Area of research
Molecular Biology · Cancer Research
Research interest
Research interests include Genetic factors in colorectal cancer, Epigenetics and DNA Methylation, Cancer Genomics and Diagnostics, and Cancer-related molecular mechanisms research.
Cost-effective solutions for high-throughput enzymatic DNA methylation sequencing
Evolution of clonal hematopoiesis on and off lenalidomide maintenance for multiple myeloma
Pandemic Social Distancing and Declines in Nasopharyngeal Carriage of Pneumococcus and Related Antimicrobial-Resistant Genes: Evidence From Household-Based Cohort Studies in Lima, Peru.
Evolution of clonal hematopoiesis on and off lenalidomide maintenance for multiple myeloma.
Coding Variants of the Genitourinary Development Gene <i>WNT9B</i> Carry High Risk for Prostate Cancer.
Subset-specific mitochondrial stress and DNA damage shape T cell responses to fever and inflammation.
HIV persists in late coronary atheroma and is associated with increased local inflammation and disease progression
Weighting of risk factors for low birth weight: a linked routine data cohort study in Wales, UK
Characteristics of Sports-Related Injuries Presenting to a Pediatric Emergency Department
Ligand-independent integrin β1 signaling supports lung adenocarcinoma development.
Differential pre-malignant programs and microenvironment chart distinct paths to malignancy in human colorectal polyps
Differential pre-malignant programs and microenvironment chart distinct paths to malignancy in human colorectal polyps.
Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer
SETD2 regulates the methylation of translation elongation factor eEF1A1 in clear cell renal cell carcinoma
CRISPR/Cas9-targeted removal of unwanted sequences from small-RNA sequencing libraries
Whole genome sequencing reveals novel IGHMBP2 variant leading to unique cryptic splice-site and Charcot-Marie-Tooth phenotype with early onset symptoms.
IgG4-related disease: Association with a rare gene variant expressed in cytotoxic T cells.
A toolkit for genetics providers in follow-up of patients with non-diagnostic exome sequencing.
Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students.
Identification of nine new susceptibility loci for endometrial cancer
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder
Genetic overlap between endometriosis and endometrial cancer: evidence from cross‐disease genetic correlation and GWAS meta‐analyses
Eosinophils Determine Dermal Thickening and Water Loss in an MC903 Model of Atopic Dermatitis
Discovery and Validation of Circulating Biomarkers of Colorectal Adenoma by High-Depth Small RNA Sequencing
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome
The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease
A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3
Genomic regulation of invasion by STAT3 in triple negative breast cancer
Geospatial Resolution of Human and Bacterial Diversity with City-Scale Metagenomics
Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1