Tessa Homfray

Tessa Homfray

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Tessa Homfray

Tessa Homfray

Publications by authors named "Tessa Homfray"

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42Publications

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Obstetric complications in pregnancies with life-limiting malformations.

Curr Opin Obstet Gynecol 2019 Dec;31(6):375-387

The Royal London Hospital, Barts Health NHS Trust.

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http://dx.doi.org/10.1097/GCO.0000000000000583DOI Listing
December 2019

Persistently elevated nuchal translucency and the fetal heart.

J Matern Fetal Neonatal Med 2018 Sep 4;31(18):2376-2380. Epub 2017 Jul 4.

a Harris Birthright Research Centre for Fetal Medicine, Fetal Medicine Research Institute, King's College Hospital , Denmark Hill, London , UK.

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http://dx.doi.org/10.1080/14767058.2017.1342804DOI Listing
September 2018

The Diagnostic Yield of Brugada Syndrome After Sudden Death With Normal Autopsy.

J Am Coll Cardiol 2018 03;71(11):1204-1214

Cardiology Clinical Academic Group, St. George's, University of London and St. George's University Hospitals NHS Foundation Trust, London, United Kingdom, European Reference Network for rare and low prevalence diseases of the heart, Guard-Heart.

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http://dx.doi.org/10.1016/j.jacc.2018.01.031DOI Listing
March 2018

Estimation of Detection Rates of Aneuploidy in High-Risk Pregnancy Using an Approach Based on Nuchal Translucency and Non-Invasive Prenatal Testing: A Cohort Study.

Fetal Diagn Ther 2015 30;38(4):254-61. Epub 2015 Apr 30.

Fetal Medicine Unit, Academic Department of Obstetrics and Gynaecology, St George's University of London, London, UK.

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http://dx.doi.org/10.1159/000381182DOI Listing
October 2016

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

Nat Genet 2016 09 1;48(9):1060-5. Epub 2016 Aug 1.

Wellcome Trust Sanger Institute, Cambridge, UK.

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http://dx.doi.org/10.1038/ng.3627DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988037PMC
September 2016

Severe micrognathia with rib dysplasia: cerebro-costo-mandibular syndrome.

Arch Dis Child Fetal Neonatal Ed 2016 Jan 3;101(1):F85. Epub 2015 Aug 3.

Neonatal Unit, St George's Hospital, London, UK.

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http://dx.doi.org/10.1136/archdischild-2014-307855DOI Listing
January 2016

Replacing the combined test by cell-free DNA testing in screening for trisomies 21, 18 and 13: impact on the diagnosis of other chromosomal abnormalities.

Fetal Diagn Ther 2014 8;35(3):174-84. Epub 2014 Feb 8.

Harris Birthright Research Centre of Fetal Medicine, King's College Hospital, London, UK.

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http://dx.doi.org/10.1159/000358388DOI Listing
February 2015

Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism.

J Med Genet 2014 Oct 14;51(10):659-68. Epub 2014 Aug 14.

MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.

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http://dx.doi.org/10.1136/jmedgenet-2014-102573DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173748PMC
October 2014

Cerebral organoids model human brain development and microcephaly.

Nature 2013 Sep 28;501(7467):373-9. Epub 2013 Aug 28.

Institute of Molecular Biotechnology of the Austrian Academy of Science, Vienna 1030, Austria.

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http://dx.doi.org/10.1038/nature12517DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817409PMC
September 2013

Prenatal diagnosis of non-immune hydrops fetalis: what do we tell the parents?

Prenat Diagn 2011 Feb 4;31(2):186-95. Epub 2011 Jan 4.

Fetal Medicine Unit, Academic Department of Obstetrics and Gynaecology, St George's Hospital Medical School, London, UK.

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http://dx.doi.org/10.1002/pd.2677DOI Listing
February 2011

Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia.

Hum Genet 2010 Feb 13;127(2):231-41. Epub 2009 Nov 13.

Medical Genetics Unit, Clinical Developmental Sciences, St George's University of London, Cranmer Terrace, London SW17 0RE, UK.

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http://dx.doi.org/10.1007/s00439-009-0766-yDOI Listing
February 2010

Congenital vascular malformations: a series of five prenatally diagnosed cases.

Am J Med Genet A 2008 Oct;146A(20):2673-80

South West Thames Regional Genetics Unit, St George's University of London, Cranmer Terrace, London, United Kingdom.

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http://dx.doi.org/10.1002/ajmg.a.32502DOI Listing
October 2008

Familial T-cell non-Hodgkin lymphoma caused by biallelic MSH2 mutations.

J Med Genet 2007 Jul;44(7):e83

Section of Cancer Genetics, Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey, UK, SM2 5NG.

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http://dx.doi.org/10.1136/jmg.2007.048942DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2597999PMC
July 2007

Heterozygous missense mutations in steroidogenic factor 1 (SF1/Ad4BP, NR5A1) are associated with 46,XY disorders of sex development with normal adrenal function.

J Clin Endocrinol Metab 2007 Mar 2;92(3):991-9. Epub 2007 Jan 2.

Developmental Endocrinology Research Group, Clinical and Molecular Genetics Unit, UCL Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, United Kingdom.

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http://dx.doi.org/10.1210/jc.2006-1672DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1872053PMC
March 2007

A newly recognized autosomal recessive syndrome with abnormal vertebral ossification, rib abnormalities, and nephrogenic rests.

Am J Med Genet A 2003 Jul;120A(3):386-8

Fetal Medicine Unit, Department of Obstetrics and Gynaecology, St. George's Hospital Medical School, London, United Kingdom.

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http://dx.doi.org/10.1002/ajmg.a.20097DOI Listing
July 2003