Mariza de Andrade
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Brazilian-American biostatistician
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Mariza de Andrademathematics Degrees
Mathematics
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Applied Mathematics
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#409
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Statistics
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Measure Theory
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Mathematics
Mariza de Andrade's Degrees
- Bachelors Statistics University of São Paulo
- PhD Biostatistics Stanford University
Why Is Mariza de Andrade Influential?
(Suggest an Edit or Addition)According to Wikipedia, Mariza de Andrade is a Brazilian-American biostatistician who works as a professor of biostatistics at the Mayo Clinic, and is known for her work on statistical genetics and precision medicine. Early life De Andrade earned a bachelor's degree in mathematics from the Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto in São Paulo and a master's degree in statistics at the Instituto Nacional de Matemática Pura e Aplicada in Rio de Janeiro. She moved to the University of Washington for additional graduate study, earning a second master's degree and Ph.D. in biostatistics there. Her 1990 dissertation, Estimation of the Genotypic Parameters under Non- Normal Models, was supervised by Elizabeth A. Thompson.
Mariza de Andrade's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) (1567)
- GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) (803)
- Increased risk of cognitive impairment or dementia in women who underwent oophorectomy before menopause (2007) (660)
- Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X. (2005) (571)
- High-resolution whole-genome association study of Parkinson disease. (2005) (535)
- Detectable clonal mosaicism from birth to old age and its relationship to cancer (2012) (514)
- Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease. (2006) (505)
- Survival patterns after oophorectomy in premenopausal women: a population-based cohort study. (2006) (488)
- Probability of pancreatic cancer following diabetes: a population-based study. (2005) (472)
- Pancreatic cancer-associated diabetes mellitus: prevalence and temporal association with diagnosis of cancer. (2008) (427)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- A Genomic Pathway Approach to a Complex Disease: Axon Guidance and Parkinson Disease (2007) (367)
- Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation. (2008) (310)
- Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy. (2009) (294)
- A major lung cancer susceptibility locus maps to chromosome 6q23-25. (2004) (292)
- Increased risk of parkinsonism in women who underwent oophorectomy before menopause (2008) (291)
- Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction (2011) (286)
- PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study (2017) (283)
- The Prevalence of BRCA2 Mutations in Familial Pancreatic Cancer (2007) (281)
- Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies. (2011) (248)
- Mitochondrial DNA content: its genetic heritability and association with renal cell carcinoma. (2008) (240)
- International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways (2015) (233)
- Human brain derived neurotrophic factor (BDNF) genes, splicing patterns, and assessments of associations with substance abuse and Parkinson's Disease (2005) (229)
- Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms. (1991) (225)
- Genetic variants and risk of lung cancer in never smokers: a genome-wide association study. (2010) (224)
- Recovery of trait heritability from whole genome sequence data (2019) (223)
- Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism. (2015) (216)
- CUBN is a gene locus for albuminuria. (2011) (214)
- Inherited Causes of Clonal Hematopoiesis in 97,691 TOPMed Whole Genomes (2020) (184)
- Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function (2012) (180)
- Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease (2016) (179)
- UCHL1 is a Parkinson's disease susceptibility gene (2004) (173)
- alpha-Synuclein gene haplotypes are associated with Parkinson's disease. (2001) (164)
- Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer. (2008) (157)
- Long-term risk of depressive and anxiety symptoms after early bilateral oophorectomy (2008) (153)
- Adrenomedullin is up-regulated in patients with pancreatic cancer and causes insulin resistance in β cells and mice. (2012) (143)
