Intranasal oxytocin in children and adolescents with autism spectrum disorder L Sikich, A Kolevzon, BH King, CJ McDougle, KB Sanders, SJ Kim, ... New England Journal of Medicine 385 (16), 1462-1473, 2021 | 215 | 2021 |
Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations S De Rubeis, PM Siper, A Durkin, J Weissman, F Muratet, D Halpern, ... Molecular autism 9, 1-20, 2018 | 191 | 2018 |
Congenital heart disease and neurodevelopment: clinical manifestations, genetics, mechanisms, and implications SN Nattel, L Adrianzen, EC Kessler, G Andelfinger, M Dehaes, ... Canadian Journal of Cardiology 33 (12), 1543-1555, 2017 | 125 | 2017 |
Examining the efficacy of a family peer advocate model for black and hispanic caregivers of children with autism spectrum disorder JM Jamison, E Fourie, PM Siper, MP Trelles, J George-Jones, ... Journal of autism and developmental disorders 47, 1314-1322, 2017 | 109 | 2017 |
Loop gating of connexin hemichannels involves movement of pore-lining residues in the first extracellular loop domain VK Verselis, MP Trelles, C Rubinos, TA Bargiello, M Srinivas Journal of Biological Chemistry 284 (7), 4484-4493, 2009 | 104 | 2009 |
Prospective investigation of FOXP1 syndrome PM Siper, S De Rubeis, MP Trelles, A Durkin, D Di Marino, F Muratet, ... Molecular autism 8, 1-16, 2017 | 83 | 2017 |
Psychiatric illness and regression in individuals with Phelan-McDermid syndrome TM Kohlenberg, MP Trelles, B McLarney, C Betancur, A Thurm, ... Journal of Neurodevelopmental Disorders 12, 1-17, 2020 | 76 | 2020 |
Framework for assessing individuals with rare genetic disorders associated with profound intellectual and multiple disabilities (PIMD): the example of Phelan McDermid Syndrome L Soorya, J Leon, MP Trelles, A Thurm The Clinical Neuropsychologist 32 (7), 1226-1255, 2018 | 71 | 2018 |
Bilingualism in autism spectrum disorder: Finding meaning in translation MP Trelles, K Castro Journal of the American Academy of Child and Adolescent Psychiatry 58 (11), 1035, 2019 | 36 | 2019 |
Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome A Kolevzon, MS Breen, PM Siper, D Halpern, Y Frank, H Rieger, ... Molecular Autism 13 (1), 17, 2022 | 31 | 2022 |
Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms MP Trelles, T Levy, B Lerman, P Siper, R Lozano, D Halpern, H Walker, ... Molecular Autism 12, 1-15, 2021 | 30 | 2021 |
Triarylmethanes, a new class of Cx50 inhibitors SB Bodendiek, C Rubinos, MP Trelles, N Coleman, DP Jenkins, H Wulff, ... Frontiers in Pharmacology 3, 106, 2012 | 15 | 2012 |
Visual evoked potential abnormalities in phelan-mcdermid syndrome PM Siper, MA Rowe, SB Guillory, AA Rouhandeh, JL George-Jones, ... Journal of the American Academy of Child & Adolescent Psychiatry 61 (4), 565 …, 2022 | 11 | 2022 |
Genetic and epigenetic signatures associated with plasma oxytocin levels in children and adolescents with autism spectrum disorder SK Siecinski, SN Giamberardino, M Spanos, AC Hauser, JR Gibson, ... Autism Research 16 (3), 502-523, 2023 | 10 | 2023 |
Social visual attentional engagement and memory in Phelan-McDermid syndrome and autism spectrum disorder: a pilot eye tracking study SB Guillory, VZ Baskett, HE Grosman, CS McLaughlin, EL Isenstein, ... Journal of Neurodevelopmental Disorders 13, 1-11, 2021 | 10 | 2021 |
A prospective study of neurological abnormalities in Phelan-McDermid syndrome M Yitzchak Frank, JM Jamison, T Tavassoli, M Kolevzon Journal of Rare Disorders 5 (1), 1, 2017 | 8 | 2017 |
Social visual attentional engagement and memory in Phelan-McDermid syndrome and autism spectrum disorder: An eye-tracking study S Guillory, VZ Baskett, HE Grosman, CS McLaughlin, EL Isenstein, ... OSF, 2020 | 2 | 2020 |
Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome T Levy, J Gluckman, PM Siper, D Halpern, J Zweifach, R Filip-Dhima, ... Journal of Neurodevelopmental Disorders 16 (1), 25, 2024 | 1 | 2024 |
T63. Parsing Attention Dysfunction in Children With Autism Spectrum Disorder and Attention Deficit/Hyperactivity Disorder S Nattel, E Wilkinson, M Kristin, E Isenstein, A Kolevzon, MP Trelles Biological Psychiatry 83 (9), S153, 2018 | 1 | 2018 |
Molecular basis for the block of connexin channels by quinine and its derivatives MP Trelles, M Srinivas BIOPHYSICAL JOURNAL, 442A-442A, 2007 | 1 | 2007 |