Physician
Internal Medicine
Dr. Ravi K. Duggirala, MD
|
|
Give Review
Ravi Duggirala practices Internal Medicine. He studied medicine at Kakatiya Medical College NTR. He received 1 awards: "CMS Meaningful Use Stage 1 Certification". Ravi K. Duggirala, MD is a published doctor. He published 99 publications, including: 'Variant in sulfonylurea receptor-1 gene is associated with high insulin concentrations in non-diabetic Mexican Americans: SUR-1 gene variant and hyperinsulinemia.' Ravi K. Duggirala, MD is registered with Medicare.
Publications
- Exome Sequence Data From Multigenerational Families Implicate AMPA Receptor Trafficking in Neurocognitive Impairment and Schizophrenia Risk.
- Genome-wide linkage on chromosome 10q26 for a dimensional scale of major depression.
- Recurrent major depression and right hippocampal volume: A bivariate linkage and association study.
- Heritability of fractional anisotropy in human white matter: A comparison of Human Connectome Project and ENIGMA-DTI data.
- Non-crossover gene conversions show strong GC bias and unexpected clustering in humans.
- Pleiotropic locus for emotion recognition and amygdala volume identified using univariate and bivariate linkage.
- Shared genetic factors influence amygdala volumes and risk for alcoholism.
- Metabolites as novel biomarkers for childhood obesity-related traits in Mexican-American children.
- Discovering Schizophrenia Endophenotypes in Randomly Ascertained Pedigrees.
- Novel QTL at chromosome 6p22 for alcohol consumption: Implications for the genetic liability of alcohol use disorders.
- Common genetic variants and gene expression associated with white matter microstructure in the human brain.
- Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: Comparing meta and megaanalytical approaches for data pooling.
- Waist circumference is genetically correlated with incident Type 2 diabetes in Mexican-American families.
- Influence of age, sex and genetic factors on the human brain.
- Genome-wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition.
- Genetic basis of neurocognitive decline and reduced white-matter integrity in normal human brain aging.
- Transcriptomics of cortical gray matter thickness decline during normal aging.
- Localization of a major susceptibility locus influencing preterm birth on chromosome 18q in Mexican Americans.
- Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group.
- Shared genetic variance between obesity and white matter integrity in Mexican Americans.
- A study of loss of heterozygosity at 70 loci in anaplastic astrocytoma and glioblastoma multiforme with implications for tumor evolution.
- Concordance between the CC chemokine receptor 5 genetic determinants that alter risks of transmission and disease progression in children exposed perinatally to human ...
- A major locus for fasting insulin concentrations and insulin resistance on chromosome 6q with strong pleiotropic effects on obesity-related phenotypes in nondiabetic M...
- Genetic basis of acanthosis nigricans in Mexican Americans and its association with phenotypes related to type 2 diabetes.
- Birth weight and the metabolic syndrome: thrifty phenotype or thrifty genotype?
- A major susceptibility locus influencing plasma triglyceride concentrations is located on chromosome 15q in Mexican Americans.
- Smoking behavior is under the influence of a major quantitative trait locus on human chromosome 5q.
- Linkage of type 2 diabetes mellitus and of age at onset to a genetic location on chromosome 10q in Mexican Americans.
- Genetic determinants of variation in gallbladder disease in the Mexican-American population.
- Variant in sulfonylurea receptor-1 gene is associated with high insulin concentrations in non-diabetic Mexican Americans: SUR-1 gene variant and hyperinsulinemia.
- Statistical properties of a variance components method for quantitative trait linkage analysis in nuclear families and extended pedigrees.
- A variance component approach to dichotomous trait linkage analysis using a threshold model.
- Genetic structure of the indigenous populations of Siberia.
- Evidence for linkage of regions on chromosomes 6 and 11 to plasma glucose concentrations in Mexican Americans.
- Quantitative variation in obesity-related traits and insulin precursors linked to the OB gene region on human chromosome 7.
- Genetic basis of variation in carotid artery wall thickness.
- Population genetics and structure of Buryats from the Lake Baikal Region of Siberia.
- Population structure of the Chenchu and other south Indian tribal groups: relationships between genetic, anthropometric, dermatoglyphic, geographic, and linguistic dis...
- Population relationships among historical and modern indigenous Siberians based on anthropometric characters.
- Digital dermatoglyphic patterns of Eskimo and Amerindian populations: relationships between geographic, dermatoglyphic, genetic, and linguistic distances.
- Fishing for pleiotropic QTLs in a polygenic sea.
- Power to localize the major gene for disease liability is increased after accounting for the effects of related quantitative phenotypes.
- A genome-wide linkage scan for genes controlling variation in urinary albumin excretion in type II diabetes.
- Association between variants in the genes for adiponectin and its receptors with insulin resistance syndrome (IRS)-related phenotypes in Mexican Americans.
- Heritability of the severity of diabetic retinopathy: the FIND-Eye study.
- Genetic control over the resting brain.
- Genetics of microstructure of cerebral white matter using diffusion tensor imaging.
- Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND).
- Blood pressure and cerebral white matter share common genetic factors in Mexican Americans.
- Whole brain and regional hyperintense white matter volume and blood pressure: overlap of genetic loci produced by bivariate, whole-genome linkage analyses.
- Common genetic influences on depression, alcohol, and substance use disorders in Mexican-American families.
- Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes.
- Evaluation of tight junction protein 1 encoding zona occludens 1 as a candidate gene for albuminuria in a Mexican American population.
- High dimensional endophenotype ranking in the search for major depression risk genes.
- Genetic factors influence serological measures of common infections.
- Wide disparity in genetic admixture among Mexican Americans from San Antonio, TX.
- Heritability and linkage analysis of hand, foot, and eye preference in Mexican Americans.
- Genomewide linkage scan for diabetic renal failure and albuminuria: the FIND study.
- Genetic variants in transient receptor potential cation channel, subfamily M 1 (TRPM1) and their risk of albuminuria-related traits in Mexican Americans.
- Genome-wide linkage screen for systolic blood pressure in the Veterans Administration Genetic Epidemiology Study (VAGES) of Mexican-Americans and confirmation of a maj...
- A multimodal assessment of the genetic control over working memory.
- On the genetic architecture of cortical folding and brain volume in primates.
- Identification of a locus modulating serum C-reactive protein levels on chromosome 5p15.
- Meta-analysis of genome-wide linkage studies of quantitative lipid traits in families ascertained for type 2 diabetes.
- P2 promoter variants of the hepatocyte nuclear factor 4alpha gene are associated with type 2 diabetes in Mexican Americans.
- Haplotypes of transcription factor 7-like 2 (TCF7L2) gene and its upstream region are associated with type 2 diabetes and age of onset in Mexican Americans.
- A genome-wide linkage scan for genes controlling variation in renal function estimated by serum cystatin C levels in extended families with type 2 diabetes.
- Effects of covariates and interactions on a genome-wide association analysis of rheumatoid arthritis.
- Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies.
- Analysis of genetic variability and whole genome linkage of whole-brain, subcortical, and ependymal hyperintense white matter volume.
- Genome-wide linkage scans for type 2 diabetes mellitus in four ethnically diverse populations-significant evidence for linkage on chromosome 4q in African Americans: t...
- Evaluation of gremlin 1 (GREM1) as a candidate susceptibility gene for albuminuria-related traits in Mexican Americans with type 2 diabetes mellitus.
- Genome-wide linkage scan for genes influencing plasma triglyceride levels in the Veterans Administration Genetic Epidemiology Study.
- Endothelial nitric oxide synthase (eNOS) gene polymorphisms and their association with type 2 diabetes-related traits in Mexican Americans.
- Autosomal genome-wide linkage analysis to identify loci for gallbladder wall thickness in Mexican Americans.
