1. A critique of the second consensus criteria for multiple system atrophy. Issue 7 (29th April 2019) Authors: Stankovic, Iva; Quinn, Niall; Vignatelli, Luca; Antonini, Angelo; Berg, Daniela; Coon, Elizabeth; Cortelli, Pietro; Fanciulli, Alessandra; Ferreira, Joaquim J.; Freeman, Roy; Halliday, Glenda; Höglinger, Günter U.; Iodice, Valeria; Kaufmann, Horacio; Klockgether, Thomas; Kostic, Vladimir; Krismer... Journal: Movement disorders Issue: Volume 34:Issue 7(2019) Page Start: 975 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A genome-wide association study in multiple system atrophy. (11th October 2016) Authors: Sailer, Anna; Scholz, Sonja W.; Nalls, Michael A.; Schulte, Claudia; Federoff, Monica; Price, T. Ryan; Lees, Andrew; Ross, Owen A.; Dickson, Dennis W.; Mok, Kin; Mencacci, Niccolo E.; Schottlaender, Lucia; Chelban, Viorica; Ling, Helen; O'Sullivan, Sean S.; Wood, Nicholas W.; Traynor, Bryan J.; F... Journal: Neurology Issue: Volume 87:Number 15(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource. Issue 8 (7th May 2021) Authors: Iwaki, Hirotaka; Leonard, Hampton L.; Makarious, Mary B.; Bookman, Matt; Landin, Barry; Vismer, David; Casey, Bradford; Gibbs, J. Raphael; Hernandez, Dena G.; Blauwendraat, Cornelis; Vitale, Daniel; Song, Yeajin; Kumar, Dinesh; Dalgard, Clifton L.; Sadeghi, Mahdiar; Dong, Xianjun; Misquitta, Leon... Journal: Movement disorders Issue: Volume 36:Issue 8(2021) Page Start: 1795 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies. Issue 2 (17th December 2016) Authors: Blauwendraat, Cornelis; Nalls, Mike A.; Federoff, Monica; Pletnikova, Olga; Ding, Jinhui; Letson, Christopher; Geiger, Joshua T.; Gibbs, J. Raphael; Hernandez, Dena G.; Troncoso, Juan C.; Simón‐Sánchez, Javier; Scholz, Sonja W. Journal: Movement disorders Issue: Volume 32:Issue 2(2017) Page Start: 298 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Author response: A genome-wide association study in multiple system atrophy. (28th March 2017) Authors: Scholz, Sonja W.; Houlden, Henry Journal: Neurology Issue: Volume 88:Number 13(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Classification of GBA Variants and Their Effects in Synucleinopathies. Issue 10 (18th October 2019) Authors: Gan‐Or, Ziv; Alcalay, Roy N.; Makarious, Mary B.; Scholz, Sonja W.; Blauwendraat, Cornelis Journal: Movement disorders Issue: Volume 34:Issue 10(2019) Page Start: 1581 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis. (26th December 2022) Authors: Calvo, Andrea; Canosa, Antonio; Moglia, Cristina; Manera, Umberto; Grassano, Maurizio; Vasta, Rosario; Palumbo, Francesca; Cugnasco, Paolo; Gallone, Salvatore; Brunetti, Maura; De Marchi, Fabiola; Arena, Vincenzo; Pagani, Marco; Dalgard, Clifton; Scholz, Sonja W.; Chia, Ruth; Corrado, Lucia; Dalf... Journal: Neurology Issue: Volume 8:Number 6(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Conjugal multiple system atrophy: Rethinking numbers of probability. (August 2020) Authors: Mitterer, Wolfgang; Lanser, Lukas; Fodor, Margot; Weiss, Johannes; Scholz, Sonja W.; Wenning, Gregor K. Journal: Parkinsonism & related disorders Issue: Volume 77(2020) Page Start: 176 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Evaluation of SORL1 in Lewy Body Dementia Identifies No Significant Associations. Issue 11 (26th August 2022) Authors: Ray, Anindita; Reho, Paolo; Shah, Zalak; Scholz, Sonja W. Journal: Movement disorders Issue: Volume 37:Issue 11(2022) Page Start: 2312 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. GBA mutations and Parkinson disease: When genotype meets phenotype. (3rd March 2015) Authors: Scholz, Sonja W.; Jeon, Beom S. Journal: Neurology Issue: Volume 84:Number 9(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