Varaico: Literature-Extracted Genetic Variants

Gene:BDNF
Variant:p.V66M
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BDNF

NM_001709.5:p.V66M

Associated Papers

Next-generation sequencing study identifies the first genes associated with Alzheimer's disease in Bangladeshi population: The CARED study.

Hakim M et al.

Journal of Alzheimer's Disease : Jad, 2026

The Genetic Mosaic of Depression: Linking Polymorphisms to Neuroplasticity and Stress Regulation.

Bednářová A et al.

Pharmaceuticals (basel, Switzerland), 2026

BDNF Val66Met protects oxaliplatin-induced peripheral neuropathy in patients with colorectal cancer.

Chen LH et al.

Science Translational Medicine, 2026

Exploring the Association Between DTC Obesity-Related Gene Polymorphisms and Obesity Risk Factors in Koreans: Focus on BDNF.

Kim J et al.

Nutrients, 2026

Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) gene and its association with select anxiety-related disorders: an updated systematic review and meta-analysis.

Tiongco RE et al.

Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals, 2026

BDNF Val66Met Variant as a Genetic Risk Factor for Major Depressive Disorder in Saudis.

Binmahfouz LS et al.

Genetic Testing and Molecular Biomarkers, 2026

Genetics and Epigenetics of Obsessive-Compulsive Disorder.

Bernoni d'Aversa F et al.

Genes, 2026

Correlation investigation between BDNF (Val66Met/rs6265) polymorphism and attention deficit hyperactivity disorder susceptibility in Chinese mainland population: a meta-analysis.

Lu Y

Psychology, Health & Medicine, 2026

Impact of Brain-Derived Neurotrophic Factor (BDNF) Variants on Cardiometabolic Profiles: A Systematic Review and Meta-Analysis of Coronary Artery Disease and Obesity.

Luo Z et al.

Obesity Reviews : an Official Journal of the International Association for the Study of Obesity, 2026

PTSD and appetite dysregulation: mTOR-dependent modulation of fear memory and satiety circuits.

Krattli SN et al.

Neuroscience and Biobehavioral Reviews, 2026

Plasma BDNF levels, BDNF Val66Met polymorphism, and their association with phenoconversion in isolated REM sleep behavior disorder.

Zang Y et al.

European Neurology, 2026

The association of Alzheimer's disease-related SNPs with mild cognitive impairment susceptibility in the Chinese population.

Xie Z et al.

Scientific Reports, 2026

Loss aversion and genetic variants influence food choice: Implications for healthier dietary decisions.

Graham CA et al.

Nutrition and Health, 2026

Longitudinal implications of BDNF rs6265 polymorphism on motor and non-motor features of Parkinson's disease in Korean population.

Yoo SW et al.

Journal of Movement Disorders, 2026

Sex Differences in Genetic Modifiers of Traumatic Brain Injury and Late-Life Cognitive Decline: The Cache County Study.

Drewel MA et al.

The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences, 2026

The Impact of Brain-Derived Neurotrophic Factor Polymorphism and Stimulation Parameters on the Response to Repetitive Transcranial Magnetic Stimulation: A Systematic Review.

Kuo YL et al.

American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2026

Differential Impact of BMI-Associated Genetic Variants on Breast Cancer Risk: Insights From Mediation Analysis.

Ando Y et al.

Cancer Science, 2026

Genetic Risk Factors for Poor Cognitive Outcome Following Brain Insult-A Systematic Review.

Dunås T et al.

Brain and Behavior, 2026

Genetic analysis of LRRK2 variants in Han Chinese patients with Parkinson's disease.

Deng X et al.

Plos One, 2026

41505438 (PubMed )
Supplement: pone.0340448.s004.pdf

15 years of longitudinal genetic, clinical, cognitive, imaging, and biochemical measures in DIAN.

Daniels AJ et al.

Npj Dementia, 2026

41709913 (PubMed )
Supplement: 44400_2025_47_MOESM1_ESM.pdf

The Mental Roots of Performance: A Preliminary Meta-Analysis of Cognitive Genes and Athlete Status.

İpekoğlu G et al.

Molecular Neurobiology, 2025

Role of Genetic and Epigenetic Biomarkers in Treatment-Resistant Depression: A Literature Review.

Sulić P et al.

Genes, 2025

Val66Met polymorphism in the BDNF gene and antidepressant response in depression: an updated meta-analysis.

Tiongco RE et al.

Personalized Medicine, 2025

Genetic and epigenetic determinants of fetal alcohol spectrum disorders: Toward a precision medicine approach.

