Matthew Hurles

27PUBLICATIONS
237CO-AUTHORS
Infant and child healthGene expression (incl. microarray and other genome-wide approaches)Molecular evolutionGene mappingNeurogenetics
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Publications (27)

|Jul 10, 2026
Common and rare genetic variant associations with cognitive performance across development in British birth cohorts.

|Jul 09, 2026
Copy number variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders-the DDD-Africa study.

|Jun 09, 2026
Improved discovery of de novo mutations using TrioDNM and VRFS.

|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

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Frequent Collaborators

8 joint publications

Hilary C Martin

6 joint publications

Sarah Lindsay

6 joint publications

Caroline F Wright

6 joint publications

Eugene J Gardner