Publications by authors named "Glen Brice"

39Publications

Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.

Authors:
Elisavet Fotiou Silvia Martin-Almedina Michael A Simpson Shin Lin Kristiana Gordon Glen Brice Giles Atton Iona Jeffery David C Rees Cyril Mignot Julie Vogt Tessa Homfray Michael P Snyder Stanley G Rockson Steve Jeffery Peter S Mortimer Sahar Mansour Pia Ostergaard

Nat Commun 2019 Apr 26;10(1):1951. Epub 2019 Apr 26.

Cardiovascular and Cell Sciences Institute, St. George's University of London, Cranmer Terrace, London, SW17 0RE, UK.

View Article and Find Full Text PDF
April 2019

Human venous valve disease caused by mutations in FOXC2 and GJC2.

Authors:
Oliver Lyons Prakash Saha Christopher Seet Adam Kuchta Andrew Arnold Steven Grover Victoria Rashbrook Amélie Sabine Gema Vizcay-Barrena Ash Patel Francesca Ludwinski Soundrie Padayachee Tsutomu Kume Brenda R Kwak Glen Brice Sahar Mansour Pia Ostergaard Peter Mortimer Steve Jeffery Nigel Brown Taija Makinen Tatiana V Petrova Bijan Modarai Alberto Smith

J Exp Med 2017 Aug;214(8):2437-2452

Academic Department of Vascular Surgery, Cardiovascular Division, BHF Centre of Research Excellence, King's College London, St Thomas' Hospital, London, England, UK.

View Article and Find Full Text PDF
August 2017

EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis.

Authors:
Silvia Martin-Almedina Ines Martinez-Corral Rita Holdhus Andres Vicente Elisavet Fotiou Shin Lin Kjell Petersen Michael A Simpson Alexander Hoischen Christian Gilissen Heather Jeffery Giles Atton Christina Karapouliou Glen Brice Kristiana Gordon John W Wiseman Marianne Wedin Stanley G Rockson Steve Jeffery Peter S Mortimer Michael P Snyder Siren Berland Sahar Mansour Taija Makinen Pia Ostergaard

J Clin Invest 2016 08 11;126(8):3080-8. Epub 2016 Jul 11.

View Article and Find Full Text PDF
August 2016

Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.

Authors:
Elisavet Fotiou Silvia Martin-Almedina Michael A Simpson Shin Lin Kristiana Gordon Glen Brice Giles Atton Iona Jeffery David C Rees Cyril Mignot Julie Vogt Tessa Homfray Michael P Snyder Stanley G Rockson Steve Jeffery Peter S Mortimer Sahar Mansour Pia Ostergaard

Nat Commun 2015 Sep 3;6:8085. Epub 2015 Sep 3.

Cardiovascular and Cell Sciences Institute, St. George's University of London, Cranmer Terrace, London SW17 0RE, UK.

View Article and Find Full Text PDF
September 2015

The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome.

Authors:
Sarah Joyce Kristiana Gordon Glen Brice Pia Ostergaard Rani Nagaraja John Short Sandra Moore Peter Mortimer Sahar Mansour

Eur J Hum Genet 2016 May 5;24(5):690-6. Epub 2015 Aug 5.

SW Thames Regional Genetics Service, St George's Healthcare NHS Trust, London, UK.

View Article and Find Full Text PDF
May 2016

The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review.

Authors:
Giles Atton Kristiana Gordon Glen Brice Vaughan Keeley Katie Riches Pia Ostergaard Peter Mortimer Sahar Mansour

Eur J Hum Genet 2015 Dec 25;23(12):1634-9. Epub 2015 Mar 25.

South West Thames Regional Genetics Service, St George's Healthcare NHS Trust, London, UK.

View Article and Find Full Text PDF
December 2015

Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.

Authors:
Gabriela E Jones Pia Ostergaard Anthony T Moore Fiona C Connell Denise Williams Oliver Quarrell Angela F Brady Isabel Spier Filiz Hazan Oana Moldovan Dagmar Wieczorek Barbara Mikat Florence Petit Christine Coubes Robert A Saul Glen Brice Kristiana Gordon Steve Jeffery Peter S Mortimer Pradeep C Vasudevan Sahar Mansour

Eur J Hum Genet 2014 Jul 27;22(7):881-7. Epub 2013 Nov 27.

