D. Rao

发表

Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

Benjamin D. Heavner, May E. Montasser, M. Fornage, 2022, Hypertension.

Testing causal hypotheses in multivariate linkage analysis of quantitative traits: General formulation and application to sibpair data

M. Province, G. Vogler, A. Heath, 1998, Genetic epidemiology.

Genotype Imputation for African Americans Using Data From HapMap Phase II Versus 1000 Genomes Projects

H. Tiwari, C. Gu, D. Arnett, 2012, Genetic epidemiology.

Human epithelial Na (cid:2) channel missense variants identiﬁed in the GenSalt study alter channel activity

D. Gu, T. Kelly, J. Hixson, 2016 .

The power of genetic diversity in genome-wide association studies of lipids

Christopher D. Brown, Aaron F. McDaid, M. P. Concas, 2021, Nature.

Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

Jennifer G. Robinson, Nicholette D. Palmer, Christine A. Williams, 2019 .

Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk

Tom R. Gaunt, Yan V. Sun, S. R. Kulkarni, 2011, Nature.

Multi-omics insights into the biological mechanisms underlying statistical gene-by-lifestyle interactions with smoking and alcohol consumption

C. Rotimi, D. Chasman, Michael Province, 2022, Frontiers in Genetics.

Population differences in the pattern of familial aggregation for sex hormone‐binding globulin and its response to exercise training: The HERITAGE family study

C. Bouchard, I. Borecki, T. Rice, 2001, American journal of human biology : the official journal of the Human Biology Council.

Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals

Andrew D. Johnson, Benjamin D. Heavner, Michael E. Hall, 2022, Nature Communications.

Edinburgh Research Explorer Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Tom R. Gaunt, Andrew D. Johnson, Nicholette D. Palmer, 2022 .

Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk

Christian Gieger, Xiaofeng Zhu, Paolo Vineis, 2011, Nature.

Single nucleotide polymorphism-single nucleotide polymorphism interactions among inflammation genes in the genetic architecture of blood pressure in the Framingham Heart Study.

L. de las Fuentes, Jacob J Basson, D. Rao, 2015, American journal of hypertension.

Population sequencing data reveal a compendium of mutational processes in human germline

Ryan D. Hernandez, Nicholette D. Palmer, S. Redline, 2020, bioRxiv.

Linkage analysis of complex traits using affected sibpairs: Effects of single‐locus approximations on estimates of the required sample size

I. Borecki, A. Todorov, D. Rao, 1997, Genetic epidemiology.

CAT scans, PET scans, and genomic scans

D C Rao, D. Rao, 1998, Genetic epidemiology.

Meta‐analysis methodology for combining non‐parametric sibpair linkage results: Genetic homogeneity and identical markers

Michael Province, C. Gu, A. Todorov, 1998, Genetic epidemiology.

Trade‐off between false positives and false negatives in the linkage analysis of complex traits

D C Rao, A A Todorov, A. Todorov, 1997, Genetic epidemiology.

A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries

Aaron F. McDaid, Yan V. Sun, Cassandra N. Spracklen, 2022 .

Tree‐based recursive partitioning methods for subdividing sibpairs into relatively more homogeneous subgroups

M A Province, D C Rao, M. Province, 2001, Genetic epidemiology.

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Ivana V. Yang, Sebastian M. Armasu, Andrew D. Johnson, 2020, Nature.

Variation in Genes that Regulate Blood Pressure Are Associated with Glomerular Filtration Rate in Chinese

May E. Montasser, P. Whelton, T. Rice, 2014, PloS one.

Gene-lifestyle interactions in the genomics of human complex traits

C. Rotimi, D. Chasman, A. Kraja, 2022, European Journal of Human Genetics.

Optimum designs for next‐generation sequencing to discover rare variants for common complex disease

Gang Shi, D C Rao, Gang Shi, 2011, Genetic epidemiology.

Heritability of LDL peak particle diameter in the Quebec Family Study

Y. Bossé, C. Bouchard, J. Després, 2003, Genetic epidemiology.

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).

G. Jean-Louis, T. Rice, D. Jeffe, 2017, Ethnicity & disease.

An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP)

R. Olshen, E. Boerwinkle, N. Schork, 2007, Human Genetics.

Meta‐analysis of genetic linkage to quantitative trait loci with study‐specific covariates: A mixed‐effects model

M. Province, C. Gu, D. Rao, 1999, Genetic epidemiology.

Random effects model for meta‐analysis of multiple quantitative sibpair linkage studies

Zhaohai Li, D. Rao, 1996, Genetic epidemiology.

