1. Shin, Minhye, Vaughn, Amanda, Momb, Jessica, Appling, Dean R. 2019. Deletion of neural tube defect-associated gene Mthfd1l causes reduced cranial mesenchyme density. In Birth defects research, 111, 1520-1534. doi:10.1002/bdr2.1591. https://pubmed.ncbi.nlm.nih.gov/31518072/
2. Ren, Ru-Jing, Wang, Li-Ling, Fang, Rong, Wang, Gang, Chen, Sheng-Di. 2011. The MTHFD1L gene rs11754661 marker is associated with susceptibility to Alzheimer's disease in the Chinese Han population. In Journal of the neurological sciences, 308, 32-4. doi:10.1016/j.jns.2011.06.036. https://pubmed.ncbi.nlm.nih.gov/21741665/
3. Al-Eitan, Laith N, Almasri, Ayah Y, Khasawneh, Rame H, Alghamdi, Mansour A. 2020. Influence of SH2B3, MTHFD1L, GGCX, and ITGB3 Gene Polymorphisms on theVariability on Warfarin Dosage Requirements and Susceptibility to CVD in the Jordanian Population. In Journal of personalized medicine, 10, . doi:10.3390/jpm10030117. https://pubmed.ncbi.nlm.nih.gov/32916786/
4. Ramírez-Lorca, Reposo, Boada, Mercé, Antúnez, Carmen, Real, Luis M, Ruiz, Agustín. . The MTHFD1L gene rs11754661 marker is not associated with Alzheimer's disease in a sample of the Spanish population. In Journal of Alzheimer's disease : JAD, 25, 47-50. doi:10.3233/JAD-2011-101983. https://pubmed.ncbi.nlm.nih.gov/21383495/
5. Yi, Dandan, Yilihamu, Yiminu'er, Jiang, Chaoyu, Sang, Jianfeng, Su, Lei. 2022. MTHFD1L knockdown diminished cells growth in papillary thyroid cancer. In Tissue & cell, 77, 101869. doi:10.1016/j.tice.2022.101869. https://pubmed.ncbi.nlm.nih.gov/35870426/
6. Bryant, Joshua D, Sweeney, Shannon R, Sentandreu, Enrique, Tiziani, Stefano, Appling, Dean R. 2018. Deletion of the neural tube defect-associated gene Mthfd1l disrupts one-carbon and central energy metabolism in mouse embryos. In The Journal of biological chemistry, 293, 5821-5833. doi:10.1074/jbc.RA118.002180. https://pubmed.ncbi.nlm.nih.gov/29483189/
7. Hubacek, J A, Staněk, V, Gebauerová, M, Adámková, V, Pitˇha, J. 2015. Rs6922269 marker at the MTHFD1L gene predict cardiovascular mortality in males after acute coronary syndrome. In Molecular biology reports, 42, 1289-93. doi:10.1007/s11033-015-3870-1. https://pubmed.ncbi.nlm.nih.gov/25809277/
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