Works matching AU Hakon Hakonarson

Results: 375
    1
    2
    3

    Loci identified by a genome‐wide association study of carotid artery stenosis in the eMERGE network.

    Published in:
    Genetic Epidemiology, 2021, v. 45, n. 1, p. 4, doi. 10.1002/gepi.22360
    By:
    • Palmer, Melody R.;
    • Kim, Daniel S.;
    • Crosslin, David R.;
    • Stanaway, Ian B.;
    • Rosenthal, Elisabeth A.;
    • Carrell, David S.;
    • Cronkite, David J.;
    • Gordon, Adam;
    • Du, Xiaomeng;
    • Li, Yatong K.;
    • Williams, Marc S.;
    • Weng, Chunhua;
    • Feng, Qiping;
    • Li, Rongling;
    • Pendergrass, Sarah A.;
    • Hakonarson, Hakon;
    • Fasel, David;
    • Sohn, Sunghwan;
    • Sleiman, Patrick;
    • Handelman, Samuel K.
    Publication type:
    Article
    4

    Cover Image.

    Published in:
    Prenatal Diagnosis, 2023, v. 43, n. 13, p. i, doi. 10.1002/pd.6513
    By:
    • Martin, Kimberly;
    • Norton, Mary E.;
    • MacPherson, Cora;
    • Demko, Zachary;
    • Egbert, Melissa;
    • Haeri, Sina;
    • Malone, Fergal;
    • Wapner, Ronald J.;
    • Roman, Ashley S.;
    • Khalil, Asma;
    • Faro, Revital;
    • Madankumar, Rajeevi;
    • Strong, Noel;
    • Silver, Robert;
    • Vohra, Nidhi;
    • Hyett, Jon;
    • Kao, Charlly;
    • Hakonarson, Hakon;
    • Jacobson, Bo;
    • Dar, Pe'er
    Publication type:
    Article
    5

    Impact of high‐risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study.

    Published in:
    Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1574, doi. 10.1002/pd.6483
    By:
    • Martin, Kimberly;
    • Norton, Mary E.;
    • MacPherson, Cora;
    • Demko, Zachary;
    • Egbert, Melissa;
    • Haeri, Sina;
    • Malone, Fergal;
    • Wapner, Ronald J.;
    • Roman, Ashley S.;
    • Khalil, Asma;
    • Faro, Revital;
    • Madankumar, Rajeevi;
    • Strong, Noel;
    • Silver, Robert;
    • Vohra, Nidhi;
    • Hyett, Jon;
    • Kao, Charlly;
    • Hakonarson, Hakon;
    • Jacobson, Bo;
    • Dar, Pe'er
    Publication type:
    Article
    6
    7
    8
    9
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19
    20
    21

    Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study.

    Published in:
    Genes, 2023, v. 14, n. 1, p. 62, doi. 10.3390/genes14010062
    By:
    • Ron, Hayley A.;
    • Crowley, Terrence Blaine;
    • Liu, Yichuan;
    • Unolt, Marta;
    • Schindewolf, Erica;
    • Moldenhauer, Julie;
    • Rychik, Jack;
    • Goldmuntz, Elizabeth;
    • Emanuel, Beverly S.;
    • Ryba, Douglas;
    • Gaynor, James William;
    • Zackai, Elaine H.;
    • Hakonarson, Hakon;
    • McDonald-McGinn, Donna M.
    Publication type:
    Article
    22
    23
    24
    25
    26
    27
    28

    Genome-wide association study implicates novel loci and reveals candidate effector genes for longitudinal pediatric bone accrual.

    Published in:
    Genome Biology, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s13059-020-02207-9
    By:
    • Cousminer, Diana L.;
    • Wagley, Yadav;
    • Pippin, James A.;
    • Elhakeem, Ahmed;
    • Way, Gregory P.;
    • Pahl, Matthew C.;
    • McCormack, Shana E.;
    • Chesi, Alessandra;
    • Mitchell, Jonathan A.;
    • Kindler, Joseph M.;
    • Baird, Denis;
    • Hartley, April;
    • Howe, Laura;
    • Kalkwarf, Heidi J.;
    • Lappe, Joan M.;
    • Lu, Sumei;
    • Leonard, Michelle E.;
    • Johnson, Matthew E.;
    • Hakonarson, Hakon;
    • Gilsanz, Vicente
    Publication type:
    Article
    29

    A vascular endothelial growth factor A genetic variant is associated with improved ventricular function and transplant-free survival after surgery for non-syndromic CHD.

