Works matching AU Mathieson, Iain


Results: 28
    1

    Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies.

    Published in:
    Journal of Human Genetics, 2012, v. 57, n. 1, p. 70, doi. 10.1038/jhg.2011.128
    By:
    • Pagnamenta, Alistair T;
    • Lise, Stefano;
    • Harrison, Victoria;
    • Stewart, Helen;
    • Jayawant, Sandeep;
    • Quaghebeur, Gerardine;
    • Deng, Alexander T;
    • Murphy, Valerie Elizabeth;
    • Akha, Elham Sadighi;
    • Rimmer, Andy;
    • Mathieson, Iain;
    • Knight, Samantha JL;
    • Kini, Usha;
    • Taylor, Jenny C;
    • Keays, David A
    Publication type:
    Article
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    Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits.

    Published in:
    PLoS Genetics, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pgen.1003500
    By:
    • Randall, Joshua C.;
    • Winkler, Thomas W.;
    • Kutalik, Zoltán;
    • Berndt, Sonja I.;
    • Jackson, Anne U.;
    • Monda, Keri L.;
    • Kilpeläinen, Tuomas O.;
    • Esko, Tõnu;
    • Mägi, Reedik;
    • Li, Shengxu;
    • Workalemahu, Tsegaselassie;
    • Feitosa, Mary F.;
    • Croteau-Chonka, Damien C.;
    • Day, Felix R.;
    • Fall, Tove;
    • Ferreira, Teresa;
    • Gustafsson, Stefan;
    • Locke, Adam E.;
    • Mathieson, Iain;
    • Scherag, Andre
    Publication type:
    Article
    5

    Predicting skeletal stature using ancient DNA.

    Published in:
    American Journal of Biological Anthropology, 2022, v. 177, n. 1, p. 162, doi. 10.1002/ajpa.24426
    By:
    • Cox, Samantha L.;
    • Moots, Hannah M.;
    • Stock, Jay T.;
    • Shbat, Andrej;
    • Bitarello, Bárbara D.;
    • Nicklisch, Nicole;
    • Alt, Kurt W.;
    • Haak, Wolfgang;
    • Rosenstock, Eva;
    • Ruff, Christopher B.;
    • Mathieson, Iain
    Publication type:
    Article
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    Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome.

    Published in:
    Nature Communications, 2015, v. 6, n. 9, p. 8464, doi. 10.1038/ncomms9464
    By:
    • Day, Felix R.;
    • Hinds, David A.;
    • Tung, Joyce Y.;
    • Stolk, Lisette;
    • Styrkarsdottir, Unnur;
    • Saxena, Richa;
    • Bjonnes, Andrew;
    • Broer, Linda;
    • Dunger, David B.;
    • Halldorsson, Bjarni V.;
    • Lawlor, Debbie A.;
    • Laval, Guillaume;
    • Mathieson, Iain;
    • McCardle, Wendy L.;
    • Louwers, Yvonne;
    • Meun, Cindy;
    • Ring, Susan;
    • Scott, Robert A.;
    • Sulem, Patrick;
    • Uitterlinden, André G.
    Publication type:
    Article
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    What is ancestry?

    Published in:
    PLoS Genetics, 2020, v. 16, n. 3, p. 1, doi. 10.1371/journal.pgen.1008624
    By:
    • Mathieson, Iain;
    • Scally, Aylwyn
    Publication type:
    Article
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    Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements.

    Published in:
    Journal of Child Neurology, 2021, v. 36, n. 2, p. 93, doi. 10.1177/0883073820953001
    By:
    • Abdelmoumen, Imane;
    • Jimenez, Sandra;
    • Valencia, Ignacio;
    • Melvin, Joseph;
    • Legido, Agustin;
    • Diaz-Diaz, Mayela M.;
    • Griffith, Christopher;
    • Massingham, Lauren J.;
    • Yelton, Melissa;
    • Rodríguez-Hernández, Janice;
    • Schnur, Rhonda E.;
    • Walsh, Laurence E.;
    • Cristancho, Ana G.;
    • Bergqvist, Christina A.;
    • McWalter, Kirsty;
    • Mathieson, Iain;
    • Belbin, Gillian M.;
    • Kenny, Eimear E.;
    • Ortiz-Gonzalez, Xilma R.;
    • Schneider, Michael C.
    Publication type:
    Article
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