1. Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease. Issue 1 (24th September 2020) Authors: Yu, Eric; Rudakou, Uladzislau; Krohn, Lynne; Mufti, Kheireddin; Ruskey, Jennifer A.; Asayesh, Farnaz; Estiar, Mehrdad A.; Spiegelman, Dan; Surface, Matthew; Fahn, Stanley; Waters, Cheryl H.; Greenbaum, Lior; Espay, Alberto J.; Dauvilliers, Yves; Dupré, Nicolas; Rouleau, Guy A.; Hassin‐Baer, Sharo... Journal: Movement disorders Issue: Volume 36:Issue 1(2021) Page Start: 178 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype. Issue 3 (15th January 2020) Authors: Estiar, Mehrdad A.; Leveille, Etienne; Spiegelman, Dan; Dupre, Nicolas; Trempe, Jean-François; Rouleau, Guy A.; Gan‐Or, Ziv Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 3(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Evaluation of DNA methylation status of toll‐like receptors 2 and 4 promoters in Behcet's disease. (12th June 2020) Authors: Kolahi, Sousan; Rashtchizadeh, Nadereh; Mahdavi, Aida Malek; Farhadi, Jafar; Khabbazi, Alireza; Sakhinia, Ebrahim; Bahavarnia, Neda; Farajzadeh Polsangi, Mohammad Jahed; Babaloo, Zohreh; Estiar, Mehrdad A. Journal: Journal of gene medicine Issue: Volume 22:Number 10(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. 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) ↗
5. GCH1 mutations in hereditary spastic paraplegia. Issue 1 (18th March 2021) Authors: Varghaei, Parizad; Yoon, Grace; Estiar, Mehrdad A.; Veyron, Simon; Leveille, Etienne; Dupré, Nicolas; Trempe, Jean‐François; Rouleau, Guy A.; Gan‐Or, Ziv Journal: Clinical genetics Issue: Volume 100:Issue 1(2021) Page Start: 51 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic and Epidemiological Study of Adult Ataxia and Spastic Paraplegia in Eastern Quebec. (5th September 2021) Authors: Haj Salem, Ikhlass; Beaudin, Marie; Stumpf, Monica; Estiar, Mehrdad A.; Côté, Pierre-Olivier; Brunet, Francis; Gamache, Pierre-Luc; Rouleau, Guy A.; Mourabit-Amari, Karim; Gan-Or, Ziv; Dupré, Nicolas Journal: Canadian journal of neurological sciences Issue: Volume 48:Number 5(2021) Page Start: 655 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetic, structural and clinical analysis of spastic paraplegia 4. (May 2022) Authors: Varghaei, Parizad; Estiar, Mehrdad A.; Ashtiani, Setareh; Veyron, Simon; Mufti, Kheireddin; Leveille, Etienne; Yu, Eric; Spiegelman, Dan; Rioux, Marie-France; Yoon, Grace; Tarnopolsky, Mark; Boycott, Kym M.; Dupre, Nicolas; Suchowersky, Oksana; Trempe, Jean-François; Rouleau, Guy A.; Gan-Or, Ziv Journal: Parkinsonism & related disorders Issue: Volume 98(2022) Page Start: 62 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Hereditary spastic paraplegia initially diagnosed as cerebral palsy. (2021) Authors: Suchowersky, Oksana; Ashtiani, Setareh; Au, Ping-Yee Billie; McLeod, Scott; Estiar, Mehrdad A.; Gan-Or, Ziv; Rouleau, Guy A. Journal: Clinical parkinsonism & related disorders Issue: Volume 5(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Heterozygous De Novo KPNA3 Mutations Cause Complex Hereditary Spastic Paraplegia. Issue 5 (14th December 2021) Authors: Estiar, Mehrdad A.; Lail, Noor; Dyment, David A.; Varghaei, Parizad; Hartley, Taila; Gillespie, Meredith K.; Yoon, Grace; Boycott, Kym M.; Rouleau, Guy A.; Gan‐Or, Ziv Journal: Annals of neurology Issue: Volume 91:Issue 5(2022) Page Start: 730 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Lack of Causal Effects or Genetic Correlation between Restless Legs Syndrome and Parkinson's Disease. Issue 8 (11th May 2021) Authors: Estiar, Mehrdad A.; Senkevich, Konstantin; Yu, Eric; Varghaei, Parizad; Krohn, Lynne; Bandres‐Ciga, Sara; Noyce, Alastair J.; Rouleau, Guy A.; Gan‐Or, Ziv Journal: Movement disorders Issue: Volume 36:Issue 8(2021) Page Start: 1967 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