Works matching IS 10614036 AND DT 2011 AND VI 43 AND IP 4

Results: 27
    1

    Erratum: Genome-wide association identifies multiple ulcerative colitis susceptibility loci.

    Published in:
    2011
    By:
    • McGovern, Dermot P. B.;
    • Gardet, Agnès;
    • Törkvist, Leif;
    • Goyette, Philippe;
    • Essers, Jonah;
    • Taylor, Kent D.;
    • Neale, Benjamin M.;
    • Ong, Rick T. H.;
    • Lagacé, Caroline;
    • Li, Chun;
    • Green, Todd;
    • Stevens, Christine R.;
    • Beauchamp, Claudine;
    • Fleshner, Phillip R.;
    • Carlson, Marie;
    • D'Amato, Mauro;
    • Halfvarson, Jonas;
    • Hibberd, Martin L.;
    • Lördal, Mikael;
    • Padyukov, Leonid
    Publication type:
    Correction Notice
    2

    Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 365, doi. 10.1038/ng.780
    By:
    • Goudie, David R.;
    • D'Alessandro, Mariella;
    • Merriman, Barry;
    • Lee, Hane;
    • Szeverényi, Ildikó;
    • Avery, Stuart;
    • O'Connor, Brian D.;
    • Nelson, Stanley F.;
    • Coats, Stephanie E.;
    • Stewart, Arlene;
    • Christie, Lesley;
    • Pichert, Gabriella;
    • Friedel, Jean;
    • Hayes, Ian;
    • Burrows, Nigel;
    • Whittaker, Sean;
    • Gerdes, Anne-Marie;
    • Broesby-Olsen, Sigurd;
    • Ferguson-Smith, Malcolm A.;
    • Verma, Chandra
    Publication type:
    Article
    3
    4

    Research highlights.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 293, doi. 10.1038/ng0411-293
    Publication type:
    Article
    5
    6

    Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 333, doi. 10.1038/ng.784
    By:
    • Schunkert, Heribert;
    • König, Inke R.;
    • Kathiresan, Sekar;
    • Reilly, Muredach P.;
    • Assimes, Themistocles L.;
    • Holm, Hilma;
    • Preuss, Michael;
    • Stewart, Alexandre F. R.;
    • Barbalic, Maja;
    • Gieger, Christian;
    • Absher, Devin;
    • Aherrahrou, Zouhair;
    • Allayee, Hooman;
    • Altshuler, David;
    • Anand, Sonia S;
    • Andersen, Karl;
    • Anderson, Jeffrey L.;
    • Ardissino, Diego;
    • Ball, Stephen G.;
    • Balmforth, Anthony J.
    Publication type:
    Article
    7

    Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 329, doi. 10.1038/ng.789
    By:
    • Mells, George F.;
    • Floyd, James A. B.;
    • Morley, Katherine I.;
    • Cordell, Heather J.;
    • Franklin, Christopher S.;
    • So-Youn Shin;
    • Heneghan, Michael A.;
    • Neuberger, James M.;
    • Donaldson, Peter T.;
    • Day, Darren B.;
    • Ducker, Samantha J.;
    • Muriithi, Agnes W.;
    • Wheater, Elizabeth F.;
    • Hammond, Christopher J.;
    • Dawwas, Muhammad F.;
    • Jones, David E.;
    • Peltonen, Leena;
    • Alexander, Graeme J.;
    • Sandford, Richard N.;
    • Anderson, Carl A.
    Publication type:
    Article
    8

    Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 306, doi. 10.1038/ng.778
    By:
    • Isidor, ,13Bertrand;
    • Lindenbaum, Pierre;
    • Pichon, Olivier;
    • Bézieau, Stéphane;
    • Dina, Christian;
    • Jacquemont, Sébastien;
    • Martin-Coignard, Dominique;
    • Thauvin-Robinet, Christel;
    • Le Merrer, Martine;
    • Mandel, Jean-Louis;
    • David, Albert;
    • Faivre, Laurence;
    • Cormier-Daire, Valérie;
    • Redon, Richard;
    • Le Caignec, Cédric
    Publication type:
    Article
    9
    10

    Silencing of microRNA families by seed-targeting tiny LNAs.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 371, doi. 10.1038/ng.786
    By:
    • Obad, Susanna;
    • dos Santos, Camila O.;
    • Petri, Andreas;
    • Heidenblad, Markus;
    • Broom, Oliver;
    • Ruse, Cristian;
    • Cexiong Fu;
    • Lindow, Morten;
    • Stenvang, Jan;
    • Straarup, Ellen Marie;
    • Hansen, Henrik Frydenlund;
    • Koch, Troels;
    • Pappin, Darryl;
    • Hannon, Gregory J.;
    • Kauppinen, Sakari
    Publication type:
    Article
    11

    Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.

