FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Mauricio Arcos-Burgos

Research Profile

Geographic Areas

Colombia

Disorders

Physiology

Concepts & Ideas

Genes & Molecular Sequences

Procedures

Anatomy

Brain

Chemicals & Drugs

Co-author Network

Publications

TOP 3
Andreas J Fallgatter; Christian P Jacob; Mauricio Arcos-Burgos; Thomas Dresler; Ann-Christine Ehlis; Maximilian Muenke; Andreas Reif; Klaus-Peter Lesch
Influence of a Latrophilin 3 (LPHN3) risk haplotype on event-related potential measures of cognitive response control in attention-deficit hyperactivity disorder (ADHD).
J I Vélez; N Acosta-Baena; Daniel Camilo Aguirre-Acevedo; Settara C Chandrasekharappa; J C Correa; G Garcia; U Harper; E Henao; M C Jaramillo-Elorza; M Jones; K S Kosik; Francisco Lopera; C M Lopera-Gómez; L Lopez; A F Martinez; D Rivera; N J Schork; B D Solomon; J M Swanson; Mauricio Arcos-Burgos
Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease.
Mauricio Arcos-Burgos; Francisco Xavier Castellanos; Ana C Londoño; Francisco Lopera; Maria T Acosta; Andres Arbelaez; Juan David Palacio; David A Pineda; Jorge I Vélez; Maximilian Muenke
Analysis of brain metabolism by proton magnetic resonance spectroscopy (1H-MRS) in attention-deficit/hyperactivity disorder suggests a generalized differential ontogenic pattern from controls.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Mauricio Arcos-Burgos (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Andreas J Fallgatter; Christian P Jacob; Mauricio Arcos-Burgos; Thomas Dresler; Ann-Christine Ehlis; Maximilian Muenke; Andreas Reif; Klaus-Peter Lesch
Influence of a Latrophilin 3 (LPHN3) risk haplotype on event-related potential measures of cognitive response control in attention-deficit hyperactivity disorder (ADHD).
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2013;23(6):458-68.
2013: J I Vélez; N Acosta-Baena; Daniel Camilo Aguirre-Acevedo; Settara C Chandrasekharappa; J C Correa; G Garcia; U Harper; E Henao; M C Jaramillo-Elorza; M Jones; K S Kosik; Francisco Lopera; C M Lopera-Gómez; L Lopez; A F Martinez; D Rivera; N J Schork; B D Solomon; J M Swanson; Mauricio Arcos-Burgos
Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease.
Molecular psychiatry 2013;18(5):568-75.
2012: Mauricio Arcos-Burgos; Francisco Xavier Castellanos; Ana C Londoño; Francisco Lopera; Maria T Acosta; Andres Arbelaez; Juan David Palacio; David A Pineda; Jorge I Vélez; Maximilian Muenke
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 and hyperactivity disorders 2012;4(4):205-12.
2012: Matthew A Lalli; L Madrigal; Mary Luz Arcila; Mauricio Arcos-Burgos; Gloria Garcia; Kenneth S Kosik; Francisco Lopera
Exploratory data from complete genomes of familial alzheimer disease age-at-onset outliers.
Human mutation 2012;33(12):1630-4.
2012: Juan-Manuel Anaya; JOHN ENRIQUE CASTIBLANCO; Ricard Cervera; Carlos Dias; Juan Esteban Gallo; José Gómez-Puerta; Roger A Levy; Ruben D Mantilla; Ricardo Pineda-Tamayo; Adriana Rojas-Villarraga; Yehuda Shoenfeld; Mauricio Arcos-Burgos
The multiple autoimmune syndromes. A clue for the autoimmune tautology.
Clinical reviews in allergy & immunology 2012;43(3):256-64.
2012: Mauricio Camargo; Settara C Chandrasekharappa; Ursula Harper; Marypat Jones; Andrew C Lidral; Ariel F Martinez; Lina Moreno; Dora Rivera; Erich Roessler; Benjamin D Solomon; Jorge I Vélez; Mauricio Arcos-Burgos
GWAS reveals new recessive loci associated with non-syndromic facial clefting.
European journal of medical genetics 2012;55(10):510-4.
