B. Bonné‐Tamir

发表

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

C. Petit, A. Adato, B. Bonné-Tamir, 2000, European Journal of Human Genetics.

Usher syndrome in the Samaritans: strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders.

V. Sheffield, A. Adato, E. Seroussi, 1997, American journal of physical anthropology.

Analysis of biochemical genetic data on Jewish populations: II. Results and interpretations of heterogeneity indices and distance measures with respect to standards.

S. Karlin, B. Bonné-Tamir, B. Bonné‐Tamir, 1979, American journal of human genetics.

Gm and Inv [Km] allotypes among Libyan and Ashkenazi Jews, and Armenians living in Israel

A. Steinberg, B. Bonné‐Tamir, 2004, Human Genetics.

The HGDP Can Be and Should Be Pursued in Harmony with Its Subjects: An Account of the Israeli Experience

B. Bonné‐Tamir, 1999, Politics and the Life Sciences.

Medical genetics in Israel.

Y. Shiloh, G. Bach, G. Barkai, 1988, Journal of medical genetics.

Analysis of biochemical genetic data on Jewish populations. III. The application of individual phenotype measurements for population comparisons.

S. Karlin, D. Carmelli, B. Bonné‐Tamir, 1982, American journal of human genetics.

HLA polymorphism in Israel. 9. An overall comparative analysis.

J. Bodmer, W. Bodmer, B. Bonné-Tamir, 1978, Tissue antigens.

Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus.

L. Farrer, M. Frydman, P. Conneally, 1985, Proceedings of the National Academy of Sciences of the United States of America.

USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses

Tsviya Olender, Doron Lancet, Shmuel Pietrokovski, 2002, European Journal of Human Genetics.

Ethnic communities in Israel: the genetic blood markers of the Babylonian Jews.

B. Bonné-Tamir, B. Bonné‐Tamir, S. Ashbel, 1978, American journal of physical anthropology.

Polymorphic microsatellites and Wilson disease (WD).

E. Stewart, P. S. St George-Hyslop, M. Giagheddu, 1993, American journal of human genetics.

Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.

K. Kidd, L. Cavalli-Sforza, A. Bowcock, 1987, American journal of human genetics.

Genetic diversity among Jews : diseases and markers at the DNA level

B. Bonné-Tamir, B. Bonné‐Tamir, A. Adam, 1992 .

Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.

K. Kidd, S. Iyengar, M. Korostishevsky, 1997, Journal of medical genetics.

A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations.

K K Kidd, A Goldman, J R Kidd, 1998, American journal of human genetics.

Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains

S. Antonarakis, R. Lyle, K. Kawasaki, 2001, Human Genetics.

Usher Syndrome in the Samaritans: Strengths and Limitations of Using Inbred Isolated Populations to Identify Genes Causing Recessive Disorders

V. Sheffield, A. Adato, E. Seroussi, 1997 .

Human gene mutations

B. Bonné-Tamir, P. Erlich, B. Bonné‐Tamir, 1999, Human Genetics.

The Habbanite isolate: demography and its genetic implications.

B. Bonné-Tamir, B. Bonné‐Tamir, S. Ashbel, 1978 .

Molecular analysis of HLA class II polymorphisms among different ethnic groups in Israel.

C. Witt, U. Motro, B. Bonné-Tamir, 1999, Human immunology.

Distinctive genetic signatures in the Libyan Jews.

M W Feldman, M. Feldman, J. Pritchard, 2001, Proceedings of the National Academy of Sciences of the United States of America.

The genome-wide structure of the Jewish people

Saharon Rosset, David Comas, Michael F. Hammer, 2010, Nature.

Genetic affinities of Ethiopian Jews.

A. Ticher, A. Zoossmann-Diskin, B. Bonné‐Tamir, 1991, Israel journal of medical sciences.

Genetic markers in Libyan Jews

B. Bonné-Tamir, B. Bonné‐Tamir, J. Modai, 1977, Human Genetics.

Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3.

