A novel PTRH2 missense mutation causing IMNEPD: a case report
Khamirani, Hossein Jafari, Zoghi, Sina, Dianatpour, Mehdi, Jankhah, Aria, Tabei, Seyed Sajjad, Mohammadi, Sanaz, Dastgheib, Seyed Alireza
Published in Human genome variation (10.06.2021)
Published in Human genome variation (10.06.2021)
Get full text
Journal Article
Meta-analysis of the frequency of intrauterine growth restriction and preterm premature rupture of the membranes in pregnant women with COVID-19
Bahrami, Reza, Schwartz, David A, Karimi-Zarchi, Mojgan, Javaheri, Atiyeh, Dastgheib, Seyed Alireza, Ferdosian, Farzad, Noorishadkam, Mahmood, Mirjalili, Seyed Reza, Neamatzadeh, Hossein
Published in Turkish journal of obstetrics and gynecology (27.09.2021)
Published in Turkish journal of obstetrics and gynecology (27.09.2021)
Get full text
Journal Article
Exome sequencing identified a de novo frameshift pathogenic variant of CTBP1 in an extremely rare case of HADDTS
Khamirani, Hossein Jafari, Zoghi, Sina, Sichani, Ali Saber, Dianatpour, Mehdi, Mohammadi, Sanaz, Tabei, Seyed Mohammad Bagher, Dastgheib, Seyed Alireza
Published in Journal of genetics (2021)
Published in Journal of genetics (2021)
Get full text
Journal Article
A meta-analysis for the risk and prevalence of preeclampsia among pregnant women with COVID-19
Karimi-Zarchi, Mojgan, Schwartz, David A, Bahrami, Reza, Dastgheib, Seyed Alireza, Javaheri, Atiyeh, Tabatabaiee, Razieh Sadat, Ferdosian, Farzad, Asadian, Fatemeh, Neamatzadeh, Hossein
Published in Turkish journal of obstetrics and gynecology (01.09.2021)
Published in Turkish journal of obstetrics and gynecology (01.09.2021)
Get full text
Journal Article
EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature review
Abbasi, Zahra, Jafari Khamirani, Hossein, Tabei, Seyed Mohammad Bagher, Manoochehri, Jamal, Dianatpour, Mehdi, Dastgheib, Seyed Alireza
Published in Human genome variation (13.01.2023)
Published in Human genome variation (13.01.2023)
Get full text
Journal Article
Two novel Warburg micro syndrome 1 cases caused by pathogenic variants in RAB3GAP1
Alavi, Omid, Khamirani, Hossein Jafari, Zoghi, Sina, Feili, Afrooz, Dastgheib, Seyed Alireza, Tabei, Seyed Mohammad Bagher, Manoochehri, Jamal, Panahandeh, Seyed Mehdi, Kamali, Majid, Dianatpour, Mehdi
Published in Human genome variation (26.10.2021)
Published in Human genome variation (26.10.2021)
Get full text
Journal Article
A meta-analysis of the association of the ACE I/D and PAI-1 4G/5G polymorphisms with recurrent pregnancy loss in Iranian women: Are the investigations adequate?
Seyed Alireza Dastgheib, Karimi-Zarchi, Mojgan, Bahrami, Reza, Razieh Sadat Tabatabaei, Javaheri, Atiyeh, Noorishadkam, Mahmood, Mirjalili, Seyed Reza, Neamatzadeh, Hossein
Published in Turkish journal of obstetrics and gynecology (01.06.2021)
Published in Turkish journal of obstetrics and gynecology (01.06.2021)
Get full text
Journal Article
A single-amino-acid in-frame deletion in CYP17A1 results in combined 17-hydroxylase and 17,20-lyase deficiency in an Iranian family despite the protein mutation site
Habib, Ashkan, Shojazadeh, Alireza, Molayemat, Mohadeseh, Jafari Khamirani, Hossein, Zoghi, Sina, Dastgheib, Seyed Alireza, Habib, Asadollah
Published in Human genome variation (21.07.2021)
Published in Human genome variation (21.07.2021)
Get full text
Journal Article
A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case report
Manoochehri, Jamal, Dastgheib, Seyed Alireza, Khamirani, Hossein Jafari, Mollaie, Maryam, Sharifi, Zahra, Zoghi, Sina, Tabei, Seyed Mohammad Bagher, Mohammadi, Sanaz, Dehghanian, Fatemeh, Farbod, Zahra, Dianatpour, Mehdi
Published in Human genome variation (12.08.2021)
Published in Human genome variation (12.08.2021)
Get full text
Journal Article
Correction: A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): a case report
Manoochehri, Jamal, Dastgheib, Seyed Alireza, Khamirani, Hossein Jafari, Mollaie, Maryam, Sharifi, Zahra, Zoghi, Sina, Tabei, Seyed Mohammad Bagher, Mohammadi, Sanaz, Dehghanian, Fatemeh, Farbod, Zahra, Dianatpour, Mehdi
Published in Human genome variation (22.11.2021)
Published in Human genome variation (22.11.2021)
Get full text
Journal Article
A novel nonsense variant in the ATL3 gene is associated with disturbed pain sensitivity, numbness of distal limbs and muscle weakness
