Works matching IS 10614036 AND DT 2007 AND VI 39 AND IP 7

Results: 28
    1
    2
    3
    4
    5

    Guilt beyond a reasonable doubt.

    Published in:
    Nature Genetics, 2007, v. 39, n. 7, p. 813, doi. 10.1038/ng0707-813
    By:
    • Altshuler, David;
    • Daly, Mark
    Publication type:
    Article
    6
    7
    8
    9
    10

    Touching base.

    Published in:
    Nature Genetics, 2007, v. 39, n. 7, p. 823, doi. 10.1038/ng0707-823
    By:
    • E. N.;
    • K. V.
    Publication type:
    Article
    11
    12

    The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.

    Published in:
    Nature Genetics, 2007, v. 39, n. 7, p. 875, doi. 10.1038/ng2039
    By:
    • Delous, Marion;
    • Baala, Lekbir;
    • Salomon, Rémi;
    • Laclef, Christine;
    • Vierkotten, Jeanette;
    • Tory, Kàlmàn;
    • Golzio, Christelle;
    • Lacoste, Tiphanie;
    • Besse, Laurianne;
    • Ozilou, Catherine;
    • Moutkine, Imane;
    • Hellman, Nathan E.;
    • Anselme, Isabelle;
    • Silbermann, Flora;
    • Vesque, Christine;
    • Gerhardt, Christoph;
    • Rattenberry, Eleanor;
    • Wolf, Matthias T. F.;
    • Gubler, Marie Claire;
    • Martinovic, Jéléna
    Publication type:
    Article
    13
    14
    15

    Deficiency of PORCN, a regulator of Wnt signaling, is associated with focal dermal hypoplasia.

    Published in:
    Nature Genetics, 2007, v. 39, n. 7, p. 833, doi. 10.1038/ng2052
    By:
    • Grzeschik, Karl-Heinz;
    • Bornholdt, Dorothea;
    • Oeffner, Frank;
    • König, Arne;
    • del Carmen Boente, María;
    • Enders, Herbert;
    • Fritz, Barbara;
    • Hertl, Michael;
    • Grasshoff, Ute;
    • Höfling, Katja;
    • Oji, Vinzenz;
    • Paradisi, Mauro;
    • Schuchardt, Christian;
    • Szalai, Zsuzsanna;
    • Tadini, Gianluca;
    • Traupe, Heiko;
    • Happle, Rudolf
    Publication type:
    Article
    16

    Comparative genomic analysis of three Leishmania species that cause diverse human disease.

    Published in:
    Nature Genetics, 2007, v. 39, n. 7, p. 839, doi. 10.1038/ng2053
    By:
    • Peacock, Christopher S.;
    • Seeger, Kathy;
    • Harris, David;
    • Murphy, Lee;
    • Ruiz, Jeronimo C.;
    • Quail, Michael A.;
    • Peters, Nick;
    • Adlem, Ellen;
    • Tivey, Adrian;
    • Aslett, Martin;
    • Kerhornou, Arnaud;
    • Ivens, Alasdair;
    • Fraser, Audrey;
    • Rajandream, Marie-Adele;
    • Carver, Tim;
    • Norbertczak, Halina;
    • Chillingworth, Tracey;
    • Hance, Zahra;
    • Jagels, Kay;
    • Moule, Sharon
    Publication type:
    Article
    17

    A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.

    Published in:
    Nature Genetics, 2007, v. 39, n. 7, p. 827, doi. 10.1038/ng2058
    By:
    • van Heel, David A.;
    • Franke, Lude;
    • Hunt, Karen A.;
    • Gwilliam, Rhian;
    • Zhernakova, Alexandra;
    • Inouye, Mike;
    • Wapenaar, Martin C.;
    • Barnardo, Martin C. N. M.;
    • Bethel, Graeme;
    • Holmes, Geoffrey K. T.;
    • Feighery, Con;
    • Jewell, Derek;
    • Kelleher, Dermot;
    • Kumar, Parveen;
    • Travis, Simon;
    • Walters, Julian R. F.;
    • Sanders, David S.;
    • Howdle, Peter;
    • Swift, Jill;
    • Playford, Raymond J.
    Publication type:
    Article
    18

    Tissue-specific and reversible RNA interference in transgenic mice.

    Published in:
    Nature Genetics, 2007, v. 39, n. 7, p. 914, doi. 10.1038/ng2045
    By:
    • Dickins, Ross A.;
    • McJunkin, Katherine;
    • Hernando, Eva;
    • Premsrirut, Prem K.;
    • Krizhanovsky, Valery;
    • Burgess, Darren J.;
    • Sang Yong Kim;
    • Cordon-Cardo, Carlos;
    • Zender, Lars;
    • Hannon, Gregory J.;
    • Lowe, Scott W.
    Publication type:
    Article
    19
    20
    21

    Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.

