Get started
Author

Michal Sagi

A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews
2001 · Israela Lerer, Michal Sagi, et al. · Human Mutation · 221
PDF
Deletion of the ANKRD15 gene at 9p24.3 causes parent-of-origin-dependent inheritance of familial cerebral palsy
2005 · Israela Lerer, Michal Sagi, et al. · Human Molecular Genetics · 133
PDF
Cancer Genetic Testing and Assisted Reproduction
2006 · Kenneth Offit, Kelly Kohut, et al. · Journal of Clinical Oncology · 115
Genome‐wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment
2011 · Lauren J. Francey, Laura K. Conlin, et al. · American Journal of Medical Genetics Part A · 106
Uniparental disomy in fetuses diagnosed with balanced Robertsonian translocations: risk estimate
2002 · Shira Silverstein, Israela Lerer, et al. · Prenatal Diagnosis · 95
Fanconi Anemia: Prenatal Diagnosis in 30 Fetuses at Risk
1985 · Arleen D. Auerbach, Michal Sagi, et al. · PEDIATRICS · 92
Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT
2000 · Israela Lerer, Michal Sagi, et al. · American Journal of Medical Genetics · 82
Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies
2015 · Avigail Beryozkin, Elia Shevah, et al. · Scientific Reports · 79
PDF
Carrier Screening for Gaucher Disease
2007 · Shachar Zuckerman, Amnon Lahad, et al. · JAMA · 79
Preimplantation Genetic Diagnosis for Cancer Syndromes
2006 · Kenneth Offit, Michal Sagi, et al. · JAMA · 78
Effect of framing on the perception of genetic recurrence risks
1989 · Shoshana Shiloh, Michal Sagi · American Journal of Medical Genetics · 77
Clinical and genetic heterogeneity of congenital adrenal hypoplasia due to NR0B1 gene mutations
2009 · Zohar Landau, Aaron Hanukoglu, et al. · Clinical Endocrinology · 71
The Jewish Ashkenazi Founder Mutations in the BRCA1/BRCA2 Genes Are Not Found at an Increased Frequency in Ashkenazi Patients with Prostate Cancer
1999 · Ayala Hubert, Tamar Peretz, et al. · The American Journal of Human Genetics · 68
Complete remission, in BRCA2 mutation carrier with metastatic pancreatic adenocarcinoma, treated with cisplatin based therapy
2011 · Amir Sonnenblick, Luna Kadouri, et al. · Cancer Biology & Therapy · 63
PDF
Prenatal diagnosis of sex chromosome aneuploidy: possible reasons for high rates of pregnancy termination
2001 · Michal Sagi, Vardiella Meiner, et al. · Prenatal Diagnosis · 63
Identification of Mutations Causing Inherited Retinal Degenerations in the Israeli and Palestinian Populations Using Homozygosity Mapping
2014 · Avigail Beryozkin, Lina Zelinger, et al. · Investigative Ophthalmology & Visual Science · 55
Application of the health belief model in a study on parents' intentions to utilize prenatal diagnosis of cleft lip and/or palate
1992 · Michal Sagi, Shoshana Shiloh, et al. · American Journal of Medical Genetics · 55
Genetic predisposition to radiation induced sarcoma: possible role for BRCA and p53 mutations
2013 · Luna Kadouri, Michal Sagi, et al. · Breast Cancer Research and Treatment · 52
Presentation Format Affects Comprehension and Risk Assessment: The Case of Prenatal Screening
2009 · Talya Miron-Shatz, Yaniv Hanoch, et al. · Journal of Health Communication · 51
On not wanting to know and not wanting to inform others: choices regarding predictive genetic testing
2004 · Ilan Yaniv, Deborah Benador, et al. · Risk Decision and Policy · 47
Mutation spectrum in Jewish cystic fibrosis patients in Israel: Implication to carrier screening
2005 · Adina Quint, Israela Lerer, et al. · American Journal of Medical Genetics Part A · 45
A deletion/insertion mutation in the BRCA2 gene in a breast cancer family: A possible role of the Alu‐polyA tail in the evolution of the deletion
2001 · Tieling Wang, Israela Lerer, et al. · Genes Chromosomes and Cancer · 42
Language in boys with fragile X syndrome
2006 · YONATA LEVY, RIKI GOTTESMAN, et al. · Journal of Child Language · 40
Incorporating information regarding preimplantation genetic diagnosis into discussions concerning testing and risk management for BRCA1/2 mutations
2012 · Karen Hurley, Lisa R. Rubin, et al. · Cancer · 37
‘TheBRCAClock is Ticking!’: Negotiating medical concerns and reproductive goals in preimplantation genetic diagnosis
2014 · Lisa R. Rubin, Allison Werner-Lin, et al. · Human Fertility · 36
Works count: 73
Citation count: 2,541
H-index: 32
I10-index: 52
Year
Topic
Type