Works matching IS 10614036 AND DT 2010 AND VI 42 AND IP 10

Results: 26
    1

    Research highlights.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 825, doi. 10.1038/ng1010-825
    By:
    • Bachall, Orli;
    • Colosimo, Pamela;
    • Niemitz, Emily;
    • Vogan, Kyle
    Publication type:
    Article
    2

    Public data archives for genomic structural variation.

    Published in:
    2010
    By:
    • Church, Deanna M.;
    • Lappalainen, Ilkka;
    • Sneddon, Tam P.;
    • Hinton, Jonathan;
    • Maguire, Michael;
    • Lopez, John;
    • Garner, John;
    • Paschall, Justin;
    • DiCuccio, Michael;
    • Yaschenko, Eugene;
    • Scherer, Stephen W;
    • Feuk, Lars;
    • Flicek, Paul
    Publication type:
    Letter
    3
    4

    High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 851, doi. 10.1038/ng.659
    By:
    • Calvo, Sarah E.;
    • Tucker, Elena J.;
    • Compton, Alison G.;
    • Kirby, Denise M.;
    • Crawford, Gabriel;
    • Burtt, Noel P.;
    • Rivas, Manuel;
    • Guiducci, Candace;
    • Bruno, Damien L.;
    • Goldberger, Olga A.;
    • Redman, Michelle C.;
    • Wiltshire, Esko;
    • Wilson, Callum J.;
    • Altshuler, David;
    • Gabriel, Stacey B.;
    • Daly, Mark J.;
    • Thorburn, David R.;
    • Mootha, Vamsi K.
    Publication type:
    Article
    5
    6
    7

    A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 897, doi. 10.1038/ng.663
    By:
    • Solouki, Abbas M.;
    • Verhoeven, Virginie J. M.;
    • van Duijn, Cornelia M.;
    • Verkerk, Annemieke J. M. H.;
    • Ikram, M. Kamran;
    • Hysi, Pirro G.;
    • Despriet, Dominiek D. G.;
    • van Koolwijk, Leonieke M.;
    • Lintje Ho;
    • Ramdas, Wishal D.;
    • Czudowska, Monika;
    • Kuijpers, Robert W. A. M.;
    • Amin, Najaf;
    • Struchalin, Maksim;
    • Aulchenko, Yurii S.;
    • van Rij, Gabriel;
    • Riemslag, Frans C. C.;
    • Young, Terri L.;
    • Mackey, David A.;
    • Spector, Timothy D.
    Publication type:
    Article
    8

    Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 869, doi. 10.1038/ng.652
    By:
    • Anttila, Verneri;
    • Stefansson, Hreinn;
    • Kallela, Mikko;
    • Todt, Unda;
    • Terwindt, Gisela M.;
    • Calafato, M. Stella;
    • Nyholt, Dale R.;
    • Dimas, Antigone S.;
    • Freilinger, Tobias;
    • Müller-Myhsok, Bertram;
    • Artto, Ville;
    • Inouye, Michael;
    • Alakurtti, Kirsi;
    • Kaunisto, Mari A.;
    • Hämäläinen, Eija;
    • de Vries, Boukje;
    • Stam, Anine H.;
    • Weller, Claudia M.;
    • Heinze, Axel;
    • Heinze-Kuhn, Katja
    Publication type:
    Article
    9

    Common variants at 19p13 are associated with susceptibility to ovarian cancer.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 880, doi. 10.1038/ng.666
    By:
    • Bolton, Kelly L.;
    • Tyrer, Jonathan;
    • Song, Honglin;
    • Ramus, Susan J.;
    • Notaridou, Maria;
    • Jones, Chris;
    • Sher, Tanya;
    • Gentry-Maharaj, Aleksandra;
    • Wozniak, Eva;
    • Ya-Yu Tsai;
    • Weidhaas, Joanne;
    • Paik, Daniel;
    • Van Den Berg, David J.;
    • Stram, Daniel O.;
    • Pearce, Celeste Leigh;
    • Wu, Anna H.;
    • Brewster, Wendy;
    • Anton-Culver, Hoda;
    • Ziogas, Argyrios;
    • Narod, Steven A.
    Publication type:
    Article
    10

    Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 906, doi. 10.1038/ng.661
    By:
    • Thorleifsson, Gudmar;
    • Walters, G. Bragi;
    • Hewitt, Alex W.;
    • Masson, Gisli;
    • Helgason, Agnar;
    • DeWan, Andrew;
    • Sigurdsson, Asgeir;
    • Jonasdottir, Adalbjorg;
    • Gudjonsson, Sigurjon A.;
    • Magnusson, Kristinn P.;
    • Stefansson, Hreinn;
    • Lam, Dennis S. C.;
    • Tam, Pancy O. S.;
    • Gudmundsdottir, Gudrun J.;
    • Southgate, Laura;
    • Burdon, Kathryn P.;
    • Gottfredsdottir, Maria Soffia;
    • Aldred, Micheala A.;
    • Mitchell, Paul;
    • Clair, David St.
    Publication type:
    Article
    11

    A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 874, doi. 10.1038/ng.668
    By:
    • Goode, Ellen L.;
    • Chenevix-Trench, Georgia;
    • Song, Honglin;
    • Ramus, Susan J.;
    • Notaridou, Maria;
    • Lawrenson, Kate;
    • Widschwendter, Martin;
    • Vierkant, Robert A.;
    • Larson, Melissa C.;
    • Kjaer, Susanne K.;
    • Birrer, Michael J.;
    • Berchuck, Andrew;
    • Schildkraut, Joellen;
    • Tomlinson, Ian;
    • Kiemeney, Lambertus A,;
    • Cook, Linda S.;
    • Gronwald, Jacek;
    • Garcia-Closas, Montserrat;
    • Gore, Martin E.;
    • Campbell, Ian
    Publication type:
    Article
    12

