Cemile Koçoğlu

<i>ATXN1</i> repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization

Gijs H P Tazelaar, Steven Boeynaems, Mathias De Decker et al. · Brain Communications · 2020 · 56 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

Life Sciences, Genetics, Neurology +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 · 19 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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 · 19 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

Life Sciences, Genetics, Molecular Genetics +17