Works matching AU Dickson, Dennis W.

Results: 624
    1

    TDP‐43 Cryptic RNAs in Perry Syndrome: Differences across Brain Regions and TDP‐43 Proteinopathies.

    Published in:
    Movement Disorders, 2025, v. 40, n. 4, p. 662, doi. 10.1002/mds.30104
    By:
    • Pickles, Sarah R.;
    • Gonzalez Bejarano, Jesus;
    • Narayan, Anand;
    • Daughrity, Lillian;
    • Maroto Cidfuentes, Candela;
    • Reeves, Madison M.;
    • Yue, Mei;
    • Castellanos Otero, Paula;
    • Estades Ayuso, Virginia;
    • Dunmore, Judy;
    • Song, Yuping;
    • Tong, Jimei;
    • DeTure, Michael;
    • Rawlinson, Bailey;
    • Castanedes‐Casey, Monica;
    • Dulski, Jaroslaw;
    • Cerquera‐Cleves, Catalina;
    • Zhang, Yongjie;
    • Josephs, Keith A.;
    • Dickson, Dennis W.
    Publication type:
    Article
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    ProtPipe: A Multifunctional Data Analysis Pipeline for Proteomics and Peptidomics Open Access.

    Published in:
    Genomics, Proteomics & Bioinformatics, 2024, v. 22, n. 6, p. 1, doi. 10.1093/gpbjnl/qzae083
    By:
    • Li, Ziyi;
    • Weller, Cory A;
    • Shah, Syed;
    • Johnson, Nicholas L;
    • Hao, Ying;
    • Jarreau, Paige B;
    • Roberts, Jessica;
    • Guha, Deyaan;
    • Bereda, Colleen;
    • Klaisner, Sydney;
    • Machado, Pedro;
    • Zanovello, Matteo;
    • Prudencio, Mercedes;
    • Oskarsson, Björn;
    • Staff, Nathan P;
    • Dickson, Dennis W;
    • Fratta, Pietro;
    • Petrucelli, Leonard;
    • Narayan, Priyanka;
    • Cookson, Mark R
    Publication type:
    Article
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    ATP13A2 variability in Parkinson disease.

    Published in:
    Human Mutation, 2009, v. 30, n. 3, p. 406, doi. 10.1002/humu.20877
    By:
    • Vilariño-Güell, Carles;
    • Soto, Alexandra I.;
    • Lincoln, Sarah J.;
    • Yahmed, Samia Ben;
    • Kefi, Mounir;
    • Heckman, Michael G.;
    • Hulihan, Mary M.;
    • Chai, Hua;
    • Diehl, Nancy N.;
    • Amouri, Rim;
    • Rajput, Alex;
    • Mash, Deborah C.;
    • Dickson, Dennis W.;
    • Middleton, Lefkos T.;
    • Gibson, Rachel A.;
    • Hentati, Faycal;
    • Farrer, Matthew J.
    Publication type:
    Article
    8

    Neuronal intranuclear inclusion disease is genetically heterogeneous.

    Published in:
    Annals of Clinical & Translational Neurology, 2020, v. 7, n. 9, p. 1716, doi. 10.1002/acn3.51151
    By:
    • Chen, Zhongbo;
    • Yan Yau, Wai;
    • Jaunmuktane, Zane;
    • Tucci, Arianna;
    • Sivakumar, Prasanth;
    • Gagliano Taliun, Sarah A.;
    • Turner, Chris;
    • Efthymiou, Stephanie;
    • Ibáñez, Kristina;
    • Sullivan, Roisin;
    • Bibi, Farah;
    • Athanasiou‐Fragkouli, Alkyoni;
    • Bourinaris, Thomas;
    • Zhang, David;
    • Revesz, Tamas;
    • Lashley, Tammaryn;
    • DeTure, Michael;
    • Dickson, Dennis W.;
    • Josephs, Keith A.;
    • Gelpi, Ellen
    Publication type:
    Article
    9

    Microglia in frontotemporal lobar degeneration with progranulin or C9ORF72 mutations.

