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Page 1
Anxiety in children and youth: Part 1-Diagnosis.
Klein B, Rajendram R, Hrycko S, Poynter A, Ortiz-Alvarez O, Saunders N, Andrews D. Klein B, et al. Among authors: rajendram r. Paediatr Child Health. 2023 Feb 28;28(1):37-51. doi: 10.1093/pch/pxac102. eCollection 2023 Feb. Paediatr Child Health. 2023. PMID: 36865762 Free PMC article. Review.
DNA Methylation of the Oxytocin Receptor Across Neurodevelopmental Disorders.
Siu MT, Goodman SJ, Yellan I, Butcher DT, Jangjoo M, Grafodatskaya D, Rajendram R, Lou Y, Zhang R, Zhao C, Nicolson R, Georgiades S, Szatmari P, Scherer SW, Roberts W, Anagnostou E, Weksberg R. Siu MT, et al. Among authors: rajendram r. J Autism Dev Disord. 2021 Oct;51(10):3610-3623. doi: 10.1007/s10803-020-04792-x. Epub 2021 Jan 4. J Autism Dev Disord. 2021. PMID: 33394241
Glutamate Genetics in Obsessive-Compulsive Disorder: A Review.
Rajendram R, Kronenberg S, Burton CL, Arnold PD. Rajendram R, et al. J Can Acad Child Adolesc Psychiatry. 2017 Fall;26(3):205-213. Epub 2017 Oct 1. J Can Acad Child Adolesc Psychiatry. 2017. PMID: 29056983 Free PMC article.
Serotonin system gene variants and regional brain volume differences in pediatric OCD.
Sinopoli VM, Erdman L, Burton CL, Easter P, Rajendram R, Baldwin G, Peterman K, Coste J, Shaheen SM, Hanna GL, Rosenberg DR, Arnold PD. Sinopoli VM, et al. Among authors: rajendram r. Brain Imaging Behav. 2020 Oct;14(5):1612-1625. doi: 10.1007/s11682-019-00092-w. Brain Imaging Behav. 2020. PMID: 31187473 Free PMC article.
Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C.
Grafodatskaya D, Chung BH, Butcher DT, Turinsky AL, Goodman SJ, Choufani S, Chen YA, Lou Y, Zhao C, Rajendram R, Abidi FE, Skinner C, Stavropoulos J, Bondy CA, Hamilton J, Wodak S, Scherer SW, Schwartz CE, Weksberg R. Grafodatskaya D, et al. Among authors: rajendram r. BMC Med Genomics. 2013 Jan 28;6:1. doi: 10.1186/1755-8794-6-1. BMC Med Genomics. 2013. PMID: 23356856 Free PMC article.
Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.
Gazzellone MJ, Zarrei M, Burton CL, Walker S, Uddin M, Shaheen SM, Coste J, Rajendram R, Schachter RJ, Colasanto M, Hanna GL, Rosenberg DR, Soreni N, Fitzgerald KD, Marshall CR, Buchanan JA, Merico D, Arnold PD, Scherer SW. Gazzellone MJ, et al. Among authors: rajendram r. J Neurodev Disord. 2016 Oct 18;8:36. doi: 10.1186/s11689-016-9170-9. eCollection 2016. J Neurodev Disord. 2016. PMID: 27777633 Free PMC article.