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Number of items: 8.


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. 475111-.


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-.


Bandres-Ciga, Sara ORCID: 0000-0003-0056-1361, Faghri, Faraz ORCID: 0000-0001-5744-8728, Majounie, Elisa, Koretsky, Mathew J ORCID: 0000-0003-4341-3991, Kim, Jeffrey ORCID: 0000-0003-0738-0512, Levine, Kristin S, Leonard, Hampton ORCID: 0000-0003-2390-8110, Makarious, Mary B ORCID: 0000-0002-7978-1051, Iwaki, Hirotaka ORCID: 0000-0002-8982-7885, Crea, Peter Wild ORCID: 0000-0001-8944-5716
et al (show 24 more authors) (2023) NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations. medRxiv, 4 (11-20). 2023.11.06.23298176-.


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) <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.


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 Mar 23 22:28:51 2024 GMT.