Works matching AU Myers, Richard M.

Results: 100
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    Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects.

    Published in:
    Nature Genetics, 2008, v. 40, n. 8, p. 963, doi. 10.1038/ng.188
    By:
    • McGowan, Kelly A.;
    • Li, Jun Z.;
    • Park, Christopher Y.;
    • Beaudry, Veronica;
    • Tabor, Holly K.;
    • Sabnis, Amit J.;
    • Weibin Zhang;
    • Fuchs, Helmut;
    • Angelis, Martin Hrabé de;
    • Myers, Richard M.;
    • Attardi, Laura D.;
    • Barsh, Gregory S.
    Publication type:
    Article
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    Mitochondria DNA copy number, mitochondria DNA total somatic deletions, Complex I activity, synapse number, and synaptic mitochondria number are altered in schizophrenia and bipolar disorder.

    Published in:
    Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02127-1
    By:
    • Das, Sujan C.;
    • Hjelm, Brooke E.;
    • Rollins, Brandi L.;
    • Sequeira, Adolfo;
    • Morgan, Ling;
    • Omidsalar, Audrey A.;
    • Schatzberg, Alan F.;
    • Barchas, Jack D.;
    • Lee, Francis S.;
    • Myers, Richard M.;
    • Watson, Stanley J.;
    • Akil, Huda;
    • Bunney, William E.;
    • Vawter, Marquis P.
    Publication type:
    Article
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    Mitochondrial involvement in psychiatric disorders.

    Published in:
    Annals of Medicine, 2008, v. 40, n. 4, p. 281, doi. 10.1080/07853890801923753
    By:
    • Shao, Ling;
    • Martin, Maureen V.;
    • Watson, Stanley J.;
    • Schatzberg, Alan;
    • Akil, Huda;
    • Myers, Richard M.;
    • Jones, Edward G.;
    • Bunney, William E.;
    • Vawter, Marquis P.
    Publication type:
    Article
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    Mitochondrial Mutations in Subjects with Psychiatric Disorders.

    Published in:
    PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0127280
    By:
    • Sequeira, Adolfo;
    • Rollins, Brandi;
    • Magnan, Christophe;
    • van Oven, Mannis;
    • Baldi, Pierre;
    • Myers, Richard M.;
    • Barchas, Jack D.;
    • Schatzberg, Alan F.;
    • Watson, Stanley J.;
    • Akil, Huda;
    • Bunney, William E.;
    • Vawter, Marquis P.
    Publication type:
    Article
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    PEA15 loss of function and defective cerebral development in the domestic cat.

    Published in:
    PLoS Genetics, 2020, v. 16, n. 12, p. 1, doi. 10.1371/journal.pgen.1008671
    By:
    • Graff, Emily C.;
    • Cochran, J. Nicholas;
    • Kaelin, Christopher B.;
    • Day, Kenneth;
    • Gray-Edwards, Heather L.;
    • Watanabe, Rie;
    • Koehler, Jey W.;
    • Falgoust, Rebecca A.;
    • Prokop, Jeremy W.;
    • Myers, Richard M.;
    • Cox, Nancy R.;
    • Barsh, Gregory S.;
    • Martin, Douglas R.
    Publication type:
    Article
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    Neurotransmission-related gene expression in the frontal pole is altered in subjects with bipolar disorder and schizophrenia.

    Published in:
    Translational Psychiatry, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41398-023-02418-1
    By:
    • Medina, Adriana M.;
    • Hagenauer, Megan Hastings;
    • Krolewski, David M.;
    • Hughes, Evan;
    • Forrester, Liam Cannon Thew;
    • Walsh, David M.;
    • Waselus, Maria;
    • Richardson, Evelyn;
    • Turner, Cortney A.;
    • Sequeira, P. Adolfo;
    • Cartagena, Preston M.;
    • Thompson, Robert C.;
    • Vawter, Marquis P.;
    • Bunney, Blynn G.;
    • Myers, Richard M.;
    • Barchas, Jack D.;
    • Lee, Francis S.;
    • Schatzberg, Alan F.;
    • Bunney, William E.;
    • Akil, Huda
    Publication type:
    Article
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    Exclusion of Linkage to the HLA Region in Ninety Multiplex Sibships with Autism.

