Lista de obras - Michael Barmada - Dominio Público Uruguay

"Predicting" parental longevity from offspring endophenotypes: data from the Long Life Family Study (LLFS).

artículo científico publicado en 2010

A Bayesian method for identifying genetic interactions.

artículo científico publicado en 2009

A Gene for Autosomal Dominant Congenital Nystagmus Localizes to 6p12

article

A Genome Scan in 260 Inflammatory Bowel Disease-Affected Relative Pairs

artículo científico publicado en 2004

A Genome Scan in 260 Inflammatory Bowel Disease-Affected Relative Pairs

scientific article published on 01 September 2004

A bayesian method for evaluating and discovering disease loci associations

artículo científico publicado en 2011

A fast algorithm for learning epistatic genomic relationships ⬇️

artículo científico publicado el 13 de noviembre de 2010

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

artículo científico publicado en 2006

A novel locus for familial migraine on Xp22.

artículo científico publicado en 2010

A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.

artículo científico publicado en 2006

A rare duplication on chromosome 16p11.2 is identified in patients with psychosis in Alzheimer's disease

artículo científico publicado en 2014

A systems biology approach to genetic studies of pancreatitis and other complex diseases.

artículo científico publicado en 2007

African ancestry and lung function in Puerto Rican children

artículo científico publicado en 2012

Alcohol consumption, cigarette smoking, and the risk of recurrent acute and chronic pancreatitis.

artículo científico publicado en 2009

An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29.

artículo científico publicado en 2008

Analysis of tumor necrosis factor-alpha, transforming growth factor-beta 1, interleukin-10, and interferon-gamma polymorphisms in patients with alcoholic chronic pancreatitis

artículo científico publicado en 2004

Associating Symptom Phenotype and Genotype in Preeclampsia

artículo científico publicado en 2018

Association of CLU and PICALM variants with Alzheimer's disease.

artículo científico publicado en 2010

Association of MHC region SNPs with irritant susceptibility in healthcare workers

artículo científico publicado en 2016

Association of the peroxisome proliferator-activated receptor gamma gene with type 2 diabetes mellitus varies by physical activity among non-Hispanic whites from Colorado.

artículo científico publicado en 2007

Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24.

artículo científico publicado en 2003

Biogenetic mechanisms predisposing to complex phenotypes in parents may function differently in their children

artículo científico publicado en 2012

Challenges of Examining Complex Genetic Disorders like GERD

artículo científico publicado en 2005

Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3.

artículo científico publicado en 2002

Clinical characterization of patients with idiopathic chronic pancreatitis and SPINK1 Mutations

artículo científico publicado en 2004

Combined bicarbonate conductance-impairing variants in CFTR and SPINK1 variants are associated with chronic pancreatitis in patients without cystic fibrosis

artículo científico publicado en 2010

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

artículo científico publicado en 2012

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

artículo científico publicado en 2011

Comprehensive Analysis of HLA-G: Implications for Recurrent Spontaneous Abortion

article

Comprehensive evaluation of the association of APOE genetic variation with plasma lipoprotein traits in U.S. whites and African blacks

artículo científico publicado en 2014

Connecting the dots: potential of data integration to identify regulatory SNPs in late-onset Alzheimer's disease GWAS findings.

artículo científico publicado en 2014

Does the pain-protective GTP cyclohydrolase haplotype significantly alter the pattern or severity of pain in humans with chronic pancreatitis?

artículo científico publicado en 2008

Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study

artículo científico publicado en 2014

Erratum: Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

scholarly article published in Nature Genetics

Evaluating de novo locus-disease discoveries in GWAS using the signal-to-noise ratio.

artículo científico publicado en 2011

Evaluating disorders with a complex genetics basis. the future roles of meta-analysis and systems biology

artículo científico publicado en 2005

Evidence for an inflammatory bowel disease locus on chromosome 3p26: linkage, transmission/disequilibrium and partitioning of linkage

article

Functional polymorphisms of the coagulation factor II gene (F2) and susceptibility to systemic lupus erythematosus

artículo científico publicado en 2011

Genetic Determinants of Survival in Patientswith Alzheimer’s Disease.

artículo científico publicado en 2015

Genetic analysis of the glutathione s-transferase genes MGST1, GSTM3, GSTT1, and GSTM1 in patients with hereditary pancreatitis

artículo científico publicado en 2004

Genetic and environmental influences on thyroid hormone variation in Mexican Americans

artículo científico publicado en 2004

Genetic association and differential expression of PITX2 with acute appendicitis

artículo científico publicado en 2018

Genetic basis of irritant susceptibility in health care workers

artículo científico publicado en 2016

Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study.

