Matthew Hurles

25PUBLICATIONS

234CO-AUTHORS

Molecular evolutionGenetics not elsewhere classifiedGene expression (incl. microarray and other genome-wide approaches)Gene mappingNeurogenetics

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Publications (25)

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|Jun 09, 2026

Improved discovery of de novo mutations using TrioDNM and VRFS.

|Feb 17, 2026

Author Correction: Complex de novo structural variants are an underestimated cause of rare disorders.

Hyunchul Jung, Tsun-Po Yang, Susan Walker

|Feb 12, 2026

Copy Number Variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders - the DDD-Africa study.

Nadja Louw, Prince Makay, Phelelani T Mpangase

|Nov 03, 2025

Complex de novo structural variants are an underestimated cause of rare disorders.

Hyunchul Jung, Tsun-Po Yang, Susan Walker

|Oct 08, 2025

Sperm sequencing reveals extensive positive selection in the male germline.

Matthew D C Neville, Andrew R J Lawson, Rashesh Sanghvi

|Nov 20, 2024

Examining the role of common variants in rare neurodevelopmental conditions.

Qin Qin Huang, Emilie M Wigdor, Daniel S Malawsky

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Frequent Collaborators

Hilary C Martin

Caroline F Wright

Eugene J Gardner

Matthew Neville

Kaitlin E Samocha

Sarah Lindsay

Sebastian S Gerety

Ruth Y Eberhardt

David J Adams

Raheleh Rahbari

Frequent Collaborators

Hilary C Martin

Caroline F Wright

Eugene J Gardner

Matthew Neville