Kyproula Christodoulou

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).

Performance evaluation of pipelines for mapping, variant calling and interval padding, for the analysis of NGS germline panels

George M. Spyrou, Maria Zanti, Kyriaki Michailidou, 2021, BMC Bioinformatics.

A Novel GBA2 Gene Missense Mutation in Spastic Ataxia

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

Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2

Aldo Quattrone, Antonio Gambardella, Anthony P. Monaco, 2000, Nature Genetics.

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

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

Fundamental Gating Mechanism of Nicotinic Receptor Channel Revealed by Mutation Causing a Congenital Myasthenic Syndrome

Lefkos T. Middleton, Kinji Ohno, Andrew G. Engel, 2000, The Journal of general physiology.

The Cypriot and Iranian National Mutation Frequency Databases

George P Patrinos, Marina Kleanthous, Kyproula Christodoulou, 2006, Human mutation.