Product
Help
Pricing
About
Jobs
Log in
Get started
Author
Add to collection
Caner Çağlar
Observed names:
C Caglar,
Caglar, Caner,
Caner Caglar,
Çağlar, Caner
Institutions:
Bezmiâlem Vakıf Üniversitesi,
Yale University
Observed institutions:
Memorial Sloan Kettering Cancer Center,
Howard Hughes Medical Institute,
Selçuk University,
Bezmiâlem Vakıf Üniversitesi,
Acıbadem University,
Yale University,
Rockefeller University
show all 7
ORCID:
0000-0002-5857-757X
Observed ORCID:
0000-0002-5857-757X
OpenAlex ID:
A5030171078
CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration
2014
·
Ashleigh E. Schaffer
, Veerle R.C. Eggens
, et al.
·
Cell
·
294
PDF
Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors
2014
·
Ketu Mishra-Gorur
, Ahmet Okay Çağlayan
, et al.
·
Neuron
·
121
PDF
Somatic POLE mutations cause an ultramutated giant cell high-grade glioma subtype with better prognosis
2015
·
E. Zeynep Erson-Omay
, Ahmet Okay Çağlayan
, et al.
·
Neuro-Oncology
·
120
The genetic structure of the Turkish population reveals high levels of variation and admixture
2021
·
M. Ece Kars
, A. Nazlı Başak
, et al.
·
Proceedings of the National Academy of Sciences
·
117
NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy
2014
·
Ahmet Okay Caglayan
, Sinan Comu
, et al.
·
European Journal of Medical Genetics
·
86
Brain Malformations Associated With Knobloch Syndrome—Review of Literature, Expanding Clinical Spectrum, and Identification of Novel Mutations
2014
·
Ahmet Okay Caglayan
, Jacob F. Baranoski
, et al.
·
Pediatric Neurology
·
73
Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly
2016
·
Julie Jerber
, Maha S. Zaki
, et al.
·
The American Journal of Human Genetics
·
47
PDF
Functional analysis reveals differential effects of glutamate and MCH neuropeptide in MCH neurons
2018
·
Marc Schneeberger
, Keith Tan
, et al.
·
Molecular Metabolism
·
46
PDF
Longitudinal analysis of treatment-induced genomic alterations in gliomas
2017
·
E. Zeynep Erson-Omay
, Octavian Henegariu
, et al.
·
Genome Medicine
·
26
PDF
Dysregulation of mTOR signalling is a converging mechanism in lissencephaly
2025
·
Ce Zhang
, Dan Liang
, et al.
·
Nature
·
22
Restriction of food intake by PPP1R17-expressing neurons in the DMH
2021
·
Caner Caglar
, Jeffrey Friedman
·
Proceedings of the National Academy of Sciences
·
13
Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors
2015
·
Ketu Mishra-Gorur
, Ahmet Okay Çağlayan
, et al.
·
Neuron
·
10
PDF
A new patient with Andermann syndrome: an underdiagnosed clinical genetics entity?
2013
·
A Degerliyurt
, G Akgumus
, et al.
·
PubMed
·
4
The genetic structure of the Turkish population
2021
·
Kars, Meltem Ece
, A. Nazli Basak
, et al.
·
Zenodo (CERN European Organization for Nuclear Research)
·
1
The genetic structure of the Turkish population reveals high levels of variation and admixture
2021
·
Kars, Meltem Ece
, Basak, Ayse Nazli
, et al.
·
Figshare
Karma Eğitim Sisteminin Öğrenci Görüşleri İle Değerlendirilmesi (Sakarya Üniversitesi Örneği)
2010
·
Sakarya Üniversitesi, Sosyal Bilimler Enstitüsü, Bilgisayar ve Öğretim Teknolojileri Eğitimi Anabilim Dalı, Bilgisayar ve Öğretim Teknolojileri Eğitimi Bilim Dalı
, Çağlar, Caner
, et al.
·
Sakarya Üniversitesi Kurumsal Açık Akademik Arşivi
Show more works
View as search
Works count:
24
Citation count:
980
H-index:
11
I10-index:
12
Year
Topic
Type