Inga Prokopenko - Genetic Mutations

Author Information

Inga Prokopenko is currently affiliated with the Wellcome Centre for Human Genetics at the University of Oxford, Oxford, UK. Dr. Prokopenko has made significant contributions to the field of genetics, with a particular focus on the genetic factors involved in metabolic and cardiovascular diseases. Her research seeks to understand the complex interplay between genetics and various disease states, aiming to uncover novel insights and potential therapeutic targets.

Research Contributions

Dr. Inga Prokopenko has contributed extensively to the understanding of genetic influences on various health conditions, including metabolic disorders, cardiovascular diseases, and diabetes. Some of her notable works include the study of dynamic longitudinal exposome trajectories in cardiovascular and metabolic noncommunicable diseases, the enrichment of Bifidobacterium in the gut microbiome of Kashmiri women with Polycystic Ovary Syndrome, and the role of physical activity and sedentary behavior in disease prevention. She has also addressed ethical concerns in the use of polygenic risk scores in pre-implantation genetic testing and contributed to integrative genomic analyses implicating DNA methylation in human obesity and diabetes.

Aliases

Dr. Inga Prokopenko is also known by the aliases "I. Prokopenko" and "Inga Prokopenko".

Publication and Citation Metrics

Metric Value
Citation Count 48,987
h-index 85
Paper Count 275

Publications:

DOI: 10.1097/EE9.0000000000000184

Year: 2022

DOI: 10.3390/genes13020379

Year: 2022

DOI: 10.1038/s41431-022-01067-0

Year: 2022

DOI: 10.21203/rs.3.rs-1129252/v1

Year: 2021

DOI: 10.1038/s41431-021-01000-x

Year: 2021

DOI: 10.1038/s41467-021-21276-3

Year: 2021

DOI: 10.1016/j.jad.2021.05.031

Year: 2021

DOI: 10.1101/2021.12.20.21266893

Year: 2021

DOI: 10.3390/genes12010064

Year: 2021

DOI: 10.1101/2021.04.17.21255471

Year: 2021

Frequently asked queries:
Can Genetic Susceptibility Influence Mutation Risk?
What are Autism Spectrum Disorders?
What is the CFTR Gene?
How is Cystic Fibrosis Inherited?
How do Inversions Occur?
What is the Molecular Basis of Genetic Diseases?
How are Missense Mutations Detected?
What is Third Generation Sequencing?
What are Targeted Therapies?
What are Viral Vectors?
Follow Us
Top Searches
Autism Spectrum Disorder Congenital Heart Disease Cystic Fibrosis DNA Cloning Fragile X Syndrome Huntington’s Disease Livestock Lynch Syndrome Neurodegenerative Diseases Sickle Cell Disease Thalassemia Patients

Partnered Content Networks

Relevant Topics