Publications by authors named "Fiona Connell"

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Visceral adipose tissue secretome from early and late-stage oesophageal cancer patients differentially affects effector and regulatory T cells.
Maria Davern, Dara Bracken-Clarke, Noel E Donlon, Andrew D Sheppard, Fiona O' Connell

J Cancer Res Clin Oncol· August 2023

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FLOT and CROSS chemotherapy regimens alter the frequency of CD27 and CD69 T cells in oesophagogastric adenocarcinomas: implications for combination with immunotherapy.
Maria Davern, Noel E Donlon, Andrew S Sheppard, Klaudia D Majcher, Fiona O' Connell

J Cancer Res Clin Oncol· July 2023

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Chemotherapy regimens induce inhibitory immune checkpoint protein expression on stem-like and senescent-like oesophageal adenocarcinoma cells.
Maria Davern, Noel E Donlon, Andrew Sheppard, Fiona O' Connell, Conall Hayes

Transl Oncol· June 2021

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Clinical and molecular consequences of disease-associated de novo mutations in SATB2.
Hemant Bengani, Mark Handley, Mohsan Alvi, Rita Ibitoye, Melissa Lees, Fiona Connell

Genet Med· August 2017

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Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.
Gabriela E Jones, Pia Ostergaard, Anthony T Moore, Fiona C Connell, Denise Williams

Eur J Hum Genet· July 2014

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Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations.
Chiara Migliore, Emmanouil Athanasakis, Sophie Dahoun, Ambroise Wonkam, Melissa Lees, Fiona Connell

Eur J Med Genet· August 2013

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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.
Kristiana Gordon, Dörte Schulte, Glen Brice, Michael A Simpson, M Guy Roukens, Fiona Connell

Circ Res· March 2013

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FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update.
Kristiana Gordon, Sarah L Spiden, Fiona C Connell, Glen Brice, Sally Cottrell

Hum Mutat· January 2013

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Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy.
Pia Ostergaard, Michael A Simpson, Antonella Mendola, Pradeep Vasudevan, Fiona C Connell

Am J Hum Genet· February 2012

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Pierpont syndrome: a collaborative study.
Emma M M Burkitt Wright, Mohnish Suri, Susan M White, Nicole de Leeuw, Anneke T Vulto-van Silfhout, Fiona C Connell

Am J Med Genet A· September 2011

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Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome).
Pia Ostergaard, Michael A Simpson, Fiona C Connell, Colin G Steward, Glen Brice

Nat Genet· September 2011

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Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype.
Pia Ostergaard, Michael A Simpson, Glen Brice, Sahar Mansour, Fiona C Connell

J Med Genet· April 2011

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Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new cases.
Sahar Mansour, Fiona Connell, Colin Steward, Pia Ostergaard, Glen Brice

Am J Med Genet A· September 2010

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Re: "conjunctival edema and distichiasis in association with congenital lymphedema of the lower legs".
Glen Brice, Fiona Connell, Sahar Mansour, Steve Jeffery, Peter Mortimer

Ophthalmic Plast Reconstr Surg· July 2010

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Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia.
Fiona Connell, Kamini Kalidas, Pia Ostergaard, Glen Brice, Tessa Homfray

Hum Genet· February 2010

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Congenital vascular malformations: a series of five prenatally diagnosed cases.
Fiona Connell, Tessa Homfray, Baskaran Thilaganathan, Amarnath Bhide, Iona Jeffrey

Am J Med Genet A· October 2008

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Phenotypic characterization of primary lymphedema.
Fiona Connell, Glen Brice, Peter Mortimer

Ann N Y Acad Sci· July 2008

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Our evolving understanding of 22q.11 deletion syndrome.
Fiona Connell, Shirley Hodgson

Dev Med Child Neurol· December 2005

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