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IAN KRANTZ, M.D.

M.D.

NPI: 1306860325IndividualAccepts Medicare

Specialties, Licenses & Credentials

Clinical Cytogenetics Physician

Medical Genetics — Clinical Cytogenetics

Code: 207SC0300X

MD052766L(PA)
Clinical Genetics (M.D.) PhysicianPrimary

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

MD052766L(PA)
Pediatrics Physician

Pediatrics

Code: 208000000X

MD052766L(PA)

CMS Specialties

PrimaryMEDICAL GENETICS AND GENOMICS

Education

OTHER

Class of 1991

Research & Publications (20)

Novel microdeletion syndromes.
PMID 17910074·Am J Med Genet C Semin Med Genet·2007
6-review
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B.
PMID 15146186·Nat Genet·2004
4-observational
Alagille syndrome: chipping away at the tip of the iceberg.
PMID 12244549·Am J Med Genet·2002
8-other
Exclusion of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange syndrome.
PMID 11391654·Am J Med Genet·2001
8-other
Screening for postpartum depression with the Edinburgh Postnatal Depression Scale (EPDS): an ethical analysis.
PMID 18519287·Scand J Public Health·2008
8-other
Ethics and vaccination.
PMID 15204177·Scand J Public Health·2004
8-other
Ethics of screening for asymptomatic herpes virus type 2 infection.
PMID 15361449·BMJ·2004
6-review
FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation.
PMID 19668217·Nat Genet·2009
8-other
Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA.
PMID 18996922·Hum Mol Genet·2009
8-other
SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation.
PMID 19058200·Hum Mutat·2009
8-other
On the molecular etiology of Cornelia de Lange syndrome.
PMID 19154515·Ann N Y Acad Sci·2009
6-review
Dosage effects of cohesin regulatory factor PDS5 on mammalian development: implications for cohesinopathies.
PMID 19412548·PLoS One·2009
7-preclinical
Transcriptional dysregulation in NIPBL and cohesin mutant human cells.
PMID 19468298·PLoS Biol·2009
8-other
A way of measuring poverty that could further a change for the better.
PMID 18568259·Bull World Health Organ·2008
8-other
Cohesin and human disease.
PMID 18767966·Annu Rev Genomics Hum Genet·2008
6-review
Bile duct anomalies in a male child with Noonan syndrome: a case for ras and notch pathway synergism.
PMID 18080325·Am J Med Genet A·2008
5-case
Fine-mapping subtelomeric deletions and duplications by comparative genomic hybridization in 42 individuals.
PMID 18257100·Am J Med Genet A·2008
8-other
Mutations in the chromatin-associated protein ATRX.
PMID 18409179·Hum Mutat·2008
8-other
Parental narratives of genetic testing for hearing loss: audiologic implications for clinical work with children and families.
PMID 17562755·Am J Audiol·2007
8-other
Natural history of aging in Cornelia de Lange syndrome.
PMID 17640042·Am J Med Genet C Semin Med Genet·2007
5-case

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
3401 CIVIC CENTER BLVD
PHILADELPHIA, PA 19104

Location

Practice Location

3401 CIVIC CENTER BLVD, PHILADELPHIA, PA
(215) 590-2920

Quick Facts

NPI
1306860325
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
3
Locations
1
Years in Practice
35
Publications
20

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