Enrique Ramos

High-throughput discovery of rare insertions and deletions in large cohorts.

Francesco Vallania, T. Druley, Enrique Ramos, 2010, Genome research.

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER

Francesco Vallania, T. Druley, Enrique Ramos, 2012, Journal of visualized experiments : JoVE.

Adaptation of the targeted capture Methyl-Seq platform for the mouse genome identifies novel tissue-specific DNA methylation patterns of genes involved in neurodevelopment

J. Potash, T. Druley, Enrique Ramos, 2015, Epigenetics.

Age-specific changes in genome-wide methylation enrich for Foxa2 and estrogen receptor alpha binding sites

T. Druley, Enrique Ramos, Nishanth Uli, 2018, PloS one.

Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing

Francesco Vallania, T. Druley, Enrique Ramos, 2012, BMC Genomics.

Traditional and targeted exome sequencing reveals common, rare and novel functional deleterious variants in RET-signaling complex in a cohort of living US patients with urinary tract malformations

T. Druley, Enrique Ramos, R. Mitra, 2012, Human Genetics.

Candidate gene resequencing to identify rare, pedigree-specific variants influencing healthy aging phenotypes in the long life family study

Qunyuan Zhang, T. Druley, Enrique Ramos, 2016, BMC Geriatrics.