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Number of items: 15.


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-+.


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 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.


Blauwendraat, Cornelis ORCID: 0000-0001-9358-8111, Iwaki, Hirotaka ORCID: 0000-0002-8982-7885, Makarious, Mary B, Bandres-Ciga, Sara, Leonard, Hampton L, Grenn, Francis P, Lake, Julie ORCID: 0000-0002-3441-2455, Krohn, Lynne ORCID: 0000-0001-6554-1666, Tan, Manuela, Kim, Jonggeol J
et al (show 28 more authors) (2021) Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease. Annals of neurology, 90 (1). pp. 35-42.


Ling, Helen, Morris, Huw R, Neal, James W, Lees, Andrew J ORCID: 0000-0002-2476-4385, Hardy, John, Holton, Janice L, Revesz, Tamas and Williams, David DR
(2017) Mixed pathologies including chronic traumatic encephalopathy account for dementia in retired association football (soccer) players. ACTA NEUROPATHOLOGICA, 133 (3). pp. 337-352.


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.


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.


Lamb, Ruth, Rohrer, Jonathan D, Lees, Andrew J ORCID: 0000-0002-2476-4385 and Morris, Huw R
(2016) Progressive Supranuclear Palsy and Corticobasal Degeneration: Pathophysiology and Treatment Options. CURRENT TREATMENT OPTIONS IN NEUROLOGY, 18 (9). 42-.


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). pp. 768-773.


Jabbari, Edwin, Woodside, John, Tan, Manuela MX, Shoai, Maryam, Pittman, Alan, Ferrari, Raffaele, Mok, Kin Y, Zhang, David, Reynolds, Regina H, de Silva, Rohan
et al (show 13 more authors) (2018) Variation at the <i>TRIM11</i> locus modifies progressive supranuclear palsy phenotype. ANNALS OF NEUROLOGY, 84 (4). pp. 485-496.


Magdalinou, Nadia K, Golden, Hannah L, Nicholas, Jennifer M, Witoonpanich, Pirada, Mummery, Catherine J, Morris, Huw R, Djamshidian, Atbin, Warner, Tom T, Warrington, Elizabeth K, Lees, Andrew J ORCID: 0000-0002-2476-4385
et al (show 1 more authors) (2018) Verbal adynamia in parkinsonian syndromes: behavioral correlates and neuroanatomical substrate. NEUROCASE, 24 (4). pp. 204-212.


Jabbari, Edwin ORCID: 0000-0001-6844-882X, Woodside, John, Tan, Manuela MX ORCID: 0000-0001-5835-669X, Pavese, Nicola ORCID: 0000-0002-6801-6194, Bandmann, Oliver, Ghosh, Boyd CP, Massey, Luke A, Capps, Erica, Warner, Tom T ORCID: 0000-0001-6195-6995, Lees, Andrew J ORCID: 0000-0002-2476-4385
et al (show 5 more authors) (2019) The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy. Movement disorders : official journal of the Movement Disorder Society, 34 (9). pp. 1307-1314.


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 35 more authors) (2016) A genome-wide association study in multiple system atrophy. NEUROLOGY, 87 (15). pp. 1591-1598.


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 Sun Jan 14 09:59:27 2024 GMT.