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Investigation of the role of TCF4 rare sequence variants in schizophrenia.
Basmanav FB, Forstner AJ, Fier H, Herms S, Meier S, Degenhardt F, Hoffmann P, Barth S, Fricker N, Strohmaier J, Witt SH, Ludwig M, Schmael C, Moebus S, Maier W, Mössner R, Rujescu D, Rietschel M, Lange C, Nöthen MM, Cichon S. Basmanav FB, et al. Among authors: fricker n. Am J Med Genet B Neuropsychiatr Genet. 2015 Jul;168B(5):354-62. doi: 10.1002/ajmg.b.32318. Epub 2015 May 22. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 26010163
Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate.
Nasser E, Mangold E, Tradowsky DC, Fier H, Becker J, Boehmer AC, Herberz R, Fricker N, Barth S, Wahle P, Nowak S, Reutter H, Reich RH, Lauster C, Braumann B, Kreusch T, Hemprich A, Pötzsch B, Hoffmann P, Kramer FJ, Knapp M, Lange C, Nöthen MM, Ludwig KU. Nasser E, et al. Among authors: fricker n. Birth Defects Res A Clin Mol Teratol. 2012 Nov;94(11):925-33. doi: 10.1002/bdra.23078. Epub 2012 Oct 18. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 23081944
Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology.
Heilmann S, Kiefer AK, Fricker N, Drichel D, Hillmer AM, Herold C, Tung JY, Eriksson N, Redler S, Betz RC, Li R, Kárason A, Nyholt DR, Song K, Vermeulen SH, Kanoni S, Dedoussis G, Martin NG, Kiemeney LA, Mooser V, Stefansson K, Richards JB, Becker T, Brockschmidt FF, Hinds DA, Nöthen MM. Heilmann S, et al. Among authors: fricker n. J Invest Dermatol. 2013 Jun;133(6):1489-96. doi: 10.1038/jid.2013.43. Epub 2013 Jan 28. J Invest Dermatol. 2013. PMID: 23358095 Free article.
Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway.
Al Chawa T, Ludwig KU, Fier H, Pötzsch B, Reich RH, Schmidt G, Braumann B, Daratsianos N, Böhmer AC, Schuencke H, Alblas M, Fricker N, Hoffmann P, Knapp M, Lange C, Nöthen MM, Mangold E. Al Chawa T, et al. Among authors: fricker n. Birth Defects Res A Clin Mol Teratol. 2014 Jun;100(6):493-8. doi: 10.1002/bdra.23244. Epub 2014 Apr 7. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 24706492
Characterizing the genetic basis of innate immune response in TLR4-activated human monocytes.
Kim S, Becker J, Bechheim M, Kaiser V, Noursadeghi M, Fricker N, Beier E, Klaschik S, Boor P, Hess T, Hofmann A, Holdenrieder S, Wendland JR, Fröhlich H, Hartmann G, Nöthen MM, Müller-Myhsok B, Pütz B, Hornung V, Schumacher J. Kim S, et al. Among authors: fricker n. Nat Commun. 2014 Oct 20;5:5236. doi: 10.1038/ncomms6236. Nat Commun. 2014. PMID: 25327457 Free article.
Genome-wide transcriptome induced by nickel in human monocytes.
Gölz L, Buerfent BC, Hofmann A, Rühl H, Fricker N, Stamminger W, Oldenburg J, Deschner J, Hoerauf A, Nöthen MM, Schumacher J, Hübner MP, Jäger A. Gölz L, et al. Among authors: fricker n. Acta Biomater. 2016 Oct 1;43:369-382. doi: 10.1016/j.actbio.2016.07.047. Epub 2016 Jul 28. Acta Biomater. 2016. PMID: 27477848
Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus.
Schulz H, Ruppert AK, Herms S, Wolf C, Mirza-Schreiber N, Stegle O, Czamara D, Forstner AJ, Sivalingam S, Schoch S, Moebus S, Pütz B, Hillmer A, Fricker N, Vatter H, Müller-Myhsok B, Nöthen MM, Becker AJ, Hoffmann P, Sander T, Cichon S. Schulz H, et al. Among authors: fricker n. Nat Commun. 2017 Nov 15;8(1):1511. doi: 10.1038/s41467-017-01818-4. Nat Commun. 2017. PMID: 29142228 Free PMC article.
Nonsyndromic cleft palate: An association study at GWAS candidate loci in a multiethnic sample.
Ishorst N, Francheschelli P, Böhmer AC, Khan MFJ, Heilmann-Heimbach S, Fricker N, Little J, Steegers-Theunissen RPM, Peterlin B, Nowak S, Martini M, Kruse T, Dunsche A, Kreusch T, Gölz L, Aldhorae K, Halboub E, Reutter H, Mossey P, Nöthen MM, Rubini M, Ludwig KU, Knapp M, Mangold E. Ishorst N, et al. Among authors: fricker n. Birth Defects Res. 2018 Jun 1;110(10):871-882. doi: 10.1002/bdr2.1213. Epub 2018 Mar 2. Birth Defects Res. 2018. PMID: 29498243
Insights into Male Androgenetic Alopecia: Differential Gene Expression Profiling of Plucked Hair Follicles and Integration with Genetic Data.
Hochfeld LM, Keller A, Anhalt T, Fricker N; Meta-analysis for Androgenetic Alopecia Novel determinants (MAAN) Consortium; Nöthen MM, Heilmann-Heimbach S. Hochfeld LM, et al. Among authors: fricker n. J Invest Dermatol. 2019 Jan;139(1):235-238. doi: 10.1016/j.jid.2018.06.182. Epub 2018 Jul 21. J Invest Dermatol. 2019. PMID: 30009830 Free article. No abstract available.
22 results