Browse by People


Up a level
Export as [feed] RSS [feed] RSS 2.0 Short Author List
Number of items: 16.


Towns, Clodagh, Richer, Madeleine, Jasaityte, Simona, Stafford, Eleanor J, Joubert, Julie, Antar, Tarek, Martinez-Carrasco, Alejandro, Makarious, Mary B, Casey, Bradford, Vitale, Dan
et al (show 14 more authors) (2023) Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2). NPJ Parkinson's disease, 9 (1). p. 131.


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.


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. 475111-.


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.


Grover, Sandeep, Kumar Sreelatha, Ashwin Ashok, Pihlstrom, Lasse, Domenighetti, Cloe, Schulte, Claudia, Sugier, Pierre-Emmanuel, Radivojkov-Blagojevic, Milena, Lichtner, Peter, Mohamed, Oceane, Portugal, Berta
et al (show 73 more authors) (2022) Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease Evidence From the COURAGE-PD Consortium. NEUROLOGY, 99 (7). E698-E710.


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.


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-.


Kim, Jonggeol Jeffrey ORCID: 0000-0003-0738-0512, Vitale, Dan, Otani, Diego Véliz, Lian, Michelle Mulan, Heilbron, Karl, 23andMe Research Team, , Iwaki, Hirotaka, Lake, Julie ORCID: 0000-0002-3441-2455, Solsberg, Caroline Warly ORCID: 0000-0001-7049-6281, Leonard, Hampton
et al (show 10 more authors) (2024) Multi-ancestry genome-wide association meta-analysis of Parkinson's disease. Nature genetics, 56 (1). pp. 27-36.


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, 4 (11-20). 2023.11.06.23298176-.


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.


Grenn, Francis P, Kim, Jonggeol J, Makarious, Mary B, Iwaki, Hirotaka, Illarionova, Anastasia, Brolin, Kajsa, Kluss, Jillian H, Schumacher-Schuh, Artur F, Leonard, Hampton, Faghri, Faraz
et al (show 14 more authors) (2020) The Parkinson's DiseaseGenome-WideAssociation Study Locus Browser. MOVEMENT DISORDERS, 35 (11). pp. 2056-2067.


Liu, Hui ORCID: 0000-0001-5308-0874, Dehestani, Mohammad, Blauwendraat, Cornelis ORCID: 0000-0001-9358-8111, Makarious, Mary B, Leonard, Hampton, Kim, Jonggeol J, Schulte, Claudia, Noyce, Alastair ORCID: 0000-0003-3027-5497, Jacobs, Benjamin M, Foote, Isabelle ORCID: 0000-0002-0253-4116
et al (show 6 more authors) (2022) Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors. Annals of neurology, 92 (2). pp. 270-278.


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.


van der Lee, Sven J ORCID: 0000-0003-1606-8643, Conway, Olivia J, Jansen, Iris, Carrasquillo, Minerva M, Kleineidam, Luca ORCID: 0009-0006-3309-6856, van den Akker, Erik, Hernández, Isabel, van Eijk, Kristel R, Stringa, Najada, Chen, Jason A
et al (show 98 more authors) (2019) A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity. Acta neuropathologica, 138 (2). pp. 237-250.

This list was generated on Sat Apr 6 12:36:40 2024 BST.