alexa Haris Kokotas | Institute of Child Health (Athens)
ISSN: 2157-7412

Journal of Genetic Syndromes & Gene Therapy
Open Access

Like us on:
OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations

700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Haris Kokotas

Haris Kokotas Haris Kokotas
Department of Genetics
Institute of Child Health Athens

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


Global Speakers in the subject

Global Experts in the subject


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
Peer Reviewed Journals
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version