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Depression, anxiety, and stress among Iranian nurses in COVID-19 care wards.
Sharifi A, Fallahi-Khoshknab M, Mohammadi S, Zeraati M, Jamshidi Z, Aghabeygi-Arani M, Mirzaei N, Fallahi-Khoshknab N, Rasooli P. Sharifi A, et al. Among authors: rasooli p. BMC Psychol. 2022 Aug 20;10(1):205. doi: 10.1186/s40359-022-00911-8. BMC Psychol. 2022. PMID: 35987839 Free PMC article.
Signal regulators of human naïve pluripotency.
Taei A, Rasooli P, Braun T, Hassani SN, Baharvand H. Taei A, et al. Among authors: rasooli p. Exp Cell Res. 2020 Apr 15;389(2):111924. doi: 10.1016/j.yexcr.2020.111924. Epub 2020 Feb 26. Exp Cell Res. 2020. PMID: 32112799 Review.
A Comprehensive, Epidemiological and Ecological Descriptive Study on Vitamin D Status in Iran (308005 People, from 2009-2018).
Farhud DD, Mehrabi A, Sarafnejad A, Sadeghipour HR, Rahimiforoushani A, Rokni MB, Majidi K, Alizadeh A, Zarif-Yeganeh M, Jalali M, Jalali M, Amir Zargar AA, Khosravi F, Momeni A, Khazeni M, Hendiani A, Ahmadi M, Dehshiri A, Rasooli P. Farhud DD, et al. Among authors: rasooli p. Iran J Public Health. 2019 Apr;48(4):644-654. Iran J Public Health. 2019. PMID: 31110974 Free PMC article.
COL18A1 is a candidate eye iridocorneal angle-closure gene in humans.
Suri F, Yazdani S, Chapi M, Safari I, Rasooli P, Daftarian N, Jafarinasab MR, Ghasemi Firouzabadi S, Alehabib E, Darvish H, Klotzle B, Fan JB, Turk C, Elahi E. Suri F, et al. Among authors: rasooli p. Hum Mol Genet. 2018 Nov 1;27(21):3772-3786. doi: 10.1093/hmg/ddy256. Hum Mol Genet. 2018. PMID: 30007336
Identification of mutation in GTPBP2 in patients of a family with neurodegeneration accompanied by iron deposition in the brain.
Jaberi E, Rohani M, Shahidi GA, Nafissi S, Arefian E, Soleimani M, Rasooli P, Ahmadieh H, Daftarian N, Carrami EM, Klotzle B, Fan JB, Turk C, Steemers F, Elahi E. Jaberi E, et al. Among authors: rasooli p. Neurobiol Aging. 2016 Feb;38:216.e11-216.e18. doi: 10.1016/j.neurobiolaging.2015.10.034. Epub 2015 Nov 6. Neurobiol Aging. 2016. PMID: 26675814
Mutation in ST6GALNAC5 identified in family with coronary artery disease.
InanlooRahatloo K, Parsa AF, Huse K, Rasooli P, Davaran S, Platzer M, Kramer M, Fan JB, Turk C, Amini S, Steemers F, Gunderson K, Ronaghi M, Elahi E. InanlooRahatloo K, et al. Among authors: rasooli p. Sci Rep. 2014 Jan 8;4:3595. doi: 10.1038/srep03595. Sci Rep. 2014. PMID: 24399302 Free PMC article.
Mutation in CYP27A1 identified in family with coronary artery disease.
Inanloorahatloo K, Zand Parsa AF, Huse K, Rasooli P, Davaran S, Platzer M, Fan JB, Amini S, Steemers F, Elahi E. Inanloorahatloo K, et al. Among authors: rasooli p. Eur J Med Genet. 2013 Dec;56(12):655-60. doi: 10.1016/j.ejmg.2013.09.008. Epub 2013 Sep 28. Eur J Med Genet. 2013. PMID: 24080357