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Sarcoidosis is associated with a truncating splice site mutation in BTNL2.
Valentonyte R, Hampe J, Huse K, Rosenstiel P, Albrecht M, Stenzel A, Nagy M, Gaede KI, Franke A, Haesler R, Koch A, Lengauer T, Seegert D, Reiling N, Ehlers S, Schwinger E, Platzer M, Krawczak M, Müller-Quernheim J, Schürmann M, Schreiber S. Valentonyte R, et al. Among authors: schwinger e. Nat Genet. 2005 Apr;37(4):357-64. doi: 10.1038/ng1519. Epub 2005 Feb 27. Nat Genet. 2005. PMID: 15735647
CFTR gene mutations in sarcoidosis.
Schürmann M, Albrecht M, Schwinger E, Stuhrmann M. Schürmann M, et al. Among authors: schwinger e. Eur J Hum Genet. 2002 Nov;10(11):729-32. doi: 10.1038/sj.ejhg.5200868. Eur J Hum Genet. 2002. PMID: 12404105
CARD15 gene mutations in sarcoidosis.
Schürmann M, Valentonyte R, Hampe J, Müller-Quernheim J, Schwinger E, Schreiber S. Schürmann M, et al. Among authors: schwinger e. Eur Respir J. 2003 Nov;22(5):748-54. doi: 10.1183/09031936.03.00040602. Eur Respir J. 2003. PMID: 14621080 Free article.
Study of Toll-like receptor gene loci in sarcoidosis.
Schürmann M, Kwiatkowski R, Albrecht M, Fischer A, Hampe J, Müller-Quernheim J, Schwinger E, Schreiber S. Schürmann M, et al. Among authors: schwinger e. Clin Exp Immunol. 2008 Jun;152(3):423-31. doi: 10.1111/j.1365-2249.2008.03621.x. Epub 2008 Apr 16. Clin Exp Immunol. 2008. PMID: 18422738 Free PMC article.
HLA-DQB1 and HLA-DPB1 genotypes in familial sarcoidosis.
Schürmann M, Bein G, Kirsten D, Schlaak M, Müller-Quernheim J, Schwinger E. Schürmann M, et al. Among authors: schwinger e. Respir Med. 1998 Apr;92(4):649-52. doi: 10.1016/s0954-6111(98)90512-1. Respir Med. 1998. PMID: 9659531 Free article.
Results from a genome-wide search for predisposing genes in sarcoidosis.
Schürmann M, Reichel P, Müller-Myhsok B, Schlaak M, Müller-Quernheim J, Schwinger E. Schürmann M, et al. Among authors: schwinger e. Am J Respir Crit Care Med. 2001 Sep 1;164(5):840-6. doi: 10.1164/ajrccm.164.5.2007056. Am J Respir Crit Care Med. 2001. PMID: 11549543
Familial sarcoidosis is linked to the major histocompatibility complex region.
Schürmann M, Lympany PA, Reichel P, Müller-Myhsok B, Wurm K, Schlaak M, Müller-Quernheim J, du Bois RM, Schwinger E. Schürmann M, et al. Among authors: schwinger e. Am J Respir Crit Care Med. 2000 Sep;162(3 Pt 1):861-4. doi: 10.1164/ajrccm.162.3.9901099. Am J Respir Crit Care Med. 2000. PMID: 10988096
Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease.
Arolt V, Lencer R, Nolte A, Müller-Myhsok B, Purmann S, Schürmann M, Leutelt J, Pinnow M, Schwinger E. Arolt V, et al. Among authors: schwinger e. Am J Med Genet. 1996 Nov 22;67(6):564-79. doi: 10.1002/(SICI)1096-8628(19961122)67:6<564::AID-AJMG10>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8950416
242 results