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Author Details

Mariza de Andrade
Mayo Clinic
1991
330
74
PMIDPaper TitleJournal TitlePublished Year
36639314Corrigendum to: "An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs" [J Hepatol 75 (2021) 572-581].J Hepatol2023
37968452Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.Sci Rep2023
37898691Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.Sci Rep2023
37348055Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.Genetics2023
37196047Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.PLoS One2023
37126548The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.Sci Adv2023
37046083Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.Nature2023
36960714Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.Circ Genom Precis Med2023
36778406Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.bioRxiv2023
36639314Corrigendum to: "An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs" [J Hepatol 75 (2021) 572-581].J Hepatol2023
37898691Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.Sci Rep2023
37968452Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.Sci Rep2023
37348055Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.Genetics2023
37046083Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.Nature2023
37196047Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.PLoS One2023
37126548The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.Sci Adv2023
36960714Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.Circ Genom Precis Med2023
36778406Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.bioRxiv2023
35915169Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer.Nat Genet2022
35927319Rare genetic variants explain missing heritability in smoking.Nat Hum Behav2022
35915169Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer.Nat Genet2022
35592775The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.Front Endocrinol (Lausanne)2022
35385311Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.Sci Adv2022
36568030Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants.HGG Adv2022
36477530Genetic diversity fuels gene discovery for tobacco and alcohol use.Nature2022
36154123Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.Circulation2022
35592775The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.Front Endocrinol (Lausanne)2022
35385311Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.Sci Adv2022
36477530Genetic diversity fuels gene discovery for tobacco and alcohol use.Nature2022
36568030Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants.HGG Adv2022
35927319Rare genetic variants explain missing heritability in smoking.Nat Hum Behav2022
36154123Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.Circulation2022
34282949Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry.Circ Genom Precis Med2021
33720349Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries.Genetics2021
33594163Rare deleterious germline variants and risk of lung cancer.NPJ Precis Oncol2021
34282949Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry.Circ Genom Precis Med2021
34125579Outcomes of COVID-19 in Patients With Cancer: A Closer Look at Pre-Emptive Routine Screening Strategies.JCO Oncol Pract2021
33853833Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer.Cancer Res2021
33720349Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries.Genetics2021
33853833Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer.Cancer Res2021
33594163Rare deleterious germline variants and risk of lung cancer.NPJ Precis Oncol2021
34125579Outcomes of COVID-19 in Patients With Cancer: A Closer Look at Pre-Emptive Routine Screening Strategies.JCO Oncol Pract2021
32374294Bivariate traits association analysis using generalized estimating equations in family data.Stat Appl Genet Mol Biol2020
32952248COVID-19 pandemic and pediatric dentistry: Fear, eating habits and parent's oral health perceptions.Child Youth Serv Rev2020
32374345Identification of Susceptibility Loci for Spontaneous Coronary Artery Dissection.JAMA Cardiol2020
32374294Bivariate traits association analysis using generalized estimating equations in family data.Stat Appl Genet Mol Biol2020
32300485A Digital Health Weight Loss Program in 250,000 Individuals.J Obes2020
32180992A digital health weight-loss intervention in severe obesity.Digit Health2020
31826912Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q.Cancer Epidemiol Biomarkers Prev2020
31826912Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q.Cancer Epidemiol Biomarkers Prev2020
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Collaborators

Baylor College of Medicine
Co-authored papers 44
Mayo Clinic
Co-authored papers 41
Baylor College of Medicine
Co-authored papers 40
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Co-authored papers 36
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Co-authored papers 33
School of Public Health, University of Michigan ann arbor
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Co-authored papers 28
University of Washington Medical Center
Co-authored papers 26
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 26
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Co-authored papers 22
University of Michigan School of Public Health ann arbor
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University of Washington Medical Center
Co-authored papers 21
Mayo Clinic
Co-authored papers 21
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Co-authored papers 18
Harvard Medical School, Harvard University
Co-authored papers 18
Vanderbilt University
Co-authored papers 18
Co-authored papers 17
Co-authored papers 17
Kaiser Permanente Washington Health Research Institute
Co-authored papers 17
University of Washington
Co-authored papers 16
Co-authored papers 16
Co-authored papers 15
Erasmus University Medical Center
Co-authored papers 15
Mayo Clinic
Co-authored papers 15
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Co-authored papers 15
Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers 15
Harvard T.H. Chan School of Public Health
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University of Minnesota Medical School, 1035 University Drive duluth
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