Schreiber S - Search Results

1

Identification of probable genotyping errors by consideration of haplotypes.

Becker T, Valentonyte R, Croucher PJ, Strauch K, Schreiber S, Hampe J, Knapp M. Becker T, et al. Among authors: schreiber s. Eur J Hum Genet. 2006 Apr;14(4):450-8. doi: 10.1038/sj.ejhg.5201565. Eur J Hum Genet. 2006. PMID: 16435001

2

Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations.

Croucher PJ, Mascheretti S, Hampe J, Huse K, Frenzel H, Stoll M, Lu T, Nikolaus S, Yang SK, Krawczak M, Kim WH, Schreiber S. Croucher PJ, et al. Among authors: schreiber s. Eur J Hum Genet. 2003 Jan;11(1):6-16. doi: 10.1038/sj.ejhg.5200897. Eur J Hum Genet. 2003. PMID: 12529700 Free article.

3

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

4

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.

Hillmer AM, Hanneken S, Ritzmann S, Becker T, Freudenberg J, Brockschmidt FF, Flaquer A, Freudenberg-Hua Y, Jamra RA, Metzen C, Heyn U, Schweiger N, Betz RC, Blaumeiser B, Hampe J, Schreiber S, Schulze TG, Hennies HC, Schumacher J, Propping P, Ruzicka T, Cichon S, Wienker TF, Kruse R, Nothen MM. Hillmer AM, et al. Among authors: schreiber s. Am J Hum Genet. 2005 Jul;77(1):140-8. doi: 10.1086/431425. Epub 2005 May 18. Am J Hum Genet. 2005. PMID: 15902657 Free PMC article.

5

Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations.

Medici V, Mascheretti S, Croucher PJ, Stoll M, Hampe J, Grebe J, Sturniolo GC, Solberg C, Jahnsen J, Moum B, Schreiber S, Vatn MH. Medici V, et al. Among authors: schreiber s. Eur J Hum Genet. 2006 Apr;14(4):459-68. doi: 10.1038/sj.ejhg.5201576. Eur J Hum Genet. 2006. PMID: 16493449

6

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

7

No association between microsomal triglyceride transfer protein (MTP) haplotype and longevity in humans.

Nebel A, Croucher PJ, Stiegeler R, Nikolaus S, Krawczak M, Schreiber S. Nebel A, et al. Among authors: schreiber s. Proc Natl Acad Sci U S A. 2005 May 31;102(22):7906-9. doi: 10.1073/pnas.0408670102. Epub 2005 May 23. Proc Natl Acad Sci U S A. 2005. PMID: 15911777 Free PMC article.

8

Sirtuin 1 (SIRT1) sequence variation is not associated with exceptional human longevity.

Flachsbart F, Croucher PJ, Nikolaus S, Hampe J, Cordes C, Schreiber S, Nebel A. Flachsbart F, et al. Among authors: schreiber s. Exp Gerontol. 2006 Jan;41(1):98-102. doi: 10.1016/j.exger.2005.09.008. Epub 2005 Oct 27. Exp Gerontol. 2006. PMID: 16257164

9

PopGen: population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships.

Krawczak M, Nikolaus S, von Eberstein H, Croucher PJ, El Mokhtari NE, Schreiber S. Krawczak M, et al. Among authors: schreiber s. Community Genet. 2006;9(1):55-61. doi: 10.1159/000090694. Community Genet. 2006. PMID: 16490960 Review.

10

Technology-specific error signatures in the 1000 Genomes Project data.

Nothnagel M, Herrmann A, Wolf A, Schreiber S, Platzer M, Siebert R, Krawczak M, Hampe J. Nothnagel M, et al. Among authors: schreiber s. Hum Genet. 2011 Oct;130(4):505-16. doi: 10.1007/s00439-011-0971-3. Epub 2011 Feb 23. Hum Genet. 2011. PMID: 21344269

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