Georgios Koutsis

Associate Professor of Neurology and Neurogenetics

Ethniko kai Kapodistriako Panepistemio Athenon Iatrike Schole

Greece

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About

Georgios Koutsis is an Associate Professor of Neurology and Neurogenetics at Ethniko kai Kapodistriako Panepistemio Athenon Iatrike Schole, Greece. His research areas include dementia pathology, Friedreich ataxia, neurodevelopmental disorders, and the implications of genetic variations in various neurological conditions. His recent publications reflect a strong focus on the genetic characterization of neurological diseases and health-related quality of life among affected populations.

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Collaborators (21)

Paola Borgia

Istituto Giannina Gaslini

ITALY

Georgios Koutsis

Research Interests

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Articles (22)

Genetic Prοpensity for Different Aspects of Dementia Pathology and Cognitive Decline in a Community Elderly Population

Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder

Longitudinal analysis of anthropometric measures over 5 years in patients with Friedreich ataxia in the EFACTS natural history study.

Cerebral Amyloidosis in Individuals with Subjective Cognitive Decline: From Genetic Predisposition to Actual Cerebrospinal Fluid Measurements

Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome

Alternative splicing expands the clinical spectrum of NDUFS6-related mitochondrial disorders.

The FGF14 GAA repeat expansion in Greek patients with late-onset cerebellar ataxia and an overview of the SCA27B phenotype across populations.

Health-Related Quality of Life in Patients with Friedreich Ataxia Using Mobility Assistive Technologies: Limited Fit of the EQ-5D-3L Mobility Dimension.

Screening for SCA27B, CANVAS and other repeat expansion disorders in Greek patients with late-onset cerebellar ataxia suggests a need to update current diagnostic algorithms.

Implication of Apolipoprotein E gene variants in pediatric-onset multiple sclerosis: Possible association with disease susceptibility and its clinical characteristics, in a Hellenic cohort.

Longitudinal changes of <scp>SARA</scp> scale in Friedreich ataxia: Strong influence of baseline score and age at onset

Pure cerebellar ataxia due to bi‐allelic PRDX3 variants including recurring p.Asp202Asn

Transthyretin (Pro24Ser) variant amyloidosis: A case report of the first patient in Greece.

Screening for the FMR1 premutation in Greek patients with late-onset movement disorders

Mutational screening of Greek patients with axonal Charcot-Marie-Tooth disease using targeted next-generation sequencing: Clinical and molecular spectrum delineation.

Transthyretin Amyloidosis Cardiomyopathy in Greece: Clinical Insights from the National Referral Center.

A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease

A Greek National Cross-Sectional Study on Myotonic Dystrophies

Cholesterol levels in plasma and cerebrospinal fluid in patients with clinically isolated syndrome and relapsing-remitting multiple sclerosis.

Expanding the spectrum of C9ORF72-related neurodegenerative disorders in the Greek population.

High Hereditary Transthyretin-Related Amyloidosis Prevalence in Crete: Genetic Heterogeneity and Distinct Phenotypes.

Prevalence and clinical outcomes of transthyretin amyloidosis: a systematic review and meta-analysis.

Collaborators (21)

Paola Borgia

Cleanthe Spanaki

Mohmad Farooq Shaikh

Mary Yannakoulia

Pietro FERRARA

Gabriela Elena Oprea

Lara Menzies

Pipitsa Valsamaki

Christalena Sofocleous

Leonidas Stefanis

Evangelos Anagnostou

Mariella Valenzise

Alistair Pagnamenta

Mary Kosmidis

German Moris

roberta battini

Vasilios Kimiskidis

Siddharth Banka

Francesco Brancati

Francesc Palau

Jan Traeger-Synodinos

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