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SNP-based analysis of genetic substructure in the German population.
Steffens M, Lamina C, Illig T, Bettecken T, Vogler R, Entz P, Suk EK, Toliat MR, Klopp N, Caliebe A, König IR, Köhler K, Ludemann J, Diaz Lacava A, Fimmers R, Lichtner P, Ziegler A, Wolf A, Krawczak M, Nūrnberg P, Hampe J, Schreiber S, Meitinger T, Wichmann HE, Roeder K, Wienker TF, Baur MP. Steffens M, et al. Among authors: schreiber s. Hum Hered. 2006;62(1):20-9. doi: 10.1159/000095850. Epub 2006 Sep 21. Hum Hered. 2006. PMID: 17003564
A comprehensive evaluation of SNP genotype imputation.
Nothnagel M, Ellinghaus D, Schreiber S, Krawczak M, Franke A. Nothnagel M, et al. Among authors: schreiber s. Hum Genet. 2009 Mar;125(2):163-71. doi: 10.1007/s00439-008-0606-5. Epub 2008 Dec 17. Hum Genet. 2009. PMID: 19089453
Technology-specific error signatures in the 1000 Genomes Project data.
Nothnagel M, Herrmann A, Wolf A, Schreiber S, Platzer M, Siebert R, Krawczak M, Hampe J. Nothnagel M, et al. Among authors: schreiber s. Hum Genet. 2011 Oct;130(4):505-16. doi: 10.1007/s00439-011-0971-3. Epub 2011 Feb 23. Hum Genet. 2011. PMID: 21344269
Linkage disequilibrium patterns and tagSNP transferability among European populations.
Mueller JC, Lõhmussaar E, Mägi R, Remm M, Bettecken T, Lichtner P, Biskup S, Illig T, Pfeufer A, Luedemann J, Schreiber S, Pramstaller P, Pichler I, Romeo G, Gaddi A, Testa A, Wichmann HE, Metspalu A, Meitinger T. Mueller JC, et al. Among authors: schreiber s. Am J Hum Genet. 2005 Mar;76(3):387-98. doi: 10.1086/427925. Epub 2005 Jan 6. Am J Hum Genet. 2005. PMID: 15637659 Free PMC article.
Efficacy assessment of SNP sets for genome-wide disease association studies.
Wollstein A, Herrmann A, Wittig M, Nothnagel M, Franke A, Nürnberg P, Schreiber S, Krawczak M, Hampe J. Wollstein A, et al. Among authors: schreiber s. Nucleic Acids Res. 2007;35(17):e113. doi: 10.1093/nar/gkm621. Epub 2007 Aug 28. Nucleic Acids Res. 2007. PMID: 17726055 Free PMC article.
2,824 results