Literature DB >> 22379996

Institutional Profile: Golden Helix Institute of Biomedical Research: interdisciplinary research and educational activities in pharmacogenomics and personalized medicine.

Konstantinos Mitropoulos1, Federico Innocenti, Ron H van Schaik, Alexander Lezhava, Giannis Tzimas, Panagoula Kollia, Milan Macek, Paolo Fortina, George P Patrinos.   

Abstract

The Golden Helix Institute of Biomedical Research is an international nonprofit scientific organization with interdisciplinary research and educational activities in the field of genome medicine in Europe, Asia and Latin America. These activities are supervised by an international scientific advisory council, consisting of world leaders in the field of genomics and translational medicine. Research activities include the regional coordination of the Pharmacogenomics for Every Nation Initiative in Europe, in an effort to integrate pharmacogenomics in developing countries, the development of several national/ethnic genetic databases and related web services and the critical assessment of the impact of genetics and genomic medicine on society in various countries. Educational activities also include the organization of the Golden Helix Symposia(®), which are high-profile scientific research symposia in the field of personalized medicine and the Golden Helix Pharmacogenomics Days, an international educational activity focused on pharmacogenomics, as part of its international pharmacogenomics education and outreach efforts.

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Year:  2012        PMID: 22379996      PMCID: PMC3858958          DOI: 10.2217/pgs.12.7

Source DB:  PubMed          Journal:  Pharmacogenomics        ISSN: 1462-2416            Impact factor:   2.533


  18 in total

1.  Region-specific genetic heterogeneity of HBB mutation distribution in South-Western Greece.

Authors:  Adamantia Papachatzopoulou; Alexandra Kourakli; Eleana F Stavrou; Ekaterini Fragou; Apostolos Vantarakis; George P Patrinos; Aglaia Athanassiadou
Journal:  Hemoglobin       Date:  2010       Impact factor: 0.849

2.  Large-scale population genetic analysis for hemoglobinopathies reveals different mutation spectra in central Greece compared to the rest of the country.

Authors:  Maria Samara; Ioanna Chiotoglou; Angelos Kalamaras; Sophia Likousi; Christos Chassanidis; Andromahi Vagena; Christos Vagenas; Eftichios Eftichiadis; Nikolaos Vamvakopoulos; George P Patrinos; Panagoula Kollia
Journal:  Am J Hematol       Date:  2007-07       Impact factor: 10.047

3.  Pharmacogenomics: paving the path to personalized medicine.

Authors:  George P Patrinos; Federico Innocenti
Journal:  Pharmacogenomics       Date:  2010-02       Impact factor: 2.533

4.  Hellenic National Mutation database: a prototype database for mutations leading to inherited disorders in the Hellenic population.

Authors:  George P Patrinos; Sjozef van Baal; Michael B Petersen; Manoussos N Papadakis
Journal:  Hum Mutat       Date:  2005-04       Impact factor: 4.878

5.  The cypriot and Iranian National Mutation Frequency Databases.

Authors:  Marina Kleanthous; Philippos C Patsalis; Anthi Drousiotou; Mehdi Motazacker; Kyproula Christodoulou; Marios Cariolou; Erol Baysal; Kimia Khrizi; Babak Moghimi; Farzin Pourfarzad; Sjozef van Baal; Constantinos Deltas; Hossein Najmabadi; George P Patrinos
Journal:  Hum Mutat       Date:  2006-06       Impact factor: 4.878

6.  Documentation of inherited disorders and mutation frequencies in the different religious communities in Israel in the Israeli National Genetic Database.

Authors:  Joël Zlotogora; Sjozef van Baal; George P Patrinos
Journal:  Hum Mutat       Date:  2007-10       Impact factor: 4.878

7.  ETHNOS : A versatile electronic tool for the development and curation of national genetic databases.

Authors:  Sjozef van Baal; Joël Zlotogora; George Lagoumintzis; Vassiliki Gkantouna; Ioannis Tzimas; Konstantinos Poulas; Athanassios Tsakalidis; Giovanni Romeo; George P Patrinos
Journal:  Hum Genomics       Date:  2010-06       Impact factor: 4.639

8.  FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide.

Authors:  Sjozef van Baal; Polynikis Kaimakis; Manyphong Phommarinh; Daphne Koumbi; Harry Cuppens; Francesca Riccardino; Milan Macek; Charles R Scriver; George P Patrinos
Journal:  Nucleic Acids Res       Date:  2006-11-28       Impact factor: 16.971

9.  Copy number variation and genomic alterations in health and disease.

Authors:  George P Patrinos; Michael B Petersen
Journal:  Genome Med       Date:  2009-02-20       Impact factor: 11.117

10.  Copy number variation goes clinical.

Authors:  Cédric Le Caignec; Richard Redon
Journal:  Genome Biol       Date:  2009-01-23       Impact factor: 13.583

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  2 in total

1.  Pharmacogenomic assessment of Mexican and Peruvian populations.

Authors:  Sharon Marsh; Cristi R King; Derek J Van Booven; Jane Y Revollo; Robert H Gilman; Howard L McLeod
Journal:  Pharmacogenomics       Date:  2015       Impact factor: 2.533

2.  6th Golden Helix Pharmacogenomics Day: pharmacogenomics and individualized therapy.

Authors:  Maja Stojiljkovic; Amira Fazlagic; Lidija Dokmanovic-Krivokapic; Gordana Nikcevic; George P Patrinos; Sonja Pavlovic; Branka Zukic
Journal:  Hum Genomics       Date:  2012-09-25       Impact factor: 4.639

  2 in total

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