ISSN: 2157-7412

Journal of Genetic Syndromes & Gene Therapy
Open Access

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Haris Kokotas
Haris Kokotas

Haris Kokotas
Department of Genetics
Institute of Child Health Athens
Greece

Biography

Haris Kokotas, Molecular Geneticist, received his BSc from the Faculty of Biology, University of Athens, Greece and earned his PhD in Molecular Genetics of Deafness from the Athens University Medical School. He has gained experience on cytogenetic and molecular techniques and he has focused his research on the genetics of the head, including hearing loss and eye diseases. He is currently the principal investigator or co-investigator in several research projects which are being performed at the Department of Genetics, Institute of Child Health, Athens, Greece. He has presented in several national and international conferences and has published numerous articles in national and international peer-reviewed scientific journals. He has also taken the task of the managing editor for a special issue dedicated to the genetics of sensorineural hearing loss. Haris is a member of the Hellenic Association of Medical Geneticists, the European Society of Human Genetics (ESHG), and the American Society of Human Genetics (ASHG).

Research Interest

Molecular genetics of deafness and blindness

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Publications

Molecular Genetics and Gene Therapy Aspects of Phenylalanine Hydroxylase (PAH) Related Hyperphenylalaninemias

Maria Grigoriadou, Kleopatra H Schulpis and Haris Kokotas

Editorial: J Genet Syndr Gene Ther 2014, 5: e125
doi: 10.4172/2157-7412.1000e125
 
Molecular Genetics of Pseudoexfoliation Syndrome (PXFS) and Glaucoma(PXFG)

Christos Kroupis, Dimitrios Chiras, Konstantina Tzika and Haris Kokotas

Editorial: J Genet Syndr Gene Ther 2013, 4:e118
doi: 10.4172/2157-7412.1000e118
 
Human Nondisjunction and Mouse Models in Down Syndrome

Haris Kokotas

Editorial: J Genet Syndr Gene Ther 2012, 3:e108
doi: 10.4172/2157-7412.1000e108
 

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