Jenny Taylor

Jenny Taylor

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Remission of Inflammatory Bowel Disease in Glucose-6-Phosphatase 3 Deficiency by Allogeneic Haematopoietic Stem Cell Transplantation.

J Crohns Colitis 2020 Jan;14(1):142-147

Translational Gastroenterology Unit, NIHR Oxford Biomedical Research Centre, Nuffield Department of Experimental Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.

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https://academic.oup.com/ecco-jcc/advance-article/doi/10.109
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http://dx.doi.org/10.1093/ecco-jcc/jjz112DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930000PMC
January 2020

Do health professionals value genomic testing? A discrete choice experiment in inherited cardiovascular disease.

Eur J Hum Genet 2019 Nov 11;27(11):1639-1648. Epub 2019 Jun 11.

Health Economics Research Centre, Nuffield Department of Population Health, University of Oxford, Old Road Campus, Oxford, OX3 7LF, UK.

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http://dx.doi.org/10.1038/s41431-019-0452-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6870981PMC
November 2019

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy.

Am J Hum Genet 2019 Jun 9;104(6):1210-1222. Epub 2019 May 9.

Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2019.03.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556837PMC
June 2019

Classical and Non-classical Presentations of Complement Factor I Deficiency: Two Contrasting Cases Diagnosed via Genetic and Genomic Methods.

Front Immunol 2019 7;10:1150. Epub 2019 Jun 7.

Clinical Immunology Service, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.

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http://dx.doi.org/10.3389/fimmu.2019.01150DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6568211PMC
June 2019

Clinical spectrum of -related epileptic disorders.

Neurology 2019 03 8;92(11):e1238-e1249. Epub 2019 Feb 8.

From the University of Tübingen (S. Wolking, J.M., Y.G.W., H.L., J.S.), Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, Tübingen, Germany; Luxembourg Centre for Systems Biomedicine (P.M.), University of Luxembourg, Esch-sur-Alzette; Pediatric Neurology and Neurogenetics Unit and Laboratories (D.M., R.G., C.M.), Children's Hospital Anna Meyer, University of Florence, Italy; Danish Epilepsy Centre (R.S.M.), Dianalund; Institute for Regional Health Services (R.S.M.), University of Southern Denmark, Odense; Department of Clinical and Experimental Epilepsy (S.B.), UCL Institute of Neurology and Epilepsy Society, UK, London; Division of Neurology (K.L.H., I.H.), Children's Hospital of Philadelphia, PA; Department of Pediatric Neurology (C.D.A.), Centre de Compétences Maladies Rares, CHU Besançon; Service de Génétique (N.C.), Hospices Civils des Lyon, Bron; GENDEV Team (N.C.), Neurosciences Research Center of Lyon, Bron, France; Neuropediatric Clinic and Clinic for Neurorehabilitation (K.S.), Epilepsy Center for Children and Adolescents, Schoen Klinik Vogtareuth, Germany; Beaumont Hospital (P.W.-W.), Dublin, Ireland; Department of Pediatrics, Division of Medical Genetics, Institute of Human Genetics (B.A.M.), Departments of Neurology and Pediatrics (A.N.), and Departments of Neurology and Pediatrics, and Institute of Human Genetics (M.R.C.), University of California, San Francisco; Department of Neurology (W.V.P.), University Hospitals Leuven, Belgium; Department of Pediatrics (L.L.S.), Hvidovre Hospital, Denmark; King's College Hospital (S.O., E.H., S.G., D.K.P.), London; Evelina London Children's Hospital (S.O., E.H., S.G.), London, UK; Section of Genetics (K.B., M.S.S.), Department of Pediatrics, University of Colorado and Children's Hospital Colorado, Aurora; Clinique Bernoise Montana (T.D.), Crans-Montana, Switzerland; Department of Neuropediatrics (H.M.), University Medical Center Schleswig-Holstein, Christian-Albrechts University, Kiel, Germany; National Institute for Health Research Oxford Biomedical Research Centre, Wellcome Centre for Human Genetics (A.T.P., S.J.L.K., J.C.T.) and Department of Oncology (D.V.V.), University of Oxford, UK; Epilepsy Center (M.P.C.), Health Sciences Department, San Paolo Hospital, University of Milan; Child Neuropsychiatry (F.D.), Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Italy; Departments of Neurology and Clinical Genomics (R.H.G.) and Health Sciences Research and Clinical Genomics (E.W.K., C.K.), Mayo Clinic, Rochester, MN; Ambry Genetics (Z.P.), Aliso Viejo, CA; Department of Clinical Neuroscience (S.T.), King's College London; New Medicines (M.A., D.M.), UCB Pharma, Slough, UK; Neuropediatric Clinic and Clinic for Neurorehabilitation (G.J.K.), Epilepsy Center for Children and Adolescents, Schoen Klinik Vogtareuth, Germany; Research Institute for Rehabilitation, Transition and Palliation (G.J.K.), PMU Salzburg, Austria; Department of Neurology (D.H.L.), University of California, San Francisco; Neurogenetics Group (S. Weckhuysen), Center for Molecular Neurology, VIB, Antwerp; Laboratory of Neurogenetics (S. Weckhuysen), Institute Born-Bunge, University of Antwerp; Department of Neurology (S. Weckhuysen), Antwerp University Hospital, Antwerp, Belgium; Department of Basic & Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience (D.K.P.), MRC Centre for Neurodevelopmental Disorders (D.K.P.), King's College London, UK; Evelina London Children's Hospital (D.K.P.), London, UK; Department of Neuropediatrics (I.H.), University Medical Center Schleswig-Holstein, Christian-Albrechts University, Kiel, Germany; Institute of Neuroscience (R.H.T.), Henry Wellcome Building, Newcastle University; Neurology Research Group (M.I.R.), Institute of Life Science, Swansea University Medical School, Swansea, UK; Service de Génétique (G.L.), Hospices Civils des Lyon, Bron; GENDEV Team (G.L.), Neurosciences Research Center of Lyon, Bron, France; NIHR University College London Hospitals Biomedical Research Centre (S.M.S.), UCL Institute of Neurology, London, UK; Cologne Center for Genomics (D.L.), University of Cologne, Germany; Stanley Center for Psychiatric Research (D.L.) and Program in Medical and Population Genetics (D.L.), Broad Institute of MIT and Harvard, Cambridge; Psychiatric and Neurodevelopmental Genetics Unit (D.L.), Massachusetts General Hospital and Harvard Medical School, Boston.

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http://dx.doi.org/10.1212/WNL.0000000000007089DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511102PMC
March 2019

Deep learning for detecting tumour-infiltrating lymphocytes in testicular germ cell tumours.

J Clin Pathol 2019 Feb 5;72(2):157-164. Epub 2018 Dec 5.

Nuffield Department of Surgical Sciences and NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1136/jclinpath-2018-205328DOI Listing
February 2019

Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature.

Genet Med 2018 10 15;20(10):1122-1130. Epub 2018 Feb 15.

Health Economics Research Centre, Nuffield Department of Population Health, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1038/gim.2017.247DOI Listing
October 2018

From Genotype to Phenotype.

Circ Genom Precis Med 2018 10;11(10):e002316

Division of Cardiovascular Medicine, Radcliffe Department of Medicine (M.M., H.W., E.O.), University of Oxford, United Kingdom.

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http://dx.doi.org/10.1161/CIRCGEN.118.002316DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217934PMC
October 2018

Mutation burden and other molecular markers of prognosis in colorectal cancer treated with curative intent: results from the QUASAR 2 clinical trial and an Australian community-based series.

Lancet Gastroenterol Hepatol 2018 09 2;3(9):635-643. Epub 2018 Jul 2.

Oxford Centre for Cancer Gene Research, Wellcome Trust Centre for Human Genetics, Oxford, UK; Genomic Medicine Theme, National Institute for Health Research Oxford Biomedical Research Centre, Wellcome Trust Centre for Human Genetics, Oxford, UK; Cancer Genetics and Evolution Laboratory, Institute of Cancer and Genomic Sciences, University of Birmingham, Edgbaston, Birmingham, UK.

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http://dx.doi.org/10.1016/S2468-1253(18)30117-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6088509PMC
September 2018

A homozygous variant disrupting the PIGH start-codon is associated with developmental delay, epilepsy, and microcephaly.

Hum Mutat 2018 06 30;39(6):822-826. Epub 2018 Mar 30.

National Institute for Health Research Oxford Biomedical Research Centre, Wellcome Centre for Human Genetics, University of Oxford, Oxford, Oxfordshire, UK.

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http://dx.doi.org/10.1002/humu.23420DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001798PMC
June 2018

Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study.

Eur J Hum Genet 2018 05 13;26(5):652-659. Epub 2018 Feb 13.

Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1038/s41431-018-0106-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945590PMC
May 2018

A high throughput screen for active human transposable elements.

BMC Genomics 2018 02 1;19(1):115. Epub 2018 Feb 1.

Wellcome Trust Centre for Human Genetics, Oxford, UK.

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http://dx.doi.org/10.1186/s12864-018-4485-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796560PMC
February 2018

Hierarchical probabilistic models for multiple gene/variant associations based on next-generation sequencing data.

Bioinformatics 2017 Oct;33(19):3058-3064

National Health Service Translational Molecular Diagnostics Centre, Oxford University Hospitals, John Radcliffe Hospital, Oxford, OX3 9DU UK.

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http://dx.doi.org/10.1093/bioinformatics/btx355DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637939PMC
October 2017

Insights from early experience of a Rare Disease Genomic Medicine Multidisciplinary Team: a qualitative study.

Eur J Hum Genet 2017 06 22;25(6):680-686. Epub 2017 Mar 22.

Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1038/ejhg.2017.37DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427178PMC
June 2017

ReliableGenome: annotation of genomic regions with high/low variant calling concordance.

Bioinformatics 2017 01 7;33(2):155-160. Epub 2016 Sep 7.

Wellcome Trust Centre of Human Genetics, University of Oxford, Oxford OX3 7BN, UK.

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http://dx.doi.org/10.1093/bioinformatics/btw587DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903559PMC
January 2017

Autosomal dominant osteopetrosis associated with renal tubular acidosis is due to a CLCN7 mutation.

Am J Med Genet A 2016 11 19;170(11):2988-2992. Epub 2016 Aug 19.

Academic Endocrine Unit, Oxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, University of Oxford, Oxford, United Kingdom.

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http://dx.doi.org/10.1002/ajmg.a.37755DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5132132PMC
November 2016

Activation of an exonic splice-donor site in exon 30 of in a patient with severe microcephaly and pigmentary abnormalities.

Clin Case Rep 2016 Oct 23;4(10):952-956. Epub 2016 Aug 23.

Department of Clinical Genetics Oxford University Hospitals NHS Foundation Trust Oxford UK.

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http://dx.doi.org/10.1002/ccr3.663DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054469PMC
October 2016

De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation.

Cell Rep 2016 06 26;15(10):2251-2265. Epub 2016 May 26.

EMBL Australia, The Australian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800, Australia; The Harry Perkins Institute of Medical Research, QEII Medical Centre and Centre for Medical Research, the University of Western Australia, Nedlands, WA 6009, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2016.04.090DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906373PMC
June 2016

Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome.

J Med Genet 2016 Mar 5;53(3):152-62. Epub 2015 Nov 5.

INSIGNEO Institute for in silico medicine, Sheffield University, Sheffield, UK Sheffield Institute for Translational Neuroscience, Sheffield University, Sheffield, UK Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield, UK.

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http://dx.doi.org/10.1136/jmedgenet-2015-103393DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789813PMC
March 2016

Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgE.

Clin Immunol 2016 Feb 8;163:17-21. Epub 2015 Dec 8.

Nuffield Department of Medicine, Experimental Medicine Division, University of Oxford, UK; Oxford NIHR Biomedical Research Centre, John Radcliffe Hospital, Oxford, UK.

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http://dx.doi.org/10.1016/j.clim.2015.12.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4758821PMC
February 2016

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders.

Authors:
Jenny C Taylor Hilary C Martin Stefano Lise John Broxholme Jean-Baptiste Cazier Andy Rimmer Alexander Kanapin Gerton Lunter Simon Fiddy Chris Allan A Radu Aricescu Moustafa Attar Christian Babbs Jennifer Becq David Beeson Celeste Bento Patricia Bignell Edward Blair Veronica J Buckle Katherine Bull Ondrej Cais Holger Cario Helen Chapel Richard R Copley Richard Cornall Jude Craft Karin Dahan Emma E Davenport Calliope Dendrou Olivier Devuyst Aimée L Fenwick Jonathan Flint Lars Fugger Rodney D Gilbert Anne Goriely Angie Green Ingo H Greger Russell Grocock Anja V Gruszczyk Robert Hastings Edouard Hatton Doug Higgs Adrian Hill Chris Holmes Malcolm Howard Linda Hughes Peter Humburg David Johnson Fredrik Karpe Zoya Kingsbury Usha Kini Julian C Knight Jonathan Krohn Sarah Lamble Craig Langman Lorne Lonie Joshua Luck Davis McCarthy Simon J McGowan Mary Frances McMullin Kerry A Miller Lisa Murray Andrea H Németh M Andrew Nesbit David Nutt Elizabeth Ormondroyd Annette Bang Oturai Alistair Pagnamenta Smita Y Patel Melanie Percy Nayia Petousi Paolo Piazza Sian E Piret Guadalupe Polanco-Echeverry Niko Popitsch Fiona Powrie Chris Pugh Lynn Quek Peter A Robbins Kathryn Robson Alexandra Russo Natasha Sahgal Pauline A van Schouwenburg Anna Schuh Earl Silverman Alison Simmons Per Soelberg Sørensen Elizabeth Sweeney John Taylor Rajesh V Thakker Ian Tomlinson Amy Trebes Stephen Rf Twigg Holm H Uhlig Paresh Vyas Tim Vyse Steven A Wall Hugh Watkins Michael P Whyte Lorna Witty Ben Wright Chris Yau David Buck Sean Humphray Peter J Ratcliffe John I Bell Andrew Om Wilkie David Bentley Peter Donnelly Gilean McVean

