Method
Predicting human genes susceptible to genomic instability associated with Alu/Alu-mediated rearrangements
- First Published June 15, 2018
Research
Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing alleles
- First Published May 16, 2013
Research
NAHR-mediated copy-number variants in a clinical population: Mechanistic insights into both genomic disorders and Mendelizing traits
- First Published May 8, 2013
Research
Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes
- First Published January 4, 2011
Letter
Complex selection on 5′ splice sites in intron-rich organisms
- First Published September 10, 2009
LETTER
Copy number variation at the breakpoint region of isochromosome 17q
- First Published August 19, 2008
LETTER
Three distinct modes of intron dynamics in the evolution of eukaryotes
- First Published May 10, 2007
LETTER
Evolutionarily conserved genes preferentially accumulate introns
- First Published May 10, 2007
LETTER
AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12
- First Published February 6, 2007