Lista de obras - Mauricio Arcos-Burgos - Dominio Público Uruguay

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.

artículo científico publicado en 2016

A Mutation in DAOA Modifies the Age of Onset in PSEN1 E280A Alzheimer's Disease

artículo científico publicado en 2016

A New Method for Detecting Significant p-values with Applications to Genetic Data

A common genetic network underlies substance use disorders and disruptive or externalizing disorders

artículo científico publicado en 2012

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication

artículo científico publicado en 2010

A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD.

artículo científico publicado en 2011

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

artículo científico publicado en 2010

A latent genetic subtype of major depression identified by whole-exome genotyping data in a Mexican-American cohort

artículo científico publicado en 2017

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

scientific article published on 30 March 2016

A multigenerational pedigree of late-onset Alzheimer's disease implies new genetic causes

artículo científico publicado en 2005

A novel alteration in metaxin 1, F202L, is associated with N370S in Gaucher disease

artículo científico publicado en 2004

A two-locus genetic interaction between LPHN3 and 11q predicts ADHD severity and long-term outcome

artículo científico publicado en 2011

ADHD Endophenotypes in Caribbean Families.

artículo científico publicado en 2018

ADHD latent class clusters: DSM-IV subtypes and comorbidity

artículo científico publicado en 2009

APOE*E2 allele delays age of onset in PSEN1 E280A Alzheimer's disease

artículo científico publicado en 2015

An 1H-MRS framework predicts the onset of Alzheimer's disease symptoms in PSEN1 mutation carriers

artículo científico publicado en 2013

An Ultraconserved Brain-Specific Enhancer Within ADGRL3 (LPHN3) Underpins Attention-Deficit/Hyperactivity Disorder Susceptibility

artículo científico publicado en 2016

Analysis of brain metabolism by proton magnetic resonance spectroscopy (1H-MRS) in attention-deficit/hyperactivity disorder suggests a generalized differential ontogenic pattern from controls

artículo científico publicado en 2012

Attention deficit/hyperactivity disorder (ADHD): complex phenotype, simple genotype?

artículo científico publicado en 2004

Attention-Deficit/Hyperactivity Disorder

Attention-Deficit/Hyperactivity Disorder and Comorbid Disruptive Behavior Disorders: Evidence of Pleiotropy and New Susceptibility Loci

article

Attention-deficit/hyperactivity disorder (ADHD): feasibility of linkage analysis in a genetic isolate using extended and multigenerational pedigrees

article

Attention-deficit/hyperactivity disorder and comorbidities in 18 Paisa Colombian multigenerational families

artículo científico publicado en 2004

Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.

artículo científico publicado en 2004

CRISPLD2: a novel NSCLP candidate gene

article

Candidate gene discovery in autoimmunity by using extreme phenotypes, next generation sequencing and whole exome capture

artículo científico publicado en 2014

Chagas' disease susceptibility/resistance: linkage disequilibrium analysis suggests epistasis between major histocompatibility complex and interleukin-10.

artículo científico publicado en 2004

Clinical features of multiple sclerosis in a genetically homogeneous tropical population

artículo científico publicado en 2001

Clinical outcomes and genome-wide association for a brain methylation site in an antidepressant pharmacogenetics study in Mexican Americans

artículo científico publicado en 2014

Clonal population structure of Colombian sylvatic Trypanosoma cruzi.

artículo científico publicado en 1998

Complex segregation analysis of non-myoclonic idiopathic generalized epilepsy in families ascertained from probands affected with idiopathic epilepsy with tonic-clonic seizures in Antioquia, Colombia

artículo científico publicado en 1996

Complex segregation analysis of nonsyndromic cleft lip/palate in a Chilean population

article

Congenital Leptin Deficiency and Leptin Gene Missense Mutation Found in Two Colombian Sisters with Severe Obesity.

