These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
103 related articles for article (PubMed ID: 22659238)
1. Population-ethnic group specific genome variation allele frequency data: a querying and visualization journey. Viennas E; Gkantouna V; Ioannou M; Georgitsi M; Rigou M; Poulas K; Patrinos GP; Tzimas G Genomics; 2012 Aug; 100(2):93-101. PubMed ID: 22659238 [TBL] [Abstract][Full Text] [Related]
2. Population-specific documentation of pharmacogenomic markers and their allelic frequencies in FINDbase. Georgitsi M; Viennas E; Gkantouna V; Christodoulopoulou E; Zagoriti Z; Tafrali C; Ntellos F; Giannakopoulou O; Boulakou A; Vlahopoulou P; Kyriacou E; Tsaknakis J; Tsakalidis A; Poulas K; Tzimas G; Patrinos GP Pharmacogenomics; 2011 Jan; 12(1):49-58. PubMed ID: 21174622 [TBL] [Abstract][Full Text] [Related]
3. FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide. van Baal S; Kaimakis P; Phommarinh M; Koumbi D; Cuppens H; Riccardino F; Macek M; Scriver CR; Patrinos GP Nucleic Acids Res; 2007 Jan; 35(Database issue):D690-5. PubMed ID: 17135191 [TBL] [Abstract][Full Text] [Related]
4. A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software. Zaimidou S; van Baal S; Smith TD; Mitropoulos K; Ljujic M; Radojkovic D; Cotton RG; Patrinos GP Hum Mutat; 2009 Mar; 30(3):308-13. PubMed ID: 19021233 [TBL] [Abstract][Full Text] [Related]
5. National and ethnic mutation databases: recording populations' genography. Patrinos GP Hum Mutat; 2006 Sep; 27(9):879-87. PubMed ID: 16868936 [TBL] [Abstract][Full Text] [Related]
7. Documentation of clinically relevant genomic biomarker allele frequencies in the next-generation FINDbase worldwide database. Kounelis F; Kanterakis A; Kanavos A; Pandi MT; Kordou Z; Manusama O; Vonitsanos G; Katsila T; Tsermpini EE; Lauschke VM; Koromina M; van der Spek PJ; Patrinos GP Hum Mutat; 2020 Jun; 41(6):1112-1122. PubMed ID: 32248568 [TBL] [Abstract][Full Text] [Related]
8. FINDbase: a worldwide database for genetic variation allele frequencies updated. Georgitsi M; Viennas E; Antoniou DI; Gkantouna V; van Baal S; Petricoin EF; Poulas K; Tzimas G; Patrinos GP Nucleic Acids Res; 2011 Jan; 39(Database issue):D926-32. PubMed ID: 21113021 [TBL] [Abstract][Full Text] [Related]
9. Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies. Viennas E; Komianou A; Mizzi C; Stojiljkovic M; Mitropoulou C; Muilu J; Vihinen M; Grypioti P; Papadaki S; Pavlidis C; Zukic B; Katsila T; van der Spek PJ; Pavlovic S; Tzimas G; Patrinos GP Nucleic Acids Res; 2017 Jan; 45(D1):D846-D853. PubMed ID: 27924022 [TBL] [Abstract][Full Text] [Related]
10. Documentation of inherited disorders and mutation frequencies in the different religious communities in Israel in the Israeli National Genetic Database. Zlotogora J; van Baal S; Patrinos GP Hum Mutat; 2007 Oct; 28(10):944-9. PubMed ID: 17492749 [TBL] [Abstract][Full Text] [Related]
11. SNP-VISTA: an interactive SNP visualization tool. Shah N; Teplitsky MV; Minovitsky S; Pennacchio LA; Hugenholtz P; Hamann B; Dubchak IL BMC Bioinformatics; 2005 Dec; 6():292. PubMed ID: 16336665 [TBL] [Abstract][Full Text] [Related]
12. Genomics made easier: an introductory tutorial to genome datamining. Schattner P Genomics; 2009 Mar; 93(3):187-95. PubMed ID: 19041391 [TBL] [Abstract][Full Text] [Related]
13. Browsing isolated population data. Mancosu G; Cosso M; Marras F; Borlino CC; Ledda G; Manias T; Adamo M; Serra D; Melis P; Pirastu M BMC Bioinformatics; 2005 Dec; 6 Suppl 4(Suppl 4):S17. PubMed ID: 16351743 [TBL] [Abstract][Full Text] [Related]
14. The cypriot and Iranian National Mutation Frequency Databases. Kleanthous M; Patsalis PC; Drousiotou A; Motazacker M; Christodoulou K; Cariolou M; Baysal E; Khrizi K; Moghimi B; Pourfarzad F; van Baal S; Deltas C; Najmabadi H; Patrinos GP Hum Mutat; 2006 Jun; 27(6):598-9. PubMed ID: 16705699 [TBL] [Abstract][Full Text] [Related]
17. cPath: open source software for collecting, storing, and querying biological pathways. Cerami EG; Bader GD; Gross BE; Sander C BMC Bioinformatics; 2006 Nov; 7():497. PubMed ID: 17101041 [TBL] [Abstract][Full Text] [Related]
18. Frequency Finder: a multi-source web application for collection of public allele frequencies of SNP markers. Nguyen TH; Liu C; Gershon ES; McMahon FJ Bioinformatics; 2004 Feb; 20(3):439-43. PubMed ID: 14960477 [TBL] [Abstract][Full Text] [Related]
19. Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome. Zhang J; Feuk L; Duggan GE; Khaja R; Scherer SW Cytogenet Genome Res; 2006; 115(3-4):205-14. PubMed ID: 17124402 [TBL] [Abstract][Full Text] [Related]
20. Lightweight genome viewer: portable software for browsing genomics data in its chromosomal context. Faith JJ; Olson AJ; Gardner TS; Sachidanandam R BMC Bioinformatics; 2007 Sep; 8():344. PubMed ID: 17877794 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]