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記憶力
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記憶力
6 個討論
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嗯，完全記不住東西，各種往事，結果 還是 記憶力不錯。。。我是不是被封印了。。
jessica89
? 最后回復
變態的ACTN3
?
2021-11-04 21:00
5714
7
? 來自相關小組
回寄忘了記單號沒事吧？
hua2358518
? 最后回復
pony24
?
2018-03-17 12:07
3258
1
? 來自相關小組
啥時候才能出報告啊 等的焦急的一匹
MAIKEBYE
? 最后回復
ouyangke
?
2018-01-28 16:26
3068
3
? 來自相關小組
為什么我的報告里面沒有記憶力這項呢？有人知道嗎？
何濤
? 最后回復
wuxiang
?
2016-12-17 16:16
4017
3
? 來自相關小組
我的記憶力一直不錯，大家的結果如何？
zhengqiang
? 最后回復
謙遜的PKHD1基因
?
2016-10-24 13:37
6107
13
? 來自相關小組
好記憶抵得上爛筆頭
zk8848
? 2016-06-29 14:35
3245
0
? 來自相關小組
發起討論
記憶力
6 個討論
相關基因
WWC1
位點：RS17070145
COMT
位點：RS4680
Papassotiropoulos A, et al. Common Kibra alleles are associated with human memory performance. 2006
Schaper K, et al. KIBRA gene variants are associated with episodic memory in healthy elderly. 2008
Zhang H, et al. Cognitive flexibility is associated with KIBRA variant and modulated by recent tobacco use. 2009
Galecki P, et al. Single nucleotide polymorphism of the KIBRA gene in recurrent depressive disorders. 2015
Vassos E, et al. Evidence of association of KIBRA genotype with episodic memory in families of psychotic patients and controls. 2010
Yasuda Y, et al. Association study of KIBRA gene with memory performance in a Japanese population. 2010
Burgess JD, et al. Association of common KIBRA variants with episodic memory and AD risk. 2011
Kauppi K, et al. KIBRA polymorphism is related to enhanced memory and elevated hippocampal processing. 2011
Witte AV, et al. Interaction of BDNF and COMT polymorphisms on paired-associative stimulation-induced cortical plasticity. 2012
Rodríguez-Rodríguez E, et al. Age-dependent association of KIBRA genetic variation and Alzheimer's disease risk. 2009
Seshadri S, et al. Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. 2007
Almeida OP, et al. KIBRA genetic polymorphism influences episodic memory in later life, but does not increase the risk of mild cognitive impairment. 2008
Need AC, et al. Failure to replicate effect of Kibra on human memory in two large cohorts of European origin. 2008
Corneveaux JJ, et al. Evidence for an association between KIBRA and late-onset Alzheimer's disease. 2010
Bates TC, et al. Association of KIBRA and memory. 2009
Vázquez-Higuera JL, et al. Caspase-1 genetic variation is not associated with Alzheimer's disease risk. 2010
Schneider A, et al. KIBRA: A New Gateway to Learning and Memory? 2010
Wersching H, et al. Impact of common KIBRA allele on human cognitive functions. 2011
Sédille-Mostafaie N, et al. The role of memory-related gene polymorphisms, KIBRA and CLSTN2, on replicate memory assessment in the elderly. 2012
Wang D, et al. KIBRA gene variants are associated with synchronization within the default-mode and executive control networks. 2013
Palombo DJ, et al. KIBRA polymorphism is associated with individual differences in hippocampal subregions: evidence from anatomical segmentation using high-resolution MRI. 2013
Wagner AK, et al. Association of KIBRA rs17070145 polymorphism and episodic memory in individuals with severe TBI. 2012
Milnik A, et al. Association of KIBRA with episodic and working memory: a meta-analysis. 2012
Schuck NW, et al. Aging and KIBRA/WWC1 genotype affect spatial memory processes in a virtual navigation task. 2013
Duning K, et al. Common exonic missense variants in the C2 domain of the human KIBRA protein modify lipid binding and cognitive performance. 2013
Stein DJ, et al. Warriors versus worriers: the role of COMT gene variants. 2006
Gellekink H, et al. Catechol-O-methyltransferase genotype is associated with plasma total homocysteine levels and may increase venous thrombosis risk. 2007
Caspi A, et al. Moderation of the effect of adolescent-onset cannabis use on adult psychosis by a functional polymorphism in the catechol-O-methyltransferase gene: longitudinal evidence of a gene X environment interaction. 2005
Onay UV, et al. Combined effect of CCND1 and COMT polymorphisms and increased breast cancer risk. 2008
Lohoff FW, et al. Association between the catechol-O-methyltransferase Val158Met polymorphism and cocaine dependence. 2008
Benedetti F, et al. The catechol-O-methyltransferase Val(108/158)Met polymorphism affects antidepressant response to paroxetine in a naturalistic setting. 2009
Mier D, et al. Neural substrates of pleiotropic action of genetic variation in COMT: a meta-analysis. 2010
Honea R, et al. Impact of interacting functional variants in COMT on regional gray matter volume in human brain. 2009
Gupta M, et al. Genetic susceptibility to schizophrenia: role of dopaminergic pathway gene polymorphisms. 2009
Bodenmann S, et al. Pharmacogenetics of modafinil after sleep loss: catechol-O-methyltransferase genotype modulates waking functions but not recovery sleep. 2009
Heinz A, et al. The effects of catechol O-methyltransferase genotype on brain activation elicited by affective stimuli and cognitive tasks. 2015
