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Matthew D. C. Neville

wellcome sanger institute

12H-index
30Paper Count
1.0KCitation Count
Published Papers 10
Publication Date
Long-read sequencing reveals pre-meiotic gene conversion in sperm
errNature
IF48.5
err2026-08-26
err0
errOAAI
errRegev Schweiger; Sangjin Lee; Chenxi Zhou; Tsun-Po Yang; Stacy Li; Rashesh Sanghvi; Matthew Neville; Katie Smith; Kirsty Roberts; Ayrun Nessa; Sam Wadge; Kerrin S. Small; Peter J. Campbell; Kristian Almstrup; Peter H. Sudmant; Raheleh Rahbari; Richard Durbin
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Author Correction: Complex de novo structural variants are an underestimated cause of rare disorders
err2026-02-17
err0
errOAAI
errHyunchul Jung; Tsun-Po Yang; Susan Walker; Petr Danecek; O. Isaac Garcia-Salinas; Matthew D. C. Neville; Joseph Christopher; Isidro Cortés-Ciriano; Helen Firth; Aylwyn Scally; Matthew Hurles; Peter Campbell; Raheleh Rahbari
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Complex de novo structural variants are an underestimated cause of rare disorders
err2025-11-03
err0
errOAAI
errHyunchul Jung; Tsun-Po Yang; Susan Walker; Petr Danecek; O. Isaac Garcia-Salinas; Matthew D. C. Neville; Joseph Christopher; Isidro Cortés-Ciriano; Helen Firth; Aylwyn Scally; Matthew Hurles; Peter Campbell; Raheleh Rahbari
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Somatic mutation and selection at population scale
errNature
IF48.5
err2025-10-08
err0
errOAAI
errAndrew R. J. Lawson; Federico Abascal; Pantelis A. Nicola; Stefanie V. Lensing; Amy L. Roberts; Georgios Kalantzis; Adrian Baez-Ortega; Natalia Brzozowska; Julia S. El-Sayed Moustafa; Dovile Vaitkute; Belma Jakupovic; Ayrun Nessa; Samuel Wadge; Marc F. Österdahl; Anna L. Paterson; Doris M. Rassl; Raul E. Alcantara; Laura O’Neill; Sara Widaa; Siobhan Austin-Guest; Matthew D. C. Neville; Moritz J. Przybilla; Wei Cheng; Maria Morra; Lucy Sykes; Matthew Mayho; Nicole Müller-Sienerth; Nicholas Williams; Diana Alexander; Luke M. R. Harvey; Thomas Clarke; Alex Byrne; Jamie R. Blundell; Matthew D. Young; Krishnaa T. A. Mahbubani; Kourosh Saeb-Parsy; Hilary C. Martin; Michael R. Stratton; Peter J. Campbell; Raheleh Rahbari; Kerrin S. Small; Iñigo Martincorena
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Sperm sequencing reveals extensive positive selection in the male germline
errNature
IF48.5
err2025-10-08
err0
errOAAI
errMatthew D. C. Neville; Andrew R. J. Lawson; Rashesh Sanghvi; Federico Abascal; My H. Pham; Alex Cagan; Pantelis A. Nicola; Tetyana Bayzetinova; Adrian Baez-Ortega; Kirsty Roberts; Stefanie V. Lensing; Sara Widaa; Raul E. Alcantara; María Paz García; Sam Wadge; Michael R. Stratton; Peter J. Campbell; Kerrin Small; Iñigo Martincorena; Matthew E. Hurles; Raheleh Rahbari
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Hotspots of human mutation point to clonal expansions in spermatogonia
errNature
IF48.5
err2025-10-08
err0
PREAI
errVladimir Seplyarskiy; Mikhail A. Moldovan; Evan Koch; Prathitha Kar; Matthew D. C. Neville; Raheleh Rahbari; Shamil Sunyaev
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The impact of ancestral, genetic, and environmental influences on germline de novo mutation rates and spectra
err2025-05-15
err0
errOAAI
errGarcia-Salinas, O. Isaac; Hwang, Seongwon; Huang, Qin Qin; Sanghvi, Rashesh; Malawsky, Daniel S.; Kaplanis, Joanna; Neville, Matthew D. C.; Day, Felix R.; Rahbari, Raheleh; Scally, Aylwyn; Martin, Hilary C.
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Clonal diversification and histogenesis of malignant germ cell tumours
err2022-08-11
err9
errOAAI
errOliver, Thomas R. W.; Chappell, Lia; Sanghvi, Rashesh; Deighton, Lauren; Ansari-Pour, Naser; Dentro, Stefan C.; Young, Matthew D.; Coorens, Tim H. H.; Jung, Hyunchul; Butler, Tim; Neville, Matthew D. C.; Leongamornlert, Daniel; Sanders, Mathijs A.; Hooks, Yvette; Cagan, Alex; Mitchell, Thomas J.; Cortes-Ciriano, Isidro; Warren, Anne Y.; Wedge, David C.; Heer, Rakesh; Coleman, Nicholas; Murray, Matthew J.; Campbell, Peter J.; Rahbari, Raheleh; Behjati, Sam
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The contribution of X-linked coding variation to severe developmental disorders
err2021-01-27
err31
errOAAI
errMartin, Hilary C.; Gardner, Eugene J.; Samocha, Kaitlin E.; Kaplanis, Joanna; Akawi, Nadia; Sifrim, Alejandro; Eberhardt, Ruth Y.; Tavares, Ana Lisa Taylor; Neville, Matthew D. C.; Niemi, Mari E. K.; Gallone, Giuseppe; McRae, Jeremy; Wright, Caroline F.; FitzPatrick, David R.; Firth, Helen V.; Hurles, Matthew E.
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A platform for curated products from novel open reading frames prompts reinterpretation of disease variants
err2021-01-19
err15
errOAAI
errNeville, Matthew D. C.; Kohze, Robin; Erady, Chaitanya; Meena, Narendra; Hayden, Matthew; Cooper, David N.; Mort, Matthew; Prabakaran, Sudhakaran
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