Works by Goate, Alison M.


Results: 182
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    Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis.

    Published in:
    JAMA Neurology, 2021, v. 78, n. 1, p. 102, doi. 10.1001/jamaneurol.2020.3536
    By:
    • Kunkle, Brian W.;
    • Schmidt, Michael;
    • Klein, Hans-Ulrich;
    • Naj, Adam C.;
    • Hamilton-Nelson, Kara L.;
    • Larson, Eric B.;
    • Evans, Denis A.;
    • De Jager, Phil L.;
    • Crane, Paul K.;
    • Buxbaum, Joe D.;
    • Ertekin-Taner, Nilufer;
    • Barnes, Lisa L.;
    • Fallin, M. Daniele;
    • Manly, Jennifer J.;
    • Go, Rodney C. P.;
    • Obisesan, Thomas O.;
    • Kamboh, M. Ilyas;
    • Bennett, David A.;
    • Hall, Kathleen S.;
    • Goate, Alison M.
    Publication type:
    Article
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    The Role of Cardiovascular Risk Factors and Stroke in Familial Alzheimer Disease.

    Published in:
    JAMA Neurology, 2016, v. 73, n. 10, p. 1231, doi. 10.1001/jamaneurol.2016.2539
    By:
    • Tosto, Giuseppe;
    • Bird, Thomas D.;
    • Bennett, David A.;
    • Boeve, Bradley F.;
    • Brickman, Adam M.;
    • Cruchaga, Carlos;
    • Faber, Kelley;
    • Foroud, Tatiana M.;
    • Farlow, Martin;
    • Goate, Alison M.;
    • Graff-Radford, Neill R.;
    • Lantigua, Rafael;
    • Manly, Jennifer;
    • Ottman, Ruth;
    • Rosenberg, Roger;
    • Schaid, Daniel J.;
    • Schupf, Nicole;
    • Stern, Yaakov;
    • Sweet, Robert A.;
    • Mayeux, Richard
    Publication type:
    Article
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    TREM2 Variant p.R47H as a Risk Factor for Sporadic Amyotrophic Lateral Sclerosis.

    Published in:
    JAMA Neurology, 2014, v. 71, n. 4, p. 449, doi. 10.1001/jamaneurol.2013.6237
    By:
    • Cady, Janet;
    • Koval, Erica D.;
    • Benitez, Bruno A.;
    • Zaidman, Craig;
    • Jockel-Balsarotti, Jennifer;
    • Allred, Peggy;
    • Baloh, Robert H.;
    • Ravits, John;
    • Simpson, Ericka;
    • Appel, Stanley H.;
    • Pestronk, Alan;
    • Goate, Alison M.;
    • Miller, Timothy M.;
    • Cruchaga, Carlos;
    • Harms, Matthew B.
    Publication type:
    Article
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    C9orf72 Hexanucleotide Repeat Expansions in Clinical Alzheimer Disease.

    Published in:
    JAMA Neurology, 2013, v. 70, n. 6, p. 736, doi. 10.1001/2013.jamaneurol.537
    By:
    • Harms, Matthew;
    • Benitez, Bruno A.;
    • Cairns, Nigel;
    • Cooper, Breanna;
    • Cooper, Paul;
    • Mayo, Kevin;
    • Carrell, David;
    • Faber, Kelley;
    • Williamson, Jennifer;
    • Bird, Tom;
    • Diaz-Arrastia, Ramon;
    • Foroud, Tatiana M.;
    • Boeve, Bradley F.;
    • Graff-Radford, Neill R.;
    • Mayeux, Richard;
    • Chakraverty, Sumitra;
    • Goate, Alison M.;
    • Cruchaga, Carlos
    Publication type:
    Article
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    Investigation of convergent and divergent genetic influences underlying schizophrenia and alcohol use disorder.

    Published in:
    Psychological Medicine, 2023, v. 53, n. 4, p. 1196, doi. 10.1017/S003329172100266X
    By:
    • Johnson, Emma C.;
    • Kapoor, Manav;
    • Hatoum, Alexander S.;
    • Zhou, Hang;
    • Polimanti, Renato;
    • Wendt, Frank R.;
    • Walters, Raymond K.;
    • Lai, Dongbing;
    • Kember, Rachel L.;
    • Hartz, Sarah;
    • Meyers, Jacquelyn L.;
    • Peterson, Roseann E.;
    • Ripke, Stephan;
    • Bigdeli, Tim B.;
    • Fanous, Ayman H.;
    • Pato, Carlos N.;
    • Pato, Michele T.;
    • Goate, Alison M.;
    • Kranzler, Henry R.;
    • O'Donovan, Michael C.
    Publication type:
    Article
    11

    Report of the APOE4 National Institute on Aging/Alzheimer Disease Sequencing Project Consortium Working Group: Reducing APOE4 in Carriers is a Therapeutic Goal for Alzheimer's Disease.