Smolka MN, et al. Catechol-O-methyltransferase val158met genotype affects processing of emotional stimuli in the amygdala and prefrontal cortex. 2005
Zubieta JK, et al. COMT val158met genotype affects mu-opioid neurotransmitter responses to a pain stressor. 2003
Szekely A, et al. Association between hypnotizability and the catechol-O-methyltransferase (COMT) polymorphism. 2010
Hoenicka J, et al. Gender-specific COMT Val158Met polymorphism association in Spanish schizophrenic patients. 2010
Chien YL, et al. Association of the 3' region of COMT with schizophrenia in Taiwan. 2009
Mier D, et al. Neural substrates of pleiotropic action of genetic variation in COMT: a meta-analysis. 2010
Gupta M, et al. Association studies of catechol-O-methyltransferase (COMT) gene with schizophrenia and response to antipsychotic treatment. 2009
Liao SY, et al. Genetic variants in COMT and neurocognitive impairment in families of patients with schizophrenia. 2009
Secher A, et al. Antidepressive-drug-induced bodyweight gain is associated with polymorphisms in genes coding for COMT and TPH1. 2009
Tu HP, et al. Monoamine oxidase A gene polymorphisms and enzyme activity associated with risk of gout in Taiwan aborigines. 2010
Pálmason H, et al. Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant. 2010
Illi A, et al. Catechol-O-methyltransferase val108/158met genotype, major depressive disorder and response to selective serotonin reuptake inhibitors in major depressive disorder. 2010
Amstadter AB, et al. Association between COMT, PTSD, and increased smoking following hurricane exposure in an epidemiologic sample. 2009
Kring SI, et al. Polymorphisms of serotonin receptor 2A and 2C genes and COMT in relation to obesity and type 2 diabetes. 2009
Peterson NB, et al. Association of COMT haplotypes and breast cancer risk in caucasian women. 2010
Salo J, et al. The interaction between serotonin receptor 2A and catechol-O-methyltransferase gene polymorphisms is associated with the novelty-seeking subscale impulsiveness. 2010
Costas J, et al. Heterozygosity at catechol-O-methyltransferase Val158Met and schizophrenia: new data and meta-analysis. 2011
Voisey J, et al. HapMap tag-SNP analysis confirms a role for COMT in schizophrenia risk and reveals a novel association. 2012
Nicholl BI, et al. No evidence for a role of the catechol-O-methyltransferase pain sensitivity haplotypes in chronic widespread pain. 2010
Miller DK, et al. Acute intravenous synaptamine complex variant KB220? "normalizes" neurological dysregulation in patients during protracted abstinence from alcohol and opiates as observed using quantitative electroencephalographic and genetic analysis for reward polymorphisms: part 1, pilot study with 2 case reports. 2010
Dumas I, et al. Polymorphisms in genes involved in the estrogen pathway and mammographic density. 2010
Barbosa FR, et al. Influence of catechol-O-methyltransferase (COMT) gene polymorphisms in pain sensibility of Brazilian fibromialgia patients. 2012
Finan PH, et al. COMT moderates the relation of daily maladaptive coping and pain in fibromyalgia. 2011
Inoue-Choi M, et al. Genetic Association Between the COMT Genotype and Urinary Levels of Tea Polyphenols and Their Metabolites among Daily Green Tea Drinkers. 1300
Yilmaz Z, et al. COMT Val158Met variant and functional haplotypes associated with childhood ADHD history in women with bulimia nervosa. 2011
Eisenberg J, et al. Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype. 1999
Michaelovsky E, et al. Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS. 2008
Costas J, et al. Interaction between COMT haplotypes and cannabis in schizophrenia: a case-only study in two samples from Spain. 2011
Malaguti A, et al. Role of COMT, 5-HT(1A) , and SERT genetic polymorphisms on antidepressant response to Transcranial Magnetic Stimulation. 2011
Cerne JZ, et al. Estrogen metabolism genotypes, use of long-term hormone replacement therapy and risk of postmenopausal breast cancer. 2011
Laugsand EA, et al. Clinical and genetic factors associated with nausea and vomiting in cancer patients receiving opioids. 2011
Ancín I, et al. Sensory gating deficit is associated with catechol-O-methyltransferase polymorphisms in bipolar disorder. 2011
Schreiner F, et al. Association of COMT genotypes with S-COMT promoter methylation in growth-discordant monozygotic twins and healthy adults. 2011
Jugurnauth SK, et al. A COMT gene haplotype associated with methamphetamine abuse. 2011
Schosser A, et al. The impact of COMT gene polymorphisms on suicidality in treatment resistant major depressive disorder--a European multicenter study. 2012
Schulz S, et al. When control fails: influence of the prefrontal but not striatal dopaminergic system on behavioural flexibility in a change detection task. 2012
Zammit S, et al. Cannabis, COMT and psychotic experiences. 2011
