1. Assessing the relationship between monoallelic PRKN mutations and Parkinson's risk. Issue 1 (15th January 2021) Authors: Lubbe, Steven J; Bustos, Bernabe I; Hu, Jing; Krainc, Dimitri; Joseph, Theresita; Hehir, Jason; Tan, Manuela; Zhang, Weijia; Escott-Price, Valentina; Williams, Nigel M; Blauwendraat, Cornelis; Singleton, Andrew B; Morris, Huw R Journal: Human molecular genetics Issue: Volume 30:Issue 1(2021) Page Start: 78 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. CHCHD2 and Parkinson's disease. Issue 7 (July 2015) Authors: Jansen, Iris E; Bras, Jose M; Lesage, Suzanne; Schulte, Claudia; Gibbs, J Raphael; Nalls, Mike A; Brice, Alexis; Wood, Nicholas W; Morris, Huw; Hardy, John A; Singleton, Andrew B; Gasser, Thomas; Heutink, Peter; Sharma, Manu; IPDGC, † Journal: Lancet neurology Issue: Volume 14:Issue 7(2015:Jul.) Page Start: 678 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical-genetic model predicts incident impulse control disorders in Parkinson's disease. Issue 10 (13th April 2016) Authors: Kraemmer, Julia; Smith, Kara; Weintraub, Daniel; Guillemot, Vincent; Nalls, Mike A; Cormier-Dequaire, Florence; Moszer, Ivan; Brice, Alexis; Singleton, Andrew B; Corvol, Jean-Christophe Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 87:Issue 10(2016) Page Start: 1106 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data. Issue 6 (May 2016) Authors: Mok, Kin Y; Sheerin, Una; Simón-Sánchez, Javier; Salaka, Afnan; Chester, Lucy; Escott-Price, Valentina; Mantripragada, Kiran; Doherty, Karen M; Noyce, Alastair J; Mencacci, Niccolo E; Lubbe, Steven J; Williams-Gray, Caroline H; Barker, Roger A; van Dijk, Karin D; Berendse, Henk W; Heutink, Peter;... Journal: Lancet neurology Issue: Volume 15:Issue 6(2016:May) Page Start: 585 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study. Issue 10 (October 2015) Authors: Nalls, Mike A; McLean, Cory Y; Rick, Jacqueline; Eberly, Shirley; Hutten, Samantha J; Gwinn, Katrina; Sutherland, Margaret; Martinez, Maria; Heutink, Peter; Williams, Nigel M; Hardy, John; Gasser, Thomas; Brice, Alexis; Price, T Ryan; Nicolas, Aude; Keller, Margaux F; Molony, Cliona; Gibbs, J Rap... Journal: Lancet neurology Issue: Volume 14:Issue 10(2015:Oct.) Page Start: 1002 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Evidence for GRN connecting multiple neurodegenerative diseases. Issue 2 (1st May 2021) Authors: Nalls, Mike A; Blauwendraat, Cornelis; Sargent, Lana; Vitale, Dan; Leonard, Hampton; Iwaki, Hirotaka; Song, Yeajin; Bandres-Ciga, Sara; Menden, Kevin; Faghri, Faraz; Heutink, Peter; Cookson, Mark R; Singleton, Andrew B Journal: Brain communications Issue: Volume 3:Issue 2(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson's disease. Issue 5 (29th November 2019) Authors: Leonard, Hampton; Blauwendraat, Cornelis; Krohn, Lynne; Faghri, Faraz; Iwaki, Hirotaka; Ferguson, Glen; Day-Williams, Aaron G; Stone, David J; Singleton, Andrew B; Nalls, Mike A; Gan-Or, Ziv Other Names: author non-byline.; Adarmes-Gómez Astrid D author non-byline.; Aguilar Miquel author non-byline.; Aitkulova Akbota author non-byline.; Akhmetzhanov Vadim author non-byline.; Alcalay Roy N author non-byline.; Alvarez Ignacio author non-byline.; Alvarez Victoria author non-byline.; Bandres-Ciga Sa... Journal: Journal of medical genetics Issue: Volume 57:Issue 5(2020) Page Start: 331 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. Issue 12 (December 2019) Authors: Nalls, Mike A; Blauwendraat, Cornelis; Vallerga, Costanza L; Heilbron, Karl; Bandres-Ciga, Sara; Chang, Diana; Tan, Manuela; Kia, Demis A; Noyce, Alastair J; Xue, Angli; Bras, Jose; Young, Emily; von Coelln, Rainer; Simón-Sánchez, Javier; Schulte, Claudia; Sharma, Manu; Krohn, Lynne; Pihlstrøm, L... Journal: Lancet neurology Issue: Volume 18:Issue 12(2019) Page Start: 1091 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. LRP10 in α-synucleinopathies. Issue 12 (December 2018) Authors: Kia, Demis A; Sabir, Marya S; Ahmed, Sarah; Trinh, Joanne; Bandres-Ciga, Sara; Noyce, Alastair J; Kaiyrzhanov, Rauan; Middlehurst, Ben; Kia, Demis A; Tan, Manuela; Houlden, Henry; Morris, Huw R; Plun-Favreau, Helene; Holmans, Peter; Hardy, John; Trabzuni, Daniah; Bras, Jose; Quinn, John; Mok, Kin... Journal: Lancet neurology Issue: Volume 17:Issue 12(2018) Page Start: 1032 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. LRP10 in α-synucleinopathies. Issue 12 (December 2018) Authors: Pihlstrøm, Lasse; Schottlaender, Lucia; Chelban, Viorica; Houlden, Henry; Al-Sarraj, Safa; Arzberger, Thomas; Bettencourt, Conceicao; Bhatia, Kailash; Dickson, Dennis W; Federoff, Monica; Gelpi, Ellen; Gentleman, Steve; Hardy, John; Holton, Janice; Huitinga, Inge; Levey, Allan; Mann, David; Meiss... Journal: Lancet neurology Issue: Volume 17:Issue 12(2018) Page Start: 1033 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