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Batsheva Bonne-Tamir

Research Profile

Physiology

Concepts & Ideas

Chemicals & Drugs

Occupations

Genetics, Population

Living Beings

Jews

Genes & Molecular Sequences

Procedures

Co-author Network

Publications

TOP 3
Doron M Behar; Bayazit Yunusbayev; Mait Metspalu; Ene Metspalu; Saharon Rosset; Jüri Parik; Siiri Rootsi; Gyaneshwer Chaubey; Ildus Kutuev; Guennady Yudkovsky; Elza Khusnutdinova; Oleg Balanovsky; Ornella Semino; Luisa Pereira; David Comas; David Gurwitz; Batsheva Bonne-Tamir; Tudor Parfitt; Michael F Hammer; Karl Skorecki; Richard Villems
The genome-wide structure of the Jewish people.
Doron M Behar; Ene Metspalu; Toomas Kivisild; Saharon Rosset; Shay Tzur; Yarin Hadid; Guennady Yudkovsky; Dror Rosengarten; Luisa Pereira; António Amorim; Ildus Kutuev; David Gurwitz; Batsheva Bonne-Tamir; Richard Villems; Karl Skorecki
Counting the founders: the matrilineal genetic ancestry of the Jewish Diaspora.
Doron M Behar; Ene Metspalu; Toomas Kivisild; Alessandro Achilli; Yarin Hadid; Shay Tzur; Luisa Pereira; António Amorim; Lluis Quintana-Murci; Kari Majamaa; Corinna Herrnstadt; Neil Howell; Oleg Balanovsky; Ildus Kutuev; Andrey Pshenichnov; David Gurwitz; Batsheva Bonne-Tamir; Antonio Torroni; Richard Villems; Karl Skorecki
The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event.

