| Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran CM Sloan-Heggen, M Babanejad, M Beheshtian, AC Simpson, KT Booth, ... Journal of medical genetics 52 (12), 823-829, 2015 | 116 | 2015 |
| Effect of inbreeding on intellectual disability revisited by trio sequencing K Kahrizi, H Hu, M Hosseini, VM Kalscheuer, Z Fattahi, M Beheshtian, ... Clinical genetics 95 (1), 151-159, 2019 | 68 | 2019 |
| Distinct genetic variation and heterogeneity of the Iranian population Z Mehrjoo, Z Fattahi, M Beheshtian, M Mohseni, H Poustchi, F Ardalani, ... PLoS genetics 15 (9), e1008385, 2019 | 50 | 2019 |
| Association Study of the TREM2 Gene and Identification of a Novel Variant in Exon 2 in Iranian Patients with Late-Onset Alzheimer's Disease Z Mehrjoo, A Najmabadi, SS Abedini, M Mohseni, K Kamali, H Najmabadi, ... Medical Principles and Practice 24 (4), 351-354, 2015 | 25 | 2015 |
| Two novel mutations in ILDR1 gene cause autosomal recessive nonsyndromic hearing loss in consanguineous Iranian families Z Mehrjoo, M Babanejad, K Kahrizi, H Najmabadi Journal of genetics 94, 483-487, 2015 | 17 | 2015 |
| Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities K Najafi, Z Mehrjoo, F Ardalani, S Ghaderi-Sohi, A Kariminejad, ... Scientific Reports 11 (1), 6952, 2021 | 16 | 2021 |
| Limbic system associated membrane protein mutation in an iranian family diagnosed with ménière’s disease Z Mehrjoo, K Kahrizi, M Mohseni, M Akbari, S Arzhangi, K Jalalvand, ... Archives of Iranian Medicine 23 (5), 319, 2020 | 11 | 2020 |
| Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran M Mohseni, M Babanejad, KT Booth, P Jamali, K Jalalvand, B Davarnia, ... Clinical genetics 100 (1), 59-78, 2021 | 8 | 2021 |
| Carrier Testing in Known Autosomal Recessive Intellectual Disability Genes in an Iranian Healthy Individual Using Exome Sequencing Z Mehrjoo, MR Akbari, SS Abedini, S Vaziri, K Kahrizi, H Najmabadi Archives of Iranian medicine 18 (10), 643-669, 2015 | 3 | 2015 |
| Refining diagnosis of renal cell carcinoma subtypes through single-cell resolution transcriptomic signatures M Kim, A Madrigal, Z Mehrjoo, KI Glennon, M Arseneault, M Park, F Brimo, ... Cancer Research 84 (6_Supplement), 3500-3500, 2024 | | 2024 |
| Investigating the heterogeneity and clinical significance of tumor-associated macrophages in renal cell carcinoma milieu EM Zavacky, M Kim, A Madrigal, Z Mehrjoo, J Spicer, S Tanguay, F Brimo, ... CANCER RESEARCH 83 (16), 2023 | | 2023 |
| Abstract A012: Investigating the heterogeneity and clinical significance of tumor-associated macrophages in renal cell carcinoma milieu EM Zavacky, M Kim, A Madrigal, Z Mehrjoo, J Spicer, S Tanguay, F Brimo, ... Cancer Research 83 (16_Supplement), A012-A012, 2023 | | 2023 |
| Abstract B011: An atlas of cellular heterogeneity in primary and metastatic renal cell carcinomas A Madrigal, M Kim, A Osakwe, T Lu, Z Mehrjoo, E Moslemi, R Farouni, ... Cancer Research 83 (16_Supplement), B011-B011, 2023 | | 2023 |
| Abstract PR005: An atlas of cellular heterogeneity in primary and metastatic renal cell carcinomas A Madrigal, M Kim, A Osakwe, T Lu, Z Mehrjoo, E Moslemi, R Farouni, ... Cancer Research 83 (16_Supplement), PR005-PR005, 2023 | | 2023 |
| Distinct genetic diversity and heterogeneity of the Iranian population Z Mehrjoo, Z Fattahi, M Beheshtian, M Mohseni, H Poustchi, F Ardalani, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1914-1915, 2019 | | 2019 |
| Distinct Human Genetic Variation in Iran Z Mehrjoo, Z Fattahi, M Beheshtian, Y Gossmann, B Helwing, LM Niestroj, ... Hum. Hered. 83 (5), 241-242, 2017 | | 2017 |