artículo científico publicado en 2015

Genetic determinants of disease progression in Alzheimer's disease

artículo científico publicado en 2015

Genetic variants associated with susceptibility to psychosis in late-onset Alzheimer's disease families

artículo científico publicado en 2015

Genetic variants in major histocompatibility complex-linked genes associate with pediatric liver transplant rejection.

artículo científico publicado en 2008

Genetic variants within the MHC region are associated with immune responsiveness to childhood vaccinations

artículo científico publicado en 2013

Genetic variation in C-reactive protein (CRP) gene may be associated with risk of systemic lupus erythematosus and CRP concentrations

artículo científico publicado en 2008

Genetic variation in fatty acid-binding protein-4 and peroxisome proliferator-activated receptor gamma interactively influence insulin sensitivity and body composition in males

artículo científico publicado en 2004

Genetic variation in uncoupling protein 3 is associated with dietary intake and body composition in females

artículo científico publicado en 2004

Genetics of gastroesophageal reflux disease: a review

artículo científico publicado en 2002

Genome-Wide Association Study and Linkage Analysis of the Healthy Aging Index

artículo científico publicado en 2015

Genome-wide association analysis of age-at-onset in Alzheimer's disease

artículo científico publicado en 2011

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

artículo científico publicado en 2008

Genome-wide association scan for childhood caries implicates novel genes

scientific journal article

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

artículo científico publicado en 2007

Genome-wide association study of Alzheimer's disease

artículo científico publicado en 2012

Genome-wide association study of antiphospholipid antibodies

artículo científico publicado en 2013

Genome-wide copy-number variation study of psychosis in Alzheimer's disease.

artículo científico publicado en 2015

Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13

article

Genomewide association analysis of respiratory syncytial virus infection in mice

artículo científico publicado en 2009

Hereditary, familial, and idiopathic chronic pancreatitis are not associated with polymorphisms in the tumor necrosis factor α (TNF-α) promoter region or the TNF receptor 1 (TNFR1) gene

article

Heritability of and mortality prediction with a longevity phenotype: the healthy aging index

artículo científico publicado en 2013

Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry

artículo científico publicado en 2015

Identifying genetic interactions in genome-wide data using Bayesian networks

artículo científico publicado en 2010

Impact of genetic variants in human scavenger receptor class B type I (SCARB1) on plasma lipid traits.

artículo científico publicado en 2014

Increasing incidence of acute pancreatitis at an American pediatric tertiary care center: is greater awareness among physicians responsible?

artículo científico publicado en 2010

Investigation of oxidized LDL-receptor 1 (OLR1) as the candidate gene for Alzheimer's disease on chromosome 12.

artículo científico publicado en 2002

Is the monocyte chemotactic protein-1 -2518 G allele a risk factor for severe acute pancreatitis?

artículo científico publicado en 2005

Keratin 8 Mutations Are Not Associated with Familial, Sporadic and Alcoholic Pancreatitis in a Population from the United States

artículo científico publicado en 2005

Learning genetic epistasis using Bayesian network scoring criteria

artículo científico publicado en 2011

Limited contribution of the SPINK1 N34S mutation to the risk and severity of alcoholic chronic pancreatitis: a report from the United States

artículo científico publicado en 2003

Lipoprotein lipase gene sequencing and plasma lipid profile

artículo científico publicado en 2013

Mechanisms of CFTR functional variants that impair regulated bicarbonate permeation and increase risk for pancreatitis but not for cystic fibrosis

artículo científico publicado en 2014

Multicenter approach to recurrent acute and chronic pancreatitis in the United States: the North American Pancreatitis Study 2 (NAPS2).

artículo científico publicado en 2008

Needs Assessment for Research Use of High-Throughput Sequencing at a Large Academic Medical Center

artículo científico publicado en 2015

Novel late-onset Alzheimer disease loci variants associate with brain gene expression

artículo científico publicado en 2012

Parental attitudes toward newborn screening for Duchenne/Becker muscular dystrophy and spinal muscular atrophy

artículo científico publicado en 2014

Pathways to injury in chronic pancreatitis: decoding the role of the high-risk SPINK1 N34S haplotype using meta-analysis

artículo científico publicado en 2008

Perinuclear neutrophil antibodies are not markers for genetic susceptibility or indicators of genetic heterogeneity in familial ulcerative colitis

artículo científico publicado en 2002

Phenotype-stratified genetic linkage study demonstrates that IBD2 is an extensive ulcerative colitis locus.

artículo científico publicado en 2006

Physical activity levels in American-Indian adults: the Strong Heart Family Study

artículo científico publicado en 2009

Physical and mental quality of life in chronic pancreatitis: a case-control study from the North American Pancreatitis Study 2 cohort.

