Works matching AU Hakon Hakonarson

Results: 372
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    N-Acetylcysteine for Hereditary Cystatin C Amyloid Angiopathy: A Nonrandomized Clinical Trial.

    Published in:
    JAMA Neurology, 2025, v. 82, n. 5, p. 486, doi. 10.1001/jamaneurol.2025.0326
    By:
    • Snorradottir, Asbjorg Osk;
    • Gutierrez-Uzquiza, Alvaro;
    • Bragado, Paloma;
    • March, Michael E.;
    • Kao, Charlly;
    • Arkink, Enrico Bernardo;
    • Jonsdottir, Solveig;
    • Sigurdardottir, Arna;
    • Isaksson, Helgi J.;
    • Mariasdóttir, Hekla Liv;
    • Bjorgvinsdottir, Olga Yr;
    • Kowal, Natalia M.;
    • Heimisdottir, Hugrun L.;
    • Sverrisdottir, Astros;
    • Palsdottir, Astridur;
    • Bjornsson, Hans Tomas;
    • Hakonarson, Hakon
    Publication type:
    Article
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    Cover.

    Published in:
    Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2137
    By:
    • Maj, Mary;
    • Taylor, Christie L.;
    • Landau, Kevin;
    • Toriello, Helga V.;
    • Li, Dong;
    • Bhoj, Elizabeth J.;
    • Hakonarson, Hakon;
    • Nelson, Beverly;
    • Gluschitz, Sarah;
    • Walker, Ruth H.;
    • Sobering, Andrew K.
    Publication type:
    Article
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    Cover.

    Published in:
    Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 4, p. 1, doi. 10.1002/mgg3.1956
    By:
    • Verdi, Giavanna;
    • Li, Dong;
    • Elsea, Sarah H.;
    • Nelson, Beverly;
    • Bhoj, Elizabeth J.;
    • Hakonarson, Hakon;
    • Yearwood, Katherine R.;
    • Upadhya, Sharmila;
    • Gluschitz, Sarah;
    • Smith, Janice L.;
    • Sobering, Andrew K.
    Publication type:
    Article
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    Improved genetic risk scoring algorithm for type 1 diabetes prediction.

    Published in:
    Pediatric Diabetes, 2022, v. 23, n. 3, p. 320, doi. 10.1111/pedi.13310
    By:
    • Qu, Hui‐Qi;
    • Qu, Jingchun;
    • Glessner, Joseph;
    • Liu, Yichuan;
    • Mentch, Frank;
    • Chang, Xiao;
    • March, Michael;
    • Li, Jin;
    • Roizen, Jeffrey D.;
    • Connolly, John J.;
    • Sleiman, Patrick;
    • Hakonarson, Hakon
    Publication type:
    Article
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    Genome‐wide association analysis of psoriasis patients treated with anti‐TNF drugs.

    Published in:
    Experimental Dermatology, 2020, v. 29, n. 12, p. 1225, doi. 10.1111/exd.14215
    By:
    • Ovejero‐Benito, María C.;
    • Muñoz‐Aceituno, Ester;
    • Sabador, David;
    • Almoguera, Berta;
    • Prieto‐Pérez, Rocío;
    • Hakonarson, Hakon;
    • Coto‐Segura, Pablo;
    • Carretero, Gregorio;
    • Reolid, Alejandra;
    • Llamas‐Velasco, Mar;
    • Abad‐Santos, Francisco;
    • Daudén, Esteban
    Publication type:
    Article
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    Genome‐wide single nucleotide polymorphism‐based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa.

    Published in:
    Experimental Dermatology, 2019, v. 28, n. 10, p. 1118, doi. 10.1111/exd.13501
    By:
    • Vahidnezhad, Hassan;
    • Youssefian, Leila;
    • Saeidian, Amir Hossein;
    • Zeinali, Sirous;
    • Touati, Andrew;
    • Abiri, Maryam;
    • Sotoudeh, Soheila;
    • Norouz‐zadeh, Sara;
    • Amirinezhad, Niloufar;
    • Mozafari, Nikoo;
    • Daneshpazhooh, Maryam;
    • Mahmoudi, Hamidreza;
    • Hamid, Mohammad;
    • Bradfield, Jonathan P.;
    • Kim, Cecilia E.;
    • Hakonarson, Hakon;
    • Uitto, Jouni
    Publication type:
    Article
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    The Tehran longitudinal family-based cardiometabolic cohort study sheds new light on dyslipidemia transmission patterns.