- Germ line Fanconi anemia complementation group C mutations and pancreatic cancer. (2005) (143)
- Alpha1-antitrypsin deficiency carriers, tobacco smoke, chronic obstructive pulmonary disease, and lung cancer risk. (2008) (140)
- Multiethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI (2015) (139)
- Pancreatic Cancer Genetic Epidemiology Consortium (2006) (138)
- Parkin variants in North American Parkinson's disease: Cases and controls (2003) (136)
- A genome‐wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q (2012) (136)
- Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci (2017) (135)
- Imputation and quality control steps for combining multiple genome-wide datasets (2014) (130)
- Familial segregation of venous thromboembolism (2004) (129)
- Increased prevalence of antimitochondrial antibodies in first‐degree relatives of patients with primary biliary cirrhosis (2007) (128)
- Heritability of Leukoaraiosis in Hypertensive Sibships (2004) (124)
- Random‐effects Cox proportional hazards model: General variance components methods for time‐to‐event data (2005) (121)
- Polymorphisms in DNA repair genes, smoking, and pancreatic adenocarcinoma risk. (2008) (121)
- Education and occupations preceding Parkinson disease (2005) (118)
- Genetic Association for Renal Traits among Participants of African Ancestry Reveals New Loci for Renal Function (2011) (117)
- Genome-wide association study of kidney function decline in individuals of European descent (2014) (114)
- Relationship of the apolipoprotein E polymorphism with carotid artery atherosclerosis. (1995) (111)
- Glutathione pathway genes and lung cancer risk in young and old populations. (2004) (108)
- Genomic and Transcriptomic Association Studies Identify 16 Novel Susceptibility Loci for Venous Thromboembolism. (2019) (107)
- Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection. (2019) (106)
- Comparison of Multivariate Tests for Genetic Linkage (2001) (101)
- EGFR-T790M is a rare lung cancer susceptibility allele with enhanced kinase activity. (2007) (99)
- Heritability of cardiovascular risk factors in a Brazilian population: Baependi Heart Study (2008) (97)
- Fine Mapping of Chromosome 6q23-25 Region in Familial Lung Cancer Families Reveals RGS17 as a Likely Candidate Gene (2009) (96)
- Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale (2020) (93)
- Characterization of large structural genetic mosaicism in human autosomes. (2015) (91)
- Genetics of cardiovascular disease: Importance of sex and ethnicity. (2015) (89)
- Chemical exposures and Parkinson's disease: A population‐based case–control study (2006) (89)
- Homozygosity Mapping and Exome Sequencing Reveal GATAD1 Mutation in Autosomal Recessive Dilated Cardiomyopathy (2011) (88)
- Fine mapping of the alpha-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees. (2003) (84)
- Alopecia areata in families: association with the HLA locus. (1999) (84)
- Effect of Emphysema on Lung Cancer Risk in Smokers: A Computed Tomography–Based Assessment (2010) (83)
- Mitochondrial Genetic Polymorphisms and Pancreatic Cancer Risk (2007) (83)
- Heritability of Longitudinal Measures of Body Mass Index and Lipid and Lipoprotein Levels in Aging Twins (2007) (83)
- Risk of malignancy in first‐degree relatives of patients with pancreatic carcinoma (2005) (82)
- Leukocyte DNA Methylation Signature Differentiates Pancreatic Cancer Patients from Healthy Controls (2011) (82)
- Obesity adversely affects survival in pancreatic cancer patients (2010) (81)
- Men transmit MS more often to their children vs women (2006) (80)
- Irritable bowel syndrome aggregates strongly in families: a family‐based case‐control study (2008) (80)
- Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease (2017) (78)
- Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits. (2019) (77)
- Genetic regulation of the capacity to make immunoglobulin G to pneumococcal capsular polysaccharides. (1997) (75)
- Association of APOE polymorphisms with disease severity in MS is limited to women (2004) (73)
- Mutagen sensitivity has high heritability: evidence from a twin study. (2006) (72)
- Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality (2011) (71)
- Segregation analysis of cancer in families of glioma patients (2001) (69)
- Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2021) (68)
- Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. (2012) (67)
- Genetic variation within the anticoagulant, procoagulant, fibrinolytic and innate immunity pathways as risk factors for venous thromboembolism (2011) (66)
- Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes (2019) (66)
- Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. (2011) (64)
- Elevated amyloid beta protein (Abeta42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator gene. (2005) (63)
- Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndrome (2015) (62)
- Immune Cell Infiltration May Be a Key Determinant of Long-Term Survival in Small Cell Lung Cancer. (2019) (60)
- Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data (2022) (60)
- Genetic variation associated with circulating monocyte count in the eMERGE Network. (2013) (59)
- Segregation analysis of idiopathic talipes equinovarus in a Texan population. (1998) (57)
- A genetic association study of 5‐HTT LPR and GNβ3 C825T polymorphisms with irritable bowel syndrome (2007) (57)
- The endothelial protein C receptor (PROCR) Ser219Gly variant and risk of common thrombotic disorders: a HuGE review and meta-analysis of evidence from observational studies. (2012) (57)
- Cerebral small vessel disease genomics and its implications across the lifespan (2020) (56)
- Cystic fibrosis transmembrane regulator gene carrier status is a risk factor for young onset pancreatic adenocarcinoma (2005) (56)
- A recurrent mutation in PARK2 is associated with familial lung cancer. (2015) (54)
- Genetic variation in the HLA region is associated with susceptibility to herpes zoster (2014) (53)
- A susceptibility locus on chromosome 6q greatly increases lung cancer risk among light and never smokers. (2010) (52)
- A genome-wide linkage scan for ankle-brachial index in African American and non-Hispanic white subjects participating in the GENOA study. (2006) (51)
- Mutagen Sensitivity and Genetic Variants in Nucleotide Excision Repair Pathway: Genotype-Phenotype Correlation (2007) (50)
- The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype (2018) (48)
- Haplotype and cell proliferation analyses of candidate lung cancer susceptibility genes on chromosome 15q24-25.1. (2009) (48)
- Extension of variance components approach to incorporate temporal trends and longitudinal pedigree data analysis (2002) (48)
- Genetic linkage methods for quantitative traits (2001) (47)
- Clinical outcomes and changes in lung function after segmentectomy versus lobectomy for lung cancer cases. (2014) (47)
- Allelic associations of two polymorphic microsatellites in intron 40 of the human von Willebrand factor gene. (1994) (47)
- Interaction of α‐synuclein and tau genotypes in Parkinson's disease (2005) (46)
- Genomic Susceptibility Loci for Brain Atrophy in Hypertensive Sibships From the GENOA Study (2005) (46)
- Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study (2017) (45)
- Nucleotide Excision Repair Pathway Polymorphisms and Pancreatic Cancer Risk: Evidence for role of MMS19L (2009) (45)
- Comparison of model‐free linkage mapping strategies for the study of a complex trait (1997) (45)
- Thrombomodulin gene polymorphisms or haplotypes as potential risk factors for venous thromboembolism: a population‐based case–control study (2005) (44)
- The genetics of alopecia areata. (2001) (44)
- P-selectin and subclinical and clinical atherosclerosis: the Multi-Ethnic Study of Atherosclerosis (MESA). (2015) (44)
- Genetic Variants That Confer Resistance to Malaria Are Associated with Red Blood Cell Traits in African-Americans: An Electronic Medical Record-based Genome-Wide Association Study (2013) (42)
- Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network (2015) (42)
- The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study (2014) (42)
- Influence of genomic loci on measures of chronic kidney disease in hypertensive sibships. (2006) (42)
- Multiple-level validation identifies PARK2 in the development of lung cancer and chronic obstructive pulmonary disease (2016) (41)
- Alpha1-antitrypsin and neutrophil elastase imbalance and lung cancer risk. (2005) (41)
- Environmental tobacco smoke exposure in women with lung cancer. (2004) (40)
- Genome-wide association study of familial lung cancer (2018) (40)
- Two Major QTLs and Several Others Relate to Factors of Metabolic Syndrome in the Family Blood Pressure Program (2005) (40)
- Methods to estimate genetic components of variance for quantitative traits in family studies (1999) (40)
- &agr;-Synuclein, pesticides, and Parkinson disease: A case–control studySYMBOL (2008) (40)
- Reliability of self-reported ancestry among siblings: implications for genetic association studies. (2006) (39)
- Major histocompatibility complex class I chain-related gene A polymorphisms and extended haplotypes are associated with familial alopecia areata. (2006) (38)
- Assessment of genotype imputation methods (2009) (38)
