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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
2005 4
2006 3
2007 1
2008 2
2009 4
2010 4
2011 1
2012 8
2013 9
2014 6
2015 6
2016 6
2017 10
2018 6
2019 8
2020 5
2021 8
2022 11
2023 10
2024 3

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110 results

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Page 1
Current practice in diagnostic genetic testing of the epilepsies.
Krey I, Platzer K, Esterhuizen A, Berkovic SF, Helbig I, Hildebrand MS, Lerche H, Lowenstein D, Møller RS, Poduri A, Sadleir L, Sisodiya SM, Weckhuysen S, Wilmshurst JM, Weber Y, Lemke JR, Berkovic SF, Cross JH, Helbig I, Lerche H, Lowenstein D, Mefford HC, Perucca P, Tan NC, Caglayan H, Helbig K, Singh G, Weber Y, Weckhuysen S. Krey I, et al. Among authors: caglayan h. Epileptic Disord. 2022 Oct 1;24(5):765-786. doi: 10.1684/epd.2022.1448. Epileptic Disord. 2022. PMID: 35830287 Free PMC article.
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.
Masnada S, Hedrich UBS, Gardella E, Schubert J, Kaiwar C, Klee EW, Lanpher BC, Gavrilova RH, Synofzik M, Bast T, Gorman K, King MD, Allen NM, Conroy J, Ben Zeev B, Tzadok M, Korff C, Dubois F, Ramsey K, Narayanan V, Serratosa JM, Giraldez BG, Helbig I, Marsh E, O'Brien M, Bergqvist CA, Binelli A, Porter B, Zaeyen E, Horovitz DD, Wolff M, Marjanovic D, Caglayan HS, Arslan M, Pena SDJ, Sisodiya SM, Balestrini S, Syrbe S, Veggiotti P, Lemke JR, Møller RS, Lerche H, Rubboli G. Masnada S, et al. Among authors: caglayan hs. Brain. 2017 Sep 1;140(9):2337-2354. doi: 10.1093/brain/awx184. Brain. 2017. PMID: 29050392 Free article.
Humidity- and Temperature-Tunable Metal-Hydrogel-Metal Reflective Filters.
Chervinskii S, Issah I, Lahikainen M, Rashed AR, Kuntze K, Priimagi A, Caglayan H. Chervinskii S, et al. Among authors: caglayan h. ACS Appl Mater Interfaces. 2021 Oct 27;13(42):50564-50572. doi: 10.1021/acsami.1c15616. Epub 2021 Oct 13. ACS Appl Mater Interfaces. 2021. PMID: 34643385 Free PMC article.
A diagnostic challenge: dilated pupil.
Caglayan HZ, Colpak IA, Kansu T. Caglayan HZ, et al. Curr Opin Ophthalmol. 2013 Nov;24(6):550-7. doi: 10.1097/ICU.0000000000000005. Curr Opin Ophthalmol. 2013. PMID: 24100369 Review.
Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies.
Krüger J, Schubert J, Kegele J, Labalme A, Mao M, Heighway J, Seebohm G, Yan P, Koko M, Aslan-Kara K, Caglayan H, Steinhoff BJ, Weber YG, Keo-Kosal P, Berkovic SF, Hildebrand MS, Petrou S, Krause R, May P, Lesca G, Maljevic S, Lerche H. Krüger J, et al. Among authors: caglayan h. EBioMedicine. 2022 Oct;84:104244. doi: 10.1016/j.ebiom.2022.104244. Epub 2022 Sep 9. EBioMedicine. 2022. PMID: 36088682 Free PMC article.
New Horizons in Near-Zero Refractive Index Photonics and Hyperbolic Metamaterials.
Lobet M, Kinsey N, Liberal I, Caglayan H, Huidobro PA, Galiffi E, Mejía-Salazar JR, Palermo G, Jacob Z, Maccaferri N. Lobet M, et al. Among authors: caglayan h. ACS Photonics. 2023 Oct 23;10(11):3805-3820. doi: 10.1021/acsphotonics.3c00747. eCollection 2023 Nov 15. ACS Photonics. 2023. PMID: 38027250 Free PMC article. Review.
Intestinal-Cell Kinase and Juvenile Myoclonic Epilepsy.
Lerche H, Berkovic SF, Lowenstein DH; EuroEPINOMICS-CoGIE Consortium; EpiPGX Consortium; Epi4K Consortium/Epilepsy Phenome/Genome Project. Lerche H, et al. N Engl J Med. 2019 Apr 18;380(16):e24. doi: 10.1056/NEJMc1805100. N Engl J Med. 2019. PMID: 30995385 No abstract available.
De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies.
Manivannan SN, Roovers J, Smal N, Myers CT, Turkdogan D, Roelens F, Kanca O, Chung HL, Scholz T, Hermann K, Bierhals T, Caglayan HS, Stamberger H; MAE Working Group of EuroEPINOMICS RES Consortium; Mefford H, de Jonghe P, Yamamoto S, Weckhuysen S, Bellen HJ. Manivannan SN, et al. Among authors: caglayan hs. Brain. 2022 Jun 3;145(5):1684-1697. doi: 10.1093/brain/awab409. Brain. 2022. PMID: 34788397 Free PMC article.
110 results