Lionel Willatt
Addenbrooke's Hospital(GB)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Congenital heart defects research, Chromosomal and Genetic Variations, Prenatal Screening and Diagnostics
Most-Cited Works
- → Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes(2008)806 cited
- → Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations(2009)527 cited
- → Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability(2006)372 cited
- → Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome(2009)370 cited
- → 3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome(2005)296 cited
- → Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome(2005)255 cited
- → Long-term tripotent differentiation capacity of human neural stem (NS) cells in adherent culture(2008)231 cited
- → Clinical and molecular delineation of the 17q21.31 microdeletion syndrome(2008)217 cited
- → ASOX9Duplication and Familial 46,XX Developmental Testicular Disorder(2011)190 cited
- → High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings(2009)158 cited