artículo científico publicado en 2019

Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study

artículo científico publicado en 2010

Cross validation of pooling/resampling GWAS using the WTCCC data

Definition of mutations in polyautoimmunity

artículo científico publicado en 2016

Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest

artículo científico publicado en 2016

Early interstitial lung disease in familial pulmonary fibrosis

artículo científico publicado en 2007

Environmental influences that affect attention deficit/hyperactivity disorder: study of a genetic isolate

artículo científico publicado en 2007

Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations

artículo científico publicado en 2009

Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

artículo científico publicado en 2010

Exploratory data from complete genomes of familial alzheimer disease age-at-onset outliers

artículo científico publicado en 2012

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate

artículo científico publicado en 2009

Factorial and discriminant analyses of neuropsychological variables in familial and sporadic late onset Alzheimer disease

Familial Alzheimer's Disease and Recessive Modifiers

scientific article published on 29 October 2019

From the black widow spider to human behavior: Latrophilins, a relatively unknown class of G protein-coupled receptors, are implicated in psychiatric disorders

artículo científico publicado en 2010

GWAS reveals new recessive loci associated with non-syndromic facial clefting

artículo científico publicado en 2012

Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio

article

Genetics of non-syndromic childhood obesity and the use of high-throughput DNA sequencing technologies.

artículo científico publicado en 2017

Genetics of population isolates.

artículo científico publicado en 2002

Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results

scientific article published on 11 June 2009

Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p

artículo científico publicado en 2010

Influence of a latrophilin 3 (LPHN3) risk haplotype on event-related potential measures of cognitive response control in attention-deficit hyperactivity disorder (ADHD).

artículo científico publicado en 2012

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

artículo científico publicado en 2004

LPHN3 and attention-deficit/hyperactivity disorder: a susceptibility and pharmacogenetic study

artículo científico publicado en 2015

Latent class subtyping of attention-deficit/hyperactivity disorder and comorbid conditions

artículo científico publicado en 2008

Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C

artículo científico publicado en 2010

Linkage and association analysis of ADHD endophenotypes in extended and multigenerational pedigrees from a genetic isolate.

artículo científico publicado en 2015

Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?

Low-frequency and rare variants may contribute to elucidate the genetics of major depressive disorder.

artículo científico publicado en 2018

Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.

artículo científico publicado en 2004

Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder

artículo científico publicado en 2008

Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome

artículo científico publicado en 2014

Multiple sclerosis in the tropics: genetic association to STR's loci spanning the HLA and TNF.

artículo científico publicado en 2002

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

artículo científico publicado en 2002

Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder

artículo científico publicado en 2004

Mutations in sphingolipid metabolism genes are associated with ADHD

artículo científico publicado en 2020

Mutations modifying sporadic Alzheimer's disease age of onset

artículo científico publicado en 2016

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Comprehensive Review

scientific article published on 07 August 2019

Neural Plasticity during Aging

artículo científico publicado en 2019

Neural Plasticity in Obesity and Psychiatric Disorders

artículo científico publicado en 2016

Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren's syndrome

artículo científico publicado en 2015

Origin of the PSEN1 E280A mutation causing early-onset Alzheimer's disease

artículo científico publicado en 2014

Pedigree disequilibrium test (PDT) replicates association and linkage between DRD4 and ADHD in multigenerational and extended pedigrees from a genetic isolate.

artículo científico publicado en 2004

Pharmacogenetic impact of VKORC1 and CYP2C9 allelic variants on warfarin dose requirements in a hispanic population isolate.

artículo científico publicado en 2009

Planning in borderline personality disorder: evidence for distinct subpopulations

artículo científico publicado en 2009

Polyautoimmunity in Sjögren Syndrome

artículo científico publicado en 2016

Polymorphisms in the neural nicotinic acetylcholine receptor α4 subunit (CHRNA4) are associated with ADHD in a genetic isolate

artículo científico publicado en 2009

Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease

artículo científico publicado en 2012

Potential cognitive endophenotypes in multigenerational families: segregating ADHD from a genetic isolate

artículo científico publicado en 2011

Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors

artículo científico publicado en 2012

Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study.

