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Detection of arthritis-susceptibility loci, including Ncf1, and variable effects of the major histocompatibility complex region depending on genetic background in rats.

Rintisch C, Förster M, Holmdahl R. Rintisch C, et al. Among authors: forster m. Arthritis Rheum. 2009 Feb;60(2):419-27. doi: 10.1002/art.24292. Arthritis Rheum. 2009. PMID: 19180494

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Epitope-specific antibody response is controlled by immunoglobulin V(H) polymorphisms.

Raposo B, Dobritzsch D, Ge C, Ekman D, Xu B, Lindh I, Förster M, Uysal H, Nandakumar KS, Schneider G, Holmdahl R. Raposo B, et al. Among authors: forster m. J Exp Med. 2014 Mar 10;211(3):405-11. doi: 10.1084/jem.20130968. Epub 2014 Feb 17. J Exp Med. 2014. PMID: 24534192 Free PMC article.

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Genetic control of antibody production during collagen-induced arthritis development in heterogeneous stock mice.

Förster M, Raposo B, Ekman D, Klaczkowska D, Popovic M, Nandakumar KS, Lindvall T, Hultqvist M, Teneva I, Johannesson M, Ahlqvist E, Holmdahl R. Förster M, et al. Arthritis Rheum. 2012 Nov;64(11):3594-603. doi: 10.1002/art.34658. Arthritis Rheum. 2012. PMID: 22886420

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High-resolution mapping of a complex disease, a model for rheumatoid arthritis, using heterogeneous stock mice.

Ahlqvist E, Ekman D, Lindvall T, Popovic M, Förster M, Hultqvist M, Klaczkowska D, Teneva I, Johannesson M, Flint J, Valdar W, Nandakumar KS, Holmdahl R. Ahlqvist E, et al. Among authors: forster m. Hum Mol Genet. 2011 Aug 1;20(15):3031-41. doi: 10.1093/hmg/ddr206. Epub 2011 May 12. Hum Mol Genet. 2011. PMID: 21565963

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Development of a high-resolution NGS-based HLA-typing and analysis pipeline.

Wittig M, Anmarkrud JA, Kässens JC, Koch S, Forster M, Ellinghaus E, Hov JR, Sauer S, Schimmler M, Ziemann M, Görg S, Jacob F, Karlsen TH, Franke A. Wittig M, et al. Among authors: forster m. Nucleic Acids Res. 2015 Jun 23;43(11):e70. doi: 10.1093/nar/gkv184. Epub 2015 Mar 9. Nucleic Acids Res. 2015. PMID: 25753671 Free PMC article.

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Vy-PER: eliminating false positive detection of virus integration events in next generation sequencing data.

Forster M, Szymczak S, Ellinghaus D, Hemmrich G, Rühlemann M, Kraemer L, Mucha S, Wienbrandt L, Stanulla M; UFO Sequencing Consortium within I-BFM Study Group, Franke A. Forster M, et al. Sci Rep. 2015 Jul 13;5:11534. doi: 10.1038/srep11534. Sci Rep. 2015. PMID: 26166306 Free PMC article.

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New technologies for DNA analysis--a review of the READNA Project.

McGinn S, Bauer D, Brefort T, Dong L, El-Sagheer A, Elsharawy A, Evans G, Falk-Sörqvist E, Forster M, Fredriksson S, Freeman P, Freitag C, Fritzsche J, Gibson S, Gullberg M, Gut M, Heath S, Heath-Brun I, Heron AJ, Hohlbein J, Ke R, Lancaster O, Le Reste L, Maglia G, Marie R, Mauger F, Mertes F, Mignardi M, Moens L, Oostmeijer J, Out R, Pedersen JN, Persson F, Picaud V, Rotem D, Schracke N, Sengenes J, Stähler PF, Stade B, Stoddart D, Teng X, Veal CD, Zahra N, Bayley H, Beier M, Brown T, Dekker C, Ekström B, Flyvbjerg H, Franke A, Guenther S, Kapanidis AN, Kaye J, Kristensen A, Lehrach H, Mangion J, Sauer S, Schyns E, Tost J, van Helvoort JM, van der Zaag PJ, Tegenfeldt JO, Brookes AJ, Mir K, Nilsson M, Willcocks JP, Gut IG. McGinn S, et al. Among authors: forster m. N Biotechnol. 2016 May 25;33(3):311-30. doi: 10.1016/j.nbt.2015.10.003. Epub 2015 Oct 26. N Biotechnol. 2016. PMID: 26514324 Review.

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Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies.

Ellinghaus D, Zhang H, Zeissig S, Lipinski S, Till A, Jiang T, Stade B, Bromberg Y, Ellinghaus E, Keller A, Rivas MA, Skieceviciene J, Doncheva NT, Liu X, Liu Q, Jiang F, Forster M, Mayr G, Albrecht M, Häsler R, Boehm BO, Goodall J, Berzuini CR, Lee J, Andersen V, Vogel U, Kupcinskas L, Kayser M, Krawczak M, Nikolaus S, Weersma RK, Ponsioen CY, Sans M, Wijmenga C, Strachan DP, McArdle WL, Vermeire S, Rutgeerts P, Sanderson JD, Mathew CG, Vatn MH, Wang J, Nöthen MM, Duerr RH, Büning C, Brand S, Glas J, Winkelmann J, Illig T, Latiano A, Annese V, Halfvarson J, D'Amato M, Daly MJ, Nothnagel M, Karlsen TH, Subramani S, Rosenstiel P, Schreiber S, Parkes M, Franke A. Ellinghaus D, et al. Among authors: forster m. Gastroenterology. 2013 Aug;145(2):339-47. doi: 10.1053/j.gastro.2013.04.040. Epub 2013 Apr 25. Gastroenterology. 2013. PMID: 23624108 Free PMC article.

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Accurate variant detection across non-amplified and whole genome amplified DNA using targeted next generation sequencing.

ElSharawy A, Warner J, Olson J, Forster M, Schilhabel MB, Link DR, Rose-John S, Schreiber S, Rosenstiel P, Brayer J, Franke A. ElSharawy A, et al. Among authors: forster m. BMC Genomics. 2012 Sep 20;13:500. doi: 10.1186/1471-2164-13-500. BMC Genomics. 2012. PMID: 22994565 Free PMC article.

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Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing.

Elsharawy A, Forster M, Schracke N, Keller A, Thomsen I, Petersen BS, Stade B, Stähler P, Schreiber S, Rosenstiel P, Franke A. Elsharawy A, et al. Among authors: forster m. BMC Genomics. 2012 Aug 22;13:417. doi: 10.1186/1471-2164-13-417. BMC Genomics. 2012. PMID: 22913592 Free PMC article.

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