Pages that link to "Q29614907"
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The following pages link to SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap (Q29614907):
Displaying 50 items.
- Genome-wide association study identifies single nucleotide polymorphism in DYRK1A associated with replication of HIV-1 in monocyte-derived macrophages (Q21135536) (← links)
- Phased whole-genome genetic risk in a family quartet using a major allele reference sequence (Q21144940) (← links)
- Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis (Q21144987) (← links)
- Genome-wide QTL mapping for three traits related to teat number in a White Duroc x Erhualian pig resource population (Q21261513) (← links)
- Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder (Q22252418) (← links)
- Genetic variants within the MHC region are associated with immune responsiveness to childhood vaccinations (Q23910391) (← links)
- Genetic variants in the major histocompatibility complex class I and class II genes are associated with diisocyanate-induced asthma (Q23910397) (← links)
- N-acetyltransferase 2 genotypes are associated with diisocyanate-induced asthma (Q23910398) (← links)
- Genetic variants in TNFa, TGFB1, PTGS1 and PTGS2 genes are associated with diisocyanate-induced asthma (Q23910400) (← links)
- Candidate gene-environment interaction research: reflections and recommendations (Q24273240) (← links)
- Circadian polymorphisms in night owls, in bipolars, and in non-24-hour sleep cycles (Q24273283) (← links)
- Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy (Q24288778) (← links)
- Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region (Q24289047) (← links)
- Investigation of rheumatoid arthritis susceptibility genes identifies association of AFF3 and CD226 variants with response to anti-tumour necrosis factor treatment (Q24310184) (← links)
- Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1 (Q24629883) (← links)
- New loci associated with kidney function and chronic kidney disease (Q24630646) (← links)
- Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder (Q24634497) (← links)
- A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation (Q24648813) (← links)
- A genomewide association study of citalopram response in major depressive disorder (Q24656746) (← links)
- Genome-wide association meta-analysis for total serum bilirubin levels (Q24658179) (← links)
- Draft Genomes of Anopheles cracens and Anopheles maculatus: Comparison of Simian Malaria and Human Malaria Vectors in Peninsular Malaysia (Q26315263) (← links)
- Candidate gene association studies: a comprehensive guide to useful in silico tools (Q26851744) (← links)
- Can knowledge of germline markers of toxicity optimize dosing and efficacy of cancer therapy? (Q26859144) (← links)
- Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals (Q27003308) (← links)
- Epigenome-guided analysis of the transcriptome of plaque macrophages during atherosclerosis regression reveals activation of the Wnt signaling pathway (Q27311648) (← links)
- Prediction of Causal Candidate Genes in Coronary Artery Disease Loci (Q27342192) (← links)
- On the association of common and rare genetic variation influencing body mass index: a combined SNP and CNV analysis (Q27496612) (← links)
- Genetic Vulnerability and Susceptibility to Substance Dependence (Q27686799) (← links)
- Genetic basis of irritant susceptibility in health care workers (Q27908551) (← links)
- Association of MHC region SNPs with irritant susceptibility in healthcare workers (Q27908640) (← links)
- Genome-wide association study reveals two new risk loci for bipolar disorder (Q28235753) (← links)
- Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction (Q28287618) (← links)
- Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits (Q28295739) (← links)
- Cooperation of DLC1 and CDK6 affects breast cancer clinical outcome (Q28385752) (← links)
- TERT gene harbors multiple variants associated with pancreatic cancer susceptibility (Q28386653) (← links)
- Deciphering associations for lung cancer risk through imputation and analysis of 12,316 cases and 16,831 controls (Q28389918) (← links)
- A Bayesian Approach to the Overlap Analysis of Epidemiologically Linked Traits (Q28392202) (← links)
- Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function (Q28392223) (← links)
- Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases (Q28394008) (← links)
- Sex Steroid Hormone Single-Nucleotide Polymorphisms, Pesticide Use, and the Risk of Prostate Cancer: A Nested Case-Control Study within the Agricultural Health Study (Q28394503) (← links)
- Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer (Q28396029) (← links)
- The Geographic Distribution of Genetic Risk as Compared to Social Risk for Chronic Diseases in the United States (Q28396517) (← links)
- Common germline variants within the CDKN2A/2B region affect risk of pancreatic neuroendocrine tumors (Q28397098) (← links)
- Drug Metabolizing Enzyme and Transporter Gene Variation, Nicotine Metabolism, Prospective Abstinence, and Cigarette Consumption (Q28397614) (← links)
- Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis (Q28480561) (← links)
- RHOA is a modulator of the cholesterol-lowering effects of statin (Q28485187) (← links)
- CYP2B6 non-coding variation associated with smoking cessation is also associated with differences in allelic expression, splicing, and nicotine metabolism independent of common amino-acid changes (Q28535164) (← links)
- Anti-TNF treatment response in rheumatoid arthritis patients is associated with genetic variation in the NLRP3-inflammasome (Q28540052) (← links)
- Genetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise (Q28548630) (← links)
- First Draft Assembly and Annotation of the Genome of a California Endemic Oak Quercus lobata Née (Fagaceae) (Q28596118) (← links)