11. 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) ↗
12. Estimation of genetic risk function with covariates in the presence of missing genotypes. (27th June 2017) Authors: Lee, Annie J.; Marder, Karen; Alcalay, Roy N.; Mejia‐Santana, Helen; Orr‐Urtreger, Avi; Giladi, Nir; Bressman, Susan; Wang, Yuanjia Journal: Statistics in medicine Issue: Volume 36:Number 22(2017) Page Start: 3533 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Estimation of genetic risk function with covariates in the presence of missing genotypes. (27th June 2017) Authors: Lee, Annie J.; Marder, Karen; Alcalay, Roy N.; Mejia‐Santana, Helen; Orr‐Urtreger, Avi; Giladi, Nir; Bressman, Susan; Wang, Yuanjia Journal: Statistics in medicine Issue: Volume 36:Number 22(2017) Page Start: 3533 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. Fall risk and gait in Parkinson's disease: The role of the LRRK2 G2019S mutation. Issue 12 (7th October 2013) Authors: Mirelman, Anat; Heman, Talia; Yasinovsky, Kira; Thaler, Avner; Gurevich, Tanya; Marder, Karen; Bressman, Susan; Bar‐Shira, Anat; Orr‐Urtreger, Avi; Giladi, Nir; Hausdorff, Jeffrey M. Journal: Movement disorders Issue: Volume 28:Issue 12(2013) Page Start: 1683 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. In memoriam: Robert E. Burke, MD, 1949–2018. Issue 1 (17th January 2019) Authors: Fahn, Stanley; Sulzer, David; Kang, Un Jung; Bressman, Susan Journal: Movement disorders Issue: Volume 34:Issue 1(2019) Page Start: 35 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. Intact working memory in non‐manifesting LRRK2 carriers – an fMRI study. (18th December 2015) Authors: Thaler, Avner; Helmich, Rick C.; Or‐Borichev, Ayelet; van Nuenen, Bart F.L.; Shapira‐Lichter, Irit; Gurevich, Tanya; Orr‐Urtreger, Avi; Marder, Karen; Bressman, Susan; Bloem, Bastiaan R.; Giladi, Nir; Hendler, Talma; Mirelman, Anat Journal: European journal of neuroscience Issue: Volume 43:Number 1(2016:Jan.) Page Start: 106 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. 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) ↗
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) ↗