Corneliu Bodea
Sanofi (United States)(US)
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Genomic variations and chromosomal abnormalities, Genomics and Rare Diseases, Gene expression and cancer classification, Inflammatory Bowel Disease
Most-Cited Works
- → Most genetic risk for autism resides with common variation(2014)1,269 cited
- → Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humans(2016)180 cited
- → Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls(2013)136 cited
- → A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies(2016)26 cited
- → PINES: phenotype-informed tissue weighting improves prediction of pathogenic noncoding variants(2018)22 cited
- → Lung gene expression and single cell analyses reveal two subsets of idiopathic pulmonary fibrosis (IPF) patients associated with different pathogenic mechanisms(2021)20 cited
- → Variants in STXBP3 are Associated with Very Early Onset Inflammatory Bowel Disease, Bilateral Sensorineural Hearing Loss and Immune Dysregulation(2021)15 cited
- → Type 2 cytokines pleiotropically modulate sensory nerve architecture and neuroimmune interactions to mediate itch(2025)12 cited
- → Phenotype-specific information improves prediction of functional impact for noncoding variants(2016)6 cited
- → Pathway specific polygenic risk scores identify pathways and patient clusters associated with inflammatory bowel disease risk, severity and treatment response(2021)3 cited