Published in J Am Acad Child Adolesc Psychiatry on December 01, 2004
Latent class subtyping of attention-deficit/hyperactivity disorder and comorbid conditions. J Am Acad Child Adolesc Psychiatry (2008) 1.17
The association between attention-deficit/hyperactivity disorder and early-onset alcohol dependence: A retrospective study. Indian J Psychiatry (2008) 0.99
Environmental influences that affect attention deficit/hyperactivity disorder: study of a genetic isolate. Eur Child Adolesc Psychiatry (2007) 0.93
A common genetic network underlies substance use disorders and disruptive or externalizing disorders. Hum Genet (2012) 0.92
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
GWAS reveals new recessive loci associated with non-syndromic facial clefting. Eur J Med Genet (2012) 0.88
Potential cognitive endophenotypes in multigenerational families: segregating ADHD from a genetic isolate. Atten Defic Hyperact Disord (2011) 0.86
Analysis of brain metabolism by proton magnetic resonance spectroscopy (1H-MRS) in attention-deficit/hyperactivity disorder suggests a generalized differential ontogenic pattern from controls. Atten Defic Hyperact Disord (2012) 0.85
A two-locus genetic interaction between LPHN3 and 11q predicts ADHD severity and long-term outcome. Transl Psychiatry (2011) 0.81
Toward a better understanding of ADHD: LPHN3 gene variants and the susceptibility to develop ADHD. Atten Defic Hyperact Disord (2010) 0.81
Characteristics and comorbidity of ADHD sib pairs in the Central Valley of Costa Rica. Compr Psychiatry (2011) 0.78
Neuropsychological and dimensional behavioral trait profiles in Costa Rican ADHD sib pairs: Potential intermediate phenotypes for genetic studies. Am J Med Genet B Neuropsychiatr Genet (2015) 0.78
An Ultraconserved Brain-Specific Enhancer Within ADGRL3 (LPHN3) Underpins Attention-Deficit/Hyperactivity Disorder Susceptibility. Biol Psychiatry (2016) 0.75
Linkage and association analysis of ADHD endophenotypes in extended and multigenerational pedigrees from a genetic isolate. Mol Psychiatry (2015) 0.75
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science (2008) 20.68
Dynamic mapping of human cortical development during childhood through early adulthood. Proc Natl Acad Sci U S A (2004) 17.86
Toward discovery science of human brain function. Proc Natl Acad Sci U S A (2010) 15.22
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. N Engl J Med (2004) 7.91
Neurodevelopmental trajectories of the human cerebral cortex. J Neurosci (2008) 7.14
Competition between functional brain networks mediates behavioral variability. Neuroimage (2007) 6.98
Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy. N Engl J Med (2011) 6.34
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nat Genet (2002) 6.29
The resting brain: unconstrained yet reliable. Cereb Cortex (2009) 6.20
The oscillating brain: complex and reliable. Neuroimage (2009) 5.22
Mapping the functional connectivity of anterior cingulate cortex. Neuroimage (2007) 5.12
Precuneus shares intrinsic functional architecture in humans and monkeys. Proc Natl Acad Sci U S A (2009) 4.99
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations. N Engl J Med (2009) 4.96
Functional connectivity of default mode network components: correlation, anticorrelation, and causality. Hum Brain Mapp (2009) 4.86
Developmental trajectories of brain volume abnormalities in children and adolescents with attention-deficit/hyperactivity disorder. JAMA (2002) 4.72
Reliable intrinsic connectivity networks: test-retest evaluation using ICA and dual regression approach. Neuroimage (2009) 4.47
Mapping cortical change in Alzheimer's disease, brain development, and schizophrenia. Neuroimage (2004) 4.13
Development of anterior cingulate functional connectivity from late childhood to early adulthood. Cereb Cortex (2008) 4.12
A comprehensive assessment of regional variation in the impact of head micromovements on functional connectomics. Neuroimage (2013) 3.96
Spontaneous attentional fluctuations in impaired states and pathological conditions: a neurobiological hypothesis. Neurosci Biobehav Rev (2007) 3.94
Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation. N Engl J Med (2009) 3.88
