Associated Papers
Impact of genetic variants on hippocampal volume among individuals with schizophrenia and bipolar disorders.
Toffanin T et al.
Psychiatry Research. Neuroimaging, 2026
Sex Differences on Social and Anxiety-Related Responses in Low-Density Lipoprotein Receptor Knockout Mice.
Pinho CM et al.
Molecular Neurobiology, 2026
The Genetic Mosaic of Depression: Linking Polymorphisms to Neuroplasticity and Stress Regulation.
Bednářová A et al.
Pharmaceuticals (basel, Switzerland), 2026
Vitamin D Receptor (VDR) Polymorphisms and Cardiometabolic Profiles in Orthopedic Patients: A Cluster-Based Analysis.
Larysz D et al.
International Journal of Molecular Sciences, 2026
The 22q11.2 deletion syndrome: Genetic mechanisms, clinical manifestations, and therapeutic strategies.
Yang S et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2026
Genetic Variation in Response to the Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND): A Randomized Controlled Trial.
Cornelis MC et al.
Nutrients, 2026
Genetics and Epigenetics of Obsessive-Compulsive Disorder.
Bernoni d'Aversa F et al.
Genes, 2026
Sustained HIV-1 remission after heterozygous CCR5Δ32 stem cell transplantation.
Gaebler C et al.
Nature, 2026
COMT and ACE (Epi)genetic Variation Is Associated with Cognitive and Metabolic Resilience in Swiss Tactical Athletes.
Flück M et al.
International Journal of Molecular Sciences, 2026
Gothelf's Haplotype of COMT in Parkinson's Disease: A Case-Control Study.
Červenák Z et al.
Biomedicines, 2026
Pharmacogenomics of Major Depressive Disorder in Indigenous Amazonian Populations.
Aguiar KEC et al.
Clinical Pharmacology and Therapeutics, 2026
Pharmacogenomics and Opioid Efficacy in Sickle Cell Disease.
Elshaikh RH et al.
Medicina (kaunas, Lithuania), 2026
Disordered eating in early childhood: DRD2 and COMT gene polymorphisms and behavioral features in family trios.
Pascale E et al.
Eating and Weight Disorders : Ewd, 2026
Genetic Risk Factors for Poor Cognitive Outcome Following Brain Insult-A Systematic Review.
Dunås T et al.
Brain and Behavior, 2026
Neurovascular Integration Failure and Freezing of Gait: Rethinking Parkinsonism Through a Vascular Lens.
Kim K et al.
The European Journal of Neuroscience, 2026
Sexually Dimorphic Association of Catechol-O-Methyltransferase (COMT) Functional Polymorphism with Dimensional Personality Pathology: A Preliminary Study.
Rucker JT et al.
Brain Sciences, 2025
A proof-of-concept study: investigating the impact of COMT genotype and proline on negative symptoms in Alzheimer's disease.
Clelland JD et al.
Bjpsych Open, 2025
The Mental Roots of Performance: A Preliminary Meta-Analysis of Cognitive Genes and Athlete Status.
İpekoğlu G et al.
Molecular Neurobiology, 2025
Relationship between circadian and social rhythms regulation, chronotype, COMT, CLOCK, GSK3-ß gene polymorphisms and response to valproate treatment in remitted bipolar subjects.
Ulusoy Altinoklu M et al.
Chronobiology International, 2025
The impact of single nucleotide polymorphisms on the absorption, distribution, metabolism, and excretion of dietary (poly)phenols: a critical systematic review.
Tosi N et al.
Food & Function, 2025
Genetic and Epigenetic Components in the Pathogenesis of Adenomyosis and Endometriosis in Adolescents.
Palumbo M et al.
Biomedicines, 2025
Role of Genetic and Epigenetic Biomarkers in Treatment-Resistant Depression: A Literature Review.
Sulić P et al.
Genes, 2025
Does COMT Play a Role in Parkinson's Disease Susceptibility across Diverse Ancestral Populations?
Martín-Bórnez M et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2025
Genetic and epigenetic determinants of fetal alcohol spectrum disorders: Toward a precision medicine approach.
Sessa F et al.
Experimental and Molecular Pathology, 2025
Further Investigation of Catechol-O-Methyltransferase Gene and Parkinson's Disease Susceptibility in the UK Biobank Cohort.
Hu Z et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2025
Dopaminergic Genetic Variation and Trait Impulsivity: The Role of COMT rs4680 in Mixed Behavioral and Substance Addictions.
Zdunek G et al.
Life (basel, Switzerland), 2025
COMT rs4680 and DAOA rs947267 Polymorphism Interact to Influence Cognition and Psychiatric Symptoms in Chronic Schizophrenia.
Chen P et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2025
Genetic Predisposition and Genetic Resilience Factors in Stress-Related Disorders During the Developmental Age: A Narrative Review.
Raffagnato A et al.
Genes, 2025
Novel Genetic Susceptibility Markers for Breast Cancer in Iraqi Women: First Evidence of CYP3A4*1B Protective Effects and GSTP1/MTHFR Risk Associations.
Hoidy WH et al.
Clinical Breast Cancer, 2025
The interaction of negative parenting and DRD2 gene rs1799732 polymorphism on self-control in children and adolescents: Development stage differences.
Mao J et al.
The British Journal of Developmental Psychology, 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
Clinical Utility of Urine Hormone Metabolite Testing in Personalized Medicine: A Case Report of a Male Patient with Low Testosterone.
Newman MS et al.
Integrative Medicine (encinitas, Calif.), 2025
Genetic Basis of the Negative Response to the Use of Triptans for the Treatment of Migraine-A Systematic Review and Meta-Analysis.
Andreata VG et al.
Brain and Behavior, 2025
Clinical and genetic profiling of fibromyalgia-associated dry eye: A multifactorial approach.
Vergés C et al.
The Ocular Surface, 2025
Genetic and Epigenetic Approaches to Opioid Use Disorder.
Ranadeva ND et al.
Expert Reviews in Molecular Medicine, 2025