Publications powered by Harvard Catalyst Profiles

  1. Predicting Autism Spectrum Disorder in Very Preterm Infants. Pediatrics. 2020 10; 146(4). View abstract
  2. Evaluation and Management of the Child With Autism Spectrum Disorder. Continuum (Minneap Minn). 2018 02; 24(1, Child Neurology):248-275. View abstract
  3. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder. Nat Neurosci. 2017 Apr; 20(4):602-611. View abstract
  4. Implementation of the Safety Huddle. Crit Care Nurse. 2016 Dec; 36(6):80-82. View abstract
  5. 16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort. . 2016 11; 170(11):2943-2955. View abstract
  6. CSF concentrations of 5-methyltetrahydrofolate in a cohort of young children with autism. Neurology. 2016 06 14; 86(24):2258-63. View abstract
  7. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities. JAMA Psychiatry. 2016 Jan; 73(1):20-30. View abstract
  8. Clinical phenotype of the recurrent 1q21.1 copy-number variant. Genet Med. 2016 Apr; 18(4):341-9. View abstract
  9. Clinical characteristics of children and young adults with co-occurring autism spectrum disorder and epilepsy. Epilepsy Behav. 2015 Jun; 47:183-90. View abstract
  10. A survey of seizures and current treatments in 15q duplication syndrome. Epilepsia. 2014 Mar; 55(3):396-402. View abstract
  11. The association between epilepsy and autism symptoms and maladaptive behaviors in children with autism spectrum disorder. Autism. 2014 Nov; 18(8):996-1006. View abstract
  12. Clinical characteristics of children with autism spectrum disorder and co-occurring epilepsy. PLoS One. 2013; 8(7):e67797. View abstract
  13. Compared to what? Early brain overgrowth in autism and the perils of population norms. Biol Psychiatry. 2013 Oct 15; 74(8):563-75. View abstract
  14. Mapping cortical anatomy in preschool aged children with autism using surface-based morphometry. Neuroimage Clin. 2012; 2:111-9. View abstract
  15. A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders. J Med Genet. 2012 Oct; 49(10):660-8. View abstract
  16. The co-morbidity burden of children and young adults with autism spectrum disorders. PLoS One. 2012; 7(4):e33224. View abstract
  17. Commentary from the DSM-5 Workgroup on Neurodevelopmental Disorders. J Am Acad Child Adolesc Psychiatry. 2012 Apr; 51(4):347-9. View abstract
  18. Common neurological co-morbidities in autism spectrum disorders. Curr Opin Pediatr. 2011 Dec; 23(6):609-15. View abstract
  19. Recent advances in autism spectrum disorders. Curr Opin Pediatr. 2011 Dec; 23(6):607-8. View abstract
  20. Autism. Editorial. Autism. 2011 Sep; 15(5):523-5. View abstract
  21. Testing autism interventions: trials and tribulations. Lancet. 2010 Jun 19; 375(9732):2124-5. View abstract
  22. The role of epilepsy and epileptiform EEGs in autism spectrum disorders. Pediatr Res. 2009 Jun; 65(6):599-606. View abstract
  23. Neurometabolic disorders and dysfunction in autism spectrum disorders. Curr Neurol Neurosci Rep. 2009 Mar; 9(2):129-36. View abstract
  24. Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways. Hum Mol Genet. 2007 Jul 15; 16(14):1682-98. View abstract
  25. Strong association of de novo copy number mutations with autism. Science. 2007 Apr 20; 316(5823):445-9. View abstract
  26. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet. 2007 Mar; 39(3):319-28. View abstract
  27. Stratification based on language-related endophenotypes in autism: attempt to replicate reported linkage. . 2006 Sep 05; 141B(6):591-8. View abstract
  28. Autism from developmental and neuropsychological perspectives. Annu Rev Clin Psychol. 2006; 2:327-55. View abstract
  29. beta2-adrenergic receptor activation and genetic polymorphisms in autism: data from dizygotic twins. J Child Neurol. 2005 Nov; 20(11):876-84. View abstract
  30. Autism spectrum disorder: screening, diagnosis, and medical evaluation. Semin Pediatr Neurol. 2004 Sep; 11(3):186-95. View abstract
  31. The genetics of autism. Semin Pediatr Neurol. 2004 Sep; 11(3):196-204. View abstract
  32. Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism. Biol Psychiatry. 2004 Feb 15; 55(4):413-9. View abstract
  33. A genomewide screen of 345 families for autism-susceptibility loci. Am J Hum Genet. 2003 Oct; 73(4):886-97. View abstract
  34. The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions. Am J Hum Genet. 2001 Aug; 69(2):463-6. View abstract
  35. Visual field defects and other ophthalmological disturbances associated with vigabatrin. Drug Saf. 2001; 24(5):385-404. View abstract