| Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome R Weksberg, AC Stachon, JA Squire, L Moldovan, J Bayani, S Meyn, ... Human genetics 120, 837-845, 2007 | 78 | 2007 |
| Molecular diagnosis of 22q11. 2 deletion and duplication by multiplex ligation dependent probe amplification AC Stachon, B Baskin, AC Smith, A Shugar, C Cytrynbaum, L Fishman, ... American Journal of Medical Genetics Part A 143 (24), 2924-2930, 2007 | 71 | 2007 |
| New insights into the regulatory function of CYFIP1 in the context of WAVE-and FMRP-containing complexes S Abekhoukh, HB Sahin, M Grossi, S Zongaro, T Maurin, I Madrigal, ... Disease Models & Mechanisms 10 (4), 463-474, 2017 | 68 | 2017 |
| Assessment and medication management of paediatric obsessive-compulsive disorder SE Stewart, D Hezel, AC Stachon Drugs 72, 881-893, 2012 | 21 | 2012 |
| Rett syndrome: clinical and molecular characterization of two Brazilian patients A Stachon, FB Assumpção Jr, S Raskin Arquivos de neuro-psiquiatria 65, 36-40, 2007 | 11 | 2007 |
| Anxiety disorders and perceptual disturbances in adolescents with 22q11. 2 deletion syndrome treated with SSRI: a case series AC Stachon, C De Souza Journal of the Canadian Academy of Child and Adolescent Psychiatry 20 (4), 305, 2011 | 9 | 2011 |
| 22q11. 2 microduplication: an enigmatic genetic disorder RI Kylat Journal of Pediatric Genetics 7 (03), 138-142, 2018 | 7 | 2018 |
| Drula Do Nascimento MR, Trembleau A, Arroyo I, Szatmari P, Smith IM, Milà M, Smith AC, Giangrande A, Caillé I, Bardoni B S Abekhoukh, HB Sahin, M Grossi, S Zongaro, T Maurin, I Madrigal, ... New insights into the regulatory function of CYFIP1 in the context of WAVE …, 2017 | 7 | 2017 |
| Pharmacotherapy for obsessive-compulsive and related disorders among children and adolescents. SE Stewart, AC Stachon American Psychological Association, 2014 | 4 | 2014 |
| Reflections of nursing students following Hurricane Michael BA Miller, S Mason, KH Leigh, S Kelley Creative Nursing 28 (3), 198-202, 2022 | 2 | 2022 |
| Síndrome de Rett: caracterização clínica e molecular de dois casos brasileiros A Stachon, FB Assumpção Jr, S Raskin Arquivos de Neuro-Psiquiatria 65, 36-40, 2007 | 2 | 2007 |
| Clinical and Molecular Characterization of Psychosis in 22q11 Deletion Syndrome A Stachon | | 2010 |
| Rett's syndrome-Author's response A Stachon ARQUIVOS DE NEURO-PSIQUIATRIA 65 (2 B), 544-545, 2007 | | 2007 |
| Commentary on Treatment Resistant Psychosis in an adolescent with scoliosis and a history of early feeding difficulties A Stachon Journal of the Canadian Academy of Child and Adolescent Psychiatry 16 (1), 30, 2007 | | 2007 |
| Molecular characterization of deletion breakpoints in adults with 22Q11 deletion syndrome with and without schizophrenia A Stachon, S Meyn, J Squire, L Moldovan, E Chow, A Bassett, ... AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 141 (7 …, 2006 | | 2006 |
