A second generation human haplotype map of over 3.1 million SNPs

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Items 101–200 of 1,030

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2. Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
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3. A genetic atlas of human admixture history
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4. Transcriptome genetics using second generation sequencing in a Caucasian population
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5. A Versatile Gene-Based Test for Genome-wide Association Studies
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6. Large-scale whole-genome sequencing of the Icelandic population
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7. SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies
   Zongli Xu, Jack A. Taylor · 2009 · Nucleic Acids Research
8. Natural Variations and Genome-Wide Association Studies in Crop Plants
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9. Human dectin-1 deficiency and mucocutaneous fungal infections
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11. Common Regulatory Variation Impacts Gene Expression in a Cell Type–Dependent Manner
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12. Biased gene conversion and the evolution of mammalian genomic landscapes
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13. SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations
    Unoki, Hiroyuki, Takahashi, Atsushi, Kawaguchi, Takahisa, Hara, Kazuo, Horikoshi, Momoko, Andersen, Gitte, Ng, Daniel P K, Holmkvist, Johan, Borch-Johnsen, Knut, Jørgensen, Torben et al. · 2008 · Nature Genetics
14. The Genetics of Major Depression
    Flint, Jonathan, Kendler, Kenneth S. · 2014 · Neuron
15. Linking disease associations with regulatory information in the human genome
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16. Signals of recent positive selection in a worldwide sample of human populations
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17. Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
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18. Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
    Laufey Thora Amundadottir, Peter L. Kraft, Rachael Z. Stolzenberg‐Solomon, Charles S. Fuchs, Gloria M. Petersen, Alan A. Arslan, H. Bas Bueno-de-Mesquita, Myron Gross, Kathy J. Helzlsouer, Eric J. Jacobs et al. · 2009 · Nature Genetics
19. MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis
    Jeffrey B. Kopp, Michael W. Smith, George W. Nelson, Randall C. Johnson, Barry I. Freedman, Donald W. Bowden, Tarás K. Oleksyk, Louise M. McKenzie, Hiroshi Kajiyama, Tejinder S. Ahuja et al. · 2008 · Nature Genetics
20. Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses
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21. The genetics of asthma and allergic disease: a 21st century perspective
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22. A framework for feature selection in clustering
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23. Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study
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24. Random-Effects Model Aimed at Discovering Associations in Meta-Analysis of Genome-wide Association Studies
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25. p53 polymorphisms: cancer implications
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26. Haplotype phasing: existing methods and new developments
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27. Increased accuracy of artificial selection by using the realized relationship matrix
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28. De novo assembly and genotyping of variants using colored de Bruijn graphs
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29. Whole-genome sequence variation, population structure and demographic history of the Dutch population
    Laurent C. Francioli, Androniki Menelaou, Sara L. Pulit, Clara C. Elbers, Wigard P. Kloosterman, Jessica van Setten, Isaäc J. Nijman, Ivo Renkens, Paul I. W. de Bakker, Freerk van Dijk et al. · 2014 · Nature Genetics
30. Common vs. rare allele hypotheses for complex diseases
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31. Improving the Accuracy and Efficiency of Identity-by-Descent Detection in Population Data
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32. MYH9 is associated with nondiabetic end-stage renal disease in African Americans
    W.H. Linda Kao, Michael J. Klag, Lucy A. Meoni, David Reich, Yvette Berthier‐Schaad, Man Li, Josef Coresh, Nick J. Patterson, Arti Tandon, Neil R. Powe et al. · 2008 · Nature Genetics
33. A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose
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34. DNase I sensitivity QTLs are a major determinant of human expression variation
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35. Designing Genome-Wide Association Studies: Sample Size, Power, Imputation, and the Choice of Genotyping Chip
    Chris C. A. Spencer, Zhan Su, Peter Donnelly, Jonathan Marchini · 2009 · PLoS Genetics
36. 9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response
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37. Genomic Patterns of Homozygosity in Worldwide Human Populations
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38. Meta-analysis and imputation refines the association of 15q25 with smoking quantity
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39. Estimating and interpreting F ST : The impact of rare variants
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40. Next-generation genomics: an integrative approach
    R. David Hawkins, Gary C. Hon, Bing Ren · 2010 · Nature Reviews Genetics
41. Natural selection has driven population differentiation in modern humans
    Barreiro, Luis B, Laval, Guillaume, Quach, Hélène, Patin, Etienne, Quintana-Murci, Lluís · 2008 · Nature Genetics
42. Genomic Runs of Homozygosity Record Population History and Consanguinity
    Mirna Kirin, Ruth McQuillan, Christopher S. Franklin, Harry J. Campbell, Paul McKeigue, James F. Wilson · 2010 · PLoS ONE
43. GWAMA: software for genome-wide association meta-analysis
    Reedik Mägi, Andrew P. Morris · 2010 · BMC Bioinformatics
44. A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33
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45. Detectable clonal mosaicism and its relationship to aging and cancer
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46. Bayesian inference of ancient human demography from individual genome sequences
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47. Variation in Transcription Factor Binding Among Humans
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48. Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage
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49. The MHC locus and genetic susceptibility to autoimmune and infectious diseases
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50. Genome-wide association studies in diverse populations
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51. SDM--a server for predicting effects of mutations on protein stability and malfunction
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52. Resurrecting Surviving Neandertal Lineages from Modern Human Genomes
