Works by Taylor, Jenny


Results: 94
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    Reviews.

    Published in:
    2008
    By:
    • Rush, David;
    • Morton, Stephen;
    • Taylor, Jenny Bourne;
    • Wilson, Ross;
    • Thomas Mansell;
    • Feigel, Lara;
    • Dunst, Alexander;
    • Ledger, Sally;
    • Lebeau, Vicky;
    • McCarthy, Conor;
    • Vance, Norman
    Publication type:
    Book Review
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    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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    Biallelic TMEM260 variants cause truncus arteriosus, with or without renal defects.

    Published in:
    Clinical Genetics, 2022, v. 101, n. 1, p. 127, doi. 10.1111/cge.14071
    By:
    • Pagnamenta, Alistair T.;
    • Jackson, Adam;
    • Perveen, Rahat;
    • Beaman, Glenda;
    • Petts, Gemma;
    • Gupta, Asheeta;
    • Hyder, Zerin;
    • Chung, Brian Hon‐Yin;
    • Kan, Anita Sik‐Yau;
    • Cheung, Ka Wang;
    • Kerstjens‐Frederikse, Wilhelmina S.;
    • Abbott, Kristin M.;
    • Elpeleg, Orly;
    • Taylor, Jenny C.;
    • Banka, Siddharth;
    • Ta‐Shma, Asaf
    Publication type:
    Article
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    Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 9, p. 1031, doi. 10.1038/ejhg.2013.91
    By:
    • Shanks, Morag E;
    • Downes, Susan M;
    • Copley, Richard R;
    • Lise, Stefano;
    • Broxholme, John;
    • Hudspith, Karl A Z;
    • Kwasniewska, Alexandra;
    • Davies, Wayne I L;
    • Hankins, Mark W;
    • Packham, Emily R;
    • Clouston, Penny;
    • Seller, Anneke;
    • Wilkie, Andrew O M;
    • Taylor, Jenny C;
    • Ragoussis, Jiannis;
    • Németh, Andrea H
    Publication type:
    Article
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    Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 3, p. 274, doi. 10.1038/ejhg.2012.172
    By:
    • Shanks, Morag E;
    • Downes, Susan M;
    • Copley, Richard R;
    • Lise, Stefano;
    • Broxholme, John;
    • Hudspith, Karl AZ;
    • Kwasniewska, Alexandra;
    • Davies, Wayne IL;
    • Hankins, Mark W;
    • Packham, Emily R;
    • Clouston, Penny;
    • Seller, Anneke;
    • Wilkie, Andrew OM;
    • Taylor, Jenny C;
    • Ragoussis, Jiannis;
    • Németh, Andrea H
    Publication type:
    Article
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    A genome-wide association study of global gene expression.

    Published in:
    Nature Genetics, 2007, v. 39, n. 10, p. 1202, doi. 10.1038/ng2109
    By:
    • Dixon, Anna L.;
    • Liming Liang;
    • Moffatt, Miriam F.;
    • Wei Chen;
    • Heath, Simon;
    • Wong, Kenny C. C.;
    • Taylor, Jenny;
    • Burnett, Edward;
    • Gut, Ivo;
    • Farrall, Martin;
    • Lathrop, G. Mark;
    • Abecasis, Gonçalo R.;
    • Cookson, William O. C.
    Publication type:
    Article
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    Book reviews.

    Published in:
    1994
    By:
    • Taylor, Jenny Bourne
    Publication type:
    Book Review
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    Targeted Next-Generation Sequencing of Plasma DNA from Cancer Patients: Factors Influencing Consistency with Tumour DNA and Prospective Investigation of Its Utility for Diagnosis.