2012: M Jain; K-P Lesch; Ana C Londoño; Francisco Lopera; J Meyer; Maria T Acosta; A Arbelaez; Mauricio Arcos-Burgos; J E Bailey-Wilson; Joan Z Balog; F Xavier Castellanos; J Elia; Christine M Freitag; H Hakonarson; U Hemminger; C Jacob; Juan David Palacio; Luis Palacio; H Palmason; David A Pineda; Tobias Renner; E Roessler; J Romanos; Marcel Romanos; C Seitz; J Swanson; J I Vélez; Susanne Walitza; Andreas Warnke; Maximilian Muenke
A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD.
Molecular psychiatry 2012;17(7):741-7.
2012: Mauricio Arcos-Burgos; Benjamin D Solomon; Jorge I Vélez; Maximilian Muenke
A common genetic network underlies substance use disorders and disruptive or externalizing disorders.
Human genetics 2012;131(6):917-29.
2011: David A Pineda; Daniel E Pineda-Alvarez; Isabel Puerta; Natalia Trujillo-Orrego; Jorge I Velez; Maria T Acosta; DC Aguirre-Acevedo; Clara P Arango; Liliana Hincapié-Henao; Sandra I Holzinger; John Lewis; Francisco Lopera; Ariel F Martinez; Maximilian Muenke; Juan David Palacio; Mauricio Arcos-Burgos
Potential cognitive endophenotypes in multigenerational families: segregating ADHD from a genetic isolate.
Attention deficit and hyperactivity disorders 2011;3(3):291-9.
2011: Horia C Stanescu; Mauricio Arcos-Burgos; Alan Medlar; Detlef Bockenhauer; Anna Kottgen; Liviu Dragomirescu; Catalin Voinescu; Naina Patel; Kerra Pearce; Mike Hubank; Henry A F Stephens; Valerie Laundy; Sandosh Padmanabhan; Anna Zawadzka; Julia M Hofstra; Marieke J H Coenen; Martin den Heijer; Lambertus A L M Kiemeney; Delphine Bacq-Daian; Benedicte Stengel; Stephen H Powis; Paul Brenchley; John Feehally; Andrew J Rees; Hanna Debiec; Jack F M Wetzels; Pierre Ronco; Peter W Mathieson; Robert Kleta
Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy.
The New England journal of medicine 2011;364(7):616-26.
2011: Maria T Acosta; Mauricio Arcos-Burgos; Joan Z Balog; M L Bustamante; J I Vélez; Maximilian Muenke
A two-locus genetic interaction between LPHN3 and 11q predicts ADHD severity and long-term outcome.
Translational psychiatry 2011;1():e17.
2011: Sabina Domené; Horia Stanescu; Deeann Wallis; Bradford Tinloy; Daniel E Pineda; Robert Kleta; Mauricio Arcos-Burgos; Erich Roessler; Maximilian Muenke
Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011;156B(1):11-8.
2011: Ariel F Martinez; Maximilian Muenke; Mauricio Arcos-Burgos
From the black widow spider to human behavior: Latrophilins, a relatively unknown class of G protein-coupled receptors, are implicated in psychiatric disorders.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011;156B(1):1-10.
2010: Mauricio Arcos-Burgos; Maximilian Muenke
Toward a better understanding of ADHD: LPHN3 gene variants and the susceptibility to develop ADHD.
Attention deficit and hyperactivity disorders 2010;2(3):139-47.
2010: David A Pineda; Natalia Trujillo-Orrego; DC Aguirre-Acevedo; Clara P Arango; Liliana Hincapié-Henao; David A Montoya-Arenas; Francisco Lopera; Daniel E Pineda-Alvarez; Mauricio Arcos-Burgos; Maximilian Muenke
[Utility of the Wender-Utah rating scale and the checklists for the diagnosis of familial attention deficit hyperactivity disorder in adults. Convergent and concurrent validities].
Revista de neurologia 2010;50(4):207-16.
2010: Lina Palacio; Diana Falla; Ignacio Tobon; Fernando Mejia; John Lewis; Ariel F Martinez; Mauricio Arcos-Burgos; Mauricio Camargo
Pharmacogenetic impact of VKORC1 and CYP2C9 allelic variants on warfarin dose requirements in a hispanic population isolate.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2010;16(1):83-90.