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53. A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer
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54. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
    John Campbell Chambers, Diabetes Genetics Replication and Meta-analyses (DIAGRAM+) Study, Weihua Zhang, Joban Sehmi, Xinzhong Li, Mark N. Wass, Pim van der Harst, Hilma Hólm, Serena Sanna, Maryam Kavousi et al. · 2011 · Nature Genetics
55. Revealing the architecture of gene regulation: the promise of eQTL studies
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56. Detecting shared pathogenesis from the shared genetics of immune-related diseases
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57. Natural selection and infectious disease in human populations
    Elinor K. Karlsson, Dominic P. Kwiatkowski, Pardis C. Sabeti · 2014 · Nature Reviews Genetics
58. Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome
    for UK Primary Sjögren's Syndrome Registry, Christopher J. Lessard, He Li, Indra Adrianto, John A. Ice, Astrid Rasmussen, Kiely M. Grundahl, Jennifer A. Kelly, Mikhail G. Dozmorov, Corinne Miceli‐Richard et al. · 2013 · Nature Genetics
59. Genomic evidence for the Pleistocene and recent population history of Native Americans
    Raghavan, Maanasa, Steinrücken, Matthias, Harris, Kelley, Schiffels, Stephan, Rasmussen, Simon, DeGiorgio, Michael, Albrechtsen, Anders, Valdiosera, Cristina, Ávila-Arcos, María C., Malaspinas, Anna-Sapfo et al. · 2015 · Science
60. Sensitive detection of chromosomal segments of distinct ancestry in admixed populations
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61. High-Resolution Mapping of Expression-QTLs Yields Insight into Human Gene Regulation
    Veyrieras, Jean-Baptiste, Kudaravalli, Sridhar, Kim, Su Yeon, Dermitzakis, Emmanouil T., Gilad, Yoav, Stephens, Matthew, Pritchard, Jonathan K. · 2008 · PLoS Genetics
62. Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding
    Kevin Judd McKernan, Heather E. Peckham, Gina L. Costa, Stephen F. McLaughlin, Yutao Fu, Eric F. Tsung, Christopher R. Clouser, Cisyla Duncan, Jeffrey K. Ichikawa, Clarence C. Lee et al. · 2009 · Genome Research
63. Practical aspects of imputation-driven meta-analysis of genome-wide association studies
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64. Human genetic susceptibility to infectious disease
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65. Genome-wide association study of hematological and biochemical traits in a Japanese population
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66. A framework for enhancing ethical genomic research with Indigenous communities
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67. A Composite of Multiple Signals Distinguishes Causal Variants in Regions of Positive Selection
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68. The 1001 Genomes Project for Arabidopsis thaliana
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69. Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration
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70. Genome-wide associations for birth weight and correlations with adult disease
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71. The Pathogenesis of Endometriosis: Molecular and Cell Biology Insights
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72. Effect of read-mapping biases on detecting allele-specific expression from RNA-sequencing data.
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73. A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation
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74. Multiple sclerosis
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75. Human Genome Sequencing in Health and Disease
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76. Searching for SNPs with cloud computing
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77. Narcolepsy is strongly associated with the T-cell receptor alpha locus
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78. An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data
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79. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies
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80. Web-Based, Participant-Driven Studies Yield Novel Genetic Associations for Common Traits
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81. Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations
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82. Mechanism and Regulation of Meiotic Recombination Initiation
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83. The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits
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84. SNP identification in crop plants
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85. Impact of regulatory variation from RNA to protein
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86. A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
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87. Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening
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88. A common sequence motif associated with recombination hot spots and genome instability in humans
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89. Inferring admixture histories of human populations using linkage disequilibrium
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90. Next-generation genetics in plants
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91. Ensembl variation resources
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92. Identifying Causal Variants at Loci with Multiple Signals of Association
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93. Plasma lipoproteins: genetic influences and clinical implications
    Hegele, Robert A. · 2009 · Nature Reviews Genetics
94. Widespread Genomic Signatures of Natural Selection in Hominid Evolution
    McVicker, Graham, Gordon, David, Davis, Colleen, Green, Phil · 2009 · PLoS Genetics
95. Genome-wide patterns of population structure and admixture in West Africans and African Americans
    Bryc, Katarzyna, Auton, Adam, Nelson, Matthew R., Oksenberg, Jorge R., Hauser, Stephen L., Williams, Scott, Froment, Alain, Bodo, Jean-Marie, Wambebe, Charles, Tishkoff, Sarah A. et al. · 2010 · Proceedings of the National Academy of Sciences
96. W hats H ap : Weighted Haplotype Assembly for Future-Generation Sequencing Reads
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97. Whole population, genome-wide mapping of hidden relatedness
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98. Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders
    Psychiatric GWAS Consortium Coordinating Committee · 2009 · American Journal of Psychiatry
99. Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis
    Schizophrenia Working Group of the Psychiatric Genomics Consortium, Loh, Po-Ru, Bhatia, Gaurav, Gusev, Alexander, Finucane, Hilary K, Bulik-Sullivan, Brendan K, Pollack, Samuela J, de Candia, Teresa R, Lee, Sang Hong, Wray, Naomi R et al. · 2015 · Nature Genetics
100. Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene ( LIPC )
     Neale, Benjamin M., Fagerness, Jesen, Reynolds, Robyn, Sobrin, Lucia, Parker, Margaret, Raychaudhuri, Soumya, Tan, Perciliz L., Oh, Edwin C., Merriam, Joanna E., Souied, Eric et al. · 2010 · Proceedings of the National Academy of Sciences