Associated Papers
Comprehensive analysis of the mitochondrial DNA variants using multivariate covariate and multiple-testing models to enhance reliability reveals potential associations with coronary artery disease traits and dietary preferences.
Sawant A et al.
Mitochondrion, 2025
Unveiling genetic architecture of white matter microstructure through unsupervised deep representation learning of fractional anisotropy maps.
Zhao X et al.
Research Square, 2025
The Impact of Brain-Derived Neurotrophic Factor rs6265 (Val66Met) Polymorphism on Therapeutic Electrical Stimulation for Peripheral Nerve Regeneration: A Preclinical Study of Therapy-Genotype Interactions.
Walters JB et al.
Muscle & Nerve, 2025
Association of NTRK2 gene with suicidality: a meta-analysis.
Ye W et al.
Psychiatric Genetics, 2024
The Val66Met variant of brain-derived neurotrophic factor is linked to reduced telomere length in a military population: a pilot study.
Allsopp RC et al.
Scientific Reports, 2024
Brain-Derived Neurotrophic Factor (BDNF) as a Predictor of Treatment Response in Schizophrenia and Bipolar Disorder: A Systematic Review.
Liberona A et al.
International Journal of Molecular Sciences, 2024
Brain-Derived Neurotrophic Factor Val66Met is Associated with Variation in Cortical Structure in Healthy Aging Subjects.
Shen T et al.
Aging and Disease, 2024
The effect of single nucleotide polymorphisms on depression in combination with coronary diseases: a systematic review and meta-analysis.
Zhang J et al.
Frontiers in Endocrinology, 2024
Genetic Landscape of Major Depressive Disorder: Assessment of Potential Diagnostic and Antidepressant Response Markers.
Singh P et al.
The International Journal of Neuropsychopharmacology, 2023
A Rat Model of the Brain-Derived Neurotrophic Factor Val66Met Polymorphism Shows Attenuated Motivation for Alcohol Self-Administration and Diminished Propensity for Cue-Induced Relapse in Females.
Jaehne EJ et al.
Biology, 2023
Brain-derived neurotrophic factor rs6265 (Val66Met) single nucleotide polymorphism as a master modifier of human pathophysiology.
Nguyen VT et al.
Neural Regeneration Research, 2023
Variant brain-derived neurotrophic factor val66met polymorphism engages memory-associated systems to augment olfaction.
Chao YT et al.
Scientific Reports, 2022
Interplay between genetics and lifestyle on pain susceptibility in women with fibromyalgia: the al-Ándalus project.
Estévez-López F et al.
Rheumatology (oxford, England), 2022
Genetic heterogeneity on sleep disorders in Parkinson's disease: a systematic review and meta-analysis.
Huang J et al.
Translational Neurodegeneration, 2022
Brain-derived neurotrophic factor Val66Met polymorphism modulates the effects of circadian desynchronization on activity and sleep in male mice.
Phillips DJ et al.
Frontiers in Neuroscience, 2022
The FSHR G-29A variant is not associated with the ovarian response to exogenous FSH stimulation.
Song D et al.
American Journal of Reproductive Immunology (new York, N.y. : 1989), 2021
Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study.
Fjukstad KK et al.
The Pharmacogenomics Journal, 2021
Does human serotonin-1A receptor polymorphism (rs6295) code for pain and associated symptoms in fibromyalgia syndrome?
Tanwar S et al.
Reumatismo, 2021
Genetic Influences on Patient-Oriented Outcomes in Traumatic Brain Injury: A Living Systematic Review of Non-Apolipoprotein E Single-Nucleotide Polymorphisms.
Zeiler FA et al.
Journal of Neurotrauma, 2021
Brain-Derived Neurotrophic Factor Val66Met Polymorphism and Internalizing Behaviors after Early Mild Traumatic Brain Injury.
Gagner C et al.
Journal of Neurotrauma, 2021
BDNF Genetic Variant and Its Genotypic Fluctuation in Major Depressive Disorder.
Ferreira Fratelli C et al.
Behavioural Neurology, 2021
Influence of BDNF Genetic Polymorphisms in the Pathophysiology of Aging-related Diseases.
Urbina-Varela R et al.
Aging and Disease, 2020
Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study.
Erlangsen A et al.
Molecular Psychiatry, 2020
Low brain-derived neurotrophic factor protein levels and single-nucleotide polymorphism Val66Met are associated with peripheral neuropathy in type II diabetic patients.
Azoulay D et al.
Acta Diabetologica, 2020
Genetic variants in migraine: a field synopsis and systematic re-analysis of meta-analyses.
