Works matching IS 10614036 AND DT 2011 AND VI 43 AND IP 9
Results: 29
Frequent mutations of chromatin remodeling genes in transitional cell carcinoma of the bladder.
- Published in:
- Nature Genetics, 2011, v. 43, n. 9, p. 875, doi. 10.1038/ng.907
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- Article
Neurons from Alzheimer's fibroblasts.
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- Nature Genetics, 2011, v. 43, n. 9, p. 824, doi. 10.1038/ng.929
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- Article
A20 edits ubiquitin and autoimmune paradigms.
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- Nature Genetics, 2011, v. 43, n. 9, p. 822, doi. 10.1038/ng.916
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- Article
Germline mutations in RAD51D confer susceptibility to ovarian cancer.
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- Nature Genetics, 2011, v. 43, n. 9, p. 879, doi. 10.1038/ng.893
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- Article
Admixture provides new insights into recombination.
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- Nature Genetics, 2011, v. 43, n. 9, p. 819, doi. 10.1038/ng.918
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- Article
Analysis of the coding genome of diffuse large B-cell lymphoma.
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- Nature Genetics, 2011, v. 43, n. 9, p. 830, doi. 10.1038/ng.892
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- Article
Oligodendroglioma exome sequencing.
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- Nature Genetics, 2011, v. 43, n. 9, p. 824, doi. 10.1038/ng.928
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- Article
A20 (TNFAIP3) deficiency in myeloid cells triggers erosive polyarthritis resembling rheumatoid arthritis.
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- Nature Genetics, 2011, v. 43, n. 9, p. 908, doi. 10.1038/ng.874
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- Article
A copy number variation morbidity map of developmental delay.
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- Nature Genetics, 2011, v. 43, n. 9, p. 838, doi. 10.1038/ng.909
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- Article
A genome-wide association study identifies two new risk loci for Graves' disease.
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- Nature Genetics, 2011, v. 43, n. 9, p. 897, doi. 10.1038/ng.898
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- Article
Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations.
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- Nature Genetics, 2011, v. 43, n. 9, p. 887, doi. 10.1038/ng.888
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- Article
Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population.
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- Nature Genetics, 2011, v. 43, n. 9, p. 893, doi. 10.1038/ng.887
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- Article
Increased exonic de novo mutation rate in individuals with schizophrenia.
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- Nature Genetics, 2011, v. 43, n. 9, p. 860, doi. 10.1038/ng.886
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- Article
Corrigendum: Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.
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- 2011
- Publication type:
- Correction Notice
Common variation at 10p12.31 near MLLT10 influences meningioma risk.
- Published in:
- Nature Genetics, 2011, v. 43, n. 9, p. 825, doi. 10.1038/ng.879
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- Article
Lyp breakdown and autoimmunity.
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- Nature Genetics, 2011, v. 43, n. 9, p. 821, doi. 10.1038/ng.914
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- Article
Exome sequencing supports a de novo mutational paradigm for schizophrenia.
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- Nature Genetics, 2011, v. 43, n. 9, p. 864, doi. 10.1038/ng.902
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- Article
Corrigendum: Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.
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- 2011
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- Correction Notice
Phosphoglycerate dehydrogenase diverts glycolytic flux and contributes to oncogenesis.
- Published in:
- Nature Genetics, 2011, v. 43, n. 9, p. 869, doi. 10.1038/ng.890
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- Article
Proteus syndrome exomes.
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- Nature Genetics, 2011, v. 43, n. 9, p. 824, doi. 10.1038/ng.930
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- Article
MicroRNAs can generate thresholds in target gene expression.
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- Nature Genetics, 2011, v. 43, n. 9, p. 854, doi. 10.1038/ng.905
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- Article
The genome of the extremophile crucifer Thellungiella parvula.
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- Nature Genetics, 2011, v. 43, n. 9, p. 913, doi. 10.1038/ng.889
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- Article
Recombination rates in admixed individuals identified by ancestry-based inference.
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- Nature Genetics, 2011, v. 43, n. 9, p. 847, doi. 10.1038/ng.894
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- Article
Inactivating mutations of the chromatin remodeling gene ARID2 in hepatocellular carcinoma.
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- Nature Genetics, 2011, v. 43, n. 9, p. 828, doi. 10.1038/ng.903
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- Article
Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria.
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- Nature Genetics, 2011, v. 43, n. 9, p. 883, doi. 10.1038/ng.908
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- Article
Fragile X protein stalls ribosomes.
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- Nature Genetics, 2011, v. 43, n. 9, p. 824, doi. 10.1038/ng.927
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- Article
Learning to think continentally.
- Published in:
- 2011
- Publication type:
- Editorial
Patient-derived isogenic iPSCs.
- Published in:
- Nature Genetics, 2011, v. 43, n. 9, p. 824, doi. 10.1038/ng.931
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- Article
The autoimmune disease-associated PTPN22 variant promotes calpain-mediated Lyp/Pep degradation associated with lymphocyte and dendritic cell hyperresponsiveness.
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- Nature Genetics, 2011, v. 43, n. 9, p. 902, doi. 10.1038/ng.904
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- Article