- Reduced coffee consumption among individuals with primary sclerosing cholangitis but not primary biliary cirrhosis. (2014) (38)
- Identification of a novel tumor suppressor gene p34 on human chromosome 6q25.1. (2007) (38)
- Assessing linkage on chromosome 5 using components of variance approach: Univariate versus multivariate (1997) (37)
- A Rigorous and Comprehensive Validation: Common Genetic Variations and Lung Cancer (2010) (37)
- Coffee, caffeine‐related genes, and Parkinson's disease: A case–control study (2008) (36)
- TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy. (2014) (36)
- Interleukin-1 receptor antagonist allele 2 and familial alopecia areata. (2002) (36)
- Human leukocyte antigen class II alleles are associated with risk of alopecia areata. (2008) (36)
- Genetic Variants Associated with Serum Thyroid Stimulating Hormone (TSH) Levels in European Americans and African Americans from the eMERGE Network (2014) (35)
- Interferon gamma allelic variants: sex-biased multiple sclerosis susceptibility and gene expression. (2008) (35)
- Identification of genes and haplotypes that predict rheumatoid arthritis using random forests (2009) (35)
- Long-Term Survival and Prognostic Indicators in Small (≤2 cm) Pancreatic Cancer (2008) (35)
- Common variants in Mendelian kidney disease genes and their association with renal function. (2013) (35)
- Complex interactions in Parkinson's disease: A two‐phased approach (2003) (34)
- Genomic susceptibility Loci for brain atrophy, ventricular volume, and leukoaraiosis in hypertensive sibships. (2009) (33)
- Adenocarcinoma in situ, minimally invasive adenocarcinoma, and invasive pulmonary adenocarcinoma--analysis of interobserver agreement, survival, radiographic characteristics, and gross pathology in 296 nodules. (2016) (32)
- Genetic polymorphisms associated with carotid artery intima-media thickness and coronary artery calcification in women of the Kronos Early Estrogen Prevention Study. (2013) (32)
- Identification of Susceptibility Loci for Spontaneous Coronary Artery Dissection. (2020) (32)
- A genetic association study of 5-HTT LPR and GNbeta3 C825T polymorphisms with irritable bowel syndrome. (2007) (30)
- Sex‐Specific Genetic Variants are Associated With Coronary Endothelial Dysfunction (2016) (30)
- Cumulative Effect of Multiple Loci on Genetic Susceptibility to Familial Lung Cancer (2010) (30)
- eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants (2016) (29)
- Ascertainment issues in variance components models. (2000) (29)
- Alpha-synuclein, alcohol use disorders, and Parkinson disease: a case-control study. (2009) (28)
- Genome-wide study of resistant hypertension identified from electronic health records (2017) (28)
- Pleiotropic genetic effects contribute to the correlation between HDL cholesterol, triglycerides, and LDL particle size in hypertensive sibships. (2005) (28)
- Linkage analysis of chromosome 4 in families with familial pancreatic cancer (2007) (28)
- Genetic variations and patient-reported quality of life among patients with lung cancer. (2012) (27)
- Interaction of alpha-synuclein and tau genotypes in Parkinson's disease. (2005) (27)
- Ascertainment issues in variance components models (2000) (27)
- Association between SLC2A9 transporter gene variants and uric acid phenotypes in African American and white families. (2011) (27)
- Single nucleotide polymorphisms associated with abnormal coronary microvascular function (2014) (27)
- The foundation of precision medicine: integration of electronic health records with genomics through basic, clinical, and translational research (2015) (26)
- Association of Breast Cancer Susceptibility Variants with Risk of Pancreatic Cancer (2009) (26)
- Genetic Variants Associated with the Risk of Chronic Obstructive Pulmonary Disease with and without Lung Cancer (2011) (26)
- Cohort profile: the Baependi Heart Study—a family-based, highly admixed cohort study in a rural Brazilian town (2016) (26)
- An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs (2021) (26)
- An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs (2021) (26)
- Influence of SULT1A1 genetic variation on age at menopause, estrogen levels, and response to hormone therapy in recently postmenopausal white women (2016) (26)
- Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (26)
- Genomic Loci with Pleiotropic Effects on Coronary Artery Calcification in Hypertensive Sibships (2004) (25)
- Novel Genomic Loci Influencing Plasma Homocysteine Levels (2006) (25)
- Heritability of physical activity traits in Brazilian families: the Baependi Heart Study (2011) (25)
