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Number of items: 8.


Jansen, Iris E, Ye, Hui, Heetveld, Sasja, Lechler, Marie C, Michels, Helen, Seinstra, Renée I, Lubbe, Steven J, Drouet, Valérie, Lesage, Suzanne, Majounie, Elisa
et al (show 23 more authors) (2017) Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing. Genome biology, 18 (1). 22 - ?.


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 22 more authors) (2018) Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease. JAMA NEUROLOGY, 75 (11). 1416 - 1422.


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). 1091 - 1102.


Blauwendraat, Cornelis, Faghri, Faraz, Pihlstrom, Lasse, Geiger, Joshua T, Elbaz, Alexis, Lesage, Suzanne, Corvol, Jean-Christophe, May, Patrick, Nicolas, Aude, Abramzon, Yevgeniya
et al (show 31 more authors) (2017) NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases. Neurobiology of Aging, 57. 247.e9 - 247.e13.


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 15 more authors) (2020) The Parkinson's DiseaseGenome-WideAssociation Study Locus Browser. MOVEMENT DISORDERS, 35 (11). 2056 - 2067.


Gang, Qiang, Bettencourt, Conceição, Machado, Pedro M, Brady, Stefen, Holton, Janice L, Pittman, Alan M ORCID: 0000-0002-8112-2987, Hughes, Deborah, Healy, Estelle, Parton, Matthew, Hilton-Jones, David
et al (show 20 more authors) (2016) Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis. Neurobiology of aging, 47. 218.e1 - 218.e9.


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 153 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). 1333 - 1344.


Sailer, Anna, Scholz, Sonja W, Nalls, Michael A, Schulte, Claudia, Federoff, Monica, Price, T Ryan, Lees, Andrew ORCID: 0000-0002-2476-4385, Ross, Owen A, Dickson, Dennis W, Mok, Kin
et al (show 37 more authors) (2016) A genome-wide association study in multiple system atrophy. NEUROLOGY, 87 (15). 1591 - 1598.

This list was generated on Sun May 16 16:20:01 2021 BST.