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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics

ISSN 1552-485X, 1552-4841

5 papers in the library · 98 citations · publishing 2005-2025

Papers

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Genetics of Response to ECT, TMS, Ketamine and Esketamine.

American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics June 17, 2025 Clio E Franklin, Murat Altinay, Kala Bailey et al. 2 citations

Treatment-resistant mood disorders are often managed with intensive interventions that include electroconvulsive therapy (ECT), transcranial magnetic stimulation (TMS), ketamine, and esketamine, but the role of genetics in clinical response to those interventions is yet to be clearly determined. Here, we review the current literature on the genetics of response to these treatment modalities. To...

DOI: 10.1002/ajmg.b.33038 (opens in new tab) Full text (opens in new tab) Esketamine Individualized treatment Tailored therapy Pharmacogenomics +12

Positive association of phencyclidine-responsive genes, PDE4A and PLAT, with schizophrenia.

American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics December 2011 Xiangdong Deng, Hiromi Takaki, Lixiang Wang et al.

As schizophrenia-like symptoms are produced by administration of phencyclidine (PCP), a noncompetitive antagonist of N-methyl-D-aspartate (NMDA) receptors, PCP-responsive genes could be involved in the pathophysiology of schizophrenia. We injected PCP to Wistar rats and isolated five different parts of the brain in 1 and 4 hr after the injection. We analyzed the gene expression induced by the...

The fatty acid amide hydrolase C385A (P129T) missense variant in cannabis users: studies of drug use and dependence in Caucasians.

American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics July 5, 2007 Rachel F. Tyndale, Jennifer I Payne, Alexandra L Gerber et al.

A genetic variation in fatty acid amide hydrolase (FAAH), C385A (P129T), has been previously associated with risk for problem street drug use. FAAH is a mammalian enzyme that inactivates neuromodulatory-signaling lipids including the endogenous cannabinoid 1 receptor agonist anandamide. We investigated in adult Caucasians (N = 749) whether this FAAH variant altered the risk for trying, regular...

5-HT 1A polymorphism and self-transcendence in mood disorders.

American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics August 5, 2005 Cristina Lorenzi, Alessandro Serretti, Laura Mandelli et al.

Recently, an association between serotonin 1A receptor binding potential and self-transcendence scores at the temperament and character inventory (TCI) has been reported. We tested involvement of 5-HT(1A) gene in this trait, in a sample of 40 remitted mood disorder patients. Subjects with the 5-HT(1A)*C/C genotype showed significantly lower scores at the total self-transcendence and at the...

Evidence for a common biological basis of the absorption trait, hallucinogen effects, and positive symptoms: Epistasis between 5-HT2a and COMT polymorphisms

American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics June 17, 2005 Ulrich Ott, Martin Reuter, Juergen Hennig et al. 96 citations

Absorption represents a disposition to experience altered states of consciousness characterized by intensively focused attention. It is correlated with hypnotic susceptibility and includes phenomena ranging from vivid perceptions and imaginations to mystical experiences. Based on the assumption that drug-induced and naturally occurring mystical experiences share common neural mechanisms, we...