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Behavioral and synaptic alterations relevant to obsessive-compulsive disorder in mice with increased EAAT3 expression.
Delgado-Acevedo C, Estay SF, Radke AK, Sengupta A, Escobar AP, Henríquez-Belmar F, Reyes CA, Haro-Acuña V, Utreras E, Sotomayor-Zárate R, Cho A, Wendland JR, Kulkarni AB, Holmes A, Murphy DL, Chávez AE, Moya PR. Delgado-Acevedo C, et al. Among authors: wendland jr. Neuropsychopharmacology. 2019 May;44(6):1163-1173. doi: 10.1038/s41386-018-0302-7. Epub 2018 Dec 26. Neuropsychopharmacology. 2019. PMID: 30622300 Free PMC article.
Correction: Behavioral and synaptic alterations relevant to obsessivecompulsive disorder in mice with increased EAAT3 expression.
Delgado-Acevedo C, Estay SF, Radke AK, Sengupta A, Escobar AP, Henríquez-Belmar F, Reyes CA, Haro-Acuña V, Utreras E, Sotomayor-Zárate R, Cho A, Wendland JR, Kulkarni AB, Holmes A, Murphy DL, Chávez AE, Moya PR. Delgado-Acevedo C, et al. Among authors: wendland jr. Neuropsychopharmacology. 2019 May;44(6):1177. doi: 10.1038/s41386-019-0331-x. Neuropsychopharmacology. 2019. PMID: 30787427 Free PMC article.
Dennis Luke Murphy, M.D. (1936-2017).
Moya PR, Wendland JR, Fox MA. Moya PR, et al. Among authors: wendland jr. Genes Brain Behav. 2018 Mar;17(3):e12455. doi: 10.1111/gbb.12455. Genes Brain Behav. 2018. PMID: 29596735 Free article. No abstract available.
Anxiety and affective disorder comorbidity related to serotonin and other neurotransmitter systems: obsessive-compulsive disorder as an example of overlapping clinical and genetic heterogeneity.
Murphy DL, Moya PR, Fox MA, Rubenstein LM, Wendland JR, Timpano KR. Murphy DL, et al. Among authors: wendland jr. Philos Trans R Soc Lond B Biol Sci. 2013 Feb 25;368(1615):20120435. doi: 10.1098/rstb.2012.0435. Print 2013. Philos Trans R Soc Lond B Biol Sci. 2013. PMID: 23440468 Free PMC article. Review.
Meta-analysis of association between obsessive-compulsive disorder and the 3' region of neuronal glutamate transporter gene SLC1A1.
Stewart SE, Mayerfeld C, Arnold PD, Crane JR, O'Dushlaine C, Fagerness JA, Yu D, Scharf JM, Chan E, Kassam F, Moya PR, Wendland JR, Delorme R, Richter MA, Kennedy JL, Veenstra-VanderWeele J, Samuels J, Greenberg BD, McCracken JT, Knowles JA, Fyer AJ, Rauch SL, Riddle MA, Grados MA, Bienvenu OJ, Cullen B, Wang Y, Shugart YY, Piacentini J, Rasmussen S, Nestadt G, Murphy DL, Jenike MA, Cook EH, Pauls DL, Hanna GL, Mathews CA. Stewart SE, et al. Among authors: wendland jr. Am J Med Genet B Neuropsychiatr Genet. 2013 Jun;162B(4):367-79. doi: 10.1002/ajmg.b.32137. Epub 2013 Apr 18. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23606572 Free article.
Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes.
Moya PR, Dodman NH, Timpano KR, Rubenstein LM, Rana Z, Fried RL, Reichardt LF, Heiman GA, Tischfield JA, King RA, Galdzicka M, Ginns EI, Wendland JR. Moya PR, et al. Among authors: wendland jr. Eur J Hum Genet. 2013 Aug;21(8):850-4. doi: 10.1038/ejhg.2012.245. Epub 2013 Jan 16. Eur J Hum Genet. 2013. PMID: 23321619 Free PMC article.
89 results