1. Exploration of the endo‐lysosomal pathway genes in frontotemporal dementia: The use of protein‐protein interaction networks to prioritize rare‐variant association analysis results: Genetics/molecular genetics. (7th December 2020) Authors: Kocoglu, Cemile; Manzoni, Claudia; Ferrari, Raffaele; Van Broeckhoven, Christine; van der Zee, Julie Journal: Alzheimer's & dementia Issue: Volume 16(2020)Supplement 2 Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families. (February 2018) Authors: Kocoglu, Cemile; Gundogdu, Asli; Kocaman, Gulsen; Kahraman-Koytak, Pinar; Uluc, Kayihan; Kiziltan, Gunes; Caglayan, Ahmet Okay; Bilguvar, Kaya; Vural, Atay; Basak, A. Nazli Journal: Neurology Issue: Volume 4:Number 1(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. TRIM25 nonsense mutation (p.C168*) as the probable cause of early‐onset autosomal dominant Alzheimer's disease. (1st February 2022) Authors: Gómez‐Tortosa, Estrella; Baradaran‐Heravi, Yalda; Dillen, Lubina; Agüero, Pablo; Sainz, María José; Pérez‐Pérez, Julián; Kocoglu, Cemile; Téllez, Raquel; Van Broeckhoven, Christine; van der Zee, Julie Journal: Alzheimer's & dementia Issue: Volume 17(2021)Supplement 3 Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. TRIM25 nonsense mutation (p.C168*) as the probable cause of early‐onset autosomal dominant Alzheimer's disease. (December 2021) Authors: Gómez‐Tortosa, Estrella; Baradaran‐Heravi, Yalda; Dillen, Lubina; Agüero, Pablo; Sainz, María José; Pérez‐Pérez, Julián; Kocoglu, Cemile; Téllez, Raquel; Van Broeckhoven, Christine; van der Zee, Julie Journal: Alzheimer's & dementia Issue: Volume 17(2021)Supplement 3 Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of SPG11. (October 2015) Authors: Iskender, Ceren; Kartal, Ece; Akcimen, Fulya; Kocoglu, Cemile; Ozoguz, Aslihan; Kotan, Dilcan; Eraksoy, Mefkure; Parman, Yesim G.; Basak, Ayse Nazli Journal: Neurology Issue: Volume 1:Number 3(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