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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Journal ArticleDOI
Maternal and paternal lineages of the Samaritan isolate: mutation rates and time to most recent common male ancestor.
Batsheva Bonne-Tamir,Michael Korostishevsky,Alan J. Redd,Y. Pel-Or,Matthew E. Kaplan,Michael F. Hammer +5 more
TL;DR: The haplotypes identified in Samaritan paternal lineages that belong to the same haplogroup were used to estimate the number of generations elapsed since their most recent common ancestor (MRCA), and the estimate of 80 generations corresponds with accepted traditions of the origin of this sect.
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Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region.
Asher Berry,Hamish S. Scott,Jun Kudoh,Ilana Talior,Michael Korostishevsky,Marie Wattenhofer,Michel Guipponi,Christine Barras,Colette Rossier,Kazunori Shibuya,Jun Wang,Kazuhiko Kawasaki,Shuichi Asakawa,Shinsei Minoshima,Nobuyoshi Shimizu,Stylianos E. Antonarakis,Batsheva Bonne-Tamir +16 more
TL;DR: The new microsatellite markers and single nucleotide polymorphisms identified in this study should enable the refined mapping of other genetic diseases that map to 21q22.3.
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Iraqi-Jewish Kindreds with Optic Atrophy Plus (3-Methylglutaconic Aciduria Type 3) Demonstrate Linkage Disequilibrium with the CTG Repeat in the 3′ Untranslated Region of the Myotonic Dystrophy Protein Kinase Gene
Arne M. Nystuen,Hanan Costeff,Orly Elpeleg,Naomi Apter,Batsheva Bonne-Tamir,Harvey W. Mohrenweiser,Neena B. Haider,Edwin M. Stone,Val C. Sheffield +8 more
TL;DR: The existence of multiple recombinant individuals indicates the disease interval can be further narrowed with additional markers, and linkage to chromosome 19q 13.2-q13.3 is identified, well characterized and contains several candidate genes.
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HLA Polymorphism in Israel
TL;DR: Phenotype and gene frequencies of antigens at the A and B HLA loci were determined in a sample of 89 random Libyan Jews now settled in Israel.
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Considerable haplotype diversity within the 23kb encompassing the ADH7 gene.
Yi Han,Hiroki Oota,Michael V. Osier,Andrew J. Pakstis,William C. Speed,Adekunle Odunsi,Friday Okonofua,Sylvester L.B. Kajuna,Nganyirwa J. Karoma,Selemani Kungulilo,Elena L. Grigorenko,O. V. Zhukova,Batsheva Bonne-Tamir,Ru‐B Lu,Josef Parnas,Leslie O. Schulz,Judith R. Kidd,Kenneth K. Kidd +17 more
TL;DR: The low linkage disequilibrium between these two "halves" suggests multiple recombination(s) have occurred in this region, specifically, within intron 7, and the absence of strong LD between the functional variation in ADH1B that is strongly associated with alcoholism and any of the variation inADH7 supports the genetic independence of ADH7 in association studies.