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Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies.

, , , , , , , and . Nucleic Acids Res., 32 (Database-Issue): 537-541 (2004)

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FINDbase: a worldwide database for genetic variation allele frequencies updated., , , , , , , , and . Nucleic Acids Res., 39 (Database-Issue): 926-932 (2011)A 12-gene pharmacogenetic panel to prevent adverse drug reactions: an open-label, multicentre, controlled, cluster-randomised crossover implementation study, , , , , , , , , and 248 other author(s). 401 (10374): 347--356 (2023)Genome-Based Population Clustering: Nuggets of Truth Buried in a Pile of Numbers?, , and . AIAI (2), volume 382 of IFIP Advances in Information and Communication Technology, page 602-611. Springer, (2012)Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies., , , , , , , and . Nucleic Acids Res., 32 (Database-Issue): 537-541 (2004)Information technology meets pharmacogenomics: Design specifications of an integrated personalized pharmacogenomics information system., , and . BHI, page 13-16. IEEE, (2014)Enabling pharmacogenomic services: Informatics and computational discovery aspects., , , , , and . BIBE, page 1-5. IEEE Computer Society, (2015)Development of a universal, flexible and freely available database management system for gene-centered data collection, curation and display of DNA variation., , , , , , , and . BIBE, page 1-6. IEEE, (2008)Updates of the HbVar database of human hemoglobin variants and thalassemia mutations., , , , , , , , , and 3 other author(s). Nucleic Acids Res., 42 (Database-Issue): 1063-1069 (2014)