    Published in:
    Annals of Neurology, 2024, v. 95, n. 4, p. 625, doi. 10.1002/ana.26864
    By:
    • Vance, Jeffery M.;
    • Farrer, Lindsay A.;
    • Huang, Yadong;
    • Cruchaga, Carlos;
    • Hyman, Bradley T.;
    • Pericak‐Vance, Margaret A.;
    • Goate, Alison M.;
    • Greicius, Michael D.;
    • Griswold, Anthony J.;
    • Haines, Jonathan L.;
    • TCW, Julia;
    • Schellenberg, Gerard D.;
    • Tsai, Li‐Huei;
    • Herz, Joachim;
    • Holtzman, David M.
    Publication type:
    Article
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    Causal Associations Between Modifiable Risk Factors and the Alzheimer's Phenome.

    Published in:
    Annals of Neurology, 2021, v. 89, n. 1, p. 54, doi. 10.1002/ana.25918
    By:
    • Andrews, Shea J.;
    • Fulton‐Howard, Brian;
    • O'Reilly, Paul;
    • Marcora, Edoardo;
    • Goate, Alison M.;
    • Farrer, Lindsay A.;
    • Haines, Jonathan L.;
    • Mayeux, Richard;
    • Naj, Adam C.;
    • Pericak‐Vance, Margaret A.;
    • Schellenberg, Gerard D.;
    • Wang, Li‐San
    Publication type:
    Article
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    P3-287: TDP-43 A315T mutation in familial motor neuron disease

    Published in:
    2008
    By:
    • Gitcho, Michael A.;
    • Baloh, Robert H.;
    • Chakraverty, Sumi;
    • Mayo, Kevin;
    • Norton, Joanne B.;
    • Levitch, Denise;
    • Hatanpaa, Kimmo J.;
    • White, Charles H.;
    • Bigio, Eileen H.;
    • Caselli, Richard;
    • Baker, Matt;
    • Al-Lozi, Muhammad T.;
    • Morris, John C.;
    • Pestronk, Alan;
    • Rademakers, Rosa;
    • Goate, Alison M.;
    • Cairns, Nigel J.
    Publication type:
    Abstract
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    Genome-Wide Association Study of Cardiovascular Resilience Identifies Protective Variation in the CETP Gene.

    Published in:
    Journal of the American Heart Association, 2023, v. 12, n. 21, p. 1, doi. 10.1161/JAHA.123.031459
    By:
    • Chenglong Yu;
    • Bakshi, Andrew;
    • Watts, Gerald F.;
    • Renton, Alan E.;
    • Fulton-Howard, Brian;
    • Goate, Alison M.;
    • Natarajan, Pradeep;
    • Chasman, Daniel I.;
    • Robman, Liubov;
    • Woods, Robyn L.;
    • Guymer, Robyn;
    • Wolfe, Rory;
    • Le Thi Phuong Thao;
    • McNeil, John J.;
    • Tonkin, Andrew M.;
    • Nicholls, Stephen J.;
    • Lacaze, Paul
    Publication type:
    Article
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    TDP-43 A315T mutation in familial motor neuron disease.

    Published in:
    Annals of Neurology, 2008, v. 63, n. 4, p. 535, doi. 10.1002/ana.21344
    By:
    • Gitcho, Michael A.;
    • Baloh, Robert H.;
    • Chakraverty, Sumi;
    • Mayo, Kevin;
    • Norton, Joanne B.;
    • Levitch, Denise;
    • Hatanpaa, Kimmo J.;
    • White, Charles L.;
    • Bigio, Eileen H.;
    • Caselli, Richard;
    • Baker, Matt;
    • Al-Lozi, Muhammad T.;
    • Morris, John C.;
    • Pestronk, Alan;
    • Rademakers, Rosa;
    • Goate, Alison M.;
    • Cairns, Nigel J.
    Publication type:
    Article
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    HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin‐positive, tau‐negative inclusions caused by a missense mutation in the signal peptide of progranulin.

    Published in:
    Annals of Neurology, 2006, v. 60, n. 3, p. 314
    By:
    • Odity Mukherjee;
    • Pau Pastor;
    • Nigel J. Cairns;
    • Sumi Chakraverty;
    • John S. K. Kauwe;
    • Shantia Shears;
    • Maria I. Behrens;
    • John Budde;
    • Anthony L. Hinrichs;
    • Joanne Norton;
    • Denise Levitch;
    • Lisa Taylor‐Reinwald;
    • Michael Gitcho;
    • P.‐H. Tu;
    • Lea Tenenholz Grinberg;
    • Rajka M. Liscic;
    • Javier Armendariz;
    • John C. Morris;
    • Alison M. Goate
    Publication type:
    Article
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    Discovery and validation of dominantly inherited Alzheimer's disease mutations in populations from Latin America.

