1. Shaheen, Ranad, Maddirevula, Sateesh, Ewida, Nour, Walsh, Christopher, Alkuraya, Fowzan S. 2018. Genomic and phenotypic delineation of congenital microcephaly. In Genetics in medicine : official journal of the American College of Medical Genetics, 21, 545-552. doi:10.1038/s41436-018-0140-3. https://pubmed.ncbi.nlm.nih.gov/30214071/
2. Díaz-Peña, Roberto, Julià, Raül F, Montes, Juan F, Silva, Rafael S, Olloquequi, Jordi. 2022. Polymorphisms in the FRMD4A Gene Are Associated With Chronic Obstructive Pulmonary Disease Susceptibility in a Latin American Population. In Archivos de bronconeumologia, 58, 454-456. doi:10.1016/j.arbres.2022.01.016. https://pubmed.ncbi.nlm.nih.gov/35312514/
3. Pan, Yuhua, Guo, Xiaoling, Zhou, Xiaoqiang, Xiong, Fu, Yang, Xingkun. 2021. Case Report: A Novel Compound Heterozygous Mutation of the FRMD4A Gene Identified in a Chinese Family With Global Developmental Delay, Intellectual Disability, and Ataxia. In Frontiers in pediatrics, 9, 775488. doi:10.3389/fped.2021.775488. https://pubmed.ncbi.nlm.nih.gov/34869127/
4. Zheng, Xianghuai, Jia, Bo, Lin, Xi, Chen, Jun, Zhao, Jianjiang. 2016. FRMD4A: A potential therapeutic target for the treatment of tongue squamous cell carcinoma. In International journal of molecular medicine, 38, 1443-1449. doi:10.3892/ijmm.2016.2745. https://pubmed.ncbi.nlm.nih.gov/27666346/
5. Lambert, J-C, Grenier-Boley, B, Harold, D, Williams, J, Amouyel, P. 2012. Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease. In Molecular psychiatry, 18, 461-70. doi:10.1038/mp.2012.14. https://pubmed.ncbi.nlm.nih.gov/22430674/