Robert M. Plenge
Bristol-Myers Squibb (United States)(US)
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, T-cell and B-cell Immunology, Genomics and Rare Diseases, Biomedical Text Mining and Ontologies
Most-Cited Works
- → Principal components analysis corrects for stratification in genome-wide association studies(2006)10,603 cited
- → Validating therapeutic targets through human genetics(2013)753 cited
- → Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis(2008)598 cited
- → Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus(2008)578 cited
- → Identifying Relationships among Genomic Disease Regions: Predicting Genes at Pathogenic SNP Associations and Rare Deletions(2009)430 cited
- → De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot(2009)402 cited
- → X Chromosome–Inactivation Patterns of 1,005 Phenotypically Unaffected Females(2006)353 cited
- → Electronic medical records for discovery research in rheumatoid arthritis(2010)344 cited
- → A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation(1997)295 cited
- → Skewed X-Chromosome Inactivation Is a Common Feature of X-Linked Mental Retardation Disorders(2002)262 cited