Schreiber S - Search Results

1

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: schreiber s. Nat Genet. 2005 Apr;37(4):357-64. doi: 10.1038/ng1519. Epub 2005 Feb 27. Nat Genet. 2005. PMID: 15735647

2

Genetic variation in DLG5 is associated with inflammatory bowel disease.

Stoll M, Corneliussen B, Costello CM, Waetzig GH, Mellgard B, Koch WA, Rosenstiel P, Albrecht M, Croucher PJ, Seegert D, Nikolaus S, Hampe J, Lengauer T, Pierrou S, Foelsch UR, Mathew CG, Lagerstrom-Fermer M, Schreiber S. Stoll M, et al. Among authors: schreiber s. Nat Genet. 2004 May;36(5):476-80. doi: 10.1038/ng1345. Epub 2004 Apr 11. Nat Genet. 2004. PMID: 15107852

3

Genetics of Crohn disease, an archetypal inflammatory barrier disease.

Schreiber S, Rosenstiel P, Albrecht M, Hampe J, Krawczak M. Schreiber S, et al. Nat Rev Genet. 2005 May;6(5):376-88. doi: 10.1038/nrg1607. Nat Rev Genet. 2005. PMID: 15861209 Review.

4

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.

Hampe J, Franke A, Rosenstiel P, Till A, Teuber M, Huse K, Albrecht M, Mayr G, De La Vega FM, Briggs J, Günther S, Prescott NJ, Onnie CM, Häsler R, Sipos B, Fölsch UR, Lengauer T, Platzer M, Mathew CG, Krawczak M, Schreiber S. Hampe J, et al. Among authors: schreiber s. Nat Genet. 2007 Feb;39(2):207-11. doi: 10.1038/ng1954. Epub 2006 Dec 31. Nat Genet. 2007. PMID: 17200669

5

Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis.

Hofmann S, Franke A, Fischer A, Jacobs G, Nothnagel M, Gaede KI, Schürmann M, Müller-Quernheim J, Krawczak M, Rosenstiel P, Schreiber S. Hofmann S, et al. Among authors: schreiber s. Nat Genet. 2008 Sep;40(9):1103-6. doi: 10.1038/ng.198. Nat Genet. 2008. PMID: 19165924

6

Mutation detection and physical mapping of the CD11 gene cluster in association with inflammatory bowel disease.

Frenzel H, Hampe J, Huse K, Mascheretti SM, Croucher PP, Lynch NJ, Siebert R, Platzer M, Schreiber S. Frenzel H, et al. Among authors: schreiber s. Immunogenetics. 2002 Feb;53(10-11):835-42. doi: 10.1007/s00251-001-0411-y. Epub 2002 Jan 22. Immunogenetics. 2002. PMID: 11862384

7

Entropy-based SNP selection for genetic association studies.

Hampe J, Schreiber S, Krawczak M. Hampe J, et al. Among authors: schreiber s. Hum Genet. 2003 Dec;114(1):36-43. doi: 10.1007/s00439-003-1017-2. Epub 2003 Sep 18. Hum Genet. 2003. PMID: 14505034

8

Patterns of linkage disequilibrium in the MHC region on human chromosome 6p.

Stenzel A, Lu T, Koch WA, Hampe J, Guenther SM, De La Vega FM, Krawczak M, Schreiber S. Stenzel A, et al. Among authors: schreiber s. Hum Genet. 2004 Mar;114(4):377-85. doi: 10.1007/s00439-003-1075-5. Epub 2004 Jan 22. Hum Genet. 2004. PMID: 14740295

9

Widespread occurrence of alternative splicing at NAGNAG acceptors contributes to proteome plasticity.

Hiller M, Huse K, Szafranski K, Jahn N, Hampe J, Schreiber S, Backofen R, Platzer M. Hiller M, et al. Among authors: schreiber s. Nat Genet. 2004 Dec;36(12):1255-7. doi: 10.1038/ng1469. Epub 2004 Oct 31. Nat Genet. 2004. PMID: 15516930

10

Study of C-C chemokine receptor 2 alleles in sarcoidosis, with emphasis on family-based analysis.

Valentonyte R, Hampe J, Croucher PJ, Müller-Quernheim J, Schwinger E, Schreiber S, Schürmann M. Valentonyte R, et al. Among authors: schreiber s. Am J Respir Crit Care Med. 2005 May 15;171(10):1136-41. doi: 10.1164/rccm.200405-658OC. Epub 2005 Mar 4. Am J Respir Crit Care Med. 2005. PMID: 15750046

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