Related references
Note: Only part of the references are listed.Frequencies of clinically important CYP2C19 and CYP2D6 alleles are graded across Europe
Jelena Petrovic et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2020)
Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies
Emmanouil Viennas et al.
NUCLEIC ACIDS RESEARCH (2017)
ClinVar: public archive of interpretations of clinically relevant variants
Melissa J. Landrum et al.
NUCLEIC ACIDS RESEARCH (2016)
A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics
Clint Mizzi et al.
PLOS ONE (2016)
The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine
Peter D. Stenson et al.
HUMAN GENETICS (2014)
Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies
Petros Papadopoulos et al.
NUCLEIC ACIDS RESEARCH (2014)
Updates of the HbVar database of human hemoglobin variants and thalassemia mutations
Belinda Giardine et al.
NUCLEIC ACIDS RESEARCH (2014)
Microattribution and nanopublication as means to incentivize the placement of human genome variation data into the public domain
George P. Patrinos et al.
HUMAN MUTATION (2012)
Recommendations for Genetic Variation Data Capture in Developing Countries to Ensure a Comprehensive Worldwide Data Collection
George P. Patrinos et al.
HUMAN MUTATION (2011)
LOVD v.2.0: The Next Generation in Gene Variant Databases
Ivo F. A. C. Fokkema et al.
HUMAN MUTATION (2011)
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
Belinda Giardine et al.
NATURE GENETICS (2011)
FINDbase: a worldwide database for genetic variation allele frequencies updated
Marianthi Georgitsi et al.
NUCLEIC ACIDS RESEARCH (2011)
Population-specific documentation of pharmacogenomic markers and their allelic frequencies in FINDbase
Marianthi Geogitsi et al.
PHARMACOGENOMICS (2011)
Locus-Specific Database Domain and Data Content Analysis: Evolution and Content Maturation Toward Clinical Use
Christina Mitropoulou et al.
HUMAN MUTATION (2010)
FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide
Sjozef van Baal et al.
NUCLEIC ACIDS RESEARCH (2007)
National and ethnic mutation databases: recording populations' genography
George P. Patrinos
HUMAN MUTATION (2006)