Dr. Gökhan Yigit

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unigoe
 

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  • 2015 | Journal Article | Research Paper
    ​ ​Boegershausen, Nina, I-Chun Tsai, Esther Pohl, Pelin Ozlem Simsek Kiper, Filippo Beleggia, E. Ferda Percin, Katharina Keupp et al. "RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome​." ​Journal of Clinical Investigation ​125, no. 9 (2015): ​3585​-3599​. ​https://doi.org/10.1172/JCI80102.
    ​Details  DOI  PMID  PMC  WoS 
  • 2013 | Journal Article
    ​ ​Keupp, Katharina, Yun Li, Ibrahim Vargel, Alexander Hoischen, Rebecca Richardson, Kornelia Neveling, Yasemin Alanay et al. "Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon-like craniosynostosis​." ​Molecular Genetics & Genomic Medicine ​1, no. 4 (2013): ​223​-237​. ​https://doi.org/10.1002/mgg3.28.
    ​Details  DOI 
  • 2011 | Journal Article | Research Paper
    ​ ​Li, Yun, Nina Boegershausen, Yasemin Alanay, Pelin Ozlem Simsek Kiper, Nadine Plume, Katharina Keupp, Esther Pohl et al. "A mutation screen in patients with Kabuki syndrome​." ​Human Genetics ​130, no. 6 (2011): ​715​-724​. ​https://doi.org/10.1007/s00439-011-1004-y.
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  • 2009 | Journal Article
    ​ ​Kayserili, Hülya, Elif Uz, Carien Niessen, Ibrahim Vargel, Yasemin Alanay, Gokhan Tuncbilek, Gökhan Yigit et al. "ALX4 dysfunction disrupts craniofacial and epidermal development​." ​Human Molecular Genetics ​18, no. 22 (2009): ​4357​-4366​. ​https://doi.org/10.1093/hmg/ddp391.
    ​Details  DOI  PMID  PMC  WoS 

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