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Epilepsy & Behavior : E&B|January 18, 2019
STXBP1 encephalopathy is associated with awake bruxismArezoo Rezazadeh, Mohammed Uddin, O Carter Snead, et al.Frontiers in Pharmacology|May 26, 2023
Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing dataLuciana Bertholim-Nasciben, Marilia O Scliar, Guilherme Debortoli, et al.Journal of Medical Genetics|April 5, 2003
The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndromeL Bentley, K Nakabayashi, D Monk, et al.International Psychogeriatrics|October 31, 2013
Effect of methylphenidate on attention in apathetic AD patients in a randomized, placebo-controlled trialKrista L Lanctôt, Sarah A Chau, Nathan Herrmann, et al.Biomolecules|May 24, 2024
Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD OutcomesLeo McKay, Berardino Petrelli, Molly Pind, et al.Pediatrics|December 20, 2015
Prevalence of Creatine Deficiency Syndromes in Children With Nonsyndromic AutismAndreas Schulze, Margaret Bauman, Anne Chun-Hui Tsai, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 16, 2016
The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASDAnne Claire Richard, Anne Rovelet-Lecrux, Elsa Delaby, et al.Human Mutation|September 9, 2014
A CGG-repeat expansion mutation in ZNF713 causes FRA7A: association with autistic spectrum disorder in two familiesSofie Metsu, Jacqueline K Rainger, Kim Debacker, et al.Frontiers in Cellular Neuroscience|January 31, 2024
Disruption of the autism-associated gene SCN2A alters synaptic development and neuronal signaling in patient iPSC-glutamatergic neuronsChad O Brown, Jarryll A Uy, Nadeem Murtaza, et al.Oncogene|December 22, 1999
Dysregulation of cyclin dependent kinase 6 expression in splenic marginal zone lymphoma through chromosome 7q translocationsM M Corcoran, S J Mould, J A Orchard, et al.Pageof 88