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Ian D. Krantz | Researchclopedia

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Ian D. Krantz

Northwell Health ORCID

333

Works

22,715

Citations

74

h-index

186

i10-index

Research Topics

Genomics and Chromatin Dynamics Genomic variations and chromosomal abnormalities Pediatric Hepatobiliary Diseases and Treatments

Affiliations

Tokyo Institute of Technology2010–2010

Greater Baltimore Medical Center2010–2010

Lurie Children's Hospital2004–2004

San Francisco General Hospital2021–2021

Northwell Health2026–2026

Top Works

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

David T. Miller,Margaret P Adam,et al.

20102,855 citations

RNA Research and Splicing

Genomics and Rare Diseases

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

Takaya Oda,Abdel Elkahloun,et al.

19971,156 citations

KILLER/DR5 is a DNA damage–inducible p53–regulated death receptor gene

Gen Sheng Wu,Timothy F. Burns,et al.

19971,073 citations

Rare Variants Create Synthetic Genome-Wide Associations

Samuel P. Dickson,Kai Wang,et al.

2010866 citations

NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway

Ryan M. McDaniell,Daniel M. Warthen,et al.

2006737 citations

Microduplications of 16p11.2 are associated with schizophrenia

Shane McCarthy,Vladimir Makarov,et al.

2009732 citations

Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B

Ian D. Krantz,Jennifer McCallum,et al.

2004717 citations

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis

Laura K. Conlin,Brian Thiel,et al.

2010501 citations

Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between

Gail P. Jarvik,Laura M. Amendola,et al.

2014376 citations