Özgür Çoğulu

Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease

Ender Karaca, Tamar Harel, Davut Pehli̇van et al. · Neuron · 2015 · 332 citations · Full text

A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling

Dagmar Wieczorek, Nina Bögershausen, Filippo Beleggia et al. · Human Molecular Genetics · 2013 · 227 citations · Full text

SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice

Ippei Okada, Haruka Hamanoue, Koji Terada et al. · The American Journal of Human Genetics · 2010 · 116 citations · Full text

Knockout Mouse, Developmental Biology, Ophthalmology +8

The missing “link”: an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation

Julia Schreml, Burak Durmaz, Özgür Çoğulu et al. · Human Genetics · 2013 · 77 citations

Developmental Biology, Mendelian Disorder, “ Link ” +8

Highest heterogeneity for cystic fibrosis: 36 mutations account for 75% of all CF chromosomes in Turkish patients

Vasiliki Ninis, Elif Dağlı, Mübeccel Demirkol et al. · American Journal of Medical Genetics · 2002 · 63 citations · Full text