Cemile Koçoğlu

Homozygous <i>CAPN1</i> mutations causing a spastic-ataxia phenotype in 2 families

Cemile Koçoğlu, Gülşen Kocaman, Pinar Kahraman-Koytak et al. · Neurology Genetics · 2018 · 19 citations · Full text

Mendelian Disorder, Mild Ataxia, Hereditary Spastic Paraplegias +13

Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database

Ceren Tunca, Tuncay Şeker, Fulya Akçimen et al. · Human Mutation · 2020 · 18 citations · Full text

Neurogenomics, Sporadic Als, Genetics +20

Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of <i>SPG11</i>

Ceren Iskender, Ece Kartal, Fulya Akçimen et al. · Neurology Genetics · 2015 · 17 citations · Full text

Investigating the Endo-Lysosomal System in Major Neurocognitive Disorders Due to Alzheimer’s Disease, Frontotemporal Lobar Degeneration and Lewy Body Disease: Evidence for SORL1 as a Cross-Disease Gene

Luisa Benussi, Antonio Longobardi, Cemile Koçoğlu et al. · International Journal of Molecular Sciences · 2021 · 17 citations · Full text

Genetics, Disease Gene Identification, Social Sciences +22

The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice

Atay Vural, Gülşah Şimşir, Şeyma Tekgül et al. · Movement Disorders · 2021 · 16 citations