Channel:  Aligning Science Across Parkinson's (ASAP)

458 Articles

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CNV-Finder: Streamlining Copy Number Variation Discovery
Kuznetsov, N., Daida, K., Makarious, M. B., Al-Mubarak, B., Atterling Brolin, K., Malik, L., Kouam, C., Baker, B., Real, R., Step, K., Lange, L. M., Wu, L., Ostrozovicova, M., Andersh, K. M., Kung, P.-J., Mecheri, Y., Tay, Y.-W., Soundous Malek, B., Al Tassan, N., Teresa Perinan, M., Hong, S., Koretsky, M. J., Sargeant, L., Levine, K., Blauwendraat, C., Billingsley, K. J., Bandres-Ciga, S., Leonard, H. L., Bardien, S., Morris, H. R., Singleton, A. B., Nalls, M. A., Vitale, D., The Global Parkinson's Genetics Program
10.1101/2024.11.22.624040 — Posted: 2025-07-26
Sex-stratified analysis of the potential association between PGLYRP2 rs892145 variant and Parkinson's disease across diverse ancestral populations
Avila, C. L., Chaparro Solano, H. M., Quintana-Pena, V., Aberg, K., the Global Parkinson's Genetics Program (GP2), , Atterling Brolin, K.
10.1101/2025.07.23.25331993 — Posted: 2025-07-24
DIO-SPOTlight Transgenic Mouse to Functionally Monitor Protein Synthesis Regulated by the Integrated Stress Response
Oliver, M. L., Caffall, Z. F., Eatman, C. B., Faw, T. D., Calakos, N.
10.1101/2024.10.14.618312 — Posted: 2025-07-23
Enhanced beta power emerges from simulated parkinsonian primary motorcortex
Doherty, D. W., Chen, L., Smith, Y., Wichmann, T., Chu, H.-Y., Lytton, W. W.
10.1101/2024.05.23.595566 — Posted: 2025-07-20
Genotype-phenotype association study conducted on LARGE-PD reveals novel loci associated with Parkinson's Disease.
Leal, T. P., Waldo, E., Duarte-Zambrano, F., Inca-Martinez, M., Ramchandra, J., Chaparro-Solano, H. M., Anello, A. E., Borda, V., Gouveia, M. H., Teixeira-dos-Santos, D., Reyes-Perez, P., Gatto, E. M., Santos-Lobato, B. L., Eufraseo, G., Letro, G. H., Arboleda, G., Bernal-Pacheco, O., Orozco, J., Munoz, B., Chana-Cuevas, P., Aguillon, D., Moreno, S., Torrealba-Acosta, G., Lobo-Prada, T., Muller, V., Lopez Razquin, C. M., Braga-Neto, P., Duron, R., Rodriguez-Violante, M., Hernandez-Medrano, A. J., Cervantes-Arriaga, A., Martinez-Ramirez, D., Schuh, A. F. S., de Mello Rieder, C. R., Cornejo-Oliv
10.1101/2025.07.18.25331793 — Posted: 2025-07-18
Mapping the causal chain from genetic risk variants to lipid dysmetabolism in Parkinsons disease
DePaula, R., Kim, J., Rhinn, H., Saade, H., Chavez, F., Segura, T., Lozano, M. V., Etoundi, M., Silos, K., Korchina, V., doddapaneni, h. v., Venner, E., Masdeu, J. C., Pavlik, V., Yu, M. M., Lin, C.-Y. R., Jankovic, J., Buchman, A. S., Muzny, D. M., Gibbs, R. A., Elsea, S. H., Abeliovich, A., Lansbury, P., Vanegas-Arroyave, N., Shaw, C. A., Shulman, J. M.
10.1101/2025.07.14.25331535 — Posted: 2025-07-15
The Global Landscape of Genetic Variation in Parkinson's disease: Multi-Ancestry Insights into Established Disease Genes and their Translational Relevance
Lange, L. M., Fang, Z.-H., Makarious, M. B., Kuznetsov, N., Atterling Brolin, K., Ballard, S., Bardien, S., Doquenia, M. L., Heutink, P., Houlden, H., Iwaki, H., Jasaityte, S., Jones, L., Junker, J., Kaiyrzhanov, R., Koretsky, M., Kumar, K. R., the Latin American Research Consortium on the Genetics of Parkinson's Disease (LARGE-PD), , Leonard, H., Levine, K., Lim, S.-Y., Mencacci, N. E., Mohamed, W. M. Y., Nalls, M. A., Noyce, A., Ojha, R., Okubadejo, N. U., Rehman, S. u., Screven, L., Shashkin, C., Sopromadze, S., Stafford, E. J., Tan, A. H., Tan, M., Tavadyan, Z., Trinh, J., Tserensodnom, B
10.1101/2025.07.08.25330815 — Posted: 2025-07-11
Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's Disease
Lange, L. M., Fang, Z.-H., Screven, L., Tan, A. H., Alcalay, R. N., Amouri, R., Bovenzi, R., Fenn, M., Frost, J. L. I., Jankovic, J., Jasaityte, S., Jaunmuktane, Z., Jeon, B., Keller Sarmiento, I. J., Krueger, R., Kuhlenbaeumer, G., Lin, C.-H., Pavelka, L., Perinan, M. T. M., Ben Sassi, S., Schirinzi, T., Shin, J. H., Shulman, J. M., Tay, Y. W., Uitti, R., Warner, T., Wszolek, Z. K., Wu, L., Wu, R.-M., Zeuner, K. E., Blauwendraat, C., Singleton, A., Mencacci, N. E., Morris, H., Lim, S.-Y., Lohmann, K., Klein, C., the Global Parkinson's Genetics Program (GP2)
10.1101/2025.07.10.25330831 — Posted: 2025-07-11
Cryo-electron tomography reveals the microtubule-bound form of inactive LRRK2
Chen, S., Basiashvili, T., Hutchings, J., Murillo, M. S., Suarez, A. V., Xiong, E., Louro, J. A., Leschziner, A. E., Villa, E.
10.1101/2024.06.18.599606 — Posted: 2025-07-10
Mitochondrial fission controls astrocyte morphogenesis and organization in the cortex
Salazar, M. P. R., Kolanukuduru, S., Ramirez, V., Lyu, B., Manigault, G., Sejourne, G., Sesaki, H., Yu, G., Eroglu, C.
10.1101/2024.10.22.619706 — Posted: 2025-07-03

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