    Published in:
    Annals of Clinical & Translational Neurology, 2019, v. 6, n. 9, p. 1782, doi. 10.1002/acn3.50875
    By:
    • Sakae, Nobutaka;
    • Roemer, Shanu F.;
    • Bieniek, Kevin F.;
    • Murray, Melissa E.;
    • Baker, Matthew C.;
    • Kasanuki, Koji;
    • Graff‐Radford, Neill R.;
    • Petrucelli, Leonard;
    • Van Blitterswijk, Marka;
    • Rademakers, Rosa;
    • Dickson, Dennis W.
    Publication type:
    Article
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    Clinicopathological and <sup>123</sup>I‐FP‐CIT SPECT correlations in patients with dementia.

    Published in:
    Annals of Clinical & Translational Neurology, 2018, v. 5, n. 3, p. 376, doi. 10.1002/acn3.521
    By:
    • Jung, Youngsin;
    • Jordan, III, Lennon G.;
    • Lowe, Val J.;
    • Kantarci, Kejal;
    • Parisi, Joseph E.;
    • Dickson, Dennis W.;
    • Murray, Melissa E.;
    • Reichard, Ross R.;
    • Ferman, Tanis J.;
    • Jones, David T.;
    • Graff‐Radford, Jonathan;
    • Savica, Rodolfo;
    • Machulda, Mary M.;
    • Fields, Julie A.;
    • Allen, Laura A.;
    • Drubach, Daniel A.;
    • St. Louis, Erik K.;
    • Silber, Michael H.;
    • Jack, Jr., Clifford R.;
    • Knopman, David S.
    Publication type:
    Article
    11

    Cancer in pathologically confirmed multiple system atrophy.

    Published in:
    Clinical Autonomic Research, 2023, v. 33, n. 4, p. 451, doi. 10.1007/s10286-023-00946-w
    By:
    • Cheshire, William P.;
    • Koga, Shunsuke;
    • Tipton, Philip W.;
    • Sekiya, Hiroaki;
    • Ross, Owen A.;
    • Uitti, Ryan J.;
    • Josephs, Keith A.;
    • Dickson, Dennis W.
    Publication type:
    Article
    12

    Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy.

    Published in:
    Clinical Autonomic Research, 2021, v. 31, n. 1, p. 117, doi. 10.1007/s10286-020-00759-1
    By:
    • Wernick, Anna I.;
    • Walton, Ronald L.;
    • Soto-Beasley, Alexandra I.;
    • Koga, Shunsuke;
    • Heckman, Michael G.;
    • Valentino, Rebecca R.;
    • Milanowski, Lukasz M.;
    • Hoffman-Zacharska, Dorota;
    • Koziorowski, Dariusz;
    • Hassan, Anhar;
    • Uitti, Ryan J.;
    • Cheshire, William P.;
    • Singer, Wolfgang;
    • Wszolek, Zbigniew K.;
    • Dickson, Dennis W.;
    • Low, Phillip A.;
    • Ross, Owen A.
    Publication type:
    Article
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    Association of Apolipoprotein E ε4 With Transactive Response DNA-Binding Protein 43.

    Published in:
    JAMA Neurology, 2018, v. 75, n. 11, p. 1347, doi. 10.1001/jamaneurol.2018.3139
    By:
    • Wennberg, Alexandra M.;
    • Tosakulwong, Nirubol;
    • Lesnick, Timothy G.;
    • Murray, Melissa E.;
    • Whitwell, Jennifer L.;
    • Liesinger, Amanda M.;
    • Petrucelli, Leonard;
    • Boeve, Bradley F.;
    • Parisi, Joseph E.;
    • Knopman, David S.;
    • Petersen, Ronald C.;
    • Dickson, Dennis W.;
    • Josephs, Keith A.
    Publication type:
    Article
    17

    Association Between Microinfarcts and Blood Pressure Trajectories.