Mohammadi, Sanaz, Jafari Khamirani, Hossein, Baneshi, Maryam, Kamal, Neda, Manoocheri, Jamal, Saffar, Mahsa, Dianatpour, Mehdi, Tabei, Seyed Mohammad Bagher, Dastgheib, Seyed Alireza
Published in Annals of human genetics (01.07.2023)
Published in Annals of human genetics (01.07.2023)
Get full text
Journal Article
Correlation of TNF-α polymorphisms with susceptibility to lung cancer: evidence from a meta-analysis based on 29 studies
HaghighiKian, Seyed Masoud, Shirinzadeh-Dastgiri, Ahmad, Ershadi, Reza, Vakili-Ojarood, Mohammad, Barahman, Maedeh, Dastgheib, Seyed Alireza, Asadian, Fatemeh, Shiri, Amirmasoud, Aghasipour, Maryam, Rahmani, Amirhossein, Aghili, Kazem, Neamatzadeh, Hossein
Published in BMC cancer (06.09.2024)
Published in BMC cancer (06.09.2024)
Get full text
Journal Article
A thorough analysis of data on the correlation between COL9A1 polymorphisms and the susceptibility to congenital talipes equinovarus: a meta-analysis
Golshan-Tafti, Mohammad, Dastgheib, Seyed Alireza, Alijanpour, Kamran, Bahrami, Reza, Mazaheri, Mahta, Neamatzadeh, Hossein
Published in Journal of orthopaedic surgery and research (10.06.2024)
Published in Journal of orthopaedic surgery and research (10.06.2024)
Get full text
Journal Article
Gender difference in determinant factors of being overweight among the 40-70-year-old population of Kharameh cohort study, Iran
Dastgheib, Seyed Alireza, Rezaianzadeh, Abbas, Maharlouei, Najmeh, Rahimikazerooni, Salar, Lankarani, Kamran B
Published in BMC public health (17.04.2021)
Published in BMC public health (17.04.2021)
Get full text
Journal Article
Clinical features of patients with Yin Yang 1 deficiency causing Gabriele‐de Vries syndrome: A new case and review of the literature
Khamirani, Hossein Jafari, Zoghi, Sina, Namdar, Zahra Mehdipour, Kamal, Neda, Dianatpour, Mehdi, Tabei, Seyed Mohammad Bagher, Mohammadi, Sanaz, Dehghanian, Fatemeh, Farbod, Zahra, Dastgheib, Seyed Alireza
Published in Annals of human genetics (01.01.2022)
Published in Annals of human genetics (01.01.2022)
Get full text
Journal Article
Association of IL-10 -1082A>G, -819C>T, and -592C>A polymorphisms with susceptibility to chronic and aggressive periodontitis: a systematic review and meta-analysis
Mashhadiabbas, Fatemeh, Dastgheib, Seyed Alireza, Hashemzehi, Ahmad, Bahrololoomi, Zahra, Asadian, Fatemeh, Neamatzadeh, Hossein, Zare-Shehneh, Masoud, Daliri, Karim
Published in Inflammation research (01.05.2021)
Published in Inflammation research (01.05.2021)
Get full text
Journal Article
Altered Expression of hsa_circ_0001445 and hsa_circ_0020397 in Breast Cancer Representing Associations with BMI and Reproductive Factors
Firoozi, Zahra, Mohammadisoleimani, Elham, Dastsooz, Hassan, Daraei, Abdolreza, Dastgheib, Seyed Alireza, Raoofat, Atefeh, Mansoori, Hosein, Mansoori, Yaser, Naghizadeh, Mohammad Mehdi
Published in Archives of Iranian medicine (01.12.2022)
Published in Archives of Iranian medicine (01.12.2022)
Get full text
Journal Article
A meta-analysis for association of eNOS VNTR 4b/a, – 786 T > C and + 894G > T polymorphisms with risk of recurrent pregnancy loss
Golestanpour, Hossein, Bahrami, Reza, Dastgheib, Seyed Alireza, Tabatabaei, Razieh Sadat, Javaheri, Atiyeh, Karimi-Zarchi, Mojgan, Mirjalili, Seyed Reza, Neamatzadeh, Hossein
Published in Archives of gynecology and obstetrics (01.11.2021)
Published in Archives of gynecology and obstetrics (01.11.2021)
Get full text
Journal Article
A pathogenic variant of TULP3 causes renal and hepatic fibrocystic disease
Jafari Khamirani, Hossein, Palicharla, Vivek Reddy, Dastgheib, Seyed Alireza, Dianatpour, Mehdi, Imanieh, Mohammad Hadi, Tabei, Seyed Sajjad, Besse, Whitney, Mukhopadhyay, Saikat, Liem, Jr, Karel F
Published in Frontiers in genetics (07.10.2022)
Published in Frontiers in genetics (07.10.2022)
Get full text
Journal Article
Association of ACE I/D, -240A > T and AT1R A1166C polymorphisms with susceptibility to breast cancer: a systematic review and meta-analysis based on 35 case-control studies
Dastgheib, Seyed Alireza, Asadian, Fatemeh, Farbod, Meraj, Karimi-Zarchi, Mojgan, Meibodi, Bahare, Akbarian, Elahe, Neamatzadeh, Hossein
Published in Nucleosides, nucleotides & nucleic acids (01.01.2021)
Published in Nucleosides, nucleotides & nucleic acids (01.01.2021)
Get full text
Journal Article