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All Publications

2010: Doron M Behar; Bayazit Yunusbayev; Mait Metspalu; Ene Metspalu; Saharon Rosset; Jüri Parik; Siiri Rootsi; Gyaneshwer Chaubey; Ildus Kutuev; Guennady Yudkovsky; Elza Khusnutdinova; Oleg Balanovsky; Ornella Semino; Luisa Pereira; David Comas; David Gurwitz; Batsheva Bonne-Tamir; Tudor Parfitt; Michael F Hammer; Karl Skorecki; Richard Villems
The genome-wide structure of the Jewish people.
Nature 2010;466(7303):238-42.
2008: Doron M Behar; Ene Metspalu; Toomas Kivisild; Saharon Rosset; Shay Tzur; Yarin Hadid; Guennady Yudkovsky; Dror Rosengarten; Luisa Pereira; António Amorim; Ildus Kutuev; David Gurwitz; Batsheva Bonne-Tamir; Richard Villems; Karl Skorecki
Counting the founders: the matrilineal genetic ancestry of the Jewish Diaspora.
PloS one 2008;3(4):e2062.
2006: Doron M Behar; Ene Metspalu; Toomas Kivisild; Alessandro Achilli; Yarin Hadid; Shay Tzur; Luisa Pereira; António Amorim; Lluis Quintana-Murci; Kari Majamaa; Corinna Herrnstadt; Neil Howell; Oleg Balanovsky; Ildus Kutuev; Andrey Pshenichnov; David Gurwitz; Batsheva Bonne-Tamir; Antonio Torroni; Richard Villems; Karl Skorecki
The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event.
American journal of human genetics 2006;78(3):487-97.
2005: 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; Olga V Zhukova; Batsheva Bonne-Tamir; Ru-Band Lu; Josef Parnas; Leslie O Schulz; Judith R Kidd; Kenneth K Kidd
Considerable haplotype diversity within the 23kb encompassing the ADH7 gene.
Alcoholism, clinical and experimental research 2005;29(12):2091-100.
2004: Meg A Palmatier; Andrew J Pakstis; William C Speed; Peristera Paschou; David Goldman; Adekunle Odunsi; Friday Okonofua; Sylvester L B Kajuna; Nganyirwa J Karoma; Selemani Kungulilo; Elena L Grigorenko; Olga V Zhukova; Batsheva Bonne-Tamir; Ru-Band Lu; Josef Parnas; Judith R Kidd; Mellissa M C DeMille; Kenneth K Kidd
COMT haplotypes suggest P2 promoter region relevance for schizophrenia.
Molecular psychiatry 2004;9(9):859-70.
2004: Doron M Behar; Michael F Hammer; Daniel Garrigan; Richard Villems; Batsheva Bonne-Tamir; Martin Richards; David Gurwitz; Dror Rosengarten; Matthew Kaplan; Sergio Della Pergola; Lluis Quintana-Murci; Karl Skorecki
MtDNA evidence for a genetic bottleneck in the early history of the Ashkenazi Jewish population.
European journal of human genetics : EJHG 2004;12(5):355-64.
2004: Hiroki Oota; Andrew J Pakstis; Batsheva Bonne-Tamir; David Goldman; Elena L Grigorenko; Sylvester L B Kajuna; Nganyirwa J Karoma; Selemani Kungulilo; Ru-Band Lu; Kunle Odunsi; Friday Okonofua; Olga V Zhukova; Judith R Kidd; Kenneth K Kidd
The evolution and population genetics of the ALDH2 locus: random genetic drift, selection, and low levels of recombination.
Annals of human genetics 2004;68(Pt 2):93-109.
2003: Pratima Chattopadhyay; Andrew J Pakstis; Namita Mukherjee; Sudha Iyengar; Adekunle Odunsi; Friday Okonofua; Batsheva Bonne-Tamir; William C Speed; Judith R Kidd; Kenneth K Kidd
Global survey of haplotype frequencies and linkage disequilibrium at the RET locus.
European journal of human genetics : EJHG 2003;11(10):760-9.
2002: Mellissa M C DeMille; Judith R Kidd; Valeria Ruggeri; Meg A Palmatier; David Goldman; Adekunle Odunsi; Friday Okonofua; Elena L Grigorenko; Leslie O Schulz; Batsheva Bonne-Tamir; Ru-Band Lu; Josef Parnas; Andrew J Pakstis; Kenneth K Kidd
Population variation in linkage disequilibrium across the COMT gene considering promoter region and coding region variation.
Human genetics 2002;111(6):521-37.
2002: Michael V Osier; Andrew J Pakstis; Himla Soodyall; David Comas; David Goldman; Adekunle Odunsi; Friday Okonofua; Josef Parnas; Leslie O Schulz; Jaume Bertranpetit; Batsheva Bonne-Tamir; Ru-Band Lu; Judith R Kidd; Kenneth K Kidd
A global perspective on genetic variation at the ADH genes reveals unusual patterns of linkage disequilibrium and diversity.
American journal of human genetics 2002;71(1):84-99.
2002: Avital Adato; Sarah Vreugde; Tarja Joensuu; Nili Avidan; Riikka Hamalainen; Olga Belenkiy; Tsviya Olender; Batsheva Bonne-Tamir; Edna Ben-Asher; Carmen Espinos; José M Millán; Anna-Elina Lehesjoki; John G Flannery; Karen B Avraham; Shmuel Pietrokovski; Eeva-Marja Sankila; Jacques Beckmann; Doron Lancet
USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses.
European journal of human genetics : EJHG 2002;10(6):339-50.
2001: Tamar Ben-Yosef; Marie Wattenhofer; S Riazuddin; Z M Ahmed; Hamish Scott; Jun Kudoh; Kazunori Shibuya; Stylianos E Antonarakis; Batsheva Bonne-Tamir; Uppala Radhakrishna; Sadaf Naz; Zubair M Ahmed; Sheikh Amer Riazuddin; Arti Pandya; Walter E Nance; Edward R Wilcox; Thomas B Friedman; Robert J Morell
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness.
Journal of medical genetics 2001;38(6):396-400.
