PubRank

Mauricio Arcos-Burgos

Author PubWeight™ 70.98‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. N Engl J Med 2004 7.91
2 Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy. N Engl J Med 2011 6.34
3 Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nat Genet 2002 6.29
4 Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations. N Engl J Med 2009 4.96
5 A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Nat Genet 2010 3.63
6 Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. Am J Hum Genet 2004 2.65
7 Clinical outcomes and genome-wide association for a brain methylation site in an antidepressant pharmacogenetics study in Mexican Americans. Am J Psychiatry 2014 2.26
8 Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C. Am J Med Genet B Neuropsychiatr Genet 2010 2.08
9 Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p. Blood 2010 2.00
10 Early interstitial lung disease in familial pulmonary fibrosis. Am J Respir Crit Care Med 2007 1.91
11 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. Hum Hered 2009 1.71
12 FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate. Hum Mol Genet 2009 1.55
13 Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome. N Engl J Med 2014 1.53
14 Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet 2008 1.48
15 Support for association between ADHD and two candidate genes: NET1 and DRD1. Am J Med Genet B Neuropsychiatr Genet 2005 1.47
16 Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder. Nat Genet 2004 1.45
17 CRISPLD2: a novel NSCLP candidate gene. Hum Mol Genet 2007 1.32
18 Latent class subtyping of attention-deficit/hyperactivity disorder and comorbid conditions. J Am Acad Child Adolesc Psychiatry 2008 1.17
19 Attention-deficit/hyperactivity disorder and comorbid disruptive behavior disorders: evidence of pleiotropy and new susceptibility loci. Biol Psychiatry 2006 1.12
20 Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio. Am J Med Genet A 2004 1.05
21 Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility. Am J Med Genet B Neuropsychiatr Genet 2010 0.96
22 The multiple autoimmune syndromes. A clue for the autoimmune tautology. Clin Rev Allergy Immunol 2012 0.95
23 Attention-deficit/hyperactivity disorder and comorbidities in 18 Paisa Colombian multigenerational families. J Am Acad Child Adolesc Psychiatry 2004 0.95
24 Attention deficit/hyperactivity disorder (ADHD): complex phenotype, simple genotype? Genet Med 2004 0.94
25 Environmental influences that affect attention deficit/hyperactivity disorder: study of a genetic isolate. Eur Child Adolesc Psychiatry 2007 0.93
26 ADHD latent class clusters: DSM-IV subtypes and comorbidity. Psychiatry Res 2009 0.89
27 From the black widow spider to human behavior: Latrophilins, a relatively unknown class of G protein-coupled receptors, are implicated in psychiatric disorders. Am J Med Genet B Neuropsychiatr Genet 2010 0.88
28 GWAS reveals new recessive loci associated with non-syndromic facial clefting. Eur J Med Genet 2012 0.88
29 Potential cognitive endophenotypes in multigenerational families: segregating ADHD from a genetic isolate. Atten Defic Hyperact Disord 2011 0.86
30 What is next after the genes for autoimmunity? BMC Med 2013 0.85
31 Influence of a latrophilin 3 (LPHN3) risk haplotype on event-related potential measures of cognitive response control in attention-deficit hyperactivity disorder (ADHD). Eur Neuropsychopharmacol 2012 0.85
32 Exploratory data from complete genomes of familial alzheimer disease age-at-onset outliers. Hum Mutat 2012 0.84
33 Association of PDE11A global haplotype with major depression and antidepressant drug response. Neuropsychiatr Dis Treat 2009 0.83
34 TAP, HLA-DQB1, and HLA-DRB1 polymorphism in Colombian patients with primary Sjögren's syndrome. Semin Arthritis Rheum 2002 0.82
35 Polymorphisms in the neural nicotinic acetylcholine receptor α4 subunit (CHRNA4) are associated with ADHD in a genetic isolate. Atten Defic Hyperact Disord 2009 0.81
36 D6S439 microsatellite identifies a new susceptibility region for primary Sjögren's syndrome. J Rheumatol 2003 0.80
37 A novel alteration in metaxin 1, F202L, is associated with N370S in Gaucher disease. J Hum Genet 2004 0.80
38 Pharmacogenetic impact of VKORC1 and CYP2C9 allelic variants on warfarin dose requirements in a hispanic population isolate. Clin Appl Thromb Hemost 2009 0.79
39 Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type? Am J Med Genet A 2008 0.78
40 A multigenerational pedigree of late-onset Alzheimer's disease implies new genetic causes. Brain 2005 0.78
41 Temporal gene expression in the hippocampus and peripheral organs to endotoxin-induced systemic inflammatory response in caspase-1-deficient mice. Neuroimmunomodulation 2015 0.75
42 Response to Uher et al. Am J Psychiatry 2015 0.75
43 [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]. Rev Neurol 2010 0.75
44 Planning in borderline personality disorder: evidence for distinct subpopulations. World J Biol Psychiatry 2009 0.75