Ben Anderson
Quest Diagnostics (United Kingdom)(GB)
Publications by Year
Research Areas
Congenital Heart Disease Studies, Cystic Fibrosis Research Advances, Cardiac Structural Anomalies and Repair, Prenatal Screening and Diagnostics, Congenital Ear and Nasal Anomalies
Most-Cited Works
- → FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: Insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insufficiency in the United States(2010)105 cited
- → Cystic fibrosis screening using the College panel: Platform comparison and lessons learned from the first 20,000 samples(2002)52 cited
- → Novel and recurrent rearrangements in the CFTR gene: clinical and laboratory implications for cystic fibrosis screening(2005)48 cited
- → Coagulation monitoring correlation with heparin dose in pediatric extracorporeal life support(2017)42 cited
- → Stenting of the left pulmonary artery after palliation of hypoplastic left heart syndrome(2016)32 cited
- → CFTR 5T variant has a low penetrance in females that is partially attributable to its haplotype(2006)30 cited
- → A large deletion in the CFTR gene in CBAVD(2006)30 cited
- → In Vivo Evaluation of Active and Passive Physiological Control Systems for Rotary Left and Right Ventricular Assist Devices(2016)30 cited
- → Development and validation of a high throughput SARS-CoV-2 whole genome sequencing workflow in a clinical laboratory(2022)25 cited
- → Balloon Aortic Valvuloplasty for Congenital Aortic Stenosis: A 14-Year Single Centre Review(2018)24 cited