Kimia Kahrizi
Isfahan Fertility and Infertility Center(IR)University of Social Welfare and Rehabilitation Sciences(IR)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Vestibular and auditory disorders
Most-Cited Works
- → Deep sequencing reveals 50 novel genes for recessive cognitive disorders(2011)982 cited
- → Human Male Infertility Caused by Mutations in the CATSPER1 Channel Protein(2009)276 cited
- → Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability(2012)271 cited
- → Genetics of intellectual disability in consanguineous families(2018)210 cited
- → Iranome: A catalog of genomic variations in the Iranian population(2019)185 cited
- → Mutations in LOXHD1, an Evolutionarily Conserved Stereociliary Protein, Disrupt Hair Cell Function in Mice and Cause Progressive Hearing Loss in Humans(2009)160 cited