Literature DB >> 15776445

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

George P Patrinos1, Sjozef van Baal, Michael B Petersen, Manoussos N Papadakis.   

Abstract

The exponential discovery rate of new genomic alterations, leading to inherited disorders, as well as the need for comparative studies of different population's mutation frequencies necessitates recording their population-wide spectrum in online mutation databases. We report the construction of the Hellenic National Mutation database (http://www.goldenhelix.org/hellenic), a prototype database derived from a multicenter academic initiative, aiming to provide high quality and up-to-date information on the underlying genetic heterogeneity of inherited disorders found in the Hellenic population. Database records include informative summaries of the various genetic disorders studied in the Hellenic population, focused in particular on their incidence in Greece, a comprehensive reference list, and a well-structured query interface, which provides easy access to the list of the different mutations responsible for the inherited disorders in the Hellenic population. Also, extensive links to the respective Online Mendelian Inheritance in Man (OMIM) entries and, when available, to the locus-specific databases are provided, so that the user can retrieve the maximum amount of information from a single website. Furthermore, the Hellenic National Mutation database design allows easy data entry and curation. Creation of the Hellenic National Mutation database will significantly facilitate molecular diagnosis of inherited disorders in Greece and will motivate further investigation of yet unknown genetic diseases in the Hellenic population.

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Year:  2005        PMID: 15776445     DOI: 10.1002/humu.20157

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  12 in total

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

Authors:  Konstantinos Mitropoulos; Federico Innocenti; Ron H van Schaik; Alexander Lezhava; Giannis Tzimas; Panagoula Kollia; Milan Macek; Paolo Fortina; George P Patrinos
Journal:  Pharmacogenomics       Date:  2012-03       Impact factor: 2.533

2.  Roadmap for Establishing Large-Scale Genomic Medicine Initiatives in Low- and Middle-Income Countries.

Authors:  George P Patrinos; Emmanouil Pasparakis; Erasmia Koiliari; Alexandre C Pereira; Tábita Hünemeier; Lygia V Pereira; Christina Mitropoulou
Journal:  Am J Hum Genet       Date:  2020-10-01       Impact factor: 11.025

3.  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

4.  Indian genetic disease database.

Authors:  Sanchari Pradhan; Mainak Sengupta; Anirban Dutta; Kausik Bhattacharyya; Sumit K Bag; Chitra Dutta; Kunal Ray
Journal:  Nucleic Acids Res       Date:  2010-10-30       Impact factor: 16.971

5.  FINDbase: a worldwide database for genetic variation allele frequencies updated.

Authors:  Marianthi Georgitsi; Emmanouil Viennas; Dimitris I Antoniou; Vassiliki Gkantouna; Sjozef van Baal; Emanuel F Petricoin; Konstantinos Poulas; Giannis Tzimas; George P Patrinos
Journal:  Nucleic Acids Res       Date:  2010-11-27       Impact factor: 16.971

6.  Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection.

Authors:  George P Patrinos; Jumana Al Aama; Aida Al Aqeel; Fahd Al-Mulla; Joseph Borg; Andrew Devereux; Alex E Felice; Finlay Macrae; Makia J Marafie; Michael B Petersen; Ming Qi; Rajkumar S Ramesar; Joel Zlotogora; Richard G H Cotton
Journal:  Hum Mutat       Date:  2011-01       Impact factor: 4.878

7.  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

8.  The Spectrum of Beta-Thalassemia Mutations in Syrian Refugees and Turkish Citizens.

Authors:  Ahmet Kursad Gunes; Hilmi Erdem Gozden
Journal:  Cureus       Date:  2021-06-04

9.  Comparative effects of three iron chelation therapies on the quality of life of greek patients with homozygous transfusion-dependent Beta-thalassemia.

Authors:  Vasilis Goulas; Alexandra Kourakli-Symeonidis; Charalambos Camoutsis
Journal:  ISRN Hematol       Date:  2012-12-17

10.  The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G>T) in the HBG2 gene promoter.

Authors:  Christos Chassanidis; Angelos Kalamaras; Marios Phylactides; Farzin Pourfarzad; Sophia Likousi; Vassilis Maroulis; Manoussos N Papadakis; Nikolaos K Vamvakopoulos; Vassiliki Aleporou-Marinou; George P Patrinos; Panagoula Kollia
Journal:  Ann Hematol       Date:  2008-12-03       Impact factor: 3.673

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