Associated Papers
Germline Variants in the Immune Response-Related Genes: Possible Modifying Effect on Age-Dependent BRCA1 Penetrance in Breast Cancer Patient.
Kuligina ES et al.
Cancers, 2025
The contribution of baseline circulating endocannabinoids to individual differences in human pain sensitivity: a quantitative sensory testing study.
Fatemi SA et al.
Pain, 2025
The Contribution of Baseline Circulating Endocannabinoids to Individual Differences in Human Pain Sensitivity: A Quantitative Sensory Testing Study.
Fatemi SA et al.
Biorxiv : the Preprint Server for Biology, 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
Genes, Cognition, and Their Interplay in Methamphetamine Use Disorder.
Khan R et al.
Biomolecules, 2025
Drug response is related to NR3C1 and FAAH polymorphism in Chinese pediatric epilepsy patients.
Wang H et al.
Italian Journal of Pediatrics, 2025
Clinical, ethnic and genetic risk factors associated with postoperative nausea and vomiting in patients undergoing cancer surgery: a case-control study.
Grigio TR et al.
American Journal of Translational Research, 2025
Interplays of Dietary Fat with BMI and FAAH rs324420 on HDL-C in Gender-Dependent Manner in Adolescents.
Shen YL et al.
Food Science & Nutrition, 2024
Genetic variation in endocannabinoid signaling: Anxiety, depression, and threat- and reward-related brain functioning during the transition into adolescence.
Desai S et al.
Behavioural Brain Research, 2024
Genetic Variations in Susceptibility to Traumatic Muscle Injuries and Muscle Pain among Brazilian High-Performance Athletes.
Marques IS et al.
International Journal of Molecular Sciences, 2024
Association between the FAAH C385A variant (rs324420) and obesity-related traits: a systematic review.
Lopez-Cortes OD et al.
International Journal of Obesity (2005), 2024
Single Nucleotide Variants (SNVs) of the Mesocorticolimbic System Associated with Cardiovascular Diseases and Type 2 Diabetes: A Systematic Review.
Merzah M et al.
Genes, 2024
Evolutionary history of adenomas to colorectal cancer in FAP families.
Yang C et al.
Frontiers in Genetics, 2024
Associations between methamphetamine use disorder and SLC18A1, SLC18A2, BDNF, and FAAH gene sequence variants and expression levels.
Guerin AA et al.
Dialogues in Clinical Neuroscience, 2024
Effect of donor GSTM3 rs7483 genetic variant on tacrolimus elimination in the early period after liver transplantation.
Zhang T et al.
Peerj, 2024
Plasma Endocannabinoid Levels in Patients with Borderline Personality Disorder and Healthy Controls.
Spohrs J et al.
International Journal of Molecular Sciences, 2023
FAAH rs324420 Polymorphism: Biological Pathways, Impact on Elite Athletic Performance and Insights for Sport Medicine.
Silva HH et al.
Genes, 2023
FAAH Pro129Thr Variant Is Associated with Increased Cholesterol Levels in Normal-Weight Metabolically Unhealthy Subjects.
Sierra-Ruelas E et al.
Metabolic Syndrome and Related Disorders, 2023
Somatic mutations reveal hyperactive Notch signaling and racial disparities in prurigo nodularis.
Rajeh A et al.
Medrxiv : the Preprint Server for Health Sciences, 2023
Functional Variation in the FAAH Gene Is Directly Associated with Subjective Well-Being and Indirectly Associated with Problematic Alcohol Use.
Bornscheuer L et al.
Genes, 2023
Developmental age and fatty acid amide hydrolase genetic variation converge to mediate fear regulation in female mice.
Gerhard DM et al.
Developmental Psychobiology, 2023
CYP4F2 is a human-specific determinant of circulating N-acyl amino acid levels.
Tanzo JT et al.
The Journal of Biological Chemistry, 2023
Association of FAAH rs324420 (C385A) Polymorphism with High-Level Performance in Volleyball Players.
Silva HH et al.
Genes, 2023
The study of rs324420 (C385A) polymorphism of the FAAH gene of the endocannabinoid system in patients with epilepsy and ADHD.
Anvar LH et al.
Epilepsy Research, 2023
Bi-allelic mutation in SEC16B alters collagen trafficking and increases ER stress.