    Published in:
    Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-53504-3
    By:
    • Akbarzadeh, Mahdi;
    • Riahi, Parisa;
    • Saeidian, Amir Hossein;
    • Zarkesh, Maryam;
    • Masjoudi, Sajedeh;
    • Asgarian, Sara;
    • Guity, Kamran;
    • Moheimani, Hamed;
    • Masoudi, Homayoon;
    • Roudbar, Mahmoud Amiri;
    • Khalili, Davood;
    • Hosseinpanah, Farhad;
    • Barzin, Maryam;
    • Hogan, Carolyn T.;
    • Hakonarson, Hakon;
    • Hedayati, Mehdi;
    • Daneshpour, Maryam S.;
    • Azizi, Fereidoun
    Publication type:
    Article
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    Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.

    Published in:
    2023
    By:
    • Ferar, Kathleen;
    • Hall, Taryn O.;
    • Crawford, Dana C.;
    • Rowley, Robb;
    • Satterfield, Benjamin A.;
    • Li, Rongling;
    • Gragert, Loren;
    • Karlson, Elizabeth W.;
    • de Andrade, Mariza;
    • Kullo, Iftikhar J.;
    • McCarty, Catherine A.;
    • Kho, Abel;
    • Hayes, M. Geoffrey;
    • Ritchie, Marylyn D.;
    • Crane, Paul K.;
    • Mirel, Daniel B.;
    • Carlson, Christopher;
    • Connolly, John J.;
    • Hakonarson, Hakon;
    • Crenshaw, Andrew T.
    Publication type:
    Correction Notice
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    Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.

    Published in:
    Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-45649-4
    By:
    • Ferar, Kathleen;
    • Hall, Taryn O.;
    • Crawford, Dana C.;
    • Rowley, Robb;
    • Satterfield, Benjamin A.;
    • Li, Rongling;
    • Gragert, Loren;
    • Karlson, Elizabeth W.;
    • de Andrade, Mariza;
    • Kullo, Iftikhar J.;
    • McCarty, Catherine A.;
    • Kho, Abel;
    • Hayes, M. Geoffrey;
    • Ritchie, Marylyn D.;
    • Crane, Paul K.;
    • Mirel, Daniel B.;
    • Carlson, Christopher;
    • Connolly, John J.;
    • Hakonarson, Hakon;
    • Crenshaw, Andrew T.
    Publication type:
    Article
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    Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.

    Published in:
    Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-45649-4
    By:
    • Ferar, Kathleen;
    • Hall, Taryn O.;
    • Crawford, Dana C.;
    • Rowley, Robb;
    • Satterfield, Benjamin A.;
    • Li, Rongling;
    • Gragert, Loren;
    • Karlson, Elizabeth W.;
    • de Andrade, Mariza;
    • Kullo, Iftikhar J.;
    • McCarty, Catherine A.;
    • Kho, Abel;
    • Hayes, M. Geoffrey;
    • Ritchie, Marylyn D.;
    • Crane, Paul K.;
    • Mirel, Daniel B.;
    • Carlson, Christopher;
    • Connolly, John J.;
    • Hakonarson, Hakon;
    • Crenshaw, Andrew T.
    Publication type:
    Article
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    Modeling genetic inheritance of copy number variations.

    Published in:
    Nucleic Acids Research, 2008, v. 36, n. 21, p. e138, doi. 10.1093/nar/gkn641
    By:
    • Wang, Kai;
    • Chen, Zhen;
    • Tadesse, Mahlet G.;
    • Glessner, Joseph;
    • Grant, Struan F. A.;
    • Hakonarson, Hakon;
    • Bucan, Maja;
    • Li, Mingyao
    Publication type:
    Article
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    Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39645-5
    By:
    • Gracia-Diaz, Carolina;
    • Zhou, Yijing;
    • Yang, Qian;
    • Maroofian, Reza;
    • Espana-Bonilla, Paula;
    • Lee, Chul-Hwan;
    • Zhang, Shuo;
    • Padilla, Natàlia;
    • Fueyo, Raquel;
    • Waxman, Elisa A.;
    • Lei, Sunyimeng;
    • Otrimski, Garrett;
    • Li, Dong;
    • Sheppard, Sarah E.;
    • Mark, Paul;
    • Harr, Margaret H.;
    • Hakonarson, Hakon;
    • Rodan, Lance;
    • Jackson, Adam;
    • Vasudevan, Pradeep
    Publication type:
    Article
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    Effects of a 5-Lipoxygenase–Activating Protein Inhibitor on Biomarkers Associated With Risk of Myocardial Infarction: A Randomized Trial.

