A genetic profile of contemporary Jewish populations (Q47596505)

4 February 2018

review article

1 reference

title

A genetic profile of contemporary Jewish populations (English)

1 reference

4 February 2018

author name string

H Ostrer

series ordinal

1 reference

4 February 2018

publication date

1 November 2001

1 reference

4 February 2018

published in

Nature Reviews Genetics

1 reference

4 February 2018

volume

1 reference

4 February 2018

issue

1 reference

4 February 2018

page(s)

891-898

1 reference

4 February 2018

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

cites work

1 reference

7 January 2021

Y chromosomes of Jewish priests

1 reference

7 January 2021

Origins of Old Testament priests

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

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).

1 reference

7 January 2021

Jewish diseases and origins

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Genetic disease since 1945.

1 reference

7 January 2021

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

1 reference

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

1 reference

7 January 2021

The differences among Jewish communities--maternal and paternal contributions

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Salmonella typhi uses CFTR to enter intestinal epithelial cells.

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Molecular genetics of Bloom's syndrome

1 reference

7 January 2021

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

1 reference

7 January 2021

Searching for genetic determinants in the new millennium

1 reference

7 January 2021

Allelic association between marker loci

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Genetic isolates: separate but equal?

1 reference

7 January 2021

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

1 reference

7 January 2021

Molecular genetics of the Finnish disease heritage.

1 reference

7 January 2021

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Ataxia-telangiectasia: founder effect among north African Jews

1 reference

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.

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Familial dysautonomia is caused by mutations of the IKAP gene

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

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

1 reference

7 January 2021

Molecular basis of lipoamide dehydrogenase deficiency in Ashkenazi Jews

1 reference

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Late infantile metachromatic leukodystrophy in Israel

1 reference

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

1 reference

7 January 2021

Evidence for Genetic Heterogeneity Supports Clinical Differences in Congenital Myasthenic Syndromes

1 reference

7 January 2021

Hereditary inclusion body myopathy maps to chromosome 9p1-q1

1 reference

7 January 2021

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

1 reference

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