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Lista de obras de Mariza de Andrade

179 Clinical Characteristics of Familial Irritable Bowel Syndrome (IBS) Differ from Sporadic IBS

630 Coffee Consumption Is Associated With Reduced Risk of Primary Sclerosing Cholangitis but Not Primary Biliary Cirrhosis

article by Craig Lammert et al published May 2013 in Gastroenterology

643 Temporal Association of Changes in Fasting Blood Glucose and Body Mass Index to Diagnosis of Pancreatic Cancer

A Digital Health Weight Loss Program in 250,000 Individuals

scientific article published on 26 March 2020

A NOVEL GENOMIC SUSCEPTIBILITY LOCUS FOR PERIPHERAL ARTERIAL DISEASE ON CHROMOSOME 12

A Robust e-Epidemiology Tool in Phenotyping Heart Failure with Differentiation for Preserved and Reduced Ejection Fraction: the Electronic Medical Records and Genomics (eMERGE) Network

artículo científico publicado en 2015

A comparison of software packages that assess linkage using a variance components approach

artículo científico publicado en 2001

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

artículo científico publicado en 2015

A comprehensive assessment of environmental exposures among 1000 North American patients with primary sclerosing cholangitis, with and without inflammatory bowel disease.

artículo científico publicado en 2015

A digital health weight-loss intervention in severe obesity

artículo científico publicado en 2020

A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects

artículo científico publicado en 2013

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

artículo científico publicado en 2012

A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium

scientific article published on 05 May 2013

A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33

artículo científico publicado en 2010

A genome-wide linkage scan for ankle-brachial index in African American and non-Hispanic white subjects participating in the GENOA study

artículo científico publicado en 2005

A genomic pathway approach to a complex disease: axon guidance and Parkinson disease

artículo científico publicado en 2007

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

artículo científico publicado en 2021

A new statistic for identifying batch effects in high-throughput genomic data that uses guided principal component analysis

artículo científico publicado en 2013

A novel quantitative trait locus on chromosome 1 with pleiotropic effects on HDL-cholesterol and LDL particle size in hypertensive sibships

artículo científico publicado en 2005

A phenome-wide association study to discover pleiotropic effects of , , and

A recurrent mutation in PARK2 is associated with familial lung cancer

artículo científico publicado en 2015

A rigorous and comprehensive validation: common genetic variations and lung cancer

artículo científico publicado en 2010

A second genetic variant on chromosome 15q24-25.1 associates with lung cancer

artículo científico publicado en 2010

Abstract 2757: Evaluation ofEYA4as a candidate risk locus in familial lung cancer families linked to 6q

Abstract LB-189: Genetic Epidemiology of Lung Cancer Consortium: genome-wide association study of familial lung cancer cases:

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

artículo científico publicado en 2015

Adjusting for HLA-DRbeta1 in a genome-wide association analysis of rheumatoid arthritis and related biomarkers

artículo científico publicado en 2009

Adrenomedullin is up-regulated in patients with pancreatic cancer and causes insulin resistance in β cells and mice

artículo científico publicado en 2012

Age-related DNA methylation and hemostatic factors

artículo científico publicado en 2018

Alopecia Areata in Families: Association with the HLA Locus

artículo científico publicado en 1999

Alopecia Areata is associated with MICA and an extended HLA haplotype

Alpha-1-antitrypsin deficiency and smoking as risk factors for mismatch repair deficient colorectal cancer: a study from the colon cancer family registry

artículo científico publicado en 2009

Alpha-synuclein, alcohol use disorders, and Parkinson disease: a case-control study

artículo científico publicado en 2009

Alpha1-antitrypsin and neutrophil elastase imbalance and lung cancer risk

artículo científico publicado en 2005

Alpha1-antitrypsin deficiency carriers, tobacco smoke, chronic obstructive pulmonary disease, and lung cancer risk

artículo científico publicado en 2008

An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs

artículo científico publicado en 2021

Analysis of aromatic DNA adducts and 7,8-dihydro-8-oxo- 2′-deoxyguanosine in lymphocyte DNA from a case–control study of lung cancer involving minority populations

artículo científico publicado en 2000

Analysis of aromatic DNA adducts and 7,8-dihydro-8-oxo- 2′-deoxyguanosine in lymphocyte DNA from a case–control study of lung cancer involving minority populations

article published in 2000

Analysis of aromatic DNA adducts and 7,8-dihydro-8-oxo-2? deoxyguanosine in lymphocyte DNA from a case-control study of lung cancer involving minority populations

artículo científico publicado en 2000

Analysis of variation in NF-kappaB genes and expression levels of NF-kappaB-regulated molecules

artículo científico publicado en 2007

Ascertainment issues in variance components models

Ascertainment issues in variance components models

artículo científico publicado en 2000

Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study.