2010: Nicole M Yanjanin; Jorge I Vélez; Andrea Gropman; Kelly King; Simona E Bianconi; Sandra K Conley; Carmen C Brewer; Beth Solomon; William J Pavan; Mauricio Arcos-Burgos; Marc C Patterson; Forbes D Porter
Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(1):132-40.
2009: Josephine Elia; Mauricio Arcos-Burgos; Kelly L Bolton; Paul J Ambrosini; Wade Berrettini; Maximilian Muenke
ADHD latent class clusters: DSM-IV subtypes and comorbidity.
Psychiatry research 2009;170(2-3):192-8.
2009: Lina M Moreno; M Adela Mansilla; SA Bullard; Margaret E Cooper; Tamara D Busch; Junichiro Machida; Marla K Johnson; David Brauer; Katherine Krahn; Sandra Daack-Hirsch; Jamie L'heureux; Consuelo Valencia-Ramirez; Dora Rivera; Ana Maria López; Manuel A Moreno; Anne Hing; Edward J Lammer; Marilyn Jones; Kaare Christensen; Rolv T Lie; Astanand Jugessur; Allen J Wilcox; Peter Chines; Elizabeth Pugh; Kim Doheny; Mauricio Arcos-Burgos; Mary L Marazita; Jeffrey C Murray; Andrew C Lidral
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate.
Human molecular genetics 2009;18(24):4879-96.
2009: Detlef Bockenhauer; Sally Feather; Horia C Stanescu; Sascha Bandulik; Anselm A Zdebik; Markus Reichold; Jonathan Tobin; Evelyn Lieberer; Christina Sterner; Guida Landoure; Ruchi Arora; Tony Sirimanna; Dorothy Thompson; J Helen Cross; William G Van't Hoff; Omar Al Masri; Kjell Tullus; Stella Yeung; Yair Anikster; Enriko Klootwijk; Mike Hubank; Michael J Dillon; Dirk Heitzmann; Mauricio Arcos-Burgos; Mark A Knepper; Angus Dobbie; William A Gahl; Richard Warth; Eamonn Sheridan; Robert Kleta
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations.
The New England journal of medicine 2009;360(19):1960-70.
2009: Deeann Wallis; Mauricio Arcos-Burgos; Mahim Jain; F Xavier Castellanos; Juan David Palacio; David A Pineda; Francisco Lopera; Horia Stanescu; Daniel Pineda; Kate Berg; Luis Palacio; Joan E Bailey-Wilson; Maximilian Muenke
Polymorphisms in the neural nicotinic acetylcholine receptor α4 subunit (CHRNA4) are associated with ADHD in a genetic isolate.
Attention deficit and hyperactivity disorders 2009;1(1):19-24.
2009: N Trujillo-Orrego; David A Pineda; Clara P Arango; Isabel Puerta; Francisco Lopera; DC Aguirre-Acevedo; L Hincapie-Henao; D E Pineda-Alvarez; Mauricio Arcos-Burgos; Maximilian Muenke
[Attention deficit hyperactivity behavioral phenotype dimensions of adults from Antioquian families using the Wender-Utah Scale -Spanish version].
Revista de neurologia 2009;48(8):400-6.
2009: M Leonor Bustamante; Juana Villarroel; Valeria Francesetti; Matías Ríos; Mauricio Arcos-Burgos; S Jerez; P Iturra; Aldo Solari; Herman Silva
Planning in borderline personality disorder: evidence for distinct subpopulations.
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2009;10(4 Pt 2):512-7.
2009: Huai-Rong Luo; Gui-Sheng Wu; Chuanhui Dong; Mauricio Arcos-Burgos; Luciana Ribeiro; Julio Licinio; Ma-Li Wong
Association of PDE11A global haplotype with major depression and antidepressant drug response.
Neuropsychiatric disease and treatment 2009;5():163-70.
