Resource
A platform for curated products from novel open reading frames prompts reinterpretation of disease variants
- First Published January 19, 2021
Research
Interlocus gene conversion events introduce deleterious mutations into at least 1% of human genes associated with inherited disease
- First Published November 16, 2011
Research
Loss of exon identity is a common mechanism of human inherited disease
- First Published July 12, 2011
Letter
Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts
- First Published December 30, 2008
LETTER
Abundance and length of simple repeats in vertebrate genomes are determined by their structural properties
- First Published August 7, 2008
LETTER
Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16
- First Published September 1, 2005