999) (0)
43rd European Mathematical Genetics Meeting (EMGM) 2015. April 16-17, 2015, Brest, France: Abstracts (2015) (0)
Complex segregation analysis. (1971) (0)
OS 06-04 CHANGES IN GENE EXPRESSION PATHWAYS PREDICT DELAYED SODIUM EXCRETION DURING SALINE INFUSION (2016) (0)
SCALING SUBMAXIMAL CARDIOVASCULAR DATA: THE HERITAGE FAMILY STUDY (2002) (0)
Abstract 3942: Blood Pressure Response to Cold Pressor Predicts Salt-Sensitivity in the GenSalt Study (2006) (0)
PLASMA LIPID LEVELS AND THEIR RESPONSES TO ENDURANCE TRAINING: ASSOCIATION WITH AN IGF-I GENE POLYMORPHISM (1999) (0)
MUSCLE-SPECIFIC CREATINE KINASE GENE POLYMORPHISM AND VO2max TRAINABILITY IN THE HERITAGE FAMILY STUDY 1319 (1997) (0)
GENOME-WIDE SEARCH FOR GENES RELATED TO ADIPOSITY AND ITS CHANGES WITH ENDURANCE TRAINING IN THE HERITAGE FAMILY STUDY. (1999) (0)
Abstract P232: Common Variants of the Estrogen Receptor 1 Gene Predict Decreased Blood Pressure Salt-Sensitivity in Men: The GenSalt Study (2012) (0)
A Brief History behind the journal Genetic Epidemiology and the International Genetic Epidemiology Society. (2023) (0)
Abstract 13186: Rare and Low Frequency Variants Associated With Hypertension and Systolic Blood Pressure in Taiwan Chinese Families (2016) (0)
Effect of Dietary Sodium and Potassium Intervention on Blood Glucose (2010) (0)
KCNC1 Gene Polymorphism and OV2max: The HERITAGE Family Study (2004) (0)
Subject Index Vol. 29, 2009 (2009) (0)
composition changes with training in HERITAGE study Uncoupling protein 3 gene is associated with body (2013) (0)
Abstract P027: Associations of Renin-Angiotensin-Aldosterone System Genes with Blood Pressure changes and Hypertension Incidence: The GenSalt Study (2015) (0)
Human epithelial Na (cid:2) channel missense variants identiﬁed in the GenSalt study alter channel activity (2016) (0)
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data (2019) (0)
Endurance Exercise Training and High-Molecular Weight Adiponectin: the HERITAGE Family Study: 1749 (2008) (0)
Contents Vol. 29, 2009 (2009) (0)
Abstract 3933: Genetic Linkage of Aortic Valve Sclerosis and Mitral Annular Calcification: The HyperGEN Study (2006) (0)
CETP C>->−629>A Genotypes and HDL-Cholesterol Phenotypes in the HERITAGE Family Study: 2085 (2006) (0)
ASSOCIATION BETWEEN A SOLUTE CARRIER FAMILY 25, MEMBER 4 GENE POLYMORPHISM AND VO2MAX: THE HERITAGE FAMILY STUDY. (2001) (0)

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