Works matching IS 10614036 AND DT 2008 AND VI 40 AND IP 11

Results: 33
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    Susceptibility variants for male-pattern baldness on chromosome 20p11.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1279, doi. 10.1038/ng.228
    By:
    • Hillmer, Axel M;
    • Brockschmit, Felix F;
    • Hanneken, Sandra;
    • Eigelshoven, Sibylle;
    • Steffens, Michael;
    • Flaquer, Antonia;
    • Herms, Stefan;
    • Becker, Tim;
    • Kortüm, Anne-Katrin;
    • Nyholt, Dale R;
    • Zhao, Zhen Zhen;
    • Montgomery, Grant W;
    • Martin, Nicholas G;
    • Mühleisen, Thomas W;
    • Alblas, Margrieta A;
    • Moebus, Susanne;
    • Jöckel, Karl-Heinz;
    • Bröcker-Preuss, Martina;
    • Erbel, Raimund;
    • Reinartz, Roman
    Publication type:
    Article
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    Male-pattern baldness susceptibility locus at 20p11.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1282, doi. 10.1038/ng.255
    By:
    • Richards, J Brent;
    • Yuan, Xin;
    • Geller, Frank;
    • Waterworth, Dawn;
    • Bataille, Veronique;
    • Glass, Daniel;
    • Song, Kijoung;
    • Waeber, Gerard;
    • Vollenweider, Peter;
    • Aben, Katja K H;
    • Kiemeney, Lambertus A;
    • Walters, Bragi;
    • Soranzo, Nicole;
    • Thorsteinsdottir, Unnur;
    • Kong, Augustine;
    • Rafnar, Thorunn;
    • Deloukas, Panos;
    • Sulem, Patrick;
    • Stefansson, Hreinn;
    • Stefansson, Kari
    Publication type:
    Article
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    EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1285, doi. 10.1038/ng.241
    By:
    • Abd El-Aziz, Mai M;
    • Barragan, Isabel;
    • O'Driscoll, Ciara A;
    • Goodstadt, Leo;
    • Prigmore, Elena;
    • Borrego, Salud;
    • Mena, Marcela;
    • Pieras, Juan I;
    • El-Ashry, Mohamed F;
    • Safieh, Leen Abu;
    • Shah, Amna;
    • Cheetham, Michael E;
    • Carter, Nigel P;
    • Chakarova, Christina;
    • Ponting, Chris P;
    • Bhattacharya, Shomi S;
    • Antinolo, Guillermo
    Publication type:
    Article
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    TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1288, doi. 10.1038/ng.246
    By:
    • Čížková, Alena;
    • Stránecký, Viktor;
    • Mayr, Johannes A;
    • Tesařová, Markéta;
    • Havlíčková, Vendula;
    • Paul, Jan;
    • Ivánek, Robert;
    • Kuss, Andreas W;
    • Hansíková, Hana;
    • Kaplanová, Vilma;
    • Vrbacký, Marek;
    • Hartmannová, Hana;
    • Nosková, Lenka;
    • Honzík, Tomáš;
    • Drahota, Zdeněk;
    • Magner, Martin;
    • Hejzlarová, Kateřina;
    • Sperl, Wolfgang;
    • Zeman, Jiří;
    • Houštěk, Josef
    Publication type:
    Article
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    Sequence variant on 8q24 confers susceptibility to urinary bladder cancer.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1307, doi. 10.1038/ng.229
    By:
    • Kiemeney, Lambertus A;
    • Thorlacius, Steinunn;
    • Sulem, Patrick;
    • Geller, Frank;
    • Aben, Katja K H;
    • Stacey, Simon N;
    • Gudmundsson, Julius;
    • Jakobsdottir, Margret;
    • Bergthorsson, Jon T;
    • Sigurdsson, Asgeir;
    • Blondal, Thorarinn;
    • Witjes, J Alfred;
    • Vermeulen, Sita H;
    • Hulsbergen-van de Kaa, Christina A;
    • Swinkels, Dorine W;
    • Ploeg, Martine;
    • Cornel, Erik B;
    • Vergunst, Henk;
    • Thorgeirsson, Thorgeir E;
    • Gudbjartsson, Daniel
    Publication type:
    Article
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    Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1313, doi. 10.1038/ng.234
    By:
    • Stacey, Simon N;
    • Gudbjartsson, Daniel F;
    • Sulem, Patrick;
    • Bergthorsson, Jon T;
    • Kumar, Rajiv;
    • Thorleifsson, Gudmar;
    • Sigurdsson, Asgeir;
    • Jakobsdottir, Margret;
    • Sigurgeirsson, Bardur;
    • Benediktsdottir, Kristrun R;
    • Thorisdottir, Kristin;
    • Ragnarsson, Rafn;
    • Scherer, Dominique;
    • Rudnai, Peter;
    • Gurzau, Eugene;
    • Koppova, Kvetoslava;
    • Höiom, Veronica;
    • Botella-Estrada, Rafael;
    • Soriano, Virtudes;
    • Juberías, Pablo
    Publication type:
    Article
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    Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1319, doi. 10.1038/ng.221
    By:
    • Franke, Andre;
    • Balschun, Tobias;
    • Karlsen, Tom H;
    • Sventoraityte, Jurgita;
    • Nikolaus, Susanna;
    • Mayr, Gabriele;
    • Domingues, Francisco S;
    • Albrecht, Mario;
    • Nothnagel, Michael;
    • Ellinghaus, David;
    • Sina, Christian;
    • Onnie, Clive M;
    • Weersma, Rinse K;
    • Stokkers, Pieter C F;
    • Wijmenga, Cisca;
    • Gazouli, Maria;
    • Strachan, David;
    • McArdle, Wendy L;
    • Vermeire, Séverine;
    • Rutgeerts, Paul
    Publication type:
    Article
    12

