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C. Kartanou · SciRah

Researcher profile · Semantic Scholar

C. Kartanou

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C. Kartanou — researcher profile on SciRah

h-index: 9
Works: 29
Citations: 223

Most-cited papers

C9ORF72 hexanucleotide repeat expansions are a frequent cause of Huntington disease phenocopies in the Greek population.
G. Koutsis, G. Karadima, C. Kartanou, A. Kladi +1 more
2015Neurobiology of Aging32 citations
Semantic Scholar
The FGF14 GAA repeat expansion in Greek patients with late‐onset cerebellar ataxia and an overview of the SCA27B phenotype across populations
C. Kartanou, A. Mitrousias, D. Pellerin, Zoi Kontogeorgiou +12 more
2024Clinical Genetics27 citations Open access
Semantic Scholar
Spastic paraplegia preceding PSEN1‐related familial Alzheimer's disease
V. Chelban, M. Breza, Maria Szaruga, J. Vandrovcova +20 more
2021Alzheimer's & Dementia25 citations Open access
Semantic Scholar
Biallelic RFC1 pentanucleotide repeat expansions in Greek patients with late‐onset ataxia
Zoi Kontogeorgiou, C. Kartanou, Chrysanthi Tsirligkani, E. Anagnostou +4 more
2021Clinical Genetics17 citations
Semantic Scholar
X linked Charcot-Marie-Tooth disease and multiple sclerosis: emerging evidence for an association
G. Koutsis, M. Breza, G. Velonakis, John S Tzartos +11 more
2018Journal of Neurology Neurosurgery & Psychiatry16 citations
Semantic Scholar
Expanding the Spectrum of AP5Z1‐Related Hereditary Spastic Paraplegia (HSP‐SPG48): A Multicenter Study on a Rare Disease
M. Breza, Jennifer Hirst, V. Chelban, G. Banneau +32 more
2021Movement Disorders14 citations Open access
Semantic Scholar
The different faces of the p. A53T alpha-synuclein mutation: A screening of Greek patients with parkinsonism and/or dementia.
M. Breza, G. Koutsis, G. Karadima, C. Potagas +6 more
2017Neuroscience Letters14 citations
Semantic Scholar
Elevated serum α-synuclein levels in huntington's disease patients.
M. Breza, Evangelia Emmanouilidou, Emmanouela Leandrou, C. Kartanou +6 more
2020Neuroscience12 citations
Semantic Scholar
Mutational screening of the SH3TC2 gene in Greek patients with suspected demyelinating recessive Charcot‐Marie‐Tooth disease reveals a varied and unusual phenotypic spectrum
Zoi Kontogeorgiou, Katerina Nikolaou, C. Kartanou, M. Breza +3 more
2019Journal of the peripheral nervous system10 citations
Semantic Scholar
Genotyping and Plasma/Cerebrospinal Fluid Profiling of a Cohort of Frontotemporal Dementia–Amyotrophic Lateral Sclerosis Patients
Maria Bourbouli, G. Paraskevas, M. Rentzos, L. Mathioudakis +14 more
2021Brain Science8 citations Open access
Semantic Scholar
Screening for spinocerebellar ataxia type 36 (SCA36) in the Greek population.
D. Katsimpouris, C. Kartanou, M. Breza, M. Panas +2 more
2019Journal of Neurological Sciences8 citations
Semantic Scholar
Screening for the FMR1 premutation in Greek patients with late-onset movement disorders.
C. Kartanou, Maria Seferiadi, Stella Pomoni, C. Potagas +6 more
2022Parkinsonism & Related Disorders7 citations
Semantic Scholar
Expanding the spectrum of C9ORF72-related neurodegenerative disorders in the Greek population.
C. Kartanou, Zoi Kontogeorgiou, M. Rentzos, C. Potagas +10 more
2022Journal of Neurological Sciences6 citations
Semantic Scholar
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.
G. Koutsis, C. Kartanou, Zoi Kontogeorgiou, Chrysoula Koniari +16 more
2024Journal of Neurological Sciences5 citations
Semantic Scholar
Variant transthyretin amyloidosis (ATTRv) polyneuropathy in Greece: a broad overview with a focus on non-endemic unexplored regions of the country.
G. Koutsis, E. Kastritis, Zoi Kontogeorgiou, C. Kartanou +19 more
2021Neuromuscular Disorders5 citations
Semantic Scholar
Screening for the C9ORF72 repeat expansion in a greek frontotemporal dementia cohort
C. Kartanou, G. Karadima, G. Koutsis, M. Breza +4 more