Combining extremely concordant sibpairs with extremely discordant sibpairs provides a cost effective way to linkage analysis of quantitative trait loci

D C Rao, C Gu, A Todorov, 1996, Genetic epidemiology.

The HERITAGE Family Study: A Review of the Effects of Exercise Training on Cardiometabolic Health, with Insights into Molecular Transducers

C. Bouchard, J. Després, T. Rice, 2022, Medicine and science in sports and exercise.

Smoking and Genetic Risk Variation Across Populations of European, Asian, and African American Ancestry—A Meta‐Analysis of Chromosome 15q25

Ming D. Li, John P. Rice, Yan V. Sun, 2012, Genetic epidemiology.

G protein β3 polymorphism and hemodynamic and body composition phenotypes in the HERITAGE Family Study

C. Bouchard, T. Rice, J. Wilmore, 2002 .

Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

Jennifer G. Robinson, Nicholette D. Palmer, Christine A. Williams, 2019, Nature Genetics.

General purpose model and a computer program for combined segregation and path analysis (SEGPATH): Automatically creating computer programs from symbolic language model specifications

M A Province, D C Rao, M. Province, 1995, Genetic epidemiology.

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

M. Province, E. Campbell, E. Silverman, 1990 .

A Perspective on Promoting Diversity in the Biomedical Research Workforce: The National Heart, Lung, and Blood Institute's PRIDE Program.

G. Jean-Louis, T. Rice, D. Jeffe, 2016, Ethnicity & disease.

Associations of the Serum/Glucocorticoid Regulated Kinase Genes With BP Changes and Hypertension Incidence: The Gensalt Study

T. Rice, Jianfeng Huang, D. Gu, 2017, American journal of hypertension.

Gender difference in blood pressure responses to dietary sodium intervention in the GenSalt study

P. Whelton, Ji-chun Chen, Jianfeng Huang, 2009, Journal of hypertension.

Familial risk of high blood pressure in the Canadian population

C. Bouchard, P. Katzmarzyk, T. Rankinen, 2001, American journal of human biology : the official journal of the Human Biology Council.

Sex-specific effects of ACE I/D and AGT-M235T on pulse pressure: the HyperGEN Study

J. Pankow, D. Rao, K. North, 2007, Human Genetics.

Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data

May E. Montasser, T. Assimes, A. Reiner, 2019, Human Genetics.

Heterogeneity among populations for familial aggregation of blood pressure

C. Bouchard, T. Rice, M. Province, 1991, American journal of human biology : the official journal of the Human Biology Council.

Genome screening using extremely discordant and extremely concordant sib pairs

C. Gu, A. Todorov, D. Rao, 1997, Genetic epidemiology.

Quantitative Trait Locus on 15q for a Metabolic Syndrome Variable Derived from Factor Analysis

Y. Bossé, C. Bouchard, J. Després, 2007, Obesity.

Role of gene expression microarray analysis in finding complex disease genes

G. Stormo, M. Province, D. Rao, 2002, Genetic epidemiology.

Familial aggregation of subcutaneous fat patterning: Principal components of skinfolds in the Québec family study

C. Bouchard, T. Rice, L. Pérusse, 1996, American journal of human biology : the official journal of the Human Biology Council.

Race differences in reproducibilities: The HERITAGE family study

C. Bouchard, M. Province, J. Wilmore, 1997, American journal of human biology : the official journal of the Human Biology Council.

Commingling and segregation analysis of blood pressure in consanguineous and nonconsanguineous families from Andhra Pradesh, India

T. Rice, D. Rao, A. Nirmala, 1992, American journal of human biology : the official journal of the Human Biology Council.

Prediction of physical activity and physical work capacity (PWC150) in young adulthood from childhood and adolescence with consideration of parental measures

C. Bouchard, P. Katzmarzyk, L. Pérusse, 2001, American journal of human biology : the official journal of the Human Biology Council.