- Identification of unique venous thromboembolism-susceptibility variants in African-Americans (2017) (24)
- Association of Mitotic Regulation Pathway Polymorphisms with Pancreatic Cancer Risk and Outcome (2010) (23)
- Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes (2019) (23)
- Pharmacogenomics of estrogens on changes in carotid artery intima-medial thickness and coronary arterial calcification: Kronos Early Estrogen Prevention Study. (2016) (23)
- Polygenic Overlap Between Kidney Function and Large Artery Atherosclerotic Stroke (2014) (23)
- Focused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung Cancer (2016) (23)
- A limited role for DJ1 in Parkinson disease susceptibility (2004) (22)
- Alpha-1-antitrypsin deficiency and smoking as risk factors for mismatch repair deficient colorectal cancer: a study from the colon cancer family registry. (2010) (22)
- A novel quantitative trait locus on chromosome 1 with pleiotropic effects on HDL-cholesterol and LDL particle size in hypertensive sibships. (2005) (22)
- Intraclass and interclass correlations of allele sizes within and between loci in DNA typing data. (1993) (21)
- Taller height as a risk factor for venous thromboembolism: a Mendelian randomization meta‐analysis (2017) (21)
- Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2020) (21)
- Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms (2016) (20)
- A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR (2019) (19)
- Linkage disequilibria among (CA)n polymorphisms in the human dystrophin gene and their implications in carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophies. (1994) (19)
- The challenge of detecting epistasis (G×G Interactions): Genetic Analysis Workshop 16 (2009) (19)
- Complex segregation analysis of facial clefting in Chile. (1997) (19)
- Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network (2015) (19)
- Hepatocyte growth factor demonstrates racial heterogeneity as a biomarker for coronary heart disease (2017) (19)
- Enhancing the Power of Genetic Association Studies through the Use of Silver Standard Cases Derived from Electronic Medical Records (2013) (19)
- Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll Region. (2019) (19)
- Familial Lung Cancer: A Brief History from the Earliest Work to the Most Recent Studies (2017) (19)
- Identification of gene-gene interaction using principal components (2009) (19)
- Genetic analyses of smoking initiation, persistence, quantity, and age-at-onset of regular cigarette use in Brazilian families: the Baependi Heart Study (2012) (18)
- NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality. (2017) (18)
- Genetic diversity fuels gene discovery for tobacco and alcohol use (2022) (18)
- Genome sequencing unveils a regulatory landscape of platelet reactivity (2019) (18)
- Clinical Features of Bronchioloalveolar Carcinoma with New Histologic and Staging Definitions (2010) (18)
- Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential (2022) (17)
- Association of family history of specific cancers with a younger age of onset of pancreatic adenocarcinoma. (2006) (17)
- Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer (2018) (16)
- Long-term risk of depressive and anxiety symptoms after early bilateral oophorectomy (2018) (16)
- Mitochondrial Genetic Polymorphisms Do Not Predict Survival in Patients with Pancreatic Cancer (2008) (15)
- Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed (2022) (15)
- Perceptions of lung cancer risk and beliefs in screening accuracy of spiral computed tomography among high-risk lung cancer family members. (2010) (15)
- A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program (2021) (15)
- Case‐control study of the α‐synuclein interacting protein gene and Parkinson's disease (2003) (15)
- SLCO1B1 genetic variation and hormone therapy in menopausal women (2018) (15)
- Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records (2014) (15)
- Group 6: Pleiotropy and multivariate analysis (2003) (14)
- CCR5Delta32 polymorphism effects on CCR5 expression, patterns of immunopathology and disease course in multiple sclerosis. (2005) (13)
- Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans (2005) (13)
- Assessing linkage of monoamine oxidase B in a genome‐wide scan using a univariate variance components approach (1999) (12)
- Entropy Based Genetic Association Tests and Gene-Gene Interaction Tests (2011) (12)
- Practical Application of Residuals from Survival Models in Quantitative Trait Linkage Analysis (2001) (12)
- Case-control study of the alpha-synuclein interacting protein gene and Parkinson's disease. (2003) (11)
