Robin Sherrington
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Alzheimer's disease research and treatments, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases
Most-Cited Works
- → Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease(1995)4,041 cited
- → Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene(1995)2,060 cited
- → Mutant presenilins of Alzheimer's disease increase production of 42-residue amyloid β-protein in both transfected cells and transgenic mice(1997)1,262 cited
- → Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia(2003)1,146 cited
- → Localization of a susceptibility locus for schizophrenia on chromosome 5(1988)619 cited
- → Loss‐of‐function mutations in the Na v 1.7 gene underlie congenital indifference to pain in multiple human populations(2007)452 cited
- → Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease(1998)434 cited
- → Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23(2001)373 cited
- → Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant(1996)308 cited
- → Presenilin Proteins Undergo Heterogeneous Endoproteolysis between Thr291and Ala299and Occur as Stable N- and C-Terminal Fragments in Normal and Alzheimer Brain Tissue(1997)288 cited