Works by Kirby, Andrew

Results: 97
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    Book reviews.

    Published in:
    1993
    By:
    • Kirby, Andrew
    Publication type:
    Book Review
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    Unusual norovirus and rotavirus genotypes in Ethiopia.

    Published in:
    Paediatrics & International Child Health, 2012, v. 32, n. 1, p. 51, doi. 10.1179/1465328111Y.0000000047
    By:
    • Yassin, Mohammed A;
    • Kirby, Andrew;
    • Mengistu, Abebayehu A;
    • Arbide, Isabel;
    • Dove, Winifred;
    • Beyer, Mandy;
    • Cunliffe, Nigel A;
    • Cuevas, Luis E
    Publication type:
    Article
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    Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration.

    Published in:
    Nature Genetics, 2012, v. 44, n. 4, p. 390, doi. 10.1038/ng.2202
    By:
    • Chiang, Colby;
    • Jacobsen, Jessie C;
    • Ernst, Carl;
    • Hanscom, Carrie;
    • Heilbut, Adrian;
    • Blumenthal, Ian;
    • Mills, Ryan E;
    • Kirby, Andrew;
    • Lindgren, Amelia M;
    • Rudiger, Skye R;
    • McLaughlan, Clive J;
    • Bawden, C Simon;
    • Reid, Suzanne J;
    • Faull, Richard L M;
    • Snell, Russell G;
    • Hall, Ira M;
    • Shen, Yiping;
    • Ohsumi, Toshiro K;
    • Borowsky, Mark L;
    • Daly, Mark J
    Publication type:
    Article
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    Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease.

    Published in:
    Nature Genetics, 2011, v. 43, n. 11, p. 1066, doi. 10.1038/ng.952
    By:
    • Rivas, Manuel A;
    • Beaudoin, Mélissa;
    • Gardet, Agnes;
    • Stevens, Christine;
    • Sharma, Yashoda;
    • Zhang, Clarence K;
    • Boucher, Gabrielle;
    • Ripke, Stephan;
    • Ellinghaus, David;
    • Burtt, Noel;
    • Fennell, Tim;
    • Kirby, Andrew;
    • Latiano, Anna;
    • Goyette, Philippe;
    • Green, Todd;
    • Halfvarson, Jonas;
    • Haritunians, Talin;
    • Korn, Joshua M;
    • Kuruvilla, Finny;
    • Lagacé, Caroline
    Publication type:
    Article
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    Integrated detection and population-genetic analysis of SNPs and copy number variation.

    Published in:
    Nature Genetics, 2008, v. 40, n. 10, p. 1166, doi. 10.1038/ng.238
    By:
    • McCarroll, Steven A.;
    • Kuruvilla, Finny G.;
    • Korn, Joshua M.;
    • Cawley, Simon;
    • Nemesh, James;
    • Wysoker, Alec;
    • Shapero, Michael H.;
    • de Bakker, Paul I. W.;
    • Maller, Julian B.;
    • Kirby, Andrew;
    • Elliott, Amanda L.;
    • Parkin, Melissa;
    • Hubbell, Earl;
    • Webster, Teresa;
    • Rui Mei;
    • Veitch, James;
    • Collins, Patrick J.;
    • Handsaker, Robert;
    • Lincoln, Steve;
    • Nizzari, Marcia
    Publication type:
    Article
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    Mismatch Repair Genes <i>Mlh1</i> and <i>Mlh3</i> Modify CAG Instability in Huntington's Disease Mice: Genome-Wide and Candidate Approaches.

    Published in:
    PLoS Genetics, 2013, v. 9, n. 10, p. 1, doi. 10.1371/journal.pgen.1003930
    By:
    • Pinto, Ricardo Mouro;
    • Dragileva, Ella;
    • Kirby, Andrew;
    • Lloret, Alejandro;
    • Lopez, Edith;
    • St. Claire, Jason;
    • Panigrahi, Gagan B.;
    • Hou, Caixia;
    • Holloway, Kim;
    • Gillis, Tammy;
    • Guide, Jolene R.;
    • Cohen, Paula E.;
    • Li, Guo-Min;
    • Pearson, Christopher E.;
    • Daly, Mark J.;
    • Wheeler, Vanessa C.
    Publication type:
    Article
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    DGAT1 mutation is linked to a congenital diarrheal disorder.

    Published in:
    Journal of Clinical Investigation, 2012, v. 122, n. 12, p. 4680, doi. 10.1172/JCI64873
    By:
    • Haas, Joel T.;
    • Winter, Harland S.;
    • Elaine Lim;
    • Kirby, Andrew;
    • Blumenstie, Brendan;
    • DeFelice, Matthew;
    • Gabriel, Stacey;
    • Jalas, Chaim;
    • Branski, David;
    • Grueter, Carrie A.;
    • Toporovski, Mauro S.;
    • Walther, Tobias C.;
    • Daly, Mark J.;
    • Farese Jr., Robert V.
    Publication type:
    Article
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    Genetic modifiers of hypertension in soluble guanylate cyclase α1-deficient mice.

    Published in:
    Journal of Clinical Investigation, 2012, v. 122, n. 6, p. 2316, doi. 10.1172/JCI60119
    By:
    • Buys, Emmanuel S.;
    • Raher, Michael J.;
    • Kirby, Andrew;
    • Mohd, Shahid;
    • Baron, David M.;
    • Hayton, Sarah R.;
    • Tainsh, Laurel T.;
    • Sips, Patrick Y.;
    • Rauwerdink, Kristen M.;
    • Yan, Qingshang;
    • Tainsh, Robert E. T.;
    • Shakartzi, Hannah R.;
    • Stevens, Christine;
    • Decaluwé, Kelly;
    • Rodrigues-Machado, Maria da Gloria;
    • Malhotra, Rajeev;
    • Van de Voorde, Johan;
    • Wang, Tong;
    • Brouckaert, Peter;
    • Daly, Mark J.
    Publication type:
    Article
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    A framework for the interpretation of de novo mutation in human disease.

