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Title:	Negligible impact of rare autoimmune-locus coding-region variants on missing heritability
Source:	Nature [0028-0836] Hunt, K A yr:2013

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description	2.	Ward, Lucas D. "Interpreting noncoding genetic variation in complex traits and human disease." Nature biotechnology 30.11 (2012): 1095-1106.
description	3.	Glimcher, J. "After GWAS: mice to the rescue?" Current opinion in immunology 24.5 (2012): 564-570.
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description	5.	Sawcer, S. "A high-density screen for linkage in multiple sclerosis." American journal of human genetics 77.3 (2005): 454-67.
description	6.	de Jong, A. "Advances in prenatal screening: the ethical dimension." Nature reviews. Genetics 12.9 (2011): 657-663.
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description	8.	Andreassen, O. "Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors." American journal of human genetics 92.2 (2013): 197-209.
description	9.	Pergament, E. "Reproductive decisions after fetal genetic counselling." Baillière's best practice & research. Clinical obstetrics & gynaecology 26.5 (2012): 517-529.
description	10.	Ladomery, Michael R. "MicroRNAs: their discovery, biogenesis, function and potential use as biomarkers in non-invasive prenatal diagnostics." International journal of molecular epidemiology and genetics 2.3 (2011): 253-60.
description	11.	Kachur, Robert M. "Buried in the Bedroom: Bearing Witness to Incest in Poe's "The Tell-Tale Heart."." Mosaic 41.1 (2008): 43-59.
description	12.	Plomin, R. "Common DNA Markers Can Account for More Than Half of the Genetic Influence on Cognitive Abilities." Psychological science 24.4 (2013): 562-568.
description	13.	Oetting, William S. "Getting Ready for the Human Phenome Project: The 2012 Forum of the Human Variome Project." Human mutation 34.4 (2013): 661-666.
description	14.	Aberg, Karolina A. "A Comprehensive Family-Based Replication Study of Schizophrenia Genes." JAMA psychiatry 70.2 (2013): 1-9.
description	15.	Wu, X. "Impairment of hepatic NK cell development in IFN-γ deficient mice." Cytokine 60.3 (2012): 616-625.
description	16.	Suto, J. "Quantitative trait locus mapping of genes that control body length and plasma insulin-like growth factor 1 level in mice." BMC research notes 5 (2012): 4294967295-4294967295.
description	17.	Randall, Frances E. "Effector and regulatory B cells: modulators of CD4(+) T cell immunity." Nature Reviews. Immunology 10.4 (2010): 236-47.
description	18.	Sullivan, Patrick F. "Meta-Analysis of Genome-wide Association Studies with Overlapping Subjects." American journal of human genetics 85.6 (2009): 862-872.
description	19.	Sharp, P M M. "The codon Adaptation Index--a measure of directional synonymous codon usage bias, and its potential applications." Nucleic Acids Research 15.3 (1987): 1281-1295.
description	20.	Gregersen, Jon W W. "Functional epistasis on a common MHC haplotype associated with multiple sclerosis." Nature 443.7111 (2006): 574-7.