Matthew Hurles

28PUBLICATIONS
243CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Infant and child healthMolecular evolutionGene mappingNeurogenetics
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Publications (28)

|Oct 05, 2026
Imputation of fluid intelligence scores reduces ascertainment bias and increases power for analyses of common and rare variants.

|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

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Frequent Collaborators

9 joint publications

Hilary C Martin

7 joint publications

Sarah Lindsay

6 joint publications

Caroline F Wright

6 joint publications

Eugene J Gardner