    Published in:
    PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0162809
    By:
    • Kaisaki, Pamela J.;
    • Cutts, Anthony;
    • Popitsch, Niko;
    • Camps, Carme;
    • Pentony, Melissa M.;
    • Wilson, Gareth;
    • Page, Suzanne;
    • Kaur, Kulvinder;
    • Vavoulis, Dimitris;
    • Henderson, Shirley;
    • Gupta, Avinash;
    • Middleton, Mark R.;
    • Karydis, Ioannis;
    • Talbot, Denis C.;
    • Schuh, Anna;
    • Taylor, Jenny C.
    Publication type:
    Article
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    Factors influencing success of clinical genome sequencing across a broad spectrum of disorders.

    Published in:
    Nature Genetics, 2015, v. 47, n. 7, p. 717, doi. 10.1038/ng.3304
    By:
    • Taylor, Jenny C;
    • Copley, Richard R;
    • Craft, Jude;
    • Howard, Malcolm;
    • Pagnamenta, Alistair;
    • Popitsch, Niko;
    • Tomlinson, Ian;
    • Bull, Katherine;
    • Cais, Ondrej;
    • Greger, Ingo H;
    • Cario, Holger;
    • Chapel, Helen;
    • Patel, Smita Y;
    • van Schouwenburg, Pauline A;
    • Cornall, Richard;
    • Dahan, Karin;
    • Dendrou, Calliope;
    • Fugger, Lars;
    • Devuyst, Olivier;
    • Fenwick, Aimée L
    Publication type:
    Article
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    Exploring the potential duty of care in clinical genomics under UK law.

    Published in:
    Medical Law International, 2017, v. 17, n. 3, p. 158, doi. 10.1177/0968533217721966
    By:
    • Mitchell, Colin;
    • Ploem, Corrette;
    • Chico, Victoria;
    • Ormondroyd, Elizabeth;
    • Hall, Alison;
    • Wallace, Susan;
    • Fay, Michael;
    • Goodwin, Deirdre;
    • Bell, Jessica;
    • Phillips, Simon;
    • Taylor, Jenny C.;
    • Hennekam, Raoul;
    • Kaye, Jane
    Publication type:
    Article
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    Impact of month of birth on the development of autoimmune thyroid disease in the United Kingdom and Europe.

    Published in:
    2014
    By:
    • Hamilton, Alexander;
    • Newby, Paul R;
    • Carr-Smith, Jacqueline D;
    • Disanto, Giulio;
    • Allahabadia, Amit;
    • Armitage, Mary;
    • Brix, Thomas H;
    • Chatterjee, Krishna;
    • Connell, John M;
    • Hegedüs, Laszlo;
    • Hunt, Penny J;
    • Lazarus, John H;
    • Pearce, Simon H;
    • Robinson, Bruce G;
    • Taylor, Jenny C;
    • Vaidya, Bijay;
    • Wass, John A H;
    • Wiersinga, Wilmar M;
    • Weetman, Anthony P;
    • Ramagopalan, Sreeram V
    Publication type:
    journal article
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    INTRODUCING MOOD WORK.

    Published in:
    New Formations, 2014, n. 82, p. 5, doi. 10.3898/NEWF.82.INTRODUCTION.2014
    By:
    • Highmore, Ben;
    • Taylor, Jenny Bourne
    Publication type:
    Article
    46

    Editorial.

    Published in:
    New Formations, 2009, n. 67, p. 7, doi. 10.3898/NEWF.67.Editorial.2009
    By:
    • Taylor, Jenny Bourne;
    • Kaplan, Cora
    Publication type:
    Article
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    Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series.

    Published in:
    Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0651-9
    By:
    • Taylor, John;
    • Craft, Jude;
    • Blair, Edward;
    • Wordsworth, Sarah;
    • Beeson, David;
    • Chandratre, Saleel;
    • Cossins, Judith;
    • Lester, Tracy;
    • Németh, Andrea H.;
    • Ormondroyd, Elizabeth;
    • Patel, Smita Y.;
    • Pagnamenta, Alistair T.;
    • Taylor, Jenny C.;
    • Thomson, Kate L.;
    • Watkins, Hugh;
    • Wilkie, Andrew O. M.;
    • Knight, Julian C.
    Publication type:
    Article
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