Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 140 Records) |
Query Trace: Syndrome and COMT[original query] |
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Adjunctive S-adenosylmethionine (SAMe) in treating non-remittent major depressive disorder: An 8-week double-blind, randomized, controlled trial<sup/>. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2018 8 28 (10): 1126-1136. Sarris Jerome, Byrne Gerard J, Bousman Chad, Stough Con, Murphy Jenifer, MacDonald Patricia, Adams Laura, Nazareth Sonia, Oliver Georgina, Cribb Lachlan, Savage Karen, Menon Ranjit, Chamoli Suneel, Berk Michael, Ng Chee, Mischoulon Dav |
COMT Val 108/158 Met polymorphism and treatment response to aripiprazole in patients with acute schizophrenia. Neuropsychiatric disease and treatment 2018 14 1657-1663. Kaneko Haruka, Miura Itaru, Kanno-Nozaki Keiko, Horikoshi Sho, Hino Mizuki, Yabe Hiroo |
Pharmacogenetics and prediction of adverse events in prescription opioid use disorder patients. Basic & clinical pharmacology & toxicology 2018 12 124 (4): 439-448. Muriel Javier, Margarit César, Barrachina Jordi, Ballester Pura, Flor Andrea, Morales Domingo, Horga José F, Fernández Eduardo, Peiró Ana |
Association of Fatigue With TPH2 Genetic Polymorphisms in Women With Irritable Bowel Syndrome. Biological research for nursing 2018 Oct 1099800418806055. Han Claire J, Jarrett Monica E, Cain Kevin C, Jun Sangeun, Heitkemper Margaret |
Clinical and Genetic Factors Associated with Resistance to Treatment in Patients with Schizophrenia: A Case-Control Study. International journal of molecular sciences 2019 9 20 (19): . Hajj Aline, Obeid Sahar, Sahyoun Saria, Haddad Chadia, Azar Jocelyne, Rabbaa Khabbaz Lydia, Hallit Souhe |
Functional dyspepsia susceptibility is associated with TGFB1 gene polymorphisms (RS4803455, RS1800469) in H pylori-negative Chinese population. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2019 Aug e13681. Cheung Cynthia K Y, Lan Lin Lin, Chan Yawen, Yuen Kay, Cheong Pui Kuan, Fang Fanny, Wu Justin C |
Lower [F]fallypride binding to dopamine D receptors in frontal brain areas in adults with 22q11.2 deletion syndrome: a positron emission tomography study. Psychological medicine 2019 Apr 1-9. van Duin Esther D A, Ceccarini Jenny, Booij Jan, Kasanova Zuzana, Vingerhoets Claudia, van Huijstee Jytte, Heinzel Alexander, Mohammadkhani-Shali Siamak, Winz Oliver, Mottaghy Felix, Myin-Germeys Inez, van Amelsvoort Thérè |
Association of rs4680 COMT, rs6280 DRD3, and rs7322347 5HT2A With Clinical Features of Youth-Onset Schizophrenia. Frontiers in psychiatry 2019 12 10 830. Morozova Anna, Zorkina Yana, Pavlov Konstantin, Pavlova Olga, Storozheva Zinaida, Zubkov Eugene, Zakharova Natalia, Karpenko Olga, Reznik Alexander, Chekhonin Vladimir, Kostyuk Georg |
Low prevalence of substance use in people with 22q11.2 deletion syndrome. The British journal of psychiatry : the journal of mental science 2019 1 215 (5): 661-667. Vingerhoets Claudia, van Oudenaren Mathilde J F, Bloemen Oswald J N, Boot Erik, van Duin Esther D A, Evers Laurens J M, Fiksinski Ania M, Breetvelt Elemi J, Palmer Lisa D, Vergaelen Elfi, Vogels Annick, Meijer Carin, Booij Jan, , de Haan Liewe, Swillen Ann, Vorstman Jacob A S, Bassett Anne S, van Amelsvoort Therese A M |