2009: Mary L Marazita; Andrew C Lidral; Jeffrey C Murray; L Leigh Field; Brion S Maher; Toby Goldstein McHenry; Margaret E Cooper; Manika Govil; Sandra Daack-Hirsch; Bridget Riley; Astanand Jugessur; Temis Felix; Lina Morene; M Adela Mansilla; Alexandre R Vieira; Kim Doheny; Elizabeth Pugh; Consuelo Valencia-Ramirez; Mauricio Arcos-Burgos
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.
Human heredity 2009;68(3):151-70.
2008: Mahim Jain; Deeann Wallis; Nathaniel H Robin; Fabienne Wavrant De Vrieze; John Hardy; Mohsen Ghadami; Kristin Bosse; Regina C Betz; Markus M Nöthen; Mauricio Arcos-Burgos; Maximilian Muenke
Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?
American journal of medical genetics. Part A 2008;146A(17):2308-11.
2008: Maria T Acosta; F Xavier Castellanos; Kelly L Bolton; Joan Z Balog; Patricia Eagen; Linda Nee; Janet Jones; Luis Palacio; Christopher Sarampote; Heather F Russell; Kate Berg; Mauricio Arcos-Burgos; Maximilian Muenke
Latent class subtyping of attention-deficit/hyperactivity disorder and comorbid conditions.
Journal of the American Academy of Child and Adolescent Psychiatry 2008;47(7):797-807.
2007: Ivan O Rosas; Ping Ren; Nilo A Avila; Catherine K Chow; Teri J Franks; William D Travis; J Philip McCoy; Rose M May; Hai-Ping Wu; Dao Nguyen; Mauricio Arcos-Burgos; Sandra D MacDonald; Bernadette R Gochuico
Early interstitial lung disease in familial pulmonary fibrosis.
American journal of respiratory and critical care medicine 2007;176(7):698-705.
2007: David A Pineda; Luis Palacio; Isabel Puerta; Vilma Merchán; Clara P Arango; Astrid Yuleth Galvis; Mónica Gómez; Daniel Camilo Aguirre-Acevedo; Francisco Lopera; Mauricio Arcos-Burgos
Environmental influences that affect attention deficit/hyperactivity disorder: study of a genetic isolate.
European child & adolescent psychiatry 2007;16(5):337-46.
2007: Mahim Jain; Luis Palacio; F Xavier Castellanos; Juan David Palacio; David A Pineda; Maria I Restrepo; Juan F Muñoz; Francisco Lopera; Deeann Wallis; Kate Berg; Joan E Bailey-Wilson; Mauricio Arcos-Burgos; Maximilian Muenke
Attention-deficit/hyperactivity disorder and comorbid disruptive behavior disorders: evidence of pleiotropy and new susceptibility loci.
Biological psychiatry 2007;61(12):1329-39.
2007: Mauricio Arcos-Burgos; Maria T Acosta
Tuning major gene variants conditioning human behavior: the anachronism of ADHD.
Current opinion in genetics & development 2007;17(3):234-8.
2005: J C Pérez-Póveda; Luis Palacio; Mauricio Arcos-Burgos
[Description of an endogamous, multigenerational and extensive family with benign hereditary chorea from the Paisa community].
Revista de neurologia 2005;41(2):95-8.
2005: Adriano Jimenez-Escrig; Estrella Gomez-Tortosa; Manuel Baron; Alberto Rabano; Mauricio Arcos-Burgos; Luis Guillermo Palacios; Antonio Yusta; Pilar Anta; Immaculada Perez; Margarita Hierro; David G Munoz; Sagrario Barquero
A multigenerational pedigree of late-onset Alzheimer's disease implies new genetic causes.
Brain : a journal of neurology 2005;128(Pt 7):1707-15.
2005: Aaron J Bobb; Anjene Addington; Ellen Sidransky; Michele C Gornick; Jason P Lerch; Deanna Greenstein; Liv S Clasen; Wendy S Sharp; Gale Inoff-Germain; Fabienne Wavrant-De Vrièze; Mauricio Arcos-Burgos; Richard E Straub; John Hardy; F Xavier Castellanos; Judy Rapoport
Support for association between ADHD and two candidate genes: NET1 and DRD1.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;134B(1):67-72.
