Neil Miller
BioNano Genomics (United States)(US)
Publications by Year
Research Areas
Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Cancer Genomics and Diagnostics, Pharmacogenetics and Drug Metabolism, Acute Lymphoblastic Leukemia research
Most-Cited Works
- → Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing(2011)706 cited
- → Rapid Whole-Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units(2012)669 cited
- → Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders(2014)529 cited
- → An Integrated Clinico-Metabolomic Model Improves Prediction of Death in Sepsis(2013)502 cited
- → Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis(2010)475 cited
- → The Pharmacogene Variation (PharmVar) Consortium: Incorporation of the Human Cytochrome P450 (CYP) Allele Nomenclature Database(2017)410 cited
- → Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings(2015)405 cited
- → A highly annotated whole-genome sequence of a Korean individual(2009)344 cited
- → C6/36 Aedes albopictus Cells Have a Dysfunctional Antiviral RNA Interference Response(2010)318 cited
- → A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases(2015)318 cited