Mahmoud Koko

13PUBLICATIONS
92CO-AUTHORS
Infant and child healthChild and adolescent developmentGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsDevelopmental genetics (incl. sex determination)
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Publications (13)

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

|Oct 01, 2025
Polygenic and developmental profiles of autism differ by age at diagnosis.

Xinhe Zhang, Jakob Grove, Yuanjun Gu

|Jan 22, 2025
Exome sequencing of UK birth cohorts.

Mahmoud Koko, Laurie Fabian, Iaroslav Popov

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

Qin Qin Huang, Emilie M Wigdor, Daniel S Malawsky

|May 03, 2024
Contribution of autosomal rare and de novo variants to sex differences in autism.

Mahmoud Koko, F Kyle Satterstrom, Varun Warrier

|Feb 05, 2024
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy.

Mahmoud Koko, Maha A Elseed, Inaam N Mohammed

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Frequent Collaborators

3 joint publications

Hilary Martin

3 joint publications

Varun Warrier

3 joint publications

Ashraf Yahia

2 joint publications

Giovanni Stevanin