Angela Davies
Clinical Trial Investigators(US)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Chromosomal and Genetic Variations, Prenatal Screening and Diagnostics, Genetics and Neurodevelopmental Disorders, Congenital heart defects research
Most-Cited Works
- → The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases(1993)1,455 cited
- → Genetic Analysis of the Epidermal Differentiation Complex (EDC) on Human Chromosome 1q21: Chromosomal Orientation, New Markers, and a 6-Mb YAC Contig(1996)116 cited
- → Delineation of two distinct 6p deletion syndromes(1999)113 cited
- → Characterization of terminal chromosome anomalies using multisubtelomere FISH(2003)85 cited
- → Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases(2003)68 cited
- An interstitial deletion of 6p24-p25 proximal to the FKHL7 locus and including AP-2alpha that affects anterior eye chamber development.(1999)
- → Isolation and chromosomal mapping of human glycogen synthase kinase-3 α and -3β encoding genes(1998)58 cited
- → Meiotic outcomes of three-way translocations ascertained in cleavage-stage embryos: refinement of reproductive risks and implications for PGD(2013)49 cited
- → The copy number variant involving part of the α7 nicotinic receptor gene contains a polymorphic inversion(2008)41 cited