1. A novel homozygous variant in an Iranian pedigree with cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 4. Issue 11 (17th July 2020) Authors: Mohamadian, Malihe; Ghandil, Pegah; Naseri, Mohsen; Bahrami, Afsane; Momen, Ali Akbar Journal: Journal of clinical laboratory analysis Issue: Volume 34:Issue 11(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Association between HLA-G 14bp Gene Polymorphism and Serum sHLA-G Protein Concentrations in Preeclamptic Patients and Normal Pregnant Women. (18th August 2018) Authors: Rokhafrooz, Saber; Ghadiri, Ata; Ghandil, Pegah; Ghafourian, Mehri; Hossaini, Seyed Hojjat; Daraei, Nahid; Najafian, Mahin; Rouhizadeh, Ahmad Journal: Immunological investigations Issue: Volume 47:Number 6(2018) Page Start: 558 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Association of vascular endothelial growth factor A polymorphisms and aberrant expression of connexin 43 and VEGFA with idiopathic recurrent spontaneous miscarriage. Issue 3 (30th January 2020) Authors: Sajjadi, Maryam S.; Ghandil, Pegah; Shahbazian, Nahid; Saberi, Alihossein Journal: Journal of obstetrics and gynaecology research Issue: Volume 46:Issue 3(2020) Page Start: 369 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Association study between two polymorphisms of tumor necrosis factor ligand superfamily member 15 (TNFSF15) gene and ulcerative colitis in south‐west of Iran. Issue 5 (16th December 2018) Authors: Taheri, Marzieh; Ghandil, Pegah; Hashemi, Seyyed Jalal; Ghafourian, Mehri; Masjedi Zadeh, Abdol Rahim; Ghadiri, Ata Allah Journal: Journal of cellular biochemistry Issue: Volume 120:Issue 5(2019) Page Start: 8784 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genetic association study of CTLA4 and FCεRIα polymorphisms in asthmatic patients in the southwestern region of Iran. (2nd September 2021) Authors: Roshanizadeh, Zahra; Ghandil, Pegah; Khodadadi, Ali; Tavakol, Heshmatollah; Kambiz, Ahmadi Angali; Ghadiri, Ata Journal: Nucleosides, nucleotides & nucleic acids Issue: Volume 40:Number 9(2021) Page Start: 914 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic association study of CTLA4 and FCεRIα polymorphisms in asthmatic patients in the southwestern region of Iran. (2nd September 2021) Authors: Roshanizadeh, Zahra; Ghandil, Pegah; Khodadadi, Ali; Tavakold, Heshmatollah; Angali, Kambiz Ahmadi; Ghadiri, Ata Journal: Nucleosides, nucleotides & nucleic acids Issue: Volume 40:Number 9(2021) Page Start: 914 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Identification of Cytochrome b‐245, beta‐chain gene mutations, and clinical presentations in Iranian patients with X‐linked chronic granulomatous disease. Issue 2 (23rd October 2020) Authors: Heydari, Atefeh; Abolnezhadian, Farhad; Sadeghi‐Shabestari, Mahnaz; Saberi, Alihossein; Shamsizadeh, Ahmad; Ghadiri, Ata A.; Ghandil, Pegah Journal: Journal of clinical laboratory analysis Issue: Volume 35:Issue 2(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Identification of the PRM1 gene mutations in oligoasthenoteratozoospermic men. (28th October 2020) Authors: Nasirshalal, Mahzad; Tahmasebi‐Birgani, Maryam; Dadfar, Mohammadreza; Nikbakht, Roshan; Saberi, Alihossein; Ghandil, Pegah Journal: Andrologia Issue: Volume 52:Number 11(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes. (29th September 2020) Authors: Mohamadian, Malihe; Naseri, Mohsen; Ghandil, Pegah; Bahrami, Afsane; Momen, Ali Akbar Journal: Journal of gene medicine Issue: Volume 22:Number 12(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