1. Cappelletti, Chiara, Henriksen, Sandra Pilar, Geut, Hanneke, Pihlstrøm, Lasse, Toft, Mathias. 2023. Transcriptomic profiling of Parkinson's disease brains reveals disease stage specific gene expression changes. In Acta neuropathologica, 146, 227-244. doi:10.1007/s00401-023-02597-7. https://pubmed.ncbi.nlm.nih.gov/37347276/
2. Aisagbonhi, Omonigho, Bui, Tony, Nasamran, Chanond A, Fisch, Kathleen M, Horii, Mariko. 2023. High placental expression of FLT1, LEP, PHYHIP and IL3RA - In persons of African ancestry with severe preeclampsia. In Placenta, 144, 13-22. doi:10.1016/j.placenta.2023.10.008. https://pubmed.ncbi.nlm.nih.gov/37949031/
3. Li, Juan, Pu, Ke, Li, Chunmei, Wang, Yuping, Zhou, Yongning. 2021. A Novel Six-Gene-Based Prognostic Model Predicts Survival and Clinical Risk Score for Gastric Cancer. In Frontiers in genetics, 12, 615834. doi:10.3389/fgene.2021.615834. https://pubmed.ncbi.nlm.nih.gov/33692828/
4. Durand, Julien, Lampron, Antoine, Mazzuco, Tania L, Chapman, Audrey, Bourdeau, Isabelle. 2011. Characterization of differential gene expression in adrenocortical tumors harboring beta-catenin (CTNNB1) mutations. In The Journal of clinical endocrinology and metabolism, 96, E1206-11. doi:10.1210/jc.2010-2143. https://pubmed.ncbi.nlm.nih.gov/21565795/
5. Skvortsova, Yulia V, Kondratieva, Sofia A, Zinovyeva, Marina V, Azhikina, Tatyana L, Gainetdinov, Ildar V. 2016. Intragenic Locus in Human PIWIL2 Gene Shares Promoter and Enhancer Functions. In PloS one, 11, e0156454. doi:10.1371/journal.pone.0156454. https://pubmed.ncbi.nlm.nih.gov/27248499/
6. Cosemans, Nele, Maljaars, Jarymke, Vogels, Annick, Noens, Ilse, Peeters, Hilde. 2021. 8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder. In Neurogenetics, 22, 207-213. doi:10.1007/s10048-021-00635-8. https://pubmed.ncbi.nlm.nih.gov/33683518/