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JENNIFER VELTMAN, M.D.
M.D.
Infectious Disease Physician
NPI: 1356599310IndividualAccepts Medicare
Specialties, Licenses & Credentials
Infectious Disease PhysicianPrimary
Internal Medicine — Infectious Disease
Code: 207RI0200X
4301092896(MI)A121822(CA)
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
4301092896(MI)A121822(CA)
Pediatrics Physician
Pediatrics
Code: 208000000X
4301092896(MI)
Education
WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE
Class of 2008
Research & Publications (20)
Contrast-enhanced magnetic resonance imaging of the breast: the value of pharmacokinetic parameters derived from fast dynamic imaging during initial enhancement in classifying lesions.
PMID 18270714·Eur Radiol·2008
8-other
Breast tumor characteristics of BRCA1 and BRCA2 gene mutation carriers on MRI.
PMID 18270717·Eur Radiol·2008
4-observational
Genomic copy number analysis in mental retardation: finding the needles in the haystack.
PMID 17047673·Eur J Hum Genet·2007
8-other
Diagnostic genome profiling: unbiased whole genome or targeted analysis?
PMID 17065419·J Mol Diagn·2006
6-review
Holoprosencephaly and preaxial polydactyly associated with a 1.24 Mb duplication encompassing FBXW11 at 5q35.1.
PMID 16865294·J Hum Genet·2006
5-case
Magnetic resonance-guided biopsies and localizations of the breast: initial experiences using an open breast coil and compatible intervention device.
PMID 15905725·Invest Radiol·2005
8-other
Array-based comparative genomic hybridization for genome-wide screening of DNA copy number in bladder tumors.
PMID 12782593·Cancer Res·2003
8-other
Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH.
PMID 12740760·Am J Hum Genet·2003
4-observational
High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization.
PMID 11951177·Am J Hum Genet·2002
4-observational
The additional value of three time point color coding in dynamic contrast-enhanced MRI of the breast for inexperienced and experienced readers.
PMID 19442470·Eur J Radiol·2010
8-other
Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: a multicenter study.
PMID 19388127·Hum Mutat·2009
4-observational
Forging links between human mental retardation-associated CNVs and mouse gene knockout models.
PMID 19557186·PLoS Genet·2009
7-preclinical
Genomic microarrays in mental retardation: a practical workflow for diagnostic applications.
PMID 19085936·Hum Mutat·2009
6-review
Disruption of the neurexin 1 gene is associated with schizophrenia.
PMID 18945720·Hum Mol Genet·2009
8-other
Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.
PMID 19578123·Hum Mol Genet·2009
8-other
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.
PMID 18628315·J Med Genet·2008
8-other
Reduced purifying selection prevails over positive selection in human copy number variant evolution.
PMID 18687881·Genome Res·2008
7-preclinical
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
PMID 18784092·N Engl J Med·2008
8-other
Recurrent CNVs disrupt three candidate genes in schizophrenia patients.
PMID 18940311·Am J Hum Genet·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 3901 CHRYSLER DR, SUITE 4A
DETROIT, MI 48201 - Phone
- (313) 745-4525
Quick Facts
- NPI
- 1356599310
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 5
- Locations
- 2
- Years in Practice
- 18
- Publications
- 20
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