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Biosensors & Bioelectronics|February 25, 2014
Design and characterisation of a thin-film electrode array with shared reference/counter electrodes for electrochemical detectionYildiz Uludag, Zehra Olcer, Mahmut Samil SagirogluBioinformatics (Oxford, England)|December 6, 2013
HomSI: a homozygous stretch identifier from next-generation sequencing dataZeliha Görmez, Burcu Bakir-Gungor, Mahmut Samil SagirogluIntractable & Rare Diseases Research|September 28, 2016
Coffin-Siris syndrome with café-au-lait spots, obesity and hyperinsulinism caused by a mutation in the ARID1B geneFatma Mujgan Sonmez, Eyyup Uctepe, Mehmet Gunduz, et al.Gene|April 4, 2015
Whole-exome sequencing revealed two novel mutations in Usher syndromeAsuman Koparir, Omer Faruk Karatas, Ali Timucin Atayoglu, et al.BMC Genetics|October 1, 2013
Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtypeFatih Bayrakli, Bulent Guclu, Cengiz Yakicier, et al.Journal of Human Genetics|October 2, 2015
Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 geneFatih Bayrakli, Hatice Gamze Poyrazoglu, Sirin Yuksel, et al.Pageof 1