    Published in:
    JAMA: Journal of the American Medical Association, 2005, v. 293, n. 18, p. 2245, doi. 10.1001/jama.293.18.2245
    By:
    • Hakonarson, Hakon;
    • Thorvaldsson, Sverrir;
    • Helgadottir, Anna;
    • Gudbjartsson, Daniel;
    • Zink, Florian;
    • Andresdottir, Margret;
    • Manolescu, Andrei;
    • Arnar, David O.;
    • Andersen, Karl;
    • Sigurdsson, Axel;
    • Thorgeirsson, Gestur;
    • Jonsson, Asgeir;
    • Agnarsson, Uggi;
    • Bjornsdottir, Halldora;
    • Gottskalksson, Gizur;
    • Einarsson, Atli;
    • Gudmundsdottir, Hrefna;
    • Adalsteinsdottir, Asdis E.;
    • Gudmundsson, Kolbeinn;
    • Kristjansson, Kristleifur
    Publication type:
    Article
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    Drug‐resistant epilepsy classified by a phenotyping algorithm associates with NTRK2.

    Published in:
    Acta Neurologica Scandinavica, 2019, v. 140, n. 3, p. 169, doi. 10.1111/ane.13115
    By:
    • Almoguera, Berta;
    • McGinnis, Emily;
    • Abrams, Debra;
    • Vazquez, Lyam;
    • Cederquist, Anna;
    • Sleiman, Patrick M.;
    • Dlugos, Dennis;
    • Hakonarson, Hakon;
    • Cagan, Andrew;
    • Connolly, John;
    • Gainer, Vivian S;
    • Garifallou, James;
    • Kaminski, Courtney;
    • Lee, Yvonne C.;
    • Mafra, Fernanda;
    • Mentch, Frank;
    • Pellegrino, Renata;
    • Qiu, Haijun;
    • Snyder, James;
    • Tian, Lifeng
    Publication type:
    Article
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    The novel atherosclerosis locus at 10q11 regulates plasma CXCL12 levels.

    Published in:
    European Heart Journal, 2011, v. 32, n. 8, p. 963, doi. 10.1093/eurheartj/ehr091
    By:
    • Mehta, Nehal N.;
    • Li, Mingyao;
    • William, Dilusha;
    • Khera, Amit V.;
    • DerOhannessian, Stephanie;
    • Qu, Liming;
    • Ferguson, Jane F.;
    • McLaughlin, Catherine;
    • Shaikh, Lalarukh Haris;
    • Shah, Rhia;
    • Patel, Parth N.;
    • Bradfield, Jonathan P.;
    • He, Jing;
    • Stylianou, Ioannis M.;
    • Hakonarson, Hakon;
    • Rader, Daniel J.;
    • Reilly, Muredach P.
    Publication type:
    Article
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    Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC.

    Published in:
    2020
    By:
    • Mishra, Rajashree;
    • Åkerlund, Mikael;
    • Cousminer, Diana L.;
    • Ahlqvist, Emma;
    • Bradfield, Jonathan P.;
    • Chesi, Alessandra;
    • Hodge, Kenyaita M.;
    • Guy, Vanessa C.;
    • Brillon, David J.;
    • Pratley, Richard E.;
    • Rickels, Michael R.;
    • Vella, Adrian;
    • Ovalle, Fernando;
    • Harris, Ronald I.;
    • Melander, Olle;
    • Varvel, Stephen;
    • Hakonarson, Hakon;
    • Froguel, Phillippe;
    • Lonsdale, John T.;
    • Mauricio, Didac
    Publication type:
    journal article
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    Inducible knockout of Clec16a in mice results in sensory neurodegeneration.

    Published in:
    Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-88895-0
    By:
    • Hain, Heather S.;
    • Pandey, Rahul;
    • Bakay, Marina;
    • Strenkowski, Bryan P.;
    • Harrington, Danielle;
    • Romer, Micah;
    • Motley, William W.;
    • Li, Jian;
    • Lancaster, Eunjoo;
    • Roth, Lindsay;
    • Grinspan, Judith B.;
    • Scherer, Steven S.;
    • Hakonarson, Hakon
    Publication type:
    Article
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    The polygenic architecture of left ventricular mass mirrors the clinical epidemiology.

    Published in:
    Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-64525-z
    By:
    • Mosley, Jonathan D.;
    • Levinson, Rebecca T.;
    • Farber-Eger, Eric;
    • Edwards, Todd L.;
    • Hellwege, Jacklyn N.;
    • Hung, Adriana M.;
    • Giri, Ayush;
    • Shuey, Megan M.;
    • Shaffer, Christian M.;
    • Shi, Mingjian;
    • Brittain, Evan L.;
    • Chung, Wendy K.;
    • Kullo, Iftikhar J.;
    • Arruda-Olson, Adelaide M.;
    • Jarvik, Gail P.;
    • Larson, Eric B.;
    • Crosslin, David R.;
    • Williams, Marc S.;
    • Borthwick, Ken M.;
    • Hakonarson, Hakon
    Publication type:
    Article