Follow
Hossein Daghagh
Hossein Daghagh
Verified email at stanford.edu
Title
Cited by
Cited by
Year
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
522018
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 190, 111309, 2020
322020
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
62020
Change of epigenetic modification and human reproduction
JN Nojadeh, H Daghghagh
Asian Pacific Journal of Reproduction 5 (1), 10-13, 2016
32016
Homozygous mutation in CSF1R causes brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS)
H Daghagh, HR Kafshboran, Y Daneshmandpour, MN Aghdam, ...
BioImpacts: BI 13 (3), 183, 2023
12023
Correlation of rs35753505 polymorphism in Neuregulin 1 gene with psychopathology and intelligence of people with schizophrenia
A Moradkhani, AT Jalil, MM Saleh, E Vanaki, H Daghagh, B Daghighazar, ...
Gene 867, 147285, 2023
2023
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
The system can't perform the operation now. Try again later.
Articles 1–8