    Published in:
    Nature Genetics, 2007, v. 39, n. 7, p. 830, doi. 10.1038/ng2061
    By:
    • Parkes, Miles;
    • Barrett, Jeffrey C.;
    • Prescott, Natalie J.;
    • Tremelling, Mark;
    • Anderson, Carl A.;
    • Fisher, Sheila A.;
    • Roberts, Roland G.;
    • Nimmo, Elaine R.;
    • Cummings, Fraser R.;
    • Soars, Dianne;
    • Drummond, Hazel;
    • Lees, Charlie W.;
    • Khawaja, Saud A.;
    • Bagnall, Richard;
    • Burke, Denis A.;
    • Todhunter, Catherine E.;
    • Ahmad, Tariq;
    • Onnie, Clive M.;
    • McArdle, Wendy;
    • Strachan, David
    Publication type:
    Article
    22

    Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer.

    Published in:
    Nature Genetics, 2007, v. 39, n. 7, p. 865, doi. 10.1038/ng2064
    By:
    • Stacey, Simon N.;
    • Manolescu, Andrei;
    • Sulem, Patrick;
    • Rafnar, Thorunn;
    • Gudmundsson, Julius;
    • Gudjonsson, Sigurjon A.;
    • Masson, Gisli;
    • Jakobsdottir, Margret;
    • Thorlacius, Steinunn;
    • Helgason, Agnar;
    • Aben, Katja K.;
    • Strobbe, Luc J.;
    • Albers-Akkers, Marjo T.;
    • Swinkels, Dorine W.;
    • Henderson, Brian E.;
    • Kolonel, Laurence N.;
    • Le Marchand, Loic;
    • Millastre, Esther;
    • Andres, Raquel;
    • Godino, Javier
    Publication type:
    Article
    23

    Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.

    Published in:
    Nature Genetics, 2007, v. 39, n. 7, p. 889, doi. 10.1038/ng2066
    By:
    • den Hollander, Anneke I.;
    • Koenekoop, Robert K.;
    • Mohamed, Moin D.;
    • Arts, Heleen H.;
    • Boldt, Karsten;
    • Towns, Katherine V.;
    • Sedmak, Tina;
    • Beer, Monika;
    • Nagel-Wolfrum, Kerstin;
    • McKibbin, Martin;
    • Dharmaraj, Sharola;
    • Lopez, Irma;
    • Ivings, Lenka;
    • Williams, Grange A.;
    • Springell, Kelly;
    • Woods, C. Geoff;
    • Jafri, Hussain;
    • Rashid, Yasmin;
    • Strom, Tim M.;
    • van der Zwaag, Bert
    Publication type:
    Article
    24

    Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.

    Published in:
    Nature Genetics, 2007, v. 39, n. 7, p. 857, doi. 10.1038/ng2068
    By:
    • Todd, John A.;
    • Walker, Neil M.;
    • Cooper, Jason D.;
    • Smyth, Deborah J.;
    • Downes, Kate;
    • Plagnol, Vincent;
    • Bailey, Rebecca;
    • Nejentsev, Sergey;
    • Field, Sarah F.;
    • Payne, Felicity;
    • Lowe, Christopher E.;
    • Szeszko, Jeffrey S.;
    • Hafler, Jason P.;
    • Zeitels, Lauren;
    • Yang, Jennie H. M.;
    • Vella, Adrian;
    • Nutland, Sarah;
    • Stevens, Helen E.;
    • Schuilenburg, Helen;
    • Coleman, Gillian
    Publication type:
    Article
    25

    Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.

    Published in:
    Nature Genetics, 2007, v. 39, n. 7, p. 882, doi. 10.1038/ng2069
    By:
    • Arts, Heleen H.;
    • Doherty, Dan;
    • van Beersum, Sylvia E. C.;
    • Parisi, Melissa A.;
    • Letteboer, Stef J. F.;
    • Gorden, Nicholas T.;
    • Peters, Theo A.;
    • Märker, Tina;
    • Voesenek, Krysta;
    • Kartono, Aileen;
    • Ozyurek, Hamit;
    • Farin, Federico M.;
    • Kroes, Hester Y.;
    • Wolfrum, Uwe;
    • Brunner, Han G.;
    • Cremers, Frans P. M.;
    • Glass, Ian A.;
    • Knoers, Nine V. A. M.;
    • Roepman, Ronald
    Publication type:
    Article
    26

    A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.

    Published in:
    Nature Genetics, 2007, v. 39, n. 7, p. 870, doi. 10.1038/ng2075
    By:
    • Hunter, David J.;
    • Kraft, Peter;
    • Jacobs, Kevin B.;
    • Cox, David G.;
    • Yeager, Meredith;
    • Hankinson, Susan E.;
    • Wacholder, Sholom;
    • Zhaoming Wang;
    • Welch, Robert;
    • Hutchinson, Amy;
    • Junwen Wang;
    • Kai Yu;
    • Chatterjee, Nilanjan;
    • Orr, Nick;
    • Willett, Walter C.;
    • Colditz, Graham A.;
    • Ziegler, Regina G.;
    • Berg, Christine D.;
    • Buys, Saundra S.;
    • McCarty, Catherine A.
    Publication type:
    Article
    27
    28