Resultats de la cerca - Nalls, Mike A

Uncovering the complexities of biological structures with network-based learning: An application in SARS-CoV-2 per Faghri, Faraz, Nalls, Mike A.

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Mendelian Randomization — the Key to Understanding Aspects of Parkinson's Disease Causation? per Noyce, Alastair J., Nalls, Mike A.

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The genetic architecture of Parkinson’s disease per Blauwendraat, Cornelis, Nalls, Mike A, Singleton, Andrew B

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Association of red cell distribution width with all-cause and cardiovascular-specific mortality in African American and white adults: a prospective cohort study per Tajuddin, Salman M., Nalls, Mike A., Zonderman, Alan B., Evans, Michele K.

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No Clear Support for a Role for Vitamin D in Parkinson’s Disease: A Mendelian Randomization Study per Larsson, Susanna C., Singleton, Andrew B., Nalls, Mike A., Richards, J. Brent

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The Parkinson’s phenome—traits associated with Parkinson’s disease in a broadly phenotyped cohort per Heilbron, Karl, Noyce, Alastair J., Fontanillas, Pierre, Alipanahi, Babak, Nalls, Mike A., Cannon, Paul

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Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability per Reynolds, Regina H., Botía, Juan, Nalls, Mike A., Hardy, John, Gagliano Taliun, Sarah A., Ryten, Mina

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Coding Variation in GBA Explains the Majority of the SYT11-GBA Parkinson’s Disease GWAS Locus per Blauwendraat, Cornelis, Bras, Jose M., Nalls, Mike A., Lewis, Patrick A., Hernandez, Dena G., Singleton, Andrew B.

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What Success Can Teach Us About Failure: The Plasma Metabolome of Older Adults with Superior Memory and Lessons for Alzheimer’s Disease per Mapstone, Mark, Lin, Feng, Nalls, Mike A., Cheema, Amrita K., Singleton, Andrew B., Fiandaca, Massimo S., Federoff, Howard J.

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Genetic risk and age in Parkinson’s: continuum not stratum per Nalls, Mike A., Escott-Price, Valentina, Williams, Nigel, Lubbe, Steven, Keller, Margaux F., Morris, Huw R., Singleton, Andrew B.

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Multimodal Neuroimaging and Behavioral Assessment of SNCA Polymorphism rs356219 in Older Adults per Burciu, Roxana G., Seidler, Rachael D., Shukla, Priyank, Nalls, Mike A., Singleton, Andrew B., Okun, Michael S., Vaillancourt, David E.

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Genetic variability at the PARK16 locus per Tucci, Arianna, Nalls, Mike A, Houlden, Henry, Revesz, Tamas, Singleton, Andrew B, Wood, Nicholas W, Hardy, John, Paisán-Ruiz, Coro

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Change in Epigenome-Wide DNA Methylation Over 9 Years and Subsequent Mortality: Results From the InCHIANTI Study per Moore, Ann Zenobia, Hernandez, Dena G., Tanaka, Toshiko, Pilling, Luke C., Nalls, Mike A., Bandinelli, Stefania, Singleton, Andrew B., Ferrucci, Luigi

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Finnish Parkinson’s disease study integrating protein-protein interaction network data with exome sequencing analysis per Siitonen, Ari, Kytövuori, Laura, Nalls, Mike A., Gibbs, Raphael, Hernandez, Dena G., Ylikotila, Pauli, Peltonen, Markku, Singleton, Andrew B., Majamaa, Kari

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A population scale analysis of rare SNCA variation in the UK Biobank per Blauwendraat, Cornelis, Makarious, Mary B., Leonard, Hampton L., Bandres-Ciga, Sara, Iwaki, Hirotaka, Nalls, Mike A., Noyce, Alastair J., Singleton, Andrew B.

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Proteomics and Epidemiological Models of Human Aging per Ubaida-Mohien, Ceereena, Moaddel, Ruin, Moore, Ann Zenobia, Kuo, Pei-Lun, Faghri, Faraz, Tharakan, Ravi, Tanaka, Toshiko, Nalls, Mike A., Ferrucci, Luigi

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Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk per Lake, Julie, Reed, Xylena, Langston, Rebekah G., Nalls, Mike A., Gan‐Or, Ziv, Cookson, Mark R., Singleton, Andrew B., Blauwendraat, Cornelis, Leonard, Hampton L.

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Clinical-genetic model predicts incident impulse control disorders in Parkinson’s disease per Kraemmer, Julia, Smith, Kara, Weintraub, Daniel, Guillemot, Vincent, Nalls, Mike A, Cormier-Dequaire, Florence, Moszer, Ivan, Brice, Alexis, Singleton, Andrew B, Corvol, Jean-Christophe

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Functionalization of the TMEM175 p.M393T variant as a risk factor for Parkinson disease per Jinn, Sarah, Blauwendraat, Cornelis, Toolan, Dawn, Gretzula, Cheryl A, Drolet, Robert E, Smith, Sean, Nalls, Mike A, Marcus, Jacob, Singleton, Andrew B, Stone, David J

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Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis per Johnson, Janel O., Glynn, Shannon M., Gibbs, J. Raphael, Nalls, Mike A., Sabatelli, Mario, Restagno, Gabriella, Drory, Vivian E., Chiò, Adriano, Rogaeva, Ekaterina, Traynor, Bryan J.

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