1. Frequency of GBA Variants in Autopsy‐proven Multiple System Atrophy. Issue 4 (3rd April 2017) Authors: Sklerov, Miriam; Kang, Un J.; Liong, Christopher; Clark, Lorraine; Marder, Karen; Pauciulo, Michael; Nichols, William C.; Chung, Wendy K.; Honig, Lawrence S.; Cortes, Etty; Vonsattel, Jean Paul; Alcalay, Roy N. Journal: Movement disorders clinical practice Issue: Volume 4:Issue 4(2017) Page Start: 574 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Parkinson disease phenotype in Ashkenazi jews with and without LRRK2 G2019S mutations. Issue 14 (15th October 2013) Authors: Alcalay, Roy N.; Mirelman, Anat; Saunders‐Pullman, Rachel; Tang, Ming‐X; Mejia Santana, Helen; Raymond, Deborah; Roos, Ernest; Orbe‐Reilly, Martha; Gurevich, Tanya; Bar Shira, Anat; Gana Weisz, Mali; Yasinovsky, Kira; Zalis, Maayan; Thaler, Avner; Deik, Andres; Barrett, Matthew James; Cabassa, Jo... Journal: Movement disorders Issue: Volume 28:Issue 14(2013) Page Start: 1966 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Validation of low‐coverage whole‐genome sequencing for mitochondrial DNA variants suggests mitochondrial DNA as a genetic cause of preterm birth. Issue 12 (8th September 2021) Authors: Yang, Zeyu; Slone, Jesse; Wang, Xinjian; Zhan, Jack; Huang, Yongbo; Namjou, Bahram; Kaufman, Kenneth M.; Pauciulo, Michael; Harley, John B.; Muglia, Louis J.; Chepelev, Iouri; Huang, Taosheng Journal: Human mutation Issue: Volume 42:Issue 12(2021) Page Start: 1602 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