B. Bonné-Tamir, H. Tamary, H. Shalev, 1998, American journal of human genetics.

A Pst+ Polymorphism in the HEXA Gene with an Unusual Geographic Distribution

S. Kapoor, M. Bobrow, C. Scriver, 1993, European journal of human genetics : EJHG.

Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins

S. Tishkoff, K. Kidd, N. Risch, 1996, Science.

Human mitochondrial DNA types in two Israeli populations--a comparative study at the DNA level.

L. Cavalli-Sforza, D. Wallace, B. Bonné-Tamir, 1986, American journal of human genetics.

Genetic variation of three tetrameric tandem repeats in four distinct Israeli ethnic groups.

U. Motro, C. Brautbar, S. Israel, 1999, Journal of forensic sciences.

Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites.

J. Weissenbach, L. Cavalli-Sforza, L. Cavalli-Sforza, 1994, American journal of human genetics.

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population.

K. Kidd, L. Farrer, A. De Stefano, 1995, Human molecular genetics.

Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes.

H. Ostrer, M. Hammer, M. Jobling, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Y chromosome sequence variation and the history of human populations

Li Jin, Jaume Bertranpetit, Alberto Piazza, 2000, Nature Genetics.

A Human Genome Diversity Cell Line Panel

Jonathan Scott Friedlaender, R. J. Herrera, M. Feldman, 2002, Science.

The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs.

A. Torroni, R. Scozzari, E. Vega, 1999, American journal of human genetics.

mtDNA analysis reveals a major late Paleolithic population expansion from southwestern to northeastern Europe.

H. Bandelt, P. Forster, A. Torroni, 1998, American journal of human genetics.

Counting the Founders: The Matrilineal Genetic Ancestry of the Jewish Diaspora

S. Rosset, D. Gurwitz, R. Villems, 2008, PloS one.

Maternal and Paternal Lineages of the Samaritan Isolate: Mutation Rates and Time to Most Recent Common Male Ancestor

M. Hammer, B. Bonné-Tamir, A. Redd, 2003, Annals of human genetics.

Worldwide genetic analysis of the CFTR region.

K. Kidd, J. Kidd, A. Pakstis, 2001, American journal of human genetics.

Global survey of haplotype frequencies and linkage disequilibrium at the RET locus

K. Kidd, J. Kidd, A. Pakstis, 2003, European Journal of Human Genetics.

Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

Shinsei Minoshima, Stylianos E. Antonarakis, Kazunori Shibuya, 2001, Nature Genetics.

MtDNA evidence for a genetic bottleneck in the early history of the Ashkenazi Jewish population

M. Hammer, D. Gurwitz, R. Villems, 2004, European Journal of Human Genetics.

A global perspective on genetic variation at the ADH genes reveals unusual patterns of linkage disequilibrium and diversity.

Josef Parnas, Jaume Bertranpetit, David Goldman, 2002, American journal of human genetics.

The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event.

D. Gurwitz, R. Villems, T. Kivisild, 2006, American journal of human genetics.

COMT haplotypes suggest P2 promoter region relevance for schizophrenia

K K Kidd, W Speed, J R Kidd, 2004, Molecular Psychiatry.

Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance.

H. Chaib, D. Weil, A. Adato, 1999, American journal of human genetics.

Isolation and characterization of a human chromosome 21q22.3 gene (WDR4) and its mouse homologue that code for a WD-repeat protein.

S Minoshima, S. Antonarakis, N. Shimizu, 2000, Genomics.

PGI*3(Israel), a new, unstable allele in the phosphoglucose isomerase system

B. Bonné-Tamir, B. Ramot, S. Papiha, 1987, Human Genetics.

Novel ATP7B mutations causing Wilson disease in several Israeli ethnic groups

L A Farrer, L. Farrer, R. Gershoni-baruch, 1998, Human mutation.

Familial lipoid adrenal hyperplasia: genetic marker data and an approach to prenatal diagnosis.

B. Bonné-Tamir, M. Frydman, A. Kauschansky, 1986, American journal of medical genetics.

Allele Frequencies in a Worldwide Survey of a CA Repeat in the First Intron of the CFTR Gene

K. Kidd, J. Kidd, J. Bertranpetit, 1999, Human Heredity.

The evolution and population genetics of the ALDH2 locus: random genetic drift, selection, and low levels of recombination

K. Kidd, E. Grigorenko, J. Kidd, 2004, Annals of human genetics.

Mitochondrial DNA affinity of several Jewish communities.

