نتائج البحث - Nalls, Mike A
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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 حسب Tajuddin, Salman M., Nalls, Mike A., Zonderman, Alan B., Evans, Michele K.
منشور في 2017نص -
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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 حسب Mapstone, Mark, Lin, Feng, Nalls, Mike A., Cheema, Amrita K., Singleton, Andrew B., Fiandaca, Massimo S., Federoff, Howard J.
منشور في 2016نص -
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Multimodal Neuroimaging and Behavioral Assessment of SNCA Polymorphism rs356219 in Older Adults حسب Burciu, Roxana G., Seidler, Rachael D., Shukla, Priyank, Nalls, Mike A., Singleton, Andrew B., Okun, Michael S., Vaillancourt, David E.
منشور في 2018نص -
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Change in Epigenome-Wide DNA Methylation Over 9 Years and Subsequent Mortality: Results From the InCHIANTI Study حسب Moore, Ann Zenobia, Hernandez, Dena G., Tanaka, Toshiko, Pilling, Luke C., Nalls, Mike A., Bandinelli, Stefania, Singleton, Andrew B., Ferrucci, Luigi
منشور في 2016نص -
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Finnish Parkinson’s disease study integrating protein-protein interaction network data with exome sequencing analysis حسب Siitonen, Ari, Kytövuori, Laura, Nalls, Mike A., Gibbs, Raphael, Hernandez, Dena G., Ylikotila, Pauli, Peltonen, Markku, Singleton, Andrew B., Majamaa, Kari
منشور في 2019نص -
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A population scale analysis of rare SNCA variation in the UK Biobank حسب Blauwendraat, Cornelis, Makarious, Mary B., Leonard, Hampton L., Bandres-Ciga, Sara, Iwaki, Hirotaka, Nalls, Mike A., Noyce, Alastair J., Singleton, Andrew B.
منشور في 2020نص -
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Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk حسب Lake, Julie, Reed, Xylena, Langston, Rebekah G., Nalls, Mike A., Gan‐Or, Ziv, Cookson, Mark R., Singleton, Andrew B., Blauwendraat, Cornelis, Leonard, Hampton L.
منشور في 2021نص -
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Clinical-genetic model predicts incident impulse control disorders in Parkinson’s disease حسب Kraemmer, Julia, Smith, Kara, Weintraub, Daniel, Guillemot, Vincent, Nalls, Mike A, Cormier-Dequaire, Florence, Moszer, Ivan, Brice, Alexis, Singleton, Andrew B, Corvol, Jean-Christophe
منشور في 2016نص -
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Functionalization of the TMEM175 p.M393T variant as a risk factor for Parkinson disease حسب 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
منشور في 2019نص -
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Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis حسب 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.
منشور في 2014نص