Functional connectivity of the human amygdala using resting state fMRI. Neuroimage (2008) 3.76
Structural MRI of pediatric brain development: what have we learned and where are we going? Neuron (2010) 3.74
Direct measure of the de novo mutation rate in autism and schizophrenia cohorts. Am J Hum Genet (2010) 3.69
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
Brain imaging and fluid biomarker analysis in young adults at genetic risk for autosomal dominant Alzheimer's disease in the presenilin 1 E280A kindred: a case-control study. Lancet Neurol (2012) 3.48
A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome. Neuron (2010) 3.31
Network centrality in the human functional connectome. Cereb Cortex (2011) 3.19
Cortical morphology in children and adolescents with different apolipoprotein E gene polymorphisms: an observational study. Lancet Neurol (2007) 3.19
The neural correlates of attention deficit hyperactivity disorder: an ALE meta-analysis. J Child Psychol Psychiatry (2006) 3.17
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia. Proc Natl Acad Sci U S A (2010) 3.13
Longitudinal mapping of cortical thickness and clinical outcome in children and adolescents with attention-deficit/hyperactivity disorder. Arch Gen Psychiatry (2006) 3.10
Broca's region: linking human brain functional connectivity data and non-human primate tracing anatomy studies. Eur J Neurosci (2010) 3.06
A functional screen for sonic hedgehog regulatory elements across a 1 Mb interval identifies long-range ventral forebrain enhancers. Development (2006) 2.90
Etiologic subtypes of attention-deficit/hyperactivity disorder: brain imaging, molecular genetic and environmental factors and the dopamine hypothesis. Neuropsychol Rev (2007) 2.80
Alzheimer's Prevention Initiative: a plan to accelerate the evaluation of presymptomatic treatments. J Alzheimers Dis (2011) 2.78
Growing together and growing apart: regional and sex differences in the lifespan developmental trajectories of functional homotopy. J Neurosci (2010) 2.73
Apolipoprotein Eepsilon4 modifies Alzheimer's disease onset in an E280A PS1 kindred. Ann Neurol (2003) 2.72
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
Pre-dementia clinical stages in presenilin 1 E280A familial early-onset Alzheimer's disease: a retrospective cohort study. Lancet Neurol (2011) 2.65
Florbetapir PET analysis of amyloid-β deposition in the presenilin 1 E280A autosomal dominant Alzheimer's disease kindred: a cross-sectional study. Lancet Neurol (2012) 2.65
Relationship between cingulo-insular functional connectivity and autistic traits in neurotypical adults. Am J Psychiatry (2009) 2.60
Network homogeneity reveals decreased integrity of default-mode network in ADHD. J Neurosci Methods (2007) 2.56
L-dopa modulates functional connectivity in striatal cognitive and motor networks: a double-blind placebo-controlled study. J Neurosci (2009) 2.55
Multiple hits during early embryonic development: digenic diseases and holoprosencephaly. Am J Hum Genet (2002) 2.49
Clinical and functional outcome of childhood attention-deficit/hyperactivity disorder 33 years later. Arch Gen Psychiatry (2012) 2.44
Functional brain correlates of social and nonsocial processes in autism spectrum disorders: an activation likelihood estimation meta-analysis. Biol Psychiatry (2008) 2.33
Inter-individual differences in resting-state functional connectivity predict task-induced BOLD activity. Neuroimage (2010) 2.29
Brain development and ADHD. Clin Psychol Rev (2006) 2.28
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
Aberrant striatal functional connectivity in children with autism. Biol Psychiatry (2010) 2.21
Dynamic mapping of normal human hippocampal development. Hippocampus (2006) 2.21
Toward systems neuroscience of ADHD: a meta-analysis of 55 fMRI studies. Am J Psychiatry (2012) 2.16
Mechanistic and epidemiologic considerations in the evaluation of adverse birth outcomes following gestational exposure to statins. Am J Med Genet A (2004) 2.10
Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C. Am J Med Genet B Neuropsychiatr Genet (2010) 2.08
Cerebellar development and clinical outcome in attention deficit hyperactivity disorder. Am J Psychiatry (2007) 2.08