Three Approaches to Modeling Gene‐Environment Interactions in Longitudinal Family Data: Gene‐Smoking Interactions in Blood Pressure

A. Vazquez, Y. Sung, K. Schwander, 2016, Genetic epidemiology.

Measured maximal heart rates compared to commonly used age‐based prediction equations in the heritage family study

T. Rankinen, M. Sarzynski, A. Leon, 2013, American Journal of Human Biology.

Principal components analysis of morphological measures in the Québec family study: Familial correlations

C. Bouchard, T. Rice, C. Gu, 1997, American journal of human biology : the official journal of the Human Biology Council.

Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

Jennifer G. Robinson, Nicholette D. Palmer, P. Elliott, 2019, Nature Communications.

Model‐based linkage analysis with imprinting for quantitative traits: ignoring imprinting effects can severely jeopardize detection of linkage

Yun Ju Sung, D C Rao, Y. Sung, 2008, Genetic epidemiology.

Familial aggregation of body mass index and subcutaneous fat measures in the longitudinal Québec family study

C. Bouchard, T. Rice, L. Pérusse, 1999, Genetic epidemiology.

Research Education and Mentoring Program in Cardiovascular Diseases for Under-Represented Junior Faculty From NHLBI SIPID/PRIDE.

T. Rice, D. Jeffe, J. Jobe, 2019, Journal of the American College of Cardiology.

Biological and cultural sources of familial resemblance in plasma lipids: A comparison between North America and Israel—the lipid research clinics program

K. Namboodiri, D. Rao, Y. Friedlander, 1988, Genetic epidemiology.

Heterogeneity in multifactorial inheritance of plasma lipids and lipoproteins in ethnically diverse families in Jerusalem

D. Rao, Y. Friedlander, J. Kark, 1986, Genetic epidemiology.

New genetic loci link adipose and insulin biology to body fat distribution

Tamara S. Roman, Thomas W. Mühleisen, Ellen M. Schmidt, 2014, Nature.

FTO Genotype Is Associated With Exercise Training–induced Changes in Body Composition

C. Bouchard, T. Rice, T. Rankinen, 2010, Obesity.

New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk

Ellen M. Schmidt, Cameron D. Palmer, Toshiko Tanaka, 2016, Nature Communications.

On the role of vitamin D binding globulin in glucose homeostasis: Results from the San Luis Valley diabetes study

D. Rao, G. Vogler, P. Majumder, 1989, Genetic epidemiology.

Familial clustering of insulin and abdominal visceral fat: the HERITAGE Family Study.

J. Després, T. Rice, J. Wilmore, 1998, The Journal of clinical endocrinology and metabolism.

Changes in Ventilatory Threshold with Exercise Training in a Sedentary Population: The Heritage Family Study

C. Bouchard, S. Gaskill, J. Wilmore, 2001, International journal of sports medicine.

Genomic scan for maximal oxygen uptake and its response to training in the HERITAGE Family Study.

C. Bouchard, I. Borecki, T. Rice, 2000, Journal of applied physiology.

An overview of the genetic dissection of complex traits.

D. Rao, D. Rao, 2008, Advances in genetics.

Sibling correlation of left ventricular mass and geometry in hypertensive African Americans and whites: the HyperGEN study. Hypertension Genetic Epidemiology Network.

Yuling Hong, R. Devereux, D. Arnett, 2001, American journal of hypertension.

Is adiposity at normal body weight relevant for cardiovascular disease risk?

C. Bouchard, J. Wilmore, D. Rao, 2002, International Journal of Obesity.

No linkage of the lipoprotein lipase locus to hypertension in Caucasians.

M. Leppert, M. Province, D. Rao, 1999, Journal of hypertension.

Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits.

Sebastian M. Armasu, Christine A. Williams, Audrey Y. Chu, 2019, American journal of human genetics.

Targeting the metabolic syndrome with exercise: evidence from the HERITAGE Family Study.

C. Bouchard, J. Wilmore, D. Rao, 2003, Medicine and science in sports and exercise.

Genetic insights into resting heart rate and its role in cardiovascular disease

M. P. Concas, Henry J. Lin, S. Bandinelli, 2023, Nature communications.

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

May E. Montasser, H. M. Draisma, K. Lunetta, 2014 .

Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk

Tom R. Gaunt, Andrew D. Johnson, Nicholette D. Palmer, 2011, Nature.

Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

Nicholette D. Palmer, Sina A. Gharib, M. Fornage, 2020, bioRxiv.

Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations

Xiaofeng Zhu, Tamar Sofer, Joshua C Denny, 2017, PLoS genetics.

Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans

Stephanie A. Bien, C. Carlson, M. Fornage, 2016, PloS one.

Genome-wide meta-analyses of smoking behaviors in African Americans

Gary K. Chen, J. Witte, M. Fornage, 2012, Translational Psychiatry.

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

Nicholette D. Palmer, P. Elliott, M. Fornage, 2019, bioRxiv.

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

Audrey Y. Chu, Toshiko Tanaka, S. Bandinelli, 2018, Molecular Psychiatry.

A genomewide linkage scan for abdominal subcutaneous and visceral fat in black and white families: The HERITAGE Family Study.

C. Bouchard, I. Borecki, T. Rice, 2002, Diabetes.

Methods for handling multiple testing.

Nicholas J Schork, N. Schork, T. Rice, 2008, Advances in genetics.

Melanocortin 4 receptor sequence variations are seldom a cause of human obesity: the Swedish Obese Subjects, the HERITAGE Family Study, and a Memphis cohort.

E. Snyder, C. Bouchard, L. Lönn, 2002, The Journal of clinical endocrinology and metabolism.

Racial admixture and its impact on BMI and blood pressure in African and Mexican Americans

N. Risch, N. Schork, Hua Tang, 2006, Human Genetics.

Genome-wide search for genes related to the fat-free body mass in the Québec family study.

Y. Chagnon, C. Bouchard, I. Borecki, 2000, Metabolism: clinical and experimental.

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

Yu-Han H. Hsu, Sanjay R. Patel, J. Witte, 2017, PLoS genetics.

Variants in the CD36 gene associate with the metabolic syndrome and high-density lipoprotein cholesterol.

M. Permutt, D. Rao, S. Hunt, 2008, Human molecular genetics.

Population sequencing data reveal a compendium of mutational processes in human germline

Nicholette D. Palmer, S. Redline, E. Boerwinkle, 2021, Science.

Possible linkage of a breast cancer‐susceptibility locus to the ABO locus: Sensitivity of LOD scores to a single new recombinant observation

E. Thompson, M. Skolnick, D. Rao, 1984, Genetic epidemiology.

The effect of sex, age and race on estimating percentage body fat from body mass index: The Heritage Family Study

C. Bouchard, J. Wilmore, D. Rao, 2002, International Journal of Obesity.

Possible Locus on Chromosome 18q Influencing Postural Systolic Blood Pressure Changes

J. Pankow, M. Province, D. Rao, 2000, Hypertension.

Ethnicity and human genetic linkage maps.

E. Boerwinkle, N. Risch, M. Leppert, 2005, American journal of human genetics.

Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat

M. Fornage, C. Bouchard, J. Blangero, 2015, International Journal of Obesity.

Genetic variation at the apolipoprotein gene loci contribute to response of plasma lipids to dietary change

E. Boerwinkle, Chun-Fang Xu, P. Talmud, 1990, Genetic epidemiology.

The genetic susceptibility to insulin‐dependent diabetes mellitus: Combined segregation and linkage analysis

N. Morton, D. Rao, C. Maclean, 1985, Genetic epidemiology.

On transferability of genome‐wide tagSNPs

A. Templeton, C. Gu, S. Ketkar, 2008, Genetic epidemiology.

A Genetic study of hypoalphalipoproteinemia

P. J. Byard, I. Borecki, D. Rao, 1984, Genetic epidemiology.

Familial resemblance for abdominal visceral fat: the HERITAGE family study

C. Bouchard, I. Borecki, T. Rice, 1997, International Journal of Obesity.

A saturated map of common genetic variants associated with human height

Aaron F. McDaid, M. P. Concas, Cassandra N. Spracklen, 2022, Nature.

Ignoring temporal trends in genetic effects substantially reduces power of quantitative trait linkage analysis

Gang Shi, D. Rao, 2008, Genetic epidemiology.

Evaluation of path analysis through computer simulation: Effect of incorrectly assuming independent distribution of familial correlations

R. Wette, D. Rao, M. McGue, 1984, Genetic epidemiology.

Contribution of body fatness and adipose tissue distribution to the age variation in plasma steroid hormone concentrations in men: the HERITAGE Family Study.

