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Copy number variation in patients with cervical artery dissection.
Grond-Ginsbach C, Chen B, Pjontek R, Wiest T, Jiang Y, Burwinkel B, Tchatchou S, Krawczak M, Schreiber S, Brandt T, Kloss M, Arnold ML, Hemminki K, Lichy C, Lyrer PA, Hausser I, Engelter ST. Grond-Ginsbach C, et al. Among authors: schreiber s. Eur J Hum Genet. 2012 Dec;20(12):1295-9. doi: 10.1038/ejhg.2012.82. Epub 2012 May 23. Eur J Hum Genet. 2012. PMID: 22617347 Free PMC article.
Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.
Yang R, Chen B, Pfütze K, Buch S, Steinke V, Holinski-Feder E, Stöcker S, von Schönfels W, Becker T, Schackert HK, Royer-Pokora B, Kloor M, Schmiegel WH, Büttner R, Engel C, Lascorz Puertolas J, Försti A, Kunkel N, Bugert P, Schreiber S, Krawczak M, Schafmayer C, Propping P, Hampe J, Hemminki K, Burwinkel B. Yang R, et al. Among authors: schreiber s. Carcinogenesis. 2014 Feb;35(2):315-23. doi: 10.1093/carcin/bgt344. Epub 2013 Oct 14. Carcinogenesis. 2014. PMID: 24127187
Genetic Imbalance in Patients with Cervical Artery Dissection.
Grond-Ginsbach C, Chen B, Krawczak M, Pjontek R, Ginsbach P, Jiang Y, Abboud S, Arnold ML, Bersano A, Brandt T, Caso V, Debette S, Dichgans M, Geschwendtner A, Giacalone G, Martin JJ, Metso AJ, Metso TM, Grau AJ, Kloss M, Lichy C, Pezzini A, Traenka C, Schreiber S, Thijs V, Touzé E, Del Zotto E, Tatlisumak T, Leys D, Lyrer PA, Engelter ST; CADISP group.. Grond-Ginsbach C, et al. Among authors: schreiber s. Curr Genomics. 2017 Apr;18(2):206-213. doi: 10.2174/1389202917666160805152627. Curr Genomics. 2017. PMID: 28367076 Free PMC article.
Family-Based Benchmarking of Copy Number Variation Detection Software.
Nutsua ME, Fischer A, Nebel A, Hofmann S, Schreiber S, Krawczak M, Nothnagel M. Nutsua ME, et al. Among authors: schreiber s. PLoS One. 2015 Jul 21;10(7):e0133465. doi: 10.1371/journal.pone.0133465. eCollection 2015. PLoS One. 2015. PMID: 26197066 Free PMC article.
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
2,765 results