Found: 19
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Significant association of DRD1 with nicotine dependence.
- Published in:
- Human Genetics, 2008, v. 123, n. 2, p. 133, doi. 10.1007/s00439-007-0453-9
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- Article
Gene-based analysis suggests association of the nicotinic acetylcholine receptor β1 subunit ( CHRNB1) and M1 muscarinic acetylcholine receptor ( CHRM1) with vulnerability for nicotine dependence.
- Published in:
- Human Genetics, 2006, v. 120, n. 3, p. 381, doi. 10.1007/s00439-006-0229-7
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- Article
Significant Association of Catechol-O-Methyltransferase (COMT) Haplotypes with Nicotine Dependence in Male and Female Smokers of Two Ethnic Populations.
- Published in:
- Neuropsychopharmacology, 2006, v. 31, n. 3, p. 675, doi. 10.1038/sj.npp.1300997
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- Article
Ancestry informative markers and admixture proportions in northeastern Mexico.
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- Journal of Human Genetics, 2009, v. 54, n. 9, p. 504, doi. 10.1038/jhg.2009.65
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- Article
Candidate gene association analysis of acute lymphoblastic leukemia identifies new susceptibility locus at 11p15 (LMO1).
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- Carcinogenesis, 2011, v. 32, n. 9, p. 1349, doi. 10.1093/carcin/bgr091
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- Article
Association of chromosome 8q variants with prostate cancer risk in Caucasian and Hispanic men.
- Published in:
- Carcinogenesis, 2009, v. 30, n. 8, p. 1372, doi. 10.1093/carcin/bgp148
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- Article
CYP1B1 variants are associated with prostate cancer in non-Hispanic and Hispanic Caucasians.
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- Carcinogenesis, 2008, v. 29, n. 9, p. 1751, doi. 10.1093/carcin/bgm300
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- Article
Haplotype analysis indicates an association between the DOPA decarboxylase (DDC) gene and nicotine dependence.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 12, p. 1691, doi. 10.1093/hmg/ddi177
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- Article
Ethnic- and gender-specific association of the nicotinic acetylcholine receptor α4 subunit gene (CHRNA4) with nicotine dependence.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 9, p. 1211, doi. 10.1093/hmg/ddi132
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- Article
Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing.
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- JAMA: Journal of the American Medical Association, 2014, v. 312, n. 18, p. 1869, doi. 10.1001/jama.2014.14601
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- Article
Whole-Exome Sequencing, Proteome Landscape, and Immune Cell Migration Patterns in a Clinical Context of Menkes Disease.
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- Genes, 2021, v. 12, n. 5, p. 744, doi. 10.3390/genes12050744
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- Article
Heterozygous <i>De Novo</i> and Inherited Mutations in the Smooth Muscle Actin (<i>ACTG2</i>) Gene Underlie Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 3, p. 1, doi. 10.1371/journal.pgen.1004258
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- Article
Significant Association of ANKK1 and Detection of a Functional Polymorphism with Nicotine Dependence in an African-American Sample.
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- Neuropsychopharmacology, 2009, v. 34, n. 2, p. 319, doi. 10.1038/npp.2008.37
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- Article
Wide Disparity in Genetic Admixture Among Mexican Americans from San Antonio, TX.
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- Annals of Human Genetics, 2011, v. 75, n. 4, p. 529, doi. 10.1111/j.1469-1809.2011.00655.x
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- Article
Identification of viral infections in the prostate andevaluation of their association with cancer.
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- BMC Cancer, 2010, v. 10, p. 326, doi. 10.1186/1471-2407-10-326
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- Article
Clinical and molecular characterization of de novo loss of function variants in HNRNPU.
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- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 10, p. 2680, doi. 10.1002/ajmg.a.38388
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- Article
Increased bone turnover, osteoporosis, progressive tibial bowing, fractures, and scoliosis in a patient with a final-exon SATB2 frameshift mutation.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 11, p. 3028, doi. 10.1002/ajmg.a.37847
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- Article
The spectrum of mutations in UBE3A causing Angelman syndrome.
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- Human Molecular Genetics, 1999, v. 8, n. 1, p. 129, doi. 10.1093/hmg/8.1.129
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- Article
Distal Hereditary Motor Neuropathy Type II (Distal HMN II): Mapping of a Locus to Chromosome 12q24.
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- Human Molecular Genetics, 1996, v. 5, n. 7, p. 1065, doi. 10.1093/hmg/5.7.1065
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- Article