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MATTHEW YEAGER, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1972352508Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Genetic variation in CLDN1 and susceptibility to hepatitis C virus infection.
PMID 19674288·J Viral Hepat·2010
8-other
Conceptualizing supports and the support needs of people with intellectual disability.
PMID 19368481·Intellect Dev Disabil·2009
8-other
Genetic variation in cell cycle and apoptosis related genes and multiple myeloma risk.
PMID 19362737·Leuk Res·2009
8-other
An analysis of growth, differentiation and apoptosis genes with risk of renal cancer.
PMID 19603096·PLoS One·2009
8-other
Quantitative trait loci predicting circulating sex steroid hormones in men from the NCI-Breast and Prostate Cancer Cohort Consortium (BPC3).
PMID 19574343·Hum Mol Genet·2009
4-observational
Common genetic variants in candidate genes and risk of familial lymphoid malignancies.
PMID 19573080·Br J Haematol·2009
8-other
Characteristics and needs of people with intellectual disability who have higher IQs.
PMID 19489667·Intellect Dev Disabil·2009
6-review
Common variation in genes related to innate immunity and risk of adult glioma.
PMID 19423540·Cancer Epidemiol Biomarkers Prev·2009
8-other
Common genetic variation in TP53 and risk of human papillomavirus persistence and progression to CIN3/cancer revisited.
PMID 19423538·Cancer Epidemiol Biomarkers Prev·2009
8-other
Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies.
PMID 19414860·Blood·2009
8-other
Common gene variants in the tumor necrosis factor (TNF) and TNF receptor superfamilies and NF-kB transcription factors and non-Hodgkin lymphoma risk.
PMID 19390683·PLoS One·2009
8-other
Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility.
PMID 19383797·Proc Natl Acad Sci U S A·2009
8-other
Identification of modifier genes for cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations.
PMID 19626699·Int J Cancer·2009
8-other
Risk of non-Hodgkin lymphoma associated with germline variation in genes that regulate the cell cycle, apoptosis, and lymphocyte development.
PMID 19336552·Cancer Epidemiol Biomarkers Prev·2009
4-observational
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).
PMID 19330030·Nat Genet·2009
8-other
Public policy and the enhancement of desired outcomes for persons with intellectual disability.
PMID 19650684·Intellect Dev Disabil·2009
8-other
Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer.
PMID 19644707·Hum Genet·2009
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
- 17 DAVIS BLVD STE 308
TAMPA, FL 33606 - Phone
- (813) 974-2201
Quick Facts
- NPI
- 1972352508
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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