Sari Lieberman - Concepedia

Author

Sari Lieberman

Shaare Zedek Medical Center ORCID

Also Known As

Lieberman S, Lieberman, Sari, S Shalev, S. Lieberman, Sari Lieberman

Publications

807

Citations

H-Index

Concepts

All Affiliations

Shaare Zedek Medical Center Hebrew University of Jerusalem Ben-Gurion University of the Negev Hadassah Medical Center Tel Aviv University

About

Sari Lieberman is an author at Shaare Zedek Medical Center specializing in medicine, public health, and genetic testing.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	159
2	Public Health	3	3	130
3	Arts	1	1	22
4	Epidemiology	1	1	12
5	Family Medicine	1	1	88

Sari Lieberman

Publications

690

Citations

H-Index

Page 1

	Year	Citations
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families Zippora Brownstein, Lilach M. Friedman, Hashem Shahin, Genome biology	2011	201
Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen U. Schwarze, Tim Cundy, Shawna M. Pyott, Human Molecular Genetics	2012	137
Familial communication and cascade testing among relatives of BRCA population screening participants Sari Lieberman, Amnon Lahad, Ariela Tomer, Genetics in Medicine Family MedicineGenetic TestingFamily RelationshipGenetic EpidemiologyFamilial Communication	2018	88
Population screening for BRCA1/BRCA2 founder mutations in Ashkenazi Jews: proactive recruitment compared with self-referral Sari Lieberman, Ariela Tomer, Avi Ben-Chetrit, Genetics in Medicine	2016	57
Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and Surveillance Sari Lieberman, Tom Walsh, Menachem Schechter, Gastroenterology Allelic VariantGenetic DisorderGeneticsClinical GeneticsHuman Polymorphism	2017	41
Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data Samer Khateb, Mor Hanany, Ayat Khalaileh, Journal of Medical Genetics	2016	34
Population screening for BRCA1/BRCA2 mutations: lessons from qualitative analysis of the screening experience Sari Lieberman, Amnon Lahad, Ariela Tomer, Genetics in Medicine Genetic AnalysisGenetic TestingBrca1/brca2 MutationsQualitative AnalysisMedicine	2016	30
Presymptomatic Awareness of Germline Pathogenic <i>BRCA</i> Variants and Associated Outcomes in Women With Breast Cancer Tal Hadar, Pnina Mor, Gefen Amit, JAMA Oncology	2020	28
"The Most Important Test You’ll Ever Take"?: Attitudes toward confidential carrier matching and open individual testing among modern-religious Jews in Israel Ayala Frumkin, Aviad E. Raz, Morasha Plesser-Duvdevani, Social Science & Medicine Religious PrejudiceJewish StudiesReligiosityJewish ThoughtConfidential Carrier Matching	2011	22
Variable Features of Juvenile Polyposis Syndrome With Gastric Involvement Among Patients With a Large Genomic Deletion of BMPR1A Sari Lieberman, Rachel Beeri, Tom Walsh, Clinical and Translational Gastroenterology	2019	18

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