McAloney, Kerrie
QIMR Berghofer Medical Research Institute
3 papers on CoChatORCID 0000-0002-4390-2691
Most cited papers
- Verified
Common genetic variants contribute to risk of rare severe neurodevelopmental disorders
Niemi, M. E. K., Martin, H. C., Rice, D. L., Gallone, G., Gordon, S., Kelemen, M., McAloney, K., McRae, J., Radford, E. J., Yu, S., et al. (2018) · Nature
Genetic Associations and EpidemiologyGenomics and Rare Diseases
Cited by 340
- Verified
Novel genetic loci affecting facial shape variation in humans
Xiong, Z., Dankova, G., Howe, L. J., Lee, M. K., Hysi, P. G., de Jong, M. A., Zhu, G., Adhikari, K., Li, D., Li, Y., et al. (2019) · eLife
Genetic Associations and EpidemiologyMorphological variations and asymmetry
Cited by 92
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Continuity of Genetic Risk for Aggressive Behavior Across the Life-Course
van der Laan, C. M., Morosoli-García, J. J., van de Weijer, S. G. A., Colodro-Conde, L., the ACTION Consortium, Ip, H. F., van der Laan, C. M., Krapohl, E. M. L., Brikell, I., Sánchez-Mora, C., et al. (2021) · Behavior Genetics
Genetic Associations and EpidemiologyNeurotransmitter Receptor Influence on Behavior
Cited by 24
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