Found: 8

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  • Analysis of copy number variation using quantitative interspecies competitive PCR.

    Published in:
    Nucleic Acids Research, 2008, v. 36, n. 17, p. e112, doi. 10.1093/nar/gkn495
    By:
    • Williams, Nigel M.;
    • Williams, Hywel;
    • Majounie, Elisa;
    • Norton, Nadine;
    • Glaser, Beate;
    • Morris, Huw R.;
    • Owen, Michael J.;
    • O’Donovan, Michael C.
    Publication type:
    Article

  • Genetic variation in LIN28B is associated with the timing of puberty.

    Published in:
    Nature Genetics, 2009, v. 41, n. 6, p. 729, doi. 10.1038/ng.382
    By:
    • Ong, Ken K.;
    • Elks, Cathy E.;
    • Shengxu Li;
    • Jing Hua Zhao;
    • Jian'an Luan;
    • Andersen, Lars B.;
    • Bingham, Sheila A.;
    • Brage, Soren;
    • Smith, George Davey;
    • Ekelund, Ulf;
    • Gillson, Christopher J.;
    • Glaser, Beate;
    • Golding, Jean;
    • Hardy, Rebecca;
    • Kay-Tee Khaw;
    • Kuh, Diana;
    • Luben, Robert;
    • Marcus, Michele;
    • McGeehin, Michael A.;
    • Ness, Andrew R.
    Publication type:
    Article

  • Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study.

    Published in:
    Journal of Neurodevelopmental Disorders, 2009, v. 1, n. 1, p. 46, doi. 10.1007/s11689-009-9008-9
    By:
    • Azuma, Rayna;
    • Daly, Eileen M.;
    • Campbell, Linda E.;
    • Stevens, Angela F.;
    • Deeley, Quinton;
    • Giampietro, Vincent;
    • Brammer, Michael J.;
    • Glaser, Beate;
    • Ambery, Fiona Z.;
    • Morris, Robin G.;
    • Williams, Steven C. R.;
    • Owen, Michael J.;
    • Murphy, Declan G. M.;
    • Murphy, Kieran C.
    Publication type:
    Article

  • Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study.

    Published in:
    Journal of Neurodevelopmental Disorders, 2009, v. 1, n. 1, p. 46, doi. 10.1007/s11689-009-9008-9
    By:
    • Azuma, Rayna;
    • Daly, Eileen;
    • Campbell, Linda;
    • Stevens, Angela;
    • Deeley, Quinton;
    • Giampietro, Vincent;
    • Brammer, Michael;
    • Glaser, Beate;
    • Ambery, Fiona;
    • Morris, Robin;
    • Williams, Steven;
    • Owen, Michael;
    • Murphy, Declan;
    • Murphy, Kieran
    Publication type:
    Article

  • Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy.

    Published in:
    PLoS Genetics, 2010, v. 6, n. 2, p. 1, doi. 10.1371/journal.pgen.1000856
    By:
    • Pillas, Demetris;
    • Hoggart, Clive J.;
    • Evans, David M.;
    • O'Reilly, Paul F.;
    • Sipilä, Kirsi;
    • Lähdesmäki, Raija;
    • Millwood, Iona Y.;
    • Kaakinen, Marika;
    • Netuveli, Gopalakrishnan;
    • Blane, David;
    • Charoen, Pimphen;
    • Sovio, Ulla;
    • Pouta, Anneli;
    • Freimer, Nelson;
    • Hartikainen, Anna-Liisa;
    • Laitinen, Jaana;
    • Vaara, Sarianna;
    • Glaser, Beate;
    • Crawford, Peter;
    • Timpson, Nicholas J.
    Publication type:
    Article

  • Common variants in the region around Osterix are associated with bone mineral density and growth in childhood.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 8, p. 1510, doi. 10.1093/hmg/ddp052
    By:
    • Timpson, Nicholas J.;
    • Tobias, Jon H.;
    • Richards, J. Brent;
    • Soranzo, Nicole;
    • Duncan, Emma L.;
    • Sims, Anne-Marie;
    • Whittaker, Pamela;
    • Kumanduri, Vasudev;
    • Zhai, Guangju;
    • Glaser, Beate;
    • Eisman, John;
    • Jones, Graeme;
    • Nicholson, Geoff;
    • Prince, Richard;
    • Seeman, Ego;
    • Spector, Tim D.;
    • Brown, Matthew A.;
    • Peltonen, Leena;
    • Smith, George Davey;
    • Deloukas, Panos
    Publication type:
    Article

  • Strong evidence that GNB1L is associated with schizophrenia.

    Published in:
    Human Molecular Genetics, 2008, v. 17, n. 4, p. 555, doi. 10.1093/hmg/ddm330
    By:
    • Williams, Nigel M.;
    • Glaser, Beate;
    • Norton, Nadine;
    • Williams, Hywel;
    • Pierce, Timothy;
    • Moskvina, Valentina;
    • Monks, Stephen;
    • Del Favero, Jurgen;
    • Goossens, Dirk;
    • Rujescu, Dan;
    • Giegling, Ina;
    • Kirov, George;
    • Craddock, Nicholas;
    • Murphy, Kieran C.;
    • O'Donovan, Michael C.;
    • Owen, Michael J.
    Publication type:
    Article

  • Comparison of Methods for Combining Case-Control and Family-Based Association Studies.

    Published in:
    Human Heredity, 2009, v. 68, n. 2, p. 106, doi. 10.1159/000212503
    By:
    • Glaser, Beate;
    • Holmans, Peter
    Publication type:
    Article