    Variant between CPT1B and CHKB associated with susceptibility to narcolepsy.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1324, doi. 10.1038/ng.231
    By:
    • Miyagawa, Taku;
    • Kawashima, Minae;
    • Nishida, Nao;
    • Ohashi, Jun;
    • Kimura, Ryosuke;
    • Fujimoto, Akihiro;
    • Shimada, Mihoko;
    • Morishita, Shinichi;
    • Shigeta, Takashi;
    • Lin, Ling;
    • Hong, Seung-Chul;
    • Faraco, Juliette;
    • Shin, Yoon-Kyung;
    • Jeong, Jong-Hyun;
    • Okazaki, Yuji;
    • Tsuji, Shoji;
    • Honda, Makoto;
    • Honda, Yutaka;
    • Mignot, Emmanuel;
    • Tokunaga, Katsushi
    Publication type:
    Article
    13

    Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1329, doi. 10.1038/ng.243
    By:
    • Scott, Richard H;
    • Douglas, Jenny;
    • Baskcomb, Linda;
    • Huxter, Nikki;
    • Barker, Karen;
    • Hanks, Sandra;
    • Craft, Alan;
    • Gerrard, Mary;
    • Kohler, Janice A;
    • Levitt, Gill A;
    • Picton, Sue;
    • Pizer, Barry;
    • Ronghe, Milind D;
    • Williams, Denise;
    • Cook, Jackie A;
    • Pujol, Pascal;
    • Maher, Eamonn R;
    • Birch, Jillian M;
    • Stiller, Charles A;
    • Pritchard-Jones, Kathy
    Publication type:
    Article
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    Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1335, doi. 10.1038/ng.245
    By:
    • Ahmed, Zubair M;
    • Masmoudi, Saber;
    • Kalay, Ersan;
    • Belyantseva, Inna A;
    • Mosrati, Mohamed Ali;
    • Collin, Rob W J;
    • Riazuddin, Saima;
    • Hmani-Aifa, Mounira;
    • Venselaar, Hanka;
    • Kawar, Mayya N;
    • Tlili, Abdelaziz;
    • van der Zwaag, Bert;
    • Khan, Shahid Y;
    • Ayadi, Leila;
    • Riazuddin, S Amer;
    • Morell, Robert J;
    • Griffith, Andrew J;
    • Charfedine, Ilhem;
    • Çaylan, Refik;
    • Oostrik, Jaap
    Publication type:
    Article
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    Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1341, doi. 10.1038/ng.242
    By:
    • Rahimov, Fedik;
    • Marazita, Mary L;
    • Visel, Axel;
    • Cooper, Margaret E;
    • Hitchler, Michael J;
    • Rubini, Michele;
    • Domann, Frederick E;
    • Govil, Manika;
    • Christensen, Kaare;
    • Bille, Camille;
    • Melbye, Mads;
    • Jugessur, Astanand;
    • Lie, Rolv T;
    • Wilcox, Allen J;
    • Fitzpatrick, David R;
    • Green, Eric D;
    • Mossey, Peter A;
    • Little, Julian;
    • Steegers-Theunissen, Regine P;
    • Pennacchio, Len A
    Publication type:
    Article
    16

    Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1348, doi. 10.1038/ng.230
    By:
    • Jeong, Yongsu;
    • Leskow, Federico Coluccio;
    • El-Jaick, Kenia;
    • Roessler, Erich;
    • Muenke, Maximilian;
    • Yocum, Anastasia;
    • Dubourg, Christele;
    • Li, Xue;
    • Geng, Xin;
    • Oliver, Guillermo;
    • Epstein, Douglas J
    Publication type:
    Article
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    Single-copy insertion of transgenes in Caenorhabditis elegans.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1375, doi. 10.1038/ng.248
    By:
    • Frøkjær-Jensen, Christian;
    • Wayne Davis, M;
    • Hopkins, Christopher E;
    • Newman, Blake J;
    • Thummel, Jason M;
    • Olesen, Søren-Peter;
    • Grunnet, Morten;
    • Jorgensen, Erik M
    Publication type:
    Article
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    Rice, rising.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1273, doi. 10.1038/ng1108-1273
    By:
    • Wang, Yonghong;
    • Li, Jiayang
    Publication type:
    Article
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    Research Highlights.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1277, doi. 10.1038/ng1108-1277
    Publication type:
    Article
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    Corrigendum: Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.

    Published in:
    2008
    By:
    • Kathiresan, Sekar;
    • Melander, Olle;
    • Guiducci, Candace;
    • Surti, Aarti;
    • Burtt, Noël P;
    • Rieder, Mark J;
    • Cooper, Gregory M;
    • Roos, Charlotta;
    • Voight, Benjamin F;
    • Havulinna, Aki S;
    • Wahlstrand, Björn;
    • Hedner, Thomas;
    • Corella, Dolores;
    • Tai, E Shyong;
    • Ordovas, Jose M;
    • Berglund, Göran;
    • Vartiainen, Erkki;
    • Jousilahti, Pekka;
    • Hedblad, Bo;
    • Taskinen, Marja-Riitta
    Publication type:
    Correction Notice
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