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Number of items: 6.


Blauwendraat, Cornelis, Reed, Xylena, Kia, Demis A, Gan-Or, Ziv, Lesage, Suzanne, Pihistrom, Lasse, Guerreiro, Rita, Gibbs, J Raphael, Sabir, Marya, Ahmed, Sarah
et al (show 19 more authors) (2018) Frequency of Loss of Function Variants in <i>LRRK2</i> in Parkinson Disease. JAMA NEUROLOGY, 75 (11). pp. 1416-1422.


Billingsley, Kimberley J, Ding, Jinhui, Jerez, Pilar Alvarez, Illarionova, Anastasia, Levine, Kristin, Grenn, Francis P, Makarious, Mary B, Moore, Anni, Vitale, Daniel, Reed, Xylena
et al (show 31 more authors) (2023) Genome-Wide Analysis of Structural Variants in Parkinson Disease. ANNALS OF NEUROLOGY, 93 (5). pp. 1012-1022.


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
et al (show 260 more authors) (2019) Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. The Lancet Neurology, 18 (12). pp. 1091-1102.


Grenn, Francis P, Kim, Jonggeol J, Makarious, Mary B, Iwaki, Hirotaka, Illarionova, Anastasia, Brolin, Kajsa, Kluss, Jillian H, Schumacher-Schuh, Artur F, Leonard, Hampton, Faghri, Faraz
et al (show 14 more authors) (2020) The Parkinson's DiseaseGenome-WideAssociation Study Locus Browser. MOVEMENT DISORDERS, 35 (11). pp. 2056-2067.


Hall, Ashley, Middlehurst, Ben ORCID: 0000-0002-2603-2719, Cadogan, Max AM, Reed, Xylena, Billingsley, Kimberley J, Bubb, Vivien J ORCID: 0000-0003-2763-7004 and Quinn, John P ORCID: 0000-0003-3551-7803
(2024) A SINE-VNTR-Alu at the LRIG2 locus is associated with proximal and distal gene expression in CRISPR and population models. Scientific reports, 14 (1). p. 792.


Fernandez-Santiago, Ruben, Martin-Flores, Nuria, Antonelli, Francesca, Cerquera, Catalina, Moreno, Veronica, Bandres-Ciga, Sara, Manduchi, Elisabetta, Tolosa, Eduard, Singleton, Andrew B, Moore, Jason H
et al (show 152 more authors) (2019) <i>SNCA</i> and <i>mTOR</i> Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease. MOVEMENT DISORDERS, 34 (9). pp. 1333-1344.

This list was generated on Mon Feb 26 12:21:05 2024 GMT.