Search Results - Nalls, Mike A

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

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

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The genetic architecture of Parkinson’s disease by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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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