artículo científico publicado en 2016

Reproductive success is predicted by social dynamics and kinship in managed animal populations

artículo científico publicado en 2016

Response to Uher et al.

artículo científico publicado en 2015

Retrospective assessment of childhood ADHD symptoms for diagnosis in adults: validity of a short 8-item version of the Wender-Utah Rating Scale

artículo científico publicado en 2016

Rheumatoid arthritis association in Colombian population is restricted to HLA-DRB1*04 QRRAA alleles

article

Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy

scientific journal article

Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement

artículo científico publicado en 2016

SAT0055 Exploration of Risk Factors for Rheumatoid Arthritis Using Advance Recursive Partitioning Approach

scholarly article by N. Molano-Gonzalez et al published June 2014 in Annals of the Rheumatic Diseases

Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility

artículo científico publicado en 2010

Support for association between ADHD and two candidate genes: NET1 and DRD1.

artículo científico publicado en 2005

TAP, HLA-DQB1, and HLA-DRB1 polymorphism in Colombian patients with primary Sjögren's syndrome

scientific article published on 01 June 2002

TAP1 and TAP2 polymorphisms analysis in northwestern Colombian patients with systemic lupus erythematosus

artículo científico publicado en 2003

Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's Disease.

artículo científico publicado en 2018

Temporal gene expression in the hippocampus and peripheral organs to endotoxin-induced systemic inflammatory response in caspase-1-deficient mice

artículo científico publicado en 2015

The Multiple Autoimmune Syndromes. A Clue for the Autoimmune Tautology

article

The PHF21B gene is associated with major depression and modulates the stress response.

artículo científico publicado en 2016

Toward a better understanding of ADHD: LPHN3 gene variants and the susceptibility to develop ADHD

artículo científico publicado en 2010

Tuning major gene variants conditioning human behavior: the anachronism of ADHD.

artículo científico publicado en 2007

Vitiligo: complex segregation and linkage disequilibrium analyses with respect to microsatellite loci spanning the HLA.

artículo científico publicado en 2002

What is next after the genes for autoimmunity?

artículo científico publicado en 2013

Whole exome sequencing of extreme morbid obesity patients: translational implications for obesity and related disorders

artículo científico publicado en 2014

Young adult outcomes in the follow-up of the multimodal treatment study of attention-deficit/hyperactivity disorder: symptom persistence, source discrepancy, and height suppression

artículo científico publicado en 2017

Lista de obras de Mauricio Arcos-Burgos

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.

A Mutation in DAOA Modifies the Age of Onset in PSEN1 E280A Alzheimer's Disease

A New Method for Detecting Significant p-values with Applications to Genetic Data

A common genetic network underlies substance use disorders and disruptive or externalizing disorders

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication

A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD.

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

A latent genetic subtype of major depression identified by whole-exome genotyping data in a Mexican-American cohort

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

A multigenerational pedigree of late-onset Alzheimer's disease implies new genetic causes

A novel alteration in metaxin 1, F202L, is associated with N370S in Gaucher disease

A two-locus genetic interaction between LPHN3 and 11q predicts ADHD severity and long-term outcome

ADHD Endophenotypes in Caribbean Families.

ADHD latent class clusters: DSM-IV subtypes and comorbidity

APOE*E2 allele delays age of onset in PSEN1 E280A Alzheimer's disease

An 1H-MRS framework predicts the onset of Alzheimer's disease symptoms in PSEN1 mutation carriers

An Ultraconserved Brain-Specific Enhancer Within ADGRL3 (LPHN3) Underpins Attention-Deficit/Hyperactivity Disorder Susceptibility

Analysis of brain metabolism by proton magnetic resonance spectroscopy (1H-MRS) in attention-deficit/hyperactivity disorder suggests a generalized differential ontogenic pattern from controls

Attention deficit/hyperactivity disorder (ADHD): complex phenotype, simple genotype?

