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4 results on '"Rayabarapu Pranav Chand"'

1. Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India.

Author

Rayabarapu Pranav Chand, Arramraju Sreenivas Kumar, Kapadia Anuj, Satti Vishnupriya, and Battini Mohan Reddy

Subjects
Medicine, Science
Abstract

In our attempt to comprehensively understand the nature of association of variants at 11q23.3 apolipoprotein gene cluster region, we genotyped a prioritized set of 96 informative SNPs using Fluidigm customized SNP genotyping platform in a sample of 508 coronary artery disease (CAD) cases and 516 controls. We found 12 SNPs as significantly associated with CAD at P

Published
2016
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2. Proband only exome sequencing in 403 Indian children with neurodevelopmental disorders: Diagnostic yield, utility and challenges in a resource-limited setting

Author

Rayabarapu Pranav Chand, Wankhede Vinit, Varsha Vaidya, Anand Subramaniam Iyer, Madhavi Shelke, Shagun Aggarwal, Suvarna Magar, Sumita Danda, Amita Moirangthem, Shubha Rajendra Phadke, Manisha Goyal, Prajnya Ranganath, Mehul Mistri, Parth Shah, Nidhi Shah, and Udhaya Hardik Kotecha

Subjects
Genetics, General Medicine, Genetics (clinical)
Published
2023

3. Exome Sequencing in 403 Indian Children with Neurodevelopmental Disorders: Diagnostic Yield, Utility and Challenges in a Resource-Limited Setting

Author

Rayabarapu, Pranav Chand, primary, Vinit, Wankhede, additional, Vaidya, Varsha, additional, Iyer, Anand Subramaniam, additional, Shelke, Madhavi, additional, Aggarwal, Shagun, additional, Magar, Suvarna, additional, Danda, Sumita, additional, Moirangthem, Amita, additional, Phadke, Shubha Rajendra, additional, Goyal, Manisha, additional, Ranganath, Prajnya, additional, Mistri, Mehul, additional, Shah, Parth, additional, Shah, Nidhi, additional, and Kotecha, Udhaya Hardik, additional

Published
2022
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4. Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India

Author

Arramraju Sreenivas Kumar, Kapadia Anuj, Battini Mohan Reddy, Rayabarapu Pranav Chand, and Satti Vishnupriya

Subjects
0301 basic medicine, Male, lcsh:Medicine, Gene Expression, Genome-wide association study, Disease, Coronary Artery Disease, 030204 cardiovascular system & hematology, Bioinformatics, Vascular Medicine, Biochemistry, Body Mass Index, 0302 clinical medicine, Medicine and Health Sciences, lcsh:Science, Genetics, education.field_of_study, Multidisciplinary, Chromosome Biology, Genomics, Middle Aged, Lipids, SNP genotyping, Cholesterol, Chromosomal region, Female, Research Article, Adult, Genotype, Population, India, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Chromosomes, 03 medical and health sciences, medicine, Genome-Wide Association Studies, Humans, Genetic Predisposition to Disease, Gene Regulation, education, Genetic Association Studies, Aged, Dyslipidemias, Evolutionary Biology, Population Biology, Chromosomes, Human, Pair 11, lcsh:R, Haplotype, Biology and Life Sciences, Computational Biology, Human Genetics, Cholesterol, LDL, Cell Biology, medicine.disease, Genome Analysis, 030104 developmental biology, Apolipoproteins, Haplotypes, Dyslipidemia, Metabolic Disorders, lcsh:Q, Population Genetics
Abstract

In our attempt to comprehensively understand the nature of association of variants at 11q23.3 apolipoprotein gene cluster region, we genotyped a prioritized set of 96 informative SNPs using Fluidigm customized SNP genotyping platform in a sample of 508 coronary artery disease (CAD) cases and 516 controls. We found 12 SNPs as significantly associated with CAD at P

Published
2016

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