    Published in:
    JAMA Neurology, 2018, v. 75, n. 2, p. 212, doi. 10.1001/jamaneurol.2017.3392
    By:
    • Graff-Radford, Jonathan;
    • Raman, Mekala R.;
    • Rabinstein, Alejandro A.;
    • Przybelski, Scott A.;
    • Lesnick, Timothy G.;
    • Boeve, Bradley F.;
    • Murray, Melissa E.;
    • Dickson, Dennis W.;
    • Reichard, R. Ross;
    • Parisi, Joseph E.;
    • Knopman, David S.;
    • Petersen, Ronald C.;
    • Jack, Clifford R.;
    • Kantarci, Kejal
    Publication type:
    Article
    18

    Duration and Pathologic Correlates of Lewy Body Disease.

    Published in:
    JAMA Neurology, 2017, v. 74, n. 3, p. 310, doi. 10.1001/jamaneurol.2016.4926
    By:
    • Graff-Radford, Jonathan;
    • Aakre, Jeremiah;
    • Savica, Rodolfo;
    • Boeve, Bradley;
    • Kremers, Walter K.;
    • Ferman, Tanis J.;
    • Jones, David T.;
    • Kantarci, Kejal;
    • Knopman, David S.;
    • Dickson, Dennis W.;
    • Kukull, Walter A.;
    • Petersen, Ronald C.
    Publication type:
    Article
    19

    Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease.

    Published in:
    JAMA Neurology, 2016, v. 73, n. 10, p. 1217, doi. 10.1001/jamaneurol.2016.2245
    By:
    • Davis, Marie Y.;
    • Johnson, Catherine O.;
    • Leverenz, James B.;
    • Weintraub, Daniel;
    • Trojanowski, John Q.;
    • Chen-Plotkin, Alice;
    • Van Deerlin, Vivianna M.;
    • Quinn, Joseph F.;
    • Chung, Kathryn A.;
    • Peterson-Hiller, Amie L.;
    • Rosenthal, Liana S.;
    • Dawson, Ted M.;
    • Albert, Marilyn S.;
    • Goldman, Jennifer G.;
    • Stebbins, Glenn T.;
    • Bernard, Bryan;
    • Wszolek, Zbigniew K.;
    • Ross, Owen A.;
    • Dickson, Dennis W.;
    • Eidelberg, David
    Publication type:
    Article
    20

    Clinical Correlations With Lewy Body Pathology in LRRK2-Related Parkinson Disease.

    Published in:
    JAMA Neurology, 2015, v. 72, n. 1, p. 100, doi. 10.1001/jamaneurol.2014.2704
    By:
    • Kalia, Lorraine V.;
    • Lang, Anthony E.;
    • Hazrati, Lili-Naz;
    • Fujioka, Shinsuke;
    • Wszolek, Zbigniew K.;
    • Dickson, Dennis W.;
    • Ross, Owen A.;
    • Van Deerlin, Vivianna M.;
    • Trojanowski, John Q.;
    • Hurtig, Howard I.;
    • Alcalay, Roy N.;
    • Marder, Karen S.;
    • Clark, Lorraine N.;
    • Gaig, Carles;
    • Tolosa, Eduardo;
    • Ruiz-Martínez, Javier;
    • Marti-Masso, Jose F.;
    • Ferrer, Isidre;
    • López de Munain, Adolfo;
    • Goldman, Samuel M.
    Publication type:
    Article
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    Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia.

    Published in:
    Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2013, v. 14, n. 5/6, p. 463, doi. 10.3109/21678421.2013.787630
    By:
    • van Blitterswijk, Marka;
    • Baker, Matthew C.;
    • Bieniek, Kevin F.;
    • Knopman, David S.;
    • Josephs, Keith A.;
    • Boeve, Bradley;
    • Caselli, Richard;
    • Wszolek, Zbigniew K.;
    • Petersen, Ronald;
    • Graff-Radford, Neill R.;
    • Boylan, Kevin B.;
    • Dickson, Dennis W.;
    • Rademakers, Rosa
    Publication type:
    Article
    23

    Clinical and electrophysiologic variability in amyotrophic lateral sclerosis within a kindred harboring the C9ORF72 repeat expansion.

