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Profile Details
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USD 60 /hr
Hire Dr. Jane H.
United Kingdom
USD 60 /hr
Molecular genetics expert and next generation sequencing specialist
Profile Summary
Subject Matter Expertise
Services
Writing
Technical Writing,
General Proofreading & Editing
Research
Fact Checking,
Scientific and Technical Research,
Systematic Literature Review
Consulting
Scientific and Technical Consulting
Product Development
Stability/Shelf Life Testing,
Product Evaluation,
Product Validation,
Concept Development,
Product Launch Support,
Packaging Design
Work Experience
Field application scientist
biomodal Ltd (formerly Cambridge Epigenetix)
February 2022 - January 2025
Field application scientist
Nonacus Ltd
July 2019 - January 2022
Senior Bioscientist
AstraZeneca
June 2017 - June 2019
Translational Scientist
Molecular Genetics Laboratory Great Ormond Street Hospital
May 2016 - June 2017
PostdoctoralResearcher
University College London
September 2014 - April 2016
Postdoctoral R&D Scientist
National Hospital for Neurology and Neurosurgery
September 2013 - September 2014
Education
PhD Molecular Genetics
University College London, University of London - United Kingdom
September 2009 - September 2013
Molecular Pathology & Genomics
Barts Cancer Institute (Queen Mary University of London
September 2008 - September 2009
Biomedical Sciences
London Metropolitan University
September 2004 - June 2008
Certifications
- Certification details not provided.
Publications
JOURNAL ARTICLE
Hayward, J., Chitty, L.S.(2018). Beyond screening for chromosomal abnormalities: Advances in non-invasive diagnosis of single gene disorders and fetal exome sequencing . Seminars in Fetal and Neonatal Medicine. 23. (2). p. 94-101.
Fassad, M.R., Shoemark, A., le Borgne, P., Koll, F., Patel, M., Dixon, M., Hayward, J., Richardson, C., Frost, E., Jenkins, L., et al.(2018). C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia . American Journal of Human Genetics. 102. (5). p. 956-972.
Irving, S., Dixon, M., Fassad, M.R., Frost, E., Hayward, J., Kilpin, K., Ollosson, S., Onoufriadis, A., Patel, M.P., Scully, J., et al.(2018). Primary Ciliary Dyskinesia Due to Microtubular Defects is Associated with Worse Lung Clearance Index . Lung. 196. (2). p. 231-238.
et al.(2017). High prevalence of CCDC103 p.His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigations . Thorax.
et al.(2017). X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3 . Nature communications.
et al.(2015). Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer . Journal of the National Cancer Institute.
(2015). Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population . Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
Song, H., Dicks, E., Ramus, S.J., Tyrer, J.P., Intermaggio, M.P., Song, H., Dicks, E., Ramus, S.J., Tyrer, J.P., Intermaggio, M.P., et al.(2015). Contribution of germline mutations in the RAD51B, RAD51C, and RAD51D genes to ovarian cancer in the population . Journal of Clinical Oncology. 33. (26). p. 2901-2907.
et al.(2013). Role of DNA methylation and epigenetic silencing of HAND2 in endometrial cancer development . PLoS medicine.
Widschwendter, M., Rosenthal, A.N., Philpott, S., Rizzuto, I., Fraser, L., Hayward, J., Intermaggio, M.P., Edlund, C.K., Ramus, S.J., Gayther, S.A., et al.(2013). The sex hormone system in carriers of BRCA1/2 mutations: A case-control study . The Lancet Oncology. 14. (12). p. 1226-1232.