Zhao Y et al.
The Journal of Headache and Pain, 2020
Catechol-O-methyltransferase gene Val158Met polymorphism and obsessive compulsive disorder susceptibility: a meta-analysis.
Kumar P et al.
Metabolic Brain Disease, 2020
The brain-derived neurotrophic factor Val66Met genotype does not influence the grey or white matter structures underlying recognition memory.
McKay NS et al.
Neuroimage, 2019
The prevalence of ADH1B and OPRM1 alleles predisposing for alcohol consumption are increased in the Hungarian psoriasis population.
Szentkereszty-Kovács Z et al.
Archives of Dermatological Research, 2019
Symptom Science: Advocating for Inclusion of Functional Genetic Polymorphisms.
Knisely MR et al.
Biological Research for Nursing, 2019
Depression in multiple sclerosis: effect of brain derived neurotrophic factor Val66Met polymorphism and disease perception.
Unknown Author
European Journal of Neurology, 2019
Genome-wide association meta-analysis of functional outcome after ischemic stroke.
Söderholm M et al.
Neurology, 2019
Is BDNF-Val66Met polymorphism associated with psychotic experiences and psychotic disorder outcome? Evidence from a 6 years prospective population-based cohort study.
Kirli U et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2019
Brain-Derived Neurotrophic Factor Val66Met Polymorphism Is Associated With a Reduced ERP Component Indexing Emotional Recollection.
Jones R et al.
Frontiers in Psychology, 2019
BDNF gene and obsessive compulsive disorder risk, symptom dimensions and treatment response.
Taj M J RJ et al.
Asian Journal of Psychiatry, 2018
Recent developments in the genetics of attention-deficit hyperactivity disorder.
Grimm O et al.
Psychiatry and Clinical Neurosciences, 2018
GABRA2 rs279858-linked variants are associated with disrupted structural connectome of reward circuits in heroin abusers.
Sun Y et al.
Translational Psychiatry, 2018
Sex Differences in Risk for Alzheimer's Disease Related to Neurotrophin Gene Polymorphisms: The Cache County Memory Study.
Matyi J et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences, 2017
Genetic predisposition toward suicidal ideation in patients with acute coronary syndrome.
Kang HJ et al.
Oncotarget, 2017
Association of C677T polymorphism (rs1801133) in MTHFR gene with depression.
Rai V
Cellular and Molecular Biology (noisy-le-grand, France), 2017
Associations of NEUROD2 polymorphisms and change of cognitive dysfunctions in schizophrenia and schizoaffective disorder after eight weeks of antipsychotic treatment.
Spellmann I et al.
Cognitive Neuropsychiatry, 2017
Brain-derived neurotrophic factor Val66Met polymorphism in depression and thrombosis: SIRT1 as a possible mediator.
Stein S et al.
European Heart Journal, 2017
Brain-Derived Neurotrophic Factor Val66Met Gene Polymorphism Impacts on Migraine Susceptibility: A Meta-analysis of Case-Control Studies.
Terrazzino S et al.
Frontiers in Neurology, 2017
The Analysis of Two BDNF Polymorphisms G196A/C270T in Chinese Sporadic Amyotrophic Lateral Sclerosis.
Xu L et al.
Frontiers in Aging Neuroscience, 2017
Preliminary evidence for association of genetic variants in pri-miR-34b/c and abnormal miR-34c expression with attention deficit and hyperactivity disorder.
Garcia-Martínez I et al.
Translational Psychiatry, 2016
Effects of polymorphisms of serotonin transporter promoter (5-HTTLPR) and brain derived neurotrophic factor gene (G196A rs6265) on the risk of major depressive disorder in the Chinese Han population.
Sun N et al.
European Review for Medical and Pharmacological Sciences, 2016
The influence of 5-HTTLPR and Val66Met polymorphisms on cortical thickness and volume in limbic and paralimbic regions in depression: a preliminary study.
Jaworska N et al.
Bmc Psychiatry, 2016
Genetic variation and dopamine D2 receptor availability: a systematic review and meta-analysis of human in vivo molecular imaging studies.
Gluskin BS et al.
Translational Psychiatry, 2016
Candidate-gene analysis of white matter hyperintensities on neuroimaging.
Tran T et al.
Journal of Neurology, Neurosurgery, and Psychiatry, 2016
Association between BDNF gene polymorphisms and attention deficit hyperactivity disorder in Korean children.
Kwon HJ et al.
Genetic Testing and Molecular Biomarkers, 2015