Found: 19
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Use of microarray hybrid capture and next-generation sequencing to identify the anatomy of a transgene.
- Published in:
- Nucleic Acids Research, 2013, v. 41, n. 6, p. e70, doi. 10.1093/nar/gks1463
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- Publication type:
- Article
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion.
- Published in:
- Nature Genetics, 2013, v. 45, n. 2, p. 197, doi. 10.1038/ng.2507
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- Publication type:
- Article
Common variants in the GDF5-UQCC region are associated with variation in human height.
- Published in:
- Nature Genetics, 2008, v. 40, n. 2, p. 198, doi. 10.1038/ng.74
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- Publication type:
- Article
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
- Published in:
- PLoS Genetics, 2017, v. 13, n. 10, p. 1, doi. 10.1371/journal.pgen.1007079
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- Publication type:
- Article
Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns.
- Published in:
- Human Genetics, 2005, v. 118, n. 2, p. 245, doi. 10.1007/s00439-005-0046-4
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- Publication type:
- Article
Addressing Bias in Small RNA Library Preparation for Sequencing: A New Protocol Recovers MicroRNAs that Evade Capture by Current Methods.
- Published in:
- Frontiers in Genetics, 2015, p. 1, doi. 10.3389/fgene.2015.00352
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- Publication type:
- Article
The genetic regulatory signature of type 2 diabetes in human skeletal muscle.
- Published in:
- Nature Communications, 2016, v. 7, n. 6, p. 11764, doi. 10.1038/ncomms11764
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- Publication type:
- Article
BoostMe accurately predicts DNA methylation values in whole-genome bisulfite sequencing of multiple human tissues.
- Published in:
- BMC Genomics, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12864-018-4766-y
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- Publication type:
- Article
Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 9, p. 1664, doi. 10.1093/hmg/ddy067
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- Publication type:
- Article
Comprehensive Association Study of Type 2 Diabetes and Related Quantitative Traits With 222 Candidate Genes.
- Published in:
- Diabetes, 2008, v. 57, n. 11, p. 3136, doi. 10.2337/db07-1731
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- Publication type:
- Article
Screening of 134 Single Nucleotide Polymorphisms (SNPs) Previously Associated With Type 2 Diabetes Replicates Association With 12 SNPs in Nine Genes.
- Published in:
- Diabetes, 2007, v. 56, n. 1, p. 256, doi. 10.2337/db06-0461
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- Publication type:
- Article
Association of Transcription Factor 7-Like 2 (TCF7L2) Variants With Type 2 Diabetes in a Finnish Sample.
- Published in:
- Diabetes, 2006, v. 55, n. 9, p. 2649, doi. 10.2337/db06-0341
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- Publication type:
- Article
Common Variants in Maturity-Onset Diabetes of the Young Genes Contribute to Risk of Type 2 Diabetes in Finns.
- Published in:
- Diabetes, 2006, v. 55, n. 9, p. 2534, doi. 10.2337/db06-0178
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- Publication type:
- Article
Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes.
- Published in:
- 2004
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- Publication type:
- journal article
The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits.
- Published in:
- PLoS Genetics, 2012, v. 8, n. 8, p. 1, doi. 10.1371/journal.pgen.1002793
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- Publication type:
- Article
LocusZoom: regional visualization of genome-wide association scan results.
- Published in:
- Bioinformatics, 2010, v. 26, n. 18, p. 2336, doi. 10.1093/bioinformatics/btq419
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- Publication type:
- Article
Interactions between genetic variation and cellular environment in skeletal muscle gene expression.
- Published in:
- PLoS ONE, 2018, v. 13, n. 4, p. 1, doi. 10.1371/journal.pone.0195788
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- Publication type:
- Article
25-OR: Investigating a Candidate Causal Allele in Type 2 Diabetes Susceptibility Gene PAM as a Cause of Neonatal Diabetes Mellitus.
- Published in:
- Diabetes, 2019, v. 68, p. N.PAG, doi. 10.2337/db19-25-OR
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- Publication type:
- Article
Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 Mutation.
- Published in:
- Diabetes, 2013, v. 62, n. 11, p. 3943, doi. 10.2337/db13-0571
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- Publication type:
- Article