Mauricio Arcos Burgos

Summary

Affiliation: National Institutes of Health
Country: USA

Publications

  1. ncbi request reprint Vitiligo: complex segregation and linkage disequilibrium analyses with respect to microsatellite loci spanning the HLA
    Mauricio Arcos-Burgos
    Medical Genetics Branch, National Human Genome Research Institute, National Institute of Health, 10 Center Drive MSC 1852, Building 10, Room 10C107, Bethesda, MD 20892 1852, USA
    Hum Genet 110:334-42. 2002
  2. ncbi request reprint Tuning major gene variants conditioning human behavior: the anachronism of ADHD
    Mauricio Arcos-Burgos
    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892 1852, USA
    Curr Opin Genet Dev 17:234-8. 2007
  3. ncbi request reprint Support for association between ADHD and two candidate genes: NET1 and DRD1
    Aaron J Bobb
    Child Psychiatry Branch, NIMH, NIH, Bethesda, Maryland 20892 1600, USA
    Am J Med Genet B Neuropsychiatr Genet 134:67-72. 2005
  4. ncbi request reprint Attention-deficit/hyperactivity disorder and comorbid disruptive behavior disorders: evidence of pleiotropy and new susceptibility loci
    Mahim Jain
    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892 3717, USA
    Biol Psychiatry 61:1329-39. 2007
  5. pmc Latent class subtyping of attention-deficit/hyperactivity disorder and comorbid conditions
    Maria T Acosta
    National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892 3717, USA
    J Am Acad Child Adolesc Psychiatry 47:797-807. 2008
  6. ncbi request reprint D6S439 microsatellite identifies a new susceptibility region for primary Sjögren's syndrome
    Juan Manuel Anaya
    Cellular Biology and Immunogenetic Unit, Corporacion para Investigaciones Biologicas CIB, Cra 72 A No 78 B 141, Medellin, Colombia
    J Rheumatol 30:2152-6. 2003
  7. ncbi request reprint Attention deficit/hyperactivity disorder (ADHD): complex phenotype, simple genotype?
    Maria Teresa Acosta
    Department of Neurology, Children s National Medical Center, Washington, DC, USA
    Genet Med 6:1-15. 2004
  8. ncbi request reprint Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio
    Lina M Moreno
    Dows Institute for Dental Research, University of Iowa, Iowa City, Iowa 52242, USA
    Am J Med Genet A 125:135-44. 2004
  9. ncbi request reprint Environmental influences that affect attention deficit/hyperactivity disorder: study of a genetic isolate
    David A Pineda
    Neuropsychology and Conduct Disorder Group, Faculty of Psychology, Master Program of Neuropsychology, University of San Buenaventura, Medellin, Colombia
    Eur Child Adolesc Psychiatry 16:337-46. 2007
  10. ncbi request reprint Attention-deficit/hyperactivity disorder and comorbidities in 18 Paisa Colombian multigenerational families
    Juan D Palacio
    Neurosciences Group, University of Antioquia, Medellin, Colombia
    J Am Acad Child Adolesc Psychiatry 43:1506-15. 2004