- Identification of genes involved in alcohol consumption and cigarettes smoking (2005) (11)
- Evaluating gene by sex and age interactions on cardiovascular risk factors in Brazilian families (2010) (10)
- Polymorphic Variants in Hereditary Pancreatic Cancer Genes Are Not Associated with Pancreatic Cancer Risk (2009) (10)
- Impact of adiposity on cellular adhesion: The Multi‐Ethnic Study of atherosclerosis (MESA) (2016) (10)
- A Digital Health Weight Loss Program in 250,000 Individuals (2020) (10)
- EGFR mediates activation of RET in lung adenocarcinoma with neuroendocrine differentiation characterized by ASCL1 expression (2017) (10)
- A digital health weight-loss intervention in severe obesity (2020) (10)
- Comparison of tagging single-nucleotide polymorphism methods in association analyses (2007) (10)
- Ordered Subset Analysis Identifies Loci Influencing Lung Cancer Risk on Chromosomes 6q and 12q (2010) (9)
- The Mayo Clinic Cohort Study of Personality and Aging: Design and Sampling, Reliability and Validity of Instruments, and Baseline Description (2006) (9)
- Linkage analysis of obesity phenotypes in pre- and post-menopausal women from a United States mid-western population (2010) (9)
- Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci (2007) (9)
- Genome-Wide Association Study of Peripheral Artery Disease (2021) (9)
- Plasma and serum L-selectin and clinical and subclinical cardiovascular disease: the Multi-Ethnic Study of Atherosclerosis (MESA). (2014) (9)
- Analysis of variation in NF-κB genes and expression levels of NF-κB-regulated molecules (2007) (8)
- Quantitative trait loci influencing low density lipoprotein particle size in African Americans Published, JLR Papers in Press, April 19, 2006. (2006) (8)
- A genome‐wide search for susceptibility genes linked to alcohol dependence (1999) (8)
- A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program (2020) (8)
- Rare deleterious germline variants and risk of lung cancer (2021) (8)
- Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q (2019) (7)
- An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels (2018) (7)
- The impact of population admixture on traditional linkage analysis. (2001) (7)
- Parametric Linkage Analysis Identifies Five Novel Genome-Wide Significant Loci for Familial Lung Cancer (2017) (7)
- An Efficient Test for Gene-Environment Interaction in Generalized Linear Mixed Models with Family Data (2017) (6)
- Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer (2022) (6)
- Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children with asthma. (2019) (6)
- Evaluating the Influence of Quality Control Decisions and Software Algorithms on SNP Calling for the Affymetrix 6.0 SNP Array Platform (2011) (6)
- External validation of the United Kingdom‐primary biliary cholangitis risk scores of patients with primary biliary cholangitis treated with ursodeoxycholic acid (2018) (5)
- Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry (2021) (5)
- Genetic Analysis of Age-at-Onset for Cardiovascular Risk Factors in a Brazilian Family Study (2009) (5)
- A second genetic variant on chromosome 15q24-25.1 associates with lung cancer. (2010) (5)
- Global Individual Ancestry Using Principal Components for Family Data (2015) (5)
- Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors (2022) (5)
- Using Item Response Theory to Model Multiple Phenotypes and Their Joint Heritability in Family Data (2014) (5)
- Missing phenotype data imputation in pedigree data analysis (2008) (4)
- Outcomes of COVID-19 in Patients With Cancer: A Closer Look at Pre-Emptive Routine Screening Strategies. (2021) (4)
- α-Synuclein, pesticides, and Parkinson disease (2008) (4)
- Estimation of quantitative genetic parameters under non-normal models. (1995) (4)
- Rare genetic variants explain missing heritability in smoking (2022) (4)
- Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies (2022) (4)
- Clinical Correlates of Autosomal Chromosomal Abnormalities in an Electronic Medical Record–Linked Genome-Wide Association Study (2013) (4)
- Clinical Correlates of Autosomal Chromosomal Abnormalities in an Electronic Medical Record–Linked Genome-Wide Association Study (2013) (3)
- Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries (2020) (3)
- Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals (2022) (3)
- Admixture effects in the traditional linkage analysis of admixed families. (2002) (3)
- Association of TNFSF8 polymorphisms with peripheral neutrophil count. (2011) (3)
- Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer (2021) (2)