2004: Luis Palacio; Jorge Luis Sánchez; ME Jiménez; D Rivera Valencia; I Jiménez-Ramírez; Mauricio Arcos-Burgos
[Linkage analysis of the 15q25-15q22 region in an extended multigenerational family segregating for idiopathic epilepsy].
Revista de neurologia 2004;39(11):1021-5.
2004: Juan David Palacio; F Xavier Castellanos; David A Pineda; Francisco Lopera; Mauricio Arcos-Burgos; Yakeel T Quiroz; Gloria C Henao; Isabel Puerta; Dora L Ramírez; Judy Rapoport; Joan E Bailey-Wilson; Kate Berg; Maximilian Muenke
Attention-deficit/hyperactivity disorder and comorbidities in 18 Paisa Colombian multigenerational families.
Journal of the American Academy of Child and Adolescent Psychiatry 2004;43(12):1506-15.
2004: Mauricio Arcos-Burgos; F Xavier Castellanos; David A Pineda; Francisco Lopera; Juan David Palacio; Luis Palacio; Judy Rapoport; Kate Berg; Joan E Bailey-Wilson; Maximilian Muenke
Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.
American journal of human genetics 2004;75(6):998-1014.
2004: Robert Kleta; Elisa Romeo; Zorica Ristic; Toshihiro Ohura; Caroline Stuart; Mauricio Arcos-Burgos; Mital H Dave; Carsten A Wagner; Simone R M Camargo; Sumiko Inoue; Norio Matsuura; Amanda Helip-Wooley; Detlef Bockenhauer; Richard Warth; Isa Bernardini; Gepke Visser; Thomas Eggermann; Philip Lee; Arthit Chairoungdua; Promsuk Jutabha; Ellappan Babu; Sirinun Nilwarangkoon; Naohiko Anzai; Yoshikatsu Kanai; François Verrey; William A Gahl; Akio Koizumi
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.
Nature genetics 2004;36(9):999-1002.
2004: Theresa M Zucchero; Margaret E Cooper; Brion S Maher; Sandra Daack-Hirsch; Buena Nepomuceno; Lucilene Ribeiro; Diana Caprau; Kaare Christensen; Yasushi Suzuki; Junichiro Machida; Nagato Natsume; Koh-ichiro Yoshiura; Alexandre R Vieira; Iêda M Orioli; Eduardo E Castilla; Lina Moreno; Mauricio Arcos-Burgos; Andrew C Lidral; L Leigh Field; You-e Liu; Ajit Ray; Toby Goldstein; Rebecca E Schultz; Min Shi; Marla K Johnson; Shinji Kondo; Brian C Schutte; Mary L Marazita; Jeffrey C Murray
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.
The New England journal of medicine 2004;351(8):769-80.
2004: Mary L Marazita; Jeffrey C Murray; Andrew C Lidral; Mauricio Arcos-Burgos; Margaret E Cooper; Toby Goldstein; Brion S Maher; Sandra Daack-Hirsch; Rebecca Schultz; M Adela Mansilla; L Leigh Field; You-e Liu; Natalie Prescott; Sue Malcolm; Robin Winter; Ajit Ray; Lina Moreno; Consuelo Valencia; Katherine Neiswanger; Diego F Wyszynski; Joan E Bailey-Wilson; Hasan Albacha-Hejazi; Terri H beaty; Iain McIntosh; Jacqueline B Hetmanski; Gökhan Tunçbilek; Matthew Edwards; Louise Harkin; Rodney Scott; Laurence G Roddick
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.
American journal of human genetics 2004;75(2):161-73.
2004: M Moreno; E L Silva; L E Ramírez; Luis Palacio; Dora Rivera; Mauricio Arcos-Burgos
Chagas' disease susceptibility/resistance: linkage disequilibrium analysis suggests epistasis between major histocompatibility complex and interleukin-10.
Tissue antigens 2004;64(1):18-24.
2004: Mauricio Arcos-Burgos; F Xavier Castellanos; D Konecki; Francisco Lopera; David A Pineda; Juan David Palacio; Judy Rapoport; Kate Berg; Joan E Bailey-Wilson; Maximilian Muenke
Pedigree disequilibrium test (PDT) replicates association and linkage between DRD4 and ADHD in multigenerational and extended pedigrees from a genetic isolate.
Molecular psychiatry 2004;9(3):252-9.
2004: Lina M Moreno; Mauricio Arcos-Burgos; Mary L Marazita; Katherine Krahn; Brion S Maher; Margaret E Cooper; Consuelo R Valencia-Ramirez; Andrew C Lidral
Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio.
American journal of medical genetics. Part A 2004;125A(2):135-44.
2004: Mary E LaMarca; Mona Goldstein; Nahid Tayebi; Mauricio Arcos-Burgos; Brian M Martin; Ellen Sidransky
A novel alteration in metaxin 1, F202L, is associated with N370S in Gaucher disease.
Journal of human genetics 2004;49(4):220-2.
2004: Maria T Acosta; Mauricio Arcos-Burgos; Maximilian Muenke
Attention deficit/hyperactivity disorder (ADHD): complex phenotype, simple genotype?
Genetics in medicine : official journal of the American College of Medical Genetics 2004;6(1):1-15.
2003: Juan-Manuel Anaya; Dora Rivera; Luis Palacio; Mauricio Arcos-Burgos; Paula A Correa
D6S439 microsatellite identifies a new susceptibility region for primary Sjögren's syndrome.
The Journal of rheumatology 2003;30(10):2152-6.
2003: Paula A Correa; José F Molina; L F Pinto; Mauricio Arcos-Burgos; M Herrera; Juan-Manuel Anaya
TAP1 and TAP2 polymorphisms analysis in northwestern Colombian patients with systemic lupus erythematosus.
Annals of the rheumatic diseases 2003;62(4):363-5.
2002: Shinji Kondo; Brian C Schutte; Rebecca J Richardson; Bryan Bjork; Alexandra S Knight; Yoriko Watanabe; Emma Howard; Renata L L Ferreira de Lima; Sandra Daack-Hirsch; Achim Sander; Donna M McDonald-McGinn; Elaine H Zackai; Edward J Lammer; Arthur S Aylsworth; Holly H Ardinger; Andrew C Lidral; Barbara R Pober; Lina Moreno; Mauricio Arcos-Burgos; Consuelo Valencia; Claude Houdayer; Michel Bahuau; Danilo Moretti-Ferreira; Antonio Richieri-Costa; Michael J Dixon; Jeffrey C Murray
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.
Nature genetics 2002;32(2):285-9.
2002: Joseph F Arboleda-Velasquez; Francisco Lopera; E Lopez; M P Frosch; D Sepulveda-Falla; J E Gutierrez; S Vargas; Miguel Medina; C Martinez De Arrieta; R V Lebo; S A Slaugenhaupt; Rebecca A Betensky; A Villegas; Mauricio Arcos-Burgos; Dora Rivera; J C Restrepo; Kenneth S Kosik
C455R notch3 mutation in a Colombian CADASIL kindred with early onset of stroke.
Neurology 2002;59(2):277-9.
2002: Juan-Manuel Anaya; Paula A Correa; Ruben D Mantilla; Mauricio Arcos-Burgos
TAP, HLA-DQB1, and HLA-DRB1 polymorphism in Colombian patients with primary Sjögren's syndrome.
Seminars in arthritis and rheumatism 2002;31(6):396-405.
2002: Luis Palacio; Dora Rivera; Juan José Builes; ME Jiménez; M Salgar; Juan-Manuel Anaya; I Jiménez; M Camargo; Mauricio Arcos-Burgos; Jorge Luis Sánchez
Multiple sclerosis in the tropics: genetic association to STR's loci spanning the HLA and TNF.
Multiple sclerosis (Houndmills, Basingstoke, England) 2002;8(3):249-55.
2002: Mauricio Arcos-Burgos; F Xavier Castellanos; Francisco Lopera; David A Pineda; Juan David Palacio; M Garcia; Gloria C Henao; Luis Palacio; Kate Berg; Joan E Bailey-Wilson; Maximilian Muenke
Attention-deficit/hyperactivity disorder (ADHD): feasibility of linkage analysis in a genetic isolate using extended and multigenerational pedigrees.
Clinical genetics 2002;61(5):335-43.
2002: Mauricio Arcos-Burgos; Maximilian Muenke
Genetics of population isolates.
Clinical genetics 2002;61(4):233-47.
2002: Mauricio Arcos-Burgos; Elba Parodi; Marta Salgar; Elina Bedoya; Juan José Builes; Diego Jaramillo; Gabriel Ceballos; Alberto Uribe; Natalia Rivera; Dora Rivera; Idalyd Fonseca; Mauricio Camargo; Guillermo Palacio
Vitiligo: complex segregation and linkage disequilibrium analyses with respect to microsatellite loci spanning the HLA.
Human genetics 2002;110(4):334-42.
2002: Juan-Manuel Anaya; Paula A Correa; Ruben D Mantilla; Mauricio Arcos-Burgos
Rheumatoid arthritis association in Colombian population is restricted to HLA-DRB1*04 QRRAA alleles.
Genes and immunity 2002;3(1):56-8.
2001: Jorge Luis Sánchez; Luis Palacio; Carlos Santiago Uribe; Ana C Londoño; A Villa; M Jiménez; Juan-Manuel Anaya; I Jiménez; M Camargo; Mauricio Arcos-Burgos
Clinical features of multiple sclerosis in a genetically homogeneous tropical population.
Multiple sclerosis (Houndmills, Basingstoke, England) 2001;7(4):227-9.
2001: Francisco Lopera; N Rivera; J Arboleda; T Restrepo; Mauricio Arcos-Burgos
[Analysis of complex segregation in a large family with hereditary cerebrovascular disease in Antioquia, Colombia].
Revista de neurologia 2001;32(3):222-5.
2000: Francisco Lopera; J Arboleda; Sonia Moreno; N Almeida; M Cuartas; Mauricio Arcos-Burgos
[Clinical characteristics of hereditary cerebrovascular disease in a large family from Colombia].
Revista de neurologia 2000;31(10):901-7.
2000: M Velásquez; Mauricio Arcos-Burgos; M E Toro; Amanda Castaño; L Madrigal; Sonia Moreno; Nicolas Jaramillo-O; Francisco Lopera
[Factorial and discriminant analyses of neuropsychological variables in familial and sporadic late onset Alzheimer disease].
Revista de neurologia 2000;31(6):501-6.
2000: Mauricio Arcos-Burgos; Luis Palacio; O Mora; Jorge Luis Sánchez; M Jiménez; I Jiménez
[Molecular genetic aspects of the susceptibility to develop idiopathic epilepsy].
Revista de neurologia 2000;30(2):173-7.
2000: Jorge Luis Sánchez; Luis Palacio; Ana C Londoño; Carlos Santiago Uribe; ME Jiménez; Luis A Villa; Juan-Manuel Anaya; M Luisa Bravo; Nicolas Jaramillo-O; Gabriel Bedoya; Claudia Espinal; I Jiménez; Mauricio Arcos-Burgos
[Multiple sclerosis: epidemiological-genetic studies in the population of Antioquia, Colombia. Disequilibrium of HLA DQ alpha].
Revista de neurologia 2000;30(2):170-3.
1999: Nicolas Jaramillo-O; J Moreno; Omar Triana; Mauricio Arcos-Burgos; S Muñoz; A Solari
Genetic structure and phylogenetic relationships of Colombian Trypanosoma cruzi populations as determined by schizodeme and isoenzyme markers.
The American journal of tropical medicine and hygiene 1999;61(6):986-93.
1999: Mauricio Arcos-Burgos; Luis Palacio; Jorge Luis Sánchez; ME Jiménez; O Mora; Lina Zuluaga; Carlos Santiago Uribe; G López-Gartner; I Jiménez
[Genetic anticipation in idiopathic epilepsies].
Revista de neurologia 1999;29(7):597-9.
1999: Francisco Lopera; N Tobón; Mauricio Arcos-Burgos; S Vargas; J E Gutiérrez; Mónica Rosselli; Alfredo Ardila
[Image characterization of Alzheimer's disease associated with the E280A-PS1 mutation. Case-control study: MRI findings].
Revista de neurologia 1999;29(1):6-12.
1999: A Duque-Castaño; M I Roldán; JC Arango-Viana; Mauricio Arcos-Burgos; H Cubillo; Francisco Lopera
[Neuropathological findings in early-onset Alzheimer's disease (E280a-PS1 mutation)].
