Variants in CIB2 cause DFNB48 and not USH1J KT Booth, K Kahrizi, M Babanejad, H Daghagh, G Bademci, S Arzhangi, ... Clinical genetics 93 (4), 812-821, 2018 | 27 | 2018 |
Change of epigenetic modification and human reproduction JN Nojadeh, H Daghghagh Asian Pacific Journal of Reproduction 5 (1), 10-13, 2016 | 2 | 2016 |
The role of epigenetics and non-coding RNAs in autophagy: A new perspective for thorough understanding S Talebian, H Daghagh, B Yousefi, Y Ȍzkul, K Ilkhani, F Seif, MR Alivand Mechanisms of ageing and development, 111309, 2020 | 1 | 2020 |
A new report of autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation (APLAID) with a homozygous pattern from Iran A Khabbazi, HR Kafshboran, MN Aghdam, JN Nojadeh, H Daghagh, ... Immunology letters 221, 27-32, 2020 | | 2020 |
Efforts to decipher novel genes in 25 Iranian families presenting hereditary hearing loss using whole exome sequencing M Babanejad, M Mohseni, S Arzhangi, K Jalalvand, H Daghagh, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 847-847, 2018 | | 2018 |
FIFTEEN YEARS INVESTIGATION TO ELUCIDATE THE GENETIC HETEROGENEITY OF HEARING LOSS IN IRANIAN POPULATION H NAJMABADI, M BABANEJAD, M BEHESHTIAN, F ARDALANI, ... GENETICS IN THE 3RD MILLENNIUM 14 (1), 0-0, 2016 | | 2016 |