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Article
Open AccessWhole exome sequencing in Alopecia Areata identifies rare variants in KRT82
Alopecia areata is a complex genetic disease that results in hair loss due to the autoimmune-mediated attack of the hair follicle. We previously defined a role for both rare and common variants in our earlier ...
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Article
Open AccessPublisher Correction: TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
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Article
Open AccessTCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes
The association between several Single Nucleotide Polymorphisms (SNPs) within the transcription factor 7-like 2 (TCF7L2) gene and Type 2 Diabetes (T2D) as well as additional T2D-related traits is well established...
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Article
Noncoding deletions reveal a gene that is critical for intestinal function
Large-scale genome sequencing is poised to provide a substantial increase in the rate of discovery of disease-associated mutations, but the functional interpretation of such mutations remains challenging. Here...