Kerry Setchfield
University of Nottingham(GB)
Publications by Year
Research Areas
Congenital heart defects research, Congenital Heart Disease Studies, Genomic variations and chromosomal abnormalities, Cellular Mechanics and Interactions, Optical Imaging and Spectroscopy Techniques
Most-Cited Works
- → Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing(2016)464 cited
- → Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease(2012)337 cited
- → Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot(2019)193 cited
- → Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans(2014)185 cited
- → Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16(2013)165 cited
- → Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls(2011)164 cited
- → Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot(2013)109 cited
- → Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations(2011)94 cited
- → Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects(2017)56 cited
- → Effect of skin color on optical properties and the implications for medical optical technologies: a review(2024)55 cited