PubRank

Wendy Roberts

Author PubWeight™ 144.58‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Structural variation of chromosomes in autism spectrum disorder. Am J Hum Genet 2008 15.51
2 Functional impact of global rare copy number variation in autism spectrum disorders. Nature 2010 14.66
3 Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet 2007 14.05
4 Behavioral manifestations of autism in the first year of life. Int J Dev Neurosci 2005 6.56
5 Contribution of SHANK3 mutations to autism spectrum disorder. Am J Hum Genet 2007 5.04
6 Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation. Nat Genet 2010 3.73
7 A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet 2010 3.42
8 Human chromosome 7: DNA sequence and biology. Science 2003 3.02
9 Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature 2011 2.59
10 Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Hum Mol Genet 2012 2.46
11 A prospective case series of high-risk infants who developed autism. J Autism Dev Disord 2007 2.35
12 Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD. Sci Transl Med 2011 2.29
13 Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder. J Med Genet 2009 2.27
14 Type 1 diabetes and autism: is there a link? Diabetes Care 2005 2.24
15 Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia. Am J Hum Genet 2006 2.14
16 Early language and communication development of infants later diagnosed with autism spectrum disorder. J Dev Behav Pediatr 2006 1.93
17 A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism. Proc Natl Acad Sci U S A 2012 1.85
18 Investigating the structure of the restricted, repetitive behaviours and interests domain of autism. J Child Psychol Psychiatry 2006 1.81
19 Autism spectrum disorder: advances in evidence-based practice. CMAJ 2014 1.76
20 Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability. Sci Transl Med 2010 1.75
21 Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. Am J Med Genet A 2006 1.70
22 SHANK1 Deletions in Males with Autism Spectrum Disorder. Am J Hum Genet 2012 1.59
23 Rare deletions at the neurexin 3 locus in autism spectrum disorder. Am J Hum Genet 2011 1.56
24 Immunizations and autism: a review of the literature. Can J Neurol Sci 2006 1.56
25 Synthetic peptide analogs derived from bcr/abl fusion proteins and the induction of heteroclitic human T-cell responses. Haematologica 2005 1.50
26 Temperament and its relationship to autistic symptoms in a high-risk infant sib cohort. J Abnorm Child Psychol 2009 1.43
27 Sex differences in children with autism spectrum disorder identified within a high-risk infant cohort. J Autism Dev Disord 2012 1.39
28 A prospective study of autistic-like traits in unaffected siblings of probands with autism spectrum disorder. JAMA Psychiatry 2013 1.33
29 A discovery resource of rare copy number variations in individuals with autism spectrum disorder. G3 (Bethesda) 2012 1.30
30 Validating the Repetitive Behavior Scale-revised in young children with autism spectrum disorder. J Autism Dev Disord 2010 1.29
31 Auditory evoked fields predict language ability and impairment in children. Int J Psychophysiol 2008 1.29
32 Stereotyped motor behaviors associated with autism in high-risk infants: a pilot videotape analysis of a sibling sample. J Autism Dev Disord 2007 1.26
33 Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. Hum Mol Genet 2013 1.26
34 Magnetoencephalography identifies rapid temporal processing deficit in autism and language impairment. Neuroreport 2005 1.25
35 Language lateralization development in children with autism: insights from the late field magnetoencephalogram. Neurosci Lett 2005 1.23
36 Investigating phenotypic heterogeneity in children with autism spectrum disorder: a factor mixture modeling approach. J Child Psychol Psychiatry 2012 1.23
37 The prevalence of autistic spectrum disorder in children surveyed in a tertiary care epilepsy clinic. Epilepsia 2005 1.17
38 Structure of the autism symptom phenotype: A proposed multidimensional model. J Am Acad Child Adolesc Psychiatry 2007 1.13
39 Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures. Hum Mol Genet 2013 1.11
40 Using the preschool language scale, fourth edition to characterize language in preschoolers with autism spectrum disorders. Am J Speech Lang Pathol 2011 1.11
41 Inhibition of motor responses in siblings concordant and discordant for attention deficit hyperactivity disorder. Am J Psychiatry 2005 1.09
42 Delayed mismatch field for speech and non-speech sounds in children with autism. Neuroreport 2005 1.06
43 Prominence of M50 auditory evoked response over M100 in childhood and autism. Neuroreport 2004 1.02
