Vassos Neocleous - Neurology

Author Information

Vassos Neocleous is affiliated with the Department of Molecular Genetics, Function and Therapy at The Cyprus Institute of Neurology and Genetics in Nicosia, Cyprus. His work predominantly focuses on the genetic and molecular aspects of various medical conditions, contributing significantly to the understanding and management of these disorders.

Research Contributions

Vassos Neocleous has made substantial contributions to the fields of genetics and neurology, as evidenced by his extensive research output. His work spans a range of topics, including prenatal treatment strategies, molecular modeling for obesity, and the genetic underpinnings of diseases such as cystic fibrosis, central precocious puberty, hearing impairment, juvenile myoclonic epilepsy, and steroid deficiencies. His research has been instrumental in advancing the understanding of these conditions and improving patient care strategies.

Aliases

Throughout his career, Vassos Neocleous has been cited and recognized under various names, including V Neocleous and V. Neocleous. These aliases reflect the different ways his name may appear in academic publications and databases.

Publication and Citation Metrics

Metric	Value
Total Citation Count	929
H-index	16
Total Number of Papers	99

Publications:

Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe

DOI: 10.1530/EJE-21-0554

Year: 2022

Molecular modelling of novel ADCY3 variant predicts a molecular target for tackling obesity

DOI: 10.3892/ijmm.2021.5065

Year: 2022

Demographic Characteristics, Clinical and Laboratory Features, and The Distribution of Pathogenic Variants In the Cftr Gene In the Cypriot Cystic Fibrosis (Cf) Population Demonstrate The Utility of a National Cf Patient Registry

DOI: 10.21203/RS.3.RS-413045/V1

Year: 2021

WS03.4 Notable cystic fibrosis cases of Greek-Cypriot originwith rare or unique CFTR genotypes

DOI: 10.1016/S1569-1993(21)00930-9

Year: 2021

Demographic characteristics, clinical and laboratory features, and the distribution of pathogenic variants in the CFTR gene in the Cypriot cystic fibrosis (CF) population demonstrate the utility of a national CF patient registry

DOI: 10.1186/s13023-021-02049-z

Year: 2021

Pathogenic and Low-Frequency Variants in Children With Central Precocious Puberty

DOI: 10.3389/fendo.2021.745048

Year: 2021

Audiological features in Serbian patients with hearing impairment identified with c.35delG in the GJB2 gene

DOI: 10.2298/sarh201117098d

Year: 2021

Neurophysiological and Genetic Findings in Patients With Juvenile Myoclonic Epilepsy

DOI: 10.3389/fnint.2020.00045

Year: 2020

Dehydration and electrolyte imbalance: a common presenting manifestation of cystic fibrosis in Cyprus

DOI: 10.1183/13993003.congress-2020.2770

Year: 2020

Late diagnosis of 3β-Hydroxysteroid dehydrogenase deficiency: the pivotal role of gas chromatography-mass spectrometry urinary steroid metabolome analysis and a novel homozygous nonsense mutation in the HSD3B2 gene

DOI: 10.1515/jpem-2020-0245

Year: 2020

What is the Prognosis for PPMS?

What is Cognitive Behavioral Therapy (CBT)?

How Does the Mediterranean Diet Impact Brain Health?

What is the Role of Genetics in Neurological Disorders?

How Do Genetic Mutations Influence Neurological Pathways?

How are Oligoclonal Bands Detected?

How is VR Used in Neurocare?

Can the Mediterranean Diet Reduce the Risk of Neurodegenerative Diseases?

When to Seek Medical Attention?

How important is patient education and support?

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