1. Felício, Daniela, du Mérac, Tanguy Rubat, Amorim, António, Martins, Sandra. 2023. Functional implications of paralog genes in polyglutamine spinocerebellar ataxias. In Human genetics, 142, 1651-1676. doi:10.1007/s00439-023-02607-4. https://pubmed.ncbi.nlm.nih.gov/37845370/
2. Liang, L, Mao, Y, Zhang, J R, Zhang, S C, Yang, H X. . [Analysis of genes related to hypothyroidism during pregnancy]. In Zhonghua yi xue za zhi, 99, 3350-3354. doi:10.3760/cma.j.issn.0376-2491.2019.42.015. https://pubmed.ncbi.nlm.nih.gov/31715674/
3. Gamage, Thilini H, Misceo, Doriana, Fannemel, Madeleine, Frengen, Eirik. 2013. A balanced de novo inv(7)(p14.3q22.3) disrupting PDE1C and ATXN7L1 in a 14-year old developmentally delayed boy. In European journal of medical genetics, 56, 361-4. doi:10.1016/j.ejmg.2013.04.005. https://pubmed.ncbi.nlm.nih.gov/23664928/
4. Ashktorab, Hassan, Daremipouran, M, Goel, Ajay, Sun, Xueguang, Brim, Hassan. 2014. DNA methylome profiling identifies novel methylated genes in African American patients with colorectal neoplasia. In Epigenetics, 9, 503-12. doi:10.4161/epi.27644. https://pubmed.ncbi.nlm.nih.gov/24441198/
5. Stangeland, Biljana, Mughal, Awais A, Grieg, Zanina, Vik Mo, Einar O, Langmoen, Iver A. . Combined expressional analysis, bioinformatics and targeted proteomics identify new potential therapeutic targets in glioblastoma stem cells. In Oncotarget, 6, 26192-215. doi:10.18632/oncotarget.4613. https://pubmed.ncbi.nlm.nih.gov/26295306/
6. Bensenor, Isabela, Padilha, Kallyandra, Lima, Isabella Ramos, Lotufo, Paulo A, Pereira, Alexandre C. 2021. Genome-Wide Association of Proprotein Convertase Subtilisin/Kexin Type 9 Plasma Levels in the ELSA-Brasil Study. In Frontiers in genetics, 12, 728526. doi:10.3389/fgene.2021.728526. https://pubmed.ncbi.nlm.nih.gov/34659352/