C. Bouchard, J. Wilmore, D. Rao, 2000, The Journal of clinical endocrinology and metabolism.

Repeated‐measures model for the investigation of temporal trends using longitudinal family studies: Application to systolic blood pressure

M. Province, D. Rao, L. Eaves, 1989, Genetic epidemiology.

Association and linkage between an insulin-like growth FACTOR-1 GENE polymorphism and fat free mass in the HERITAGE Family Study

Y. Chagnon, C. Bouchard, I. Borecki, 1999, International Journal of Obesity.

Genetic analysis combining path analysis with regressive models: The beta path model of polygenic and familial environmental transmission

Zhaohai Li, G. Bonney, D. Rao, 1994, Genetic epidemiology.

A Monte Carlo evaluation of three statistical methods used in path analysis

R. Wette, D. Rao, M. McGue, 1987, Genetic epidemiology.

The analysis of Schizophrenia family data

D. Rao, I. Gottesman, M. McGue, 1986, Behavior genetics.

Family History of Coronary Heart Disease and Hemostatic Variables in Middle-Aged Adults

J. Pankow, A. Folsom, M. Province, 1997, Thrombosis and Haemostasis.

Polymorphisms in the GNB3 and ADD1 genes and blood pressure in a Chinese population

P. Whelton, T. Rice, Jianfeng Huang, 2010, Human Genetics.

Familial aggregation of amount and distribution of subcutaneous fat and their responses to exercise training in the HERITAGE family study.

C. Bouchard, T. Rice, M. Province, 2000, Obesity research.

Genome-wide linkage scan for exercise stroke volume and cardiac output in the HERITAGE Family Study.

C. Bouchard, T. Rice, J. Wilmore, 2002, Physiological genomics.

Complex segregation analysis of low levels of plasma high‐density lipoprotein cholesterol in a sample of nuclear families in Jerusalem

D. Rao, Y. Friedlander, J. Kark, 1986, Genetic epidemiology.

Meta-analysis for model-free methods.

M. Province, C. Gu, D. Rao, 2001, Advances in genetics.

A dopamine D2 receptor gene polymorphism and physical activity in two family studies

C. Bouchard, J. Wilmore, D. Rao, 2003, Physiology & Behavior.

Smoking and Genetic Risk Variation Across Populations of European, Asian, and African American Ancestry—A Meta‐Analysis of Chromosome 15q25

Ming D. Li, John P. Rice, Sarah M. Hartz, 2012, Genetic epidemiology.

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study

May E. Montasser, Nicholette D. Palmer, M. Fornage, 2023, medRxiv.

Familial risk of high blood pressure in the Canadian population

C. Bouchard, P. Katzmarzyk, T. Rankinen, 2001, American Journal of Human Biology.

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

Audrey Y. Chu, S. Bandinelli, D. Hernandez, 2018, Molecular Psychiatry.

A general autosomal/X‐linked model

M. Skolnick, S. Hasstedt, D. Rao, 1984, Genetic epidemiology.

The impact of energy intake and energy expenditure of activity on the familial transmission of adiposity in an indian population

T. Rice, L. E. Mitchell, D. Rao, 1993, American journal of human biology : the official journal of the Human Biology Council.

Assessment of adiposity in an Indian population: Familial correlations

T. Rice, L. E. Mitchell, D. Rao, 1993, Genetic epidemiology.

Heterogeneity among populations for familial aggregation of blood pressure

C. Bouchard, T. Rice, M. Province, 1991, American journal of human biology : the official journal of the Human Biology Council.

G. Jean-Louis, T. Rice, D. Jeffe, 2017, Ethnicity & disease.

Genome screening using extremely discordant and extremely concordant sib pairs

C. Gu, A. Todorov, D. Rao, 1997, Genetic epidemiology.

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

K. Kidd, J. Kidd, A. Pakstis, 1986, Genetic epidemiology.

HLA antigens and acute rheumatic fever: Evidence for a recessive susceptibility gene linked to HLA

A. Chakravarti, D. Rao, M. Hafez, 1985, Genetic epidemiology.

A commingling analysis of obesity in the Tecumseh community health study

M. Province, M. Higgins, J. Keller, 1991, American journal of human biology : the official journal of the Human Biology Council.

Performance of Genotype Imputations Using Data from the 1000 Genomes Project

Claude Bouchard, Yun Ju Sung, Tuomo Rankinen, 2011, Human Heredity.

A new model for the resolution of cultural and biological inheritance in the presence of temporal trends: Application to systolic blood pressure

M. Province, D. Rao, J. Maccluer, 1985, Genetic epidemiology.