Kerra Pearce
Dorset County Hospital(GB)
Publications by Year
Research Areas
Glioma Diagnosis and Treatment, Bioinformatics and Genomic Networks, RNA Research and Splicing, Protein Degradation and Inhibitors, Blood groups and transfusion
Most-Cited Works
- → Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease(2011)857 cited
- → Identification of mutations in CUL7 in 3-M syndrome(2005)172 cited
- → Targeting acute myeloid leukemia by drug-induced c-MYB degradation(2017)114 cited
- → Genome-wide DNA methylation analysis of archival formalin-fixed paraffin-embedded tissue using the Illumina Infinium HumanMethylation27 BeadChip(2010)103 cited
- → Molecular study of 33 families with Fraser syndrome new data and mutation review(2008)85 cited
- → Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome(2010)62 cited
- → Mutations in linker for activation of T cells (LAT) lead to a novel form of severe combined immunodeficiency(2016)55 cited
- → De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes(2019)50 cited
- → Hearing in 44–45 year olds with m.1555A>G, a genetic mutation predisposing to aminoglycoside-induced deafness: a population based cohort study(2012)45 cited
- → Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry(2011)43 cited