E. M. Prager, B. Bonné-Tamir, M. Groß, 1993, Human biology.

Linkage analysis and the inheritance of arches in a Habbanite isolate.

E. Thompson, D. Carmelli, B. Bonné-Tamir, 1979, American journal of human genetics.

The inheritance of fingerprint patterns.

B. Bonné-Tamir, H. Slatis, H M Slatis, 1976, American journal of human genetics.

High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim.

B. Bonné-Tamir, K. Avraham, A. Berry, 1999, American journal of medical genetics.

Genetic evolution of the Samaritans

M. Cazes, B. Bonné‐Tamir, 1984, Journal of Biosocial Science.

Analysis of genetic data on Jewish populations. I. Historical background, demographic features, and genetic markers.

S Karlin, S. Karlin, B Bonné-Tamir, 1979, American journal of human genetics.

A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus

Hongyu Zhao, Trefor Jenkins, David Goldman, 1998, Human Genetics.

Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.

L. Farrer, A. DeStefano, C. Baldwin, 1996, American journal of human genetics.

Predictive testing for Wilson's disease using tightly linked and flanking DNA markers

L. Cavalli-Sforza, L. Cavalli-Sforza, J. Hebert, 1991, Neurology.

Wilson's disease in Israel: a genetic and epidemiological study

L. Cavalli-Sforza, A. Bowcock, B. Bonné-Tamir, 1990, Annals of human genetics.

Population variation in linkage disequilibrium across the COMT gene considering promoter region and coding region variation

K. Kidd, E. Grigorenko, J. Kidd, 2002, Human Genetics.

Evidence for linkage between Wilson disease and esterase D in three kindreds: Detection of linkage for an autosomal recessive disorder by the family study method

L. Farrer, D. Rao, B. Bonné-Tamir, 1986, Genetic epidemiology.

Considerable haplotype diversity within the 23kb encompassing the ADH7 gene.

K. Kidd, E. Grigorenko, J. Kidd, 2005, Alcoholism, clinical and experimental research.

Evolution of haplotypes at the DRD2 locus.

A J Pakstis, E L Grigorenko, E. Grigorenko, 1995, American journal of human genetics.

Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.

C. Petit, D. Weil, A. Adato, 1997, American journal of human genetics.

Genetic studies in a family with inverted nipples (mammillae invertita)

R. Shafir, H. Tsur, R. Goodman, 1979, Clinical genetics.

Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

A. Pandya, S. Antonarakis, J. Kudoh, 2001, Journal of medical genetics.

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.

S. Antonarakis, N. Shimizu, K. Kawasaki, 2000, Genomics.

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.

S. Antonarakis, N. Shimizu, K. Kawasaki, 2000, Genomics.

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.

V. Sheffield, H. Mohrenweiser, E. Stone, 1997, Human molecular genetics.

DRD2 haplotypes containing the TaqI A1 allele: implications for alcoholism research.

K. Kidd, J. Kidd, A. Pakstis, 1996, Alcoholism, clinical and experimental research.

Genetic mapping of the gene for Usher syndrome: linkage analysis in a large Samaritan kindred.

E. Seroussi, M. Korostishevsky, V. Godel, 1994, Genomics.

HLA Polymorphism in Israel

J. Bodmer, B. Bonné‐Tamir, J. Modai, 1978 .

HLA polymorphism in Israel. 3. Ashkenazi Jews of German descent.

J. Bodmer, B. Bonné‐Tamir, J. Modai, 1978, Tissue antigens.

Genetic polymorphisms among Ethiopian Jews in Israel.

B. Bonné‐Tamir, S. Ashbel, Z. Goldwitch, 1987, Gene geography : a computerized bulletin on human gene frequencies.

Ethnic communities in Israel: the genetic blood markers of the Moroccan Jews.

B. Bonné-Tamir, B. Bonné‐Tamir, S. Ashbel, 1978, American journal of physical anthropology.

Isolation, Migration and Health: Genetic distance analyses in Israeli groups using classical markers and DNA polymorphisms in the β globin gene

A. Oppenheim, A. Ticher, A. Zoossmann-Diskin, 1992 .