Sirous Zeinali
Title
Cited by
Cited by
Year
Thalassemia in Iran: epidemiology, prevention, and management
H Abolghasemi, A Amid, S Zeinali, MH Radfar, P Eshghi, MS Rahiminejad, ...
Journal of Pediatric Hematology/Oncology 29 (4), 233-238, 2007
2752007
Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients.
F Peyvandi, PM Mannucci, M Lak, M Abdoullahi, S Zeinali, R Sharifian, ...
British journal of haematology 102 (2), 626-628, 1998
1361998
Missense mutations in the human β fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion
S Duga, R Asselta, E Santagostino, S Zeinali, T Simonic, M Malcovati, ...
Blood, The Journal of the American Society of Hematology 95 (4), 1336-1341, 2000
1342000
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations
N Mahdieh, B Rabbani, S Wiley, MT Akbari, S Zeinali
Journal of human genetics 55 (10), 639-648, 2010
1062010
Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiency
F Peyvandi, VP Jenkins, PM Mannucci, A Billio, S Zeinali, SJ Perkins, ...
Thrombosis and haemostasis 84 (08), 250-257, 2000
902000
Generation and characterization of a functional Nanobody against the vascular endothelial growth factor receptor-2; angiogenesis cell receptor
M Behdani, S Zeinali, H Khanahmad, M Karimipour, N Asadzadeh, ...
Molecular immunology 50 (1-2), 35-41, 2012
892012
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families
R Harripaul, N Vasli, A Mikhailov, MA Rafiq, K Mittal, C Windpassinger, ...
Molecular psychiatry 23 (4), 973-984, 2018
842018
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort
G Bademci, J Foster, N Mahdieh, M Bonyadi, D Duman, FB Cengiz, ...
Genetics in Medicine 18 (4), 364-371, 2016
832016
Novel mutations in the BRCA1 and BRCA2genes in Iranian women with early-onset breast cancer
VR Yassaee, S Zeinali, I Harirchi, S Jarvandi, MA Mohagheghi, ...
Breast Cancer Research 4 (4), R6, 2002
732002
MicroRNA-148b and microRNA-152 reactivate tumor suppressor genes through suppression of DNA methyltransferase-1 gene in pancreatic cancer cell lines
M Azizi, L Teimoori-Toolabi, MK Arzanani, K Azadmanesh, ...
Cancer biology & therapy 15 (4), 419-427, 2014
722014
Multipotent mesenchymal stromal cells: optimization and comparison of five cationic polymer-based gene delivery methods
Y Gheisari, M Soleimani, K Azadmanesh, S Zeinali, Y Gheisari, ...
Cytotherapy 10 (8), 815-823, 2008
722008
A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract
CE Willoughby, S Arab, R Gandhi, S Zeinali, S Arab, D Luk, G Billingsley, ...
Journal of medical genetics 40 (11), e124-e124, 2003
722003
A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract
CE Willoughby, S Arab, R Gandhi, S Zeinali, S Arab, D Luk, G Billingsley, ...
Journal of medical genetics 40 (11), e124-e124, 2003
722003
Development of VEGFR2-specific Nanobody Pseudomonas exotoxin A conjugated to provide efficient inhibition of tumor cell growth
M Behdani, S Zeinali, M Karimipour, H Khanahmad, S Schoonooghe, ...
New biotechnology 30 (2), 205-209, 2013
702013
The molecular analysis of β-thalassemia mutations in Lorestan Province, Iran
AA Kiani, Y Mortazavi, S Zeinali, Y Shirkhani
Hemoglobin 31 (3), 343-349, 2007
652007
Genetic Modification of Mesenchymal Stem Cells to Overexpress CXCR4 and CXCR7 Does Not Improve the Homing and Therapeutic Potentials of These Cells iná…
Y Gheisari, K Azadmanesh, N Ahmadbeigi, SM Nassiri, AF Golestaneh, ...
Stem cells and development 21 (16), 2969-2980, 2012
522012
Genetic polymorphisms in three Iranian populations with different risks of esophageal cancer, an ecologic comparison
A Sepehr, F Kamangar, CC Abnet, S Fahimi, A Pourshams, H Poustchi, ...
Cancer letters 213 (2), 195-202, 2004
492004
Variable expressivity and high penetrance of CYP1B1 mutations associated with primary congenital glaucoma
F Suri, S Yazdani, M Narooie-Nejhad, SJ Zargar, SH Paylakhi, S Zeinali, ...
Ophthalmology 116 (11), 2101-2109, 2009
482009
The locus for combined factor V-factor VIII deficiency (F5F8D) maps to 18q21, between D18S849 and D18S1103
M Neerman-Arbez, SE Antonarakis, JL Blouin, S Zeinali, M Akhtari, ...
The American Journal of Human Genetics 61 (1), 143-150, 1997
441997
Thrombophilic mutations in Iran
S Zeinali, F Duca, B Zarbakhsh, L Tagliabue, PM Mannucci
Thrombosis and haemostasis 83 (02), 351-352, 2000
412000
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