Ian D. Krantz
Northwell Health(US)Hofstra University(US)Cohen Children's Medical Center(US)
Publications by Year
Research Areas
Genomics and Chromatin Dynamics, Genomic variations and chromosomal abnormalities, Pediatric Hepatobiliary Diseases and Treatments, RNA Research and Splicing, Genomics and Rare Diseases
Most-Cited Works
- → Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies(2010)2,854 cited
- → Mutations in the human Jagged1 gene are responsible for Alagille syndrome(1997)1,156 cited
- → KILLER/DR5 is a DNA damage–inducible p53–regulated death receptor gene(1997)1,073 cited
- → Rare Variants Create Synthetic Genome-Wide Associations(2010)866 cited
- → NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway(2006)737 cited
- → Microduplications of 16p11.2 are associated with schizophrenia(2009)732 cited