CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration AE Schaffer, VRC Eggens, AO Caglayan, MS Reuter, E Scott, NG Coufal, ... Cell 157 (3), 651-663, 2014 | 278 | 2014 |
Somatic POLE mutations cause an ultramutated giant cell high-grade glioma subtype with better prognosis EZ Erson-Omay, AO Çağlayan, N Schultz, N Weinhold, SB Omay, ... Neuro-oncology 17 (10), 1356-1364, 2015 | 120 | 2015 |
Mutations in KATNB1 cause complex cerebral malformations by disrupting asymmetrically dividing neural progenitors K Mishra-Gorur, AO Çağlayan, AE Schaffer, C Chabu, O Henegariu, ... Neuron 84 (6), 1226-1239, 2014 | 117 | 2014 |
NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy AO Caglayan, S Comu, JF Baranoski, Y Parman, H Kaymakçalan, ... European journal of medical genetics 58 (1), 39-43, 2015 | 96 | 2015 |
The genetic structure of the Turkish population reveals high levels of variation and admixture ME Kars, AN Başak, OE Onat, K Bilguvar, J Choi, Y Itan, C Çağlar, ... Proceedings of the National Academy of Sciences 118 (36), e2026076118, 2021 | 57 | 2021 |
Brain malformations associated with Knobloch syndrome—review of literature, expanding clinical spectrum, and identification of novel mutations AO Caglayan, JF Baranoski, F Aktar, W Han, B Tuysuz, A Guzel, B Guclu, ... Pediatric neurology 51 (6), 806-813. e8, 2014 | 50 | 2014 |
Functional analysis reveals differential effects of glutamate and MCH neuropeptide in MCH neurons M Schneeberger, K Tan, AR Nectow, L Parolari, C Caglar, E Azevedo, ... Molecular metabolism 13, 83-89, 2018 | 38 | 2018 |
Biallelic mutations in TMTC3, encoding a transmembrane and TPR-containing protein, lead to cobblestone lissencephaly J Jerber, MS Zaki, JY Al-Aama, RO Rosti, T Ben-Omran, E Dikoglu, ... The American Journal of Human Genetics 99 (5), 1181-1189, 2016 | 36 | 2016 |
Longitudinal analysis of treatment-induced genomic alterations in gliomas EZ Erson-Omay, O Henegariu, SB Omay, AS Harmancı, MW Youngblood, ... Genome medicine 9, 1-10, 2017 | 25 | 2017 |
Restriction of food intake by PPP1R17-expressing neurons in the DMH C Caglar, J Friedman Proceedings of the National Academy of Sciences 118 (13), e2100194118, 2021 | 7 | 2021 |
Longitudinal analysis of treatment-induced genomic alterations in gliomas. Genome Med 9 (1): 12 EZ Erson-Omay, O Henegariu, SB Omay, AS Harmancı, MW Youngblood, ... | 6 | 2017 |
A new patient with Andermann syndrome: an underdiagnosed clinical genetics entity? A Degerliyurt, G Akgumus, C Caglar, K Bilguvar, AO Caglayan Genetic counseling 24 (3), 283, 2013 | 6 | 2013 |