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Number of items: 7.


Billingsley, Kimberley, Quinn, John ORCID: 0000-0003-3551-7803 and Bubb, Vivien ORCID: 0000-0003-2763-7004
(2019) Analysis of repetitive element expression in the blood and skin of patients with Parkinson’s disease identifies differential expression of satellite elements. Scientific Reports, 9 (1). 4369-.


Billingsley, Kimberley, Barbosa, Ines, Bandrés-Ciga, Sara, Quinn, John ORCID: 0000-0003-3551-7803, Bubb, Vivien, Deshpande, Charu, Botia, Juan, Reynolds, Regina, Zhang, David, Simpson, Michael ORCID: 0000-0002-8539-8753
et al (show 8 more authors) (2018) Genetic variation within genes associated with mitochondrial function is significantly associated with later age at onset of Parkinson disease and contributes to disease risk. BioRxiv.


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.


Quinn, JP ORCID: 0000-0003-3551-7803, Billingsley, Kimberley, Reynolds, Regina H, Botia, Juan, Nalls, Mike A, Hardy, John, Gagliano Taliun, Sarah A and Ryten, Mina
(2019) Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability. npj Parkinson's Disease, 5 (1). 6-.


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.


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) SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease. MOVEMENT DISORDERS, 34 (9). pp. 1333-1344.


Quinn, JP ORCID: 0000-0003-3551-7803, Billingsley, Kimberley, Chang, D, Nalls, MA, Hallgrímsdóttir, IB, Hunkapiller, J, van der Brug, M, Cai, F, International Parkinson's Disease Genomics Consortium, , 23andMe Research Team,
et al (show 9 more authors) (2017) A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci. Nature Genetics, 49 (10). pp. 1511-1516.

This list was generated on Sat May 27 06:48:59 2023 BST.