South West Thames Regional Genetics Service, St George's Healthcare NHS Trust, London, UK.

View Article and Find Full Text PDF
July 2014

Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedema.

Authors:
Kristiana Gordon Dörte Schulte Glen Brice Michael A Simpson M Guy Roukens Andreas van Impel Fiona Connell Kamini Kalidas Steve Jeffery Peter S Mortimer Sahar Mansour Stefan Schulte-Merker Pia Ostergaard

Circ Res 2013 Mar 14;112(6):956-60. Epub 2013 Feb 14.

Human Genetics Research Centre, Biomedical Sciences, St George's University of London, London, United Kingdom.

View Article and Find Full Text PDF
March 2013

Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer.

Authors:
Elise Ruark Katie Snape Peter Humburg Chey Loveday Ilirjana Bajrami Rachel Brough Daniel Nava Rodrigues Anthony Renwick Sheila Seal Emma Ramsay Silvana Del Vecchio Duarte Manuel A Rivas Margaret Warren-Perry Anna Zachariou Adriana Campion-Flora Sandra Hanks Anne Murray Naser Ansari Pour Jenny Douglas Lorna Gregory Andrew Rimmer Neil M Walker Tsun-Po Yang Julian W Adlard Julian Barwell Jonathan Berg Angela F Brady Carole Brewer Glen Brice Cyril Chapman Jackie Cook Rosemarie Davidson Alan Donaldson Fiona Douglas Diana Eccles D Gareth Evans Lynn Greenhalgh Alex Henderson Louise Izatt Ajith Kumar Fiona Lalloo Zosia Miedzybrodzka Patrick J Morrison Joan Paterson Mary Porteous Mark T Rogers Susan Shanley Lisa Walker Martin Gore Richard Houlston Matthew A Brown Mark J Caufield Panagiotis Deloukas Mark I McCarthy John A Todd Clare Turnbull Jorge S Reis-Filho Alan Ashworth Antonis C Antoniou Christopher J Lord Peter Donnelly Nazneen Rahman

Nature 2013 Jan 16;493(7432):406-10. Epub 2012 Dec 16.

Division of Genetics & Epidemiology, The Institute of Cancer Research, Sutton SM2 5NG, UK.

View Article and Find Full Text PDF
January 2013

FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update.

Authors:
Kristiana Gordon Sarah L Spiden Fiona C Connell Glen Brice Sally Cottrell John Short Rohan Taylor Steve Jeffery Peter S Mortimer Sahar Mansour Pia Ostergaard

Hum Mutat 2013 Jan 16;34(1):23-31. Epub 2012 Oct 16.

Department of Cardiac and Vascular Sciences, St George's University of London, London, United Kingdom.

View Article and Find Full Text PDF
January 2013

Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy.

Authors:
Pia Ostergaard Michael A Simpson Antonella Mendola Pradeep Vasudevan Fiona C Connell Andreas van Impel Anthony T Moore Bart L Loeys Arash Ghalamkarpour Alexandros Onoufriadis Ines Martinez-Corral Sophie Devery Jules G Leroy Lut van Laer Amihood Singer Martin G Bialer Meriel McEntagart Oliver Quarrell Glen Brice Richard C Trembath Stefan Schulte-Merker Taija Makinen Miikka Vikkula Peter S Mortimer Sahar Mansour Steve Jeffery

Am J Hum Genet 2012 Feb 26;90(2):356-62. Epub 2012 Jan 26.

Medical Genetics Unit, Biomedical Sciences, St. George's University of London, UK.

View Article and Find Full Text PDF
February 2012

Gene-gene interactions in breast cancer susceptibility.

Authors:
Clare Turnbull Sheila Seal Anthony Renwick Margaret Warren-Perry Deborah Hughes Anna Elliott David Pernet Susan Peock Julian W Adlard Julian Barwell Jonathan Berg Angela F Brady Carole Brewer Glen Brice Cyril Chapman Jackie Cook Rosemarie Davidson Alan Donaldson Fiona Douglas Lynn Greenhalgh Alex Henderson Louise Izatt Ajith Kumar Fiona Lalloo Zosia Miedzybrodzka Patrick J Morrison Joan Paterson Mary Porteous Mark T Rogers Susan Shanley Lisa Walker Munaza Ahmed Diana Eccles D Gareth Evans Peter Donnelly Douglas F Easton Michael R Stratton Nazneen Rahman

Hum Mol Genet 2012 Feb 9;21(4):958-62. Epub 2011 Nov 9.

