Back to Search
PHILLIP LENNON, M.S.W., PH.D.
M.S.W., PH.D.
Clinical Social Worker
NPI: 1326182924Individual
Specialties, Licenses & Credentials
Clinical Social WorkerPrimary
Social Worker — Clinical
Code: 1041C0700X
00485(IA)
Research & Publications (20)
Chronic myeloid leukemia in blast phase associated with t(3;8)(q26;q24).
PMID 19665075·Cancer Genet Cytogenet·2009
5-case
Sonic hedgehog signaling pathway is activated in ALK-positive anaplastic large cell lymphoma.
PMID 19244133·Cancer Res·2009
8-other
Bacterial artificial chromosome array-based comparative genomic hybridization using paired formalin-fixed, paraffin-embedded and fresh frozen tissue specimens in multiple myeloma.
PMID 19109814·Cancer·2009
8-other
Translocation (18;22)(q21;q11) in B-cell lymphomas: a report of 4 cases and review of the literature.
PMID 18656237·Hum Pathol·2008
5-case
Splenic marginal zone lymphomas are characterized by loss of interstitial regions of chromosome 7q, 7q31.32 and 7q36.2 that include the protection of telomere 1 (POT1) and sonic hedgehog (SHH) genes.
PMID 18492102·Br J Haematol·2008
8-other
Activity of tyrosine kinase inhibitors against human NUP214-ABL1-positive T cell malignancies.
PMID 18401417·Leukemia·2008
7-preclinical
Validation of a targeted DNA microarray for the clinical evaluation of recurrent abnormalities in chronic lymphocytic leukemia.
PMID 18161787·Am J Hematol·2008
3-trial
Therapy may unmask hypoplastic myelodysplastic syndrome that mimics aplastic anemia.
PMID 17701956·Cancer·2007
8-other
Aberrant EVI1 expression in acute myeloid leukemias associated with the t(3;8)(q26;q24).
PMID 17693189·Cancer Genet Cytogenet·2007
8-other
Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review.
PMID 17330859·Am J Med Genet A·2007
5-case
A novel 8.5 MB dup(1)(p34.1p34.3) characterized by FISH in a child presenting with congenital heart defect and dysmorphic features.
PMID 16892326·Am J Med Genet A·2006
5-case
Array-based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation.
PMID 16688748·Am J Med Genet A·2006
5-case
WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH.
PMID 16646034·Am J Med Genet A·2006
5-case
The use of epicardial echocardiography as an adjunct to transesophageal echocardiography for the detection of pulmonary embolism.
PMID 16492819·Anesth Analg·2006
5-case
Web enabling technology for the design, enumeration, optimization and tracking of compound libraries.
PMID 16101417·Curr Top Med Chem·2005
6-review
Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array-based comparative genomic hybridization in a patient with mental retardation and dysmorphic features.
PMID 16015583·Am J Med Genet A·2005
5-case
Inhibition of IKK-2 by 2-[(aminocarbonyl)amino]-5-acetylenyl-3-thiophenecarboxamides.
PMID 15911271·Bioorg Med Chem Lett·2005
8-other
Regulation of endothelial CD73 by adenosine: paracrine pathway for enhanced endothelial barrier function.
PMID 11046060·J Immunol·2000
8-other
Interactive computer technology for skin cancer prevention targeting children.
PMID 10808985·Am J Prev Med·2000
3-trial
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2020 OGDEN AVE, SUITE 400
AURORA, IL 60504 - Phone
- (630) 499-4703
Quick Facts
- NPI
- 1326182924
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile