Gillian Turner

Gillian Turner

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Gillian Turner

Gillian Turner

Publications by authors named "Gillian Turner"

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Ibrutinib plus Venetoclax for the Treatment of Mantle-Cell Lymphoma.

N Engl J Med 2018 03;378(13):1211-1223

From the Peter MacCallum Cancer Centre, Melbourne, VIC (C.S.T., M.A.A., R.A., S.H., R.J.H., K.B., G.T., J.D.I., M.B., D.W., S.L., S.-J.D., M.A.D., J.F.S., A.W.R.), and the Victorian Comprehensive Cancer Centre (C.S.T., M.A.A., R.A., S.H., R.J.H., K.B., D.W., S.-J.D., M.A.D., J.F.S., A.W.R.), the Faculty of Medicine (C.S.T., R.J.H., S.-J.D., M.A.D., J.F.S., A.W.R.) and Centre for Cancer Research (S.-J.D., M.A.D.), University of Melbourne, the Department of Clinical Haematology and Bone Marrow Transplantation, the Royal Melbourne Hospital (C.S.T., M.A.A., K.B., J.F.S., A.W.R.), and the Division of Cancer and Haematology, Walter and Eliza Hall Institute of Medical Research (M.A.A., A.W.R.), Parkville, VIC - all in Australia; and the University Hospital of Schleswig-Holstein, Kiel (C.P.), and Klinikum der Universität, Ludwig-Maximilian University of Munich, Munich (M.D.) - both in Germany.

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http://dx.doi.org/10.1056/NEJMoa1715519DOI Listing
March 2018

A non-coding variant in the 5' UTR of DLG3 attenuates protein translation to cause non-syndromic intellectual disability.

Eur J Hum Genet 2016 11 25;24(11):1612-1616. Epub 2016 May 25.

School of Medicine and the Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.

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http://dx.doi.org/10.1038/ejhg.2016.46DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5110046PMC
November 2016

Addressing childhood obesity at school entry: Qualitative experiences of school health professionals.

J Child Health Care 2016 09 23;20(3):304-13. Epub 2015 Jun 23.

Physical Activity Exchange, Research Institute for Sport and Exercise Sciences, Liverpool John Moores University, Liverpool, UK

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http://dx.doi.org/10.1177/1367493515587061DOI Listing
September 2016

Resolution of Roth spots in chronic myeloid leukaemia after treatment with imatinib.

Br J Haematol 2015 Sep 28;170(6):744. Epub 2015 Jun 28.

Department of Haematology at Norfolk & Norwich University Hospital NHS Trust, Norwich, UK.

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http://dx.doi.org/10.1111/bjh.13546DOI Listing
September 2015

Outcomes of a cystic fibrosis carrier testing clinic for couples.

Med J Aust 2009 Nov;191(9):499-501

Hunter Genetics, Newcastle, NSW, Australia.

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November 2009

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.

Nat Genet 2009 May 19;41(5):535-43. Epub 2009 Apr 19.

Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK.

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http://dx.doi.org/10.1038/ng.367DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2872007PMC
May 2009

Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation.

Am J Hum Genet 2008 May 1;82(5):1150-7. Epub 2008 May 1.

Laboratoire de Génétique et Epigénétique des Maladies Métaboliques, Neurosensorielles et du Développement (INSERM U781), Université Paris Descartes, Hôpital Necker-Enfants Malades, F-75015 Paris, France.

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http://dx.doi.org/10.1016/j.ajhg.2008.03.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2427205PMC
May 2008

X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11.

Eur J Hum Genet 2007 Jan 13;15(1):68-75. Epub 2006 Sep 13.

Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany.

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http://dx.doi.org/10.1038/sj.ejhg.5201714DOI Listing
January 2007

The Börjeson-Forssman-Lehman syndrome (BFLS, MIM #301900).

Eur J Hum Genet 2006 Dec 16;14(12):1233-7. Epub 2006 Aug 16.

Neurogenetics Laboratory, Department of Genetic Medicine, Women's and Children's Hospital, North Adelaide, SA 5006, Australia.

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http://dx.doi.org/10.1038/sj.ejhg.5201639DOI Listing
December 2006

Multicentre study of delirium in ICU patients using a simple screening tool.

Aust Crit Care 2005 Feb;18(1):6, 8-9, 11-4 passim

ICU, Sir Charles Gairdner Hospital, Perth, WA.

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February 2005

Emerging concerns related to CJD.

Authors:
Gillian Turner

Nurs Times 2004 Aug 24-30;100(34):28-30

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November 2004

Syndromic form of X-linked mental retardation with marked hypotonia in early life, severe mental handicap, and difficult adult behavior maps to Xp22.

Am J Med Genet A 2003 Mar;117A(3):245-50

Hunter Genetics, University of Newcastle, PO Box 84, Waratah, New South Wales 2298, Australia.

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http://dx.doi.org/10.1002/ajmg.a.10005DOI Listing
March 2003

Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome.

Nat Genet 2002 Dec 4;32(4):661-5. Epub 2002 Nov 4.

Department of Cytogenetics and Molecular Genetics, Centre for Medical Genetics, Women's and Children's Hospital, 72 King William Rd., North Adelaide, SA 5006, Australia.

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http://www.nature.com/articles/ng1040
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http://dx.doi.org/10.1038/ng1040DOI Listing
December 2002

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy.

Nat Genet 2002 Apr 11;30(4):441-5. Epub 2002 Mar 11.

Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital, North Adelaide, South Australia 5006, Australia.

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http://dx.doi.org/10.1038/ng862DOI Listing
April 2002

Personal recollections of Professor Michael Hull.

Hum Fertil (Camb) 2002 Feb;5(1 Suppl):S72-5

Department of Reproductive Medicine St Mary's Hospital, Whitworth Park, Manchester.

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February 2002

Best Foot Forward.

Authors:
Gillian F Turner

J R Coll Physicians Lond 1993 Oct;27(4):476-477

Member, Standing Committee of Members 1989-93.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396723PMC
October 1993

Members' Column.

Authors:
Gillian Turner

J R Coll Physicians Lond 1992 Jan;26(1 Suppl):9-10

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5375405PMC
January 1992