Product
Help
Pricing
About
Jobs
Log in
Get started
Author
Add to collection
Jessica Woodley
Observed name:
J. Woodley
Institution:
Birmingham Women’s and Children’s NHS Foundation Trust
Observed institutions:
Churchill Hospital,
Queen Alexandra Hospital,
University of Oxford,
Birmingham Women's Hospital,
Birmingham Women’s and Children’s NHS Foundation Trust,
Integrated DNA Technologies (United States)
show all 6
ORCID:
0009-0006-3076-6471
Observed ORCID:
0009-0006-3076-6471
OpenAlex ID:
A5016570901
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
2016
·
Roddy Walsh
, Kate L. Thomson
, et al.
·
Genetics in Medicine
·
746
PDF
Optimized design parameters for CRISPR Cas9 and Cas12a homology-directed repair
2021
·
Mollie S. Schubert
, Bernice Thommandru
, et al.
·
Scientific Reports
·
136
PDF
Reevaluation of the South Asian MYBPC3 Δ25bp Intronic Deletion in Hypertrophic Cardiomyopathy
2020
·
Andrew R. Harper
, Michael Bowman
, et al.
·
Circulation Genomic and Precision Medicine
·
44
PDF
Kosaki overgrowth syndrome: A novel pathogenic variant in PDGFRB and expansion of the phenotype including cerebrovascular complications
2020
·
Alison Foster
, Basile Chalot
, et al.
·
Clinical Genetics
·
32
PDF
Inherited predisposition to pneumothorax: estimating the frequency of Birt-Hogg-Dub� syndrome from genomics and population cohorts
2025
·
Bryndis Yngvadottir
, Lucy Richman
, et al.
·
Thorax
·
20
ACKR1 /Duffy‐null genotype testing for clozapine: A guideline developed by the UK Centre of Excellence in Regulatory Science and Innovation in Pharmacogenomics (CERSI‐PGx)
2026
·
Stephen Murtough
, Oriella Stellakis
, et al.
·
British Journal of Clinical Pharmacology
·
6
Effect of CYP1A2, CYP2D6, and CYP3A4 Variation on Antipsychotic Treatment Outcomes
2025
·
Lauren Varney
, Stephen Murtough
, et al.
·
Pharmaceuticals
·
4
PDF
ACKR1 genetic testing should be offered before starting clozapine treatment
2026
·
Stephen Murtough
, Daisy Mills
, et al.
·
Nature Mental Health
·
3
Identification of novel 3D-genome altering and complex structural variants underlying retinitis pigmentosa type 17 through a multistep and high-throughput approach
2024
·
Suzanne E. de Bruijn
, Daan M. Panneman
, et al.
·
Frontiers in Genetics
·
3
PDF
67. A rare case of aortitis as the presenting feature of haematological malignancy
2018
·
Laura Spooner
, Gurdeep Dulay
, et al.
·
Rheumatology Advances in Practice
·
1
Standardized Methods in Ipsc for Crispr-based Editing and Homology-directed Repair (hdr)
2024
·
K. Murugan
, B.C. Thommandru
, et al.
·
Cytotherapy
Improved Knock-in in Primary T Cells With Optimized Cas9 Hdr Methods and Reagents
2024
·
B.C. Thommandru
, K. Murugan
, et al.
·
Cytotherapy
Pb1786: Comparison of Optical Genome Mapping With Standard of Care Testing to Investigate Genomic Abnormalities in Leukaemias: the Experience of the Central and South Genomic Laboratory Hub, Uk
2022
·
M. Muraru
, A. Skowronska
, et al.
·
HemaSphere
The Nature, Prevalence and Clinical Significance of Anderson-Fabry Disease in a UK Hypertrophic Cardiomyopathy (HCM) Cohort
2012
·
Jeffrey Taylor
, Jessica Woodley
, et al.
·
Journal of Medical Genetics
Expansion of a diagnostic service for hypertrophic cardiomyopathy using next generation sequencing
2011
·
Suzanne Kamel Reid
, Jessica Woodley
, et al.
·
Journal of Medical Genetics
Show more works
View as search
Works count:
15
Citation count:
995
H-index:
6
I10-index:
5
Year
Topic
Type