Works matching IS 10614036 AND DT 2010 AND VI 42 AND IP 1
Results: 23
Exome sequencing identifies the cause of a mendelian disorder.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 30, doi. 10.1038/ng.499
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- Publication type:
- Article
Genome-wide association study identifies five loci associated with lung function.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 36, doi. 10.1038/ng.501
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- Publication type:
- Article
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 45, doi. 10.1038/ng.500
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- Article
Preferential associations between co-regulated genes reveal a transcriptional interactome in erythroid cells.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 53, doi. 10.1038/ng.496
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- Publication type:
- Article
Variant in PNPLA3 is associated with alcoholic liver disease.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 21, doi. 10.1038/ng.488
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- Publication type:
- Article
A restricted spectrum of NRAS mutations causes Noonan syndrome.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 27, doi. 10.1038/ng.497
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- Publication type:
- Article
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 24, doi. 10.1038/ng.506
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- Publication type:
- Article
Geographical genomics of human leukocyte gene expression variation in southern Morocco.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 62, doi. 10.1038/ng.495
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- Publication type:
- Article
The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 68, doi. 10.1038/ng.493
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- Publication type:
- Article
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 72, doi. 10.1038/ng.505
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- Publication type:
- Article
Somatic mutations of the Parkinson's disease–associated gene PARK2 in glioblastoma and other human malignancies.
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- Nature Genetics, 2010, v. 42, n. 1, p. 77, doi. 10.1038/ng.491
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- Publication type:
- Article
Skp2 is required for survival of aberrantly proliferating Rb1-deficient cells and for tumorigenesis in Rb1<sup>+/−</sup> mice.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 83, doi. 10.1038/ng.498
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- Publication type:
- Article
Wt1 is required for cardiovascular progenitor cell formation through transcriptional control of Snail and E-cadherin.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 89, doi. 10.1038/ng.494
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- Publication type:
- Article
Integrating with integrity.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 1, doi. 10.1038/ng0110-1
- Publication type:
- Article
Exome sequencing makes medical genomics a reality.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 13, doi. 10.1038/ng0110-13
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- Publication type:
- Article
Lung function and airway diseases.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 14, doi. 10.1038/ng0110-14
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- Publication type:
- Article
Getting connected in the globin interactome.
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- Nature Genetics, 2010, v. 42, n. 1, p. 16, doi. 10.1038/ng0110-16
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- Publication type:
- Article
Research highlights.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 19, doi. 10.1038/ng0110-19
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- Article
No evidence for a role of CLCN2 variants in idiopathic generalized epilepsy.
- Published in:
- 2010
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- Publication type:
- Letter
Reassessing the abundance of H3K9me2 chromatin domains in embryonic stem cells.
- Published in:
- 2010
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- Publication type:
- Letter
Reply to “Reassessing the abundance of H3K9me2 chromatin domains in embryonic stem cells”.
- Published in:
- 2010
- By:
- Publication type:
- Letter
Evolutionary flux of canonical microRNAs and mirtrons in Drosophila.
- Published in:
- 2010
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- Publication type:
- Letter
Reply to “Evolutionary flux of canonical microRNAs and mirtrons in Drosophila”.
- Published in:
- 2010
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- Publication type:
- Letter