2001: Marie Wattenhofer; Kazunori Shibuya; Jun Kudoh; Robert Lyle; Joäelle Michaud; Colette Rossier; K Kawasaki; Shuichi Asakawa; Shinsei Minoshima; A Berry; Batsheva Bonne-Tamir; Nobuyoshi Shimizu; Stylianos E Antonarakis; Hamish Scott
Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains.
Human genetics 2001;108(2):140-7.
2001: Hamish Scott; Jun Kudoh; Marie Wattenhofer; Kazunori Shibuya; A Berry; R Chrast; Michel Guipponi; J Wang; K Kawasaki; Shuichi Asakawa; Shinsei Minoshima; F Younus; S Qasim Mehdi; Uppala Radhakrishna; MP Papasavvas; Corinne Gehrig; Colette Rossier; Michael Korostishevsky; A Gal; Nobuyoshi Shimizu; Batsheva Bonne-Tamir; Stylianos E Antonarakis
Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness.
Nature genetics 2001;27(1):59-63.
2000: Lucia Bartoloni; Marie Wattenhofer; Jun Kudoh; A Berry; Kazunori Shibuya; K Kawasaki; J Wang; Shuichi Asakawa; Ilana Talior; Batsheva Bonne-Tamir; Colette Rossier; Joäelle Michaud; Edward RB McCabe; Shinsei Minoshima; Nobuyoshi Shimizu; Hamish Scott; Stylianos E Antonarakis
Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiency.
Genomics 2000;70(2):190-200.
2000: Joäelle Michaud; Jun Kudoh; A Berry; Batsheva Bonne-Tamir; Maria D Lalioti; Colette Rossier; Kazunori Shibuya; K Kawasaki; Shuichi Asakawa; Shinsei Minoshima; Nobuyoshi Shimizu; Stylianos E Antonarakis; Hamish Scott
Isolation and characterization of a human chromosome 21q22.3 gene (WDR4) and its mouse homologue that code for a WD-repeat protein.
Genomics 2000;68(1):71-9.
2000: Michael F Hammer; Alan J Redd; Elizabeth T Wood; M R Bonner; H Jarjanazi; Tatiana M Karafet; S Santachiara-Benerecetti; A Oppenheim; M A Jobling; T Jenkins; Harry Ostrer; Batsheva Bonne-Tamir
Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(12):6769-74.
2000: Avital Adato; L Raskin; Christine Petit; Batsheva Bonne-Tamir
Deafness heterogeneity in a Druze isolate from the Middle East: novel OTOF and PDS mutations, low prevalence of GJB2 35delG mutation and indication for a new DFNB locus.
European journal of human genetics : EJHG 2000;8(6):437-42.
1999: Batsheva Bonne-Tamir
The HGDP can be and should be pursued in harmony with its subjects: an account of the Israeli experience.
Politics and the life sciences : the journal of the Association for Politics and the Life Sciences 1999;18(2):291-3.
1999: Avital Adato; H Kalinski; Dominique Weil; Hassan Chaib; Michael Korostishevsky; Batsheva Bonne-Tamir
Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance.
American journal of human genetics 1999;65(1):261-5.
1998: Kenneth K Kidd; Bharti Morar; CM Castiglione; H Zhao; Andrew J Pakstis; William C Speed; Batsheva Bonne-Tamir; Ru-Band Lu; David Goldman; C Lee; Y S Nam; David K Grandy; T Jenkins; Judith R Kidd
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus.
Human genetics 1998;103(2):211-27.
1998: Sarah A Tishkoff; A Goldman; Francesc Calafell; William C Speed; Amos S Deinard; Batsheva Bonne-Tamir; Judith R Kidd; Andrew J Pakstis; T Jenkins; Kenneth K Kidd
A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations.
American journal of human genetics 1998;62(6):1389-402.
1998: Hannah Tamary; Lea Shalmon; Hanna Shalev; A Halil; D Dobrushin; N Ashkenazi; Meira Zoldan; Peretz Resnitzky; Michael Korostishevsky; Batsheva Bonne-Tamir; Rina Zaizov
Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3.
American journal of human genetics 1998;62(5):1062-9.
1998: H Kalinsky; A Funes; A Zeldin; Y Pel-Or; Michael Korostishevsky; Ruth Gershoni-Baruch; Lindsay A Farrer; Batsheva Bonne-Tamir
Novel ATP7B mutations causing Wilson disease in several Israeli ethnic groups.
Human mutation 1998;11(2):145-51.
1997: Avital Adato; Dominique Weil; H Kalinski; Y Pel-Or; Hammadi Ayadi; Christine Petit; Michael Korostishevsky; Batsheva Bonne-Tamir
Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.
American journal of human genetics 1997;61(4):813-21.
1997: S Iyengar; H Kalinsky; S Weiss; Michael Korostishevsky; M Sadeh; Y Zhao; Kenneth K Kidd; Batsheva Bonne-Tamir
Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.
Journal of medical genetics 1997;34(5):391-4.
1996: Kenneth K Kidd; Andrew J Pakstis; C M Castiglione; Judith R Kidd; William C Speed; David Goldman; W C Knowler; Ru-Band Lu; Batsheva Bonne-Tamir
DRD2 haplotypes containing the TaqI A1 allele: implications for alcoholism research.
Alcoholism, clinical and experimental research 1996;20(4):697-705.
1995: C M Castiglione; Amos S Deinard; William C Speed; Giorgio Sirugo; H C Rosenbaum; Y Zhang; David K Grandy; Elena L Grigorenko; Batsheva Bonne-Tamir; Andrew J Pakstis
Evolution of haplotypes at the DRD2 locus.
American journal of human genetics 1995;57(6):1445-56.
1991: A Zoossmann-Diskin; A Ticher; I Hakim; Z Goldwitch; Ardon Rubinstein; Batsheva Bonne-Tamir
Genetic affinities of Ethiopian Jews.
Israel journal of medical sciences 1991;27(5):245-51.