Bryan Paeper
Publications by Year
Research Areas
Liver Disease Diagnosis and Treatment, Hepatitis C virus research, Pancreatic function and diabetes, RNA Research and Splicing, Gene expression and cancer classification
Most-Cited Works
- → The contribution of de novo coding mutations to autism spectrum disorder(2014)2,750 cited
- → Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse(2001)2,563 cited
- → Bone Dysplasia Sclerosteosis Results from Loss of the SOST Gene Product, a Novel Cystine Knot–Containing Protein(2001)1,008 cited
- → A 52‐kb deletion in the SOST‐MEOX1 intergenic region on 17q12‐q21 is associated with van Buchem disease in the Dutch population(2002)300 cited
- → De Novo Mutations in NALCN Cause a Syndrome Characterized by Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay(2015)157 cited
- → Systems biology and the host response to viral infection(2007)135 cited
- → Polymorphisms in the Sclerosteosis/van Buchem Disease Gene (SOST) Region Are Associated with Bone-Mineral Density in Elderly Whites(2004)132 cited
- → Genomic Analysis Reveals a Potential Role for Cell Cycle Perturbation in HCV-Mediated Apoptosis of Cultured Hepatocytes(2009)113 cited
- → Proteomic profiling of human liver biopsies: Hepatitis C virus–induced fibrosis and mitochondrial dysfunction(2007)111 cited
- → Sequencing and expression analysis of the serine protease gene cluster located in chromosome 19q13 region(2000)100 cited