Associated Papers
Novel NARS2 variants in a patient with early-onset status epilepticus: case study and literature review.
Yang N et al.
Bmc Pediatrics, 2024
The serotonin receptor 3E variant is a risk factor for female IBS-D.
Fritz N et al.
Journal of Molecular Medicine (berlin, Germany), 2022
Serotonin type 3 receptor subunit gene polymorphisms associated with psychosomatic symptoms in irritable bowel syndrome: A multicenter retrospective study.
Berens S et al.
World Journal of Gastroenterology, 2022
Pharmacogenetics of antiemetics for chemotherapy-induced nausea and vomiting: A systematic review and meta-analysis.
Eliasen A et al.
Critical Reviews in Oncology/hematology, 2020
Abnormalities of mucosal serotonin metabolism and 5-HT3 receptor subunit 3C polymorphism in irritable bowel syndrome with diarrhoea predict responsiveness to ondansetron.
Gunn D et al.
Alimentary Pharmacology & Therapeutics, 2019
Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese.
Tang FY et al.
Investigative Ophthalmology & Visual Science, 2017
A review of genetic alterations in the serotonin pathway and their correlation with psychotic diseases and response to atypical antipsychotics.
Baou M et al.
Schizophrenia Research, 2016
5-HT3 receptor influences the washing phenotype and visual organization in obsessive-compulsive disorder supporting 5-HT3 receptor antagonists as novel treatment option.
Lennertz L et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology, 2014
A coding variant of the novel serotonin receptor subunit 5-HT3E influences sustained attention in schizophrenia patients.
Lennertz L et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology, 2010
Influence of 5-HT3 receptor subunit genes HTR3A, HTR3B, HTR3C, HTR3D and HTR3E on treatment response to antipsychotics in schizophrenia.
Schuhmacher A et al.
Pharmacogenetics and Genomics, 2009
Allelic variants in HTR3C show association with autism.
Rehnström K et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2009