van Baal S - Search Results

1

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. Kleanthous M, et al. Among authors: van baal s. Hum Mutat. 2006 Jun;27(6):598-9. doi: 10.1002/humu.9422. Hum Mutat. 2006. PMID: 16705699

2

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

Patrinos GP, van Baal S, Petersen MB, Papadakis MN. Patrinos GP, et al. Among authors: van baal s. Hum Mutat. 2005 Apr;25(4):327-33. doi: 10.1002/humu.20157. Hum Mutat. 2005. PMID: 15776445

3

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. Zlotogora J, et al. Among authors: van baal s. Hum Mutat. 2007 Oct;28(10):944-9. doi: 10.1002/humu.20551. Hum Mutat. 2007. PMID: 17492749

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. Zaimidou S, et al. Among authors: van baal s. Hum Mutat. 2009 Mar;30(3):308-13. doi: 10.1002/humu.20857. Hum Mutat. 2009. PMID: 19021233

5

The Israeli National Genetic Database.

Zlotogora J, van Baal S, Patrinos GP. Zlotogora J, et al. Among authors: van baal s. Isr Med Assoc J. 2009 Jun;11(6):373-5. Isr Med Assoc J. 2009. PMID: 19697591 Free article. Review.

6

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

van Baal S, Zlotogora J, Lagoumintzis G, Gkantouna V, Tzimas I, Poulas K, Tsakalidis A, Romeo G, Patrinos GP. van Baal S, et al. Hum Genomics. 2010 Jun;4(5):361-8. doi: 10.1186/1479-7364-4-5-361. Hum Genomics. 2010. PMID: 20650823 Free PMC article.

7

HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update.

Giardine B, van Baal S, Kaimakis P, Riemer C, Miller W, Samara M, Kollia P, Anagnou NP, Chui DH, Wajcman H, Hardison RC, Patrinos GP. Giardine B, et al. Among authors: van baal s. Hum Mutat. 2007 Feb;28(2):206. doi: 10.1002/humu.9479. Hum Mutat. 2007. PMID: 17221864

8

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 Jr, Scriver CR, Patrinos GP. van Baal S, et al. Nucleic Acids Res. 2007 Jan;35(Database issue):D690-5. doi: 10.1093/nar/gkl934. Epub 2006 Nov 28. Nucleic Acids Res. 2007. PMID: 17135191 Free PMC article.

9

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

Georgitsi M, Viennas E, Antoniou DI, Gkantouna V, van Baal S, Petricoin EF 3rd, Poulas K, Tzimas G, Patrinos GP. Georgitsi M, et al. Among authors: van baal s. Nucleic Acids Res. 2011 Jan;39(Database issue):D926-32. doi: 10.1093/nar/gkq1236. Epub 2010 Nov 27. Nucleic Acids Res. 2011. PMID: 21113021 Free PMC article.

10

Chromosomal localization of genes encoding CAN/Nup214-interacting proteins--human CRM1 localizes to 2p16, whereas Nup88 localizes to 17p13 and is physically linked to SF2p32.

Fornerod M, van Baal S, Valentine V, Shapiro DN, Grosveld G. Fornerod M, et al. Among authors: van baal s. Genomics. 1997 Jun 15;42(3):538-40. doi: 10.1006/geno.1997.4767. Genomics. 1997. PMID: 9205132 No abstract available.

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