(Q47596505)

4 February 2018

review article

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title

A genetic profile of contemporary Jewish populations (English)

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4 February 2018

author name string

H Ostrer

series ordinal

1

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4 February 2018

publication date

1 November 2001

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4 February 2018

published in

Nature Reviews Genetics

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4 February 2018

volume

2

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4 February 2018

issue

11

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4 February 2018

page(s)

891-898

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4 February 2018

https://scigraph.springernature.com/pub.10.1038/35098506

exact match

0 references

cites work

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

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7 January 2021

Y chromosomes of Jewish priests

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Origins of Old Testament priests

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Y chromosomes traveling south: the cohen modal haplotype and the origins of the Lemba--the "Black Jews of Southern Africa"

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7 January 2021

Genetic studies on Cochin Jews in Israel: 1. Population data, blood groups, isoenzymes, and HLA determinants

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7 January 2021

Genetic studies on Cochin Jews in Israel: 2. Gm and Inv data--polymorphism for Gm3 and for Gm1,17,21 without Gm(26).

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7 January 2021

Jewish diseases and origins

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7 January 2021

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness

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7 January 2021

Diversity of alpha-globin mutations and clinical presentation of alpha-thalassemia in Israel

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Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in Israel

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Mendelian diseases among Roman Jews: implications for the origins of disease alleles.

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7 January 2021

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

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7 January 2021

ACTIVATED PROTEIN C RESISTANCE CAUSED BY A COMMON FACTOR V MUTATION HAS A SINGLE ORIGIN

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7 January 2021

Age estimates of two common mutations causing factor XI deficiency: recent genetic drift is not necessary for elevated disease incidence among Ashkenazi Jews

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7 January 2021

The 185delAG BRCA1 mutation originated before the dispersion of Jews in the diaspora and is not limited to Ashkenazim

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7 January 2021

Mutations in the ER-Golgi intermediate compartment protein ERGIC-53 cause combined deficiency of coagulation factors V and VIII

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7 January 2021

Genetic disease since 1945.

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7 January 2021

Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations

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7 January 2021

Recent origin and spread of a common Lithuanian mutation, G197del LDLR, causing familial hypercholesterolemia: positive selection is not always necessary to account for disease incidence among Ashkenazi Jews

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7 January 2021

The differences among Jewish communities--maternal and paternal contributions

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7 January 2021

Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene

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7 January 2021

Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease

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7 January 2021

Identification of the 185delAG BRCA1 mutation in a Spanish Gypsy population

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7 January 2021

The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestry

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7 January 2021

High frequencies of human genetic diseases: founder effect with genetic drift or selection?

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7 January 2021

Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan

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7 January 2021

The genetic advantage hypothesis in cystic fibrosis heterozygotes: a murine study

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7 January 2021

Salmonella typhi uses CFTR to enter intestinal epithelial cells.

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7 January 2021

Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes

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7 January 2021

Population-based genetic screening for reproductive counseling: the Tay-Sachs disease model

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7 January 2021

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

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7 January 2021

Molecular genetics of Bloom's syndrome

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7 January 2021

Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31

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7 January 2021

Searching for genetic determinants in the new millennium

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7 January 2021

Allelic association between marker loci

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7 January 2021

The extent of linkage disequilibrium in four populations with distinct demographic histories

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7 January 2021

Prospects for whole-genome linkage disequilibrium mapping of common disease genes

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7 January 2021

Genetic isolates: separate but equal?

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7 January 2021

Patterns of inter- and intra-group genetic diversity in the Vlax Roma as revealed by Y chromosome and mitochondrial DNA lineages

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Molecular genetics of the Finnish disease heritage.

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7 January 2021

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Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families

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Phenotype-genotype relationships in monogenic disease: lessons from the thalassaemias.

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7 January 2021

The common, Near-Eastern origin of Ashkenazi and Sephardi Jews supported by Y-chromosome similarity

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7 January 2021

Ataxia-telangiectasia: founder effect among north African Jews

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7 January 2021

Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population.

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7 January 2021

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

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7 January 2021

The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%

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7 January 2021

Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.

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7 January 2021

Familial dysautonomia is caused by mutations of the IKAP gene

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7 January 2021

Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia

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7 January 2021

Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.

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7 January 2021

Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studies

1 reference

7 January 2021

Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population

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7 January 2021

Molecular basis of lipoamide dehydrogenase deficiency in Ashkenazi Jews

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7 January 2021

Mucolipidosis type IV: novel MCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish population

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7 January 2021

Niemann-Pick disease: mutation update, genotype/phenotype correlations, and prospects for genetic testing

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7 January 2021

Tay-Sachs screening in the Jewish Ashkenazi population: DNA testing is the preferred procedure

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7 January 2021

Late infantile metachromatic leukodystrophy in Israel

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7 January 2021

Mutations in human 11 beta-hydroxylase genes: 11 beta-hydroxylase deficiency in Jews of Morocco and corticosterone methyl-oxidase II deficiency in Jews of Iran

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7 January 2021

Evidence for Genetic Heterogeneity Supports Clinical Differences in Congenital Myasthenic Syndromes

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7 January 2021

Hereditary inclusion body myopathy maps to chromosome 9p1-q1

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7 January 2021

Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT

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7 January 2021

Frameshift and splice-junction mutations in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis in Jews or Moroccan origin

1 reference

7 January 2021

High prevalence of complement C7 deficiency among healthy blood donors of Moroccan Jewish ancestry

1 reference

7 January 2021

Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation

1 reference

7 January 2021

A single origin of phenylketonuria in Yemenite Jews

1 reference

7 January 2021

Identifiers

DOI

10.1038/35098506

1 reference

4 February 2018

1 reference

4 February 2018