artículo científico publicado en 2017

Assessment of genotype imputation methods

artículo científico publicado en 2009

Association between SLC2A9 transporter gene variants and uric acid phenotypes in African American and white families ⬇️

artículo científico publicado el 24 de diciembre de 2010

Association of APOE polymorphisms with disease severity in MS is limited to women.

artículo científico publicado en 2004

Association of TNFSF8 polymorphisms with peripheral neutrophil count

artículo científico publicado en 2011

Association of breast cancer susceptibility variants with risk of pancreatic cancer

artículo científico publicado en 2009

Association of family history of specific cancers with a younger age of onset of pancreatic adenocarcinoma

artículo científico publicado en 2006

Association of mitotic regulation pathway polymorphisms with pancreatic cancer risk and outcome

artículo científico publicado en 2010

Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection

artículo científico publicado en 2019

Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry

artículo científico publicado en 2021

Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

article

Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel

scientific article published on 20 March 2019

Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation.

artículo científico publicado en 2008

Autosomal mutations affecting Y chromosome loops in Drosophila melanogaster

artículo científico publicado en 2008

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

artículo científico publicado en 2016

Beta-synuclein gene variants and Parkinson's disease: a preliminary case-control study

artículo científico publicado en 2007

Biochemical response to ursodeoxycholic acid predicts survival in a North American cohort of primary biliary cirrhosis patients.

artículo científico publicado en 2013

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

artículo científico publicado en 2015

Bivariate traits association analysis using generalized estimating equations in family data

scientific article published on 05 May 2020

Brazilian urban population genetic structure reveals a high degree of admixture.

artículo científico publicado en 2011

CCR5Delta32 polymorphism effects on CCR5 expression, patterns of immunopathology and disease course in multiple sclerosis.

artículo científico publicado en 2005

CD95 polymorphisms are associated with susceptibility to MS in women

artículo científico publicado en 2004

CTLA4 is associated with susceptibility to multiple sclerosis

CUBN is a gene locus for albuminuria

artículo científico publicado en 2011

Case-control genetic association studies in gastrointestinal disease: review and recommendations.

artículo científico publicado en 2006

Case-control study of the ?-synuclein interacting protein gene and Parkinson's disease

article

Characterization of large structural genetic mosaicism in human autosome

artículo científico publicado en 2015

Chemical exposures and Parkinson's disease: a population-based case-control study

artículo científico publicado en 2006

Clinical Correlates of Autosomal Chromosomal Abnormalities in an Electronic Medical Record-Linked Genome-Wide Association Study: A Case Series

artículo científico publicado en 2013

Clinical Correlates of Autosomal Chromosomal Abnormalities in an Electronic Medical Record-Linked Genome-Wide Association Study: A Case Series.

artículo científico publicado en 2013

Clinical features of bronchioloalveolar carcinoma with new histologic and staging definitions

artículo científico publicado en 2010

Clinical outcomes and changes in lung function after segmentectomy versus lobectomy for lung cancer cases

artículo científico publicado en 2014

Coffee, caffeine-related genes, and Parkinson's disease: a case-control study

artículo científico publicado en 2008

Cohort profile: the Baependi Heart Study—a family-based, highly admixed cohort study in a rural Brazilian town

artículo científico publicado en 2016

Collaborative Analysis of α-Synuclein Gene Promoter Variability and Parkinson Disease

artículo científico publicado en 2006

Common variants in Mendelian kidney disease genes and their association with renal function

artículo científico publicado en 2013

Comparison of Multivariate Tests for Genetic Linkage

scientific article published on 01 January 2001

Comparison of longitudinal variance components and regression-based approaches for linkage detection on chromosome 17 for systolic blood pressure

artículo científico publicado en 2003

Comparison of tagging single-nucleotide polymorphism methods in association analyses

artículo científico publicado en 2007

Comparison of variable and model selection methods for genetic association studies using the GAW15 simulated data

artículo científico publicado en 2007

Complex interactions in Parkinson's disease: a two-phased approach.

