Yayınlar & Eserler

Yayın Ağı
Makaleler 13
Tümü (13)
SCI-E, SSCI, AHCI (13)
SCI-E, SSCI, AHCI, ESCI (13)
Scopus (13)

1. Dysregulation of mTOR signalling is a converging mechanism in lissencephaly

Zhang C., Liang D., Ercan-Sencicek A. G., Bulut A. S., Cortes J., Cheng I. Q., et al.
NATURE , cilt.638, sa.8049, ss.172-181, 2025 (SCI-Expanded, Scopus) identifier identifier identifier

2. Symposium 1.3. Restriction of Food Intake by Dorsomedial Hypothalamus

ÇAĞLAR C.
ACTA PHYSIOLOGICA , ss.11, 2023 (SCI-Expanded, Scopus) identifier

3. The genetic structure of the Turkish population reveals high levels of variation and admixture

Kars M. E., Basak A. N., ONAT O. E., Bilguvar K., Choi J., Itan Y., et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , sa.36, 2021 (SCI-Expanded, SSCI, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

4. Restriction of food intake by PPP1R17-expressing neurons in the DMH

Caglar C., Friedman J.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , cilt.118, sa.13, 2021 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

5. Functional analysis reveals differential effects of glutamate and MCH neuropeptide in MCH neurons

Schneeberger M., Tan K., Nectow A. R., Parolari L., Caglar C., Azevedo E., et al.
MOLECULAR METABOLISM , cilt.13, ss.83-89, 2018 (SCI-Expanded, Scopus) identifier identifier identifier

6. Longitudinal analysis of treatment-induced genomic alterations in gliomas

Erson-Omay E. Z., Henegariu O., Omay S. B., Harmanci A. S., Youngblood M. W., Mishra-Gorur K., et al.
GENOME MEDICINE , cilt.9, 2017 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

7. Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly

Jerber J., Zaki M. S., Al-Aama J. Y., Rosti R. O., Ben-Omran T., Dikoglu E., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , cilt.99, sa.5, ss.1181-1189, 2016 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

8. Somatic POLE mutations cause an ultramutated giant cell high-grade glioma subtype with better prognosis

Erson-Omay E. Z., Caglayan A. O., Schultz N., Weinhold N., Omay S. B., ÖZDUMAN K., et al.
NEURO-ONCOLOGY , cilt.17, sa.10, ss.1356-1364, 2015 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

9. NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy

Caglayan A. O., Comu S., Baranoski J. F., Parman Y., Kaymakcalan H., Akgumus G. T., et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS , cilt.58, sa.1, ss.39-43, 2015 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

10. Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors

Mishra-Gorur K., Caglayan A. O., Schaffer A. E., Chabu C., Henegariu O., Vonhoff F., et al.
NEURON , cilt.84, sa.6, ss.1226-1239, 2014 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

11. Brain Malformations Associated With Knobloch Syndrome-Review of Literature, Expanding Clinical Spectrum, and Identification of Novel Mutations

Caglayan A. O., Baranoski J. E., Aktar F., Han W., Tuysuz B., Guzel A., et al.
PEDIATRIC NEUROLOGY , cilt.51, sa.6, ss.806-813, 2014 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

12. CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration

Schaffer A. E., Eggens V. R. C., Caglayan A. O., Reuter M. S., Scott E., Coufal N. G., et al.
CELL , cilt.157, sa.3, ss.651-663, 2014 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

13. A NEW PATIENT WITH ANDERMANN SYNDROME: AN UNDERDIAGNOSED CLINICAL GENETICS ENTITY?

Degerliyurt A., Akgumus G., Caglar C., Bilguvar K., Caglayan A. O.
GENETIC COUNSELING , cilt.24, sa.3, ss.283-289, 2013 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier
Kitaplar 2

1. Chapter 00282: Bioinformatic Applications in Neuroscience

Çağlar C.
Encyclopedia of Bioinformatics and Computational Biology, 2nd Edition, Asıf Khan, Editör, Elsevier Science, Oxford/Amsterdam , London, ss.525-550, 2025

2. Clinical Application of Next Generation Sequencing: Complex Diseases

Çağlar C.
NEXT GENERATION SEQUENCING AND ITS CLINICAL APPLICATIONS, Prof. Dr. Ahmet Okay Çağlayan, Editör, Güneş Tıp Kitabevi, Ankara, ss.1, 2022
Metrikler

Yayın

15

Yayın (WoS)

13

Yayın (Scopus)

13

Atıf (WoS)

710

H-İndeks (WoS)

10

Atıf (Scopus)

744

H-İndeks (Scopus)

10

Atıf (Scholar)

1054

H-İndeks (Scholar)

11

Proje

3

Açık Erişim

8
BM Sürdürülebilir Kalkınma Amaçları