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Page 1
Reduction of PCR-amplifiable DNA by ethylene oxide treatment of forensic consumables.
Neureuther K, Rohmann E, Hilken M, Sonntag ML, Herdt S, Koennecke T, Jacobs R, Adamski M, Reisbacher S, Alfs K, Strain P, Bastisch I. Neureuther K, et al. Among authors: rohmann e. Forensic Sci Int Genet. 2014 Sep;12:185-91. doi: 10.1016/j.fsigen.2014.06.006. Epub 2014 Jun 17. Forensic Sci Int Genet. 2014. PMID: 25005741
Activating somatic FGFR2 mutations in breast cancer.
Reintjes N, Li Y, Becker A, Rohmann E, Schmutzler R, Wollnik B. Reintjes N, et al. Among authors: rohmann e. PLoS One. 2013;8(3):e60264. doi: 10.1371/journal.pone.0060264. Epub 2013 Mar 20. PLoS One. 2013. PMID: 23527311 Free PMC article.
Mutations in different components of FGF signaling in LADD syndrome.
Rohmann E, Brunner HG, Kayserili H, Uyguner O, Nürnberg G, Lew ED, Dobbie A, Eswarakumar VP, Uzumcu A, Ulubil-Emeroglu M, Leroy JG, Li Y, Becker C, Lehnerdt K, Cremers CW, Yüksel-Apak M, Nürnberg P, Kubisch C, Schlessinger J, van Bokhoven H, Wollnik B. Rohmann E, et al. Nat Genet. 2006 Apr;38(4):414-7. doi: 10.1038/ng1757. Epub 2006 Feb 26. Nat Genet. 2006. PMID: 16501574
Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.
Kalay E, Li Y, Uzumcu A, Uyguner O, Collin RW, Caylan R, Ulubil-Emiroglu M, Kersten FF, Hafiz G, van Wijk E, Kayserili H, Rohmann E, Wagenstaller J, Hoefsloot LH, Strom TM, Nürnberg G, Baserer N, den Hollander AI, Cremers FP, Cremers CW, Becker C, Brunner HG, Nürnberg P, Karaguzel A, Basaran S, Kubisch C, Kremer H, Wollnik B. Kalay E, et al. Among authors: rohmann e. Hum Mutat. 2006 Jul;27(7):633-9. doi: 10.1002/humu.20368. Hum Mutat. 2006. PMID: 16752389
BTNL2 gene variant and sarcoidosis.
Li Y, Wollnik B, Pabst S, Lennarz M, Rohmann E, Gillissen A, Vetter H, Grohé C. Li Y, et al. Among authors: rohmann e. Thorax. 2006 Mar;61(3):273-4. doi: 10.1136/thx.2005.056564. Thorax. 2006. PMID: 16517590 Free PMC article. No abstract available.
65 results