Ferda Emriye Perçin

Ferda Emriye Perçin

Gazi University - Ankara / Türkiye
Medical and Health Sciences / Medical Genetics
AD Scientific Index ID: 184226
Gazi Üniversitesi
person_outline Ferda Emriye Perçin's MOST POPULAR ARTICLES
1-) Human microphthalmia associated with mutations in the retinal homeobox gene CHX10E Ferda Percin, LA Ploder, JJ Yu, K Arici, D Jonathan Horsford, ...Nature genetics 25 (4), 397-401, 20003162000
2-) Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndromeH van Bokhoven, J Celli, H Kayserili, E van Beusekom, S Balci, W Brussel, ...Nature genetics 25 (4), 423-426, 20003022000
3-) Blood-derived human iPS cells generate optic vesicle–like structures with the capacity to form retinal laminae and develop synapsesMJ Phillips, KA Wallace, SJ Dickerson, MJ Miller, AD Verhoeven, ...Investigative ophthalmology & visual science 53 (4), 2007-2019, 20122262012
4-) LRP4 mutations alter Wnt/β-catenin signaling and cause limb and kidney malformations in Cenani-Lenz syndromeY Li, B Pawlik, N Elcioglu, M Aglan, H Kayserili, G Yigit, F Percin, ...The American Journal of Human Genetics 86 (5), 696-706, 20101882010
5-) Modeling human retinal development with patient-specific induced pluripotent stem cells reveals multiple roles for visual system homeobox 2MJ Phillips, ET Perez, JM Martin, ST Reshel, KA Wallace, EE Capowski, ...Stem cells 32 (6), 1480-1492, 20141402014