Evidence map›Paper›PMID 17652939›Full record

ArticleHuman heredity2008

Haplotype diversity in four genes (CLCNKA, CLCNKB, BSND, NEDD4L) involved in renal salt reabsorption.

Saba Sile, Digna R Velez, Niloufar B Gillani, Charles A Alexander, Charles R Alexander, Alfred L George, Scott M Williams

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Human heredity, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
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, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Common Variants for Heart Failure.Current genomics · 2015
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

  • Erratum issued
    Alexander, Charles R [corrected to Alexander, Charles A]
5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Saba SileDepartment of Medicine, Vanderbilt University, Nashville, Tenn 37232-0275, USA. saba.sile@vanderbilt.edu
Digna R Velez
Niloufar B Gillani
Charles A Alexander
Charles R Alexander
Alfred L George
Scott M Williams
Vanderbilt University · USCenter for Human Genetics · US

Funding

Training Program on Genetic Variation and Human PhenotypesT32GM080178 · NIGMS · VANDERBILT UNIVERSITY · PI COX, NANCY J, SAMUELS, DAVID C · 2007 to 2021
$3.1M
Renal Cl channel polymorphisms and blood pressureK08DK071742 · NIDDK · VANDERBILT UNIVERSITY · PI SILE, SABA · 2005 to 2007
$283k
NIDDK NIH HHS DK071742NIDDK NIH HHS K08 DK071742NIGMS NIH HHS T32 GM080178
6 · The paper itself

Abstract

objectiveDifferences exist among various populations with regards to hypertension prevalence, severity, progression and response to therapy. Such differences may be due to genetic or environmental factors. We characterized the genetic variation and haplotype diversity of four hypertension candidate genes (CLCNKA, CLCNKB, BSND, NEDD4L) in four different ethnic groups (Caucasian Americans, African-Americans, Han Chinese, and Mexican-Americans).

methodsWe genotyped 42 single nucleotide polymorphisms across the four genes in equal numbers of each ethnically defined population, then tested for linkage disequilibrium, computed allelic and haplotype frequencies, and compared data across the different ethnic groups.

resultsWe identified significant genotype and allele frequency differences among ethnic groups. The strongest differences were observed between African-American and Mexican-Americans and between Caucasian and Mexican-Americans. In addition, haplotype blocks were defined for BSND, CLCNKA_B and NEDD4L in the four populations examined. Completely mismatched ('yin yang') haplotypes were also observed. We found that the number of inferred halpotypes varied gene to gene and in some instances between the populations for a given gene indicating substantial haplotype diversity. The haplotype diversity among the various ethnic populations observed in our study was greater than that reported in Perlegen database.

conclusionsHaplotype diversity in hypertension candidate genes has important implications for designing and evaluating candidate gene or genome-wide blood pressure association studies that consider these genes.

Indexed as

HaplotypesChloride ChannelsEndosomal Sorting Complexes Required for TransportGene FrequencyGenotypeHumansHypertensionKidneyMembrane ProteinsNedd4 Ubiquitin Protein LigasesPolymorphism, Single NucleotideSodium ChlorideUbiquitin-Protein LigasesBSND protein, humanChloride ChannelsCLCNKA protein, humanCLCNKB protein, humanEndosomal Sorting Complexes Required for TransportMembrane ProteinsNedd4L protein, humanNedd4 Ubiquitin Protein LigasesSodium ChlorideUbiquitin-Protein Ligases

Identifiers

PMID17652939
PMCPMC2862756
OpenAlexW2014109177

What OpenQuestion holds

Textmetadata
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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.