Sessa F et al.

Experimental and Molecular Pathology, 2025

Association of BDNF Val66Met genotype with obesity indicators and metabolic parameters.

İnan CM et al.

International Journal of Food Sciences and Nutrition, 2025

Brain-Derived Neurotrophic Factor Trafficking via the Regulated Secretory Pathway: Mechanisms and Disease Implications.

Ewell SN

Molecular Neurobiology, 2025

Genetic Predisposition and Genetic Resilience Factors in Stress-Related Disorders During the Developmental Age: A Narrative Review.

Raffagnato A et al.

Genes, 2025

BDNF gene polymorphisms and substance use disorders: a systematic review.

Peregud D et al.

Reviews in the Neurosciences, 2025

Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population.

Enzan N et al.

Nature Communications, 2025

41184235 (PubMed )
Supplement: 41467_2025_64659_MOESM3_ESM.xlsx › SD38

Genetic Association Study of Brain-Derived Neurotrophic Factor (BDNF) and Serotonin-Related Gene Variants in Suicide Attempters with Major Depressive Disorder and Control Persons.

Kim T et al.

Genes, 2025

Biomarker Discovery in Wilson's Disease-A Path Toward Improved Diagnosis and Management: A Comprehensive Review.

Wolska M et al.

Molecular Neurobiology, 2025

A Model of Traumatic Brain Injury Oligomerizes Tau in Cortical Organoids and Induces Clinically Relevant Pathologies that Synergize with MAPT Mutation.

Shiravi S et al.

Journal of Neurotrauma, 2025

Genetic perspectives on transient global amnesia: A narrative review.

Komiotis C et al.

Clinical Neurology and Neurosurgery, 2025

LRRK2 and the fragile synapse: a molecular prelude to Parkinson's disease?

Masotti B et al.

The Biochemical Journal, 2025

An In silico Multi-Omics Investigation of Alzheimer's Disease Linking Gene Dysregulation, Mutations, and Protein Networks to Core Pathologies.

Abd-Alkareem MA et al.

Current Alzheimer Research, 2025

BDNF genotype associated with changes in cortical thickness, severity of symptoms, and cognitive impairments in mild traumatic brain injury.

Shi L et al.

Molecular Brain, 2025

Characterization of prevalent genetic variants in the Estonian Biobank body-mass index GWAS.

Abner E et al.

Nature Communications, 2025

41062462 (PubMed )
Supplement: 41467_2025_64006_MOESM6_ESM.xlsx › Figure1a

Potential Genetic Intersections Between ADHD and Alzheimer's Disease: A Systematic Review.

Borgonovo R et al.

Neurosci, 2025

Genetics of Response to ECT, TMS, Ketamine and Esketamine.

Franklin CE et al.

American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2025

Interactive effect of BDNF rs10835210 polymorphism and childhood maltreatment on cognitive functioning in Chinese male patients with methamphetamine use disorder.

Jiang L et al.

European Archives of Psychiatry and Clinical Neuroscience, 2025

The Role of Genetics in Stroke Risk and Outcome: A Review of Current Evidence.

Oyovwi MO et al.

Brain and Behavior, 2025

Comments on "An Observational Case-control Study for BDNF Val66Met Polymorphism and Serum BDNF in Patients with Major Depressive Disorder (MDD)".

Ajay S et al.

Indian Journal of Psychological Medicine, 2025

Unveiling genetic architecture of white matter microstructure through unsupervised deep representation learning of fractional anisotropy maps.

Zhao X et al.

Research Square, 2025

Pharmacogenetics and the Response to Antidepressants in Major Depressive Disorder.

Bertollo AG et al.

Pharmaceuticals (basel, Switzerland), 2025

Association of catechol-O-methyltransferase genetic polymorphism with neuromodulation treatment response in women with fecal or urinary incontinence.

Florian-Rodriguez ME et al.

American Journal of Obstetrics and Gynecology, 2025

Personalized Response to Empagliflozin in Heart Failure: Association of BDNF and ATP2A2 Variants in a South Asian Cohort.

Ain QT et al.

Biomedicines, 2025

The Influence of Genetic Polymorphisms and Psychosocial Determinants on Suicidal Behaviors: A Case-Control Study of CRHR1, NTRK2, and FKBP5.

Cîmpianu ME et al.

International Journal of Molecular Sciences, 2025

A Comparative Analysis of Genetic and Epigenetic Factors in METH Addiction: A Focus on SLC (SLC6A4) and COMT Genes.

Hussain HK et al.

Frontiers in Bioscience (landmark Edition), 2025

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."