Publications J Wirth 2009

Publications Jutta Wirth till 2009 (30 Articles)
  • Kirchhoff M, Rose H, Maahr J, Gerdes T, Bugge M, Tommerup N, Tumer Z, Lespinasse J, Jensen PK, Wirth J, Lundsteen C. High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes. Eur J Hum Genet 2000; 8(9):661-8.


  • Vollmer M, Kremer M, Ruf R, Miot S, Nothwang HG, Wirth J, Otto E, Krapf R, Hildebrandt F. Molecular cloning of the critical region for glomerulopathy with fibronectin deposits (GFND) and evaluation of candidate genes. Genomics 2000; 68(2):127-35.


  • Heller A, Seidel J, Hubler A, Starke H, Beensen V, Senger G, Rocchi M, Wirth J, Chudoba I, Claussen U, Liehr T. Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review. J Med Genet 2000; 37(7):529-32.


  • Scheer MP, van der Maarel S, Kubart S, Schulz A, Wirth J, Schweiger S, Ropers H, Nothwang HG. DXS6673E encodes a predominantly nuclear protein, and its mouse ortholog DXHXS6673E is alternatively spliced in a developmental- and tissue-specific manner. Genomics 2000;63(1):123-32.


  • Stumm M, Koch A, Wieacker PF, Phillip C, Steinbach F, Allhoff EP, Buhtz P, Walter H, Tonnies H, Wirth J. Partial monosomy 2p as the single chromosomal anomaly in a case of renal metanephric adenoma. Cancer Genet Cytogenet 1999; 115(1):82-5.


Subject: Human cancer


  • Stumm M, Koch A, Wieacker PF, Phillip C, Steinbach F, Allhoff EP, Buhtz P, Walter H, Tonnies H, Wirth J. Partial monosomy 2p as the single chromosomal anomaly in a case of renal metanephric adenom. Cancer Genet Cytogenet 1999; 115(1):82-5.


  • Wirth J, Nothwang HG, van der Maarel S, Menzel C, Borck G, Lopez-Pajares I, Brondum-Nielsen K, Tommerup N, Bugge M, Ropers HH, Haaf T. Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes. J Med Genet 1999; 36(4):271-8.


  • Silahtaroglu A, Hol FA, Jensen PK, Erdel M, Duba HC, Geurds MP, Knoers NV, Mariman EC, Tumer Z, Utermann G, Wirth J, Bugge M, Tommerup N. Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome. Eur J Hum Genet 1999; 7(1):68-76.


  • Caubit X, Thangarajah R, Theil T, Wirth J, Nothwang HG, Ruther U, Krauss S. Mouse Dac, a novel nuclear factor with homology to Drosophila dachshund shows a dynamic expression in the neural crest, the eye, the neocortex, and the limb bud.Dev Dyn 1999;214(1):66-80.


Subject: Human genetics


  • Duba HC, Erdel M, Loffler J, Wirth J, Utermann B, Utermann G. Nail patella syndrome in a cytogenetically balanced t(9;17)(q34.1;q25) carrier. Eur J Hum Genet 1998; 6(1):75-9.


  • Silahtaroglu AN, Hacihanefioglu S, Guven GS, Cenani A, Wirth J, Tommerup N, Tumer Z. Not para-, not peri-, but centric inversion of chromosome 12. J Med Genet 1998;35(8):682-4.


  • Nothwang HG, Wirth J, Brandl B, Haaf T, Nielsen KB, Tommerup N, Ropers HH. Identification of positional candidates for neurological disorders on chromsome 13q14–>q22.Cytogenet Cell Genet 1997; 79(3-4):293-7.


  • Kingsley K, Wirth J, van der Maarel S, Freier S, Ropers HH, Haaf T. Complex FISH probes for the subtelomeric regions of all human chromosomes: comparative hybridization of CEPH YACs to chromosomes of the Old World monkey Presbytis cristata and great apes. Cytogenet Cell Genet 1997; 78(1):12-9.


Subject: Sex determination


  • Wagner T, Tommerup N, Wirth J, Leffers H, Zimmer J, Back E, Weissenbach J, Scherer G. A somatic cell hybrid panel for distal 17q: GDIA1 maps to 17q25.3. Cytogenet Cell Genet 1997; 76(3-4):172-5.


  • Wirth J, Wagner T, Meyer J, Pfeiffer RA, Tietze HU, Schempp W, Scherer G. Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9. Hum Genet 1996; 97(2):186-93.


  • Meyer J, Wirth J, Held M, Schempp W, Scherer G. SOX20, a new member of the SOX gene family, is located on chromosome 17p13.Cytogenet Cell Genet 1996; 72(2-3):246-9.


  • Wagner T, Wirth J, Meyer J, Zabel B, Held M, Zimmer J, Pasantes J, Bricarelli FD, Keutel J, Hustert E, et al. Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9. Cell 1994; 79(6):1111-20.