Association between conformational mutations in neuroserpin and onset and severity of dementia. Lancet (2002) 2.02
Making data sharing work: the FCP/INDI experience. Neuroimage (2012) 2.02
Regional variation in interhemispheric coordination of intrinsic hemodynamic fluctuations. J Neurosci (2008) 2.00
Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p. Blood (2010) 2.00
Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features. Proc Natl Acad Sci U S A (2003) 1.98
Management of clozapine-induced fever in a child. Am J Psychiatry (2014) 1.97
A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics. Am J Hum Genet (2005) 1.96
Distinct neural mechanisms of risk and ambiguity: a meta-analysis of decision-making. Neuroimage (2006) 1.96
Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia. Proc Natl Acad Sci U S A (2002) 1.92
Toward reliable characterization of functional homogeneity in the human brain: preprocessing, scan duration, imaging resolution and computational space. Neuroimage (2012) 1.92
Early interstitial lung disease in familial pulmonary fibrosis. Am J Respir Crit Care Med (2007) 1.91
A previously unidentified amino-terminal domain regulates transcriptional activity of wild-type and disease-associated human GLI2. Hum Mol Genet (2005) 1.89
Distinct neural signatures detected for ADHD subtypes after controlling for micro-movements in resting state functional connectivity MRI data. Front Syst Neurosci (2013) 1.88
Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis. Am J Hum Genet (2002) 1.88
Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancer. Am J Hum Genet (2002) 1.86
Imaging human connectomes at the macroscale. Nat Methods (2013) 1.82
Residual functional connectivity in the split-brain revealed with resting-state functional MRI. Neuroreport (2008) 1.80
Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly. Hum Genet (2002) 1.80
Characterizing variation in the functional connectome: promise and pitfalls. Trends Cogn Sci (2012) 1.77
Brain gray matter deficits at 33-year follow-up in adults with attention-deficit/hyperactivity disorder established in childhood. Arch Gen Psychiatry (2011) 1.77
Temporal and probabilistic discounting of rewards in children and adolescents: effects of age and ADHD symptoms. Neuropsychologia (2005) 1.76
A preliminary study of functional connectivity in comorbid adolescent depression. Neurosci Lett (2009) 1.74
Deformation-based surface morphometry applied to gray matter deformation. Neuroimage (2003) 1.71
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
Detecting disease-specific patterns of brain structure using cortical pattern matching and a population-based probabilistic brain atlas. Inf Process Med Imaging (2001) 1.70
Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics. Hum Genet (2006) 1.70
Polymorphisms of the dopamine D4 receptor, clinical outcome, and cortical structure in attention-deficit/hyperactivity disorder. Arch Gen Psychiatry (2007) 1.70
Three-dimensional brain growth abnormalities in childhood-onset schizophrenia visualized by using tensor-based morphometry. Proc Natl Acad Sci U S A (2008) 1.65
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nat Genet (2011) 1.63
Simple models of human brain functional networks. Proc Natl Acad Sci U S A (2012) 1.63
Genetic variation in the 22q11 locus and susceptibility to schizophrenia. Proc Natl Acad Sci U S A (2002) 1.60
Covert matching of unfamiliar faces in a case of prosopagnosia: an ERP study. Cortex (2003) 1.58
Adverse birth outcome among mothers with low serum cholesterol. Pediatrics (2007) 1.58
The molecular genetics of holoprosencephaly. Am J Med Genet C Semin Med Genet (2010) 1.57
Diagnosis and management of fragile X syndrome. Am Fam Physician (2005) 1.57
The pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection (PANDAS) subgroup: separating fact from fiction. Pediatrics (2004) 1.56
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate. Hum Mol Genet (2009) 1.55
A convergent functional architecture of the insula emerges across imaging modalities. Neuroimage (2012) 1.55
Novel mutation in sonic hedgehog in non-syndromic colobomatous microphthalmia. Am J Med Genet A (2003) 1.54