artículo científico publicado en 2013

Pooling-based genome-wide association study implicates gamma-glutamyltransferase 1 (GGT1) gene in pancreatic carcinogenesis

artículo científico publicado en 2010

Prostaglandin E2 and IL-23 plus IL-1β differentially regulate the Th1/Th17 immune response of human CD161(+) CD4(+) memory T cells

artículo científico publicado en 2011

Rarity of the Alzheimer disease-protective APP A673T variant in the United States

artículo científico publicado en 2015

Replication of European Rheumatoid Arthritis Loci in a Pakistani Population

scientific article published on 01 February 2013

Replication study of genome-wide associated SNPs with late-onset Alzheimer's disease

artículo científico publicado en 2011

Resequencing of LPL in African Blacks and associations with lipoprotein-lipid levels

artículo científico publicado en 2015

Resequencing of the CETP gene in American whites and African blacks: Association of rare and common variants with HDL-cholesterol levels

artículo científico publicado en 2015

SPINK1/PSTI mutations are associated with tropical pancreatitis and type II diabetes mellitus in Bangladesh

artículo científico publicado en 2002

Stability of exploratory multivariate data modeling in longitudinal data

artículo científico publicado en 2003

TCGA Expedition: A Data Acquisition and Management System for TCGA Data

artículo científico publicado en 2016

The C161-->T polymorphism in peroxisome proliferator-activated receptor gamma, but not P12A, is associated with insulin resistance in Hispanic and non-Hispanic white women: evidence for another functional variant in peroxisome proliferator-activated

artículo científico publicado en 2005

The IBD International Genetics Consortium Provides Further Evidence for Linkage to IBD4 and Shows Gene-Environment Interaction

article

The MCP-1 ᐠ2518 A/G Polymorphism Is Not a Susceptibility Factor for Chronic Pancreatitis

article

The PPARgamma Pro12Ala polymorphism is not associated with body mass index or waist circumference among Hispanics from Colorado.

artículo científico publicado en 2007

The SPINK1 N34S mutation is not associated with Type 2 diabetes mellitus in a population of the USA.

artículo científico publicado en 2005

The application of network label propagation to rank biomarkers in genome-wide Alzheimer's data

artículo científico publicado en 2014

The peroxisome proliferator-activated receptor gamma coactivator-1 alpha gene (PGC-1alpha) is not associated with type 2 diabetes mellitus or body mass index among Hispanic and non Hispanic Whites from Colorado.

artículo científico publicado en 2007

Transforming growth factor-β1, interleukin-10 and interferon-γ cytokine polymorphisms in patients with hereditary, familial and sporadic chronic pancreatitis

artículo científico publicado en 2004

Type of pain, pain-associated complications, quality of life, disability and resource utilisation in chronic pancreatitis: a prospective cohort study.

artículo científico publicado en 2011

Ulcerative colitis is more strongly linked to chromosome 12 than Crohn's disease

artículo científico publicado en 2001

Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

artículo científico publicado en 2009

Variation in the FABP2 promoter alters transcriptional activity and is associated with body composition and plasma lipid levels

artículo científico publicado en 2003

Vitamin D insufficiency and severe asthma exacerbations in Puerto Rican children

artículo científico publicado en 2012

Whole exome sequencing identifies multiple, complex etiologies in an idiopathic hereditary pancreatitis kindred

artículo científico publicado en 2012

X-linked infantile spinal muscular atrophy: clinical definition and molecular mapping

artículo científico publicado en 2007

Lista de obras de Michael Barmada

"Predicting" parental longevity from offspring endophenotypes: data from the Long Life Family Study (LLFS).

A Bayesian method for identifying genetic interactions.

A Gene for Autosomal Dominant Congenital Nystagmus Localizes to 6p12

A Genome Scan in 260 Inflammatory Bowel Disease-Affected Relative Pairs

A Genome Scan in 260 Inflammatory Bowel Disease-Affected Relative Pairs

A bayesian method for evaluating and discovering disease loci associations

A fast algorithm for learning epistatic genomic relationships ⬇️

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

A novel locus for familial migraine on Xp22.

A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.

A rare duplication on chromosome 16p11.2 is identified in patients with psychosis in Alzheimer's disease

A systems biology approach to genetic studies of pancreatitis and other complex diseases.

African ancestry and lung function in Puerto Rican children

Alcohol consumption, cigarette smoking, and the risk of recurrent acute and chronic pancreatitis.

An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29.

Analysis of tumor necrosis factor-alpha, transforming growth factor-beta 1, interleukin-10, and interferon-gamma polymorphisms in patients with alcoholic chronic pancreatitis

Associating Symptom Phenotype and Genotype in Preeclampsia

Association of CLU and PICALM variants with Alzheimer's disease.

Association of MHC region SNPs with irritant susceptibility in healthcare workers

Association of the peroxisome proliferator-activated receptor gamma gene with type 2 diabetes mellitus varies by physical activity among non-Hispanic whites from Colorado.

Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24.

Biogenetic mechanisms predisposing to complex phenotypes in parents may function differently in their children

Challenges of Examining Complex Genetic Disorders like GERD

Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3.

Clinical characterization of patients with idiopathic chronic pancreatitis and SPINK1 Mutations

Combined bicarbonate conductance-impairing variants in CFTR and SPINK1 variants are associated with chronic pancreatitis in patients without cystic fibrosis

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

Comprehensive Analysis of HLA-G: Implications for Recurrent Spontaneous Abortion

Comprehensive evaluation of the association of APOE genetic variation with plasma lipoprotein traits in U.S. whites and African blacks

Connecting the dots: potential of data integration to identify regulatory SNPs in late-onset Alzheimer's disease GWAS findings.

Does the pain-protective GTP cyclohydrolase haplotype significantly alter the pattern or severity of pain in humans with chronic pancreatitis?

Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study

Erratum: Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

Evaluating de novo locus-disease discoveries in GWAS using the signal-to-noise ratio.

Evaluating disorders with a complex genetics basis. the future roles of meta-analysis and systems biology

Evidence for an inflammatory bowel disease locus on chromosome 3p26: linkage, transmission/disequilibrium and partitioning of linkage

Functional polymorphisms of the coagulation factor II gene (F2) and susceptibility to systemic lupus erythematosus

Genetic Determinants of Survival in Patientswith Alzheimer’s Disease.

Genetic analysis of the glutathione s-transferase genes MGST1, GSTM3, GSTT1, and GSTM1 in patients with hereditary pancreatitis

Genetic and environmental influences on thyroid hormone variation in Mexican Americans

Genetic association and differential expression of PITX2 with acute appendicitis

Genetic basis of irritant susceptibility in health care workers

Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study.

Genetic determinants of disease progression in Alzheimer's disease

Genetic variants associated with susceptibility to psychosis in late-onset Alzheimer's disease families

Genetic variants in major histocompatibility complex-linked genes associate with pediatric liver transplant rejection.

Genetic variants within the MHC region are associated with immune responsiveness to childhood vaccinations

Genetic variation in C-reactive protein (CRP) gene may be associated with risk of systemic lupus erythematosus and CRP concentrations

Genetic variation in fatty acid-binding protein-4 and peroxisome proliferator-activated receptor gamma interactively influence insulin sensitivity and body composition in males

Genetic variation in uncoupling protein 3 is associated with dietary intake and body composition in females

Genetics of gastroesophageal reflux disease: a review

Genome-Wide Association Study and Linkage Analysis of the Healthy Aging Index

Genome-wide association analysis of age-at-onset in Alzheimer's disease

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

Genome-wide association scan for childhood caries implicates novel genes

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

Genome-wide association study of Alzheimer's disease

Genome-wide association study of antiphospholipid antibodies

Genome-wide copy-number variation study of psychosis in Alzheimer's disease.

Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13

Genomewide association analysis of respiratory syncytial virus infection in mice

Hereditary, familial, and idiopathic chronic pancreatitis are not associated with polymorphisms in the tumor necrosis factor α (TNF-α) promoter region or the TNF receptor 1 (TNFR1) gene

Heritability of and mortality prediction with a longevity phenotype: the healthy aging index

Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry

Identifying genetic interactions in genome-wide data using Bayesian networks

Impact of genetic variants in human scavenger receptor class B type I (SCARB1) on plasma lipid traits.

Increasing incidence of acute pancreatitis at an American pediatric tertiary care center: is greater awareness among physicians responsible?

Investigation of oxidized LDL-receptor 1 (OLR1) as the candidate gene for Alzheimer's disease on chromosome 12.

Is the monocyte chemotactic protein-1 -2518 G allele a risk factor for severe acute pancreatitis?

Keratin 8 Mutations Are Not Associated with Familial, Sporadic and Alcoholic Pancreatitis in a Population from the United States

Learning genetic epistasis using Bayesian network scoring criteria

Limited contribution of the SPINK1 N34S mutation to the risk and severity of alcoholic chronic pancreatitis: a report from the United States

Lipoprotein lipase gene sequencing and plasma lipid profile

Mechanisms of CFTR functional variants that impair regulated bicarbonate permeation and increase risk for pancreatitis but not for cystic fibrosis

Multicenter approach to recurrent acute and chronic pancreatitis in the United States: the North American Pancreatitis Study 2 (NAPS2).

Needs Assessment for Research Use of High-Throughput Sequencing at a Large Academic Medical Center

Novel late-onset Alzheimer disease loci variants associate with brain gene expression

Parental attitudes toward newborn screening for Duchenne/Becker muscular dystrophy and spinal muscular atrophy