    A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 864, doi. 10.1038/ng.660
    By:
    • Yamauchi, Toshimasa;
    • Hara, Kazuo;
    • Maeda, Shiro;
    • Yasuda, Kazuki;
    • Takahashi, Atsushi;
    • Horikoshi, Momoko;
    • Nakamura, Masahiro;
    • Fujita, Hayato;
    • Grarup, Niels;
    • Cauchi, Stephane;
    • Ng, Daniel P. K.;
    • Ma, Ronald C. W.;
    • Tsunoda, Tatsuhiko;
    • Kubo, Michiaki;
    • Watada, Hirotaka;
    • Maegawa, Hiroshi;
    • Okada-Iwabu, Miki;
    • Iwabu, Masato;
    • Shojima, Nobuhiro;
    • Hyoung Doo Shin
    Publication type:
    Article
    13

    Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 840, doi. 10.1038/ng.662
    By:
    • Otto, Edgar A.;
    • Hurd, Toby W;
    • Airik, Rannar;
    • Chaki, Moumita;
    • Zhou, Weibin;
    • Stoetzel, Corinne;
    • Patil, Suresh B;
    • Levy, Shawn;
    • Ghosh, Amiya K;
    • Murga-Zamalloa, Carlos A;
    • van Reeuwijk, Jeroen;
    • Letteboer, Stef J F;
    • Sang, Liyun;
    • Giles, Rachel H;
    • Liu, Qin;
    • Coene, Karlien L M;
    • Estrada-Cuzcano, Alejandro;
    • Collin, Rob W J;
    • McLaughlin, Heather M;
    • Held, Susanne
    Publication type:
    Article
    14

    Harvesting the apple genome.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 822, doi. 10.1038/ng1010-822
    By:
    • Giovannoni, James
    Publication type:
    Article
    15
    16

    A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 885, doi. 10.1038/ng.669
    By:
    • Antoniou, Antonis C.;
    • Xianshu Wang;
    • Fredericksen, Zachary S.;
    • McGuffog, Lesley;
    • Tarre, Robert;
    • Sinilnikova, Olga M.;
    • Healey, Sue;
    • Morrison, Jonathan;
    • Kartsonaki, Christiana;
    • Lesnick, Timothy;
    • Ghoussaini, Maya;
    • Barrowdale, Daniel;
    • Brace, Em;
    • Peock, Susan;
    • Cook, Margaret;
    • Oliver, Clare;
    • Frost, Debra;
    • Eccles, Diana;
    • Evans, D. Gareth;
    • Eeles, Ros
    Publication type:
    Article
    17

    Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 827, doi. 10.1038/ng.653
    By:
    • Krawitz, Peter M.;
    • Schweiger, Michal R.;
    • Rödelsperger, Christian;
    • Marcelis, Carlo;
    • Kölsch, Uwe;
    • Meisel, Christian;
    • Stephani, Friederike;
    • Kinoshita, Taroh;
    • Murakami, Yoshiko;
    • Bauer, Sebastian;
    • Isau, Melanie;
    • Fischer, Axel;
    • Dahl, Andreas;
    • Kerick, Martin;
    • Hecht, Jochen;
    • Köhler, Sebastian;
    • Jäger, Marten;
    • Grünhagen, Johannes;
    • de Condor, Birgit Jonske;
    • Doelken, Sandra
    Publication type:
    Article
    18

    PRDM9 marks the spot.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 821, doi. 10.1038/ng1010-821
    By:
    • McVean, Gil;
    • Myers, Simon
    Publication type:
    Article
    19

    A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 902, doi. 10.1038/ng.664
    By:
    • Hysi, Pirro G.;
    • Young, Terri L.;
    • Mackey, David A.;
    • Andrew, Toby;
    • Fernández-Medarde, Alberto;
    • Solouki, Abbas M.;
    • Hewitt, Alex W.;
    • Macgregor, Stuart;
    • Vingerling, Johannes R.;
    • Yi-Ju Li;
    • Ikram, M. Kamran;
    • Lee Yiu Fai;
    • Sham, Pak C.;
    • Manyes, Lara;
    • Porteros, Angel;
    • Lopes, Margarida C.;
    • Carbonaro, Francis;
    • Fahy, Samantha J.;
    • Martin, Nicholas G.;
    • van Duijn, Cornelia M.
    Publication type:
    Article
    20
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    23

    The genome of the domesticated apple (Malus × domestica Borkh.).

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 833, doi. 10.1038/ng.654
    By:
    • Velasco, Riccardo;
    • Zharkikh, Andrey;
    • Affourtit, Jason;
    • Dhingra, Amit;
    • Cestaro, Alessandro;
    • Kalyanaraman, Ananth;
    • Fontana, Paolo;
    • Bhatnagar, Satish K.;
    • Troggio, Michela;
    • Pruss, Dmitry;
    • Salvi, Silvio;
    • Pindo, Massimo;
    • Baldi, Paolo;
    • Castelletti, Sara;
    • Cavaiuolo, Marina;
    • Coppola, Giuseppina;
    • Costa, Fabrizio;
    • Cova, Valentina;
    • Dal Ri, Antonio;
    • Goremykin, Vadim
    Publication type:
    Article
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