Evidence map›Paper›PMID 27010569›Full record

ArticlePloS one2016

The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry.

Yedael Y Waldman, Arjun Biddanda, Natalie R Davidson, Paul Billing-Ross, Maya Dubrovsky, Christopher L Campbell, Carole Oddoux, Eitan Friedman, Gil Atzmon, Eran Halperin and 2 more

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. A comprehensive Y-STR portrait of Yousafzai's population.International journal of legal medicine · 2017
    Article
  9. Ancient X chromosomes reveal contrasting sex bias in Neolithic and Bronze Age Eurasian migrations.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  10. Article
  11. 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

12 authors.

Yedael Y WaldmanDepartment of Biological Statistics and Computational Biology, Cornell University, Ithaca, NY, United States of America.
Arjun BiddandaDepartment of Biological Statistics and Computational Biology, Cornell University, Ithaca, NY, United States of America.
Natalie R DavidsonDepartment of Biological Statistics and Computational Biology, Cornell University, Ithaca, NY, United States of America.
Paul Billing-RossDepartment of Biological Statistics and Computational Biology, Cornell University, Ithaca, NY, United States of America.
Maya DubrovskyDanek Gertner Institute of Human Genetics, Chaim Sheba Medical Center, Tel-Hashomer, Israel.
Christopher L CampbellDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY, United States of America.
Carole OddouxDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY, United States of America.
Eitan FriedmanDanek Gertner Institute of Human Genetics, Chaim Sheba Medical Center, Tel-Hashomer, Israel.
Gil AtzmonDepartments of Medicine and Genetics, Albert Einstein College of Medicine, Bronx, NY, United States of America.
Eran HalperinDepartment of Molecular Microbiology and Biotechnology, Tel Aviv University, Ramat Aviv, Tel Aviv, Israel.
Harry OstrerDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY, United States of America.
Alon KeinanDepartment of Biological Statistics and Computational Biology, Cornell University, Ithaca, NY, United States of America.

Funding

Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
Tri-Institutional Training Program in Computational Biology & MedicineT32GM083937 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI CHRISTINI, DAVID J. · 2009 to 2018
$3.1M
The X-factor of complex disease: From population genetics to GWAS of Chromosome XR01HG006849 · NHGRI · CORNELL UNIVERSITY · PI CLARK, ANDREW G · 2013 to 2020
$2.3M
Population Genetic Consequences of Recent Explosive Population Growth in HumansR01GM108805 · NIGMS · CORNELL UNIVERSITY · PI CLARK, ANDREW G, KEINAN, ALON · 2014 to 2017
$2.2M
NHGRI NIH HHS R01 HG006849NHGRI NIH HHS R01HG006849NIDDK NIH HHS P30 DK020541NIGMS NIH HHS 1T32GM083937NIGMS NIH HHS R01 GM108805NIGMS NIH HHS R01GM108805NIGMS NIH HHS T32 GM083937
6 · The paper itself

Abstract

The Bene Israel Jewish community from West India is a unique population whose history before the 18th century remains largely unknown. Bene Israel members consider themselves as descendants of Jews, yet the identity of Jewish ancestors and their arrival time to India are unknown, with speculations on arrival time varying between the 8th century BCE and the 6th century CE. Here, we characterize the genetic history of Bene Israel by collecting and genotyping 18 Bene Israel individuals. Combining with 486 individuals from 41 other Jewish, Indian and Pakistani populations, and additional individuals from worldwide populations, we conducted comprehensive genome-wide analyses based on FST, principal component analysis, ADMIXTURE, identity-by-descent sharing, admixture linkage disequilibrium decay, haplotype sharing and allele sharing autocorrelation decay, as well as contrasted patterns between the X chromosome and the autosomes. The genetics of Bene Israel individuals resemble local Indian populations, while at the same time constituting a clearly separated and unique population in India. They are unique among Indian and Pakistani populations we analyzed in sharing considerable genetic ancestry with other Jewish populations. Putting together the results from all analyses point to Bene Israel being an admixed population with both Jewish and Indian ancestry, with the genetic contribution of each of these ancestral populations being substantial. The admixture took place in the last millennium, about 19-33 generations ago. It involved Middle-Eastern Jews and was sex-biased, with more male Jewish and local female contribution. It was followed by a population bottleneck and high endogamy, which can lead to increased prevalence of recessive diseases in this population. This study provides an example of how genetic analysis advances our knowledge of human history in cases where other disciplines lack the relevant data to do so.

Indexed as

Genetics, PopulationAsian PeopleFemaleGenome-Wide Association StudyGenotypeHaplotypesHumansIndiaIsraelJewsLinkage DisequilibriumMalePakistan

Identifiers

PMID27010569
PMCPMC4806850

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Registered trials

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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.