artículo científico publicado en 2003

Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndrome

artículo científico publicado en 2015

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

artículo científico publicado en 2014

Correction to: Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study

artículo científico publicado en 2018

Cumulative effect of multiple loci on genetic susceptibility to familial lung cancer

artículo científico publicado en 2010

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

artículo científico publicado en 2012

Diagnostic tools in linkage analysis for quantitative traits

artículo científico publicado en 2003

EGFR mediates activation of RET in lung adenocarcinoma with neuroendocrine differentiation characterized by ASCL1 expression

artículo científico publicado en 2017

EGFR-T790M is a rare lung cancer susceptibility allele with enhanced kinase activity

artículo científico publicado en 2007

Effect of emphysema on lung cancer risk in smokers: a computed tomography-based assessment

artículo científico publicado en 2010

Elevated Levels of Adhesion Proteins Are Associated With Low Ankle-Brachial Index

artículo científico publicado en 2016

Elevated amyloid beta protein (Abeta42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator gene

artículo científico publicado en 2004

Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records

artículo científico publicado en 2013

Entropy based genetic association tests and gene-gene interaction tests

artículo científico

Erratum: Corrigendum: Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk

scientific article published in Nature Communications

Estimation of quantitative genetic parameters under non-normal models

scientific article published on 01 January 1995

Evaluating gene by sex and age interactions on cardiovascular risk factors in Brazilian families.

artículo científico publicado en 2010

Evaluating the influence of quality control decisions and software algorithms on SNP calling for the affymetrix 6.0 SNP array platform

artículo científico publicado en 2011

Extension of variance components approach to incorporate temporal trends and longitudinal pedigree data analysis.

artículo científico publicado en 2002

External validation of the United Kingdom-primary biliary cholangitis risk scores of patients with primary biliary cholangitis treated with ursodeoxycholic acid.

artículo científico publicado en 2018

Familial Lung Cancer: A Brief History from the Earliest Work to the Most Recent Studies

artículo científico publicado en 2017

Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer

artículo científico publicado en 2008

Familial aggregation of irritable bowel syndrome: a family case-control study.

artículo científico publicado en 2010

Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury

artículo científico publicado en 2006

Fine mapping of chromosome 6q23-25 region in familial lung cancer families reveals RGS17 as a likely candidate gene

artículo científico publicado en 2009

Fine mapping of the -T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees ⬇️

artículo científico publicado el 14 de octubre de 2003

Focused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung Cancer

artículo científico publicado en 2016

Fruit and vegetable consumption is inversely associated with having pancreatic cancer

artículo científico publicado en 2011

GAW20: methods and strategies for the new frontiers of epigenetics and pharmacogenomics

GPC5 rs2352028 variant and risk of lung cancer in never smokers – Authors' reply

GWAS of 126,559 individuals identifies genetic variants associated with educational attainment

artículo científico publicado en 2013

Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans

artículo científico publicado en 2005

Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci

artículo científico publicado en 2007

Genetic Variants Associated with the Risk of Chronic Obstructive Pulmonary Disease with and without Lung Cancer ⬇️

artículo científico publicado el 1 de noviembre de 2011

Genetic Variations and Patient-Reported Quality of Life Among Patients With Lung Cancer ⬇️

artículo científico publicado el 26 de marzo de 2012

Genetic analyses of smoking initiation, persistence, quantity, and age-at-onset of regular cigarette use in Brazilian families: the Baependi Heart Study

artículo científico publicado en 2012

Genetic analysis of age-at-onset for cardiovascular risk factors in a Brazilian family study.

artículo científico publicado en 2009

Genetic association for renal traits among participants of African ancestry reveals new loci for renal function

artículo científico publicado en 2011

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

artículo científico publicado en 2016

Genetic polymorphisms associated with carotid artery intima-media thickness and coronary artery calcification in women of the Kronos Early Estrogen Prevention Study

artículo científico publicado en 2012

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

artículo científico publicado en 2010

Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network

artículo científico publicado en 2014

Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network

artículo científico publicado en 2011

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

artículo científico publicado en 2013

Genetic variation associated with circulating monocyte count in the eMERGE Network

artículo científico publicado en 2013

Genetics of cardiovascular disease: Importance of sex and ethnicity

artículo científico publicado en 2015

Genome partitioning of genetic variation for complex traits using common SNPs

artículo científico publicado en 2011

Genome scans for genetic predisposition to alcoholism by use of transmission disequilibrium test analyses

article

Genome-wide association and functional follow-up reveals new loci for kidney function

artículo científico publicado en 2012

Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction

artículo científico publicado en 2011

Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk

artículo científico publicado en 2014

Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer

artículo científico publicado en 2009

Genome-wide association study of familial lung cancer

Genome-wide association study of kidney function decline in individuals of European descent