Collaborators

Detail Information

Publications15

  1. ncbi request reprint Vitiligo: complex segregation and linkage disequilibrium analyses with respect to microsatellite loci spanning the HLA
    Mauricio Arcos-Burgos
    Medical Genetics Branch, National Human Genome Research Institute, National Institute of Health, 10 Center Drive MSC 1852, Building 10, Room 10C107, Bethesda, MD 20892 1852, USA
    Hum Genet 110:334-42. 2002
    ....
  2. ncbi request reprint Tuning major gene variants conditioning human behavior: the anachronism of ADHD
    Mauricio Arcos-Burgos
    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892 1852, USA
    Curr Opin Genet Dev 17:234-8. 2007
    ..Recent molecular and clinical evidence supports Thom Hartmann's Hunter-Farmer theory, reaffirming that ADHD might be an anachronic behavioral trait...
  3. ncbi request reprint Support for association between ADHD and two candidate genes: NET1 and DRD1
    Aaron J Bobb
    Child Psychiatry Branch, NIMH, NIH, Bethesda, Maryland 20892 1600, USA
    Am J Med Genet B Neuropsychiatr Genet 134:67-72. 2005
    ..Because family-based and case-control methods gave divergent results, both should be used in genetic studies of ADHD...
  4. ncbi request reprint Attention-deficit/hyperactivity disorder and comorbid disruptive behavior disorders: evidence of pleiotropy and new susceptibility loci
    Mahim Jain
    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892 3717, USA
    Biol Psychiatry 61:1329-39. 2007
    ..Attention-deficit/hyperactivity disorder (ADHD) comorbid with oppositional defiant disorder (ODD) or conduct disorder (CD) and substance abuse/dependence seems to represent a specific subset within the phenotypic ADHD spectrum...
  5. pmc Latent class subtyping of attention-deficit/hyperactivity disorder and comorbid conditions
    Maria T Acosta
    National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892 3717, USA
    J Am Acad Child Adolesc Psychiatry 47:797-807. 2008
    ..The aim of this study was to perform LCA in a sample of 1,010 individuals from a nationwide recruitment of unilineal nuclear families with at least one child with ADHD and another child either affected or clearly unaffected...
  6. ncbi request reprint D6S439 microsatellite identifies a new susceptibility region for primary Sjögren's syndrome
    Juan Manuel Anaya
    Cellular Biology and Immunogenetic Unit, Corporacion para Investigaciones Biologicas CIB, Cra 72 A No 78 B 141, Medellin, Colombia
    J Rheumatol 30:2152-6. 2003
    ....
  7. ncbi request reprint Attention deficit/hyperactivity disorder (ADHD): complex phenotype, simple genotype?
    Maria Teresa Acosta
    Department of Neurology, Children s National Medical Center, Washington, DC, USA
    Genet Med 6:1-15. 2004
    ..We also will discuss genetic models underlying the complexity of this behavioral phenotype and the probable role of epistatic interactions between major genes contributing to the ADHD phenotype...
  8. ncbi request reprint Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio
    Lina M Moreno
    Dows Institute for Dental Research, University of Iowa, Iowa City, Iowa 52242, USA
    Am J Med Genet A 125:135-44. 2004
    ..This article contains supplementary material, which may be viewed at the American Journal of Medical Genetics website at http://www.interscience.wiley.com/jpages/0148-7299/suppmat/index.html...
  9. ncbi request reprint Environmental influences that affect attention deficit/hyperactivity disorder: study of a genetic isolate
    David A Pineda
    Neuropsychology and Conduct Disorder Group, Faculty of Psychology, Master Program of Neuropsychology, University of San Buenaventura, Medellin, Colombia
    Eur Child Adolesc Psychiatry 16:337-46. 2007
    ..0, P < 0.05). Future studies on the risk of developing ADHD must include these environmental factors as covariates...
  10. ncbi request reprint Attention-deficit/hyperactivity disorder and comorbidities in 18 Paisa Colombian multigenerational families
    Juan D Palacio
    Neurosciences Group, University of Antioquia, Medellin, Colombia
    J Am Acad Child Adolesc Psychiatry 43:1506-15. 2004
    ..This report describes the inclusion strategy and clinical features of participants to facilitate comparisons with other data sets...
  11. pmc Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11
    Mauricio Arcos-Burgos
    National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892 3717, USA
    Am J Hum Genet 75:998-1014. 2004
    ..The concordance between results from different analytical methods of linkage and the replication of data between two independent studies suggest that these loci truly harbor ADHD susceptibility genes...
  12. ncbi request reprint Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate
    Theresa M Zucchero
    University of Iowa, Iowa City 52242, USA
    N Engl J Med 351:769-80. 2004
    ..We searched for a specific genetic factor contributing to this complex trait by examining large numbers of affected patients and families and evaluating a specific candidate gene...
  13. pmc Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35
    Mary L Marazita
    Center for Craniofacial and Dental Genetics, Division of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA 15219, USA
    Am J Hum Genet 75:161-73. 2004
    ..0004). These are the first genomewide significant linkage results ever reported for CL/P, and they represent an unprecedented demonstration of the power of linkage analysis to detect multiple genes simultaneously for a complex disorder...
  14. ncbi request reprint TAP, HLA-DQB1, and HLA-DRB1 polymorphism in Colombian patients with primary Sjögren's syndrome
    Juan Manuel Anaya
    Rheumatology Unit, Corporacion para Investigaciones Biologicas CIB, Medellin, Colombia
    Semin Arthritis Rheum 31:396-405. 2002
    ..Thus, we investigated the influence of transporters associated with antigen processing (TAP), human leukocyte antigen (HLA)-DQB1, and HLA-DRB1 gene polymorphism in mestizo Colombian patients with pSS...
  15. pmc Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?
    Mahim Jain
    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA
    Am J Med Genet A 146:2308-11. 2008