Wieczorek D - Search Results

1

Altered development of NKT cells, γδ T cells, CD8 T cells and NK cells in a PLZF deficient patient.

Eidson M, Wahlstrom J, Beaulieu AM, Zaidi B, Carsons SE, Crow PK, Yuan J, Wolchok JD, Horsthemke B, Wieczorek D, Sant'Angelo DB. Eidson M, et al. Among authors: wieczorek d. PLoS One. 2011;6(9):e24441. doi: 10.1371/journal.pone.0024441. Epub 2011 Sep 6. PLoS One. 2011. PMID: 21915328 Free PMC article.

2

Classification and visualization based on derived image features: application to genetic syndromes.

Balliu B, Würtz RP, Horsthemke B, Wieczorek D, Böhringer S. Balliu B, et al. Among authors: wieczorek d. PLoS One. 2014 Nov 18;9(11):e109033. doi: 10.1371/journal.pone.0109033. eCollection 2014. PLoS One. 2014. PMID: 25405460 Free PMC article.

3

Histone acetylation dependent allelic expression imbalance of BAPX1 in patients with the oculo-auriculo-vertebral spectrum.

Fischer S, Lüdecke HJ, Wieczorek D, Böhringer S, Gillessen-Kaesbach G, Horsthemke B. Fischer S, et al. Among authors: wieczorek d. Hum Mol Genet. 2006 Feb 15;15(4):581-7. doi: 10.1093/hmg/ddi474. Epub 2006 Jan 11. Hum Mol Genet. 2006. PMID: 16407370

4

Computer-based recognition of dysmorphic faces.

Loos HS, Wieczorek D, Würtz RP, von der Malsburg C, Horsthemke B. Loos HS, et al. Among authors: wieczorek d. Eur J Hum Genet. 2003 Aug;11(8):555-60. doi: 10.1038/sj.ejhg.5200997. Eur J Hum Genet. 2003. PMID: 12891374

5

Automated syndrome detection in a set of clinical facial photographs.

Boehringer S, Guenther M, Sinigerova S, Wurtz RP, Horsthemke B, Wieczorek D. Boehringer S, et al. Among authors: wieczorek d. Am J Med Genet A. 2011 Sep;155A(9):2161-9. doi: 10.1002/ajmg.a.34157. Epub 2011 Aug 3. Am J Med Genet A. 2011. PMID: 21815261

6

Reproduction abnormalities and twin pregnancies in parents of sporadic patients with oculo-auriculo-vertebral spectrum/Goldenhar syndrome.

Wieczorek D, Ludwig M, Boehringer S, Jongbloet PH, Gillessen-Kaesbach G, Horsthemke B. Wieczorek D, et al. Hum Genet. 2007 May;121(3-4):369-76. doi: 10.1007/s00439-007-0336-0. Epub 2007 Feb 13. Hum Genet. 2007. PMID: 17297623

7

Angelman Syndrome-Affected Individual with a Numerically Normal Karyotype and Isodisomic Paternal Uniparental Disomy of Chromosome 15 due to Maternal Robertsonian Translocation (14;15) by Monosomy Rescue.

Bramswig NC, Buiting K, Bechtel N, Horsthemke B, Rostasy K, Wieczorek D. Bramswig NC, et al. Among authors: wieczorek d. Cytogenet Genome Res. 2018;156(1):9-13. doi: 10.1159/000490838. Epub 2018 Jul 18. Cytogenet Genome Res. 2018. PMID: 30016768

8

Impact of geometry and viewing angle on classification accuracy of 2D based analysis of dysmorphic faces.

Vollmar T, Maus B, Wurtz RP, Gillessen-Kaesbach G, Horsthemke B, Wieczorek D, Boehringer S. Vollmar T, et al. Among authors: wieczorek d. Eur J Med Genet. 2008 Jan-Feb;51(1):44-53. doi: 10.1016/j.ejmg.2007.10.002. Epub 2007 Oct 12. Eur J Med Genet. 2008. PMID: 18054308

9

Genome-Wide Analysis of the Nucleosome Landscape in Individuals with Coffin-Siris Syndrome.

Kalmbach A, Schröder C, Klein-Hitpass L, Nordström K, Ulz P, Heitzer E, Speicher MR, Rahmann S, Wieczorek D, Horsthemke B, Bramswig NC. Kalmbach A, et al. Among authors: wieczorek d. Cytogenet Genome Res. 2019;159(1):1-11. doi: 10.1159/000503266. Epub 2019 Oct 26. Cytogenet Genome Res. 2019. PMID: 31658463 Free article.

10

Syndrome identification based on 2D analysis software.

Boehringer S, Vollmar T, Tasse C, Wurtz RP, Gillessen-Kaesbach G, Horsthemke B, Wieczorek D. Boehringer S, et al. Among authors: wieczorek d. Eur J Hum Genet. 2006 Oct;14(10):1082-9. doi: 10.1038/sj.ejhg.5201673. Epub 2006 Jun 14. Eur J Hum Genet. 2006. PMID: 16773127

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