| 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 | 1051 | 2011 |
| A defect in the TUSC3 gene is associated with autosomal recessive mental retardation M Garshasbi, V Hadavi, H Habibi, K Kahrizi, R Kariminejad, F Behjati, ... The American Journal of Human Genetics 82 (5), 1158-1164, 2008 | 178 | 2008 |
| Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci H Najmabadi, MM Motazacker, M Garshasbi, K Kahrizi, A Tzschach, ... Human genetics 121, 43-48, 2007 | 150 | 2007 |
| A clinical and molecular genetic study of 112 Iranian families with primary microcephaly H Darvish, S Esmaeeli-Nieh, GB Monajemi, M Mohseni, ... Journal of medical genetics 47 (12), 823-828, 2010 | 120 | 2010 |
| Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humans CH Pak, M Garshasbi, K Kahrizi, C Gross, LH Apponi, JJ Noto, SM Kelly, ... Proceedings of the National Academy of Sciences 108 (30), 12390-12395, 2011 | 98 | 2011 |
| SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly M Garshasbi, MM Motazacker, K Kahrizi, F Behjati, SS Abedini, SE Nieh, ... Human genetics 118, 708-715, 2006 | 97 | 2006 |
| Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots AW Kuss, M Garshasbi, K Kahrizi, A Tzschach, F Behjati, H Darvish, ... Human genetics 129, 141-148, 2011 | 74 | 2011 |
| The genotoxic and cytotoxic effects of bisphenol-A (BPA) in MCF-7 cell line and amniocytes SM Aghajanpour-Mir, E Zabihi, H Akhavan-Niaki, E Keyhani, ... International journal of molecular and cellular medicine 5 (1), 19, 2016 | 66 | 2016 |
| Prognostic value of chromosome 1 and 8 copy number in invasive ductal breast carcinoma among Iranian women: an interphase FISH analysis F Behjati, M Atri, H Najmabadi, K Nouri, M Zamani, P Mehdipour Pathology & Oncology Research 11, 157-163, 2005 | 48 | 2005 |
| Accurate breakpoint mapping in apparently balanced translocation families with discordant phenotypes using whole genome mate-pair sequencing C Aristidou, C Koufaris, A Theodosiou, M Bak, MM Mehrjouy, F Behjati, ... PLoS One 12 (1), e0169935, 2017 | 45 | 2017 |
| Overexpression of her-2/neu in malignant mammary tumors; translation of clinicopathological features from dog to human A Muhammadnejad, E Keyhani, P Mortazavi, F Behjati, IS Haghdoost Asian Pac J Cancer Prev 13 (12), 6415-21, 2012 | 45 | 2012 |
| Improvement of hepatogenic differentiation of iPS cells on an aligned polyethersulfone compared to random nanofibers M Mahmoodinia Maymand, HR Soleimanpour-Lichaei, A Ardeshirylajimi, ... Artificial cells, nanomedicine, and biotechnology 46 (4), 853-860, 2018 | 36 | 2018 |
| Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome SG Firouzabadi, R Kariminejad, R Vameghi, H Darvish, H Ghaedi, ... Molecular neurobiology 54, 7019-7027, 2017 | 30 | 2017 |
| Human leukocyte antigens and circulating immunoglobulin levels in Indian patients with pulmonary tuberculosis SS Papiha, J Wentzel, F Behjati, SS Agarwal Tubercle 66 (1), 25-33, 1985 | 29 | 1985 |
| Investigation of primary microcephaly in Bushehr province of Iran: novel STIL and ASPM mutations E Papari, M Bastami, A Farhadi, S Abedini, M Hosseini, I Bahman, ... Clinical Genetics: an international journal of genetics in medicine 83 (5 …, 2013 | 28 | 2013 |
| Angiogenesis markers in breast cancer-potentially useful tools for priority setting of anti-angiogenic agents E Keyhani, A Muhammadnejad, F Behjati, F Sirati, F Khodadadi, ... Asian Pacific Journal of Cancer Prevention 14 (12), 7651-7656, 2013 | 27 | 2013 |
| Chromosomal studies in infertile men. P Kalantari, H Sepehri, F Behjati, ZO Ashtiani, MT Akbari Tsitologiia i Genetika 35 (6), 50-54, 2001 | 27 | 2001 |
| miRNA-Related Polymorphisms in miR-423 (rs6505162) and PEX6 (rs1129186) and Risk of Esophageal Squamous Cell Carcinoma in an Iranian Cohort Z Nariman-Saleh-Fam, M Bastami, MH Somi, F Behjati, Y Mansoori, ... Genetic Testing and Molecular Biomarkers 21 (6), 382-390, 2017 | 24 | 2017 |
| BOD1 Is Required for Cognitive Function in Humans and Drosophila S Esmaeeli-Nieh, M Fenckova, IM Porter, MM Motazacker, B Nijhof, ... PLoS Genetics 12 (5), e1006022, 2016 | 24 | 2016 |
| Detection of HER2 status in breast cancer: comparison of current methods with MLPA and real-time RT-PCR R Pazhoomand, E Keyhani, M Banan, H Najmabadi, F Khodadadi, ... Asian Pac J Cancer Prev 14 (12), 7621-8, 2013 | 24 | 2013 |