44 Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genes. Neurogenetics 2007 1.02
45 Measures of cortical grey matter structure and development in children with autism spectrum disorder. J Autism Dev Disord 2012 1.00
46 Clinical practice pathways for evaluation and medication choice for attention-deficit/hyperactivity disorder symptoms in autism spectrum disorders. Pediatrics 2012 0.99
47 Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 region. J Autism Dev Disord 2007 0.92
48 Characterization of a novel cation transporter ATPase gene (ATP13A4) interrupted by 3q25-q29 inversion in an individual with language delay. Genomics 2005 0.91
49 The norepinephrine transporter gene and attention-deficit hyperactivity disorder. Am J Med Genet 2002 0.91
50 Parents' perspectives on participating in genetic research in autism. J Autism Dev Disord 2013 0.91
51 Phenotypic overlap between core diagnostic features and emotional/behavioral problems in preschool children with autism spectrum disorder. J Autism Dev Disord 2011 0.90
52 Sequence variation in the 3'-untranslated region of the dopamine transporter gene and attention-deficit hyperactivity disorder (ADHD). Am J Med Genet B Neuropsychiatr Genet 2005 0.89
53 The interaction of escitalopram and R-citalopram at the human serotonin transporter investigated in the mouse. Psychopharmacology (Berl) 2014 0.89
54 White matter and development in children with an autism spectrum disorder. Autism 2012 0.87
55 Sequence variants within exon 1 of MECP2 occur in females with mental retardation. Am J Med Genet B Neuropsychiatr Genet 2007 0.85
56 Attention deficit hyperactivity disorder and the gene for dopamine Beta-hydroxylase. Am J Psychiatry 2002 0.85
57 Positive affect in infant siblings of children diagnosed with autism spectrum disorder. J Abnorm Child Psychol 2015 0.84
58 The NeuroDevNet Autism Spectrum Disorders Demonstration Project. Semin Pediatr Neurol 2011 0.83
59 Copy number variation analysis and sequencing of the X-linked mental retardation gene TSPAN7/TM4SF2 in patients with autism spectrum disorder. Psychiatr Genet 2009 0.83
60 Influence of reporting effects on the association between maternal depression and child autism spectrum disorder behaviors. J Child Psychol Psychiatry 2011 0.82
61 Trisomy 15q25.2-qter in an autistic child: genotype-phenotype correlations. Am J Med Genet A 2005 0.82
62 Skin cancer in skin of color: an update on current facts, trends, and misconceptions. J Drugs Dermatol 2013 0.82
63 Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum Disorder. Eur J Med Genet 2011 0.82
64 Prospective preliminary analysis of the development of autism and epilepsy in children with infantile spasms. J Child Neurol 2003 0.81
65 Factor analysis of the Parenting Stress Index-Short Form with parents of young children with autism spectrum disorders. Autism Res 2011 0.81
66 Immunization uptake in younger siblings of children with autism spectrum disorder. Autism 2012 0.80
67 The serotonin receptor HTR1B: gene polymorphisms in attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet 2007 0.80
68 Examination of bidirectional relationships between parent stress and two types of problem behavior in children with autism spectrum disorder. J Autism Dev Disord 2014 0.79
69 Placebo-controlled study examining effects of selegiline in children with attention-deficit/hyperactivity disorder. J Child Adolesc Psychopharmacol 2006 0.79
70 Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the desmocollin gene cluster on 18q. Am J Med Genet B Neuropsychiatr Genet 2009 0.79
71 Brief report: assessment of early sensory processing in infants at high-risk of autism spectrum disorder. J Autism Dev Disord 2014 0.79
72 Investigating the measurement properties of the social responsiveness scale in preschool children with autism spectrum disorders. J Autism Dev Disord 2013 0.78
73 Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism. Am J Med Genet B Neuropsychiatr Genet 2004 0.77
74 Stability and Change in the Cognitive and Adaptive Behaviour Scores of Preschoolers with Autism Spectrum Disorder. J Autism Dev Disord 2015 0.77
75 Replication test for association of the IL-1 receptor antagonist gene, IL1RN, with attention-deficit/hyperactivity disorder. Neuropsychobiology 2004 0.76
76 The early detection of autism in clinical practice. Paediatr Child Health 2004 0.75
77 Immunization uptake in siblings of children with autism. Pediatrics 2008 0.75
78 The Effects of a Daily Skincare Regimen on Maintaining the Benefits Obtained from Previous Chemical Resurfacing Treatments. J Drugs Dermatol 2016 0.75
79 Modeling the phenotypic architecture of autism symptoms from time of diagnosis to age 6. J Autism Dev Disord 2014 0.75