Works matching AU Dixon, J. Michael

Results: 127
    1
    2
    3
    4
    5
    6
    7
    8
    9

    Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome.

    Published in:
    Nature Genetics, 2011, v. 43, n. 1, p. 20, doi. 10.1038/ng.724
    By:
    • Dauwerse, Johannes G.;
    • Dixon, Jill;
    • Seland, Saskia;
    • Ruivenkamp, Claudia A. L.;
    • van Haeringen, Arie;
    • Hoefsloot, Lies H.;
    • Peters, Dorien J. M.;
    • Boers, Agnes Clement-de;
    • Daumer-Haas, Cornelia;
    • Maiwald, Robert;
    • Zweier, Christiane;
    • Kerr, Bronwyn;
    • Cobo, Ana M.;
    • Toral, Joaquín F.;
    • Hoogeboom, A. Jeannette M.;
    • Lohmann, Dietmar R.;
    • Hehr, Ute;
    • Dixon, Michael J.;
    • Breuning, Martijn H.;
    • Wieczorek, Dagmar
    Publication type:
    Article
    10
    11
    12
    13

    Treacher Collins syndrome.

    Published in:
    2007
    By:
    • Dixon, J.;
    • Trainor, P.;
    • Dixon, M. J.;
    • Dixon, Jill;
    • Trainor, Paul;
    • Dixon, Michael J
    Publication type:
    journal article
    14
    15
    16

    Authors' reply.

    Published in:
    Histopathology, 1982, v. 6, n. 6, p. 816, doi. 10.1111/j.1365-2559.1982.tb02779.x
    By:
    • Dixon, J. Michael;
    • Anderson, Thomas J.;
    • Page, David L.;
    • Lee, D.;
    • Duffy, Stephen W.
    Publication type:
    Article
    17
    18
    19
    20

    Maastricht Delphi consensus on event Definitions for classification of recurrence in Breast cancer research.

    Published in:
    JNCI: Journal of the National Cancer Institute, 2014, v. 106, n. 12, p. 1, doi. 10.1093/jnci/dju288
    By:
    • Moossdorff, Martine;
    • van Roozendaal, Lori M.;
    • Strobbe, Luc J. A.;
    • Aebi, Stefan;
    • Cameron, David A.;
    • Dixon, J. Michael;
    • Giuliano, Armando E.;
    • Haffty, Bruce G.;
    • Hickey, Brigid E.;
    • Hudis, Clifford A.;
    • Klimberg, V. Suzanne;
    • Koczwara, Bogda;
    • Kühn, Thorsten;
    • Lippman, Marc E.;
    • Lucci, Anthony;
    • Piccart, Martine;
    • Smith, Benjamin D.;
    • Tjan-Heijnen, Vivianne C. G.;
    • van deVelde, Cornelis J. H.;
    • Van Zee, Kimberly J.
    Publication type:
    Article
    21

    Maastricht Delphi Consensus on Event Definitions for Classification of Recurrence in Breast Cancer Research.

    Published in:
    JNCI: Journal of the National Cancer Institute, 2014, v. 106, n. 12, p. 1, doi. 10.1093/jnci/dju288
    By:
    • Moossdorff, Martine;
    • van Roozendaal, Lori M.;
    • Strobbe, Luc J. A.;
    • Aebi, Stefan;
    • Cameron, David A.;
    • Dixon, J. Michael;
    • Giuliano, Armando E.;
    • Haffty, Bruce G.;
    • Hickey, Brigid E.;
    • Hudis, Clifford A.;
    • Klimberg, V. Suzanne;
    • Koczwara, Bogda;
    • Kühn, Thorsten;
    • Lippman, Marc E.;
    • Lucci, Anthony;
    • Piccart, Martine;
    • Smith, Benjamin D.;
    • Tjan-Heijnen, Vivianne C. G.;
    • van de Velde, Cornelis J. H.;
    • Van Zee, Kimberly J.
    Publication type:
    Article
    22
    23

    Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.

