You are here

paper published

  • Kazeminasab S, Taşkıran II, Fattahi Z, Bazzazzadegan N, Hosseini M, Rahimi M, Olaad Nabi M, Haddadi M, Çelik A, Ropers HH, Najmabadi H, and K Kahrizi K (2018) CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177(8):691-699. doi: 10.1002/ajmg.b.32648
  • Fattahi Z, Sheikh T, Musante L, Rasheed M, Taşkıran II, Harripaul R, Hu H, Kazeminasab S, Alam MR, Hosseini M, Larti F, Ghaderi Z, Çelik A, Ayub M, Ansar M, Haddadi M, Wienker TF, Ropers HH, Kahrizi K, Vincent JB, and H Najmabadi (2018) Biallelic missense variants in ZBTB11 can cause intellectual disability in human. Human Molecular Genetics 27(18):3177-3188. doi: 10.1093/hmg/ddy220.
  • Bayramlı X, Kocagöz Y, Sakızlı U, and Fuss SH (2017) Patterned Arrangements of Olfactory Receptor Gene Expression in Zebrafish are Established by Radial Migration of Specified Olfactory Sensory Neurons. Scientific Reports, Jul 17;7(1):5572. doi: 10.1038/s41598-017-06041-1.
  • Köstler S, Alaybeyoğlu B, Weichenberger CX, and Çelik A (2015) FlyOde – a platform for community curation and interactive visualization of dynamic gene regulatory networks in Drosophila eye development. F1000Research 4:1484-9.
  • Potier D, Davie K, Hulselmans G, Sanchez MN, Haagen L, Huynh-Thu VA, Koldere D, Çelik A, Geurts P, Christiaens V, and Aerts S (2014) Mapping gene regulatory networks in Drosophila eye development by large-scale transcriptome perturbations and motif inference. Cell Reports 9:1-14.
  • Tsachaki M, Mishra AK, Rister J, Shy D, Ng J, Çelik A, and Sprecher SG (2013) Interplay of Sens and Php13 controls photoreceptor development, differentiation and transformation in Drosophila. PLoS Genetics 9(12):e1004027.
  • Li X, Erclik T, Chen Z, Venkatesh S, Morante J, Çelik A, and Desplan C, (2013) Temporal specification of neuroblasts controls neuronal diversity in the Drosophila medulla. Nature 498(7455):456-62.
  • Stefan H. Fuss, Yan Zhu, and Peter Mombaerts (2013) Odorant receptor gene choice and axonal wiring in mice with deletion mutations in the odorant receptor gene SR1. Mol Cell Neurosci. 2013 May 17. [Epub ahead of print]
  • Theme by Danetsoft and Danang Probo Sayekti inspired by Maksimer