JacquelineHarrisMD

PubMed

• Arrhythmias including atrial fibrillation and congenital heart disease in Kleefstra syndrome: a possible epigenetic link.
  Sunil K Vasireddi, Tanja Zdolsek Draksler, Arianne Bouman, Joost Kummeling, Matthew Wheeler, Chloe Reuter, Siddharth Srivastava, Jacqueline Harris, Paul G Fisher, Sanj...> ;Europace. 2023 Dec 28
• 1 citations
  Development of webcam-collected and artificial-intelligence-derived social and cognitive performance measures for neurodevelopmental genetic syndromes.
  Thomas W Frazier, Robyn M Busch, Patricia Klaas, Katherine Lachlan, Shafali Jeste, Alexander Kolevzon, Eva Loth, Jacqueline Harris, Leslie Speer, Tom Pepper, Kristin A...> ;American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 2023 Sep 1
• 2 citations
  Development of informant-report neurobehavioral survey scales for PTEN hamartoma tumor syndrome and related neurodevelopmental genetic syndromes.
  Frazier, T., Busch, R., Klaas, P., Lachlan, K., Jeste, S., Kolevzon, A., Loth, E., Harris, J., Speer, L., Pepper, T., Anthony, K., Graglia, J., Delagrammatikas, C., Be...> ;American Journal of Medical Genetics. Part A. 2023 Jul 1
• 3 citations
  Epigenetics of cognition and behavior: insights from Mendelian disorders of epigenetic machinery.
  Rowena Ng, Allison Kalinousky, Jacqueline Harris> ;Journal of Neurodevelopmental Disorders. 2023 May 27
• Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome.
  Dima Qu'd, Lauren M Schmitt, Amber Leston, Jacqueline R Harris, Anne Slavotinek, Ilka Riddle, Diana S Brightman, Brittany N Simpson> ;Frontiers in Genetics. 2023 Jan 1
• Pandemic intake questionnaire to improve quality, effectiveness, and efficiency of outpatient neurologic and developmental care at the Kennedy Krieger institute during...
  Menon, D. U., Pooja Vedmurthy, Connor Murray, Belinda Chen, Akua Asiedu, Kristin Baranano, Mihee Bay, Harolyn Belcher, Vera Burton, Charles Conlon, Amena Fine, Ryan Gi...> ;Frontiers in Rehabilitation Sciences. 2022 Jan 1
• 34 citations
  Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome
  , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,...> ;American Journal of Medical Genetics. Part A. 2021 Mar 30
• 3 citations
  Characterization of an unbalanced translocation causing 3q28qter duplication and 10q26.2qter deletion in a patient with global developmental delay and self-injury.
  Ikeoluwa A. Osei-Owusu, Alexis L. Norris, Anya T. Joynt, Jeremy Thorpe, Soonweng Cho, Elaine Tierney, Jonathan D. Schmidt, Louis P. Hagopian, Jacqueline Harris, Jonath...> ;Cold Spring Harbor Molecular Case Studies. 2020 Dec 17
• 18 citations
  De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder.
  , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , > ;Genetics in Medicine. 2020 Mar 1
• 24 citations
  Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability
  Benjamin Cogné, Sophie Ehresmann, Eliane Beauregard-Lacroix, Justine Rousseau, Thomas Besnard, Thomas Garcia, Slavé Petrovski, Shiri Avni, Kirsty McWalter, Patrick R. ...> ;American Journal of Human Genetics. 2019 Mar 7
• 3 citations
  Disrupted epigenetics in the Sotos syndrome neurobehavioral phenotype
  Jacqueline Harris, Jill A. Fahrner> ;Current Opinion in Psychiatry. 2019 Mar 1
• 15 citations
  Abnormalities of the DNA methylation mark and its machinery: an emerging cause of neurologic dysfunction.
  Jacqueline Weissman, Sakkubai Naidu, Hans T. Bjornsson> ;Seminars in Neurology. 2014 Jul 1
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