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JOSEPH DUMANSKI, D.M.D.
D.M.D.
General Practice Dentistry
NPI: 1922440569Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
34398(NY)
Research & Publications (20)
Genome-wide high-resolution analysis of DNA copy number alterations in NF1-associated malignant peripheral nerve sheath tumors using 32K BAC array.
PMID 19603524·Genes Chromosomes Cancer·2009
8-other
Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array.
PMID 19304958·Neuro Oncol·2009
8-other
Tissue-specific variation in DNA methylation levels along human chromosome 1.
PMID 19505295·Epigenetics Chromatin·2009
8-other
Genome-wide microarray-based comparative genomic hybridization analysis of lymphoplasmacytic lymphomas reveals heterogeneous aberrations.
PMID 19672776·Leuk Lymphoma·2009
8-other
Somatic mosaicism for copy number variation in differentiated human tissues.
PMID 18570184·Hum Mutat·2008
8-other
The mechanism of cystic fibrosis transmembrane conductance regulator transcriptional repression during the unfolded protein response.
PMID 18319256·J Biol Chem·2008
8-other
Autoantibodies to glutathione S-transferase theta 1 in patients with primary sclerosing cholangitis and other autoimmune diseases.
PMID 18242955·J Autoimmun·2008
8-other
High-resolution DNA copy number profiling of malignant peripheral nerve sheath tumors using targeted microarray-based comparative genomic hybridization.
PMID 18281533·Clin Cancer Res·2008
8-other
A segmental maximum a posteriori approach to genome-wide copy number profiling.
PMID 18204059·Bioinformatics·2008
8-other
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles.
PMID 18304490·Am J Hum Genet·2008
4-observational
Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array.
PMID 18058796·Hum Mutat·2008
4-observational
Detection of copy number changes at the NF1 locus with improved high-resolution array CGH.
PMID 17718862·Clin Genet·2007
4-observational
Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation.
PMID 17901693·Cytogenet Genome Res·2007
5-case
A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients.
PMID 18000907·Am J Med Genet A·2007
5-case
Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus.
PMID 17222329·BMC Genomics·2007
8-other
Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter).
PMID 17603794·Am J Med Genet A·2007
5-case
A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene.
PMID 17676630·Am J Med Genet A·2007
5-case
Chromosome 22 array-CGH profiling of breast cancer delimited minimal common regions of genomic imbalances and revealed frequent intra-tumoral genetic heterogeneity.
PMID 16964389·Int J Oncol·2006
4-observational
Array-CGH and multipoint FISH to decode complex chromosomal rearrangements.
PMID 17196103·BMC Genomics·2006
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
- 1879 ROUTE 112 STE 3
CORAM, NY 11727 - Phone
- (631) 474-0410
Quick Facts
- NPI
- 1922440569
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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