Revista de neurologia 1999;29(1):1-6.
1999: O Mora; I Jiménez; Luis Palacio; M Jiménez; Jorge Luis Sánchez; Lina Zuluaga; Carlos Santiago Uribe; R Isaza; ALVARO MUNOZ; Mauricio Arcos-Burgos
[Mode of inheritance of idiopathic generalized non-myoclonic epilepsy in families investigated by studying members with idiopathic epilepsy with tonic-clonic crises on waking. Antioquia, Colombia].
Revista de neurologia 1999;28(8):768-71.
1999: Francisco Lopera; Luis Palacio; I Jiménez; P Villegas; Isabel Puerta; David A Pineda; M Jiménez; Mauricio Arcos-Burgos
[Discrimination between genetic factors in attention deficit].
Revista de neurologia 1999;28(7):660-4.
1999: Mauricio Arcos-Burgos; Guillermo Palacio; Jorge Luis Sánchez; Ana C Londoño; Carlos Santiago Uribe; M Jiménez; A Villa; Juan-Manuel Anaya; M Luisa Bravo; Nicolas Jaramillo-O; Claudia Espinal; Juan José Builes; Manuel Moreno; I Jiménez
Multiple sclerosis: association to HLA DQalpha in a tropical population.
Experimental and clinical immunogenetics 1999;16(3):131-8.
1998: E Márquez; Mauricio Arcos-Burgos; Omar Triana; J Moreno; Nicolas Jaramillo-O
Clonal population structure of Colombian sylvatic Trypanosoma cruzi.
The Journal of parasitology 1998;84(6):1143-9.
1998: Jorge Luis Sánchez; I Jiménez; Luis Palacio; M Jiménez; O Mora; Lina Zuluaga; Carlos Santiago Uribe; R Isaza; A Villa; R Blanco; Mauricio Arcos-Burgos
[Comparison of the multifactorial model as a hereditary mechanism of non-myoclonic generalized idiopathic epilepsy and partial idiopathic epilepsy].
Revista de neurologia 1998;26(153):739-44.
1998: Mauricio Arcos-Burgos; Luis Palacio; I Jiménez; N Pineda; O Mora; Jorge Luis Sánchez; M Jiménez; ALVARO MUNOZ; V Brancolini; M Devoto; Andres Ruiz-Linares
[Antiochian genealogies in which idiopathic epilepsy presents familial conglomeration. Simulations of power for the detection of genetic linkage].
Revista de neurologia 1998;26(149):50-2.
1997: Francisco Lopera; A Ardilla; A Martínez; L Madrigal; JC Arango-Viana; Cynthia A Lemere; Juan Carlos Arango Lasprilla; L Hincapíe; Mauricio Arcos-Burgos; Jorge E Ossa; I M Behrens; Joanne Norton; Corinne Lendon; Alison Goate; Andres Ruiz-Linares; Mónica Rosselli; Kenneth S Kosik
Clinical features of early-onset Alzheimer disease in a large kindred with an E280A presenilin-1 mutation.
JAMA : the journal of the American Medical Association 1997;277(10):793-9.
1996: I Jiménez; O Mora; M Jiménez; Lina Zuluaga; R Isaza; Jorge Luis Sánchez; Carlos Santiago Uribe; Rafael Blanco; Mauricio Arcos-Burgos
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.
Human genetics 1996;98(2):214-8.
1996: I Jiménez; O Mora; G Lopez; ME Jiménez; L Zuluga; R Isaza; J L Sanchez; Carlos Santiago Uribe; Carlos Y Valenzuela; Rafael Blanco; Mauricio Arcos-Burgos
Idiopathic epilepsy with generalized tonic clonic seizures in Antioquia, Colombia: is the joint Amerindian and Negroid racial admixture the cause of its high prevalence?
Biological research 1996;29(3):297-304.
1996: Pilar Herrera; Mauricio Arcos-Burgos; Carlos Y Valenzuela; J P Pandey
Gm and Km allotypes and typhoid fever.
Experimental and clinical immunogenetics 1996;13(3-4):121-5.