Michal Sagi - Concepedia

Author

Michal Sagi

Hadassah Medical Center

Also Known As

M Sagi, MICHAL SAGI, Michal Sagi

Publications

2.5K

Citations

H-Index

126

Concepts

All Affiliations

Hadassah Medical Center Hebrew University of Jerusalem Tel Aviv University Sheba Medical Center Rabin Medical Center

About

Michal Sagi is an author at Hadassah Medical Center specializing in medicine, pathology, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	25	945
2	Public Health	10	10	440
3	Arts	2	2	116
4	Natural Sciences	1	1	43
5	Nursing	1	1	31

Michal Sagi

Publications

2.1K

Citations

H-Index

Page 1

	Year	Citations
A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews Israela Lerer, Michal Sagi, Ziva Ben‐Neriah, Human Mutation	2001	220
Deletion of the ANKRD15 gene at 9p24.3 causes parent-of-origin-dependent inheritance of familial cerebral palsy Israela Lerer, Michal Sagi, Vardiella Meiner, Human Molecular Genetics	2005	132
Genome‐wide SNP genotyping identifies the <i>Stereocilin</i> (<i>STRC</i>) gene as a major contributor to pediatric bilateral sensorineural hearing impairment Lauren J. Francey, Laura K. Conlin, Hanna E. Kadesch, American Journal of Medical Genetics Part A	2011	104
Uniparental disomy in fetuses diagnosed with balanced Robertsonian translocations: risk estimate Shira Silverstein, Israela Lerer, Michal Sagi, Prenatal Diagnosis FertilityCytogeneticsGeneticsReproductive HealthGynecology	2002	96
Fanconi Anemia: Prenatal Diagnosis in 30 Fetuses at Risk Arleen D. Auerbach, Michal Sagi, Barbara Adler PEDIATRICS MedicineChromosomal Breakage StudiesHematologyReproductive HealthGynecology	1985	93
Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT Israela Lerer, Michal Sagi, Esther Malamud, American Journal of Medical Genetics Ashkenazi PatientsAllergyMendelian DisorderGenetic DisorderGenetics	2000	82
Carrier Screening for Gaucher Disease Shachar Zuckerman, Amnon Lahad, Amir Shmueli, JAMA	2007	80
Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies Avigail Beryozkin, Elia Shevah, Adva Kimchi, Scientific Reports	2015	78
Effect of framing on the perception of genetic recurrence risks Shoshana Shiloh, Michal Sagi American Journal of Medical Genetics	1989	77
Clinical and genetic heterogeneity of congenital adrenal hypoplasia due to <i>NR0B1</i> gene mutations Zohar Landau, Aaron Hanukoglu, Joseph Sack, Clinical Endocrinology	2009	70

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