    Published in:
    Nature Genetics, 2014, v. 46, n. 9, p. 944, doi. 10.1038/ng.3050
    By:
    • Samocha, Kaitlin E;
    • Robinson, Elise B;
    • Sanders, Stephan J;
    • Stevens, Christine;
    • Sabo, Aniko;
    • McGrath, Lauren M;
    • Kosmicki, Jack A;
    • Rehnström, Karola;
    • Mallick, Swapan;
    • Kirby, Andrew;
    • Wall, Dennis P;
    • MacArthur, Daniel G;
    • Gabriel, Stacey B;
    • DePristo, Mark;
    • Purcell, Shaun M;
    • Palotie, Aarno;
    • Boerwinkle, Eric;
    • Buxbaum, Joseph D;
    • Cook, Edwin H;
    • Gibbs, Richard A
    Publication type:
    Article
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    Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.

    Published in:
    Nature Genetics, 2013, v. 45, n. 3, p. 299, doi. 10.1038/ng.2543
    By:
    • Kirby, Andrew;
    • Gnirke, Andreas;
    • Jaffe, David B;
    • Barešová, Veronika;
    • Pochet, Nathalie;
    • Blumenstiel, Brendan;
    • Ye, Chun;
    • Aird, Daniel;
    • Stevens, Christine;
    • Robinson, James T;
    • Cabili, Moran N;
    • Gat-Viks, Irit;
    • Kelliher, Edward;
    • Daza, Riza;
    • DeFelice, Matthew;
    • Hůlková, Helena;
    • Sovová, Jana;
    • Vylet'al, Petr;
    • Antignac, Corinne;
    • Guttman, Mitchell
    Publication type:
    Article
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    Imaging polysaccharides by atomic force microscopy.

    Published in:
    Biopolymers, 1996, v. 38, n. 3, p. 355, doi. 10.1002/(SICI)1097-0282(199603)38:3&lt;355::AID-BIP8&gt;3.0.CO;2-T
    By:
    • Kirby, Andrew R.;
    • Gunning, A. Patrick;
    • Morris, Victor J.
    Publication type:
    Article
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    An approach to ideology.

    Published in:
    Journal of Geography in Higher Education, 1980, v. 4, n. 2, p. 16, doi. 10.1080/03098268008708768
    By:
    • Kirby, Andrew
    Publication type:
    Article
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    Book notes.

    Published in:
    1995
    By:
    • Kirby, Andrew
    Publication type:
    Book Review
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    Book Notes.

    Published in:
    Political Studies, 1992, v. 40, n. 3, p. 597, doi. 10.1111/j.1467-9248.1992.tb00713.x
    By:
    • Moxon-Browne, Edward;
    • Borthwick, R. L.;
    • Kirby, Andrew;
    • Forman, F. N.;
    • Studlar, Donley T.;
    • Lee, Simon;
    • Zimmerman, Ekkart;
    • Bealey, Frank;
    • Aughey, Arthur;
    • Brown, William;
    • Seyd, Patrick;
    • Gamble, Andrew;
    • Chandler, J. A.;
    • Chapman, Richard;
    • Durham, Martin;
    • Parry, Geraint;
    • Watt, Ian;
    • Hampton, W. A.;
    • Waddington, P. A. J.;
    • Jordan, Bill
    Publication type:
    Article
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    Book reviews.

    Published in:
    1996
    By:
    • Kirby, Andrew
    Publication type:
    Book Review
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    Same-Sex Marriage: A Dilemma for Parish Clergy.

    Published in:
    Sexuality & Culture, 2017, v. 21, n. 3, p. 901, doi. 10.1007/s12119-017-9414-1
    By:
    • Kirby, Andrew;
    • McKenzie-Green, Barbara;
    • McAra-Couper, Judith;
    • Nayar, Shoba
    Publication type:
    Article
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    Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty.

    Published in:
    Journal of Clinical Endocrinology & Metabolism, 2017, p. 1557, doi. 10.1210/jc.2016-3677
    By:
    • Dauber, Andrew;
    • Cunha-Silva, Marina;
    • Macedo, Delanie B.;
    • Brito, Vinicius N.;
    • Paula Abreu, Ana;
    • Roberts, Stephanie A.;
    • Montenegro, Luciana R.;
    • Andrew, Melissa;
    • Kirby, Andrew;
    • Weirauch, Matthew T.;
    • Labilloy, Guillaume;
    • Bessa, Danielle S.;
    • Carroll, Rona S.;
    • Jacobs, Dakota C.;
    • Chappell, Patrick E.;
    • Mendonca, Berenice B.;
    • Haig, David;
    • Kaiser, Ursula B.;
    • Latronico, Ana Claudia
    Publication type:
    Article
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    Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty.

    Published in:
    2017
    By:
    • Dauber, Andrew;
    • Cunha-Silva, Marina;
    • Macedo, Delanie B;
    • Brito, Vinicius N;
    • Abreu, Ana Paula;
    • Roberts, Stephanie A;
    • Montenegro, Luciana R;
    • Andrew, Melissa;
    • Kirby, Andrew;
    • Weirauch, Matthew T;
    • Labilloy, Guillaume;
    • Bessa, Danielle S;
    • Carroll, Rona S;
    • Jacobs, Dakota C;
    • Chappell, Patrick E;
    • Mendonca, Berenice B;
    • Haig, David;
    • Kaiser, Ursula B;
    • Latronico, Ana Claudia
    Publication type:
    journal article
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