    Published in:
    2018
    By:
    • Mavroudis, Constantine D.;
    • Seung Kim, Daniel;
    • Burnham, Nancy;
    • Morss, Alexandra H.;
    • Kim, Jerry H.;
    • Burt, Amber A.;
    • Crosslin, David R.;
    • McDonald-McGinn, Donna M.;
    • Zackai, Elaine H.;
    • Cohen, Meryl S.;
    • Nicolson, Susan C.;
    • Spray, Thomas L.;
    • Stanaway, Ian B.;
    • Nickerson, Deborah A.;
    • Russell, Mark W.;
    • Hakonarson, Hakon;
    • Jarvik, Gail P.;
    • Gaynor, J. William
    Publication type:
    journal article
    30

    Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR).

    Published in:
    BioData Mining, 2015, v. 8, p. 1, doi. 10.1186/s13040-015-0074-0
    By:
    • De, Rishika;
    • Verma, Shefali S.;
    • Drenos, Fotios;
    • Holzinger, Emily R.;
    • Holmes, Michael V.;
    • Hall, Molly A.;
    • Crosslin, David R.;
    • Carrell, David S.;
    • Hakonarson, Hakon;
    • Jarvik, Gail;
    • Larson, Eric;
    • Pacheco, Jennifer A.;
    • Rasmussen-Torvik, Laura J.;
    • Moore, Carrie B.;
    • Asselbergs, Folkert W.;
    • Moore, Jason H.;
    • Ritchie, Marylyn D.;
    • Keating, Brendan J.;
    • Gilbert-Diamond, Diane
    Publication type:
    Article
    31
    32
    33
    34
    35
    36

    Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1126, doi. 10.1038/ng.2387
    By:
    • Diskin, Sharon J;
    • Capasso, Mario;
    • Schnepp, Robert W;
    • Cole, Kristina A;
    • Attiyeh, Edward F;
    • Hou, Cuiping;
    • Diamond, Maura;
    • Carpenter, Erica L;
    • Winter, Cynthia;
    • Lee, Hanna;
    • Jagannathan, Jayanti;
    • Latorre, Valeria;
    • Iolascon, Achille;
    • Hakonarson, Hakon;
    • Devoto, Marcella;
    • Maris, John M
    Publication type:
    Article
    37

    Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer.

    Published in:
    Nature Genetics, 2009, v. 41, n. 7, p. 811, doi. 10.1038/ng.393
    By:
    • Kanetsky, Peter A.;
    • Mitra, Nandita;
    • Vardhanabhuti, Saran;
    • Li, Mingyao;
    • Vaughn, David J.;
    • Letrero, Richard;
    • Ciosek, Stephanie L.;
    • Doody, David R.;
    • Smith, Lauren M.;
    • Weaver, JoEllen;
    • Albano, Anthony;
    • Chu Chen;
    • Starr, Jacqueline R.;
    • Rader, Daniel J.;
    • Godwin, Andrew K.;
    • Reilly, Muredach P.;
    • Hakonarson, Hakon;
    • Schwartz, Stephen M.;
    • Nathanson, Katherine L.
    Publication type:
    Article
    38
    39
    40

    A Mendelian Randomization Approach Using 3-HMG-Coenzyme-A Reductase Gene Variation to Evaluate the Association of Statin-Induced Low-Density Lipoprotein Cholesterol Lowering With Noncardiovascular Disease Phenotypes.

    Published in:
    JAMA Network Open, 2021, v. 4, n. 6, p. e2112820, doi. 10.1001/jamanetworkopen.2021.12820
    By:
    • Liu, Ge;
    • Shi, Mingjian;
    • Mosley, Jonathan D.;
    • Weng, Chunhua;
    • Zhang, Yanfei;
    • Lee, Ming Ta Michael;
    • Jarvik, Gail P.;
    • Hakonarson, Hakon;
    • Namjou-Khales, Bahram;
    • Sleiman, Patrick;
    • Luo, Yuan;
    • Mentch, Frank;
    • Denny, Joshua C.;
    • Linton, MacRae F.;
    • Wei, Wei-Qi;
    • Stein, C. Michael;
    • Feng, QiPing
    Publication type:
    Article
    41

    Genetic predisposition to longer telomere length and risk of childhood, adolescent and adult-onset ependymoma.

    Published in:
    Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01038-w
    By:
    • Zhang, Chenan;
    • Ostrom, Quinn T.;
    • Semmes, Eleanor C.;
    • Ramaswamy, Vijay;
    • Hansen, Helen M.;
    • Morimoto, Libby;
    • de Smith, Adam J.;
    • Pekmezci, Melike;
    • Vaksman, Zalman;
    • Hakonarson, Hakon;
    • Diskin, Sharon J.;
    • Metayer, Catherine;
    • The Glioma International Case-Control Study (GICC);
    • Claus, Elizabeth B.;
    • Il'yasova, Dora;
    • Walsh, Kyle M.;
    • Schildkraut, Joellen;
    • Barnholtz-Sloan, Jill S.;
    • Olson, Sara H.;
    • Bernstein, Jonine L.
    Publication type:
    Article
    42
    43
    44

    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
    45

    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
    46
    47
    48
    49
    50