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Ian D. Krantz

Northwell Health(US)

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333

Papers

22.7K

Citations

74

h-index

186

i10-index

Ian D. Krantz is an academic researcher from Northwell Health. The author has contributed to research in topics: Genomics and Chromatin Dynamics & Genomic variations and chromosomal abnormalities & Pediatric Hepatobiliary Diseases and Treatments. The author has an h-index of 74, co-authored 284 publications.

ORCID: 0000-0003-2442-1128

Research Topics

Genomics and Chromatin Dynamics Genomic variations and chromosomal abnormalities Pediatric Hepatobiliary Diseases and Treatments RNA Research and Splicing Genomics and Rare Diseases

Papers by this author

works

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

2010 · The American Journal of Human Genetics · 2,835 citations

https://doi.org/10.1016/j.ajhg.2010.04.006

David T. Miller Margaret P Adam Swaroop Aradhya Leslie G. Biesecker

Spectrum and Frequency of Jagged1 (JAG1) Mutations in Alagille Syndrome Patients and Their Families

1998 · The American Journal of Human Genetics · 232 citations

https://doi.org/10.1086/301875

Ian D. Krantz Raymond P. Colliton Anna Genin Elizabeth B. Rand

International electronic health record-derived COVID-19 clinical course profiles: the 4CE consortium

2020 · npj Digital Medicine · 212 citations

https://doi.org/10.1038/s41746-020-00308-0

Gabriel A. Brat Griffin M. Weber Nils Gehlenborg Paul Avillach

Mutations in the chromatin-associated protein ATRX

2008 · Human Mutation · 184 citations

https://doi.org/10.1002/humu.20734

Richard J. Gibbons Takahito Wada Christopher A. Fisher N Malik

Cohesin and Human Disease

2008 · Annual Review of Genomics and Human Genetics · 128 citations

https://doi.org/10.1146/annurev.genom.9.081307.164211

Jinglan Liu Ian D. Krantz

Mutant cohesin affects RNA polymerase II regulation in Cornelia de Lange syndrome

2015 · Scientific Reports · 73 citations

https://doi.org/10.1038/srep16803

Linda Mannini Fabien C. Lamaze Francesco Cucco Clelia Amato

Research topics

topics

Genomics and Chromatin Dynamics

Genomic variations and chromosomal abnormalities

Pediatric Hepatobiliary Diseases and Treatments

RNA Research and Splicing

Genomics and Rare Diseases

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