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JOHN VELTMAN, MD

General Practice Physician

NPI: 1740239771Individual

Specialties, Licenses & Credentials

General Practice PhysicianPrimary

General Practice

Code: 208D00000X

18089(WV)

Research & Publications (20)

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
Disruption of the neurexin 1 gene is associated with schizophrenia.
PMID 18945720·Hum Mol Genet·2009
8-other
Forging links between human mental retardation-associated CNVs and mouse gene knockout models.
PMID 19557186·PLoS Genet·2009
7-preclinical
Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.
PMID 19578123·Hum Mol Genet·2009
8-other
Genomic microarrays in mental retardation: a practical workflow for diagnostic applications.
PMID 19085936·Hum Mutat·2009
6-review
Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: a multicenter study.
PMID 19388127·Hum Mutat·2009
4-observational
Breast tumor characteristics of BRCA1 and BRCA2 gene mutation carriers on MRI.
PMID 18270717·Eur Radiol·2008
4-observational
Mapping of 5q35 chromosomal rearrangements within a genomically unstable region.
PMID 18628311·J Med Genet·2008
8-other
Recurrent CNVs disrupt three candidate genes in schizophrenia patients.
PMID 18940311·Am J Hum Genet·2008
8-other
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.
PMID 18628315·J Med Genet·2008
8-other
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
The value of MRI compared to mammography in the assessment of tumour extent in invasive lobular carcinoma of the breast.
PMID 17574805·Eur J Surg Oncol·2008
4-observational
Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype.
PMID 18452192·Am J Med Genet A·2008
8-other
CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.
PMID 17646849·Mol Psychiatry·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
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.
PMID 17546029·Nat Genet·2007
7-preclinical
Genome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysis.
PMID 17363414·DNA Res·2007
8-other
Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarrays.
PMID 18055821·Invest Ophthalmol Vis Sci·2007
8-other
Genomic copy number analysis in mental retardation: finding the needles in the haystack.
PMID 17047673·Eur J Hum Genet·2007
8-other

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

Contact & Hours

Address
35 AIKENS CENTER, PANHANDLE MEDICINE
MARTINSBURG, WV 25401

Location

Practice Location

35 AIKENS CENTER, MARTINSBURG, WV
(304) 264-2290

Quick Facts

NPI
1740239771
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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