Soeiro-de-Souza MG, et al. COMT Met (158) modulates facial emotion recognition in bipolar I disorder mood episodes. 2012
Jacobsen LM, et al. The COMT rs4680 Met allele contributes to long-lasting low back pain, sciatica and disability after lumbar disc herniation. 2012
Narasimhan S, et al. Variation in the catechol-O-methyltransferase (COMT) gene and treatment response to venlafaxine XR in generalized anxiety disorder. 2012
Choudhry Z, et al. Catechol-o-methyltransferase gene and executive function in children with ADHD. 2014
Barnes A, et al. No association of COMT (Val158Met) genotype with brain structure differences between men and women. 2012
Liang S, et al. Association between Val158Met functional polymorphism in the COMT gene and risk of preeclampsia in a Chinese population. 2012
Martínez-Jauand M, et al. Pain sensitivity in fibromyalgia is associated with catechol-O-methyltransferase (COMT) gene. 2013
Voisey J, et al. A novel SNP in COMT is associated with alcohol dependence but not opiate or nicotine dependence: a case control study. 2011
Hill LD, et al. Catechol-O-methyltransferase (COMT) single nucleotide polymorphisms and haplotypes are not major risk factors for polycystic ovary syndrome. 2012
Zhang Y, et al. Association between polymorphisms in COMT, PLCH1, and CYP17A1, and non-small-cell lung cancer risk in Chinese nonsmokers. 2013
Bray NJ, et al. A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain. 2003
Palmatier MA, et al. COMT haplotypes suggest P2 promoter region relevance for schizophrenia. 2004
Chen X, et al. Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families. 2004
Zhu G, et al. Differential expression of human COMT alleles in brain and lymphoblasts detected by RT-coupled 5' nuclease assay. 2004
Chen J, et al. Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain. 2004
Handoko HY, et al. Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia. 2005
Zhao J, et al. An entropy-based statistic for genomewide association studies. 2005
Stein MB, et al. COMT polymorphisms and anxiety-related personality traits. 2005
Sweet RA, et al. Catechol-O-methyltransferase haplotypes are associated with psychosis in Alzheimer disease. 2005
Funke B, et al. COMT genetic variation confers risk for psychotic and affective disorders: a case control study. 2005
Fallin MD, et al. Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios. 2005
Hawi Z, et al. Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder. 2005
Beuten J, et al. Significant association of catechol-O-methyltransferase (COMT) haplotypes with nicotine dependence in male and female smokers of two ethnic populations. 2006
Kristensen VN, et al. Multilocus analysis of SNP and metabolic data within a given pathway. 2006
Rissling I, et al. Daytime sleepiness and the COMT val158met polymorphism in patients with Parkinson disease. 2006
Dempster EL, et al. The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression. 2006
Gioli-Pereira L, et al. PCR screening for 22q11.2 microdeletion: development of a new cost-effective diagnostic tool. 2006
Meyer-Lindenberg A, et al. Impact of complex genetic variation in COMT on human brain function. 2006
Zhao J, et al. Nonlinear tests for genomewide association studies. 2006
Oberacher H, et al. Direct molecular haplotyping of multiple polymorphisms within exon 4 of the human catechol-O-methyltransferase gene by liquid chromatography-electrospray ionization time-of-flight mass spectrometry. 2006
Borroni B, et al. Haplotypes in cathechol-O-methyltransferase gene confer increased risk for psychosis in Alzheimer disease. 2007
Kim H, et al. Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans. 2006
Nicodemus KK, et al. Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia. 2007
Cotterchio M, et al. Dietary phytoestrogen intake is associated with reduced colorectal cancer risk. 2006
Lang UE, et al. Gender-dependent association of the functional catechol-O-methyltransferase Val158Met genotype with sensation seeking personality trait. 2007
Molero P, et al. Clinical involvement of catechol-O-methyltransferase polymorphisms in schizophrenia spectrum disorders: influence on the severity of psychotic symptoms and on the response to neuroleptic treatment. 2007
Yu R, et al. Association analysis of COMT polymorphisms and schizophrenia in a Chinese Han population: a case-control study. 2007
Long JR, et al. Genetic polymorphisms in estrogen-metabolizing genes and breast cancer survival. 2007
Zhang K, et al. An association study between cathechol-O-methyltransferase gene and mental retardation in the Chinese Han population. 2007
Ton TG, et al. Genetic polymorphisms in dopamine-related genes and smoking cessation in women: a prospective cohort study. 2007
Nunokawa A, et al. No associations exist between five functional polymorphisms in the catechol-O-methyltransferase gene and schizophrenia in a Japanese population. 2007
Yacubian J, et al. Gene-gene interaction associated with neural reward sensitivity. 2007
