1. A new splice-site mutation in SLC12A6 causing Andermann syndrome with motor neuronopathy. Issue 10 (21st December 2017) Authors: Akçakaya, Nihan Hande; Yapıcı, Zuhal; Tunca, Ceren İskender; Tektürk, Pınar; Akçimen, Fulya; Başak, Ayşe Nazlı Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 89:Issue 10(2018) Page Start: 1123 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Assessment of the corticospinal fiber integrity in mirror movement disorder. (August 2018) Authors: Solmaz, Bilgehan; Özyurt, Mustafa Görkem; Ata, Demir Berk; Akçimen, Fulya; Shabsog, Mohammed; Türker, Kemal Sıtkı; Dalçik, Hakkı; Algin, Oktay; Başak, Ayşe Nazlı; Özgür, Merve; Çavdar, Safiye Journal: Journal of clinical neuroscience Issue: Volume 54(2018) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical and molecular characterization and response to acitretin in three families with Sjögren‐Larsson syndrome. (27th April 2018) Authors: Vural, Seçil; Vural, Atay; Akçimen, Fulya; Bağci, Işın S.; Tunca, Ceren; Gündoğdu Eken, Asli; Ruzicka, Thomas; Başak, A. Nazli Journal: International journal of dermatology Issue: Volume 57:Number 7(2018) Page Start: 843 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cover, Volume 41, Issue 8. Issue 8 (27th July 2020) Authors: Tunca, Ceren; Şeker, Tuncay; Akçimen, Fulya; Coşkun, Cemre; Bayraktar, Elif; Palvadeau, Robin; Zor, Seyit; Koçoğlu, Cemile; Kartal, Ece; Şen, Nesli Ece; Hamzeiy, Hamid; Özoğuz Erimiş, Aslıhan; Norman, Utku; Karakahya, Oğuzhan; Olgun, Gülden; Akgün, Tahsin; Durmuş, Hacer; Şahin, Erdi; Çakar, Arman... Journal: Human mutation Issue: Volume 41:Issue 8(2020) Page Start: iv Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Evidence for Non‐Mendelian Inheritance in Spastic Paraplegia 7. Issue 7 (17th February 2021) Authors: Estiar, Mehrdad A.; Yu, Eric; Haj Salem, Ikhlass; Ross, Jay P.; Mufti, Kheireddin; Akçimen, Fulya; Leveille, Etienne; Spiegelman, Dan; Ruskey, Jennifer A.; Asayesh, Farnaz; Dagher, Alain; Yoon, Grace; Tarnopolsky, Mark; Boycott, Kym M.; Dupre, Nicolas; Dion, Patrick A.; Suchowersky, Oksana; Tremp... Journal: Movement disorders Issue: Volume 36:Issue 7(2021) Page Start: 1664 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project. Issue 2 (7th November 2020) Authors: Akçimen, Fulya; Ross, Jay P.; Liao, Calwing; Spiegelman, Dan; Dion, Patrick A.; Rouleau, Guy A. Journal: Movement disorders Issue: Volume 36:Issue 2(2021) Page Start: 514 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetic and epidemiological characterization of restless legs syndrome in Québec. Issue 4 (30th October 2019) Authors: Akçimen, Fulya; Ross, Jay P; Sarayloo, Faezeh; Liao, Calwing; De Barros Oliveira, Rachel; Ruskey, Jennifer A; Bourassa, Cynthia V; Dion, Patrick A; Xiong, Lan; Gan-Or, Ziv; Rouleau, Guy A Journal: Sleep Issue: Volume 43:Issue 4(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor. Issue 7 (6th April 2020) Authors: Liao, Calwing; Sarayloo, Faezeh; Rochefort, Daniel; Houle, Gabrielle; Akçimen, Fulya; He, Qin; Laporte, Alexandre D.; Spiegelman, Dan; Poewe, Werner; Berg, Daniela; Müller, Stefanie; Hopfner, Franziska; Deuschl, Günther; Kuhlenbäeumer, Gregor; Rajput, Alex; Dion, Patrick A.; Rouleau, Guy A. Journal: Movement disorders Issue: Volume 35:Issue 7(2020) Page Start: 1153 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Outside Back Cover, Volume 41, Issue 8. Issue 8 (27th July 2020) Authors: Tunca, Ceren; Şeker, Tuncay; Akçimen, Fulya; Coşkun, Cemre; Bayraktar, Elif; Palvadeau, Robin; Zor, Seyit; Koçoğlu, Cemile; Kartal, Ece; Şen, Nesli Ece; Hamzeiy, Hamid; Özoğuz Erimiş, Aslıhan; Norman, Utku; Karakahya, Oğuzhan; Olgun, Gülden; Akgün, Tahsin; Durmuş, Hacer; Şahin, Erdi; Çakar, Arman... Journal: Human mutation Issue: Volume 41:Issue 8(2020) Page Start: iv Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Questioning the Association of the STMN2 Dinucleotide Repeat With Amyotrophic Lateral Sclerosis. (13th August 2022) Authors: Ross, Jay P.; Akçimen, Fulya; Liao, Calwing; Spiegelman, Dan; Weisburd, Ben; Dupré, Nicolas; Dion, Patrick A.; Rouleau, Guy A.; Farhan, Sali M.K. Journal: Neurology Issue: Volume 8:Number 4(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