Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

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Items 601–700 of 1,000

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8. To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies?
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9. Cardiovascular Genomics and Oxidative Stress
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17. Searching High-Order SNP Combinations for Complex Diseases Based on Energy Distribution Difference
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18. Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia
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19. Exome Sequencing of Germline DNA from Non-BRCA1/2 Familial Breast Cancer Cases Selected on the Basis of aCGH Tumor Profiling
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20. Nonsynonymous Coding Single-Nucleotide Polymorphisms Spanning the Genome in Relation to Glioblastoma Survival and Age at Diagnosis
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22. Genome-Wide Mapping Of Copy Number Variations using SNP Arrays
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23. Fine mapping of a major locus on Chromosome 10 for exploratory and fear-like behavior in mice
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28. Genetic variation in immune function and susceptibility to human filariasis
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29. Fine Mapping Functional Sites or Regions from Case‐Control Data Using Haplotypes of Multiple Linked SNPs
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30. Variation resources at UC Santa Cruz
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31. Commentary: Understanding sources of complexity in chronic diseases—the importance of integration of genetics and epidemiology
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32. Jumping on the Train of Personalized Medicine: A Primer for Non- Geneticist Clinicians: Part 3. Clinical Applications in the Personalized Medicine Area
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33. Added Value of Whole-Exome and Transcriptome Sequencing for Clinical Molecular Screenings of Advanced Cancer Patients With Solid Tumors
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34. Clinical utility in infants with suspected monogenic conditions through next‐generation sequencing
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37. Thought Disorder in Schizophrenia and Bipolar Disorder Probands, Their Relatives, and Nonpsychiatric Controls
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38. The RA-MAP Consortium: a working model for academia–industry collaboration
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39. Scuba: scalable kernel-based gene prioritization
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40. Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss
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41. Periodicity of SNP distribution around transcription start sites
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42. Sequence diversity, natural selection and linkage disequilibrium in the human T cell receptor alpha/delta locus
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43. Global Genetic Analysis
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44. Genome-Wide Association Studies: Progress in Identifying Genetic Biomarkers in Common, Complex Diseases
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45. Quantitative trait loci for IQ and other complex traits: single‐nucleotide polymorphism genotyping using pooled DNA and microarrays
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46. Cardiovascular pharmacogenomics
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47. Genetic architecture reconciles linkage and association studies of complex traits
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48. PhenoHM: human–mouse comparative phenome–genome server
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49. Genome Wide Association Scan shows Genetic Variants in the FTO gene are Associated with Obesity Related Traits
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50. Disease Gene Prioritization
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51. In Silico profiling of deleterious amino acid substitutions of potential pathological importance in haemophlia A and haemophlia B
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52. GWASeq: targeted re-sequencing follow up to GWAS
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53. Two SNAP-25 genetic variants in the binding site of multiple microRNAs and susceptibility of ADHD: A meta-analysis
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54. Naturally Segregating Variation at Ugt86Dd Contributes to Nicotine Resistance in Drosophila melanogaster
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55. The Icelandic Cancer Project – a population-wide approach to studying cancer
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56. Nanoparticle carrying a single probe for target DNA detection and single nucleotide discrimination
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57. Basic helix–loop–helix transcription factor NEUROG1 and schizophrenia: Effects on illness susceptibility, MRI brain morphometry and cognitive abilities☆
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60. MALDI-TOF MS: a platform technology for genetic discovery
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61. Linkage disequilibrium on chromosome 6 in Australian Holstein-Friesian cattle
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62. Determination of haplotypes from single DNA molecules: a method for single-molecule barcoding
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63. Progress toward personalized medicine for glaucoma
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64. Robotic microinjection enables large-scale transgenic studies of Caenorhabditis elegans
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65. Prioritization of candidate genes for a South African family with Parkinson’s disease using in-silico tools
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66. The False Dawn of Polygenic Risk Scores for Human Disease Prediction
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67. A Haplotype-Based Test of Association Using Data from Cohort and Nested Case-Control Epidemiologic Studies
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69. Classical Twin Design in Modern Pharmacogenomics Studies
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71. Heterogeneity Analysis of Esophageal Squamous Cell Carcinoma in Cell Lines, Tumor Tissues and Patient-Derived Xenografts
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72. Immunoglobulin Gene Analysis in Chronic Lymphocytic Leukemia
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73. From mouse to humans: discovery of the CACNG2 pain susceptibility gene
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74. Role of genetics in prevention of coronary atherosclerosis
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75. Down-regulation of pancreatic and duodenal homeobox-1 by somatostatin receptor subtype 5: a novel mechanism for inhibition of cellular proliferation and insulin secretion by somatostatin
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76. Toll‐like receptor polymorphisms and allergic disease: interpreting the evidence from genetic studies
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77. Neurogenetics II: complex disorders
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82. Genome-wide homozygosity and multiple sclerosis in Orkney and Shetland Islanders
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92. Prioritization of candidate disease genes by combining topological similarity and semantic similarity
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93. A Bayesian Hierarchical Model for Detecting Haplotype-Haplotype and Haplotype-Environment Interactions in Genetic Association Studies
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96. Molecular correlates of emotional learning using genetically selected rat lines
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97. Linkage Disequilibrium and Association Mapping
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