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The population genetics of the Jewish people

Human genetics, 2013-02, Vol.132 (2), p.119-127

2013

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De novo mutation rates at the single-mutation resolution in a human HBB gene region associated with adaptation and genetic disease

Genome research, 2022-03, Vol.32 (3), p.488

2022

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Mitochondrial Hsp60 Chaperonopathy Causes an Autosomal-Recessive Neurodegenerative Disorder Linked to Brain Hypomyelination and Leukodystrophy

American journal of human genetics, 2008-07, Vol.83 (1), p.30-42

2008

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The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, and Muslims in the Iberian Peninsula

American journal of human genetics, 2008-12, Vol.83 (6), p.725-736

2008

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Reprogramming of telomeric regions during the generation of human induced pluripotent stem cells and subsequent differentiation into fibroblast-like derivatives

Epigenetics, 2011-01, Vol.6 (1), p.63-75

2011

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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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Admixture mapping of end stage kidney disease genetic susceptibility using estimated mutual information ancestry informative markers

BMC genomics, 2010-10, Vol.3 (1), p.47-47, Article 47

2010

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Y Chromosomes Traveling South: The Cohen Modal Haplotype and the Origins of the Lemba—the “Black Jews of Southern Africa”

American journal of human genetics, 2000-02, Vol.66 (2), p.674-686

2000

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Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions

Human molecular genetics, 2008-09, Vol.17 (18), p.2776-2789

2008

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Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene

Human genetics, 2010-09, Vol.128 (3), p.345-350

2010

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Replication and/or separation of some human telomeres is delayed beyond S-phase in pre-senescent cells

Chromosoma, 2002-09, Vol.111 (3), p.147-155

2002

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Most of the extant mtDNA boundaries in south and southwest Asia were likely shaped during the initial settlement of Eurasia by anatomically modern humans

BMC genetics, 2004-08, Vol.5, p.26

2004

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Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestry

American journal of medical genetics. Part A, 2021-11, Vol.185 (11), p.3390-3400

2021

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African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans

Human molecular genetics, 2010-05, Vol.19 (9), p.1816-1827

2010

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Extended Y chromosome haplotypes resolve multiple and unique lineages of the Jewish priesthood

Human genetics, 2009-11, Vol.126 (5), p.707-717

2009

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Panel construction for mapping in admixed populations via expected mutual information

Genome Research, 2008-04, Vol.18 (4), p.661-667

2008

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Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations

Human genetics, 2004-03, Vol.114 (4), p.354-365

2004

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Multiple Origins of Ashkenazi Levites: Y Chromosome Evidence for Both Near Eastern and European Ancestries

American journal of human genetics, 2003-10, Vol.73 (4), p.768-779

2003

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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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The association of DNA sequence variation at the MAOA genetic locus with quantitative behavioural traits in normal males

Human genetics, 2006-11, Vol.120 (4), p.447-459

2006

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Dichotomy of single-nucleotide polymorphism haplotypes in olfactory receptor genes and pseudogenes

Nature genetics, 2000-10, Vol.26 (2), p.221-224

2000

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RAS is required for epidermal growth factor-stimulated arachidonic acid release in rat-1 fibroblasts

Oncogene, 1993-12, Vol.8 (12), p.3249-3255

1993

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The population genetics of the Jewish people

De novo mutation rates at the single-mutation resolution in a human HBB gene region associated with adaptation and genetic disease

Mitochondrial Hsp60 Chaperonopathy Causes an Autosomal-Recessive Neurodegenerative Disorder Linked to Brain Hypomyelination and Leukodystrophy

The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, and Muslims in the Iberian Peninsula

Reprogramming of telomeric regions during the generation of human induced pluripotent stem cells and subsequent differentiation into fibroblast-like derivatives

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

Admixture mapping of end stage kidney disease genetic susceptibility using estimated mutual information ancestry informative markers

Y Chromosomes Traveling South: The Cohen Modal Haplotype and the Origins of the Lemba—the “Black Jews of Southern Africa”

Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions

Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene

Replication and/or separation of some human telomeres is delayed beyond S-phase in pre-senescent cells

Most of the extant mtDNA boundaries in south and southwest Asia were likely shaped during the initial settlement of Eurasia by anatomically modern humans

Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestry

African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans

No Evidence from Genome-Wide Data of a Khazar Origin for the Ashkenazi Jews

Extended Y chromosome haplotypes resolve multiple and unique lineages of the Jewish priesthood

Panel construction for mapping in admixed populations via expected mutual information

Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations

Multiple Origins of Ashkenazi Levites: Y Chromosome Evidence for Both Near Eastern and European Ancestries

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

The association of DNA sequence variation at the MAOA genetic locus with quantitative behavioural traits in normal males

Dichotomy of single-nucleotide polymorphism haplotypes in olfactory receptor genes and pseudogenes

RAS is required for epidermal growth factor-stimulated arachidonic acid release in rat-1 fibroblasts

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