- Association of genetic variation in ENPP1 with obesity-related phenotypes.
- The Cys(311)Ser polymorphism of paraoxonase 2 (PON2) is associated with albumin-to-creatinine ratio (ACR) in Mexican Americans.
- Genetic polymorphisms in the renin-angiotensin system (RAS) genes and their association analysis with type 2 diabetes and related traits in Mexican Americans.
- Genetic polymorphisms in OGG1 and their association with angiomyolipoma, a benign kidney tumor in patients with tuberous sclerosis.
- Meta-analysis of genome-wide linkage studies in BMI and obesity.
- Genotype by diabetes interaction effects on the detection of linkage of glomerular filtration rate to a region on chromosome 2q in Mexican Americans.
- Association of neuropeptide Y receptor Y5 polymorphisms with dyslipidemia in Mexican Americans.
- Fasting insulin and obesity-related phenotypes are linked to chromosome 2p: the Strong Heart Family Study.
- A quantitative trait locus (QTL) on chromosome 6q influences birth weight in two independent family studies.
- Effect of genotype x alcoholism interaction on linkage analysis of an alcoholism-related quantitative phenotype.
- A novel missense mutation in ADRB3 increases risk for type 2 diabetes in a Mexican American family.
- A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans.
- Genetic basis of diabetic nephropathy.
- Bivariate linkage analysis of the insulin resistance syndrome phenotypes on chromosome 7q.
- Linkage of high-density lipoprotein-cholesterol concentrations to a locus on chromosome 9p in Mexican Americans.
- Genome-wide linkage analyses of type 2 diabetes in Mexican Americans: the San Antonio Family Diabetes/Gallbladder Study.
- A single nucleotide polymorphism in MGEA5 encoding O-GlcNAc-selective N-acetyl-beta-D glucosaminidase is associated with type 2 diabetes in Mexican Americans.
- Evidence for bivariate linkage of obesity and HDL-C levels in the Framingham Heart Study.
- Evidence of a novel quantitative-trait locus for obesity on chromosome 4p in Mexican Americans.
- Further evidence for a type 2 diabetes susceptibility locus on chromosome 11q.
- Genetic basis of variation in carotid artery plaque in the San Antonio Family Heart Study.
- Genetic determination of biological age in the Mennonites of the Midwestern United States.
- Heritability of anthropometric phenotypes in caste populations of Visakhapatnam, India.
Schools
Kakatiya Medical College Ntr University Of Health Sciences
Doctors Specialties
- Internal Medicine
Accepted Insurances
Awards
- CMS Meaningful Use Stage 1 Certification
Education
-
Bronx-Lebanon Hospital Center -
Kakatiya Medical College NTR
Drug Facts
| NPI NUMBER | 1275607392 | |
| NPPES Provider LastName | DUGGIRALA | |
| NPPES Provider FirstName | RAVI | |
| NPPES Provider ZIPCode | 33761 | |
| NPPES Provider State | FL | |
| Specialty Description | Internal Medicine | |
| Total Claim Count | 4292.0 | |
| Distinct Opioid Count | 5.0 | |
| Opioid Claim Count | 164.0 | |
| Percent Opioid Claims | 3.82 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1275607392 |
| Last Name Of The Provider | DUGGIRALA |
| First Name Of The Provider | RAVI |
| View All |
Similar Doctors
|
Dr. Neisa I. Diaz, MD
 This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Mark H. Smitherman, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Elizabeth A. Rommel, MD
This Doctor is OpenDoctor Recommended.
|
|
Dr. Alfred B. Chapman, DO
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Kyle McWhirter, DO
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Dennis P. Deruelle, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Ewa D. Piszczek, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. William R. Valdez Bautista, MD |
|
|
Dr. Francisco J. Rey, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Mohammad Iqbal, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Salman Ahmed, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Beth A. Hanrahan, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Mari S. Tofani, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Julieta Gilson, MD
This Doctor is OpenDoctor Recommended.
|