Jamie M Ellingford (Jamie Ellingford)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 15

Top Venues

Journal of medical genetics

Science advances

European journal of human genetics : EJHG

eLife

University of Manchester (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

University of Manchester

United Kingdom

PHD :: Manchester Centre for Genomic Medicine

University of Sheffield

United Kingdom

BSC

Publications

George Joseph Burghel, Jamie M Ellingford, Ronnie Wright, Lauren Bradford, Jake Miller, Christopher Watt, Jonathan Edgerley, Farah Naeem, Siddharth Banka
Systematic reanalysis of copy number losses of uncertain clinical significance. Journal of medical genetics 61 (7) (2024)
George Joseph Burghel, Jamie M Ellingford, Ronnie Wright, Lauren Bradford, Jake Miller, Christopher Watt, Jonathan Edgerley, Farah Naeem, Siddharth Banka
Systematic reanalysis of copy number losses of uncertain clinical significance. Journal of medical genetics 61 (7) (2024)
George Joseph Burghel, Jamie M Ellingford, Ronnie Wright, Lauren Bradford, Jake Miller, Christopher Watt, Jonathan Edgerley, Farah Naeem, Siddharth Banka
Systematic reanalysis of copy number losses of uncertain clinical significance. Journal of medical genetics (2024)
Eva Lenassi, Ana Carvalho, Anja Thormann, Liam Abrahams, Gavin Arno, Tracy Fletcher, Claire Hardcastle, Javier Lopez, Sarah E Hunt, Patrick Short, Panagiotis I Sergouniotis, Michel Michaelides, Andrew Webster, Fiona Cunningham, Simon C Ramsden, Dalia Kasperaviciute, David R Fitzpatrick, null null, Graeme C Black, Jamie M Ellingford
EyeG2P: an automated variant filtering approach improves efficiency of diagnostic genomic testing for inherited ophthalmic disorders. Journal of medical genetics (2023)
Dafydd Gareth Evans, Siva Sithambaram, Elke Maria van Veen, George Joseph Burghel, Helene Schlecht, Elaine F Harkness, Helen Byers, Jamie M Ellingford, Ashu Gandhi, Sacha J Howell, Anthony Howell, Claire Forde, Fiona Lalloo, William G Newman, Miriam Jane Smith, Emma Roisin Woodward
Differential involvement of germline pathogenic variants in breast cancer genes between DCIS and low-grade invasive cancers. Journal of medical genetics (2022)
Paul W Chrystal, Nils J Lambacher, Lance P Doucette, James Bellingham, Elena R Schiff, Nicole C L Noel, Chunmei Li, Sofia Tsiropoulou, Geoffrey A Casey, Yi Zhai, Nathan J Nadolski, Mohammed H Majumder, Julia Tagoe, Fabiana D'Esposito, Maria Francesca Cordeiro, Susan Downes, Jill Clayton-Smith, Jamie M Ellingford, null null, Omar A Mahroo, Jennifer C Hocking, Michael E Cheetham, Andrew R Webster, Gert Jansen, Oliver E Blacque, W Ted Allison, Ping Yee Billie Au, Ian M MacDonald, Gavin Arno, Michel R Leroux
The inner junction protein CFAP20 functions in motile and non-motile cilia and is critical for vision. Nature communications 13 (1) (2022)
Ranjay Jayadev, Mychel Raony P T Morais, Jamie M Ellingford, Sandhya Srinivasan, Richard W Naylor, Craig Lawless, Anna S Li, Jack F Ingham, Eric Hastie, Qiuyi Chi, Maryline Fresquet, Nikki-Maria Koudis, Huw B Thomas, Raymond T O'Keefe, Emily Williams, Antony D Adamson, Helen M Stuart, Siddharth Banka, Damian Smedley, null null, David R Sherwood, Rachel Lennon
A basement membrane discovery pipeline uncovers network complexity, regulators, and human disease associations. Science advances 8 (20) (2022)
