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American Journal of Human Genetics|July 26, 2016
Biallelic Mutations in Citron Kinase Link Mitotic Cytokinesis to Human Primary MicrocephalyHongda Li, Stephanie L Bielas, Maha S Zaki, et al.Genome Medicine|February 4, 2017
Longitudinal analysis of treatment-induced genomic alterations in gliomasE Zeynep Erson-Omay, Octavian Henegariu, S Bülent Omay, et al.Cell|December 3, 2016
Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum DisorderDora C Tărlungeanu, Elena Deliu, Christoph P Dotter, et al.Nature Communications|November 26, 2025
Subgroup of meningiomas involving FOS and FOSB gene fusionsKanat Yalcin, Hasan Alanya, Batur Gultekin, et al.Neuro-Oncology|October 17, 2020
Associations of meningioma molecular subgroup and tumor recurrenceMark W Youngblood, Danielle F Miyagishima, Lan Jin, et al.Frontiers in Pediatrics|July 19, 2024
Rapid genome sequencing for critically ill infants: an inaugural pilot study from TurkeyBengisu Guner Yilmaz, Ozlem Akgun-Dogan, Ozkan Ozdemir, et al.Pediatric Neurology|December 3, 2014
Brain malformations associated with Knobloch syndrome--review of literature, expanding clinical spectrum, and identification of novel mutationsAhmet Okay Caglayan, Jacob F Baranoski, Fesih Aktar, et al.Elife|September 9, 2016
Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 allelesAndrew T Timberlake, Jungmin Choi, Samir Zaidi, et al.Brain : a Journal of Neurology|April 14, 2020
Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathyNicolas Chatron, Felicitas Becker, Heba Morsy, et al.Biological Psychiatry|December 16, 2011
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autismThomas V Fernandez, Stephan J Sanders, Ilana R Yurkiewicz, et al.Pageof 13