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List of works by Mauricio Arcos-Burgos

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

scientific article published on 22 March 2016

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

scientific article published on 5 January 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

scientific article

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

scientific article

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

scientific article

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

scientific article published in June 2010

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 5 July 2011

ADHD Endophenotypes in Caribbean Families.

scientific article published in March 2018

ADHD latent class clusters: DSM-IV subtypes and comorbidity

scientific article

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

scientific article

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

scientific article

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

scientific article published on 14 July 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

scientific article

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

scientific article (publication date: 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

scientific article published in December 2004

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

scientific article

CRISPLD2: a novel NSCLP candidate gene

article

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

scientific article

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

scientific article published in July 2004

Clinical features of multiple sclerosis in a genetically homogeneous tropical population

scientific article

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

scientific article

Clonal population structure of Colombian sylvatic Trypanosoma cruzi

scientific article published in December 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

scientific article published in August 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.

scientific article published on 7 May 2019

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

scientific article published on 4 November 2010

Cross validation of pooling/resampling GWAS using the WTCCC data

Definition of mutations in polyautoimmunity

scientific article

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

scientific article published on 21 July 2016

Early interstitial lung disease in familial pulmonary fibrosis

scientific article

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

scientific article published on August 2007

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

scientific article

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

scientific article published in August 2010

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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.

scientific article

Genetics of population isolates.

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on July 2008

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

scientific article

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

scientific article published on 24 November 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.

scientific article published on 27 March 2018

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

scientific article

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

scientific article

Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome

scientific article

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

scientific article

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

scientific article

Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder

scientific article

Mutations in sphingolipid metabolism genes are associated with ADHD

scientific article published on 13 July 2020

Mutations modifying sporadic Alzheimer's disease age of onset

scientific article published on 30 August 2016

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Comprehensive Review

scientific article published on 07 August 2019

Neural Plasticity during Aging

scientific article published on 26 March 2019

Neural Plasticity in Obesity and Psychiatric Disorders

scientific article published on 7 April 2016

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

scientific article published on 2 June 2015

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

scientific article

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

scientific article published in March 2004

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

scientific article published on 29 June 2009

Planning in borderline personality disorder: evidence for distinct subpopulations

scientific article published in January 2009

Polyautoimmunity in Sjögren Syndrome

scientific article

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

scientific article published on 25 April 2009

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

scientific article published on 19 June 2012

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 11 May 2016

Response to Uher et al.

scientific article published in April 2015

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

scientific article

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

scientific article published on 29 June 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

scientific article published on 12 November 2010

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

scientific article

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

scientific article published on April 2003

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

scientific article published on 15 August 2018

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

scientific article

The Multiple Autoimmune Syndromes. A Clue for the Autoimmune Tautology

article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 12 March 2002

What is next after the genes for autoimmunity?

scientific article

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

scientific article

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

scientific article

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