    Published in:
    Journal of Autism & Developmental Disorders, 1999, v. 29, n. 3, p. 195, doi. 10.1023/A:1023075904742
    By:
    • Rogers, Tamara;
    • Kalaydjieva, Luba;
    • Hallmayer, Joachim;
    • Petersen, P. Brent;
    • Nicholas, Peter;
    • Pingree, Carmen;
    • McMahon, William M.;
    • Spiker, Donna;
    • Lotspeich, Linda;
    • Kraemer, Helena;
    • McCague, Patty;
    • Dimiceli, Sue;
    • Nouri, Nassim;
    • Peachy, Tawna;
    • Yang, Joan;
    • Hinds, David;
    • Risch, Neil;
    • Myers, Richard M.
    Publication type:
    Article
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    Identification of cis‐regulatory elements associated with MAPT expression in human induced pluripotent stem cell derived neural cells.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.072171
    By:
    • Rogers, Brianne B.;
    • Anderson, Ashlyn G;
    • Lauzon, Shelby N.;
    • Davis, M. Natalie;
    • Hauser, Rebecca M.;
    • Roberts, Sydney C.;
    • Rodriguez‐Nunez, Ivan;
    • Trausch‐Lowther, Katie;
    • Roberts, Brian S.;
    • Barinaga, Erin A.;
    • Rizzardi, Lindsay F.;
    • Cooper, Sara J.;
    • Myers, Richard M.;
    • Cochran, J. Nicholas
    Publication type:
    Article
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    Identification of cis‐regulatory elements associated with MAPT expression in human induced pluripotent stem cell derived neural cells.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.072171
    By:
    • Rogers, Brianne B.;
    • Anderson, Ashlyn G;
    • Lauzon, Shelby N.;
    • Davis, M. Natalie;
    • Hauser, Rebecca M.;
    • Roberts, Sydney C.;
    • Rodriguez‐Nunez, Ivan;
    • Trausch‐Lowther, Katie;
    • Roberts, Brian S.;
    • Barinaga, Erin A.;
    • Rizzardi, Lindsay F.;
    • Cooper, Sara J.;
    • Myers, Richard M.;
    • Cochran, J. Nicholas
    Publication type:
    Article
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    P3‐143: UTILITY OF GENOMIC SEQUENCING IN CASES OF EARLY‐ONSET AND FAMILIAL DEMENTIA.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P986, doi. 10.1016/j.jalz.2019.06.3171
    By:
    • Cochran, Meagan E.;
    • Cochran, J. Nicholas;
    • McKinley, Emily;
    • Amaral, Michelle D.;
    • Moyer, Bryan;
    • Lasseigne, Brittany N.;
    • Gray, David;
    • Lawlor, James M.J.;
    • Prokop, Jeremy;
    • Newberry, J. Scott;
    • Worthey, Elizabeth A.;
    • Geldmacher, David S.;
    • Natelson Love, Marissa C.;
    • Myers, Richard M.;
    • Roberson, Erik D.
    Publication type:
    Article
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    P2‐126: LOSS‐OF‐FUNCTION CODING AND NON‐CODING VARIANTS IN TET2 ARE ASSOCIATED WITH NEURODEGENERATIVE DISEASES.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P620, doi. 10.1016/j.jalz.2019.06.2533
    By:
    • Cochran, J. Nicholas;
    • Geier, Ethan G.;
    • Acosta-Uribe, Juliana;
    • Thompson, Michelle L.;
    • Amaral, Michelle D.;
    • Newberry, J. Scott;
    • Lawlor, James M.J.;
    • Lasseigne, Brittany N.;
    • Cochran, Meagan E.;
    • Bonham, Luke W.;
    • Karydas, Anna M.;
    • Roberson, Erik D.;
    • Lopera, Francisco;
    • Kosik, Kenneth S.;
    • Cooper, Gregory M.;
    • Rabinovici, Gil D.;
    • Miller, Bruce L.;
    • Myers, Richard M.;
    • Yokoyama, Jennifer S.
    Publication type:
    Article
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    Genetic origin of a large family with a novel PSEN1 mutation (Ile416Thr).

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, n. 5, p. 709, doi. 10.1016/j.jalz.2018.12.010
    By:
    • Ramirez Aguilar, Laura;
    • Acosta‐Uribe, Juliana;
    • Giraldo, Margarita M.;
    • Moreno, Sonia;
    • Baena, Ana;
    • Alzate, Diana;
    • Cuastumal, Rosario;
    • Aguillón, David;
    • Madrigal, Lucía;
    • Saldarriaga, Amanda;
    • Navarro, Alexander;
    • Garcia, Gloria P.;
    • Aguirre‐Acevedo, Daniel C.;
    • Geier, Ethan G.;
    • Cochran, J. Nicholas;
    • Quiroz, Yakeel T.;
    • Myers, Richard M.;
    • Yokoyama, Jennifer S.;
    • Kosik, Kenneth S.;
    • Lopera, Francisco
    Publication type:
    Article
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    The development of sequence-tagged sites for human chromosome 4.

    Published in:
    Human Molecular Genetics, 1993, v. 2, n. 8, p. 1271
    By:
    • Goold, Richard D.;
    • diSibio, Guy L.;
    • Xu, Haidong;
    • Lang, David B.;
    • Dadgar, Jahan;
    • Magrane, Gregg G.;
    • Dugaiczyk, Achilles;
    • Smith, Kristen A.;
    • Cox, David W.;
    • Masters, Susan B.;
    • Myers, Richard M.
    Publication type:
    Article
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