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Zeynep Erson-Omay
Zeynep Erson-Omay
Assistant Professor, Yale University School of Medicine
Verified email at yale.edu - Homepage
Title
Cited by
Cited by
Year
Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO
VE Clark, EZ Erson-Omay, A Serin, J Yin, J Cotney, K Özduman, T Avşar, ...
Science, 2013
8312013
Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
VE Clark, AS Harmancı, H Bai, MW Youngblood, TI Lee, JF Baranoski, ...
Nature genetics 48 (10), 1253-1259, 2016
3112016
Integrated genomic characterization of IDH1-mutant glioma malignant progression
H Bai, AS Harmancı, EZ Erson-Omay, J Li, S Coşkun, M Simon, ...
Nature genetics 48 (1), 59-66, 2016
3032016
Integrated genomic analyses of de novo pathways underlying atypical meningiomas
AS Harmancı, MW Youngblood, VE Clark, S Coşkun, O Henegariu, ...
Nature communications 8 (1), 14433, 2017
195*2017
Correlations between genomic subgroup and clinical features in a cohort of more than 3000 meningiomas
MW Youngblood, D Duran, JD Montejo, C Li, SB Omay, K Özduman, ...
Journal of neurosurgery 133 (5), 1345-1354, 2019
1202019
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
1192015
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
1162014
Associations of meningioma molecular subgroup and tumor recurrence
MW Youngblood, DF Miyagishima, L Jin, T Gupte, C Li, D Duran, ...
Neuro-oncology 23 (5), 783-794, 2021
1092021
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
952015
Biallelic mutations in citron kinase link mitotic cytokinesis to human primary microcephaly
H Li, SL Bielas, MS Zaki, S Ismail, D Farfara, K Um, RO Rosti, EC Scott, ...
The American Journal of Human Genetics 99 (2), 501-510, 2016
802016
PATIKAweb: a Web interface for analyzing biological pathways through advanced querying and visualization
U Dogrusoz, EZ Erson, E Giral, E Demir, O Babur, A Cetintas, R Colak
Bioinformatics 22 (3), 374-375, 2006
752006
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
502014
Paediatric hepatocellular carcinoma due to somatic CTNNB1 and NFE2L2 mutations in the setting of inherited bi-allelic ABCB11 mutations
S Vilarinho*, EZ Erson-Omay*, AS Harmanci, R Morotti, G Carrion-Grant, ...
Journal of hepatology 61 (5), 1178-1183, 2014
482014
Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical behavior in IDH mutant and IDH wild-type diffuse gliomas
CB Akyerli, Ş Yüksel, Ö Can, EZ Erson-Omay, Y Oktay, E Coşgun, ...
Journal of neurosurgery 128 (4), 1102-1114, 2018
312018
IDH-mutant glioma specific association of rs55705857 located at 8q24. 21 involves MYC deregulation
Y Oktay, E Ülgen, Ö Can, CB Akyerli, Ş Yüksel, Y Erdemgil, İM Durası, ...
Scientific reports 6 (1), 27569, 2016
292016
Extent of resection of epidermoid tumors and risk of recurrence: case report and meta-analysis
BM Shear, L Jin, Y Zhang, WB David, EI Fomchenko, EZ Erson-Omay, ...
Journal of Neurosurgery 133 (2), 291-301, 2019
282019
Loss of Protocadherin‐12 Leads to Diencephalic‐Mesencephalic Junction Dysplasia Syndrome
A Guemez‐Gamboa, AO Çağlayan, V Stanley, A Gregor, MS Zaki, ...
Annals of neurology 84 (5), 638-647, 2018
252018
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
252017
PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysms in humans
T Barak, E Ristori, AG Ercan-Sencicek, DF Miyagishima, ...
Nature medicine 27 (12), 2165-2175, 2021
232021
Whole Exome Sequencing of an Exceptional Longevity Cohort
SSM Nygaard HB, Erson-Omay EZ, Wu X, Kent BA, Bernales CQ, Evans DM, Farrer ...
J Gerontol A Biol Sci Med Sci, 2018
21*2018
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