The effect of rs1076560 (DRD2) and rs4680 (COMT) on tardive dyskinesia and cognition in schizophrenia subjects. Psychiatric genetics 2020 Oct 30 (5): 125-135. Punchaichira Toyanji Joseph, Kukshal Prachi, Bhatia Triptish, Deshpande Smita Neelkanth, Thelma B |
Genetic modifiers in rare disorders: the case of fragile X syndrome. European journal of human genetics : EJHG 2020 8 29 (1): 173-183. Crawford Hayley, Scerif Gaia, Wilde Lucy, Beggs Andrew, Stockton Joanne, Sandhu Pria, Shelley Lauren, Oliver Chris, McCleery Jose |
Catechol-O-methyltransferase rs4680 and rs4818 haplotype association with treatment response to olanzapine in patients with schizophrenia. Scientific reports 2020 6 10 (1): 10049. Nikolac Perkovic Matea, Sagud Marina, Zivkovic Maja, Uzun Suzana, Nedic Erjavec Gordana, Kozumplik Oliver, Svob Strac Dubravka, Mimica Ninoslav, Mihaljevic Peles Alma, Pivac Ne |
Effect of Functional BDNF and COMT Polymorphisms on Symptoms and Regional Brain Volume in Frontotemporal Dementia and Corticobasal Syndrome. The Journal of neuropsychiatry and clinical neurosciences 2020 May appineuropsych19100211. Huey Edward D, Fremont Rachel, Manoochehri Masood, Gazes Yunglin, Lee Seonjoo, Cosentino Stephanie, Tierney Michael, Wassermann Eric M, Momeni Parastoo, Grafman Jord |
A review of the existing literature on buprenorphine pharmacogenomics. The pharmacogenomics journal 2020 11 21 (2): 128-139. Meaden Christopher W, Mozeika Alexander, Asri Rijul, Santos Cynthia |
Early-Onset Schizophrenia: A Special Phenotype of the Disease Characterized by Increased MTHFR Polymorphisms and Aggravating Symptoms. Neuropsychiatric disease and treatment 2021 8 17 2511-2525. Wan Lin, Wei Ji |
Influence of COMT polymorphism in cognitive performance on dementia in community-dwelling elderly Mexican (SADEM study). Metabolic brain disease 2021 Apr . Juárez-Cedillo Teresa, González-Figueroa Evangelina, Martínez-Rodríguez Nancy, Fragosos Jose M, Garrido-Acosta Osvaldo, Vargas-Alarcón Gilber |
Negative symptoms in schizophrenia: correlation with clinical and genetic factors. Pharmacogenomics 2021 4 22 (7): 389-399. Hajj Aline, Hallit Souheil, Chamoun Karam, Sacre Hala, Obeid Sahar, Haddad Chadia, Dollfus Sonia, Khabbaz Lydia Rabb |
Long acting aripiprazole influences cognitive functions in recent onset schizophrenia. Psychopharmacology 2021 Feb . Peitl Vjekoslav, Štefanovi? Mario, Orlovi? Ivona, Culej Jelena, Renduli? Ana, Mateši? Krunoslav, Karlovi? Dalib |
Fibromyalgia: A Review of Related Polymorphisms and Clinical Relevance. Anais da Academia Brasileira de Ciencias 2021 11 93 (suppl 4): e20210618. Janssen Luísa P, Medeiros Liciane F, Souza Andressa DE, Silva Juliana |
Role of COMT V158M Polymorphism in the Development of Dystonia after Administration of Antipsychotic Drugs. Brain sciences 2021 10 11 (10): . Nicotera Antonio Gennaro, Di Rosa Gabriella, Turriziani Laura, Costanzo Maria Cristina, Stracuzzi Emanuela, Vitello Girolamo Aurelio, Rando Rosanna Galati, Musumeci Antonino, Vinci Mirella, Musumeci Sebastiano Antonino, Calì Frances |
Working memory dysfunction in fibromyalgia is associated with genotypes of the catechol- O-methyltransferase gene: an event-related potential study. European archives of psychiatry and clinical neuroscience 2022 9 . Ferrera David, Gómez-Esquer Francisco, Peláez Irene, Barjola Paloma, Fernandes-Magalhaes Roberto, Carpio Alberto, De Lahoz María Eugenia, Martín-Buro María Carmen, Mercado Francis |
Genotypes of Pain and Analgesia in a Randomized Trial of Irritable Bowel Syndrome.