Sunayna Best, Jenny Lord, Matthew Roche, Christopher Mark Watson, James A Poulter, Roel P J Bevers, Alex Stuckey, Katarzyna Szymanska, Jamie M Ellingford, Jenny Carmichael, Helen Brittain, Carmel Toomes, Chris Inglehearn, Colin A Johnson, Gabrielle Wheway, null null
Molecular diagnoses in the congenital malformations caused by ciliopathies cohort of the 100,000 Genomes Project. Journal of medical genetics (2021)
Shalaw Rassul Sallah, Jamie M Ellingford, Panagiotis I Sergouniotis, Simon C Ramsden, Nicholas Lench, Simon C Lovell, Graeme C Black
Improving the clinical interpretation of missense variants in X linked genes using structural analysis. Journal of medical genetics (2021)
Dafydd Gareth Evans, Elke Maria van Veen, Helen J Byers, Sarah J Evans, George Joseph Burghel, Emma Roisin Woodward, Elaine F Harkness, Diana M Eccles, Stephanie L Greville-Haygate, Jamie M Ellingford, Naomi L Bowers, Marta Pereira, Andrew J Wallace, Sasha J Howell, Anthony Howell, Fiona Lalloo, William G Newman, Miriam Jane Smith
High likelihood of actionable pathogenic variant detection in breast cancer genes in women with very early onset breast cancer. Journal of medical genetics (2021)
Leslie Patricia Molina-Ramírez, Claire Kyle, Jamie M Ellingford, Ronnie Wright, Algy Taylor, Sanjeev S Bhaskar, Christopher Campbell, Harriet Jackson, Adele Fairclough, Abigail Rousseau, George Joseph Burghel, Laura Dutton, Siddharth Banka, Tracy A Briggs, Jill Clayton-Smith, Sofia Douzgou Houge, Elizabeth A Jones, Helen M Kingston, Bronwyn Kerr, John Ealing, Suresh Somarathi, Kate E Chandler, Helen M Stuart, Emma Mm Burkitt-Wright, William G Newman, Iain A Bruce, Graeme C Black, David Gokhale
Personalised virtual gene panels reduce interpretation workload and maintain diagnostic rates of proband-only clinical exome sequencing for rare disorders. Journal of medical genetics (2021)
Zeinab Fadaie, Laura Whelan, Adrian Dockery, Catherina H Z Li, L Ingeborgh van den Born, Carel B Hoyng, Christian Gilissen, Christian Gilissen, Charlie F Rowlands, Roly Megaw, Anne K Lampe, Frans P M Cremers, Gwyneth Jane Farrar, Jamie M Ellingford, Paul F Kenna, Susanne Roosing
BBS1 branchpoint variant is associated with non-syndromic retinitis pigmentosa. Journal of medical genetics (2021)
Jamie M Ellingford, Ryan George, John H McDermott, Shazaad Ahmad, Jonathan J Edgerley, David Gokhale, William G Newman, Stephen Ball, Nicholas Machin, Graeme Cm Black
Genomic and healthcare dynamics of nosocomial SARS-CoV-2 transmission. eLife 10 (2021)
Jamie M Ellingford, Christopher Campbell, Stephanie Barton, Sanjeev Bhaskar, Saurabh Gupta, Rachel L Taylor, Panagiotis I Sergouniotis, Bradley Horn, Janine A Lamb, Michel Michaelides, Andrew R Webster, William G Newman, Binay Panda, Simon C Ramsden, Graeme Cm Black
Validation of copy number variation analysis for next-generation sequencing diagnostics. European journal of human genetics : EJHG 25 (6) (2017)
Jamie M Ellingford, Bradley Horn, Christopher Campbell, Gavin Arno, Stephanie Barton, Catriona Tate, Sanjeev Bhaskar, Panagiotis I Sergouniotis, Rachel L Taylor, Keren J Carss, Lucy F L Raymond, Michel Michaelides, Simon C Ramsden, Andrew R Webster, Graeme C M Black
Assessment of the incorporation of CNV surveillance into gene panel next-generation sequencing testing for inherited retinal diseases. Journal of medical genetics 55 (2) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Jamie M Ellingford (Jamie Ellingford)