1. Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Bellenguez, Céline, Lambert, Jean-Charles. 2022. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. In Nature genetics, 54, 1786-1794. doi:10.1038/s41588-022-01208-7. https://pubmed.ncbi.nlm.nih.gov/36411364/
2. Chen, Bohong, Sun, Xinyue, Huang, Haoxiang, Chen, Wei, Wu, Dapeng. 2024. An integrated machine learning framework for developing and validating a diagnostic model of major depressive disorder based on interstitial cystitis-related genes. In Journal of affective disorders, 359, 22-32. doi:10.1016/j.jad.2024.05.061. https://pubmed.ncbi.nlm.nih.gov/38754597/
3. Nicolas, G. 2024. Lessons from genetic studies in Alzheimer disease. In Revue neurologique, 180, 368-377. doi:10.1016/j.neurol.2023.12.006. https://pubmed.ncbi.nlm.nih.gov/38429159/
4. Gao, Li, Emond, Mary J, Louie, Tin, Mathias, Rasika A, Barnes, Kathleen C. . Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing. In Arthritis & rheumatology (Hoboken, N.J.), 68, 191-200. doi:10.1002/art.39449. https://pubmed.ncbi.nlm.nih.gov/26473621/
5. Gourh, Pravitt, Remmers, Elaine F, Boyden, Steven E, Kastner, Daniel L, Wigley, Fredrick M. 2018. Brief Report: Whole-Exome Sequencing to Identify Rare Variants and Gene Networks That Increase Susceptibility to Scleroderma in African Americans. In Arthritis & rheumatology (Hoboken, N.J.), 70, 1654-1660. doi:10.1002/art.40541. https://pubmed.ncbi.nlm.nih.gov/29732714/
6. Thami, Prisca K, Choga, Wonderful T, Dandara, Collet, Gaseitsiwe, Simani, Chimusa, Emile R. 2023. Whole genome sequencing reveals population diversity and variation in HIV-1 specific host genes. In Frontiers in genetics, 14, 1290624. doi:10.3389/fgene.2023.1290624. https://pubmed.ncbi.nlm.nih.gov/38179408/
7. Nicolas, Gaël, Zaréa, Aline, Lacour, Morgane, Charbonnier, Camille, Wallon, David. 2024. Assessment of Mendelian and risk-factor genes in Alzheimer disease: A prospective nationwide clinical utility study and recommendations for genetic screening. In Genetics in medicine : official journal of the American College of Medical Genetics, 26, 101082. doi:10.1016/j.gim.2024.101082. https://pubmed.ncbi.nlm.nih.gov/38281098/
智鼠故事 
