B
Batsheva Bonne-Tamir
Researcher at Tel Aviv University
Publications - 66
Citations - 7832
Batsheva Bonne-Tamir is an academic researcher from Tel Aviv University. The author has contributed to research in topics: Haplotype & Population. The author has an hindex of 36, co-authored 66 publications receiving 7606 citations. Previous affiliations of Batsheva Bonne-Tamir include University of Geneva.
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Genetic variation of three tetrameric tandem repeats in four distinct Israeli ethnic groups.
TL;DR: The allele frequency distributions of three STR loci amplified by PCR have been studied in four Israeli communities: Ashkenazi Jews and three non-Ashkenazi groups, namely Moroccan, Yemenite, and Ethiopian Jews, and found that all loci meet the H-W expectations.
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Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.
Sudha Iyengar,Hagar Kalinsky,S. Weiss,M. Korostishevsky,Menachem Sadeh,Ying Zhao,Kenneth K. Kidd,Batsheva Bonne-Tamir +7 more
TL;DR: The kindred in this study is the first family reported in which disease is caused by homozygosity for this rare mutation in the glycogen myophosphorylase gene, and was originally reported as the first familial case of McArdle disease in the Druze.
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Gm and Inv [Km] allotypes among Libyan and Ashkenazi jews, and Armenians living in Israel.
TL;DR: The Libyan Jews have a significantly higher frequency of Inv1 than do the Ashkenazi Jews and among the latter, Inv1 is at least twice as frequent among Polish Jews as it is among Russian Jews.
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A Pst+ polymorphism in the HEXA gene with an unusual geographic distribution.
Feige Kaplan,S Kapoor,D Lee,M Fernandes,M Vienozinskis,A Mascisch,Charles R. Scriver,Charles R. Scriver,Joyce Lim-Steele,Michael M. Kaback,Karen Zeiger,A Zoossman-Diskin,Batsheva Bonne-Tamir,E C Landels,M Bobrow,Peter Hechtman,Peter Hechtman +16 more
TL;DR: A polymorphic variant in the human HEXA gene is described, which encodes the α-subunit of hexosaminidase A, the enzyme which is deficient in Tay-Sachs disease (TSD), and which occurs on 1.4% of non-TSD carrier chromosomes in Ashkenazi Jews.
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HLA polymorphism in Israel. 3. Ashkenazi Jews of German descent.
TL;DR: Seventy-three random Jewish individuals whose families have lived in Germany for at least 4-5 generations, were typed for HLA antigens at the A and B loci and the frequent haplotype (Aw24, Bw35) was previously found.