1. Analysis of dominant and recessive parkinsonism genes in REM sleep behavior disorder. (October 2020) Authors: Mufti, K.; Rudakou, U.; Yu, E.; Ruskey, J.A.; Asavesh, F.; Laurent, S.B.; Arnulf, I.; Hu, M.T.M.; Dauvilliers, Y.; Högl, B.; Stefani, A.; Holzknecht, E.; Monaca, C.C.; Abril, B.; Plazzi, G.; Antelmi, E.; Ferini-Strambi, L.; Heidbreder, A.; Young, P.; De Cock, V. Cochen Journal: Parkinsonism & related disorders Issue: Volume 79(2020) Supplement 1 Page Start: e27 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Analysis of heterozygous PRKN variants and copy number variations in Parkinson's disease. (October 2020) Authors: Yu, E.; Krohn, L.; Rudakov, U.; Mufti, K.; Ruskey, J.A.; Asayesh, F.; Estiar, M.A.; Spiegelman, D.; Greenbaum, L.; Dauvilliers, Y.; Dupre, N.; Rouleau, G.A.; Hassin-Baer, S.; Fon, E.A.; Alcalay, R.N.; Gan-Or, Z. Journal: Parkinsonism & related disorders Issue: Volume 79(2020) Supplement 1 Page Start: e28 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. GBA variants in REM sleep behavior disorder risk and conversion: a multicenter study. (October 2020) Authors: Krohn, L.; Ruskey, J.A.; Rudakou, U.; Leveille, E.; Asayesh, F.; Hu, M.T.M.; Arnulf, I.; Dauvilliers, Y.; Högl, B.; Stefani, A.; Monaca, C.C.; Abril, B.; Plazzi, G.; Antelmi, E.; Ferini-Strambi, L.; Heidbreder, A.; Boeve, B.F.; Espay, A.J.; Cochen de Cock, V.; Mollenhauer, B. Journal: Parkinsonism & related disorders Issue: Volume 79(2020) Supplement 1 Page Start: e26 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. NPC1 variants are not associated with Parkinson's disease. (October 2020) Authors: Senkevich, K.; Amar Bencheikh, B. Ouled; Rudakou, U.; Yu, E.; Mufti, K.; Ruskey, J.A.; Asayesh, F.; Laurent, S.B.; Spiegelman, D.; Fahn, S.; Waters, C.; Monchi, O.; Dauvilliers, Y.; Alcalay, R.N.; Dupré, N.; Greenbaum, L.; Hassin-Baer, S.; Espay, A.J.; Rouleau, G.A.; Fon, E.A. Journal: Parkinsonism & related disorders Issue: Volume 79(2020) Supplement 1 Page Start: e31 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. The GBA p.Trp378Gly mutation is a probable French‐Canadian founder mutation causing Gaucher disease and synucleinopathies. Issue 3 (16th July 2018) Authors: Ruskey, J.A.; Zhou, S.; Santiago, R.; Franche, L.‐A.; Alam, A.; Roncière, L.; Spiegelman, D.; Fon, E.A.; Trempe, J.‐F.; Kalia, L.V.; Postuma, R.B.; Dupre, N.; Rivard, G.‐E.; Assouline, S.; Amato, D.; Gan‐Or, Z. Journal: Clinical genetics Issue: Volume 94:Issue 3/4(2018) Page Start: 339 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. The genetic landscape of hereditary spastic paraplegia in Canada. (October 2020) Authors: Estiar, M.A.; Yu, E.; Ruskey, J.A.; Leveille, E.; Asayesh, F.; Spiegelman, D.; Trempe, J.F.; Tarnopolsky, M.; Suchowersky, O.; Dupré, N.; Boycott, K.M.; Yoon, G.; Rouleau, G.A.; Gan-Or, Z. Journal: Parkinsonism & related disorders Issue: Volume 79(2020) Supplement 1 Page Start: e110 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