Georgia Karadima

About Georgia Karadima

Georgia Karadima, With an exceptional h-index of 24 and a recent h-index of 11 (since 2020), a distinguished researcher at National and Kapodistrian University of Athens, specializes in the field of Genetics, Neurogenetics, Neurodegenerative diseases, Molecular and Genetic Diagnosis.

His recent articles reflect a diverse array of research interests and contributions to the field:

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

Parkin mRNA Expression Levels in Peripheral Blood Mononuclear Cells in Parkin‐Related Parkinson's Disease

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

Camptocormia as an Unusual Presenting Symptom of Myotonic Dystrophy Type 2: An Overlooked Cause of Axial Myopathy

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

A Greek national cross-sectional study on myotonic dystrophies

Georgia Karadima Information

University

Position

Assistant Professor of Biology &Neurogenetics Medical School

Citations(all)

2066

Citations(since 2020)

671

Cited By

1690

hIndex(all)

24

hIndex(since 2020)

11

i10Index(all)

50

i10Index(since 2020)

12

Email

University Profile Page

Google Scholar

Georgia Karadima Skills & Research Interests

Genetics

Neurogenetics

Neurodegenerative diseases

Molecular and Genetic Diagnosis

Top articles of Georgia Karadima

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

Genetics in Medicine

2024/3/6

Parkin mRNA Expression Levels in Peripheral Blood Mononuclear Cells in Parkin‐Related Parkinson's Disease

Movement Disorders

2024/2/15

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

2024/1/14

Camptocormia as an Unusual Presenting Symptom of Myotonic Dystrophy Type 2: An Overlooked Cause of Axial Myopathy

Journal of Clinical Neuromuscular Disease

2023/3/1

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

Parkinsonism & Related Disorders

2023/2/1

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

Journal of the Peripheral Nervous System

2023/12

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

Hellenic Journal of Nuclear Medicine

2023/5/1

A Greek national cross-sectional study on myotonic dystrophies

International Journal of Molecular Sciences

2022/12/7

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

Journal of the Neurological Sciences

2022/11/15

Structural and functional brain changes in X-linked Charcot-Marie-Tooth disease: insights from a multimodal neuroimaging study

Neuroradiology

2022/3/1

HINT1‐related neuropathy in Greek patients with Charcot‐Marie‐Tooth disease

Journal of the Peripheral Nervous System

2021/12

Variant transthyretin amyloidosis (ATTRv) polyneuropathy in Greece: a broad overview with a focus on non-endemic unexplored regions of the country

2021/12/1

Genotyping and Plasma/Cerebrospinal Fluid Profiling of a Cohort of Frontotemporal Dementia–Amyotrophic Lateral Sclerosis Patients

Brain Sciences

2021/9/19

Biallelic RFC1 pentanucleotide repeat expansions in Greek patients with late‐onset ataxia

Clinical Genetics

2021/7

Wide range of reduced penetrance alleles in spinal and bulbar muscular atrophy: A model-based approach

2021/6/1

Expanding the Spectrum of AP5Z1‐Related Hereditary Spastic Paraplegia (HSP‐SPG48): A Multicenter Study on a Rare Disease

Movement Disorders

2021/4

Spastic paraplegia preceding PSEN1‐related familial Alzheimer's disease

Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring

2021

Elevated serum α-synuclein levels in huntington’s disease patients

Neuroscience

2020/4/1

Evidence for cognitive deficits in X-linked Charcot-Marie-Tooth disease

Journal of the International Neuropsychological Society

2020/3

See List of Professors in Georgia Karadima University(National and Kapodistrian University of Athens)