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Genome-wide study of resistant hypertension identified from electronic health records

artículo científico publicado en 2017

Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism

artículo científico publicado en 2019

Genomic loci with pleiotropic effects on coronary artery calcification

artículo científico publicado en 2005

Genomic susceptibility Loci for brain atrophy, ventricular volume, and leukoaraiosis in hypertensive sibships

artículo científico publicado en 2009

Genomic susceptibility loci for brain atrophy in hypertensive sibships from the GENOA study

artículo científico publicado en 2005

Germ line Fanconi anemia complementation group C mutations and pancreatic cancer

artículo científico publicado en 2005

Global Individual Ancestry Using Principal Components for Family Data

artículo científico publicado en 2015

Group 6: Pleiotropy and multivariate analysis

artículo científico publicado en 2003

Haplotype and cell proliferation analyses of candidate lung cancer susceptibility genes on chromosome 15q24-25.1.

artículo científico publicado en 2009

Hepatocyte growth factor demonstrates racial heterogeneity as a biomarker for coronary heart disease

artículo científico publicado en 2017

Heritability of cardiovascular risk factors in a Brazilian population: Baependi Heart Study

article

Heritability of leukoaraiosis in hypertensive sibships

artículo científico publicado en 2004

Heritability of longitudinal measures of body mass index and lipid and lipoprotein levels in aging twins

artículo científico publicado en 2007

Heritability of physical activity traits in Brazilian families: the Baependi Heart Study.

artículo científico publicado en 2011

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

artículo científico publicado en 2005

Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathy

artículo científico publicado en 2011

Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata

artículo científico publicado en 2007

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

artículo científico publicado en 2005

IFNG polymorphisms are associated with gender differences in susceptibility to multiple sclerosis

artículo científico publicado en 2005

Identification of Genetic Interaction with Risk Factors Using a Time-To-Event Model

artículo científico publicado en 2017

Identification of Susceptibility Loci for Spontaneous Coronary Artery Dissection

scientific article published on 06 May 2020

Identification of a novel tumor suppressor gene p34 on human chromosome 6q25.1.

artículo científico publicado en 2007

Identification of gene-gene interaction using principal components

artículo científico publicado en 2009

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

artículo científico publicado en 2009

Identification of genes involved in alcohol consumption and cigarettes smoking

artículo científico publicado en 2005

Identification of unique venous thromboembolism-susceptibility variants in African-Americans

artículo científico publicado en 2017

Identifying disease modifying genes in multiple sclerosis

artículo científico publicado en 2002

Immune Cell Infiltration May Be a Key Determinant of Long-Term Survival in Small Cell Lung Cancer

artículo científico publicado en 2019

Impact of adiposity on cellular adhesion: The Multi-Ethnic Study of atherosclerosis (MESA).

artículo científico publicado en 2015

Imputation and quality control steps for combining multiple genome-wide datasets

artículo científico publicado en 2014

Imputation methods for missing data for polygenic models

artículo científico publicado en 2003

Increased prevalence of antimitochondrial antibodies in first-degree relatives of patients with primary biliary cirrhosis

artículo científico publicado en 2007

Influence of SULT1A1 genetic variation on age at menopause, estrogen levels, and response to hormone therapy in recently postmenopausal white women

artículo científico publicado en 2016

Influence of genomic loci on measures of chronic kidney disease in hypertensive sibships

artículo científico publicado en 2006

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

artículo científico publicado en 2020

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

artículo científico publicado en 2012

Interaction of ?-synuclein and tau genotypes in Parkinson's disease

artículo científico publicado en 2005

Interferon gamma allelic variants: sex-biased multiple sclerosis susceptibility and gene expression

artículo científico publicado en 2008

Interleukin-1 Receptor Antagonist Allele 2 and Familial Alopecia Areata

artículo científico publicado en 2002

Leukocyte DNA methylation signature differentiates pancreatic cancer patients from healthy controls

artículo científico publicado en 2011

Linkage Analysis, Multivariate

Linkage analysis of chromosome 4 in families with familial pancreatic cancer

artículo científico publicado en 2007

Linkage analysis of obesity phenotypes in pre- and post-menopausal women from a United States mid-western population

artículo científico publicado en 2010

Linkage analysis using principal components of gene expression data.

artículo científico publicado en 2007

Localization of genes involved in the metabolic syndrome using multivariate linkage analysis.

