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Gene|July 8, 2015
Two novel UBR1 gene mutations ın a patient with Johanson Blizzard Syndrome: A mild phenotype without mental retardationTahir Atik, Miray Karakoyun, Maja Sukalo, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 11, 2009
The relation of arterial stiffness with intrauterine growth retardationErtürk Levent, Tahir Atik, Sükran Darcan, et al.
JCEM Case Reports|April 11, 2025
A Rare Cause of Acute Pancreatitis: Two Siblings With Werner SyndromeKenan Sakar, Baris Akinci, Ilgin Yildirim Simsir, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 2, 2004
Biliary atresia in Turkish childrenSema Aydoğdu, Funda Ozgenç, Tahir AtIk, et al.
Acta Neurologica Belgica|October 14, 2016
Targeted next generation sequencing: the diagnostic value in early-onset epileptic encephalopathySarenur Gokben, Huseyin Onay, Sanem Yilmaz, et al.
European Journal of Medical Genetics|July 19, 2019
Clinical utility of a targeted next generation sequencing panel in severe and pediatric onset Mendelian diseasesEsra Isik, Huseyin Onay, Tahir Atik, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 2, 2024
Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfectaFerda Evin, Tahir Atik, Huseyin Onay, et al.
Plos One|November 13, 2015
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing LossTahir Atik, Huseyin Onay, Ayca Aykut, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 25, 2020
The utility of whole exome sequencing for identification of the molecular etiology in autosomal recessive developmental and epileptic encephalopathiesEsra Isik, Sanem Yilmaz, Tahir Atik, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|November 27, 2024
Association between the ARMS2 rs10490924 risk genotype and dry-age related macular degeneration patients with and without reticular pseudodrusen in a Turkish population: findings from a study conducted at a tertiary clinicOnur Furundaoturan, Cumali Degirmenci, Filiz Afrashi, et al.
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