11. Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism. Issue 11 (27th August 2022) Authors: Ortega, Roberto A.; Bressman, Susan B.; Raymond, Deborah; Ozelius, Laurie J.; Katsnelson, Viktoriya; Leaver, Katherine; Swan, Matthew C.; Shanker, Vicki; Miravite, Joan; Wang, Cuiling; Bennett, Steffany A.L.; Saunders‐Pullman, Rachel Journal: Movement disorders Issue: Volume 37:Issue 11(2022) Page Start: 2217 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Digitized spiral analysis may be a potential biomarker for brachial dystonia. (December 2018) Authors: Ratliff, Jeffrey; Ortega, Roberto A.; Ooi, Hwai Yin; Mirallave, Ana; Glickman, Amanda; Yu, Qiping; Raymond, Deborah; Bressman, Susan; Pullman, Seth; Saunders-Pullman, Rachel Journal: Parkinsonism & related disorders Issue: Volume 57(2018) Page Start: 16 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Disclosure of research results in genetic studies of Parkinson's disease caused by LRRK2 mutations. Issue 7 (7th May 2015) Authors: Pont‐Sunyer, Claustre; Bressman, Susan; Raymond, Deborah; Glickman, Amanda; Tolosa, Eduardo; Saunders‐Pullman, Rachel Journal: Movement disorders Issue: Volume 30:Issue 7(2015) Page Start: 904 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. Evidence for increased completed suicide in first-degree relatives of LRRK2 G2019S mutation Parkinson's disease. Issue 7 (8th November 2018) Authors: Ortega, Roberto Angel; Groves, Mark; Mirelman, Anat; Alcalay, Roy N; Raymond, Deborah; Elango, Sonya; Mejia-Santana, Helen; Giladi, Nir; Marder, Karen; Bressman, Susan B; Saunders-Pullman, Rachel Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 90:Issue 7(2019) Page Start: 843 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
15. Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease. Issue 1 (17th May 2021) Authors: Lai, Dongbing; Alipanahi, Babak; Fontanillas, Pierre; Schwantes‐An, Tae‐Hwi; Aasly, Jan; Alcalay, Roy N.; Beecham, Gary W.; Berg, Daniela; Bressman, Susan; Brice, Alexis; Brockman, Kathrin; Clark, Lorraine; Cookson, Mark; Das, Sayantan; Van Deerlin, Vivianna; Follett, Jordan; Farrer, Matthew J.; ... Journal: Annals of neurology Issue: Volume 90:Issue 1(2021) Page Start: 76 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. Glucocerebrosidase enzyme activity in GBA mutation Parkinson's disease. (June 2016) Authors: Ortega, Roberto A.; Torres, Paola A.; Swan, Matthew; Nichols, William; Boschung, Sarah; Raymond, Deborah; Barrett, Matthew J.; Johannes, Brooke A.; Severt, Lawrence; Shanker, Vicki; Hunt, Ann L.; Bressman, Susan; Pastores, Gregory M.; Saunders-Pullman, Rachel Journal: Journal of clinical neuroscience Issue: Volume 28(2016:Jun.) Page Start: 185 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
17. Heterogeneity in primary dystonia: Lessons from THAP1, GNAL, and TOR1A in Amish‐Mennonites. Issue 6 (5th February 2014) Authors: Saunders‐Pullman, Rachel; Fuchs, Tania; San Luciano, Marta; Raymond, Deborah; Brashear, Alison; Ortega, Robert; Deik, Andres; Ozelius, Laurie J.; Bressman, Susan B. Journal: Movement disorders Issue: Volume 29:Issue 6(2014) Page Start: 812 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. Interest in Genetic Testing in Ashkenazi Jewish Parkinson's Disease Patients and Their Unaffected Relatives. Issue 2 (17th August 2014) Authors: Gupte, Manisha; Alcalay, Roy N.; Mejia‐Santana, Helen; Raymond, Deborah; Saunders‐Pullman, Rachel; Roos, Ernest; Orbe‐Reily, Martha; Tang, Ming‐X; Mirelman, Anat; Ozelius, Laurie; Orr‐Urtreger, Avi; Clark, Lorraine; Giladi, Nir; Bressman, Susan; Marder, Karen Journal: Journal of genetic counseling Issue: Volume 24:Issue 2(2015) Page Start: 238 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. Low‐variance RNAs identify Parkinson's disease molecular signature in blood. Issue 6 (18th March 2015) Authors: Chikina, Maria D.; Gerald, Christophe P.; Li, Xianting; Ge, Yongchao; Pincas, Hanna; Nair, Venugopalan D.; Wong, Aaron K.; Krishnan, Arjun; Troyanskaya, Olga G.; Raymond, Deborah; Saunders‐Pullman, Rachel; Bressman, Susan B.; Yue, Zhenyu; Sealfon, Stuart C. Journal: Movement disorders Issue: Volume 30:Issue 6(2015) Page Start: 813 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
20. Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene. Issue 7 (21st March 2015) Authors: Mirelman, Anat; Alcalay, Roy N.; Saunders‐Pullman, Rachel; Yasinovsky, Kira; Thaler, Avner; Gurevich, Tanya; Mejia‐Santana, Helen; Raymond, Deborah; Gana‐Weisz, Mali; Bar‐Shira, Anat; Ozelius, Laurie; Clark, Lorraine; Orr‐Urtreger, Avi; Bressman, Susan; Marder, Karen; Giladi, Nir; the LRRK2 AJ co... Journal: Movement disorders Issue: Volume 30:Issue 7(2015) Page Start: 981 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