artículo científico publicado en 2003

Long-term risk of depressive and anxiety symptoms after early bilateral oophorectomy

artículo científico publicado en 2008

Long-term risk of depressive and anxiety symptoms after early bilateral oophorectomy

artículo científico publicado en 2018

Long-term survival and prognostic indicators in small (<or=2 cm) pancreatic cancer

scientific article published on 13 October 2008

Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X

artículo científico publicado en 2005

Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll Region

artículo científico publicado en 2019

Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata

article

Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels

artículo científico publicado en 2011

Men transmit MS more often to their children vs women: the Carter effect

artículo científico publicado en 2006

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

artículo científico publicado en 2016

Meta-Analysis of Genome-wide Linkage Studies in BMI and Obesity*

article

Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism

artículo científico publicado en 2015

Missing phenotype data imputation in pedigree data analysis

artículo científico publicado en 2008

Mitochondrial DNA content: its genetic heritability and association with renal cell carcinoma

scientific article published on 29 July 2008

Mitochondrial genetic polymorphisms and pancreatic cancer risk

scientific article published on 01 July 2007

Mitochondrial genetic polymorphisms do not predict survival in patients with pancreatic cancer

artículo científico publicado en 2008

Multi-ethnic analysis reveals soluble L-selectin may be post-transcriptionally regulated by 3'UTR polymorphism: the Multi-Ethnic Study of Atherosclerosis (MESA).

artículo científico publicado en 2015

Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI

artículo científico publicado en 2015

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

scientific article published on 13 June 2016

Multivariate linkage analysis of blood pressure and body mass index

scientific article published on 01 July 2004

Mutagen sensitivity and genetic variants in nucleotide excision repair pathway: genotype-phenotype correlation.

artículo científico publicado en 2007

Mutagen sensitivity has high heritability: evidence from a twin study

artículo científico publicado en 2006

Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy

artículo científico publicado en 2009

N-ACETYLTRANSFERASE 2 IS A SUSCEPTIBILITY LOCUS FOR PARKINSONʼS DISEASE

scholarly article by Maurizio Facheris et al published July 2004 in Epidemiology

NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality

artículo científico

New loci associated with kidney function and chronic kidney disease

artículo científico publicado en 2010

Novel genomic loci influencing plasma homocysteine levels

artículo científico publicado en 2006

Nucleotide excision repair pathway polymorphisms and pancreatic cancer risk: evidence for role of MMS19L.

artículo científico publicado en 2009

Number of children and risk of Parkinson's disease

artículo científico publicado en 2007

Nutrients from fruit and vegetable consumption reduce the risk of pancreatic cancer

artículo científico publicado en 2013

OCCUPATIONAL EXPOSURES AND PARKINSON’S DISEASE: A POPULATION-BASED, CASE-CONTROL STUDY

scholarly article by Roberta Frigerio et al published July 2004 in Epidemiology

Obesity adversely affects survival in pancreatic cancer patients

artículo científico publicado en 2010

P-selectin and subclinical and clinical atherosclerosis: the Multi-Ethnic Study of Atherosclerosis (MESA)

artículo científico publicado en 2015

P4-095 Analysis of Alzheimer's disease candidate genes on chromosome 10

article

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

artículo científico publicado en 2016

Pancreatic cancer genetic epidemiology consortium

artículo científico

Pancreatic cancer-associated diabetes mellitus: prevalence and temporal association with diagnosis of cancer

artículo científico publicado en 2007

Parametric Linkage Analysis Identifies Five Novel Genome-Wide Significant Loci for Familial Lung Cancer

artículo científico publicado en 2017

Parkin variants in North American Parkinson's disease: cases and controls.

artículo científico publicado en 2003

Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network

artículo científico publicado en 2015

Perceptions of lung cancer risk and beliefs in screening accuracy of spiral computed tomography among high-risk lung cancer family members

artículo científico publicado en 2010

Pharmacogenomics of estrogens on changes in carotid artery intima-medial thickness and coronary arterial calcification: Kronos Early Estrogen Prevention Study

artículo científico publicado en 2015

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

scientific article published on 29 October 2019

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

artículo científico publicado en 2011

Plasma and serum L-selectin and clinical and subclinical cardiovascular disease: the Multi-Ethnic Study of Atherosclerosis (MESA).

