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A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.
Meder B, Rühle F, Weis T, Homuth G, Keller A, Franke J, Peil B, Lorenzo Bermejo J, Frese K, Huge A, Witten A, Vogel B, Haas J, Völker U, Ernst F, Teumer A, Ehlermann P, Zugck C, Friedrichs F, Kroemer H, Dörr M, Hoffmann W, Maisch B, Pankuweit S, Ruppert V, Scheffold T, Kühl U, Schultheiss HP, Kreutz R, Ertl G, Angermann C, Charron P, Villard E, Gary F, Isnard R, Komajda M, Lutz M, Meitinger T, Sinner MF, Wichmann HE, Krawczak M, Ivandic B, Weichenhan D, Gelbrich G, El-Mokhtari NE, Schreiber S, Felix SB, Hasenfuß G, Pfeufer A, Hübner N, Kääb S, Arbustini E, Rottbauer W, Frey N, Stoll M, Katus HA. Meder B, et al. Among authors: krawczak m. Eur Heart J. 2014 Apr;35(16):1069-77. doi: 10.1093/eurheartj/eht251. Epub 2013 Jul 12. Eur Heart J. 2014. PMID: 23853074
A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individuals.
Nebel A, Kleindorp R, Caliebe A, Nothnagel M, Blanché H, Junge O, Wittig M, Ellinghaus D, Flachsbart F, Wichmann HE, Meitinger T, Nikolaus S, Franke A, Krawczak M, Lathrop M, Schreiber S. Nebel A, et al. Among authors: krawczak m. Mech Ageing Dev. 2011 Jun-Jul;132(6-7):324-30. doi: 10.1016/j.mad.2011.06.008. Epub 2011 Jun 29. Mech Ageing Dev. 2011. PMID: 21740922 Clinical Trial.
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: krawczak m. 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.
A comprehensive evaluation of SNP genotype imputation.
Nothnagel M, Ellinghaus D, Schreiber S, Krawczak M, Franke A. Nothnagel M, et al. Among authors: krawczak m. Hum Genet. 2009 Mar;125(2):163-71. doi: 10.1007/s00439-008-0606-5. Epub 2008 Dec 17. Hum Genet. 2009. PMID: 19089453
Case-only analysis of gene-gene interactions in inflammatory bowel disease.
Aleknonytė-Resch M, Freitag-Wolf S; International Inflammatory Bowel Disease Genetics Consortium; Schreiber S, Krawczak M, Dempfle A. Aleknonytė-Resch M, et al. Among authors: krawczak m. Scand J Gastroenterol. 2020 Aug;55(8):897-906. doi: 10.1080/00365521.2020.1790646. Epub 2020 Jul 10. Scand J Gastroenterol. 2020. PMID: 32649238
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
Franke A, Hampe J, Rosenstiel P, Becker C, Wagner F, Häsler R, Little RD, Huse K, Ruether A, Balschun T, Wittig M, Elsharawy A, Mayr G, Albrecht M, Prescott NJ, Onnie CM, Fournier H, Keith T, Radelof U, Platzer M, Mathew CG, Stoll M, Krawczak M, Nürnberg P, Schreiber S. Franke A, et al. Among authors: krawczak m. PLoS One. 2007 Aug 8;2(8):e691. doi: 10.1371/journal.pone.0000691. PLoS One. 2007. PMID: 17684544 Free PMC article.
Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.
Lascorz J, Försti A, Chen B, Buch S, Steinke V, Rahner N, Holinski-Feder E, Morak M, Schackert HK, Görgens H, Schulmann K, Goecke T, Kloor M, Engel C, Büttner R, Kunkel N, Weires M, Hoffmeister M, Pardini B, Naccarati A, Vodickova L, Novotny J, Schreiber S, Krawczak M, Bröring CD, Völzke H, Schafmayer C, Vodicka P, Chang-Claude J, Brenner H, Burwinkel B, Propping P, Hampe J, Hemminki K. Lascorz J, et al. Among authors: krawczak m. Carcinogenesis. 2010 Sep;31(9):1612-9. doi: 10.1093/carcin/bgq146. Epub 2010 Jul 7. Carcinogenesis. 2010. PMID: 20610541
376 results