Qin Qin Huang

12PUBLICATIONS
137CO-AUTHORS
Infant and child healthMolecular evolutionNeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Molecular targets
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Publications (12)

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

|May 15, 2025
The impact of ancestral, genetic, and environmental influences on germline de novo mutation rates and spectra.

O Isaac Garcia-Salinas, Seongwon Hwang, Qin Qin Huang

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

Qin Qin Huang, Emilie M Wigdor, Daniel S Malawsky

|Sep 11, 2024
Genetic links between ovarian ageing, cancer risk and de novo mutation rates.

Stasa Stankovic, Saleh Shekari, Qin Qin Huang

|Jan 04, 2024
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference.

Xiangrui Meng, Georgina Navoly, Olga Giannakopoulou

|Aug 17, 2023
Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes.

Varun Warrier, Eva-Maria Stauffer, Qin Qin Huang

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Frequent Collaborators

8 joint publications

Hilary C Martin

4 joint publications

Matthew E Hurles

3 joint publications

Karoline Kuchenbaecker

3 joint publications

Sarah Finer