Author Kaulfuß, Silke

• 2013 | Journal Article | 
  ​ ​Blockade of the PDGFR family together with SRC leads to diminished proliferation of colorectal cancer cells​
  Kaulfuß, S.; Seemann, H.; Kampe, R.; Meyer, J.; Dressel, R.; König, B. & Scharf, J.-G. et al.​ (2013) 
  Oncotarget, 4 7 pp. 1037​-1049​.​ DOI: https://doi.org/10.18632/oncotarget.1085 
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• 2014 | Journal Article | 
  ​ ​Bcl-xL mediates therapeutic resistance of a mesenchymal breast cancer cell subpopulation​
  Keitel, U.; Scheel, A.; Thomale, J.; Halpape, R.; Kaulfuß, S.; Scheel, C. & Dobbelstein, M. ​ (2014) 
  Oncotarget, 5(23) pp. 11778​-11791​.​ DOI: https://doi.org/10.18632/oncotarget.2634 
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• 2015 | Journal Article | 
  ​ ​Leupaxin stimulates adhesion and migration of prostate cancer cells through modulation of the phosphorylation status of the actin-binding protein caldesmon.​
  Dierks, S.; von Hardenberg, S.; Schmidt, T.; Bremmer, F.; Burfeind, P. & Kaulfuß, S.​ (2015) 
  Oncotarget, 6(15) pp. 13591​-13606​.​ DOI: https://doi.org/10.18632/oncotarget.3792 
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• 2018 | Journal Article | 
  ​ ​PIK3CA mutations are specifically localized to lymphatic endothelial cells of lymphatic malformations​
  Blesinger, H.; Kaulfuß, S.; Aung, T.; Schwoch, S.; Prantl, L.; Rößler, J. & Wilting, J. et al.​ (2018) 
  PLOS ONE, 13(7) art. e0200343​.​ DOI: https://doi.org/10.1371/journal.pone.0200343 
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• 2019 | Journal Article | 
  ​ ​Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification​
  Parsons, M. T.; Tudini, E.; Li, H.; Hahnen, E.; Wappenschmidt, B.; Feliubadaló, L. & Aalfs, C. M. et al.​ (2019) 
  Human Mutation, 40(9) pp. 1557​-1578​.​ DOI: https://doi.org/10.1002/humu.23818 
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• 2019 | Journal Article | 
  ​ ​Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer​
  Weber-Lassalle, N.; Borde, J.; Weber-Lassalle, K.; Horváth, J.; Niederacher, D.; Arnold, N. & Kaulfuß, S. et al.​ (2019) 
  Breast Cancer Research, 21(1) art. 55​.​ DOI: https://doi.org/10.1186/s13058-019-1137-9 
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• 2021 | Journal Article | Research Paper | 
  ​ ​Familial cleft tongue caused by a unique translation initiation codon variant in TP63​
  Schmidt, J.; Schreiber, G.; Altmüller, J.; Thiele, H.; Nürnberg, P.; Li, Y. & Kaulfuß, S. et al.​ (2021) 
  European Journal of Human Genetics, 30(2) pp. 211​-218​.​ DOI: https://doi.org/10.1038/s41431-021-00967-x 
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• 2022 | Journal Article | Research Paper | 
  ​ ​Phenotypic spectrum of BLM‐ and RMI1‐related Bloom syndrome​
  Gönenc, I. I.; Elcioglu, N. H.; Martinez Grijalva, C.; Aras, S.; Großmann, N.; Praulich, I. & Altmüller, J. et al.​ (2022) 
  Clinical Genetics, 101(5-6) pp. 559​-564​.​ DOI: https://doi.org/10.1111/cge.14125 
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• 2023 | Journal Article
  ​ ​Moebius syndrome and gastroschisis—The second case of a rare association​
  Brockmann, K. & Kaulfuß, S.​ (2023) 
  American Journal of Medical Genetics Part A, art. ajmg.a.63411​.​ DOI: https://doi.org/10.1002/ajmg.a.63411 
  ​Details  DOI 

• 2024 | Journal Article
  ​ ​Expansion of the complex genotypic and phenotypic spectrum of FGFR2-associated neurocutaneous syndromes​
  Schmidt, J.; Kaulfuß, S.; Ott, H.; Gaubert, M.; Reintjes, N.; Bremmer, F. & Dreha-Kulaczewski, S. et al.​ (2024) 
  Human Genetics,.​ DOI: https://doi.org/10.1007/s00439-023-02634-1 
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