Publications by authors named "Victoria Harrison"

Claim this Profile
G
Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism.
Luisa Marsili, Matthieu Mantecon, Christelle Arrondel, Giulia Barcia, Zahra Assouline, Victoria Harrison

Pediatr Nephrol· September 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Delivery of a national prenatal exome sequencing service in England: a mixed methods study exploring healthcare professionals' views and experiences.
Michelle Peter, Rhiannon Mellis, Hannah McInnes-Dean, Morgan Daniel, Holly Walton, Victoria Harrison

Front Genet· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Diagnosis of inborn errors of metabolism through prenatal exome sequencing with targeted analysis for fetal structural anomalies.
Stephanie K Allen, Natalie J Chandler, Esther Kinning, Victoria Harrison, Shona L C Brothwell

Prenat Diagn· April 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
Z
ZTTK syndrome: Clinical and molecular findings of 15 cases and a review of the literature.
Sulagna Tina Kushary, Anya Revah-Politi, Subit Barua, Mythily Ganapathi, Andrea Accogli, Victoria Harrison

Am J Med Genet A· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome.
Marjolein J A Weerts, Kristina Lanko, Francisco J Guzmán-Vega, Adam Jackson, Reshmi Ramakrishnan, Victoria Harrison

Genet Med· November 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy.
David A Parry, Carol-Anne Martin, Philip Greene, Joseph A Marsh, , Victoria Harrison

Genet Med· February 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidine.
Víctor Faundes, Martin D Jennings, Siobhan Crilly, Sarah Legraie, Sarah E Withers, Victoria Harrison

Nat Commun· February 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of UBAP1 mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project.
Thomas Bourinaris, Damian Smedley, Valentina Cipriani, Isabella Sheikh, Alkyoni Athanasiou-Fragkouli, Victoria Harrison

Eur J Hum Genet· December 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SCN3A-Related Neurodevelopmental Disorder: A Spectrum of Epilepsy and Brain Malformation.
Tariq Zaman, Katherine L Helbig, Jérôme Clatot, Christopher H Thompson, Seok Kyu Kang, Victoria Harrison

Ann Neurol· August 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
Z
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder.
Raphael Carapito, Ekaterina L Ivanova, Aurore Morlon, Linyan Meng, Anne Molitor, Victoria Harrison

Am J Hum Genet· January 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome.
Francesco Vetrini, Shane McKee, Jill A Rosenfeld, Mohnish Suri, Andrea M Lewis, Victoria Harrison

Genome Med· March 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
Z
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder.
Raphael Carapito, Ekaterina L Ivanova, Aurore Morlon, Linyan Meng, Anne Molitor, Victoria Harrison

Am J Hum Genet· February 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome.
Francesco Vetrini, Shane McKee, Jill A Rosenfeld, Mohnish Suri, Andrea M Lewis, Victoria Harrison

Genome Med· February 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder.
Anne Gregor, Lynette G Sadleir, Reza Asadollahi, Silvia Azzarello-Burri, Agatino Battaglia, Victoria Harrison

Am J Hum Genet· August 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De novo mutation associated with mitochondrial epilepsy syndrome with fever sensitivity.
Emma Ladds, Andrea Whitney, Eszter Dombi, Monika Hofer, Geetha Anand, Victoria Harrison

Neurol Genet· August 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Incomplete penetrance, variable expressivity, or dosage insensitivity in four families with directly transmitted unbalanced chromosome abnormalities.
Mark S Bateman, Morag N Collinson, David J Bunyan, Amanda L Collins, Philippa Duncan, Victoria Harrison

Am J Med Genet A· February 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Magnetic barcode imaging for contrast agents.
Andy H Hung, Laura M Lilley, Fengqin Hu, Victoria S R Harrison, Thomas J Meade

Magn Reson Med· March 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Interprofessional enhanced skills training in periodontology: a qualitative study of one London pilot.
Eloise Radcliffe, Swapnil G Ghotane, Victoria Harrison, Jennifer E Gallagher

BDJ Open· February 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Multimeric Near IR-MR Contrast Agent for Multimodal In Vivo Imaging.
Victoria S R Harrison, Christiane E Carney, Keith W MacRenaris, Emily A Waters, Thomas J Meade

J Am Chem Soc· July 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Long-term patterns of dental attendance and caries experience among British adults: a retrospective analysis.
Arwa Aldossary, Victoria E Harrison, Eduardo Bernabé

Eur J Oral Sci· February 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism.
Morad Ansari, Gemma Poke, Quentin Ferry, Kathleen Williamson, Roland Aldridge, Victoria Harrison

J Med Genet· October 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A multimeric MR-optical contrast agent for multimodal imaging.
Victoria S R Harrison, Christiane E Carney, Keith W Macrenaris, Thomas J Meade

Chem Commun (Camb)· October 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Sense of coherence and incidence of periodontal disease in adults.
Jai Kanhai, Victoria E Harrison, Anna L Suominen, Matti Knuuttila, Antti Uutela

J Clin Periodontol· August 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Multimodal imaging enables early detection and characterization of changes in tumor permeability of brain metastases.
Frits Thorsen, Brett Fite, Lisa M Mahakian, Jai W Seo, Shengping Qin, Victoria Harrison

J Control Release· December 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel nonsense CDK5RAP2 mutation in a Somali child with primary microcephaly and sensorineural hearing loss.
Alistair T Pagnamenta, Jennie E Murray, Grace Yoon, Elham Sadighi Akha, Victoria Harrison

Am J Med Genet A· October 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis