Y chromosome sequence variation and the history of human populations
Cavalli-Sforza, L. Luca, Francalacci, Paolo, Jenkins, Trefor, Passarino, Giuseppe, Yang, Wei H, Davis, Ronald W, Bertranpetit, Jaume, Kauffman, Erin, Underhill, Peter A, Ibrahim, Muntaser, Jin, Li, Seielstad, Mark T, Piazza, Alberto, Kidd, Judith R, Wells, R. Spencer, Bonné-Tamir, Batsheva, Lin, Alice A, Feldman, Marcus W, Shen, Peidong, Mehdi, S. Qasim, Oefner, Peter. J
Published in Nature genetics (01.11.2000)
Published in Nature genetics (01.11.2000)
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The Emerging Tree of West Eurasian mtDNAs: A Synthesis of Control-Region Sequences and RFLPs
Macaulay, Vincent, Richards, Martin, Hickey, Eileen, Vega, Emilce, Cruciani, Fulvio, Guida, Valentina, Scozzari, Rosaria, Bonné-Tamir, Batsheva, Sykes, Bryan, Torroni, Antonio
Published in American journal of human genetics (1999)
Published in American journal of human genetics (1999)
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Jewish and Middle Eastern Non-Jewish Populations Share a Common Pool of Y-Chromosome Biallelic Haplotypes
Hammer, M. F., Redd, A. J., Wood, E. T., Bonner, M. R., Jarjanazi, H., Karafet, T., Santachiara-Benerecetti, S., Oppenheim, A., Jobling, M. A., Jenkins, T., Ostrer, H., Bonne-Tamir, B.
Published in Proceedings of the National Academy of Sciences - PNAS (06.06.2000)
Published in Proceedings of the National Academy of Sciences - PNAS (06.06.2000)
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Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins
Tishkoff, S. A., Dietzsch, E., Speed, W., Pakstis, A. J., Kidd, J. R., Cheung, K., Bonné-Tamir, B., Santachiara-Benerecetti, A. S., Moral, P., Krings, M., Pääbo, S., Watson, E., Risch, N., Jenkins, T., Kidd, K. K.
Published in Science (American Association for the Advancement of Science) (08.03.1996)
Published in Science (American Association for the Advancement of Science) (08.03.1996)
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mtDNA Analysis Reveals a Major Late Paleolithic Population Expansion from Southwestern to Northeastern Europe
Torroni, Antonio, Bandelt, Hans-Jürgen, D'Urbano, Leila, Lahermo, Päivi, Moral, Pedro, Sellitto, Daniele, Rengo, Chiara, Forster, Peter, Savontaus, Marja-Liisa, Bonné-Tamir, Batsheva, Scozzari, Rosaria
Published in American journal of human genetics (01.05.1998)
Published in American journal of human genetics (01.05.1998)
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Usher syndrome in the Samaritans: Strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders
Bonné-Tamir, B., Nystuen, A., Seroussi, E., Kalinsky, H., Kwitek-Black, A. E., Korostishevsky, M., Adato, A., Sheffield, V. C.
Published in American journal of physical anthropology (01.10.1997)
Published in American journal of physical anthropology (01.10.1997)
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Predictive testing for Wilson's disease using tightly linked and flanking DNA markers
Farrer, L A, Bowcock, A M, Hebert, J M, Bonné-Tamir, B, Sternlieb, I, Giagheddu, M, St George-Hyslop, P, Frydman, M, Lössner, J, Demelia, L
Published in Neurology (01.07.1991)
Published in Neurology (01.07.1991)
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Worldwide Genetic Analysis of the CFTR Region
Mateu, Eva, Calafell, Francesc, Lao, Oscar, Bonné-Tamir, Batsheva, Kidd, Judith R., Pakstis, Andrew, Kidd, Kenneth K., Bertranpetit, Jaume
Published in American journal of human genetics (01.01.2001)
Published in American journal of human genetics (01.01.2001)
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Conference Proceeding
Mutation Profile of All 49 Exons of the Human Myosin VIIA Gene, and Haplotype Analysis, in Usher 1B Families from Diverse Origins
Adato, A., Weil, D., Kalinski, H., Pel-Or, Y., Ayadi, H., Petit, C., Korostishevsky, M., Bonne-Tamir, B.
