1. Palumbo, Francesca, Moglia, Cristina, Romano, Alessandro, Calvo, Andrea, Gallone, Salvatore. 2024. EMILIN1 gene variant associated with polyneuropathy, language impairment, and motor dysfunction. In American journal of medical genetics. Part A, 194, e63808. doi:10.1002/ajmg.a.63808. https://pubmed.ncbi.nlm.nih.gov/38963291/
2. Honda, Chikako Kanno, Kurozumi, Sasagu, Fujii, Takaaki, Yokobori, Takehiko, Turtoi, Andrei. 2024. Cancer-associated fibroblast spatial heterogeneity and EMILIN1 expression in the tumor microenvironment modulate TGF-β activity and CD8+ T-cell infiltration in breast cancer. In Theranostics, 14, 1873-1885. doi:10.7150/thno.90627. https://pubmed.ncbi.nlm.nih.gov/38505604/
3. Ucaryilmaz Metin, Cemre, Ozcan, Gulnihal. 2022. Comprehensive bioinformatic analysis reveals a cancer-associated fibroblast gene signature as a poor prognostic factor and potential therapeutic target in gastric cancer. In BMC cancer, 22, 692. doi:10.1186/s12885-022-09736-5. https://pubmed.ncbi.nlm.nih.gov/35739492/
4. Shen, Chong, Lu, Xiangfeng, Li, Yun, Huang, Jianfeng, Gu, Dongfeng. 2009. Emilin1 gene and essential hypertension: a two-stage association study in northern Han Chinese population. In BMC medical genetics, 10, 118. doi:10.1186/1471-2350-10-118. https://pubmed.ncbi.nlm.nih.gov/19922630/
5. Megarbane, Andre, Bizzari, Sami, Deepthi, Asha, Delague, Valérie, Urtizberea, J Andoni. . A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort. In Journal of neuromuscular diseases, 9, 193-210. doi:10.3233/JND-210652. https://pubmed.ncbi.nlm.nih.gov/34602496/
6. Fabbro, Carla, de Gemmis, Paola, Braghetta, Paola, Bonaldo, Paolo, Bressan, Giorgio M. 2005. Analysis of regulatory regions of Emilin1 gene and their combinatorial contribution to tissue-specific transcription. In The Journal of biological chemistry, 280, 15749-60. doi:. https://pubmed.ncbi.nlm.nih.gov/15705587/
7. Capuano, Alessandra, Bucciotti, Francesco, Farwell, Kelly D, Colombatti, Alfonso, Doliana, Roberto. 2015. Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue Disease. In Human mutation, 37, 84-97. doi:10.1002/humu.22920. https://pubmed.ncbi.nlm.nih.gov/26462740/
8. Oh, V M S, Chua, B-M, Heng, C-K, Yim, O-S, Yap, E P H. 2011. Association of intronic single-nucleotide polymorphisms in the EMILIN1 gene with essential hypertension in a Chinese population. In Journal of human hypertension, 26, 553-61. doi:10.1038/jhh.2011.68. https://pubmed.ncbi.nlm.nih.gov/21753788/
9. Mengzhen, Zhang, Xinwei, Hou, Zeheng, Tan, Liucheng, Yang, Kai, Wu. 2024. Integrated machine learning-driven disulfidptosis profiling: CYFIP1 and EMILIN1 as therapeutic nodes in neuroblastoma. In Journal of cancer research and clinical oncology, 150, 109. doi:10.1007/s00432-024-05630-8. https://pubmed.ncbi.nlm.nih.gov/38427078/
10. Shimodaira, Masanori, Nakayama, Tomohiro, Sato, Naoyuki, Soma, Masayoshi, Matsumoto, Koichi. 2010. Association study of the elastin microfibril interfacer 1 (EMILIN1) gene in essential hypertension. In American journal of hypertension, 23, 547-55. doi:10.1038/ajh.2010.16. https://pubmed.ncbi.nlm.nih.gov/20186130/