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Number of items: 4.


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.


Jabbari, Edwin, Woodside, John, Guo, Tong, Magdalinou, Nadia K, Chelban, Viorica, Athauda, Dilan, Lees, Andrew J ORCID: 0000-0002-2476-4385, Foltynie, Thomas, Houlden, Henry, Church, Alistair
et al (show 4 more authors) (2019) Proximity extension assay testing reveals novel diagnostic biomarkers of atypical parkinsonian syndromes. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 90 (7). 768 - 773.


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 Sat Nov 13 17:55:19 2021 GMT.