Peter Corry
Bradford Royal Infirmary(GB)
Publications by Year
Research Areas
Prenatal Screening and Diagnostics, Microtubule and mitosis dynamics, Genomics and Rare Diseases, interferon and immune responses, Neonatal and fetal brain pathology
Most-Cited Works
- → Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus(2006)883 cited
- → Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response(2009)682 cited
- → A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size(2005)563 cited
- → Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome(2007)445 cited
- → Risk factors for congenital anomaly in a multiethnic birth cohort: an analysis of the Born in Bradford study(2013)265 cited
- → Protein-Truncating Mutations in ASPM Cause Variable Reduction in Brain Size(2003)180 cited
- → Primary Autosomal Recessive Microcephaly (MCPH1) Maps to Chromosome 8p22-pter(1998)168 cited
- → Mutation of the Variant α-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia(2009)165 cited
- → A Third Novel Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 9q34(2000)107 cited
- → Aicardi-Goutières Syndrome Displays Genetic Heterogeneity with One Locus (AGS1) on Chromosome 3p21(2000)78 cited