Zinkstok J, et al. Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia. 2008
Ma X, et al. A quantitative association study between schizotypal traits and COMT, PRODH and BDNF genes in a healthy Chinese population. 2007
Talkowski ME, et al. Dopamine genes and schizophrenia: case closed or evidence pending? 2007
Gooden KM, et al. Val153Met polymorphism of catechol-O-methyltransferase and prevalence of uterine leiomyomata. 2007
Diaz-Asper CM, et al. Genetic variation in catechol-O-methyltransferase: effects on working memory in schizophrenic patients, their siblings, and healthy controls. 2008
Vargas-Alarcón G, et al. Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia. 2015
Retz W, et al. Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults. 2007
Juckel G, et al. Association of catechol-O-methyltransferase variants with loudness dependence of auditory evoked potentials. 2008
Fung MM, et al. Genetic variation within adrenergic pathways determines in vivo effects of presynaptic stimulation in humans. 2008
Tander B, et al. Polymorphisms of the serotonin-2A receptor and catechol-O-methyltransferase genes: a study on fibromyalgia susceptibility. 2008
Aguilera M, et al. Putative role of the COMT gene polymorphism (Val158Met) on verbal working memory functioning in a healthy population. 2008
Ettinger U, et al. Catechol-O-methyltransferase (COMT) val158met genotype is associated with BOLD response as a function of task characteristic. 2008
Hirata H, et al. COMT polymorphisms affecting protein expression are risk factors for endometrial cancer. 2008
He C, et al. A prospective study of genetic polymorphism in MPO, antioxidant status, and breast cancer risk. 2009
Bombin I, et al. DRD3, but not COMT or DRD2, genotype affects executive functions in healthy and first-episode psychosis adolescents. 2008
Wray NR, et al. Association study of candidate variants of COMT with neuroticism, anxiety and depression. 2008
Kan T, et al. Rarity of Somatic Mutation and Frequency of Normal Sequence Variation Detected in Sporadic Colon Adenocarcinoma Using High-Throughput cDNA Sequencing. 1503
Prasad KM, et al. Structural cerebral variations as useful endophenotypes in schizophrenia: do they help construct "extended endophenotypes"? 2008
Hettema JM, et al. Catechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes. 2008
Shi J, et al. Neurotransmission and bipolar disorder: a systematic family-based association study. 2008
Xing C, et al. Linkage studies of catechol-O-methyltransferase (COMT) and dopamine-beta-hydroxylase (DBH) cDNA expression levels. 2007
Soronen P, et al. Association of a nonsynonymous variant of DAOA with visuospatial ability in a bipolar family sample. 2008
Shiels MS, et al. A community-based study of cigarette smoking behavior in relation to variation in three genes involved in dopamine metabolism: Catechol-O-methyltransferase (COMT), dopamine beta-hydroxylase (DBH) and monoamine oxidase-A (MAO-A). 2008
Haraldsson HM, et al. Catechol-O-methyltransferase Val 158 Met polymorphism and antisaccade eye movements in schizophrenia. 2010
Mukherjee N, et al. The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase. 2010
Westberg L, et al. Sex steroid-related candidate genes in psychiatric disorders. 2008
Diergaarde B, et al. Polymorphisms in genes involved in sex hormone metabolism, estrogen plus progestin hormone therapy use, and risk of postmenopausal breast cancer. 2008
Bialecka M, et al. The association of functional catechol-O-methyltransferase haplotypes with risk of Parkinson's disease, levodopa treatment response, and complications. 2008
Shi J, et al. Genetic associations with schizophrenia: meta-analyses of 12 candidate genes. 2008
Sheldrick AJ, et al. Effect of COMT val158met genotype on cognition and personality. 2008
Tranah GJ, et al. Genetic variation in candidate osteoporosis genes, bone mineral density, and fracture risk: the study of osteoporotic fractures. 2008
Halleland H, et al. Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults. 2009
Tempfer CB, et al. Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis. 2009
Hamaguchi M, et al. Possible difference in frequencies of genetic polymorphisms of estrogen receptor alpha, estrogen metabolism and P53 genes between estrogen receptor-positive and -negative breast cancers. 2008
Huuhka K, et al. Dopamine 2 receptor C957T and catechol-o-methyltransferase Val158Met polymorphisms are associated with treatment response in electroconvulsive therapy. 2008
Biederman J, et al. Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study. 2008
Roffman JL, et al. MTHFR 677C --> T genotype disrupts prefrontal function in schizophrenia through an interaction with COMT 158Val --> Met. 2008
Shrubsole MJ, et al. Drinking green tea modestly reduces breast cancer risk. 2009
Rakv?g TT, et al. Genetic variation in the catechol-O-methyltransferase (COMT) gene and morphine requirements in cancer patients with pain. 2008
Mas S, et al. [Effect of polymorphisms of the cathecol-O-methyltransferase on schizophrenia risk in a Spanish population]. 2008
Pearce CL, et al. Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium. 2009
Cote ML, et al. Tobacco and estrogen metabolic polymorphisms and risk of non-small cell lung cancer in women. 2009
Need AC, et al. A genome-wide investigation of SNPs and CNVs in schizophrenia. 2009
Boettiger CA, et al. Now or Later? An fMRI study of the effects of endogenous opioid blockade on a decision-making network. 2009
Mushlin RA, et al. Clique-finding for heterogeneity and multidimensionality in biomarker epidemiology research: the CHAMBER algorithm. 2009
Okochi T, et al. Meta-analysis of association between genetic variants in COMT and schizophrenia: an update. 2009
Goodyer IM, et al. Cohort profile: risk patterns and processes for psychopathology emerging during adolescence: the ROOTS project. 2010
Cross DS, et al. Development of a fingerprinting panel using medically relevant polymorphisms. 2009
Benedetti F, et al. Acute antidepressant response to sleep deprivation combined with light therapy is influenced by the catechol-O-methyltransferase Val(108/158)Met polymorphism. 2010
Quednow BB, et al. Sensorimotor gating depends on polymorphisms of the serotonin-2A receptor and catechol-O-methyltransferase, but not on neuregulin-1 Arg38Gln genotype: a replication study. 2009
Zhang Z, et al. The Val/Met functional polymorphism in COMT confers susceptibility to bipolar disorder: evidence from an association study and a meta-analysis. 2009
Gadow KD, et al. Association of COMT (Val158Met) and BDNF (Val66Met) gene polymorphisms with anxiety, ADHD and tics in children with autism spectrum disorder. 2009
Breitling LP, et al. Variants in COMT and spontaneous smoking cessation: retrospective cohort analysis of 925 cessation events. 2009
Haraldsson HM, et al. COMT val(158)met genotype and smooth pursuit eye movements in schizophrenia. 2009
Ko DC, et al. A genome-wide in vitro bacterial-infection screen reveals human variation in the host response associated with inflammatory disease. 2009
Eisenberg DP, et al. Executive function, neural circuitry, and genetic mechanisms in schizophrenia. 2010
Roe BE, et al. Financial and psychological risk attitudes associated with two single nucleotide polymorphisms in the nicotine receptor (CHRNA4) gene. 2009
Gu Y, et al. Association between COMT gene and Chinese male schizophrenic patients with violent behavior. 2009
Miko?ajczyk E, et al. The association of catechol-O-methyltransferase genotype with the phenotype of women with eating disorders. 2010
Doi N, et al. Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint. 2009
Blasi G, et al. Functional variation of the dopamine D2 receptor gene is associated with emotional control as well as brain activity and connectivity during emotion processing in humans. 2009
Benedetti F, et al. Association between catechol-O-methyltransferase Val(108/158)Met polymorphism and psychotic features of bipolar disorder. 2010
Rommelse NN, et al. Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder. 2010
Bertolino A, et al. Genetically determined measures of striatal D2 signaling predict prefrontal activity during working memory performance. 2010
Pinheiro AP, et al. The Genetics of Anorexia Nervosa: Current Findings and Future Perspectives. 2015
Nemoda Z, et al. Association between dopaminergic polymorphisms and borderline personality traits among at-risk young adults and psychiatric inpatients. 2010
Wang Y, et al. Analysis of association between the catechol-O-methyltransferase (COMT) gene and negative symptoms in chronic schizophrenia. 2010
Kocabas NA, et al. The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study. 2010
Cross DS, et al. Population based allele frequencies of disease associated polymorphisms in the Personalized Medicine Research Project. 2010
Fijal B, et al. The association of single nucleotide polymorphisms in the catechol-O-methyltransferase gene and pain scores in female patients with major depressive disorder. 2010
Calati R, et al. Catechol-o-methyltransferase gene modulation on suicidal behavior and personality traits: review, meta-analysis and association study. 2011
Demetrovics Z, et al. Association between Novelty Seeking of opiate-dependent patients and the catechol-O-methyltransferase Val(158)Met polymorphism. 2010
Dai F, et al. Association of catechol-O-methyltransferase genetic variants with outcome in patients undergoing surgical treatment for lumbar degenerative disc disease. 2010
Moreno-Galván M, et al. Impact of CYP1A1 and COMT genotypes on breast cancer risk in Mexican women: a pilot study. 2010
Huang CG, et al. Polymorphisms of COMT and XPD and risk of esophageal squamous cell carcinoma in a population of Yili Prefecture, in Xinjiang, China. 2011
Sommerfeldt L, et al. Polymorphisms of adrenergic cardiovascular control genes are associated with adolescent chronic fatigue syndrome. 2011
Munafò MR, et al. Association of COMT Val(108/158)Met genotype and cigarette smoking in pregnant women. 2011
Miller RJ, et al. The impact of the catechol-O-methyltransferase genotype on the acute responsiveness of vascular reactivity to a green tea extract. 2011
Zhang JP, et al. Pharmacogenetics and antipsychotics: therapeutic efficacy and side effects prediction. 2011
Porcelli S, et al. Pharmacogenetics of antidepressant response. 2011
Nixon DC, et al. Interactive effects of DAOA (G72) and catechol-O-methyltransferase on neurophysiology in prefrontal cortex. 2011
Das M, et al. Role of gene-gene/gene-environment interaction in the etiology of eastern Indian ADHD probands. 2011
Yang SY, et al. EGFR L858R mutation and polymorphisms of genes related to estrogen biosynthesis and metabolism in never-smoking female lung adenocarcinoma patients. 2011
Hill LD, et al. Epistasis between COMT and MTHFR in maternal-fetal dyads increases risk for preeclampsia. 2011
David SP, et al. Pharmacogenetics of smoking cessation in general practice: results from the patch II and patch in practice trials. 2011
Roten LT, et al. A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2). 2011
Brennan PA, et al. Interactions between the COMT Val108/158Met polymorphism and maternal prenatal smoking predict aggressive behavior outcomes. 2011
Doehring A, et al. Effect sizes in experimental pain produced by gender, genetic variants and sensitization procedures. 2011
Armbruster D, et al. Variation in genes involved in dopamine clearance influence the startle response in older adults. 2011
KONG FZ, et al. [An association study of COMT gene polymorphisms with schizophrenia]. 2011
Pivac N, et al. The association between catechol-O-methyl-transferase Val108/158Met polymorphism and suicide. 2011
Christofolini DM, et al. COMT polymorphism and the risk of endometriosis-related infertility. 2011
Doll BB, et al. Dopaminergic genes predict individual differences in susceptibility to confirmation bias. 2011
Massat I, et al. COMT and age at onset in mood disorders: a replication and extension study. 2011
Bhowmik AD, et al. Role of functional dopaminergic gene polymorphisms in the etiology of idiopathic intellectual disability. 2011
Ittiwut R, et al. Association between polymorphisms in catechol-O-methyltransferase (COMT) and cocaine-induced paranoia in European-American and African-American populations. 2011
Htun NC, et al. Association of the catechol-O-methyl transferase gene Val158Met polymorphism with blood pressure and prevalence of hypertension: interaction with dietary energy intake. 2011
Desmeules J, et al. Psychological distress in fibromyalgia patients: a role for catechol-O-methyl-transferase Val158met polymorphism. 2012
Gupta M, et al. Diverse facets of COMT: from a plausible predictive marker to a potential drug target for schizophrenia. 2011
Amstadter AB, et al. Genetic associations with performance on a behavioral measure of distress intolerance. 2012
Varga G, et al. Additive effects of serotonergic and dopaminergic polymorphisms on trait impulsivity. 2012
Hiyoshi M, et al. Association between the catechol-O-methyltransferase (rs4680: Val158Met) polymorphism and serum alanine aminotransferase activity. 2012
Smith CT, et al. Age modulates the effect of COMT genotype on delay discounting behavior. 2012
Brandys MK, et al. Anorexia nervosa and the Val158Met polymorphism of the COMT gene: meta-analysis and new data. 2012
Butts SF, et al. Joint effects of smoking and gene variants involved in sex steroid metabolism on hot flashes in late reproductive-age women. 2012
Huertas E, et al. C957T polymorphism of the dopamine D2 receptor gene is associated with motor learning and heart rate. 2012
Mitaki S, et al. Impact of five SNPs in dopamine-related genes on executive function. 2013
Zhang F, et al. No association of catechol-O-methyltransferase polymorphisms with schizophrenia in the Han Chinese population. 2012
Bakker PR, et al. Candidate gene-based association study of antipsychotic-induced movement disorders in long-stay psychiatric patients: a prospective study. 2012
Olfson E, et al. Convergence of genome-wide association and candidate gene studies for alcoholism. 2012
Miller RJ, et al. The impact of the catechol-O-methyltransferase genotype on vascular function and blood pressure after acute green tea ingestion. 2012
Kim B, et al. The effects of the catechol-O-methyltransferase val158met polymorphism on white matter connectivity in patients with panic disorder. 2013
Ko MK, et al. Association of COMT gene polymorphisms with systemic atherosclerosis in elderly Japanese. 2012
Omair A, et al. Genetic contribution of catechol-O-methyltransferase variants in treatment outcome of low back pain: a prospective genetic association study. 2012
Pap D, et al. Association between the COMT gene and rumination in a Hungarian sample. 2012
Landi N, et al. The COMT Val/Met polymorphism is associated with reading-related skills and consistent patterns of functional neural activation. 2013
Mutschler J, et al. Lack of association of a functional catechol-O-methyltransferase gene polymorphism with risk of tobacco smoking: results from a multicenter case-control study. 2013
Teng Y, et al. Catechol-O-methyltransferase and cytochrome P-450 1B1 polymorphisms and endometrial cancer risk: a meta-analysis. 2013
Goetz EL, et al. Genetic moderation of the association between regulatory focus and reward responsiveness: a proof-of-concept study. 2013
Soeiro-De-Souza MG, et al. Association of the COMT Met1?? allele with trait impulsivity in healthy young adults. 2013
Deuker L, et al. Playing nice: a multi-methodological study on the effects of social conformity on memory. 2013
Nikolac Perkovic M, et al. The association between the catechol-O-methyltransferase Val108/158Met polymorphism and hyperactive-impulsive and inattentive symptoms in youth. 2013
Ojeda DA, et al. Common functional polymorphisms in SLC6A4 and COMT genes are associated with circadian phenotypes in a South American sample. 2014
Ghisari M, et al. Genetic polymorphisms in CYP1A1, CYP1B1 and COMT genes in Greenlandic Inuit and Europeans. 2013
Serretti A, et al. No effect of serotoninergic gene variants on response to interpersonal counseling and antidepressants in major depression. 2013
Kontis D, et al. COMT and MTHFR polymorphisms interaction on cognition in schizophrenia: an exploratory study. 2013
Vereczkei A, et al. Multivariate analysis of dopaminergic gene variants as risk factors of heroin dependence. 2013
Passarelli MN, et al. No association between germline variation in catechol-O-methyltransferase and colorectal cancer survival in postmenopausal women. 2014
Baldinger P, et al. Impact of COMT genotype on serotonin-1A receptor binding investigated with PET. 2014
David SP, et al. Influence of a dopamine pathway additive genetic efficacy score on smoking cessation: results from two randomized clinical trials of bupropion. 2013
Kornek M, et al. COMT-Val158Met-polymorphism is not a risk factor for acute kidney injury after cardiac surgery. 2013
Shen Y, et al. Role of single nucleotide polymorphisms in estrogen-metabolizing enzymes and susceptibility to uterine leiomyoma in Han Chinese: a case-control study. 2014
Liu J, et al. Association between maternal COMT gene polymorphisms and fetal neural tube defects risk in a Chinese population. 2014
Pe?ka-Wysiecka J, et al. BDNF rs 6265 polymorphism and COMT rs 4680 polymorphism in deficit schizophrenia in Polish sample. 6265
Bühler KM, et al. Risky alcohol consumption in young people is associated with the fatty acid amide hydrolase gene polymorphism C385A and affective rating of drug pictures. 2014
Zhang Y, et al. Metabolic syndrome in patients taking clozapine: prevalence and influence of catechol-O-methyltransferase genotype. 2014
Khadzhieva MB, et al. Association of oxidative stress-related genes with idiopathic recurrent miscarriage. 2014
Hopkins SC, et al. Catechol-O-methyltransferase genotype as modifier of superior responses to venlafaxine treatment in major depressive disorder. 2013
Ji Y, et al. Association between the COMTVal158Met Genotype and Alzheimer's Disease in the Han Chinese Population. 2014
Roffman JL, et al. Genetic variation throughout the folate metabolic pathway influences negative symptom severity in schizophrenia. 2013
Thaler L, et al. Epistatic interactions implicating dopaminergic genes in bulimia nervosa (BN): relationships to eating- and personality-related psychopathology. 2012
Soeiro-de-Souza MG, et al. COMT polymorphisms as predictors of cognitive dysfunction during manic and mixed episodes in bipolar I disorder. 2012
Henker RA, et al. The associations between OPRM 1 and COMT genotypes and postoperative pain, opioid use, and opioid-induced sedation. 2013
Tammim?ki A, et al. Catechol-O-methyltransferase gene polymorphism and chronic human pain: a systematic review and meta-analysis. 2012
Shashi V, et al. Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms. 2012
Bhakta SG, et al. The COMT Met158 allele and violence in schizophrenia: a meta-analysis. 2012
Carpentier PJ, et al. Shared and unique genetic contributions to attention deficit/hyperactivity disorder and substance use disorders: a pilot study of six candidate genes. 2013
Bia?ecka M, et al. Association of COMT, MTHFR, and SLC19A1(RFC-1) polymorphisms with homocysteine blood levels and cognitive impairment in Parkinson's disease. 2012
Lanni C, et al. Influence of COMT Val158Met polymorphism on Alzheimer's disease and mild cognitive impairment in Italian patients. 2015
Lancaster TM, et al. COMT val158met predicts reward responsiveness in humans. 2012
Poletti S, et al. Catechol-O-methyltransferase (COMT) genotype biases neural correlates of empathy and perceived personal distress in schizophrenia. 2013
Martínez-Ramírez OC, et al. Polymorphisms of catechol estrogens metabolism pathway genes and breast cancer risk in Mexican women. 2013
Pap D, et al. Genetic variants in the catechol-o-methyltransferase gene are associated with impulsivity and executive function: relevance for major depression. 2012
Creese B, et al. No association of COMT val158met polymorphism and psychotic symptoms in Lewy body dementias. 2012
Suarez-Kurtz G, et al. Pharmacogenomic Diversity among Brazilians: Influence of Ancestry, Self-Reported Color, and Geographical Origin. 2012
Gaysina D, et al. The catechol-O-methyltransferase gene (COMT) and cognitive function from childhood through adolescence. 2013
Zhang X, et al. Prefrontal white matter impairment in substance users depends upon the catechol-o-methyl transferase (COMT) val158met polymorphism. 2013
Spronk DB, et al. DBH -1021C>T and COMT Val108/158Met genotype are not associated with the P300 ERP in an auditory oddball task. 2013
Landau R, et al. The effect of OPRM1 and COMT genotypes on the analgesic response to intravenous fentanyl labor analgesia. 2013
Hatzimanolis A, et al. Potential role of membrane-bound COMT gene polymorphisms in female depression vulnerability. 2013
Klebe S, et al. The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism. 2013
Wang Y, et al. COMT rs4680 Met is not always the 'smart allele': Val allele is associated with better working memory and larger hippocampal volume in healthy Chinese. 2013
Seok JH, et al. Effect of the COMT val158met polymorphism on white matter connectivity in patients with major depressive disorder. 2013
Niitsu T, et al. Pharmacogenetics in major depression: a comprehensive meta-analysis. 2013
Cargnin S, et al. An opposite-direction modulation of the COMT Val158Met polymorphism on the clinical response to intrathecal morphine and triptans. 2013
González-Castro TB, et al. Distribution of the Val108/158Met polymorphism of the COMT gene in healthy Mexican population. 2013
Soeiro-De-Souza MG, et al. Gender effects of the COMT Val 158 Met genotype on verbal fluency in healthy adults. 2013
Woods JS, et al. Genetic polymorphisms of catechol-O-methyltransferase modify the neurobehavioral effects of mercury in children. 2014
Park S, et al. Catechol-O-methyltransferase Val158-Met polymorphism and a response of hyperactive-impulsive symptoms to methylphenidate: A replication study from South Korea. 2014
Shen Y, et al. A multicenter case-control study on screening of single nucleotide polymorphisms in estrogen-metabolizing enzymes and susceptibility to uterine leiomyoma in han chinese. 2014
Jiménez-Jiménez FJ, et al. COMT gene and risk for Parkinson's disease: a systematic review and meta-analysis. 2014
Carmel M, et al. Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects. 2014
Liu X, et al. Association study of polymorphisms in the alpha 7 nicotinic acetylcholine receptor subunit and catechol-o-methyl transferase genes with sensory gating in first-episode schizophrenia. 2013
Wan GX, et al. The Catechol-O-Methyltransferase Val158Met Polymorphism Contributes to the Risk of Breast Cancer in the Chinese Population: An Updated Meta-Analysis. 2014
Parasuraman R, et al. Interactive effects of the COMT gene and training on individual differences in supervisory control of unmanned vehicles. 2014
Zozulinsky P, et al. Dopamine system genes are associated with orienting bias among healthy individuals. 2014
Park S, et al. Interactions Between Early Trauma and Catechol-O-Methyltransferase Genes on Inhibitory Deficits in Children With ADHD. 2014
Baeken C, et al. The influence of COMT Val1??Met genotype on the character dimension cooperativeness in healthy females. 2014
Iwasaki M, et al. Green tea consumption and breast cancer risk in Japanese women: a case-control study. 2013
Smith SB, et al. Epistasis between polymorphisms in COMT, ESR1, and GCH1 influences COMT enzyme activity and pain. 2014
Noohi F, et al. Association of COMT val158met and DRD2 G>T genetic polymorphisms with individual differences in motor learning and performance in female young adults. 2014
Du JZ, et al. Lack of association between the COMT rs4680 polymorphism and ovarian cancer risk: evidence from a meta-analysis of 3,940 individuals. 2015
Shibata N, et al. Association between the catechol-O-methyltransferase polymorphism Val158Met and Alzheimer's disease in a Japanese population. 2015
Shin SY, et al. An atlas of genetic influences on human blood metabolites. 2014
Niarchou M, et al. Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children. 2014
Vercammen A, et al. Common polymorphisms in dopamine-related genes combine to produce a 'schizophrenia-like' prefrontal hypoactivity. 2014
Moreau C, et al. Polymorphism of the dopamine transporter type 1 gene modifies the treatment response in Parkinson's disease. 2015
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