Published in American journal of human genetics (01.10.1997)
Published in American journal of human genetics (01.10.1997)
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Mitochondrial DNA affinity of several Jewish communities
Ritte, U, Neufeld, E, Prager, E M, Gross, M, Hakim, I, Khatib, A, Bonné-Tamir, B
Published in Human biology (01.06.1993)
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Published in Human biology (01.06.1993)
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Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3
BONNE-TAMIR, B, DESTEFANO, A. L, BRIGGS, C. E, ADAIR, R, FRANKLYN, B, WEISS, S, KOROSTISHEVSKY, M, FRYDMAN, M, BALDWIN, C. T, FARRER, L. A
Published in American journal of human genetics (01.06.1996)
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Published in American journal of human genetics (01.06.1996)
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Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population
Baldwin, C T, Weiss, S, Farrer, L A, De Stefano, A L, Adair, R, Franklyn, B, Kidd, K K, Korostishevsky, M, Bonné-Tamir, B
Published in Human molecular genetics (01.09.1995)
Published in Human molecular genetics (01.09.1995)
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Wilson's disease in Israel: a genetic and epidemiological study
BONNÉ‐TAMIR, B., FRYDMAN, M., AGGER, M. S., BEKEER, R., BOWCOCK, A. M., HEBERT, J. M., CAVALLI‐SFORZA, L. L., FARRER, L. A.
Published in Annals of human genetics (01.05.1990)
Published in Annals of human genetics (01.05.1990)
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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
Berry, Asher, Scott, Hamish S., Kudoh, Jun, Talior, Ilana, Korostishevsky, Michael, Wattenhofer, Marie, Guipponi, Michel, Barras, Christine, Rossier, Colette, Shibuya, Kazunori, Wang, Jun, Kawasaki, Kazuhiko, Asakawa, Shuichi, Minoshima, Shinsei, Shimizu, Nobuyoshi, Antonarakis, Stylianos, Bonné-Tamir, Batsheva
Published in Genomics (San Diego, Calif.) (15.08.2000)
Published in Genomics (San Diego, Calif.) (15.08.2000)
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PGI3(Israel), a new, unstable allele in the phosphoglucose isomerase system
Bonné-Tamir, B, Papiha, S S, Ashbel, S, Brok-Simoni, F, Kende, G, Ramot, B
Published in Human genetics (01.09.1987)
Published in Human genetics (01.09.1987)
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Assignment of the Gene for Wilson Disease to Chromosome 13: Linkage to the Esterase D Locus
Frydman, Moshe, Bonné-Tamir, Batsheva, Farrer, Lindsay A., Conneally, P. Michael, Magazanik, Abraham, Ashbel, Sara, Goldwitch, Zipora
Published in Proceedings of the National Academy of Sciences - PNAS (01.03.1985)
Published in Proceedings of the National Academy of Sciences - PNAS (01.03.1985)
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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
Nystuen, Arne, Costeff, Hanan, Elpeleg, Orly N., Apter, Naomi, Bonné-Tamir, Batsheva, Mohrenweiser, Harvey, Haider, Neena, Stone, Edwin M., Sheffield, Val C.
Published in Human molecular genetics (01.04.1997)
Published in Human molecular genetics (01.04.1997)
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COMT haplotypes suggest P2 promoter region relevance for schizophrenia
Palmatier, M A, Pakstis, A J, Speed, W, Paschou, P, Goldman, D, Odunsi, A, Okonofua, F, Kajuna, S, Karoma, N, Kungulilo, S, Grigorenko, E, Zhukova, O V, Bonne-Tamir, B, Lu, R-B, Parnas, J, Kidd, J R, DeMille, M M C, Kidd, K K
Published in Molecular psychiatry (01.09.2004)
Published in Molecular psychiatry (01.09.2004)
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A Global Haplotype Analysis of the Myotonic Dystrophy Locus: Implications for the Evolution of Modern Humans and for the Origin of Myotonic Dystrophy Mutations
Tishkoff, S.A., Goldman, A., Calafell, F., Speed, W.C., Deinard, A.S., Bonne-Tamir, B., Kidd, J.R., Pakstis, A.J., Jenkins, T., Kidd, K.K.
Published in American journal of human genetics (01.06.1998)
Published in American journal of human genetics (01.06.1998)
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