|
1
|
Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly.
|
Nat Biotechnol
|
2011
|
2.45
|
|
2
|
cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs.
|
Nat Methods
|
2010
|
1.41
|
|
3
|
Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype.
|
Blood
|
2013
|
1.25
|
|
4
|
Genomic ancestry and somatic alterations correlate with age at diagnosis in Hispanic children with B-cell acute lymphoblastic leukemia.
|
Am J Hematol
|
2014
|
0.92
|
|
5
|
Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.
|
PLoS One
|
2013
|
0.88
|
|
6
|
GATA3 risk alleles are associated with ancestral components in Hispanic children with ALL.
|
Blood
|
2013
|
0.87
|
|
7
|
PTPRG inhibition by DNA methylation and cooperation with RAS gene activation in childhood acute lymphoblastic leukemia.
|
Int J Cancer
|
2014
|
0.85
|
|
8
|
Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity.
|
Hum Mol Genet
|
2012
|
0.83
|
|
9
|
Investigation of the HIN200 locus in UK SLE families identifies novel copy number variants.
|
Ann Hum Genet
|
2011
|
0.77
|
|
10
|
Accurate single-nucleotide polymorphism allele assignment in trisomic or duplicated regions by using a single base-extension assay with MALDI-TOF mass spectrometry.
|
Clin Chem
|
2011
|
0.75
|