Attention-Deficit/Hyperactivity Disorder

Attention-Deficit/Hyperactivity Disorder and Comorbid Disruptive Behavior Disorders: Evidence of Pleiotropy and New Susceptibility Loci

Attention-deficit/hyperactivity disorder (ADHD): feasibility of linkage analysis in a genetic isolate using extended and multigenerational pedigrees

Attention-deficit/hyperactivity disorder and comorbidities in 18 Paisa Colombian multigenerational families

Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.

CRISPLD2: a novel NSCLP candidate gene

Candidate gene discovery in autoimmunity by using extreme phenotypes, next generation sequencing and whole exome capture

Chagas' disease susceptibility/resistance: linkage disequilibrium analysis suggests epistasis between major histocompatibility complex and interleukin-10.

Clinical features of multiple sclerosis in a genetically homogeneous tropical population

Clinical outcomes and genome-wide association for a brain methylation site in an antidepressant pharmacogenetics study in Mexican Americans

Clonal population structure of Colombian sylvatic Trypanosoma cruzi.

Complex segregation analysis of non-myoclonic idiopathic generalized epilepsy in families ascertained from probands affected with idiopathic epilepsy with tonic-clonic seizures in Antioquia, Colombia

Complex segregation analysis of nonsyndromic cleft lip/palate in a Chilean population

Congenital Leptin Deficiency and Leptin Gene Missense Mutation Found in Two Colombian Sisters with Severe Obesity.

Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study

Cross validation of pooling/resampling GWAS using the WTCCC data

Definition of mutations in polyautoimmunity

Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest

Early interstitial lung disease in familial pulmonary fibrosis

Environmental influences that affect attention deficit/hyperactivity disorder: study of a genetic isolate

Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations

Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Exploratory data from complete genomes of familial alzheimer disease age-at-onset outliers

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate

Factorial and discriminant analyses of neuropsychological variables in familial and sporadic late onset Alzheimer disease

Familial Alzheimer's Disease and Recessive Modifiers

From the black widow spider to human behavior: Latrophilins, a relatively unknown class of G protein-coupled receptors, are implicated in psychiatric disorders

GWAS reveals new recessive loci associated with non-syndromic facial clefting

Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio

Genetics of non-syndromic childhood obesity and the use of high-throughput DNA sequencing technologies.

Genetics of population isolates.

Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results

Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p

Influence of a latrophilin 3 (LPHN3) risk haplotype on event-related potential measures of cognitive response control in attention-deficit hyperactivity disorder (ADHD).

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

LPHN3 and attention-deficit/hyperactivity disorder: a susceptibility and pharmacogenetic study

Latent class subtyping of attention-deficit/hyperactivity disorder and comorbid conditions

Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C

Linkage and association analysis of ADHD endophenotypes in extended and multigenerational pedigrees from a genetic isolate.

Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?

Low-frequency and rare variants may contribute to elucidate the genetics of major depressive disorder.

Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.

Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder

Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome

Multiple sclerosis in the tropics: genetic association to STR's loci spanning the HLA and TNF.

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder

Mutations in sphingolipid metabolism genes are associated with ADHD

Mutations modifying sporadic Alzheimer's disease age of onset

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Comprehensive Review

Neural Plasticity during Aging

Neural Plasticity in Obesity and Psychiatric Disorders

Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren's syndrome

Origin of the PSEN1 E280A mutation causing early-onset Alzheimer's disease

Pedigree disequilibrium test (PDT) replicates association and linkage between DRD4 and ADHD in multigenerational and extended pedigrees from a genetic isolate.

Pharmacogenetic impact of VKORC1 and CYP2C9 allelic variants on warfarin dose requirements in a hispanic population isolate.

Planning in borderline personality disorder: evidence for distinct subpopulations

Polyautoimmunity in Sjögren Syndrome

Polymorphisms in the neural nicotinic acetylcholine receptor α4 subunit (CHRNA4) are associated with ADHD in a genetic isolate

Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease