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| Childhood trauma and genetic variation in the IBRO neuroscience reports 2022 Jun 12 45-54. Roomaney Aqeedah Abbas, Womersley Jacqueline Samantha, Swart Patricia Cathryn, Spies Georgina, Seedat Soraya, Hemmings Sian Megan Joan |
| The importance of identifying functional Val158Met polymorphism in catechol-O- Methyltransferase when assessing MRI-based volumetric measurements in major depressive disorder. Brain imaging and behavior 2020 Jan . Serrano-Sosa Mario, Sampathgiri Kruthika, Spuhler Karl Douglas, DeLorenzo Christine, Parsey Ramin, Huang Chu |
| Genetic variants and cognitive functions in patients with brain tumors. Neuro-oncology 2019 May . Correa Denise D, Satagopan Jaya, Martin Axel, Braun Erica, Kryza-Lacombe Maria, Cheung Kenneth, Sharma Ajay, Dimitriadoy Sofia, O'Connell Kelli, Leong Siok, Karimi Sasan, Lyo John, DeAngelis Lisa M, Orlow Ire |
| A DRD2/ANNK1-COMT Interaction, Consisting of Functional Variants, Confers Risk of Post-traumatic Stress Disorder in Traumatized Chinese. Frontiers in psychiatry 2018 9 170. Zhang Kunlin, Wang Li, Cao Chengqi, Li Gen, Fang Ruojiao, Liu Ping, Luo Shu, Zhang Xiangyang, Liberzon Isra |
| Association between COMT Val158Met and DAT1 polymorphisms and depressive symptoms in the obese population. Neuropsychiatric disease and treatment 2017 13 2221-2229. Bieli?ski Maciej, Jaracz Marcin, Lesiewska Natalia, Tomaszewska Marta, Sikora Marcin, Junik Roman, Kami?ska Anna, Tretyn Andrzej, Borkowska Ali |
| COMT, BDNF, and DTNBP1 polymorphisms and cognitive functions in patients with brain tumors. Neuro-oncology 2016 Apr . Correa Denise D, Satagopan Jaya, Cheung Kenneth, Arora Arshi K, Kryza-Lacombe Maria, Xu Youming, Karimi Sasan, Lyo John, DeAngelis Lisa M, Orlow Ire |
| The COMT Val158Met polymorphism moderates the association between cognitive functions and white matter microstructure in schizophrenia. Psychiatric genetics 2016 Mar . Poletti Sara, Mazza Elena, Bollettini Irene, Falini Andrea, Smeraldi Enrico, Cavallaro Roberto, Benedetti Frances |
| Ethnic differences in COMT genetic effects on striatal grey matter alterations associated with childhood ADHD: A voxel-based morphometry study in a Japanese sample. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2015 Nov 1-7. Shimada Koji, Fujisawa Takashi X, Takiguchi Shinichiro, Naruse Hiroaki, Kosaka Hirotaka, Okazawa Hidehiko, Tomoda Ake |
| Association of Single Nucleotide Polymorphisms in Catechol-O-Methyltransferase and Serine-Threonine Protein Kinase Genes in the Pakistani Schizophrenic Population: A Study with Special Emphasis on Cannabis and Smokeless Tobacco. CNS & neurological disorders drug targets 2015 Mar . Nawaz R, Siddiqui |
| Epistasis between polymorphisms in COMT, ESR1, and GCH1 influences COMT enzyme activity and pain. Pain 2014 Nov 155 (11): 2390-9. Smith Shad B, Reenilä Ilkka, Männistö Pekka T, Slade Gary D, Maixner William, Diatchenko Luda, Nackley Andrea |
| COMT Val158Met, but not BDNF Val66Met, is associated with white matter abnormalities of the temporal lobe in patients with first-episode, treatment-naïve major depressive disorder: a diffusion tensor imaging study. Neuropsychiatric disease and treatment 2014 10 1183-90. Hayashi Kenji, Yoshimura Reiji, Kakeda Shingo, Kishi Taro, Abe Osamu, Umene-Nakano Wakako, Katsuki Asuka, Hori Hikaru, Ikenouchi-Sugita Atsuko, Watanabe Keita, Ide Satoru, Ueda Issei, Moriya Junji, Iwata Nakao, Korogi Yukunori, Kubicki Marek, Nakamura J |
| Dopamine genetic risk score predicts depressive symptoms in healthy adults and adults with depression. PloS one 2014 9 (5): e93772. Pearson-Fuhrhop Kristin M, Dunn Erin C, Mortero Sarah, Devan William J, Falcone Guido J, Lee Phil, Holmes Avram J, Hollinshead Marisa O, Roffman Joshua L, Smoller Jordan W, Rosand Jonathan, Cramer Steven |
| Association of VMAT2 gene polymorphisms with alcohol dependence. Journal of neural transmission (Vienna, Austria : 1996) 2013 Aug 120 (8): 1161-9. Fehr Christoph, Sommerlad Daniel, Sander Thomas, Anghelescu Ion, Dahmen Norbert, Szegedi Armin, Mueller Christiana, Zill Peter, Soyka Michael, Preuss Ulrich |
| Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes. Journal of psychiatric research 2013 Aug . Zarchi O, Carmel M, Avni C, Attias J, Frisch A, Michaelovsky E, Patya M, Green T, Weinberger R, Weizman A, Gothelf D |
| Effect of the COMT val158met polymorphism on white matter connectivity in patients with major depressive disorder. Neuroscience letters 2013 Jun 545 35-9. Seok Jeong-Ho, Choi Sunyoung, Lim Hyun Kook, Lee Sang-Hyuk, Kim InSeong, Ham Byung-J |
| Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls. NeuroImage 2011 Aug 57 (4): 1517-23. Raznahan Armin, Greenstein Deanna, Lee Yohan, Long Robert, Clasen Liv, Gochman Pete, Addington Anjene, Giedd Jay N, Rapoport Judith L, Gogtay Nit |
| COMT Val158Met variant and functional haplotypes associated with childhood ADHD history in women with bulimia nervosa. Progress in neuro-psychopharmacology & biological psychiatry 2011 Jun 35 (4): 948-52. Yilmaz Zeynep, Kaplan Allan S, Zai Clement C, Levitan Robert D, Kennedy James |
| COMT gene polymorphism and corpus callosum morphometry in preterm born adults. NeuroImage 2011 Jan 54 (1): 148-53. Dutt Anirban, Shaikh Madiha, Ganguly Taposhri, Nosarti Chiara, Walshe Muriel, Arranz Maria, Rifkin Larry, McDonald Colm, Chaddock Christopher A, McGuire Philip, Murray Robin M, Bramon Elvira, Allin Matthew P |
| The COMT Val108/158Met polymorphism and medial temporal lobe volumetry in patients with schizophrenia and healthy adults. NeuroImage 2010 Nov 53 (3): 992-1000. Ehrlich Stefan, Morrow Eric M, Roffman Joshua L, Wallace Stuart R, Naylor Melissa, Bockholt H Jeremy, Lundquist Antonia, Yendiki Anastasia, Ho Beng-Choon, White Tonya, Manoach Dara S, Clark Vincent P, Calhoun Vince D, Gollub Randy L, Holt Daphne |
| Sympathetic nervous function and the effect of the catechol-O-methyltransferase Val(158)Met polymorphism in patients with panic disorder. Journal of affective disorders 2010 Jun 123 (1-3): 337-40. Kang Eun-Ho, Song Yoon-Jae, Kim Kyung-Jeong, Shim Hyun-Bo, Park Joo-Eon, Yu Bum-H |
| The distinct cognitive syndromes of Parkinson's disease: 5 year follow-up of the CamPaIGN cohort. Brain : a journal of neurology 2009 Nov 132 (Pt 11): 2958-69. Williams-Gray Caroline H, Evans Jonathan R, Goris An, Foltynie Thomas, Ban Maria, Robbins Trevor W, Brayne Carol, Kolachana Bhaskar S, Weinberger Daniel R, Sawcer Stephen J, Barker Roger |
| Genetic and disorder-specific aspects of resting state EEG abnormalities in schizophrenia. Schizophrenia bulletin 2009 Jul 35 (4): 826-39. Venables Noah C, Bernat Edward M, Sponheim Scott |
| Lack of influence of COMT Val158Met genotype on cognition in first-episode non-affective psychosis. Schizophrenia research 2008 Jul 102 (1-3): 206-9. Mata Ignacio, Perez-Iglesias Rocio, Pelayo-Teran Jose Maria, Rodríguez-Sanchez Jose Manuel, Gonzalez-Blanch Cesar, Carrasco-Marin Eugenio, Vazquez-Barquero Jose Luis, Crespo-Facorro Benedic |
| Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS. The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2008 May 11 (3): 351-63. Michaelovsky Elena, Gothelf Doron, Korostishevsky Michael, Frisch Amos, Burg Merav, Carmel Miri, Steinberg Tamar, Inbar Dov, Apter Alan, Weizman Abrah |
| Divergent backward masking performance in schizophrenia and bipolar disorder: association with COMT. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Mar 147B (2): 223-7. Goghari Vina M, Sponheim Scott |
| Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia. Genes, brain, and behavior 2008 Feb 7 (1): 61-9. Zinkstok J, Schmitz N, van Amelsvoort T, Moeton M, Baas F, Linszen |
| Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome. Psychological medicine 2008 Jan 38 (1): 89-100. van Amelsvoort T, Zinkstok J, Figee M, Daly E, Morris R, Owen M J, Murphy K C, De Haan L, Linszen D H, Glaser B, Murphy D G |
| The association between the Val158Met polymorphism of the catechol-O-methyl transferase gene and morphological abnormalities of the brain in chronic schizophrenia. Brain : a journal of neurology 2006 Feb 129 (Pt 2): 399-410. Ohnishi Takashi, Hashimoto Ryota, Mori Takeyuki, Nemoto Kiyotaka, Moriguchi Yoshiya, Iida Hidehiro, Noguchi Hiroko, Nakabayashi Tetsuo, Hori Hiroaki, Ohmori Mayu, Tsukue Ryoutaro, Anami Kimitaka, Hirabayashi Naotugu, Harada Seiichi, Arima Kunimasa, Saitoh Osamu, Kunugi Hiros |
| Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia. Proceedings of the National Academy of Sciences of the United States of America 2001 Jun 98 (12): 6917-22. Egan M F, Goldberg T E, Kolachana B S, Callicott J H, Mazzanti C M, Straub R E, Goldman D, Weinberger D |
| The relationship between a common catechol-O-methyltransferase (COMT) polymorphism val(158) met and fibromyalgia. Clinical and experimental rheumatology 0 27 (5 Suppl 56): S51-6. Cohen H, Neumann L, Glazer Y, Ebstein R P, Buskila |
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- Page last updated:Jan 27, 2023
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