Adam J de Smith

Author PubWeight™ 10.10^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
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