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DENNIS CALLEN, M.D.
M.D.
Family Medicine Physician
NPI: 1790787752IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
48749(MA)
Education
OTHER
Class of 1979
Research & Publications (20)
The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene.
PMID 15148587·J Hum Genet·2004
5-case
The influence of sex on limbic volume and perfusion in AD.
PMID 15165701·Neurobiol Aging·2004
4-observational
Limbic system perfusion in Alzheimer's disease measured by MRI-coregistered HMPAO SPET.
PMID 12111130·Eur J Nucl Med Mol Imaging·2002
3-trial
Expression of ZNF652, a novel zinc finger protein, in vulvar carcinomas and its relation to prognosis.
PMID 17468294·J Clin Pathol·2008
8-other
CBFA2T3-ZNF652 corepressor complex regulates transcription of the E-box gene HEB.
PMID 18456661·J Biol Chem·2008
7-preclinical
ZNF652, a novel zinc finger protein, interacts with the putative breast tumor suppressor CBFA2T3 to repress transcription.
PMID 16966434·Mol Cancer Res·2006
7-preclinical
FBXO31 is the chromosome 16q24.3 senescence gene, a candidate breast tumor suppressor, and a component of an SCF complex.
PMID 16357137·Cancer Res·2005
8-other
Partial androgen insensitivity syndrome and t(X;5): are there upstream regulatory elements of the androgen receptor gene?
PMID 15452386·Horm Res·2004
5-case
The sequence and analysis of duplication-rich human chromosome 16.
PMID 15616553·Nature·2004
4-observational
Linear width of the medial temporal lobe can discriminate Alzheimer's disease from normal aging: the Sunnybrook dementia study.
PMID 15013564·Neurobiol Aging·2004
4-observational
Absence of the Epstein-Barr virus genome in breast cancer-derived cell lines.
PMID 12928356·J Natl Cancer Inst·2003
8-other
Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: a cause of minute terminal chromosomal imbalances.
PMID 12548741·Am J Med Genet A·2003
5-case
CARD15/NOD2 risk alleles in the development of Crohn's disease in the Australian population.
PMID 12556233·Ann Hum Genet·2003
8-other
Defining regions of loss of heterozygosity of 16q in breast cancer cell lines.
PMID 11890994·Cancer Genet Cytogenet·2002
8-other
Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies.
PMID 11840484·Am J Med Genet·2002
8-other
A familial cryptic subtelomeric deletion 12p with variable phenotypic effect.
PMID 12000361·Clin Genet·2002
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
- 831 MAIN RD
WESTPORT, MA 02790 - Phone
- (508) 636-0613
Quick Facts
- NPI
- 1790787752
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 47
- Publications
- 20
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