Nat Genet 2015 Jul 18;47(7):717-726. Epub 2015 May 18.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1038/ng.3304DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4601524PMC
July 2015

Human slack potassium channel mutations increase positive cooperativity between individual channels.

Cell Rep 2014 Dec 4;9(5):1661-1672. Epub 2014 Dec 4.

Department of Pharmacology, Yale University, New Haven, CT 06520, USA; Department of Cellular and Molecular Physiology, Yale University, New Haven, CT 06520, USA. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2014.11.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4294418PMC
December 2014

Human induced pluripotent stem cell derived erythroblasts can undergo definitive erythropoiesis and co-express gamma and beta globins.

Br J Haematol 2014 Aug 16;166(3):435-48. Epub 2014 May 16.

Blood Research Laboratory, Radcliffe Department of Medicine, NHS Blood and Transplant and Nuffield Division of Clinical Laboratory Medicine, John Radcliffe Hospital, University of Oxford, Oxford, UK; Stem Cell Research Laboratory, Radcliffe Department of Medicine, NHS Blood and Transplant and Nuffield Division of Clinical Laboratory Medicine, John Radcliffe Hospital, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1111/bjh.12910DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4375519PMC
August 2014

Impact of month of birth on the development of autoimmune thyroid disease in the United Kingdom and Europe.

J Clin Endocrinol Metab 2014 Aug 19;99(8):E1459-65. Epub 2014 May 19.

Oxford Centre for Diabetes, Endocrinology, and Metabolism (A.H., J.A.H.W., S.C.L.G., M.J.S.), Department of Physiology, Anatomy, and Genetics (G.D., S.V.R.), and Oxford National Institute for Health Research Biomedical Research Centre (J.C.T.), Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7LE, United Kingdom; Centre for Endocrinology, Diabetes, and Metabolism (P.R.N., J.D.C.-S., J.A.F.), School of Clinical and Experimental Medicine, College of Medical and Dental Science, Institute of Biomedical Research, University of Birmingham, Birmingham B15 2TT, United Kingdom; Northern General Hospital (A.A.), Sheffield S5 7AU, United Kingdom; Royal Bournemouth Hospital (M.A.), Bournemouth BH7 7DW, United Kingdom; Department of Endocrinology and Metabolism (T.H.B., L.H.), Odense University Hospital, DK-5000 Odense, Denmark; Department of Medicine (K.C.), University of Cambridge, Cambridge CB2 1TN, United Kingdom; School of Medicine (J.M.C.), University of Dundee, Dundee DD1 9SY, United Kingdom; Department of Medicine (P.J.H.), University of Otago, Dunedein 9016, New Zealand; Centre for Endocrine and Diabetes Sciences (J.H.L.), Cardiff University, Cardiff C14 4XN, United Kingdom; Institute of Genetic Medicine (S.H.P.), Newcastle University, Newcastle-upon-Tyne NE1 3BZ, Newcastle, United Kingdom; Kolling Institute (B.G.R.), Royal North Shore Hospital and The University of Sydney, Sydney NSW 2006, Australia; Royal Devon and Exeter Hospital (B.V.), Exeter EX2 5DW, United Kingdom; Department of Endocrinology and Metabolism (W.M.W.), University of Amsterdam, 1100 DE Amsterdam, The Netherlands; Department of Human Metabolism (A.P.W.), University of Sheffield, Sheffield S10 2RX, United Kingdom; and Oxford National Institute for Health Research Biomedical Research Centre (S.C.L.G.), Churchill Hospital, Oxford OX3 7LE, United Kingdom.

