1. Chen, Changying, Gu, Xincheng, Liu, Fangyuan, Jiang, Yuzhang, Shen, Chong. 2023. SNP rs3803264 polymorphisms in THSD1 and abnormally expressed mRNA are associated with hemorrhagic stroke. In Frontiers in aging neuroscience, 15, 1144364. doi:10.3389/fnagi.2023.1144364. https://pubmed.ncbi.nlm.nih.gov/37139087/
2. Haasdijk, Remco A, Den Dekker, Wijnand K, Cheng, Caroline, Van Nieuw Amerongen, Geerten P, Duckers, Henricus J. 2016. THSD1 preserves vascular integrity and protects against intraplaque haemorrhaging in ApoE-/- mice. In Cardiovascular research, 110, 129-39. doi:10.1093/cvr/cvw015. https://pubmed.ncbi.nlm.nih.gov/26822228/
3. Danuta, Galetzka, Tobias, Müller, Marcus, Dittrich, Manuela, Marron, Heinz, Schmidberger. 2020. Molecular karyotyping and gene expression analysis in childhood cancer patients. In Journal of molecular medicine (Berlin, Germany), 98, 1107-1123. doi:10.1007/s00109-020-01937-4. https://pubmed.ncbi.nlm.nih.gov/32577795/
4. Santiago-Sim, Teresa, Fang, Xiaoqian, Hennessy, Morgan L, Seidman, J G, Kim, Dong H. 2016. THSD1 (Thrombospondin Type 1 Domain Containing Protein 1) Mutation in the Pathogenesis of Intracranial Aneurysm and Subarachnoid Hemorrhage. In Stroke, 47, 3005-3013. doi:. https://pubmed.ncbi.nlm.nih.gov/27895300/
5. Abdelrahman, Hanadi A, Al-Shamsi, Aisha, John, Anne, Ali, Bassam R, Al-Gazali, Lihadh. 2018. A recessive truncating variant in thrombospondin-1 domain containing protein 1 gene THSD1 is the underlying cause of nonimmune hydrops fetalis, congenital cardiac defects, and haemangiomas in four patients from a consanguineous family. In American journal of medical genetics. Part A, 176, 1996-2003. doi:10.1002/ajmg.a.40424. https://pubmed.ncbi.nlm.nih.gov/30055085/
6. Khamas, Ahmed, Ishikawa, Toshiaki, Mogushi, Kaoru, Uetake, Hiroyuki, Sugihara, Kenichi. 2012. Genome-wide screening for methylation-silenced genes in colorectal cancer. In International journal of oncology, 41, 490-6. doi:10.3892/ijo.2012.1500. https://pubmed.ncbi.nlm.nih.gov/22664866/
7. Al Rawi, Wafaa N, Ibrahim, Fatima H, El Nakeib, Omar A S, Al Zidgali, Faisal M. 2021. Manifestations of thrombospondin type-1 domain-containing protein 1 gene mutation in an extremely premature infant with nonimmune hydrops fetalis. In American journal of medical genetics. Part A, 185, 1598-1601. doi:10.1002/ajmg.a.62108. https://pubmed.ncbi.nlm.nih.gov/33569873/