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Pharmacogenetic analysis of adverse drug effect reveals genetic variant for susceptibility to liver toxicity.
- Published in:
- Pharmacogenomics Journal, 2002, v. 2, n. 5, p. 327, doi. 10.1038/sj.tpj.6500123
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- Article
CCR3: Shedding New Light on a Dark Problem?
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- Journal of Molecular Cell Biology, 2009, v. 1, n. 1, p. 17, doi. 10.1093/jmcb/mjp011
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- Publication type:
- Article
Neural-Specific Deletion of Htra2 Causes Cerebellar Neurodegeneration and Defective Processing of Mitochondrial OPA1.
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- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0115789
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- Publication type:
- Article
Protoporphyrins Enhance Oligomerization and Enzymatic Activity of HtrA1 Serine Protease.
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- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0115362
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- Publication type:
- Article
Stage and Gene Specific Signatures Defined by Histones H3K4me2 and H3K27me3 Accompany Mammalian Retina Maturation In Vivo.
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- PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0046867
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- Article
Genetic Signatures of Exceptional Longevity in Humans.
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- PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0029848
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- Publication type:
- Article
Mitochondrial DNA Variants of Respiratory Complex I that Uniquely Characterize Haplogroup T2 Are Associated with Increased Risk of Age-Related Macular Degeneration.
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- PLoS ONE, 2009, v. 4, n. 5, p. 1, doi. 10.1371/journal.pone.0005508
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- Publication type:
- Article
Mathematical multi-locus approaches to localizing complex human trait genes.
- Published in:
- Nature Reviews Genetics, 2003, v. 4, n. 9, p. 701, doi. 10.1038/nrg1155
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- Publication type:
- Article
SNP haplotype tagging from DNA pools of two individuals.
- Published in:
- BMC Bioinformatics, 2003, v. 4, p. 14, doi. 10.1186/1471-2105-4-14
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- Publication type:
- Article
Genetic Risk Score for Essential Hypertension and Risk of Preeclampsia.
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- American Journal of Hypertension, 2016, v. 29, n. 1, p. 17, doi. 10.1093/ajh/hpv069
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- Article
Genetic Predisposition to Dyslipidemia and Risk of Preeclampsia.
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- American Journal of Hypertension, 2015, v. 28, n. 7, p. 915, doi. 10.1093/ajh/hpu242
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- Article
Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis.
- Published in:
- 2009
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- Publication type:
- journal article
Interaction Between the Serotonin Transporter Gene (5-HTTLPR), Stressful Life Events, and Risk of Depression.
- Published in:
- JAMA: Journal of the American Medical Association, 2009, v. 301, n. 23, p. 2462, doi. 10.1001/jama.2009.878
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- Publication type:
- Article
A Comparison of Association Methods Correcting for Population Stratification in Case-Control Studies.
- Published in:
- Annals of Human Genetics, 2011, v. 75, n. 3, p. 418, doi. 10.1111/j.1469-1809.2010.00639.x
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- Publication type:
- Article
Systematically identifying genetic signatures including novel SNP-clusters, nonsense variants, frame-shift INDELs, and long STR expansions that potentially link to unknown phenotypes existing in dog breeds.
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- BMC Genomics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12864-023-09390-6
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- Publication type:
- Article
Origin of dendritic cells in peripheral lymphoid organs of mice.
- Published in:
- Nature Immunology, 2007, v. 8, n. 6, p. 578, doi. 10.1038/ni1462
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- Publication type:
- Article
Generation and characterization of mice with a conditional null allele of the HtrA4 gene.
- Published in:
- Molecular Medicine Reports, 2015, v. 12, n. 5, p. 6768, doi. 10.3892/mmr.2015.4291
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- Publication type:
- Article
Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients.
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- BMC Pregnancy & Childbirth, 2012, v. 12, n. 1, p. 61, doi. 10.1186/1471-2393-12-61
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- Publication type:
- Article
BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia.
- Published in:
- International Journal of Cancer, 2018, v. 143, n. 11, p. 2647, doi. 10.1002/ijc.31622
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- Publication type:
- Article
A protein kinase A–dependent molecular switch in synapsins regulates neurite outgrowth.
- Published in:
- Nature Neuroscience, 2002, v. 5, n. 5, p. 431, doi. 10.1038/nn840
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- Publication type:
- Article
GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-02596-9
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- Publication type:
- Article
Disease risk prediction with rare and common variants.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S61
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- Publication type:
- Article
Systematic review and meta-analysis of the association between complementary factor H Y402H polymorphisms and age-related macular degeneration.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 18, p. 2784, doi. 10.1093/hmg/ddl220
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- Publication type:
- Article
Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers.
- Published in:
- Genetic Epidemiology, 2003, v. 25, n. 4, p. 350, doi. 10.1002/gepi.10263
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- Publication type:
- Article
Two Approaches for Consolidating Results from Genome Scans of Complex Traits: Selection Methods and Scan Statistics.
- Published in:
- Genetic Epidemiology, 2001, v. 21, p. S403, doi. 10.1002/gepi.2001.21.s1.s403
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- Publication type:
- Article
Two Approaches for Consolidating Results from Genome Scans of Complex Traits: Selection Methods and Scan Statistics.
- Published in:
- Genetic Epidemiology, 2001, v. 21, p. S396, doi. 10.1002/gepi.2001.21.s1.s396
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- Publication type:
- Article
Statistical multilocus methods for disequilibrium analysis in complex traits.
- Published in:
- Human Mutation, 2001, v. 17, n. 4, p. 285, doi. 10.1002/humu.25
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- Publication type:
- Article
Association of Angiotensinogen Gene Polymorphisms with Essential Hypertension in African-Americans and Caucasians.
- Published in:
- Human Heredity, 2005, v. 60, n. 2, p. 89, doi. 10.1159/000088657
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- Publication type:
- Article
Ascertainment and Anticipation in Family Studies.
- Published in:
- Human Heredity, 2001, v. 51, n. 1/2, p. 23, doi. 10.1159/000022955
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- Publication type:
- Article
A Measure of Phase Ambiguity in Pairs of SNPs in the Presence ofLinkage Disequi librium.
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- Human Heredity, 2000, v. 50, n. 6, p. 359, doi. 10.1159/000022941
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- Publication type:
- Article
Complex Inheritance and Localizing Disease Genes.
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- Human Heredity, 2000, v. 50, n. 1, p. 85, doi. 10.1159/000022894
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- Publication type:
- Article
The NEI/NCBI dbGAP database: Genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-51
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- Publication type:
- Article