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Estimating ancestral proportions in a multi-ethnic US sample: implications for studies of admixed populations.
- Published in:
- Human Genomics, 2012, v. 6, n. 1, p. 1, doi. 10.1186/1479-7364-6-2
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- Publication type:
- Article
CYP2B6 SNPs are associated with methadone dose required for effective treatment of opioid addiction.
- Published in:
- Addiction Biology, 2013, v. 18, n. 4, p. 709, doi. 10.1111/j.1369-1600.2011.00349.x
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- Publication type:
- Article
Opiate addiction and cocaine addiction: underlying molecular neurobiology and genetics.
- Published in:
- Journal of Clinical Investigation, 2012, v. 122, n. 10, p. 3387, doi. 10.1172/JCI60390
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- Publication type:
- Article
OPRD1 SNPs associated with opioid addiction are cis-eQTLs for the phosphatase and actin regulator 4 gene, PHACTR4, a mediator of cytoskeletal dynamics.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01439-y
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- Publication type:
- Article
Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-21003-y
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- Publication type:
- Article
Haplotype block structure of the genomic region of the mu opioid receptor gene.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 2, p. 147, doi. 10.1038/jhg.2010.150
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- Publication type:
- Article
Synaptic Plasticity and Signal Transduction Gene Polymorphisms and Vulnerability to Drug Addictions in Populations of European or African Ancestry.
- Published in:
- CNS Neuroscience & Therapeutics, 2015, v. 21, n. 11, p. 898, doi. 10.1111/cns.12450
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- Publication type:
- Article
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia.
- Published in:
- 2005
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- Publication type:
- Letter
Search for genetic markers and functional variants involved in the development of opiate and cocaine addiction and treatment.
- Published in:
- Annals of the New York Academy of Sciences, 2010, v. 1187, n. 1, p. 184, doi. 10.1111/j.1749-6632.2009.05275.x
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- Publication type:
- Article
Association of Polymorphisms of the Mu Opioid Receptor Gene with the Severity of HIV Infection and Response to HIV Treatment.
- Published in:
- Journal of Infectious Diseases, 2012, v. 205, n. 11, p. 1745, doi. 10.1093/infdis/jis264
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- Publication type:
- Article
The genetics of the opioid system and specific drug addictions.
- Published in:
- Human Genetics, 2012, v. 131, n. 6, p. 823, doi. 10.1007/s00439-012-1172-4
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- Publication type:
- Article
Human papillomavirus DNA and p53 polymorphisms in squamous cell carcinomas from Fanconi anemia patients.
- Published in:
- 2003
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- Publication type:
- journal article
Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia.
- Published in:
- 2003
- By:
- Publication type:
- journal article
A Functional Haplotype Implicated in Vulnerability to Develop Cocaine Dependence is Associated with Reduced PDYN Expression in Human Brain.
- Published in:
- Neuropsychopharmacology, 2009, v. 34, n. 5, p. 1185, doi. 10.1038/npp.2008.187
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- Publication type:
- Article
Extreme sampling design in genetic association mapping of quantitative trait loci using balanced and unbalanced case-control samples.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-51790-w
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- Publication type:
- Article
Drug Addiction and Stress-Response Genetic Variability: Association Study in African Americans.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 4, p. 290, doi. 10.1111/ahg.12064
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- Publication type:
- Article
A 3' UTR SNP rs885863, a cis-eQTL for the circadian gene VIPR2 and lincRNA 689, is associated with opioid addiction.
- Published in:
- PLoS ONE, 2019, v. 14, n. 11, p. 1, doi. 10.1371/journal.pone.0224399
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- Publication type:
- Article
Overlapping Dopaminergic Pathway Genetic Susceptibility to Heroin and Cocaine Addictions in African Americans.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 3, p. 188, doi. 10.1111/ahg.12104
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- Publication type:
- Article
A Rapid Method for Retrovirus-Mediated Identification of Complementation Groups in Fanconi Anemia Patients
- Published in:
- Molecular Therapy, 2005, v. 12, n. 5, p. 976, doi. 10.1016/j.ymthe.2005.04.021
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- Publication type:
- Article
GST genotype may modify clinical phenotype in patients with Fanconi anaemia.
- Published in:
- British Journal of Haematology, 2005, v. 131, n. 1, p. 118, doi. 10.1111/j.1365-2141.2005.05721.x
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- Publication type:
- Article
Spectrum of sequence variations in the FANCA gene: An International Fanconi Anemia Registry (IFAR) study.
- Published in:
- Human Mutation, 2005, v. 25, n. 2, p. 142, doi. 10.1002/humu.20125
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- Publication type:
- Article
Polymorphisms in Stress-Related Genes Are Associated with Reduced Cocaine Abuse and Longer Retention in Methadone Maintenance Treatment for Opioid Use Disorder.
- Published in:
- 2021
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- Publication type:
- journal article
Alterations of expression of inflammation/immune-related genes in the dorsal and ventral striatum of adult C57BL/6J mice following chronic oxycodone self-administration: a RNA sequencing study.
- Published in:
- Psychopharmacology, 2017, v. 234, n. 15, p. 2259, doi. 10.1007/s00213-017-4657-y
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- Publication type:
- Article
ABCB1 (MDR1) genetic variants are associated with methadone doses required for effective treatment of heroin dependence.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 14, p. 2219, doi. 10.1093/hmg/ddn122
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- Publication type:
- Article
A non-coding CRHR2 SNP rs255105, a cis-eQTL for a downstream lincRNA AC005154.6, is associated with heroin addiction.
- Published in:
- PLoS ONE, 2018, v. 13, n. 6, p. 1, doi. 10.1371/journal.pone.0199951
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- Publication type:
- Article
Spectrum of sequence variation in the FANCG gene: An International Fanconi Anemia Registry (IFAR) study.
- Published in:
- 2003
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- Publication type:
- Erratum
Spectrum of sequence variation in the FANCG gene: An International Fanconi Anemia Registry (IFAR) study.
- Published in:
- Human Mutation, 2003, v. 21, n. 2, p. 158, doi. 10.1002/humu.10166
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- Publication type:
- Article
Identification of Alu-mediated deletions in the Fanconi anemia gene FAA.
- Published in:
- Human Mutation, 1998, v. 12, n. 3, p. 145, doi. 10.1002/(SICI)1098-1004(1998)12:3<145::AID-HUMU2>3.0.CO;2-G
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- Publication type:
- Article
Type A Niemann-Pick disease: A frameshift mutation in the acid sphingomyelinase gene (fsP330) occurs in Ashkenazi Jewish patients.
- Published in:
- Human Mutation, 1993, v. 2, n. 4, p. 317, doi. 10.1002/humu.1380020414
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- Publication type:
- Article
Identification of a 3′ acceptor splice site mutation (g2610c) in the acid sphingomyelinase gene of patients with Niemann - Pick disease.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 2, p. 205
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- Publication type:
- Article