| Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome KR Engelhardt, S McGhee, S Winkler, A Sassi, C Woellner, ... Journal of Allergy and Clinical Immunology 124 (6), 1289-1302. e4, 2009 | 587 | 2009 |
| Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome C Woellner, EM Gertz, AA Schäffer, M Lagos, M Perro, EO Glocker, ... Journal of Allergy and Clinical Immunology 125 (2), 424-432. e8, 2010 | 340 | 2010 |
| IgA deficiency: correlation between clinical and immunological phenotypes A Aghamohammadi, T Cheraghi, M Gharagozlou, M Movahedi, N Rezaei, ... Journal of clinical immunology 29, 130-136, 2009 | 283 | 2009 |
| The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency KR Engelhardt, ME Gertz, S Keles, AA Schäffer, EC Sigmund, C Glocker, ... Journal of Allergy and Clinical Immunology 136 (2), 402-412, 2015 | 197 | 2015 |
| Clinical, immunological and molecular characteristics of 37 Iranian patients with X-linked agammaglobulinemia A Aghamohammadi, M Fiorini, M Moin, N Parvaneh, S Teimourian, ... International archives of allergy and immunology 141 (4), 408-414, 2006 | 85 | 2006 |
| SOCS1 controls liver regeneration by regulating HGF signaling in hepatocytes Y Gui, M Yeganeh, S Ramanathan, C Leblanc, V Pomerleau, G Ferbeyre, ... Journal of hepatology 55 (6), 1300-1308, 2011 | 77 | 2011 |
| Mortality and morbidity in common variable immunodeficiency A Aghamohammadi, N Pouladi, N Parvaneh, M Yeganeh, M Movahedi, ... Journal of tropical pediatrics 53 (1), 32-38, 2007 | 77 | 2007 |
| The clinical, immunohematological, and molecular study of Iranian patients with severe congenital neutropenia N Rezaei, M Moin, Z Pourpak, A Ramyar, M Izadyar, Z Chavoshzadeh, ... Journal of clinical immunology 27, 525-533, 2007 | 60 | 2007 |
| Severe combined immunodeficiency: a cohort of 40 patients M Yeganeh, M Heidarzade, Z Pourpak, N Parvaneh, N Rezaei, ... Pediatric allergy and immunology 19 (4), 303-306, 2008 | 53 | 2008 |
| Regulation of MET receptor tyrosine kinase signaling by suppressor of cytokine signaling 1 in hepatocellular carcinoma Y Gui, M Yeganeh, YC Donates, WS Tobelaim, W Chababi, M Mayhue, ... Oncogene 34 (46), 5718-5728, 2015 | 49 | 2015 |
| Presence of idiopathic thrombocytopenic purpura and autoimmune hemolytic anemia in the patients with common variable immunodeficiency A Ramyar, A Aghamohammadi, K MOAZAMI, N Rezaei, M YEGANEH, ... IRANIAN JOURNAL OF ALLERGY, ASTHMA AND IMMUNOLOGY (IJAAI) 7 (3), 169-175, 2008 | 46 | 2008 |
| Suppressor of cytokine signaling 1-dependent regulation of the expression and oncogenic functions of p21CIP1/WAF1 in the liver M Yeganeh, Y Gui, R Kandhi, D Bobbala, WS Tobelaim, C Saucier, ... Oncogene 35 (32), 4200-4211, 2016 | 44 | 2016 |
| Novel BTK mutation presenting with vaccine-associated paralytic poliomyelitis S Mamishi, S Shahmahmoudi, H Tabatabaie, S Teimourian, B Pourakbari, ... European journal of pediatrics 167, 1335-1338, 2008 | 42 | 2008 |
| Tumour-promoting role of SOCS1 in colorectal cancer cells WS Tobelaim, C Beaurivage, A Champagne, V Pomerleau, A Simoneau, ... Scientific reports 5 (1), 14301, 2015 | 39 | 2015 |
| Analysis of RAB27A Gene in Griscelli Syndrome type 2: Novel Mutations Including a Deletion Hotspot S Mamishi, MH Modarressi, B Pourakbari, B Tamizifar, F Mahjoub, ... Journal of clinical immunology 28, 384-389, 2008 | 35 | 2008 |
| The clinical and laboratory survey of Iranian patients with hyper-IgE syndrome M Moin, A Farhoudi, M Movahedi, N Rezaei, Z Pourpak, M Yeganeh, ... Scandinavian journal of infectious diseases 38 (10), 898-903, 2006 | 32 | 2006 |
| Evaluation of humoral immune function in patients with bronchiectasis P TABATABAEI, A Aghamohammadi, S Mamishi, A Isaeian, G HEYDARI, ... IRANIAN JOURNAL OF ALLERGY, ASTHMA AND IMMUNOLOGY (IJAAI) 7 (2), 69-77, 2008 | 30 | 2008 |
| Progressive multifocal leukoencephalopathy in purine nucleoside phosphorylase deficiency N Parvaneh, MR Ashrafi, M Yeganeh, N Pouladi, F Sayarifar, L Parvaneh Brain and Development 29 (2), 124-126, 2007 | 27 | 2007 |
| Cutaneous granulomas in common variable immunodeficiency: case report and review of literature A Aghamohammadi, H Abolhassani, N Rezaei, N Kalantari, B Tamizifar, ... Acta Dermatovenerologica Croatica 18 (2), 0-0, 2010 | 26 | 2010 |
| Genotype-phenotype correlation in Bruton's tyrosine kinase deficiency S Teimourian, S Nasseri, N Pouladi, M Yeganeh, A Aghamohammadi Journal of pediatric hematology/oncology 30 (9), 679-683, 2008 | 26 | 2008 |