    Published in:
    Alzheimer's Research & Therapy, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13195-022-01052-1
    By:
    • Takada, Leonel Tadao;
    • Aláez-Verson, Carmen;
    • Burgute, Bhagyashri D.;
    • Nitrini, Ricardo;
    • Sosa, Ana Luisa;
    • Castilhos, Raphael Machado;
    • Chaves, Marcia Fagundes;
    • Longoria, Erika-Mariana;
    • Carrillo-Sánchez, Karol;
    • Brucki, Sonia Maria Dozzi;
    • Flores-Lagunes, Luis Leonardo;
    • Molina, Carolina;
    • Olivares, Marcos Jimenez;
    • Ziegemeier, Ellen;
    • Petranek, Jennifer;
    • Goate, Alison M.;
    • Cruchaga, Carlos;
    • Renton, Alan E.;
    • Fernández, Maria Victoria;
    • Day, Gregory S.
    Publication type:
    Article
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    Human apoE Isoforms Differentially Regulate Brain Amyloid-b Peptide Clearance.

    Published in:
    Science Translational Medicine, 2011, v. 3, n. 89, p. 1, doi. 10.1126/scitranslmed.3002156
    By:
    • Castellano, Joseph M.;
    • Kim, Jungsu;
    • Stewart, Floy R.;
    • Jiang, Hong;
    • DeMattos, Ronald B.;
    • Patterson, Bruce W.;
    • Fagan, Anne M.;
    • Morris, John C.;
    • Mawuenyega, Kwasi G.;
    • Cruchaga, Carlos;
    • Goate, Alison M.;
    • Bales, Kelly R.;
    • Paul, Steven M.;
    • Bateman, Randall J.;
    • Holtzman, David M.
    Publication type:
    Article
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    Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer’s Disease.

    Published in:
    PLoS ONE, 2016, v. 11, n. 6, p. 1, doi. 10.1371/journal.pone.0150079
    By:
    • Sassi, Celeste;
    • Ridge, Perry G.;
    • Nalls, Michael A.;
    • Gibbs, Raphael;
    • Ding, Jinhui;
    • Lupton, Michelle K.;
    • Troakes, Claire;
    • Lunnon, Katie;
    • Al-Sarraj, Safa;
    • Brown, Kristelle S.;
    • Medway, Christopher;
    • Lord, Jenny;
    • Turton, James;
    • null, null;
    • Morgan, Kevin;
    • Powell, John F.;
    • Kauwe, John S.;
    • Cruchaga, Carlos;
    • Bras, Jose;
    • Goate, Alison M.
    Publication type:
    Article
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    CHRNB3 is more strongly associated with Fagerström Test for Cigarette Dependence-based nicotine dependence than cigarettes per day: phenotype definition changes genome-wide association studies results.

    Published in:
    2012
    By:
    • Rice, John P.;
    • Hartz, Sarah M.;
    • Agrawal, Arpana;
    • Almasy, Laura;
    • Bennett, Siiri;
    • Breslau, Naomi;
    • Bucholz, Kathleen K.;
    • Doheny, Kimberly F.;
    • Edenberg, Howard J.;
    • Goate, Alison M.;
    • Hesselbrock, Victor;
    • Howells, William B.;
    • Johnson, Eric O.;
    • Kramer, John;
    • Krueger, Robert F.;
    • Kuperman, Samuel;
    • Laurie, Cathy;
    • Manolio, Teri A.;
    • Neuman, Rosalind J.;
    • Nurnberger, John I.
    Publication type:
    Journal Article
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    CHRNB3 is more strongly associated with Fagerström Test for Cigarette Dependence-based nicotine dependence than cigarettes per day: phenotype definition changes genome-wide association studies results.

    Published in:
    Addiction, 2012, v. 107, n. 11, p. 2019, doi. 10.1111/j.1360-0443.2012.03922.x
    By:
    • Rice, John P.;
    • Hartz, Sarah M.;
    • Agrawal, Arpana;
    • Almasy, Laura;
    • Bennett, Siiri;
    • Breslau, Naomi;
    • Bucholz, Kathleen K.;
    • Doheny, Kimberly F.;
    • Edenberg, Howard J.;
    • Goate, Alison M.;
    • Hesselbrock, Victor;
    • Howells, William B.;
    • Johnson, Eric O.;
    • Kramer, John;
    • Krueger, Robert F.;
    • Kuperman, Samuel;
    • Laurie, Cathy;
    • Manolio, Teri A.;
    • Neuman, Rosalind J.;
    • Nurnberger, John I.
    Publication type:
    Article