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http://dx.doi.org/10.1210/jc.2014-1270DOI Listing
August 2014

Mutations in PGAP3 impair GPI-anchor maturation, causing a subtype of hyperphosphatasia with mental retardation.

Am J Hum Genet 2014 Feb 16;94(2):278-87. Epub 2014 Jan 16.

Institute for Medical Genetics and Human Genetics, Charité Universitätsmedizin, 13353 Berlin, Germany; Berlin Brandenburg Center for Regenerative Therapies, Charité Universitätsmedizin, 13353 Berlin, Germany; Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany. Electronic address:

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http://www.cell.com/ajhg/pdf/S0002-9297(13)00582-X.pdf
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http://linkinghub.elsevier.com/retrieve/pii/S000292971300582
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http://dx.doi.org/10.1016/j.ajhg.2013.12.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928656PMC
February 2014

Lack of generalization of auditory learning in typically developing children.

J Speech Lang Hear Res 2012 Feb 22;55(1):168-81. Epub 2011 Dec 22.

MRC Institute of Hearing Research, University Park,Nottingham, UK.

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http://dx.doi.org/10.1044/1092-4388(2011/09-0213)DOI Listing
February 2012

Managing the long term care of inflammatory bowel disease patients: The cost to European health care providers.

J Crohns Colitis 2011 Aug 10;5(4):301-16. Epub 2011 Mar 10.

Health Economics Research Centre, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1016/j.crohns.2011.02.005DOI Listing
August 2011

Dimension-specific attention directs learning and listening on auditory training tasks.

Atten Percept Psychophys 2011 Jul;73(5):1329-35

MRC Institute of Hearing Research, University Park, Nottingham, NG7 2RD, UK.

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http://www.springerlink.com/index/10.3758/s13414-011-0148-0
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http://dx.doi.org/10.3758/s13414-011-0148-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117994PMC
July 2011

DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model.

Eur Heart J 2010 Apr 18;31(8):926-35. Epub 2010 Mar 18.

Health Economics Research Centre, University of Oxford, Old Road Campus, Oxford OX3 7LF, UK.

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http://dx.doi.org/10.1093/eurheartj/ehq067DOI Listing
April 2010

Motivation and intelligence drive auditory perceptual learning.

PLoS One 2010 Mar 23;5(3):e9816. Epub 2010 Mar 23.

Medical Research Council Institute of Hearing Research, Nottingham, United Kingdom.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0009816PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2843743PMC
March 2010

Exploring NICE guidance on how to manage gastroenteritis in young children under five.

Authors:
Jenny Taylor

Nurs Times 2009 Jun 30-Jul 6;105(25):15

Calderdale and Huddersfield NHS Foundation Trust.

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September 2009

Frequency discrimination learning in children.

J Acoust Soc Am 2008 Jun;123(6):4393-402

MRC Institute of Hearing Research, University Park, Nottingham, NG7 2RD, United Kingdom.

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http://www.psychology.nottingham.ac.uk/research/vision/paper
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http://scitation.aip.org/content/asa/journal/jasa/123/6/10.1
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http://dx.doi.org/10.1121/1.2890749DOI Listing
June 2008

A genome-wide association study of global gene expression.

Nat Genet 2007 Oct 16;39(10):1202-7. Epub 2007 Sep 16.

National Heart and Lung Institute, Imperial College London, London SW3 6LY, UK.

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http://www.nature.com/articles/ng2109
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http://dx.doi.org/10.1038/ng2109DOI Listing
October 2007

Patents and translational research in genomics.

Nat Biotechnol 2007 Jul;25(7):739-41

Oxford Genetics Knowledge Park, The Ethox Centre, DPHPC, University of Oxford, Gibson Building/Block 21, Radcliffe Infirmary, Woodstock Road, Oxford, OX2 6HA, UK.

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http://www.nature.com/articles/nbt0707-739
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http://dx.doi.org/10.1038/nbt0707-739DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1955681PMC
July 2007

Non-pharmacological management of breathlessness: a collaborative nurse--physiotherapist approach.

Int J Palliat Nurs 2003 Apr;9(4):150-6

St Christopher's at Home, St Christopher's Hospice, London, UK.

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http://www.magonlinelibrary.com/doi/10.12968/ijpn.2003.9.4.1
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http://dx.doi.org/10.12968/ijpn.2003.9.4.11499DOI Listing
April 2003