    Published in:
    2011
    By:
    • Voight, Benjamin F.;
    • Scott, Laura J.;
    • Steinthorsdottir, Valgerdur;
    • Morris, Andrew P.;
    • Dina, Christian;
    • Welch, Ryan P.;
    • Zeggini, Eleftheria;
    • Huth, Cornelia;
    • Aulchenko, Yurii S.;
    • Thorleifsson, Gudmar;
    • McCulloch, Laura J.;
    • Ferreira, Teresa;
    • Grallert, Harald;
    • Amin, Najaf;
    • Wu, Guanming;
    • Willer, Cristen J.;
    • Raychaudhuri, Soumya;
    • McCarroll, Steve A.;
    • Langenberg, Claudia;
    • Hofmann, Oliver M.
    Publication type:
    Correction Notice
    12
    13

    A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 339, doi. 10.1038/ng.782
    By:
    • Peden, John F;
    • Hopewell, Jemma C;
    • Saleheen, Danish;
    • Chambers, John C;
    • Hager, Jorg;
    • Soranzo, Nicole;
    • Collins, Rory;
    • Danesh, John;
    • Elliott, Paul;
    • Farrall, Martin;
    • Stirrups, Kathy;
    • Zhang, Weihua;
    • Hamsten, Anders;
    • Parish, Sarah;
    • Lathrop, Mark;
    • Watkins, Hugh;
    • Clarke, Robert;
    • Deloukas, Panos;
    • Kooner, Jaspal S;
    • Goel, Anuj
    Publication type:
    Article
    14

    A rare variant in MYH6 is associated with high risk of sick sinus syndrome.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 316, doi. 10.1038/ng.781
    By:
    • Holm, Hilma;
    • Gudbjartsson, Daniel F.;
    • Sulem, Patrick;
    • Masson, Gisli;
    • Helgadottir, Hafdis Th;
    • Zanon, Carlo;
    • Magnusson, Olafur Th;
    • Helgason, Agnar;
    • Saemundsdottir, Jona;
    • Gylfason, Arnaldur;
    • Stefansdottir, Hrafnhildur;
    • Gretarsdottir, Solveig;
    • Matthiasson, Stefan E.;
    • Thorgeirsson, Guðmundur;
    • Jonasdottir, Aslaug;
    • Sigurdsson, Asgeir;
    • Stefansson, Hreinn;
    • Werge, Thomas;
    • Rafnar, Thorunn;
    • Kiemeney, Lambertus A.
    Publication type:
    Article
    15
    16

    Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 303, doi. 10.1038/ng.779
    By:
    • Simpson, Michael A.;
    • Irving, Melita D.;
    • Asilmaz, Esra;
    • Gray, Mary J.;
    • Dafou, Dimitra;
    • Elmslie, Frances V.;
    • Mansour, Sahar;
    • Holder, Sue E.;
    • Brain, Caroline E.;
    • Burton, Barbara K.;
    • Kim, Katherine H.;
    • Pauli, Richard M.;
    • Aftimos, Salim;
    • Stewart, Helen;
    • Kim, Chong Ae;
    • Holder-Espinasse, Muriel;
    • Robertson, Stephen P.;
    • Drake, William M.;
    • Trembath, Richard C.
    Publication type:
    Article
    17

    Mutations in the pre-replication complex cause Meier-Gorlin syndrome.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 356, doi. 10.1038/ng.775
    By:
    • Bicknell, Louise S.;
    • Bongers, Ernie M. H. F.;
    • Leitch, Andrea;
    • Brown, Stephen;
    • Schoots, Jeroen;
    • Harley, Margaret E.;
    • Aftimos, Salim;
    • Al-Aama, Jumana Y.;
    • Bober, Michael;
    • Brown, Paul A. J.;
    • van Bokhoven, Hans;
    • Dean, John;
    • Edrees, Alaa Y.;
    • Feingold, Murray;
    • Fryer, Alan;
    • Hoefsloot, Lies H;
    • Kau, Nikolaus;
    • Knoers, Nine V. A. M.;
    • MacKenzie, James;
    • Opitz, John M.
    Publication type:
    Article
    18
    19

    Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 295, doi. 10.1038/ng.785
    By:
    • Giardine, Belinda;
    • Borg, Joseph;
    • Higgs, Douglas R.;
    • Peterson, Kenneth R.;
    • Philipsen, Sjaak;
    • Maglott, Donna;
    • Singleton, Belinda K.;
    • Anstee, David J.;
    • Basak, A. Nazli;
    • Clark, Barnaby;
    • Costa, Flavia C.;
    • Faustino, Paula;
    • Fedosyuk, Halyna;
    • Felice, Alex E.;
    • Francina, Alain;
    • Galanello, Renzo;
    • Gallivan, Monica V. E.;
    • Georgitsi, Marianthi;
    • Gibbons, Richard J.;
    • Giordano, Piero C.
    Publication type:
    Article
    20
    21
    22

    Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 350, doi. 10.1038/ng.776
    By:
    • Bicknell, Louise S.;
    • Walker, Sarah;
    • Klingseisen, Anna;
    • Stiff, Tom;
    • Leitch, Andrea;
    • Kerzendorfer, Claudia;
    • Martin, Carol-Anne;
    • Yeyati, Patricia;
    • Al Sanna, Nouriya;
    • Bober, Michael;
    • Johnson, Diana;
    • Wise, Carol;
    • Jackson, Andrew P.;
    • O'Driscoll, Mark;
    • Jeggo, Penny A.
    Publication type:
    Article
    23

    Corrigendum: Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy.

    Published in:
    2011
    By:
    • Hor, Hyun;
    • Kutalik, Zoltán;
    • Dauvilliers, Yves;
    • Valsesia, Armand;
    • Lammers, Gert J.;
    • Donjacour, Claire E. H. M.;
    • Iranzo, Alex;
    • Santamaria, Joan;
    • Adrados, Rosa Peraita;
    • Vicario, José L.;
    • Overeem, Sebastiaan;
    • Arnulf, Isabelle;
    • Theodorou, Ioannis;
    • Jennum, Poul;
    • Knudsen, Stine;
    • Bassetti, Claudio;
    • Mathis, Johannes;
    • Lecendreux, Michel;
    • Mayer, Geert;
    • Geisler, Peter
    Publication type:
    Correction Notice
    24

    Genome-wide association study identifies susceptibility loci for IgA nephropathy.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 321, doi. 10.1038/ng.787
    By:
    • Gharavi, Ali G.;
    • Kiryluk, Krzysztof;
    • Murim Choi;
    • Yifu Li;
    • Ping Hou;
    • Jingyuan Xie;
    • Sanna-Cherchi, Simone;
    • Men, Clara J.;
    • Julian, Bruce A.;
    • Wyatt, Robert J.;
    • Novak, Jan;
    • He, John C.;
    • Haiyan Wang;
    • Jicheng Lv;
    • Li Zhu;
    • Weiming Wang;
    • Zhaohui Wang;
    • Yasuno, Kasuhito;
    • Gunel, Murat;
    • Mane, Shrikant
    Publication type:
    Article
    25

    The value of data.

    Published in:
    2011
    By:
    • Mons, Barend;
    • van Haagen, Herman;
    • Chichester, Christine;
    • Hoen, Peter-Bram 't;
    • den Dunnen, Johan T;
    • van Ommen, Gertjan;
    • van Mulligen, Erik;
    • Singh, Bharat;
    • Hooft, Rob;
    • Roos, Marco;
    • Hammond, Joel;
    • Kiesel, Bruce;
    • Giardine, Belinda;
    • Velterop, Jan;
    • Groth, Paul;
    • Schultes, Erik
    Publication type:
    Opinion
    26
    27

    Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 360, doi. 10.1038/ng.777
    By:
    • Guernsey, Duane L.;
    • Matsuoka, Makoto;
    • Jiang, Haiyan;
    • Evans, Susan;
    • Macgillivray, Christine;
    • Nightingale, Mathew;
    • Perry, Scott;
    • Ferguson, Meghan;
    • LeBlanc, Marissa;
    • Paquette, Jean;
    • Patry, Lysanne;
    • Rideout, Andrea L.;
    • Thomas, Aidan;
    • Orr, Andrew;
    • McMaster, Chris R.;
    • Michaud, Jacques L.;
    • Deal, Cheri;
    • Langlois, Sylvie;
    • Superneau, Duane W.;
    • Parkash, Sandhya
    Publication type:
    Article