Evidence map›Paper›PMID 15516841›Full record

ReviewFamilial cancer2004

The Jewish people: their ethnic history, genetic disorders and specific cancer susceptibility.

Inbal Kedar-Barnes, Paul Rozen

Abstract readReview
PubMed Publisher
In one paragraph

Review in Familial cancer, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Perceived Antisemitism and Mental Health in Jewish Mothers and Their Children.Research on child and adolescent psychopathology · 2026
    Article
  4. Article
  5. Pharmacogenetics in Jewish populations.Drug metabolism and drug interactions · 2014
    Review
  6. Article
  7. Signatures of founder effects, admixture, and selection in the Ashkenazi Jewish population.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Inbal Kedar-BarnesDepartment of Medical Genetics, Rabin Medical Center, Beilinson Campus, Petach Tikva, Israel. inbalkd@clalit.org.il
Paul Rozen

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Jews are an ancient and unique group of people linked by language, religion and customs in spite of their major geographical shifts, expulsions, forced conversions and massacres throughout their entire history. As a result of these historical events that led to repeated migration, the Jewish people became dispersed into various ethnic sub-groups. Between these ethnic groups exists heterogeneity, as well as some similarities, to the populations amongst whom they lived. Rare genetic diseases have been reported to be prevalent among the different groups of Jews, which for the most part can be explained by random genetic drift together with intra-familial marriages. In this publication, we will briefly discuss the origin of the various ethnic groups and some of the genetic diseases commonly found in them, with emphasis on the Ashkenazim, their prevalent genetic diseases and cancer susceptibility.

Indexed as

FemaleGenetic Diseases, InbornGenetic Predisposition to DiseaseGenetics, PopulationHumansIsraelJewsMaleNeoplasmsPrevalenceRisk Assessment

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.