Sefer Kumandaş

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

Kaya Bilgüvar, Ali K. Ozturk, Angeliki Louvi et al. · Nature · 2010 · 490 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +8

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

Ketu Mishra-Gorur, Ahmet Okay Çağlayan, Ashleigh E. Schaffer et al. · Neuron · 2014 · 112 citations · Full text

Developmental Anomaly, Developmental Biology, Brain Development +12

Increased Serum Phthalates (MEHP, DEHP) and Bisphenol A Concentrations in Children With Autism Spectrum Disorder

Fatih Kardaş, Ayşe Kaçar Bayram, Esra Demi̇rci̇ et al. · Journal of Child Neurology · 2015 · 107 citations

Magnetic resonance imaging of childhood Guillain–Barre syndrome

Selim Doğanay, Hakan Gümüş, Hüseyin Per et al. · Child s Nervous System · 2010 · 103 citations

Neurological Disorder, Diagnosis, Pediatrics +5

Effect of Carbamezapine and Valproic Acid on Bone Mineral Density, IGF-I and IGFBP-3

Sefer Kumandaş, Esad Köklü, Hakan Gümüş et al. · Journal of Pediatric Endocrinology and Metabolism · 2006 · 71 citations