1. Fourier, Carmen, Ran, Caroline, Steinberg, Anna, Waldenlind, Elisabet, Belin, Andrea Carmine. 2019. Analysis of HCRTR2 Gene Variants and Cluster Headache in Sweden. In Headache, 59, 410-417. doi:10.1111/head.13462. https://pubmed.ncbi.nlm.nih.gov/30652302/
2. Yang, Jiao, Yu, Si-Yi, Yang, Jie, Liang, Fan-Rong, Lv, Zheng-Tao. 2020. No Association Between G1246A Polymorphism in HCRTR2 Gene and Risk of Cluster Headache: Evidence From an Updated Meta-Analysis of Observational Studies. In Frontiers in genetics, 11, 560517. doi:10.3389/fgene.2020.560517. https://pubmed.ncbi.nlm.nih.gov/33343621/
3. Papasavva, Maria, Katsarou, Martha-Spyridoula, Vikelis, Michail, Tsatsakis, Aristides M, Drakoulis, Nikolaos. 2019. Analysis of HCRTR2, GNB3, and ADH4 Gene Polymorphisms in a Southeastern European Caucasian Cluster Headache Population. In Journal of molecular neuroscience : MN, 70, 467-474. doi:10.1007/s12031-019-01439-0. https://pubmed.ncbi.nlm.nih.gov/31768945/
4. Oeser, Clarissa. 2015. Pharmacogenetics: HCRTR2 gene is associated with response to HF therapy. In Nature reviews. Cardiology, 13, 64. doi:10.1038/nrcardio.2015.195. https://pubmed.ncbi.nlm.nih.gov/26675427/
5. Firouzabadi, Negar, Navabzadeh, Niloofar, Moghimi-Sarani, Ebrahim, Haghnegahdar, Maral. 2020. Orexin/Hypocretin Type 2 Receptor (HCRTR2) Gene as a Candidate Gene in Sertraline-Associated Insomnia in Depressed Patients. In Neuropsychiatric disease and treatment, 16, 1121-1128. doi:10.2147/NDT.S250141. https://pubmed.ncbi.nlm.nih.gov/32440126/
6. Pinessi, L, Binello, E, De Martino, P, Valfrè, W, Vaula, G. 2007. The 1246G-->A polymorphism of the HCRTR2 gene is not associated with migraine. In Cephalalgia : an international journal of headache, 27, 945-9. doi:. https://pubmed.ncbi.nlm.nih.gov/17645762/
7. Dashti, Hassan S, Daghlas, Iyas, Lane, Jacqueline M, Garaulet, Marta, Saxena, Richa. 2021. Genetic determinants of daytime napping and effects on cardiometabolic health. In Nature communications, 12, 900. doi:10.1038/s41467-020-20585-3. https://pubmed.ncbi.nlm.nih.gov/33568662/
8. Baumber, L, Sjöstrand, C, Leone, M, Trembath, R C, Russell, M B. . A genome-wide scan and HCRTR2 candidate gene analysis in a European cluster headache cohort. In Neurology, 66, 1888-93. doi:. https://pubmed.ncbi.nlm.nih.gov/16801656/
9. Popescu, Cyprian. 2023. Combined genotype of HCRTR2 and CLOCK variants in a large family of cluster headache with familial periodicity phenotype. In Journal of neurology, 270, 5064-5070. doi:10.1007/s00415-023-11851-7. https://pubmed.ncbi.nlm.nih.gov/37418013/
10. Gallone, Salvatore, Boschi, Silvia, Rubino, Elisa, Pinessi, Lorenzo, Rainero, Innocenzo. 2014. Is HCRTR2 a genetic risk factor for Alzheimer's disease? In Dementia and geriatric cognitive disorders, 38, 245-53. doi:10.1159/000359964. https://pubmed.ncbi.nlm.nih.gov/24969517/
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