Physician

Family Medicine

Dr. Margaret R. Spitz, MD

Margaret Spitz practices Family Medicine. Margaret Spitz is a published doctor as well. She has 99 publications published. The latest was: Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia.

Publications

Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia.
Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer.
Characterization of large structural genetic mosaicism in human autosomes.
A recurrent mutation in PARK2 is associated with familial lung cancer.
A risk prediction model for smoking experimentation in mexican american youth.
Genome-wide Scan of 29,141 African Americans Finds No Evidence of Directional Selection since Admixture.
The Cytokinesis Blocked Micronucleus Assay as a Strong Predictor of Lung Cancer: Extension of a Lung cancer risk prediction model.
Wnt signaling pathway pharmacogenetics in non-small cell lung cancer.
Imputation and subset based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.
Inflammation-related Genetic Variations and Survival for Advanced Non-Small Cell Lung Cancer Receiving First-line Chemotherapy.
Distinct Loci in the CHRNA5/CHRNA3/CHRNB4 Gene Cluster Are Associated With Onset of Regular Smoking.
Genetic variation in the PNPLA3 gene and hepatocellular carcinoma in USA: Risk and prognosis prediction.
Symptom clusters of pain, depressed mood, and fatigue in lung cancer: assessing the role of cytokine genes.
Heme-related gene expression signatures of meat intakes in lung cancer tissues.
The Associations of Body Image, Anxiety, and Smoking Among Mexican-Origin Youth.
Transforming epidemiology for 21st century medicine and public health.
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.
Exposure to Pro-tobacco Messages and Smoking Status Among Mexican Origin Youth.
Role of selected genetic variants in lung cancer risk in african americans.
Investigating multiple candidate genes and nutrients in the folate metabolism pathway to detect genetic and nutritional risk factors for lung cancer.
"Drivers" of translational cancer epidemiology in the 21st century: needs and opportunities.
Fine-mapping of the 5p15.33, 6p22.1-p21.31, and 15q25.1 Regions Identifies Functional and Histology-Specific Lung Cancer Susceptibility Loci in African-Americans.
Cigarette experimentation and the population attributable fraction for associated genetic and non-genetic risk factors.
Use of the cytokinesis-blocked micronucleus assay to detect gender differences and genetic instability in a lung cancer case-control study.
Eliminating second-hand smoke from Mexican-American households: Outcomes from Project Clean Air-Safe Air (CASA).
Genome-wide association study reveals novel genetic determinants of DNA repair capacity in lung cancer.
Sensation seeking genes and physical activity in youth.
Genetic Variations in Interleukin-8 and Interleukin-10 are Associated With Pain, Depressed Mood, and Fatigue in Lung Cancer Patients.
Predictors of survival in never-smokers with non-small cell lung cancer: a large-scale, two-phase genetic study.
Gender differences in sociodemographic and behavioral influences of physical activity in mexican-origin adolescents.
Self-Reported Prior Lung Diseases as Risk Factors for Non-small Cell Lung Cancer in Mexican Americans.
Genome-wide gene-environment interaction analysis for asbestos exposure in lung cancer susceptibility.
Derived SNP alleles are used more frequently than ancestral alleles as risk-associated variants in common human diseases.
Roles of genetic variants in the PI3K and RAS/RAF pathways in susceptibility to endometrial cancer and clinical outcomes.
A Case-Control Study of a Sex-Specific Association between a 15q25 Variant and Lung Cancer Risk.
Cigarette Experimentation in Mexican Origin Youth: Psychosocial and Genetic Determinants.
p73 G4C14-to-A4T14 gene polymorphism and interaction with p53 exon 4 Arg72Pro on cancer susceptibility: a meta-analysis of the literature.
Common Genetic Variants in Cell Cycle Pathway Are Associated with Survival in Stage III-IV Non-Small Cell Lung Cancer.
DNA Repair Capacity in Peripheral Lymphocytes Predicts Survival of Patients With Non-Small-Cell Lung Cancer Treated With First-Line Platinum-Based Chemotherapy.
Novel genetic variants in the chromosome 5p15.33 region associate with lung cancer risk.
Hamilton et al. Respond to "Consolidating Data Harmonization"
Relationship Between CYP2A6 and CHRNA5-CHRNA3-CHRNB4 Variation and Smoking Behaviors and Lung Cancer Risk.
The PhenX Toolkit: Get the Most From Your Measures.
Association of smoking with tumor size at diagnosis in non-small cell lung cancer.
Psychosocial risk and correlates of early menarche in mexican-american girls.
Reproductive and Hormonal Factors and Lung Cancer Risk in the NIH-AARP Diet and Health Study Cohort.
Genetic variations in the transforming growth factor beta pathway as predictors of survival in advanced non-small cell lung cancer.
Genome-Wide Association Study of Survival in Non-Small Cell Lung Cancer Patients Receiving Platinum-Based Chemotherapy.
Erratum to: Assessing environmental and occupational risk factors for lung cancer in Mexican-Americans.
'Confounding' our future.
Global assessment of genetic variation influencing response to retinoid chemoprevention in head and neck cancer patients.
Sensation seeking, risk behaviors, and alcohol consumption among Mexican origin youth.
Variants in folate pathway genes as modulators of genetic instability and lung cancer risk.
A smoking-based carcinogenesis model for lung cancer risk prediction.
Cancer pharmacogenomics and pharmacoepidemiology: setting a research agenda to accelerate translation.
Nicotinic acetylcholine receptor region on chromosome 15q25 and lung cancer risk among African Americans: a case-control study.
Genetically abnormal circulating cells in lung cancer patients: an antigen-independent fluorescence in situ hybridization-based case-control study.
Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD.
A functional variant of tandem repeats in human telomerase gene was associated with survival of patients with early stages of non-small cell lung cancer.
Mediating effects of smoking and chronic obstructive pulmonary disease on the relation between the CHRNA5-A3 genetic locus and lung cancer risk.
Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium.
Chipping away at the genetics of smoking behavior.
Reduced DNA repair capacity for removing tobacco carcinogen-induced DNA adducts contributes to risk of head and neck cancer but not tumor characteristics.
Genetic variants in inflammation-related genes are associated with radiation-induced toxicity following treatment for non-small cell lung cancer.
Re: Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk.
Genetic and nongenetic covariates of pain severity in patients with adenocarcinoma of the pancreas: assessing the influence of cytokine genes.
Cognitive susceptibility to smoking: Two paths to experimenting among Mexican origin youth.
Exposure to smoking imagery in the movies and experimenting with cigarettes among Mexican heritage youth.
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
Role of inflammation gene polymorphisms on pain severity in lung cancer patients.
Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.
Novel susceptibility loci for second primary tumors/recurrence in head and neck cancer patients: large-scale evaluation of genetic variants.
Association between hypothyroidism and hepatocellular carcinoma: a case-control study in the United States.
Influence of subjective social status on the relationship between positive outcome expectations and experimentation with cigarettes.
Sociodemographic characteristics, health beliefs, and the accuracy of cancer knowledge.
Common 5p15.33 and 6p21.33 variants influence lung cancer risk.
Smoking-related genomic signatures in non-small cell lung cancer.
The CHRNA5-A3 region on chromosome 15q24-25.1 is a risk factor both for nicotine dependence and for lung cancer.
Genetic variations in cell-cycle pathway and the risk of oral premalignant lesions.
Germline genetic variations in drug action pathways predict clinical outcomes in advanced lung cancer treated with platinum-based chemotherapy.
The influence of tumor necrosis factor-alpha -308 G/A and IL-6 -174 G/C on pain and analgesia response in lung cancer patients receiving supportive care.
International Lung Cancer Consortium: pooled analysis of sequence variants in DNA repair and cell cycle pathways.
Effect of different types of smoking and synergism with hepatitis C virus on risk of hepatocellular carcinoma in American men and women: case-control study.
Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer.
Development and validation of a lung cancer risk prediction model for African-Americans.
An expanded risk prediction model for lung cancer.
3p22.1 and 10q22.3 deletions detected by fluorescence in situ hybridization (FISH): a potential new tool for early detection of non-small cell lung Cancer (NSCLC).
Dietary alpha-, beta-, gamma- and delta-tocopherols in lung cancer risk.
Mitochondrial DNA content: its genetic heritability and association with renal cell carcinoma.
Automated detection of genetic abnormalities combined with cytology in sputum is a sensitive predictor of lung cancer.
Prognostic significance of ataxia-telangiectasia mutated, DNA-dependent protein kinase catalytic subunit, and Ku heterodimeric regulatory complex 86-kD subunit express...
DNA repair capacity and lung cancer risk in never smokers.
Meta-analysis and pooled analysis of GSTM1 and CYP1A1 polymorphisms and oral and pharyngeal cancers: a HuGE-GSEC review.
Chromosome instability and risk of squamous cell carcinomas of head and neck.
Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1.
Cytokinesis-blocked micronucleus cytome assay biomarkers identify lung cancer cases amongst smokers.
Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms.

Doctors Specialties

Family Medicine

Accepted Insurances

Hospital

University of Texas M.D. Anderson Cancer Center

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