    Published in:
    Human Molecular Genetics, 2017, v. 26, n. 4, p. 829, doi. 10.1093/hmg/ddx012
    By:
    • Ludwig, Kerstin U.;
    • Böhmer, Anne C.;
    • Bowes, John;
    • Nikolić, Miloš;
    • Ishorst, Nina;
    • Wyatt, Niki;
    • Hammond, Nigel L.;
    • Gölz, Lina;
    • Thieme, Frederic;
    • Barth, Sandra;
    • Schuenke, Hannah;
    • Klamt, Johanna;
    • Spielmann, Malte;
    • Aldhorae, Khalid;
    • Rojas-Martinez, Augusto;
    • Nöthen, Markus M.;
    • Rada-Iglesias, Alvaro;
    • Dixon, Michael J.;
    • Knapp, Michael;
    • Mangold, Elisabeth
    Publication type:
    Article
    24

    Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 10, p. 2569, doi. 10.1093/hmg/ddt647
    By:
    • Rainger, Jacqueline K.;
    • Bhatia, Shipra;
    • Bengani, Hemant;
    • Gautier, Philippe;
    • Rainger, Joe;
    • Pearson, Matt;
    • Ansari, Morad;
    • Crow, Jayne;
    • Mehendale, Felicity;
    • Palinkasova, Bozena;
    • Dixon, Michael J.;
    • Thompson, Pamela J.;
    • Matarin, Mar;
    • Sisodiya, Sanjay M.;
    • Kleinjan, Dirk A.;
    • FitzPatrick, David R.
    Publication type:
    Article
    25
    26
    27

    Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders.

    Published in:
    American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 3, p. 545, doi. 10.1002/ajmg.a.36896
    By:
    • Leslie, Elizabeth J.;
    • O'Sullivan, James;
    • Cunningham, Michael L.;
    • Singh, Ankur;
    • Goudy, Steven L.;
    • Ababneh, Faroug;
    • Alsubaie, Lamia;
    • Ch'ng, Gaik‐Siew;
    • van der Laar, Ingrid M. B. H.;
    • M. Hoogeboom, A. Jeannette;
    • Dunnwald, Martine;
    • Kapoor, Seema;
    • Jiramongkolchai, Pawina;
    • Standley, Jennifer;
    • Manak, J. Robert;
    • Murray, Jeffrey C.;
    • Dixon, Michael J.
    Publication type:
    Article
    28

    Predicting response and resistance to endocrine therapy.

    Published in:
    Cancer (0008543X), 2008, v. 112, p. 689, doi. 10.1002/cncr.23187
    By:
    • Miller, William R.;
    • Larionov, Alexey;
    • Anderson, Thomas J.;
    • Dixon, J. Michael;
    • Walker, John R.;
    • Krause, Andreas;
    • Evans, Dean B.
    Publication type:
    Article
    29
    30
    31
    32
    33
    34
    35
    36

    Randomized Multicenter Trial of Sentinel Node Biopsy Versus Standard Axillary Treatment in Operable Breast Cancer: The ALMANAC Trial.

    Published in:
    JNCI: Journal of the National Cancer Institute, 2006, v. 98, n. 9, p. 599, doi. 10.1093/jnci/djj158
    By:
    • Mansel, Robert E.;
    • Fallowfield, Lesley;
    • Kissin, Mark;
    • Goyal, Amit;
    • Newcombe, Robert G.;
    • Dixon, J. Michael;
    • Yiangou, Constantinos;
    • Horgan, Kieran;
    • Bundred, Nigel;
    • Monypenny, Ian;
    • England, David;
    • Sibbering, Mark;
    • Abdullah, Tholkifl I.;
    • Barr, Lester;
    • Chetty, Utheshtra;
    • Sinnett, Dudley H.;
    • Fleissig, Anne;
    • Clarke, Dayalan;
    • Ell, Peter J.
    Publication type:
    Article
    37
    38
    39
    40
    41
    42
    43
    44
    45
    46
    47
    48
    49

    High prevalence of GPRC5A germline mutations in BRCA1-mutant breast cancer patients.

    Published in:
    International Journal of Cancer, 2014, v. 134, n. 10, p. 2352, doi. 10.1002/ijc.28569
    By:
    • Sokolenko, Anna P.;
    • Bulanova, Daria R.;
    • Iyevleva, Aglaya G.;
    • Aleksakhina, Svetlana N.;
    • Preobrazhenskaya, Elena V.;
    • Ivantsov, Alexandr O.;
    • Kuligina, Ekatherina Sh.;
    • Mitiushkina, Natalia V.;
    • Suspitsin, Evgeny N.;
    • Yanus, Grigoriy A.;
    • Zaitseva, Olga A.;
    • Yatsuk, Olga S.;
    • Togo, Alexandr V.;
    • Kota, Poojitha;
    • Dixon, J. Michael;
    • Larionov, Alexey A.;
    • Kuznetsov, Sergey G.;
    • Imyanitov, Evgeny N.
    Publication type:
    Article
    50