Frontiers in psychiatry 2022 4 13 842030. Vollert Jan, Wang Ruisheng, Regis Stephanie, Yetman Hailey, Lembo Anthony J, Kaptchuk Ted J, Cheng Vivian, Nee Judy, Iturrino Johanna, Loscalzo Joseph, Hall Kathryn T, Silvester Jocelyn |
The Associations of Single Nucleotide Polymorphisms with Risk and Symptoms of Irritable Bowel Syndrome. Journal of personalized medicine 2022 Jan 12 (2): . Zhao Tingting, Zhang Yiming, Lee Joochul, Starkweather Angela R, Young Erin E, Cong Xiaom |
Genetic Addiction Risk Severity Assessment Identifies Polymorphic Reward Genes as Antecedents to Reward Deficiency Syndrome (RDS) Hypodopaminergia's Effect on Addictive and Non-Addictive Behaviors in a Nuclear Family. Journal of personalized medicine 2022 12 12 (11): . Dennen Catherine A, Blum Kenneth, Bowirrat Abdalla, Thanos Panayotis K, Elman Igor, Ceccanti Mauro, Badgaiyan Rajendra D, McLaughlin Thomas, Gupta Ashim, Bajaj Anish, Baron David, Downs B William, Bagchi Debasis, Gold Mark |
The inconsistent mediating effect of catechol O methyl transferase ValMet polymorphism on the sex difference of cognitive impairment in schizophrenia patients. Frontiers in psychiatry 2022 10 13 993859. Xu Hang, Zhou Yongjie, Xiu Meihong, Chen Dachun, Wang Weiwen, Wang Li, Zhang Xiangya |
Genetic and epigenetic regulation of Catechol-O-methyltransferase in relation to inflammation in chronic fatigue syndrome and Fibromyalgia. Journal of translational medicine 2022 10 20 (1): 487. Polli Andrea, Hendrix Jolien, Ickmans Kelly, Bakusic Jelena, Ghosh Manosij, Monteyne Dora, Velkeniers Brigitte, Bekaert Bram, Nijs Jo, Godderis Lo |
[Irritable bowel syndrome phenotypes: leading factors of genetics and epigenetics, mechanisms of formation]. Terapevticheskii arkhiv 2023 5 95 (2): 164-172. O V Gaus, M A Livz |
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia. Molecular psychiatry 2023 3 . Lin Jhih-Rong, Zhao Yingjie, Jabalameli M Reza, Nguyen Nha, Mitra Joydeep, , Swillen Ann, Vorstman Jacob A S, Chow Eva W C, van den Bree Marianne, Emanuel Beverly S, Vermeesch Joris R, Owen Michael J, Williams Nigel M, Bassett Anne S, McDonald-McGinn Donna M, Gur Raquel E, Bearden Carrie E, Morrow Bernice E, Lachman Herbert M, Zhang Zhengdong |
Exercise-induced changes in gene expression do not mediate post exertional malaise in Gulf War illness. Brain, behavior, & immunity - health 2023 3 29 100612. Boruch Alexander E, Lindheimer Jacob B, Ninneman Jacob V, Wylie Glenn R, Alexander Thomas, Klein-Adams Jacquelyn C, Stegner Aaron J, Gretzon Nicholas P, Samy Bishoy, Falvo Michael J, Cook Dane |
Associations between Catechol-O-methyltransferase (COMT) polymorphisms and cognitive impairments, psychiatric symptoms and tardive dyskinesia in schizophrenia. Brain research 2023 12 148740. Jinghui Chi, Yanyan Ma, Menglei Shi, Chenghao Lu, Qiaona Jiang, Yanzhe Li, Xiaofei Zhang, Xiaomei Shi, Shen Li, Lili Wa |
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- Page last updated:Apr 22, 2024
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