Petros P. Petrou - Genetic Mutations

Author Information

Petros P. Petrou is a researcher affiliated with the Department of Biochemical Genetics at The Cyprus Institute of Neurology and Genetics, located in Nicosia, Cyprus. His work primarily focuses on genetic studies related to biochemical genetics and neurology.

Research Contributions

Petros P. Petrou has made significant contributions to the field of genetics, as demonstrated by his numerous publications. His research spans various topics including mitochondrial dynamics, genetic disorders such as Alport syndrome and galactosaemia, and the study of protein interactions within cellular structures. Notable studies include the investigation of mitochondrial dynamics dysregulation in diseases, the effects of glycine substitution in the Col4a3 gene related to Alport syndrome, and the role of the Stbd1 protein in glycogen clustering during endoplasmic reticulum stress. His work is well-recognized in the scientific community, contributing to advancements in understanding genetic and molecular mechanisms underlying various diseases.

Aliases

Petros P. Petrou is known by several aliases in the academic community including Petros P. Petrou, P. Petrou, Petros P Petrou, Petros Petrou, and P Petrou.

Publication and Citation Metrics

Metric	Value
Citation Count	649
H-index	12
Paper Count	31

Publications:

When the Balance Tips: Dysregulation of Mitochondrial Dynamics as a Culprit in Disease

DOI: 10.3390/ijms22094617

Year: 2021

A glycine substitution in the collagenous domain of Col4a3 in mice recapitulates late onset Alport syndrome

DOI: 10.1016/j.mbplus.2020.100053

Year: 2021

Stbd1 promotes glycogen clustering during endoplasmic reticulum stress and supports survival of mouse myoblasts.

DOI: 10.1242/jcs.244855

Year: 2020

A novel SLC30A10 missense variant associated with parkinsonism and dystonia without hypermanganesemia

DOI: 10.1016/j.jns.2020.117101

Year: 2020

Stbd1 promotes glycogen clustering during endoplasmic reticulum stress and supports survival of mouse myoblasts

DOI: 10.1242/jcs.244855

Year: 2020

Classic galactosaemia in the Greek Cypriot population: An epidemiological and molecular study

DOI: 10.1111/ahg.12318

Year: 2019

FP070PHENOTYPIC ANALYSIS OF TWO ALPORT SYNDROME MODEL MICE WITH A COL4Α3 G1332E MUTATION

DOI: 10.1093/NDT/GFZ106.FP070

Year: 2019

Mouse Stbd1 is N-myristoylated and affects ER–mitochondria association and mitochondrial morphology

DOI: 10.1242/jcs.195263

Year: 2017

The “sweet” side of ER-mitochondria contact sites

DOI: 10.1080/19420889.2017.1329787

Year: 2017

Chitotriosidase deficiency in the Cypriot population: Identification of a novel deletion in the CHIT1 gene.

DOI: 10.1016/j.clinbiochem.2016.03.013

Year: 2016

How Does Autosomal Recessive Inheritance Work?

What Are the Treatment Options?

How Does Radiation Cause Genetic Mutations?

What are Non-Coding Regions?

How Do Genes Work?

Are All Mutations Harmful?

What are Targeted Therapies?

How Do Genetic Mutations Influence ASD?

What Role Does Genetic Testing Play in Managing Infectious Diseases?

What is Third Generation Sequencing?

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