Michal Sagi
Hadassah Medical Center(IL)
Publications by Year
Research Areas
BRCA gene mutations in cancer, Prenatal Screening and Diagnostics, DNA Repair Mechanisms, Hearing, Cochlea, Tinnitus, Genetics, Cancer Genomics and Diagnostics
Most-Cited Works
- → A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews(2001)220 cited
- → Deletion of the ANKRD15 gene at 9p24.3 causes parent-of-origin-dependent inheritance of familial cerebral palsy(2005)132 cited
- → Cancer Genetic Testing and Assisted Reproduction(2006)114 cited
- → Genome‐wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment(2011)104 cited
- → Uniparental disomy in fetuses diagnosed with balanced Robertsonian translocations: risk estimate(2002)96 cited
- → Fanconi Anemia: Prenatal Diagnosis in 30 Fetuses at Risk(1985)93 cited
- → Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT(2000)82 cited
- → Carrier Screening for Gaucher Disease(2007)80 cited
- → Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies(2015)79 cited
- → Effect of framing on the perception of genetic recurrence risks(1989)77 cited