artículo científico publicado en 2014

Pleiotropic genetic effects contribute to the correlation between HDL cholesterol, triglycerides, and LDL particle size in hypertensive sibships

artículo científico publicado en 2005

Polygenic overlap between kidney function and large artery atherosclerotic stroke

artículo científico publicado en 2014

Polymorphic variants in hereditary pancreatic cancer genes are not associated with pancreatic cancer risk

scientific article published on 18 August 2009

Polymorphisms in DNA repair genes, smoking, and pancreatic adenocarcinoma risk

scientific article published on 10 June 2008

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

artículo científico publicado en 2005

Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network ⬇️

artículo científico publicado en 2015

Quality control procedures for genome-wide association studies

artículo científico publicado en 2011

Quantitative trait loci influencing low density lipoprotein particle size in African Americans

artículo científico publicado en 2006

Random-effects Cox proportional hazards model: general variance components methods for time-to-event data

artículo científico publicado en 2005

Rare variants in known susceptibility loci and their contribution to risk of lung cancer

artículo científico publicado en 2018

Reduced coffee consumption among individuals with primary sclerosing cholangitis but not primary biliary cirrhosis.

artículo científico publicado en 2014

Reliability of self-reported ancestry among siblings: implications for genetic association studies

scientific article published on 18 January 2006

Risk assessment for developing gliomas: a comparison of two cytogenetic approaches.

artículo científico publicado en 2001

Risk of malignancy in first-degree relatives of patients with pancreatic carcinoma

artículo científico publicado en 2005

SLCO1B1 genetic variation and hormone therapy in menopausal women

artículo científico publicado en 2018

SNP interaction detection with Random Forests in high-dimensional genetic data

artículo científico publicado en 2012

Screening the genome to detect an association with hypertension

artículo científico publicado en 2003

Segregation analysis of cancer in families of glioma patients

artículo científico publicado en 2001

Segregation analysis of idiopathic talipes equinovarus in a Texan population

artículo científico publicado en 1998

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

artículo científico publicado en 2019

Sex-Specific Genetic Variants are Associated With Coronary Endothelial Dysfunction

artículo científico publicado en 2016

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

artículo científico publicado en 2016

Single nucleotide polymorphisms associated with abnormal coronary microvascular function

artículo científico publicado en 2014

Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform.

artículo científico publicado en 2011

Summary of contributions to GAW Group 12: multivariate methods

artículo científico publicado en 2005

Summary of contributions to GAW15 Group 13: candidate gene association studies

artículo científico publicado en 2007

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

artículo científico publicado en 2006

T1385 Adrenomedullin: A Biomarker of Pancreatic Cancer-Associated Diabetes?

TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy

artículo científico publicado en 2014

Temporal association of changes in fasting blood glucose and body mass index with diagnosis of pancreatic cancer.

artículo científico publicado en 2009

The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study

artículo científico publicado en 2014

The Mayo Clinic cohort study of personality and aging: design and sampling, reliability and validity of instruments, and baseline description

artículo científico publicado en 2006

The association of copy number variation and percent mammographic density

artículo científico publicado en 2015

The challenge of detecting epistasis (G x G interactions): Genetic Analysis Workshop 16

artículo científico publicado en 2009

The challenge of detecting genotype-by-methylation interaction: GAW20

The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype

scientific article published on 08 October 2018

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.

artículo científico publicado en 2012

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

artículo científico publicado en 2015

The genetics of gene expression: comparison of linkage scans using two phenotype normalization methods

artículo científico publicado en 2007

The prevalence of BRCA2 mutations in familial pancreatic cancer

scientific article published on 01 February 2007

Thrombomodulin gene polymorphisms or haplotypes as potential risk factors for venous thromboembolism: a population-based case-control study

article

Trans-ethnic meta-analysis identifies common and rare variants associated with hepatocyte growth factor levels in the Multi-Ethnic Study of Atherosclerosis (MESA).

artículo científico publicado en 2015

Two major QTLs and several others relate to factors of metabolic syndrome in the family blood pressure program

artículo científico publicado en 2005

UCHL1 is a Parkinson's disease susceptibility gene

artículo científico publicado en 2004

UCHL1 is associated with Parkinson's disease: A case-unaffected sibling and case-unrelated control study

scholarly article by Maurizio Facheris et al published June 2005 in Neuroscience Letters

Using item response theory to model multiple phenotypes and their joint heritability in family data.

artículo científico publicado en 2014

Using the theory of added-variable plot for linear mixed models to decompose genetic effects in family data.

artículo científico publicado en 2014

Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies

artículo científico publicado en 2011

Variations in Primary Sclerosing Cholangitis Across the Age Spectrum

artículo científico publicado en 2017

Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q

scientific article published on 11 December 2019

eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants

artículo científico publicado en 2016

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