ArticleJournal of molecular and genetic medicine : an international journal of biomedical research2013
The Role of Copy Number Variation in African Americans with Type 2 Diabetes-Associated End Stage Renal Disease.
Article in Journal of molecular and genetic medicine : an international journal of biomedical research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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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.
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Who cites it
3 citing papers in PubMed, 6 citations in OpenAlex.
- Polymorphic Inversions Underlie the Shared Genetic Susceptibility of Obesity-Related Diseases.American journal of human genetics · 2020Article
- Genomic structural variations for cardiovascular and metabolic comorbidity.Scientific reports · 2017Article
- Obesity, starch digestion and amylase: association between copy number variants at human salivary (AMY1) and pancreatic (AMY2) amylase genes.Human molecular genetics · 2015Article
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Authors and funding
10 authors at 1 institution in 1 country.
Funding
Abstract
This study investigated the association of copy number variants (CNVs) in type 2 diabetes (T2D) and T2D-associated end-stage renal disease (ESRD) in African Americans. Using the Affymetrix 6.0 array, >900,000 CNV probes spanning the genome were interrogated in 965 African Americans with T2D-ESRD and 1029 non-diabetic African American controls. Previously identified and novel CNVs were separately analyzed and were evaluated for insertion/deletion status and then used as predictors in a logistic regression model to test for association. One common CNV insertion on chromosome 1 was significantly associated with T2D-ESRD (p=6.17×10
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Registered trials
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