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Selection for deafness?
Meyer CG, Amedofu GK, Brandner JM, Pohland D, Timmann C, Horstmann RD. Meyer CG, et al. Among authors: horstmann rd. Nat Med. 2002 Dec;8(12):1332-3. doi: 10.1038/nm1202-1332. Nat Med. 2002. PMID: 12457154 No abstract available.
Low frequency of deafness-associated GJB2 variants in Kenya and Sudan and novel GJB2 variants.
Gasmelseed NM, Schmidt M, Magzoub MM, Macharia M, Elmustafa OM, Ototo B, Winkler E, Ruge G, Horstmann RD, Meyer CG. Gasmelseed NM, et al. Among authors: horstmann rd. Hum Mutat. 2004 Feb;23(2):206-7. doi: 10.1002/humu.9216. Hum Mutat. 2004. PMID: 14722929
Connexin 26 R143W mutation associated with recessive nonsyndromic sensorineural deafness in Africa.
Brobby GW, Müller-Myhsok B, Horstmann RD. Brobby GW, et al. Among authors: horstmann rd. N Engl J Med. 1998 Feb 19;338(8):548-50. doi: 10.1056/NEJM199802193380813. N Engl J Med. 1998. PMID: 9471561 No abstract available.
Novel TMC1 structural and splice variants associated with congenital nonsyndromic deafness in a Sudanese pedigree.
Meyer CG, Gasmelseed NM, Mergani A, Magzoub MM, Muntau B, Thye T, Horstmann RD. Meyer CG, et al. Among authors: horstmann rd. Hum Mutat. 2005 Jan;25(1):100. doi: 10.1002/humu.9302. Hum Mutat. 2005. PMID: 15605408
ALOX5 variants associated with susceptibility to human pulmonary tuberculosis.
Herb F, Thye T, Niemann S, Browne EN, Chinbuah MA, Gyapong J, Osei I, Owusu-Dabo E, Werz O, Rüsch-Gerdes S, Horstmann RD, Meyer CG. Herb F, et al. Among authors: horstmann rd. Hum Mol Genet. 2008 Apr 1;17(7):1052-60. doi: 10.1093/hmg/ddm378. Epub 2008 Jan 3. Hum Mol Genet. 2008. PMID: 18174194
Two novel mutations R653H and E230K in the Mediterranean fever gene associated with disease.
Timmann C, Muntau B, Kuhne K, Gelhaus A, Horstmann RD. Timmann C, et al. Among authors: horstmann rd. Mutat Res. 2001 Aug 8;479(1-2):235-9. doi: 10.1016/s0027-5107(01)00221-4. Mutat Res. 2001. PMID: 11470495
Variability of the CD36 gene in West Africa.
Gelhaus A, Scheding A, Browne E, Burchard GD, Horstmann RD. Gelhaus A, et al. Among authors: horstmann rd. Hum Mutat. 2001 Nov;18(5):444-50. doi: 10.1002/humu.1215. Hum Mutat. 2001. PMID: 11668637
Pattern of connexin 26 (GJB2) mutations causing sensorineural hearing impairment in Ghana.
Hamelmann C, Amedofu GK, Albrecht K, Muntau B, Gelhaus A, Brobby GW, Horstmann RD. Hamelmann C, et al. Among authors: horstmann rd. Hum Mutat. 2001;18(1):84-5. doi: 10.1002/humu.1156. Hum Mutat. 2001. PMID: 11439000
A susceptibility locus for Parkinson's disease maps to chromosome 2p13.
Gasser T, Müller-Myhsok B, Wszolek ZK, Oehlmann R, Calne DB, Bonifati V, Bereznai B, Fabrizio E, Vieregge P, Horstmann RD. Gasser T, et al. Among authors: horstmann rd. Nat Genet. 1998 Mar;18(3):262-5. doi: 10.1038/ng0398-262. Nat Genet. 1998. PMID: 9500549
IL3 variant on chromosomal region 5q31-33 and protection from recurrent malaria attacks.
Meyer CG, Calixto Fernandes MH, Intemann CD, Kreuels B, Kobbe R, Kreuzberg C, Ayim M, Ruether A, Loag W, Ehmen C, Adjei S, Adjei O, Horstmann RD, May J. Meyer CG, et al. Among authors: horstmann rd. Hum Mol Genet. 2011 Mar 15;20(6):1173-81. doi: 10.1093/hmg/ddq562. Epub 2011 Jan 10. Hum Mol Genet. 2011. PMID: 21224257
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