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

Overview of attention for article published in Human Genetics, August 2009
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  • In the top 5% of all research outputs scored by Altmetric
  • Among the highest-scoring outputs from this source (#25 of 2,981)
  • High Attention Score compared to outputs of the same age (99th percentile)
  • High Attention Score compared to outputs of the same age and source (90th percentile)

Mentioned by

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1 news outlet
blogs
1 blog
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76 X users
facebook
1 Facebook page
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30 Wikipedia pages
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7 Google+ users
video
2 YouTube creators

Citations

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63 Dimensions

Readers on

mendeley
85 Mendeley
citeulike
8 CiteULike
Title
Extended Y chromosome haplotypes resolve multiple and unique lineages of the Jewish priesthood
Published in
Human Genetics, August 2009
DOI 10.1007/s00439-009-0727-5
Pubmed ID
Authors

Michael F. Hammer, Doron M. Behar, Tatiana M. Karafet, Fernando L. Mendez, Brian Hallmark, Tamar Erez, Lev A. Zhivotovsky, Saharon Rosset, Karl Skorecki

Abstract

It has been known for over a decade that a majority of men who self report as members of the Jewish priesthood (Cohanim) carry a characteristic Y chromosome haplotype termed the Cohen Modal Haplotype (CMH). The CMH has since been used to trace putative Jewish ancestral origins of various populations. However, the limited number of binary and STR Y chromosome markers used previously did not provide the phylogenetic resolution needed to infer the number of independent paternal lineages that are encompassed within the Cohanim or their coalescence times. Accordingly, we have genotyped 75 binary markers and 12 Y-STRs in a sample of 215 Cohanim from diverse Jewish communities, 1,575 Jewish men from across the range of the Jewish Diaspora, and 2,099 non-Jewish men from the Near East, Europe, Central Asia, and India. While Cohanim from diverse backgrounds carry a total of 21 Y chromosome haplogroups, 5 haplogroups account for 79.5% of Cohanim Y chromosomes. The most frequent Cohanim lineage (46.1%) is marked by the recently reported P58 T->C mutation, which is prevalent in the Near East. Based on genotypes at 12 Y-STRs, we identify an extended CMH on the J-P58* background that predominates in both Ashkenazi and non-Ashkenazi Cohanim and is remarkably absent in non-Jews. The estimated divergence time of this lineage based on 17 STRs is 3,190 +/- 1,090 years. Notably, the second most frequent Cohanim lineage (J-M410*, 14.4%) contains an extended modal haplotype that is also limited to Ashkenazi and non-Ashkenazi Cohanim and is estimated to be 4.2 +/- 1.3 ky old. These results support the hypothesis of a common origin of the CMH in the Near East well before the dispersion of the Jewish people into separate communities, and indicate that the majority of contemporary Jewish priests descend from a limited number of paternal lineages.

X Demographics

X Demographics

The data shown below were collected from the profiles of 76 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 85 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 3 4%
Australia 1 1%
United Kingdom 1 1%
Israel 1 1%
Spain 1 1%
Denmark 1 1%
Unknown 77 91%

Demographic breakdown

Readers by professional status Count As %
Researcher 25 29%
Student > Ph. D. Student 16 19%
Professor > Associate Professor 7 8%
Student > Doctoral Student 6 7%
Professor 6 7%
Other 18 21%
Unknown 7 8%
Readers by discipline Count As %
Agricultural and Biological Sciences 47 55%
Biochemistry, Genetics and Molecular Biology 13 15%
Medicine and Dentistry 4 5%
Social Sciences 4 5%
Arts and Humanities 3 4%
Other 6 7%
Unknown 8 9%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 95. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 23 April 2024.
All research outputs
#458,213
of 25,874,560 outputs
Outputs from Human Genetics
#25
of 2,981 outputs
Outputs of similar age
#1,075
of 124,832 outputs
Outputs of similar age from Human Genetics
#1
of 11 outputs
Altmetric has tracked 25,874,560 research outputs across all sources so far. Compared to these this one has done particularly well and is in the 98th percentile: it's in the top 5% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 2,981 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 6.8. This one has done particularly well, scoring higher than 99% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 124,832 tracked outputs that were published within six weeks on either side of this one in any source. This one has done particularly well, scoring higher than 99% of its contemporaries.
We're also able to compare this research output to 11 others from the same source and published within six weeks on either side of this one. This one has done particularly well, scoring higher than 90% of its contemporaries.