Christina Votsi

发表

Biochemical Characterization of the GBA2 c.1780G>C Missense Mutation in Lymphoblastoid Cells from Patients with Spastic Ataxia

A. Drousiotou, E. Chiricozzi, N. Loberto, 2018, International journal of molecular sciences.

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

A. Drousiotou, K. Christodoulou, G. Tanteles, 2020, Journal of the Neurological Sciences.

A Novel SPG7 Gene Pathogenic Variant in a Cypriot Family With Autosomal Recessive Spastic Ataxia

K. Christodoulou, Y. Christou, E. Zamba-Papanicolaou, 2022, Frontiers in Genetics.

Analyzing Gene Expression Profiles from Ataxia and Spasticity Phenotypes to Reveal Spastic Ataxia Related Pathways

Andrea C. Kakouri, G. Spyrou, K. Christodoulou, 2020, International journal of molecular sciences.

A Novel GBA2 Gene Missense Mutation in Spastic Ataxia

Marios Pantzaris, Christina Votsi, Eleni Zamba-Papanicolaou, 2014, Annals of human genetics.

Transcriptomic characterization of tissues from patients and subsequent pathway analyses reveal biological pathways that are implicated in spastic ataxia

Andrea C. Kakouri, S. Salani, G. Spyrou, 2022, Cell & bioscience.

Investigation of SCA10 in the Cypriot population: Further exclusion of SCA dynamic repeat mutations

K. Kleopa, K. Christodoulou, S. Papacostas, 2012, Journal of the Neurological Sciences.

Molecular diagnosis of autosomal recessive cerebellar ataxia in the whole exome/genome sequencing era

Christina Votsi, Kyproula Christodoulou, K. Christodoulou, 2013 .

A novel c.5308_5311delGAGA mutation in Senataxin in a Cypriot family with an autosomal recessive cerebellar ataxia

L. Middleton, K. Christodoulou, E. Zamba-Papanicolaou, 2008, BMC Medical Genetics.

A Novel CLN6 Variant Associated With Juvenile Neuronal Ceroid Lipofuscinosis in Patients With Absence of Visual Loss as a Presenting Feature

K. Christodoulou, G. Tanteles, S. Papacostas, 2021, Frontiers in Genetics.

Type 2 Diabetes Susceptibility in the Greek-Cypriot Population: Replication of Associations with TCF7L2, FTO, HHEX, SLC30A8 and IGF2BP2 Polymorphisms

A. Antoniades, C. Pattichis, K. Michailidou, 2017, Genes.

Revealing Clusters of Connected Pathways Through Multisource Data Integration in Huntington's Disease and Spastic Ataxia

George M. Spyrou, Margarita Zachariou, George Minadakis, 2019, IEEE Journal of Biomedical and Health Informatics.

The Effect of a Spastic Ataxia Associated GBA2 Mutation on Protein-Protein Interactions and Pathways

George Spyrou, Andrea C. Kakouri, Christina Votsi, 2019, 2019 IEEE 19th International Conference on Bioinformatics and Bioengineering (BIBE).