Sarah Lindsay

8PUBLICATIONS
79CO-AUTHORS
Infant and child healthMolecular evolutionNeurogeneticsNeurology and neuromuscular diseasesMolecular targets
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Publications (8)

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

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

|Nov 20, 2024
Examining the role of common variants in rare neurodevelopmental conditions.

Qin Qin Huang, Emilie M Wigdor, Daniel S Malawsky

|Sep 23, 2024
Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations.

V Kartik Chundru, Zhancheng Zhang, Klaudia Walter

|Jul 11, 2024
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.

Yuyang Chen, Ruebena Dawes, Hyung Chul Kim

|Dec 06, 2023
Saturation genome editing of DDX3X clarifies pathogenicity of germline and somatic variation.

Elizabeth J Radford, Hong-Kee Tan, Malin H L Andersson

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Frequent Collaborators

6 joint publications

Matthew E Hurles

4 joint publications

Caroline F Wright

3 joint publications

Hilary C Martin

3 joint publications

Eugene J Gardner