Division of Genetics and Epidemiology, The Institute of Cancer Research, Sutton, Surrey SM2 5NG, UK.

View Article and Find Full Text PDF
February 2012

Primary lymphedema with coarctation of the aorta: possible new syndrome or variant of Irons-Bianchi syndrome?

Authors:
John S Ferguson Shymalar Gunatheesan Glen Brice Rob Hastings Ruth Newbury-Ecob Peter S Mortimer Sahar Mansour

Am J Med Genet A 2011 Nov 22;155A(11):2762-5. Epub 2011 Sep 22.

Department of Dermatology, St George's Healthcare NHS Trust, London, UK.

View Article and Find Full Text PDF
November 2011

Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome).

Authors:
Pia Ostergaard Michael A Simpson Fiona C Connell Colin G Steward Glen Brice Wesley J Woollard Dimitra Dafou Tatjana Kilo Sarah Smithson Peter Lunt Victoria A Murday Shirley Hodgson Russell Keenan Daniela T Pilz Ines Martinez-Corral Taija Makinen Peter S Mortimer Steve Jeffery Richard C Trembath Sahar Mansour

Nat Genet 2011 Sep 4;43(10):929-31. Epub 2011 Sep 4.

Medical Genetics Unit, Biomedical Sciences, St. George's University of London, London, UK.

View Article and Find Full Text PDF
September 2011

Germline mutations in RAD51D confer susceptibility to ovarian cancer.

Authors:
Chey Loveday Clare Turnbull Emma Ramsay Deborah Hughes Elise Ruark Jessica R Frankum Georgina Bowden Bolot Kalmyrzaev Margaret Warren-Perry Katie Snape Julian W Adlard Julian Barwell Jonathan Berg Angela F Brady Carole Brewer Glen Brice Cyril Chapman Jackie Cook Rosemarie Davidson Alan Donaldson Fiona Douglas Lynn Greenhalgh Alex Henderson Louise Izatt Ajith Kumar Fiona Lalloo Zosia Miedzybrodzka Patrick J Morrison Joan Paterson Mary Porteous Mark T Rogers Susan Shanley Lisa Walker Diana Eccles D Gareth Evans Anthony Renwick Sheila Seal Christopher J Lord Alan Ashworth Jorge S Reis-Filho Antonis C Antoniou Nazneen Rahman

Nat Genet 2011 Aug 7;43(9):879-882. Epub 2011 Aug 7.

Section of Cancer Genetics, The Institute of Cancer Research, Sutton.

View Article and Find Full Text PDF
August 2011

PSENEN and NCSTN mutations in familial hidradenitis suppurativa (Acne Inversa).

Authors:
Andrew E Pink Michael A Simpson Glen W Brice Catherine H Smith Nemesha Desai Peter S Mortimer Jonathan N W N Barker Richard C Trembath

J Invest Dermatol 2011 Jul 17;131(7):1568-70. Epub 2011 Mar 17.

View Article and Find Full Text PDF
July 2011

Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype.

Authors:
Pia Ostergaard Michael A Simpson Glen Brice Sahar Mansour Fiona C Connell Alexandros Onoufriadis Anne H Child Jae Hwang Kamini Kalidas Peter S Mortimer Richard Trembath Steve Jeffery

J Med Genet 2011 Apr 25;48(4):251-5. Epub 2011 Jan 25.

Medical Genetics, St George's, University of London, and Guy's Hospital, London SW17 ORE, UK.

View Article and Find Full Text PDF
April 2011

Legius syndrome in fourteen families.

Authors:
Ellen Denayer Magdalena Chmara Hilde Brems Anneke Maat Kievit Yolande van Bever Ans M W Van den Ouweland Rick Van Minkelen Arja de Goede-Bolder Rianne Oostenbrink Phillis Lakeman Eline Beert Takuma Ishizaki Tomoaki Mori Kathelijn Keymolen Jenneke Van den Ende Elisabeth Mangold Sirkku Peltonen Glen Brice Julia Rankin Karin Y Van Spaendonck-Zwarts Akihiko Yoshimura Eric Legius

Hum Mutat 2011 Jan;32(1):E1985-98

Department of Human Genetics, Catholic University of Leuven, Belgium.

View Article and Find Full Text PDF
January 2011