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Number of items: 19.


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-.


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.


Sisodiya, Sanjay M, Whelan, Christopher D, Hatton, Sean N, Huynh, Khoa, Altmann, Andre, Ryten, Mina, Vezzani, Annamaria, Caligiuri, Maria Eugenia, Labate, Angelo, Gambardella, Antonio
et al (show 62 more authors) (2022) The ENIGMA-Epilepsy working group: Mapping disease from large data sets. HUMAN BRAIN MAPPING, 43 (1). pp. 113-128.


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, Barbosa, Ines, Bandrés-Ciga, Sara, Quinn, John ORCID: 0000-0003-3551-7803, Bubb, Vivien, Deshpande, Charu, Botia, Juan, Reynolds, Regina, Zhang, David, Simpson, Michael ORCID: 0000-0002-8539-8753
et al (show 8 more authors) (2018) Genetic variation within genes associated with mitochondrial function is significantly associated with later age at onset of Parkinson disease and contributes to disease risk. BioRxiv.


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.


Billingsley, Kimberley J, Barbosa, Ines A, Bandres-Ciga, Sara, Quinn, John P ORCID: 0000-0003-3551-7803, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Deshpande, Charu, Botia, Juan A, Reynolds, Regina H, Zhang, David, Simpson, Michael A
et al (show 136 more authors) (2019) Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset. NPJ PARKINSONS DISEASE, 5 (1). 8-.


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-.


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.


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-.


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-.


Park, Bo-yong, Lariviere, Sara, Rodriguez-Cruces, Raul, Royer, Jessica, Tavakol, Shahin, Wang, Yezhou, Caciagli, Lorenzo, Caligiuri, Maria Eugenia, Gambardella, Antonio, Concha, Luis
et al (show 77 more authors) (2022) Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy. BRAIN, 145 (4). pp. 1285-1298.


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.


Altmann, Andre ORCID: 0000-0002-9265-2393, Ryten, Mina, Di Nunzio, Martina, Ravizza, Teresa ORCID: 0000-0002-9578-018X, Tolomeo, Daniele, Reynolds, Regina, Somani, Alyma, Bacigaluppi, Marco, Iori, Valentina, Micotti, Edoardo
et al (show 88 more authors) (2018) A systems-level analysis highlights microglial activation as a modifying factor in common forms of human epilepsy. Unknown.


Altmann, Andre, Ryten, Mina, Di Nunzio, Martina, Ravizza, Teresa, Tolomeo, Daniele, Reynolds, Regina H, Somani, Alyma, Bacigaluppi, Marco, Iori, Valentina, Micotti, Edoardo
et al (show 90 more authors) (2022) A systems‐level analysis highlights microglial activation as a modifying factor in common epilepsies. Neuropathology and Applied Neurobiology, 48 (1). e12758-.

This list was generated on Sun Feb 11 06:05:26 2024 GMT.