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

Annals of human genetics, 2004-03, Vol.68 (2), p.93-109

2004

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Counting the founders: the matrilineal genetic ancestry of the Jewish Diaspora

PloS one, 2008-04, Vol.3 (4), p.e2062-e2062

2008

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The Matrilineal Ancestry of Ashkenazi Jewry: Portrait of a Recent Founder Event

American journal of human genetics, 2006-03, Vol.78 (3), p.487-497

2006

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A Global Perspective on Genetic Variation at the ADH Genes Reveals Unusual Patterns of Linkage Disequilibrium and Diversity

American journal of human genetics, 2002-07, Vol.71 (1), p.84-99

2002

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Haplotypes and Linkage Disequilibrium at the Phenylalanine Hydroxylase Locus, PAH, in a Global Representation of Populations

American journal of human genetics, 2000-06, Vol.66 (6), p.1882-1899

2000

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Considerable Haplotype Diversity within the 23kb Encompassing the ADH7 Gene

Alcoholism, clinical and experimental research, 2005-12, Vol.29 (12), p.2091-2100

2005

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Y chromosome sequence variation and the history of human populations

Nature genetics, 2000-11, Vol.26 (3), p.358-361

2000

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

Journal of medical genetics, 2001-06, Vol.38 (6), p.396-400

2001

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The Emerging Tree of West Eurasian mtDNAs: A Synthesis of Control-Region Sequences and RFLPs

American journal of human genetics, 1999, Vol.64 (1), p.232-249

1999

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A Human Genome Diversity Cell Line Panel

Science (American Association for the Advancement of Science), 2002-04, Vol.296 (5566), p.261-262

2002

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The genome-wide structure of the Jewish people

Nature (London), 2010-07, Vol.466 (7303), p.238-242

2010

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Novel ATP7B mutations causing Wilson disease in several Israeli ethnic groups

Human mutation, 1998, Vol.11 (2), p.145-151

1998

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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 (San Diego, Calif.), 2000-12, Vol.70 (2), p.190-200

2000

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mtDNA Analysis Reveals a Major Late Paleolithic Population Expansion from Southwestern to Northeastern Europe

American journal of human genetics, 1998-05, Vol.62 (5), p.1137-1152

1998

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DRD2 Haplotypes Containing the TaqI A1 Allele: Implications for Alcoholism Research

Alcoholism, clinical and experimental research, 1996-06, Vol.20 (4), p.697-705

1996

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

European journal of human genetics : EJHG, 2002-06, Vol.10 (6), p.339-350

2002

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

Politics and the life sciences, 1999-09, Vol.18 (2), p.291-293

Bonné-Tamir, Batsheva

1999

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

European journal of human genetics : EJHG, 2004-05, Vol.12 (5), p.355-364

2004

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

Human genetics, 2002-12, Vol.111 (6), p.521-537

2002

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Genetic Mapping of the Gene for Usher Syndrome: Linkage Analysis in a Large Samaritan Kindred

Genomics (San Diego, Calif.), 1994-03, Vol.20 (1), p.36-42

1994

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

Human genetics, 1998-08, Vol.103 (2), p.211-227

1998

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Worldwide Genetic Analysis of the CFTR Region

American journal of human genetics, 2001-01, Vol.68 (1), p.103-117

2001

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Preface

Mechanisms of ageing and development, 2005-02, Vol.126 (2), p.223

Bonne-Tamir, Batsheva

2005

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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, 2000-06, Vol.8 (6), p.437-442

2000

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

Counting the founders: the matrilineal genetic ancestry of the Jewish Diaspora

The Matrilineal Ancestry of Ashkenazi Jewry: Portrait of a Recent Founder Event

A Global Perspective on Genetic Variation at the ADH Genes Reveals Unusual Patterns of Linkage Disequilibrium and Diversity

Haplotypes and Linkage Disequilibrium at the Phenylalanine Hydroxylase Locus, PAH, in a Global Representation of Populations

Considerable Haplotype Diversity within the 23kb Encompassing the ADH7 Gene

Y chromosome sequence variation and the history of human populations

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

The Emerging Tree of West Eurasian mtDNAs: A Synthesis of Control-Region Sequences and RFLPs

A Human Genome Diversity Cell Line Panel

The genome-wide structure of the Jewish people

Novel ATP7B mutations causing Wilson disease in several Israeli ethnic groups

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

mtDNA Analysis Reveals a Major Late Paleolithic Population Expansion from Southwestern to Northeastern Europe

DRD2 Haplotypes Containing the TaqI A1 Allele: Implications for Alcoholism Research

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

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

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

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

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

Genetic Mapping of the Gene for Usher Syndrome: Linkage Analysis in a Large Samaritan Kindred

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

Worldwide Genetic Analysis of the CFTR Region

Preface

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

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