| Human liver sinusoidal endothelial cells but not hepatocytes contain factor VIII T Shahani, K Covens, R Lavend'Homme, N Jazouli, E Sokal, K Peerlinck, ... Journal of Thrombosis and Haemostasis 12 (1), 36-42, 2014 | 200 | 2014 |
| Activation of human endothelial cells from specific vascular beds induces the release of a FVIII storage pool T Shahani, R Lavend'homme, A Luttun, JM Saint-Remy, K Peerlinck, ... Blood, The Journal of the American Society of Hematology 115 (23), 4902-4909, 2010 | 77 | 2010 |
| A novel homozygous LRRK1 stop gain mutation in a patient suspected with osteosclerotic metaphyseal dysplasia M Miryounesi, A Nikfar, M Changi‐Ashtiani, M Shahrooei, ... Annals of Human Genetics 84 (1), 102-106, 2020 | 16 | 2020 |
| Whole exome sequencing identifies both nuclear and mitochondrial variations in an Iranian family with non-syndromic hearing loss S Khatami, H Rokni-Zadeh, N Mohsen-Pour, A Biglari, M Changi-Ashtiani, ... Mitochondrion 46, 321-325, 2019 | 15 | 2019 |
| Pure ultra-fine carbon particles do not exert pro-coagulation and inflammatory effects on microvascular endothelial cells H Dinmohammadi, Z Pirdel, L Salarilak, M Hoylaerts, R Nejatbakhsh, ... Environmental Science and Pollution Research 26, 991-999, 2019 | 7 | 2019 |
| Non-viral suicide gene therapy: Cytosine deaminase gene directed by VEGF promoter and 5-fluorocytosine as a gene directed enzyme/prodrug system in breast cancer model M Emamian, A Abbaspour, T Shahani, A Biglari, A Sharafi Drug Research 71 (07), 395-406, 2021 | 6 | 2021 |
| KH domain containing 3 like (KHDC3L) frame-shift mutation causes both recurrent pregnancy loss and hydatidiform mole N Fatemi, PF Ray, F Ramezanali, T Shahani, A Amiri-Yekta, ZE Kherraf, ... European Journal of Obstetrics & Gynecology and Reproductive Biology 259 …, 2021 | 6 | 2021 |
| GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co‐occurrence of a novel de novo translocation (5;7) and a likely pathogenic … S Kalayinia, M Maleki, H Rokni‐Zadeh, M Changi‐Ashtiani, H Ahangar, ... Journal of Clinical Laboratory Analysis 33 (7), e22923, 2019 | 6 | 2019 |
| Mosaic trisomy 22 in a 4‐year‐old boy with congenital heart disease and general hypotrophy: a case report S Kalayinia, T Shahani, A Biglari, M Maleki, H Rokni‐Zadeh, Z Razavi, ... Journal of Clinical Laboratory Analysis 33 (2), e22663, 2019 | 6 | 2019 |
| While urine and plasma decorin remain unchanged in prostate cancer, prostatic tissue decorin has a prognostic value R Rezaie, Z Falakian, S Mazloomzadeh, M Ayati, A Morakabati, ... Iranian Biomedical Journal 24 (4), 229, 2020 | 5 | 2020 |
| Patients with invasive ductal carcinoma have reduced levels of decorin expression in their breast tissue compared to patients with fibroadenoma while plasma decorin remains … Z Falakian, T Shahani, R Rezaie, S Mazloomzadeh, F Sirati, A Jalilvand, ... Archives of Iranian Medicine 21 (11), 509-517, 2018 | 4 | 2018 |
| Whole exome sequencing revealed a novel GJB1 pathogenic variant and a rare BSCL2 mutation in two Iranian large pedigrees with multiple affected cases of Charcot-Marie-Tooth N Mohsenpour, H Roknizadeh, M Maghbooli, M Changi-Ashtiani, ... International Journal of Molecular and Cellular Medicine 8 (3), 169, 2019 | 3 | 2019 |
| Extensive genetic screening of Iranian Factor FVII-deficient individuals unraveled several novel mutations and postulated founder effects in some cases S Ravanbod, M Faranoush, M Changi-Ashtiani, H Rokni-Zadeh, ... Research and Practice in Thrombosis and Haemostasis 7 (1), 100003, 2023 | 1 | 2023 |
| Pro‐haemostatic effect of DDAVP is partially derived through non‐classical (CD14dim/CD16++) monocytes residing the spleen L Salarilak, Z Pirdel, H Dinmohammadi, H Rokni‐Zadeh, ... Journal of Cellular and Molecular Medicine 27 (1), 30-35, 2023 | | 2023 |
| A Novel Non-frameshift ADA Deletion Detected by Whole Exome Sequencing in an Iranian Family with Severe Combined Immunodeficiency T Talebi, A Biglari, M Shahroeei, M Changi-Ashtiani, H Dinmohammadi, ... Iranian Journal of Allergy, Asthma and Immunology, 94-101, 2020 | | 2020 |
| Exome-first Approach Identified Novel Homozygous Dedicator of Cytokinesis 8 (DOCK8) Mutations in Three Unrelated Iranian Pedigrees Suspected with Hyper-IgE Syndrome A Aghebati-Maleki, T Shahani, T Momen, S Alyasin, M Changi-Ashtiani, ... Iranian Journal of Allergy Asthma and Immunology 19 (2), 193-199, 2020 | | 2020 |
| Genetic Analysis of Congenital Heart Disease in Iranian Pediatric Patients S Kalayinia, T Shahani, A Biglari, M Maleki, H Rokni-Zadeh, N Mahdieh International Cardiovascular Research Journal 13 (2), 62-67, 2019 | | 2019 |
| RNA-SEQ analysis of human major liver cell types reveals differential expression profile of sinusoidal versus other hepatic vascular endothelial cells T Shahani, P Zarrineh, K Covens, M Ashtiani, R Lavend'homme, ... Journal of Thrombosis and Haemostasis 13, 329-330, 2015 | | 2015 |
| Human liver sinusoidal endothelial cells but not hepatocytes contain FVIII M Jacquemin, K Covens, N Jazouli, E Sokal, K Peerlinck, T Shahani Journal of Thrombosis and Haemostasis 11, 323-323, 2013 | | 2013 |
| Exposure to carbon nanoparticles induces upregulation of factor VIII production by human pulmonary microvascular endothelial cells T Shahani, J Emmerechts, S Deckx, M Hoylaerts, M Jacquemin Journal of Thrombosis and Haemostasis 9, 486-486, 2011 | | 2011 |
Etienne SokalUniversité Catholique de Louvain, Institut de Recherche Expérimentale et Clinique (IREC), CliniquesVerified email at uclouvain.be
