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Jana Jezkova
Jana Jezkova
Clinical Scientist and Postdoctoral Fellow, AWMGS & Cardiff University
Verified email at cardiff.ac.uk
Title
Cited by
Cited by
Year
Human germ/stem cell-specific gene TEX19 influences cancer cell proliferation and cancer prognosis
V Planells-Palop, A Hazazi, J Feichtinger, J Jezkova, G Thallinger, ...
Molecular cancer 16, 1-18, 2017
232017
Brachyury identifies a class of enteroendocrine cells in normal human intestinal crypts and colorectal cancer
J Jezkova, JS Williams, F Pinto, SJ Sammut, GT Williams, S Gollins, ...
Oncotarget 7 (10), 11478, 2016
202016
Brachyury regulates proliferation of cancer cells via a p27Kip1-dependent pathway
J Jezkova, JS Williams, F Jones-Hutchins, SJ Sammut, S Gollins, I Cree, ...
Oncotarget 5 (11), 3813, 2014
162014
Rapid genome sequencing for pediatrics
J Jezkova, S Shaw, NV Taverner, HJ Williams
Human Mutation 43 (11), 1507-1518, 2022
142022
Exon-focused targeted oligonucleotide microarray design increases detection of clinically relevant variants across multiple NHS genomic centres
J Jezkova, J Heath, A Williams, D Barrell, J Norton, MN Collinson, SJ Beal, ...
NPJ genomic medicine 5 (1), 28, 2020
32020
1165 The wales infants’ and children’s genome service’(WINGS): diagnostic rapid whole genome sequencing for unwell children with a suspected rare genetic diagnosis
O Murch, J Jezkova, J Halstead, K Burke, S Oruganti, J Calvert, J Evans, ...
Archives of Disease in Childhood 106 (Suppl 1), A256-A256, 2021
22021
The role of Brachyury in colorectal cancer cells
J Jezkova
Prifysgol Bangor University, 2015
12015
Wales Infants’ and childreN’s Genome Service (WINGS): providing rapid genetic diagnoses for unwell children
E Sloper, J Jezkova, J Thomas, K Dawson, J Halstead, J Gardner, ...
Archives of Disease in Childhood, 2024
2024
The Wales Infants' and childreN's Genome Service'(WINGS): Diagnostic rapid whole genome sequencing for unwell children with a suspected rare genetic diagnosis
E Sloper, O Murch, J Jezkova, M Fealey, J Halstead, T Stoneman, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 340-341, 2022
2022
Resource type: White paper Application: Cytogenetics & rare disease
J Jezkova, J Heath, A Williams, D Barrell, J Norton, MN Collinson, SJ Beal, ...
Resource, 2020
2020
Brachyury Identifies a Class of Enteroendocrine Cells in Normal Human Small Intestinal and Colonic Crypts
JS Williams, J Jezkova, F Pinto, SJ Sammut, GT Williams, S Gollins, ...
PUBLIC HEALTH GENOMICS 19, 7-7, 2016
2016
Genetic analysis of the bearded collie breed: a causal mutation of coat color genes and the dopamine receptor gene DRD4
P Vejl, D Cilova, J Jezkova, M Melounova
Journal of Veterinary Behavior: Clinical Applications and Research 1 (6), 67, 2011
2011
Hiding in plain sight: Inherited pathogenic variants that are expanding clinical phenotypes in autosomal dominant syndromes
A Williams, A Kamath, AE Fry, J Jezkova, J Heath, DA Barrell, S Corrin, ...
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