Matthew Hurles

27PUBLICATIONS

237CO-AUTHORS

Infant and child healthGene expression (incl. microarray and other genome-wide approaches)Molecular evolutionGenetics not elsewhere classifiedGene mapping

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Publications (27)

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|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 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

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Frequent Collaborators

Hilary C Martin

Sarah Lindsay

Caroline F Wright

Eugene J Gardner

Matthew Neville

Kaitlin E Samocha

Sebastian S Gerety

Ruth Y Eberhardt

David J Adams

Qin Qin Huang

Frequent Collaborators

Hilary C Martin

Sarah Lindsay

Caroline F Wright

Eugene J Gardner