Asal Honarpour - Search Results

Your saved search

Your RSS Feed

Year	Number of Results
2014	1
2025	2
2026	1

Page 1

The First Evidence for the Role of ACVR2A Gene Fetal Genotype in Preeclampsia Susceptibility.

Honarpour A, Majd A, Sadeghi H, Jamaldini S, Rahimi M, Kazemzadeh P, Mirfakhraie R. Honarpour A, et al. Mol Genet Genomic Med. 2025 Feb;13(2):e70069. doi: 10.1002/mgg3.70069. Mol Genet Genomic Med. 2025. PMID: 39898504 Free PMC article.

Identification of a founder mutation for Pendred syndrome in families from northwest Iran.

Mohseni M, Honarpour A, Mozafari R, Davarnia B, Najmabadi H, Kahrizi K. Mohseni M, et al. Among authors: honarpour a. Int J Pediatr Otorhinolaryngol. 2014 Nov;78(11):1828-32. doi: 10.1016/j.ijporl.2014.08.035. Epub 2014 Sep 1. Int J Pediatr Otorhinolaryngol. 2014. PMID: 25239229

Both Fetal and Maternal Genotypes Affect Preeclampsia Pathogenesis in Iranian Patients.

Hashemnia V, Sadeghi H, Honarpour A, Dorraji K, Haririan N, Electriciteh Y, Mirfakhraie R. Hashemnia V, et al. Among authors: honarpour a. Biochem Genet. 2026 Feb;64(1):1201-1216. doi: 10.1007/s10528-025-11081-8. Epub 2025 Mar 13. Biochem Genet. 2026. PMID: 40080311

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Results by year

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

3 results

Results by year

Search Page

Filters

My Custom Filters

Results by year

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

3 results

Results by year