Mariza de Andrade

发表

Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records

Marylyn D. Ritchie, Dana C. Crawford, Shefali S. Verma, 2014, Front. Genet..

Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries

Brian E. Cade, Thomas W. Blackwell, Yan Gao, 2020, bioRxiv.

A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program

Brian E. Cade, Jan Graffelman, Alex P. Reiner, 2020, bioRxiv.

Bayesian Variable Selection in Multilevel Item Response Theory Models with Application in Genomics

Mariza de Andrade, Tiago M Fragoso, Alexandre C Pereira, 2016, Genetic epidemiology.

Missing phenotype data imputation in pedigree data analysis

Mariza de Andrade, Brooke L Fridley, 2008, Genetic epidemiology.

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

Dana C Crawford, Yuki Bradford, Mariza de Andrade, 2011, Genetic epidemiology.

Entropy Based Genetic Association Tests and Gene-Gene Interaction Tests

Mariza de Andrade, Xin Wang, M. de Andrade, 2011, Statistical applications in genetics and molecular biology.

Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction

Udo Hoffmann, David M Herrington, Eric Boerwinkle, 2011, Circulation.

Identification of gene-gene interaction using principal components

Mariza de Andrade, Joanna M Biernacka, J. Biernacka, 2009, BMC proceedings.

Genetic variants and risk of lung cancer in never smokers: a genome-wide association study.

Zhifu Sun, Feng Chen, Mariza de Andrade, 2010, The Lancet. Oncology.

Detectable clonal mosaicism from birth to old age and its relationship to cancer

Ingo Ruczinski, Li-e Wang, William L. Lowe, 2012, Nature Genetics.

Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network

Gerard Tromp, Dana C Crawford, Helena Kuivaniemi, 2015, Genetic epidemiology.

Identification of genes and haplotypes that predict rheumatoid arthritis using random forests

Mariza de Andrade, Joanna M Biernacka, Jason P Sinnwell, 2009, BMC proceedings.

High-resolution whole-genome association study of Parkinson disease.

Mariza de Andrade, Demetrius M Maraganore, D. Cox, 2005, American journal of human genetics.

Multiple-level validation identifies PARK2 in the development of lung cancer and chronic obstructive pulmonary disease

Zhifu Sun, Mariza de Andrade, Jason A. Wampfler, 2016, Oncotarget.

Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease

Mariza de Andrade, Andre Franke, Wolfgang Lieb, 2016, Nature Genetics.

Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function

Sylvia Stracke, Alex Doney, Yurii S. Aulchenko, 2012, PLoS genetics.

Genetic Variants Associated with Serum Thyroid Stimulating Hormone (TSH) Levels in European Americans and African Americans from the eMERGE Network

Suzette J. Bielinski, Christopher G. Chute, Marylyn D. Ritchie, 2014, PloS one.

Group 6: Pleiotropy and multivariate analysis

Peter Kraft, Mariza de Andrade, P. Kraft, 2003, Genetic epidemiology.

Genomic Susceptibility Loci for Brain Atrophy in Hypertensive Sibships From the GENOA Study

Clifford R Jack, Eric Boerwinkle, Mariza de Andrade, 2005, Hypertension.

CUBN is a gene locus for albuminuria.

Sylvia Stracke, Ming-Huei Chen, Luigi Ferrucci, 2011, Journal of the American Society of Nephrology : JASN.

International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways

Casey S. Greene, Marco Carbone, Andrew Fraser, 2015, Nature Communications.

Assessment of genotype imputation methods

Mariza de Andrade, Ellen L Goode, Brooke L Fridley, 2009, BMC proceedings.

PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

Hynek Pikhart, Fernando Pires Hartwig, Joshua C Denny, 2017, The lancet. Diabetes & endocrinology.

Ascertainment issues in variance components models

Mariza de Andrade, C. Amos, M. de Andrade, 2000 .

Effect of Emphysema on Lung Cancer Risk in Smokers: A Computed Tomography–Based Assessment

Fang Zhang, Mariza de Andrade, Ping Yang, 2010, Cancer Prevention Research.

Probability of pancreatic cancer following diabetes: a population-based study.

Mariza de Andrade, M. de Andrade, G. Petersen, 2005, Gastroenterology.

Polymorphic Variants in Hereditary Pancreatic Cancer Genes Are Not Associated with Pancreatic Cancer Risk

Mariza de Andrade, Fergus J Couch, David N. Rider, 2009, Cancer Epidemiology, Biomarkers & Prevention.

Comparison of Multivariate Tests for Genetic Linkage

Mariza de Andrade, Christopher I. Amos, C. Amos, 2001, Human Heredity.

Characterization of large structural genetic mosaicism in human autosomes.

William Wheeler, Nan Hu, Peter Kraft, 2015, American journal of human genetics.

The foundation of precision medicine: integration of electronic health records with genomics through basic, clinical, and translational research

Marylyn D. Ritchie, Helena Kuivaniemi, Mariza de Andrade, 2015, Front. Genet..

Genetics of cardiovascular disease: Importance of sex and ethnicity.

Mariza de Andrade, Virginia M Miller, Stacey J Winham, 2015, Atherosclerosis.

Adenocarcinoma in situ, minimally invasive adenocarcinoma, and invasive pulmonary adenocarcinoma--analysis of interobserver agreement, survival, radiographic characteristics, and gross pathology in 296 nodules.

Mariza de Andrade, Ping Yang, Jason A Wampfler, 2016, Human pathology.

Random‐effects Cox proportional hazards model: General variance components methods for time‐to‐event data

Terry M Therneau, Mariza de Andrade, V Shane Pankratz, 2005, Genetic epidemiology.

Leukocyte DNA Methylation Signature Differentiates Pancreatic Cancer Patients from Healthy Controls

Mariza de Andrade, Hui Tang, Ann L. Oberg, 2011, PloS one.

For Personal Use. Mass Reproduce Only with Permission from Mayo Clinic Proceedings a . Original Article Mayo Genome Consortia: a Genotype-phenotype Resource for Genome-wide Association Studies with an Application to the Analysis of Circulating Bilirubin Levels

Christopher G Chute, Jyotishman Pathak, Hugues Sicotte, 2022 .

Genome-wide association study of familial lung cancer

Paul Brennan, Mariza de Andrade, Maria Teresa Landi, 2018, Carcinogenesis.

Survival patterns after oophorectomy in premenopausal women: a population-based cohort study.

Mariza de Andrade, L. Melton, L. Melton, 2006, The Lancet. Oncology.

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function.

Sylvia Stracke, Christian Gieger, Alex Doney, 2012, Human molecular genetics.

Human brain derived neurotrophic factor (BDNF) genes, splicing patterns, and assessments of associations with substance abuse and Parkinson's Disease

Mariza de Andrade, Tomas Drgon, Demetrius M Maraganore, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The Prevalence of BRCA2 Mutations in Familial Pancreatic Cancer

Mariza de Andrade, Michael Goggins, Ralph H. Hruban, 2007, Cancer Epidemiology Biomarkers & Prevention.

Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.

Aldo Quattrone, Nobutaka Hattori, Mariza de Andrade, 2006, JAMA.

Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci

Gerard Tromp, Marylyn D. Ritchie, Dana C. Crawford, 2017, Circulation research.