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

Year Number of Results
2010 2
2011 3
2013 2
2014 3
2015 3
2016 3
2017 1
2018 3
2021 4
2022 1
2023 4
2024 1

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26 results

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Page 1
Molecular genetic study of Calpainopathy in Iran.
Mojbafan M, Khajeh A, Habibi H, Bagherian H, Zeinali S. Mojbafan M, et al. Among authors: bagherian h. Gene. 2018 Nov 30;677:259-265. doi: 10.1016/j.gene.2018.07.067. Epub 2018 Jul 27. Gene. 2018. PMID: 30056071
The Spectrum of Pathogenic Variants in Iranian Families with Hemophilia A.
Azadmehr S, Rahiminejad F, Zafarghandi Motlagh F, Jamali M, Ghazizadeh Tehrani P, Shirzadeh T, Bagherian H, Karimipoor M, Davoudi-Dehaghani E, Zeinali S. Azadmehr S, et al. Among authors: bagherian h. Arch Iran Med. 2021 Dec 1;24(12):887-896. doi: 10.34172/aim.2021.133. Arch Iran Med. 2021. PMID: 35014236 Free article.
Genetic attributes of Iranian cystic fibrosis patients: the diagnostic efficiency of CFTR mutations in over a decade.
Hosseini Nami A, Kabiri M, Zafarghandi Motlagh F, Shirzadeh T, Fakhari N, Karimi A, Bagherian H, Jamali M, Younesikhah S, Shadman S, Zeinali R, Zeinali S. Hosseini Nami A, et al. Among authors: bagherian h. Front Genet. 2023 May 18;14:1140034. doi: 10.3389/fgene.2023.1140034. eCollection 2023. Front Genet. 2023. PMID: 37274793 Free PMC article.
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.
Shirzadeh T, Saeidian AH, Bagherian H, Salehpour S, Setoodeh A, Alaei MR, Youssefian L, Samavat A, Touati A, Fallah MS, Vahidnezhad H, Karimipoor M, Azadmehr S, Raeisi M, Bandehi Sarhadi A, Zafarghandi Motlagh F, Jamali M, Zeinali Z, Abiri M, Zeinali S; Additional individual contributors. Shirzadeh T, et al. Among authors: bagherian h. J Inherit Metab Dis. 2018 Nov;41(6):1159-1167. doi: 10.1007/s10545-018-0228-6. Epub 2018 Aug 29. J Inherit Metab Dis. 2018. PMID: 30159852
Heterogeneity of hemoglobin h disease in childhood.
Zeinali S, Fallah MS, Bagherian H. Zeinali S, et al. Among authors: bagherian h. N Engl J Med. 2011 May 26;364(21):2070-1; author reply 2071. doi: 10.1056/NEJMc1103406. N Engl J Med. 2011. PMID: 21612484 No abstract available.
A decade of molecular preimplantation genetic diagnosis of 350 blastomeres for beta-thalassemia combined with HLA typing, aneuploidy screening and sex selection in Iran.
Keshvar Y, Sabeghi S, Sharifi Z, Fatemi KS, Fouladi P, Younesi Khah S, Rahiminejad F, Joudaki A, Amini M, Bagherian H, Ghaffari Novin M, Movahedin M, Mojbafan M, Zeinali S. Keshvar Y, et al. Among authors: bagherian h. BMC Pregnancy Childbirth. 2022 Apr 15;22(1):330. doi: 10.1186/s12884-022-04660-9. BMC Pregnancy Childbirth. 2022. PMID: 35428248 Free PMC article.
Biallelic variants in MESD, which encodes a WNT-signaling-related protein, in four new families with recessively inherited osteogenesis imperfecta.
Tran TT, Keller RB, Guillemyn B, Pepin M, Corteville JE, Khatib S, Fallah MS, Zeinali S, Malfait F, Symoens S, Coucke P, Witters P, Levtchenko E, Bagherian H, Nickerson DA, Bamshad MJ, Chong JX; University of Washington Center for Mendelian Genomics; Byers PH. Tran TT, et al. Among authors: bagherian h. HGG Adv. 2021 Aug 20;2(4):100051. doi: 10.1016/j.xhgg.2021.100051. eCollection 2021 Oct 14. HGG Adv. 2021. PMID: 35047842 Free PMC article.
26 results