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Number of items: 5.


Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K, Walters, Raymond K, Bras, Jose, Duncan, Laramie, Escott-Price, Valentina, Falcone, Guido J, Gormley, Padhraig, Malik, Rainer
et al (show 562 more authors) (2018) Analysis of shared heritability in common disorders of the brain. SCIENCE, 360 (6395). 1313 - +.


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.


Giri, Anamika, Mok, Kin Y, Jansen, Iris, Sharma, Manu, Tesson, Christelle, Mangone, Graziella, Lesage, Suzanne, Bras, José M, Shulman, Joshua M, Sheerin, Una-Marie
et al (show 14 more authors) (2017) Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population. Neurobiology of Aging, 50. 167.e11 - 167.e13.


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.


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.

This list was generated on Mon Apr 26 09:57:18 2021 BST.