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Number of items: 6.


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 561 more authors) (2018) Analysis of shared heritability in common disorders of the brain. SCIENCE, 360 (6395). 1313-+.


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 19 more authors) (2018) Frequency of Loss of Function Variants in <i>LRRK2</i> in Parkinson Disease. JAMA NEUROLOGY, 75 (11). pp. 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). pp. 1091-1102.


Prins, Bram P, Abbasi, Ali, Wong, Anson, Vaez, Ahmad, Nolte, Ilja, Franceschini, Nora, Stuart, Philip E, Achury, Javier Guterriez, Mistry, Vanisha, Bradfield, Jonathan P
et al (show 37 more authors) (2016) Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study. PLOS MEDICINE, 13 (6). e1001976-.


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 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.

This list was generated on Mon Mar 25 11:56:04 2024 GMT.