Bronwyn Kerr
Adelphi Group (United Kingdom)(GB)Massey University(NZ)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Protein Tyrosine Phosphatases, Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Connective tissue disorders research
Most-Cited Works
- → High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies(2017)451 cited
- → Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome(2010)366 cited
- → Fetal valproate syndrome and autism: additional evidence of an association(2001)363 cited
- → An Absence of Cutaneous Neurofibromas Associated with a 3-bp Inframe Deletion in Exon 17 of the NF1 Gene (c.2970-2972 delAAT): Evidence of a Clinically Significant NF1 Genotype-Phenotype Correlation(2006)360 cited
- → Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23.(1998)272 cited
- → Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders(2017)271 cited