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Genome-wide study of a Neolithic Wartberg grave community reveals distinct HLA variation and hunter-gatherer ancestry.
Immel A, Pierini F, Rinne C, Meadows J, Barquera R, Szolek A, Susat J, Böhme L, Dose J, Bonczarowska J, Drummer C, Fuchs K, Ellinghaus D, Kässens JC, Furholt M, Kohlbacher O, Schade-Lindig S, Franke A, Schreiber S, Krause J, Müller J, Lenz TL, Nebel A, Krause-Kyora B. Immel A, et al. Among authors: franke a. Commun Biol. 2021 Jan 25;4(1):113. doi: 10.1038/s42003-020-01627-4. Commun Biol. 2021. PMID: 33495542 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: franke a. 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.
Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2.
Franke A, Fischer A, Nothnagel M, Becker C, Grabe N, Till A, Lu T, Müller-Quernheim J, Wittig M, Hermann A, Balschun T, Hofmann S, Niemiec R, Schulz S, Hampe J, Nikolaus S, Nürnberg P, Krawczak M, Schürmann M, Rosenstiel P, Nebel A, Schreiber S. Franke A, et al. Gastroenterology. 2008 Oct;135(4):1207-15. doi: 10.1053/j.gastro.2008.07.017. Epub 2008 Jul 18. Gastroenterology. 2008. PMID: 18723019
A comprehensive evaluation of SNP genotype imputation.
Nothnagel M, Ellinghaus D, Schreiber S, Krawczak M, Franke A. Nothnagel M, et al. Among authors: franke a. Hum Genet. 2009 Mar;125(2):163-71. doi: 10.1007/s00439-008-0606-5. Epub 2008 Dec 17. Hum Genet. 2009. PMID: 19089453
Current software for genotype imputation.
Ellinghaus D, Schreiber S, Franke A, Nothnagel M. Ellinghaus D, et al. Among authors: franke a. Hum Genomics. 2009 Jul;3(4):371-80. doi: 10.1186/1479-7364-3-4-371. Hum Genomics. 2009. PMID: 19706367 Free PMC article.
1,697 results