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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 2
2004 2
2005 3
2006 4
2007 4
2008 2
2009 10
2010 12
2011 10
2012 8
2013 9
2014 6
2015 10
2016 18
2017 18
2018 22
2019 25
2020 11
2021 18
2022 12
2023 11
2024 4

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192 results

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Page 1
Cohort profile update: Tehran cardiometabolic genetic study.
Daneshpour MS, Akbarzadeh M, Lanjanian H, Sedaghati-Khayat B, Guity K, Masjoudi S, Zahedi AS, Moazzam-Jazi M, Bonab LNH, Shalbafan B, Asgarian S, Farhood GK, Javanrooh N, Zarkesh M, Riahi P, Moghaddas MR, Dehkordi PA, Ahmadi AD, Hosseini F, Farahani SJ, Hadaegh F, Mirmiran P, Tehrani FR, Ghanbarian A, Pasand MSFM, Amiri P, Valizadeh M, Hosseipanah F, Tohidi M, Ghasemi A, Zadeh-Vakili A, Piryaei M, Alamdari S, Khalili D, Momenan A, Barzin M, Zeinali S, Hedayati M, Azizi F. Daneshpour MS, et al. Among authors: zeinali s. Eur J Epidemiol. 2023 Jun;38(6):699-711. doi: 10.1007/s10654-023-01008-1. Epub 2023 May 12. Eur J Epidemiol. 2023. PMID: 37169991 Free PMC article.
Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia.
Yap ZY, Efthymiou S, Seiffert S, Vargas Parra K, Lee S, Nasca A, Maroofian R, Schrauwen I, Pendziwiat M, Jung S, Bhoj E, Striano P, Mankad K, Vona B, Cuddapah S, Wagner A, Alvi JR, Davoudi-Dehaghani E, Fallah MS, Gannavarapu S, Lamperti C, Legati A, Murtaza BN, Nadeem MS, Rehman MU, Saeidi K, Salpietro V, von Spiczak S, Sandoval A, Zeinali S, Zeviani M, Reich A; SYNaPS Study Group; University of Washington Center for Mendelian Genomics; Jang C, Helbig I, Barakat TS, Ghezzi D, Leal SM, Weber Y, Houlden H, Yoon WH. Yap ZY, et al. Among authors: zeinali s. Am J Hum Genet. 2021 Dec 2;108(12):2368-2384. doi: 10.1016/j.ajhg.2021.11.003. Epub 2021 Nov 19. Am J Hum Genet. 2021. PMID: 34800363 Free PMC article.
Efficacy and antitumor activity of a mutant type of interleukin 2.
Dehghan R, Beig Parikhani A, Zeinali S, Shokrgozar M, Amanzadeh A, Ajdary S, Ahangari Cohan R, Talebkhan Y, Behdani M. Dehghan R, et al. Among authors: zeinali s. Sci Rep. 2022 Mar 30;12(1):5376. doi: 10.1038/s41598-022-09278-7. Sci Rep. 2022. PMID: 35354847 Free PMC article.
Microsatellite Marker Analysis for Laboratory Mice Profiling.
Ahangari Cohan R, Nouri Inanlou D, Samiee Aref MH, Zeinali S, Farhoudi R. Ahangari Cohan R, et al. Among authors: zeinali s. Adv Biomed Res. 2019 Jun 28;8:40. doi: 10.4103/abr.abr_53_19. eCollection 2019. Adv Biomed Res. 2019. PMID: 31360681 Free PMC article.
Ichthyosis follicularis syndromes in patients with mutations in GJB2.
Youssefian L, Naji M, Park JS, Rajabi F, Abdollahimajd F, Mahmoudi H, Kamyab-Hesari K, Ghalamkarpour F, Zabihi M, Teimoorian M, Youssefian L, Zeinali S, Vahidnezhad H, Uitto J. Youssefian L, et al. Among authors: zeinali s. Clin Exp Dermatol. 2022 Aug;47(8):1561-1566. doi: 10.1111/ced.15217. Epub 2022 Jun 23. Clin Exp Dermatol. 2022. PMID: 35396755
A CIB1 Splice-Site Founder Mutation in Families with Typical Epidermodysplasia Verruciformis.
Vahidnezhad H, Youssefian L, Saeidian AH, Mansoori B, Jazayeri A, Azizpour A, Hesari KK, Yousefi M, Zeinali S, Jouanguy E, Casanova JL, Uitto J. Vahidnezhad H, et al. Among authors: zeinali s. J Invest Dermatol. 2019 May;139(5):1195-1198. doi: 10.1016/j.jid.2018.11.011. Epub 2018 Nov 29. J Invest Dermatol. 2019. PMID: 30503243 Free article. Review. No abstract available.
Molecular Basis of α-Thalassemia in Iran.
Valaei A, Karimipoor M, Kordafshari A, Zeinali S. Valaei A, et al. Among authors: zeinali s. Iran Biomed J. 2018 Jan 1;22(1):6-14. doi: 10.22034/ibj.22.1.6. Iran Biomed J. 2018. PMID: 29115104 Free PMC article.
192 results