2018Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration5 citations
Semantic Scholar
A Greek National Cross-Sectional Study on Myotonic Dystrophies
G. Papadimas, C. Papadopoulos, K. Kekou, C. Kartanou +15 more
2022International Journal of Molecular Sciences4 citations Open access
Semantic Scholar
HINT1‐related neuropathy in Greek patients with Charcot‐Marie‐Tooth disease
Zoi Kontogeorgiou, Charalampos Voudommatis, C. Kartanou, D. Pandis +6 more
2021Journal of the peripheral nervous system4 citations
Semantic Scholar
The novel p.A30G SNCA pathogenic variant in Greek patients with familial and sporadic Parkinson's disease
I. Alefanti, C. Koros, Viktoria Tsami, A. Simitsi +17 more
2025European Journal of Neurology2 citations Open access
Semantic Scholar
Unraveling the genetic landscape of ALS in Greece: identification of known and novel causative variants in a 353-patient cohort
C. Kartanou, Zoi Kontogeorgiou, Theodoros Loupis, D. M. Vrachnos +14 more
2025Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration2 citations
Semantic Scholar
Huntington's Disease‐like Syndrome as a Rare Presentation of CACNA1A ‐Related Disorder
P. Boumis, Constantinos Potagas, C. Koros, Vasileios Constantinides +11 more
2025Movement Disorders Clinical Practice1 citations Open access
Semantic Scholar
Mutational screening of Greek patients with axonal Charcot‐Marie‐Tooth disease using targeted next‐generation sequencing: Clinical and molecular spectrum delineation
Zoi Kontogeorgiou, C. Kartanou, M. Rentzos, P. Kokotis +7 more
2023Journal of the peripheral nervous system1 citations Open access
Semantic Scholar
Correction to: SCA27B: a treatable ataxia—from falls to independence
A. Metridis, M. Makrygianni, A. Naka, L. Florentin +4 more
2026Neurological Sciences0 citations
Semantic Scholar
In Vivo Mapping of Catecholaminergic Loss and Iron Deposition in Huntington's Disease
E. D. de Natale, Heather Wilson, E. Karavasilis, A. Liozidou +8 more
2026Movement Disorders0 citations Open access
Semantic Scholar
Cranial Nerve Involvement With Diplopia as Presenting Feature of CMT1H Caused by Recurring FBLN5 Variant
G. Koutsis, Zoi Kontogeorgiou, Charalampos Tzempetzis, Nikolaos Ragazos +8 more
2026Journal of the peripheral nervous system0 citations Open access
Semantic Scholar
Niemann Pick Type C Presenting as Familial Late‐Onset Richardson Syndrome. A Case Series of Four Siblings
V. Constantinides, C. Koros, Andreas Kyrozis, E. Papathanasiou +16 more
2026Movement Disorders Clinical Practice0 citations Open access
Semantic Scholar
The Genetic Landscape of Hereditary Spastic Paraplegia in Greece
G. Koutsis, V. Chelban, C. Kartanou, Zoi Kontogeorgiou +16 more
2025Clinical Genetics0 citations Open access
Semantic Scholar
Complex phenotype in a C9ORF72‐positive patient with high‐titer anti‐glutamic acid decarboxylase antibodies: neuroimmunology meets neurogenetics
S. Varvaressos, M. Breza, S. Marousi, M. Printzou +7 more
2019European Journal of Neurology0 citations
Semantic Scholar
J4 Huntington’s disease in the greek population: 21 years of clinical assessment and genetic testing at a national reference centre
G. Koutsis, G. Karadima, A. Kladi, M. Breza +2 more
20160 citations
Semantic Scholar

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G. Koutsis×29
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G. Koutsis — researcher profile on SciRah
G. Karadima×29
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M. Panas×18
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M. Panas — researcher profile on SciRah
Zoi Kontogeorgiou×12
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M. Breza — researcher profile on SciRah

L. Stefanis×10

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Chrysoula Koniari×7

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M. Rentzos — researcher profile on SciRah

Nikolaos Ragazos×6

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