Associated Papers
Functional genetics reveals the contribution of delta opioid receptor to type 2 diabetes and beta-cell function.
Meulebrouck S et al.
Nature Communications, 2024
Novel NARS2 variants in a patient with early-onset status epilepticus: case study and literature review.
Yang N et al.
Bmc Pediatrics, 2024
Protocol optimization of a targeted sequencing panel for genomic profiling of bronchoalveolar lavage fluid in lung cancer.
Sather CL et al.
Cancer Medicine, 2023
OPRD1 rs569356 polymorphism has an effect on plasma norbuprenorphine levels and dose/kg-normalized norbuprenorphine values in individuals with opioid use disorder.
Kaya-Akyüzlü D et al.
Environmental Toxicology and Pharmacology, 2023
Harnessing the paradoxical phenotypes of APOE ɛ2 and APOE ɛ4 to identify genetic modifiers in Alzheimer's disease.
Kim YW et al.
Alzheimer's & Dementia : the Journal of the Alzheimer's Association, 2021
Whole genome mapping and identification of single nucleotide polymorphisms of four Bangladeshi individuals and their functional significance.
Khan S et al.
Bmc Research Notes, 2021
Genetic susceptibility of opioid receptor genes polymorphism to drug addiction: A candidate-gene association study.
Al-Eitan LN et al.
Bmc Psychiatry, 2021
Molecular Imaging of Opioid and Dopamine Systems: Insights Into the Pharmacogenetics of Opioid Use Disorders.
Burns JA et al.
Frontiers in Psychiatry, 2019
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family.
Khan MJ et al.
Scientific Reports, 2018
An analysis of genetic association in opioid dependence susceptibility.
Nagaya D et al.
Journal of Clinical Pharmacy and Therapeutics, 2018
Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.
Maguire SL et al.
The Journal of Pathology, 2016
Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing.
Samorodnitsky E et al.
Human Mutation, 2015
Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan.
Ilyas M et al.
Bmc Genomics, 2015
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
An intronic variant in OPRD1 predicts treatment outcome for opioid dependence in African-Americans.
Crist RC et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology, 2013
Analyzing Interaction of μ-, δ- and κ-opioid Receptor Gene Variants on Alcohol or Drug Dependence Using a Pattern Discovery-based Method.
Li Z et al.
Journal of Addiction Research & Therapy, 2013
Case-control association analysis of polymorphisms in the δ-opioid receptor, OPRD1, with cocaine and opioid addicted populations.
Crist RC et al.
Drug and Alcohol Dependence, 2013
The genetics of the opioid system and specific drug addictions.
Levran O et al.
Human Genetics, 2012
Functional impact of a single-nucleotide polymorphism in the OPRD1 promoter region.
Zhang H et al.
Journal of Human Genetics, 2010
Mutation detection in candidate genes for benign familial infantile seizures on a novel locus.
Li N et al.
The International Journal of Neuroscience, 2010
Genetics of drug dependence.
Gelernter J et al.
Dialogues in Clinical Neuroscience, 2010
The OPRD1 and OPRK1 loci in alcohol or drug dependence: OPRD1 variation modulates substance dependence risk.
Zhang H et al.
Molecular Psychiatry, 2008
The opioid system in alcohol and drug dependence: family-based association study.
Xuei X et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2007
Analysis of SNP profiles in patients with major depressive disorder.
Kõks S et al.
The International Journal of Neuropsychopharmacology, 2006
Relationship of the delta-opioid receptor gene to heroin abuse in a large Chinese case/control sample.
Xu K et al.
American Journal of Medical Genetics, 2002