| Deep sequencing reveals 50 novel genes for recessive cognitive disorders H Najmabadi, H Hu, M Garshasbi, T Zemojtel, SS Abedini, W Chen, ... Nature 478 (7367), 57-63, 2011 | 1026 | 2011 |
| Genetics of intellectual disability in consanguineous families H Hu, K Kahrizi, L Musante, Z Fattahi, R Herwig, M Hosseini, C Oppitz, ... Molecular psychiatry 24 (7), 1027-1039, 2019 | 193 | 2019 |
| A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability F Larti, K Kahrizi, L Musante, H Hu, E Papari, Z Fattahi, N Bazazzadegan, ... European Journal of Human Genetics 23 (3), 331-336, 2015 | 27 | 2015 |
| Biallelic missense variants in ZBTB11 can cause intellectual disability in humans Z Fattahi, TI Sheikh, L Musante, M Rasheed, II Taskiran, R Harripaul, ... Human molecular genetics 27 (18), 3177-3188, 2018 | 20 | 2018 |
| Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families M Pashaei, A Davarzani, R Hajati, B Zamani, S Nafissi, F Larti, Y Nilipour, ... Journal of neurogenetics 35 (2), 84-94, 2021 | 15 | 2021 |
| YIF1B mutations cause a post-natal neurodevelopmental syndrome associated with Golgi and primary cilium alterations J Diaz, X Gérard, MB Emerit, J Areias, D Geny, J Dégardin, M Simonutti, ... Brain 143 (10), 2911-2928, 2020 | 15 | 2020 |
| New evidence for the role of calpain 10 in autosomal recessive intellectual disability: identification of two novel nonsense variants by exome sequencing in Iranian families M Oladnabi, L Musante, F Larti, H Hu, SS Abedini, TF Wienker, ... Archives of Iranian medicine 18 (3), 179-184, 2015 | 15 | 2015 |
| Prevalence of viral hepatitis in hemodialysis patients in Tehran, Iran MN Toosi, F Larti, S Seifei, A Abdollahi Journal of gastrointestinal and liver diseases: JGLD 17 (2), 233-234, 2008 | 12 | 2008 |
| Risk factors and seroprevalence of hepatitis B and C infections among hemodialysis patients in Tehran TM NASIRI, F Larti, M Rasteh, H FOROUTAN, N Salarieh, ... IRANIAN JOURNAL OF PATHOLOGY (IJP) 2 (4), 181-186, 2007 | 10 | 2007 |
| Risk factors and seroprevalence of hepatitis B and C infections among hemodialysis patients in Tehran TM NASIRI, F Larti, M Rasteh, H FOROUTAN, N Salarieh, ... IRANIAN JOURNAL OF PATHOLOGY (IJP) 2 (4), 181-186, 2007 | 10 | 2007 |
| Erratum: A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability F Larti, K Kahrizi, L Musante, H Hu, E Papari, Z Fattahi, N Bazazzadegan, ... European Journal of Human Genetics 23 (3), 416-416, 2015 | 8 | 2015 |
| Genetic Investigation of an Iranian Supercentenarian by Whole Exome Sequencing. T Akhtarkhavari, MT Joghataei, Z Fattahi, MR Akbari, F Larti, H Najmabadi, ... Archives of Iranian medicine 18 (10), 688-697, 2015 | 6 | 2015 |
| A splice-altering variant in LARP7 gene leads to exon exclusion M Hosseini, F Larti, Z Fattahi, H Najmabadi, K Kahrizi Gene Reports 15, 100375, 2019 | 2 | 2019 |
| Whole genome sequencing identifies a duplicated region encompassing Xq13. 2q13. 3 in a large Iranian family with intellectual disability S Mehvari, F Larti, H Hu, Z Fattahi, M Beheshtian, SS Abedini, S Arzhangi, ... Molecular Genetics & Genomic Medicine 8 (10), e1418, 2020 | 1 | 2020 |
| YIF1B mutations cause a post-natal neurodevelopmental syndrome associated with Golgi and primary cilium alterations (vol 143, pg 2911, 2020) J Diaz, X Gerard, MB Emerit, J Areias, D Geny, J Degardin, M Simonutti, ... Brain-A Journal of Neurology 144, --, 2021 | | 2021 |
| The benefits of whole exome sequencing data reanalysis in Intellectual disability Z Fattahi, M Babanejad, F Peymani, M Beheshtian, F Larti, K Kahrizi, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1392-1392, 2019 | | 2019 |
| Attempts to elucidate role of ZBTB11 gene in intellectual disability Z Fattahi, T Sheikh, K Kahrizi, R Harripaul, F Larti, N Bazazzadegan, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 337-338, 2018 | | 2018 |
| Investigation of relative leukocyte telomere length in Iranian healthy individuals F Larti, S Dehdahsi, F Larti, A Rad, M Mohammad-Zadeh, K Kahrizi, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 1011-1011, 2018 | | 2018 |
| INVITED SPEAKERS: I-18: IDENTIFICATION OF OVER 50 NOVEL GENES INVOLVED IN ARID BY HOMOZYGOUSITY MAPPING AND NEXT GENERATION SEQUENCING H NAJMABADI, H HU, M GARSHASBI, T ZEMOJTEL, SS ABEDINI, ... CELL JOURNAL (YAKHTEH) 13 (2), 11-11, 2011 | | 2011 |
| INVITED SPEAKERS: I-18: IDENTIFICATION OF OVER 50 NOVEL GENES INVOLVED IN ARID BY HOMOZYGOUSITY MAPPING AND NEXT GENERATION SEQUENCING H NAJMABADI, H HU, M GARSHASBI, T ZEMOJTEL, SS ABEDINI, ... CELL JOURNAL (YAKHTEH) 13 (2), 11-11, 2011 | | 2011 |
