Biayna Sukhudyan

Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration

Ashleigh E. Schaffer, Martin W. Breuss, Ahmet Okay Çağlayan et al. · Nature Genetics · 2018 · 86 citations

Neurodegenerative Diseases, Human Ctnna2, Arp2/3 Complex Overactivity +7

Effectiveness of antiepileptic therapy in patients with PCDH19 mutations

J Lotte, Thomas Bast, Peter Borusiak et al. · Seizure · 2016 · 74 citations · Full text

Mendelian Disorder, Genetic Disorder, Antiepileptic Therapy +4

Gómez–López-Hernández syndrome: reappraisal of the diagnostic criteria

Biayna Sukhudyan, Varsine Jaladyan, Gayane Melikyan et al. · European Journal of Pediatrics · 2010 · 72 citations

Down Syndrome, Mendelian Disorder, Gómez–lópez-hernández Syndrome +3

Horizontal head titubation in infants with <scp>J</scp>oubert syndrome: a new finding

Andrea Poretti, H.‐J. Christen, Lindsay Elton et al. · Developmental Medicine & Child Neurology · 2014 · 15 citations

Infantile Basal Ganglia Stroke after Mild Head Trauma Associated with Mineralizing Angiopathy of Lenticulostriate Arteries: An Under Recognized Entity

Tamara Avetisyan, Nune Kuyumjyan, Biayna Sukhudyan et al. · Neuropediatrics · 2018 · 15 citations

Neurological Disorder, Vascular Malformation, Cerebrovascular Disease +19