Found: 32
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ITGA3 and epithelial integrity.
- Published in:
- Nature Genetics, 2012, v. 44, n. 6, p. 618, doi. 10.1038/ng.2319
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- Article
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.
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- Nature Genetics, 2012, v. 44, n. 6, p. 659, doi. 10.1038/ng.2274
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- Article
CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms.
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- Nature Genetics, 2012, v. 44, n. 6, p. 714, doi. 10.1038/ng.2277
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- Article
Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.
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- Nature Genetics, 2012, v. 44, n. 6, p. 639, doi. 10.1038/ng.2262
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- Article
A genome-wide association study identifies susceptibility loci for Wilms tumor.
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- Nature Genetics, 2012, v. 44, n. 6, p. 681, doi. 10.1038/ng.2251
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- Article
Exploring the variation within.
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- Nature Genetics, 2012, v. 44, n. 6, p. 614, doi. 10.1038/ng.2311
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- Article
Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1.
- Published in:
- Nature Genetics, 2012, v. 44, n. 6, p. 699, doi. 10.1038/ng.2263
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- Article
Epigenetic activation by long RNA.
- Published in:
- Nature Genetics, 2012, v. 44, n. 6, p. 618, doi. 10.1038/ng.2321
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- Article
Detectable clonal mosaicism from birth to old age and its relationship to cancer.
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- Nature Genetics, 2012, v. 44, n. 6, p. 642, doi. 10.1038/ng.2271
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- Article
Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1.
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- Nature Genetics, 2012, v. 44, n. 6, p. 709, doi. 10.1038/ng.2259
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- Article
Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume.
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- 2012
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- Erratum
One gene's shattering effects.
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- Nature Genetics, 2012, v. 44, n. 6, p. 616, doi. 10.1038/ng.2289
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- Article
Exome sequencing and the genetic basis of complex traits.
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- Nature Genetics, 2012, v. 44, n. 6, p. 623, doi. 10.1038/ng.2303
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- Article
Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration.
- Published in:
- Nature Genetics, 2012, v. 44, n. 6, p. 704, doi. 10.1038/ng.2254
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- Article
Erratum: A transposon in tb1 drove maize domestication.
- Published in:
- 2012
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- Erratum
How do you feel?
- Published in:
- Nature Genetics, 2012, v. 44, n. 6, p. 618, doi. 10.1038/ng.2317
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- Article
Traversing the genomic landscape of prostate cancer from diagnosis to death.
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- Nature Genetics, 2012, v. 44, n. 6, p. 613, doi. 10.1038/ng.2301
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- Publication type:
- Article
Extremely low-coverage sequencing and imputation increases power for genome-wide association studies.
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- Nature Genetics, 2012, v. 44, n. 6, p. 631, doi. 10.1038/ng.2283
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- Article
piRNA, epigenetics and memory formation.
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- Nature Genetics, 2012, v. 44, n. 6, p. 618, doi. 10.1038/ng.2318
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- Article
The Pediatric Cancer Genome Project.
- Published in:
- Nature Genetics, 2012, v. 44, n. 6, p. 619, doi. 10.1038/ng.2287
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- Article
Integrated analysis of somatic mutations and focal copy-number changes identifies key genes and pathways in hepatocellular carcinoma.
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- Nature Genetics, 2012, v. 44, n. 6, p. 694, doi. 10.1038/ng.2256
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- Article
Meta-analysis identifies six new susceptibility loci for atrial fibrillation.
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- Nature Genetics, 2012, v. 44, n. 6, p. 670, doi. 10.1038/ng.2261
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- Article
Corrigendum: Arabidopsis thaliana as a model for the genetics of local adaptation.
- Published in:
- 2012
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- Erratum
Detectable clonal mosaicism and its relationship to aging and cancer.
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- Nature Genetics, 2012, v. 44, n. 6, p. 651, doi. 10.1038/ng.2270
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- Article
The '3Is' of animal experimentation.
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- Nature Genetics, 2012, v. 44, n. 6, p. 611, doi. 10.1038/ng.2322
- Publication type:
- Article
A model-based approach for analysis of spatial structure in genetic data.
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- Nature Genetics, 2012, v. 44, n. 6, p. 725, doi. 10.1038/ng.2285
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- Article
Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.
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- Nature Genetics, 2012, v. 44, n. 6, p. 676, doi. 10.1038/ng.2272
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- Article
Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer.
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- Nature Genetics, 2012, v. 44, n. 6, p. 685, doi. 10.1038/ng.2279
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- Article
Parallel domestication of the Shattering1 genes in cereals.
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- Nature Genetics, 2012, v. 44, n. 6, p. 720, doi. 10.1038/ng.2281
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- Article
Exome sequencing of liver fluke-associated cholangiocarcinoma.
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- Nature Genetics, 2012, v. 44, n. 6, p. 690, doi. 10.1038/ng.2273
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- Article
Genetics of blond hair.
- Published in:
- Nature Genetics, 2012, v. 44, n. 6, p. 618, doi. 10.1038/ng.2320
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- Publication type:
- Article
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype.
- Published in:
- Nature Genetics, 2012, v. 44, n. 6, p. 636, doi. 10.1038/ng.2257
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- Publication type:
- Article