    Published in:
    Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2013, v. 14, n. 3, p. 132, doi. 10.3109/17482968.2012.724075
    By:
    • Coon, Elizabeth A.;
    • Daube, Jasper R.;
    • Dejesus-Hernandez, Mariely;
    • Adeli, Anahita;
    • Savica, Rodolfo;
    • Parisi, Joseph E.;
    • Dickson, Dennis W.;
    • Josephs, Keith A.;
    • Baker, Matthew C.;
    • Johnson, Kris A.;
    • Ivnik, Robert J.;
    • Petersen, Ronald C.;
    • Knopman, David S.;
    • Boylan, Kevin B.;
    • Rademakers, Rosa;
    • Boeve, Bradley F.
    Publication type:
    Article
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    FTDP-17 with Pick body-like inclusions associated with a novel tau mutation, p.E372G.

    Published in:
    Brain Pathology, 2017, v. 27, n. 5, p. 612, doi. 10.1111/bpa.12428
    By:
    • Tacik, Pawel;
    • DeTure, Michael A.;
    • Carlomagno, Yari;
    • Lin, Wen‐Lang;
    • Murray, Melissa E.;
    • Baker, Matthew C.;
    • Josephs, Keith A.;
    • Boeve, Bradley F.;
    • Wszolek, Zbigniew K.;
    • Graff‐Radford, Neill R.;
    • Parisi, Joseph E.;
    • Petrucelli, Leonard;
    • Rademakers, Rosa;
    • Isaacson, Richard S.;
    • Heilman, Kenneth M.;
    • Petersen, Ronald C.;
    • Dickson, Dennis W.;
    • Kouri, Naomi
    Publication type:
    Article
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    Pick's Disease: A Modern Approach.

    Published in:
    Brain Pathology, 1998, v. 8, n. 2, p. 339, doi. 10.1111/j.1750-3639.1998.tb00158.x
    By:
    • Dickson, Dennis W.
    Publication type:
    Article
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    Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.

    Published in:
    Nature Genetics, 2011, v. 43, n. 7, p. 699, doi. 10.1038/ng.859
    By:
    • Höglinger, Günter U.;
    • Melhem, Nadine M.;
    • Dickson, Dennis W.;
    • Sleiman, Patrick M. A.;
    • Li-San Wang;
    • Klei, Lambertus;
    • Rademakers, Rosa;
    • de Silva, Rohan;
    • Litvan, Irene;
    • Riley, David E.;
    • van Swieten, John C.;
    • Heutink, Peter;
    • Wszolek, Zbigniew K.;
    • Uitti, Ryan J.;
    • Vandrovcova, Jana;
    • Hurtig, Howard I.;
    • Gross, Rachel G.;
    • Maetzler, Walter;
    • Goldwurm, Stefano;
    • Tolosa, Eduardo
    Publication type:
    Article
    48

    Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 234, doi. 10.1038/ng.536
    By:
    • Van Deerlin, Vivianna M.;
    • Sleiman, Patrick M. A.;
    • Martinez-Lage, Maria;
    • Chen-Plotkin, Alice;
    • Li-San Wang;
    • Graff-Radford, Neill R.;
    • Dickson, Dennis W.;
    • Rademakers, Rosa;
    • Boeve, Bradley F.;
    • Grossman, Murray;
    • Arnold, Steven E.;
    • Mann, David M. A.;
    • Pickering-Brown, Stuart M.;
    • Seelaar, Harro;
    • Heutink, Peter;
    • van Swieten, John C.;
    • Murrell, Jill R.;
    • Ghetti, Bernardino;
    • Spina, Salvatore;
    • Grafman, Jordan
    Publication type:
    Article
    49

    Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease.

    Published in:
    Nature Genetics, 2009, v. 41, n. 2, p. 192, doi. 10.1038/ng.305
    By:
    • Carrasquillo, Minerva M.;
    • Fanggeng Zou;
    • Pankratz, V. Shane;
    • Wilcox, Samantha L.;
    • Li Ma;
    • Walker, Louise P.;
    • Younkin, Samuel G.;
    • Younkin, Curtis S.;
    • Younkin, Linda H.;
    • Bisceglio, Gina D.;
    • Ertekin-Taner, Nilufer;
    • Crook, Julia E.;
    • Dickson, Dennis W.;
    • Petersen, Ronald C.;
    • Graff-Radford, Neill R.;
    • Younkin, Steven G.
    Publication type:
    Article
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