El-Gazzar A et al.
Embo Molecular Medicine, 2023
Genetic variation in fatty acid amide hydrolase (FAAH): Associations with early drinking and smoking behaviors.
Alsaafin A et al.
Addictive Behaviors, 2023
Cannabinoid receptor type 2 gene is associated with comorbidity of schizophrenia and cannabis dependence and fatty acid amide hydrolase gene is associated with cannabis dependence in the Spanish population.
Arias Horcajadas F et al.
Adicciones, 2023
Fatty acid amide hydrolase C385A polymorphism affects susceptibility to various diseases.
Hosseinzadeh Anvar L et al.
Biofactors (oxford, England), 2023
FAAH polymorphism (rs324420) modulates extinction recall in healthy humans: an fMRI study.
Spohrs J et al.
European Archives of Psychiatry and Clinical Neuroscience, 2022
A common genetic variant in fatty acid amide hydrolase is linked to alterations in fear extinction neural circuitry in a racially diverse, nonclinical sample of adults.
Zabik NL et al.
Journal of Neuroscience Research, 2022
Genetic variation in endocannabinoid signaling is associated with differential network-level functional connectivity in youth.
Sisk LM et al.
Journal of Neuroscience Research, 2022
Identification of sex-specific genetic associations in response to opioid analgesics in a White, non-Hispanic cohort from Southeast Minnesota.
Lopes GS et al.
The Pharmacogenomics Journal, 2022
Comprehensive analysis of important pharmacogenes in Koreans using the DMET™ platform.
Kim B et al.
Translational and Clinical Pharmacology, 2021
Computational analysis of deleterious single nucleotide polymorphisms in catechol O-Methyltransferase conferring risk to post-traumatic stress disorder.
Chitrala KN et al.
Journal of Psychiatric Research, 2021
Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome.
McGurk KA et al.
Human Molecular Genetics, 2021
Targeted transcriptome analysis using synthetic long read sequencing uncovers isoform reprograming in the progression of colon cancer.
Liu S et al.
Communications Biology, 2021
Association of the Fatty Acid Amide Hydrolase C385A Polymorphism With Alcohol Use Severity and Coping Motives in Heavy-Drinking Youth.
Best LM et al.
Alcoholism, Clinical and Experimental Research, 2021
Genetic analyses of the endocannabinoid pathway in association with affective phenotypic variants.
Lazary J et al.
Neuroscience Letters, 2021
Genetics of methamphetamine use disorder: A systematic review and meta-analyses of gene association studies.
Guerin AA et al.
Neuroscience and Biobehavioral Reviews, 2021
Endocannabinoid Gene × Gene Interaction Association to Alcohol Use Disorder in Two Adolescent Cohorts.
Elkrief L et al.
Frontiers in Psychiatry, 2021
FAAH and CNR1 Polymorphisms in the Endocannabinoid System and Alcohol-Related Sleep Quality.
Soundararajan S et al.
Frontiers in Psychiatry, 2021
Genetic Variants of Fatty Acid Amide Hydrolase Modulate Acute Inflammatory Responses to Colitis in Adult Male Mice.
Vecchiarelli HA et al.
Frontiers in Cellular Neuroscience, 2021
Racial and sex differences in the polymorphisms of the endocannabinoid receptor genes in obesity.
Thethi TK et al.
Journal of Diabetes and Its Complications, 2020
Clinical, genomics and networking analyses of a high-altitude native American Ecuadorian patient with congenital insensitivity to pain with anhidrosis: a case report.
López-Cortés A et al.
Bmc Medical Genomics, 2020
Effects of TPH2 gene variation and childhood trauma on the clinical and circuit-level phenotype of functional movement disorders.
Spagnolo PA et al.
Journal of Neurology, Neurosurgery, and Psychiatry, 2020
Genetic contributions to the etiology of anorexia nervosa: New perspectives in molecular diagnosis and treatment.
Paolacci S et al.
Molecular Genetics & Genomic Medicine, 2020
Ethnic differences in genetic polymorphism associated with irritable bowel syndrome.
Xiao QY et al.
World Journal of Gastroenterology, 2020
FAAH levels and its genetic polymorphism association with susceptibility to methamphetamine dependence.
Zhang W et al.
Annals of Human Genetics, 2020