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Author Details
Full Name
Ellen Hanson
Affiliation
Boston Children's Hospital and Harvard Medical School
ORCID
Career Start Year
2007
Papers
39
H Index
22
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37004757
Phenotypically driven subgroups of ASD display distinct metabolomic profiles.
Brain Behav Immun
2023
37246331
Autism spectrum disorder and GABA levels in children with succinic semialdehyde dehydrogenase deficiency.
Dev Med Child Neurol
2023
36138632
Neurobehavioral Associations with NREM and REM Sleep Architecture in Children with Autism Spectrum Disorder.
Children (Basel)
2022
33384013
A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants.
Am J Psychiatry
2021
33393837
Succinic Semialdehyde Dehydrogenase Deficiency: Review of the Natural History Study.
J Child Neurol
2021
32597026
Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers.
Autism Res
2020
32887777
Novel <i>ALDH5A1</i> variants and genotype: Phenotype correlation in SSADH deficiency.
Neurology
2020
32652891
Language characterization in 16p11.2 deletion and duplication syndromes.
Am J Med Genet B Neuropsychiatr Genet
2020
30945897
Impacting development in infants with tuberous sclerosis complex: Multidisciplinary research collaboration.
Am Psychol
2019
31691264
Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational study.
Epilepsia
2019
30837452
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication.
Transl Psychiatry
2019
28349640
Developmental trajectories for young children with 16p11.2 copy number variation.
Am J Med Genet B Neuropsychiatr Genet
2017
26066539
Clinical phenotype of the recurrent 1q21.1 copy-number variant.
Genet Med
2016
26629640
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
JAMA Psychiatry
2016
26579706
Behavior and Sensory Interests Questionnaire: Validation in a sample of children with autism spectrum disorder and other developmental disability.
Res Dev Disabil
2016
27207092
Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication.
J Autism Dev Disord
2016
26742926
The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.
Biol Psychiatry
2016
24954156
Quality of life in major depressive disorder before/after multiple steps of treatment and one-year follow-up.
Acta Psychiatr Scand
2015
26194566
Sleep Dependent Memory Consolidation in Children with Autism Spectrum Disorder.
Sleep
2015
25493922
The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.
JAMA Psychiatry
2015
25064419
The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Biol Psychiatry
2015
24391123
Addressing dental fear in children with autism spectrum disorders: a randomized controlled pilot study using electronic screen media.
Clin Pediatr (Phila)
2014
23065101
Brief report: prevalence of attention deficit/hyperactivity disorder among individuals with an autism spectrum disorder.
J Autism Dev Disord
2013
24048512
Factor VII antigen levels are differentially associated to etiological subtypes of ischaemic stroke.
Thromb Haemost
2013
24086496
Genetic variants of coagulation factor XI show association with ischemic stroke up to 70 years of age.
PLoS One
2013
23141846
Association between variation in ADAMTS13 and aneurysmal subarachnoid hemorrhage.
Thromb Res
2013
22065253
A multisite study of the clinical diagnosis of different autism spectrum disorders.
Arch Gen Psychiatry
2012
23227143
Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders.
PLoS One
2012
23054248
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
J Med Genet
2012
22749962
TFPI gene variation and ischemic stroke.
Thromb Res
2012
22482829
No evidence for an association between ABO blood group and overall ischemic stroke or any of the major etiologic subtypes.
Thromb Res
2012
22409238
Plasma factor VII-activating protease antigen levels and activity are increased in ischemic stroke.
J Thromb Haemost
2012
21054779
Plasma levels of von Willebrand factor in the etiologic subtypes of ischemic stroke.
J Thromb Haemost
2011
21694630
A pilot study to improve venipuncture compliance in children and adolescents with autism spectrum disorders.
J Dev Behav Pediatr
2011
20613623
Cognitive and behavioral characterization of 16p11.2 deletion syndrome.
J Dev Behav Pediatr
2010
20468056
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.
Am J Med Genet B Neuropsychiatr Genet
2010
19339759
Comment on "Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients".
J Clin Invest
2009
19765208
Association between genetic variation at the ADAMTS13 locus and ischemic stroke.
J Thromb Haemost
2009
16977497
Use of complementary and alternative medicine among children diagnosed with autism spectrum disorder.
J Autism Dev Disord
2007
1 - 39 of 39
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