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Number of items: 18.


Marini, Sandro, Crawford, Katherine, Morotti, Andrea, Lee, Myung J, Pezzini, Alessandro, Moomaw, Charles J, Flaherty, Matthew L, Montaner, Joan, Roquer, Jaume, Jimenez-Conde, Jordi
et al (show 243 more authors) (2019) Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity A Meta-analysis. JAMA NEUROLOGY, 76 (4). pp. 480-491.


Pulit, Sara L, Weng, Lu-Chen, McArdle, Patrick F, Trinquart, Ludovic, Choi, Seung Hoan, Mitchell, Braxton D, Rosand, Jonathan, de Bakker, Paul IW, Benjamin, Emelia J, Ellinor, Patrick T
et al (show 351 more authors) (2018) Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes. NEUROLOGY-GENETICS, 4 (6). e293-.


Mencacci, Niccolo E, Reynolds, Regina, Ruiz, Sonia Garcia, Vandrovcova, Jana, Forabosco, Paola, Sanchez-Ferrer, Alvaro, Volpato, Viola, Weale, Michael E, Bhatia, Kailash P, Webber, Caleb
et al (show 3 more authors) (2020) Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders. BRAIN, 143 (9). pp. 2771-2787.


Noyce, Alastair J, Kia, Demis A, Hemani, Gibran, Nicolas, Aude, Price, T Ryan, De Pablo-Fernandez, Eduardo, Haycock, Philip C, Lewis, Patrick A, Foltynie, Thomas, Smith, George Davey
et al (show 8 more authors) (2017) Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study. PLOS MEDICINE, 14 (6). e1002314-.


Walton, E, Hibar, D, Yilmaz, Z, Jahanshad, N, Cheung, J, Batury, V-L, Seitz, J, Bulik, CM, Thompson, PM, Ehrlich, Stefan
et al (show 500 more authors) (2019) Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa. MOLECULAR NEUROBIOLOGY, 56 (7). pp. 5146-5156.


Billingsley, Kimberley J, Ding, Jinhui, Jerez, Pilar Alvarez, Illarionova, Anastasia, Levine, Kristin, Grenn, Francis P, Makarious, Mary B, Moore, Anni, Vitale, Daniel, Reed, Xylena
et al (show 31 more authors) (2023) Genome-Wide Analysis of Structural Variants in Parkinson Disease. ANNALS OF NEUROLOGY, 93 (5). pp. 1012-1022.


Chen, Zhongbo ORCID: 0000-0001-6668-7202, Zhang, David, Reynolds, Regina H ORCID: 0000-0001-6470-7919, Gustavsson, Emil K ORCID: 0000-0003-0541-7537, García-Ruiz, Sonia, D'Sa, Karishma, Fairbrother-Browne, Aine ORCID: 0000-0002-7196-1410, Vandrovcova, Jana, International Parkinson’s Disease Genomics Consortium (IPDGC), , Hardy, John ORCID: 0000-0002-3122-0423
et al (show 4 more authors) (2021) Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage. Nature communications, 12 (1). 2076-.


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.


Niemi, Mari EK, Karjalainen, Juha, Daly, Mark, Ganna, Andrea, Mehtonen, Juha, Cordioli, Mattia, Kaunisto, Mari, Pigazzini, Sara, Donner, Kati, Kivinen, Katja
et al (show 3481 more authors) (2021) Mapping the human genetic architecture of COVID-19. NATURE, 600 (7889). 472-+.


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.


Quinn, JP ORCID: 0000-0003-3551-7803, Billingsley, Kimberley, Reynolds, Regina H, Botia, Juan, Nalls, Mike A, Hardy, John, Gagliano Taliun, Sarah A and Ryten, Mina
(2019) Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability. npj Parkinson's Disease, 5 (1). 6-.


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.


Hibar, Derrek P, Adams, Hieab HH, Jahanshad, Neda, Chauhan, Ganesh, Stein, Jason L, Hofer, Edith, Renteria, Miguel E, Bis, Joshua C, Arias-Vasquez, Alejandro, Ikram, M Kamran
et al (show 322 more authors) (2017) Novel genetic loci associated with hippocampal volume. NATURE COMMUNICATIONS, 8 (1). 13624-.


Noyce, Alastair J, R'Bibo, Lea, Peress, Luisa, Bestwick, Jonathan P, Adams-Carr, Kerala L, Mencacci, Niccolo E, Hawkes, Christopher H, Masters, Joseph M, Wood, Nicholas, Hardy, John
et al (show 3 more authors) (2017) PREDICT-PD: An online approach to prospectively identify risk indicators of Parkinson's disease. MOVEMENT DISORDERS, 32 (2). pp. 219-226.


Guelfi, Sebastian, D'Sa, Karishma, Botía, Juan A, Vandrovcova, Jana, Reynolds, Regina H, Zhang, David, Trabzuni, Daniah, Collado-Torres, Leonardo, Thomason, Andrew, Quijada Leyton, Pedro
et al (show 10 more authors) (2020) Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information. Nature communications, 11 (1). 1041-.


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.


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 Sat Feb 24 21:18:40 2024 GMT.