Valerie Banks
Children's Specialty Group(US)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Congenital heart defects research, Chromosomal and Genetic Variations, Genetics and Neurodevelopmental Disorders, Congenital Ear and Nasal Anomalies
Most-Cited Works
- → A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay(2010)671 cited
- → Identification of a Recurrent Microdeletion at 17q23.1q23.2 Flanked by Segmental Duplications Associated with Heart Defects and Limb Abnormalities(2010)167 cited
- → Further clinical and molecular delineation of the 15q24 microdeletion syndrome(2011)92 cited
- → Distinctive phenotype in 9 patients with deletion of chromosome 1q24‐q25(2011)62 cited
- → Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats(2011)60 cited
- → 8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients(2013)56 cited
- → Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes(2011)21 cited
- → Refinement of the Region for Split Hand/Foot Malformation 5 on 2q31.1(2010)17 cited