- Identification of Genetic Interaction with Risk Factors Using a Time-To-Event Model (2017) (2)
- Linkage analysis using principal components of gene expression data (2007) (2)
- The association of copy number variation and percent mammographic density (2015) (2)
- Bayesian Variable Selection in Multilevel Item Response Theory Models with Application in Genomics (2016) (2)
- GAW20: methods and strategies for the new frontiers of epigenetics and pharmacogenomics (2018) (2)
- Using the theory of added-variable plot for linear mixed models to decompose genetic effects in family data (2014) (2)
- Summary of contributions to GAW15 Group 13: candidate gene association studies (2007) (2)
- The genetics of gene expression: comparison of linkage scans using two phenotype normalization methods (2007) (2)
- The challenge of detecting genotype-by-methylation interaction: GAW20 (2018) (1)
- SNP interaction detection with Random Forests in high-dimensional genetic data (2012) (1)
- A Comparison of Software Packages that Assess Linkage Using a Variance Components Approach (2001) (1)
- Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program (2021) (1)
- Genome scans for genetic predisposition to alcoholism by use of transmission disequilibrium test analyses (1999) (1)
- Summary of contributions to GAW Group 12: Multivariate Methods (2005) (1)
- Comparison of variable and model selection methods for genetic association studies using the GAW15 simulated data (2007) (1)
- Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (1)
- Age-related DNA methylation and hemostatic factors. (2018) (1)
- eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants (2016) (0)
- Abstract 1452: Analyses of whole exome sequencing (WES) data of hereditary lung cancer families identify germline copy number variations (CNVs) in multiple genes (2022) (0)
- Multi-ancestry Genome- and Phenome-wide Association Studies of Diverticular Disease in Electronic Health Records with Natural Language Processing enriched phenotype algorithm (2020) (0)
- High-quality basic care and support needed in lung cancer survivors. (2012) (0)
- Deep-coverage whole genome sequences and blood lipids among 16,324 individuals (2018) (0)
- The challenge of detecting genotype-by-methylation interaction: GAW20 (2018) (0)
- Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2021) (0)
- Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program (2023) (0)
- OCCUPATIONAL EXPOSURES AND PARKINSON’S DISEASE: A POPULATION-BASED, CASE-CONTROL STUDY (2004) (0)
- Bivariate traits association analysis using generalized estimating equations in family data (2020) (0)
- The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations (2022) (0)
- Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network (2011) (0)
- A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects (2013) (0)
- Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581] (2021) (0)
- Effect of a Weight Loss Digital Health Platform on Metabolic Syndrome: A 6-Month Prospective Study in China (Preprint) (2020) (0)
- Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndrome (2015) (0)
- Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale (2020) (0)
- Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis (2023) (0)
- Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study (2017) (0)
- Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants (2023) (0)
- A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR (2019) (0)
- Clonal haematopoiesis and risk of chronic liver disease (2023) (0)
- Correction to: Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study (2018) (0)
- The genetic determinants of recurrent somatic mutations in 43,693 blood genomes (2023) (0)
- Multi-ethnic analysis reveals soluble l-selectin may be post-transcriptionally regulated by 3′UTR polymorphism: the Multi-Ethnic Study of Atherosclerosis (MESA) (2015) (0)
- Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium (2021) (0)
- Corrigendum to: "An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs" [J Hepatol 75 (2021) 572-581]. (2023) (0)
- Statistical models for analysis of cytogenetic biomarkers. (2000) (0)
- Variant-specific inflation factors for assessing population stratification at the phenotypic variance level (2021) (0)
- N-ACETYLTRANSFERASE 2 IS A SUSCEPTIBILITY LOCUS FOR PARKINSON'S DISEASE (2004) (0)
- Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants (2022) (0)
- Correction to: Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study (2018) (0)
- The association of copy number variation and percent mammographic density (2015) (0)
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