Works matching IS 10614036 AND DT 2011 AND VI 43 AND IP 12
Results: 32
Genome-wide association study identifies a susceptibility locus for schizophrenia in Han Chinese at 11p11.2.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1228, doi. 10.1038/ng.979
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- Publication type:
- Article
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1210, doi. 10.1038/ng.985
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- Publication type:
- Article
He et al. reply.
- Published in:
- 2011
- By:
- Publication type:
- Letter
A rare variant in CFH directly links age-related macular degeneration with rare glomerular nephropathies.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1176, doi. 10.1038/ng.1012
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- Publication type:
- Article
Fine points in mapping autoimmunity.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1173, doi. 10.1038/ng.1015
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- Publication type:
- Article
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1256, doi. 10.1038/ng.1004
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- Publication type:
- Article
Predicting phenotypic variation in yeast from individual genome sequences.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1270, doi. 10.1038/ng.1007
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- Publication type:
- Article
The rugged landscape of drug design.
- Published in:
- 2011
- Publication type:
- Editorial
PTEN ceRNAs in melanoma.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1178, doi. 10.1038/ng.1022
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- Publication type:
- Article
A genome-wide association study identifies new susceptibility loci for non-cardia gastric cancer at 3q13.31 and 5p13.1.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1215, doi. 10.1038/ng.978
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- Publication type:
- Article
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1193, doi. 10.1038/ng.998
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- Publication type:
- Article
Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1247, doi. 10.1038/ng.973
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- Publication type:
- Article
A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1237, doi. 10.1038/ng.974
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- Publication type:
- Article
AKT2 mutations and hypoglycemia.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1178, doi. 10.1038/ng.1024
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- Publication type:
- Article
Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1262, doi. 10.1038/ng.994
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- Publication type:
- Article
Relative overexpression of X-linked genes in mouse embryonic stem cells is consistent with Ohno's hypothesis.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Insertional mutagenesis identifies multiple networks of cooperating genes driving intestinal tumorigenesis.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1202, doi. 10.1038/ng.990
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- Publication type:
- Article
Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1186, doi. 10.1038/ng.975
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- Publication type:
- Article
Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1241, doi. 10.1038/ng.981
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- Publication type:
- Article
Personalized asthma control.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1178, doi. 10.1038/ng.1023
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- Publication type:
- Article
Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1252, doi. 10.1038/ng.1008
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- Publication type:
- Article
Parallel bacterial evolution within multiple patients identifies candidate pathogenicity genes.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1275, doi. 10.1038/ng.997
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- Publication type:
- Article
Exome sequencing identifies frequent mutation of ARID1A in molecular subtypes of gastric cancer.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1219, doi. 10.1038/ng.982
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- Publication type:
- Article
Evidence for compensatory upregulation of expressed X-linked genes in mammals, Caenorhabditis elegans and Drosophila melanogaster.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1179, doi. 10.1038/ng.948
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- Publication type:
- Article
Leishmaniasis genomes.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1178, doi. 10.1038/ng.1025
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- Publication type:
- Article
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD).
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1189, doi. 10.1038/ng.995
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- Publication type:
- Article
Evidence for dosage compensation between the X chromosome and autosomes in mammals.
- Published in:
- 2011
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- Publication type:
- Letter
Common variants on 8p12 and 1q24.2 confer risk of schizophrenia.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1224, doi. 10.1038/ng.980
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- Publication type:
- Article
Priming for chemotherapy.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1178, doi. 10.1038/ng.1021
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- Publication type:
- Article
A rare penetrant mutation in CFH confers high risk of age-related macular degeneration.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1232, doi. 10.1038/ng.976
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- Publication type:
- Article
Chance and necessity in the evolution of a bacterial pathogen.
- Published in:
- 2011
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- Publication type:
- Opinion
Natural variation in GS5 plays an important role in regulating grain size and yield in rice.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1266, doi. 10.1038/ng.977
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- Publication type:
- Article