Found: 28
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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
Newly identified loci that influence lipid concentrations and risk of coronary artery disease.
- Published in:
- Nature Genetics, 2008, v. 40, n. 2, p. 161, doi. 10.1038/ng.76
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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
Single-cell transcriptomic profiling of human pancreatic islets reveals genes responsive to glucose exposure over 24 h.
- Published in:
- Diabetologia, 2024, v. 67, n. 10, p. 2246, doi. 10.1007/s00125-024-06214-4
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- Publication type:
- Article
Association Analysis of Genetic Variants with Type 2 Diabetes in a Mongolian Population in China.
- Published in:
- Journal of Diabetes Research, 2015, v. 2015, p. 1, doi. 10.1155/2015/613236
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- Publication type:
- Article
Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences.
- Published in:
- PLoS Genetics, 2020, v. 16, n. 9, p. 1, doi. 10.1371/journal.pgen.1009019
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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
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
The Genome of a Mongolian Individual Reveals the Genetic Imprints of Mongolians on Modern Human Populations.
- Published in:
- Genome Biology & Evolution, 2014, v. 6, n. 12, p. 3122, doi. 10.1093/gbe/evu242
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- Publication type:
- Article
Colocalization of GWAS and eQTL signals at loci with multiple signals identifies additional candidate genes for body fat distribution.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4161, doi. 10.1093/hmg/ddz263
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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
A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14.
- Published in:
- 2004
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- Publication type:
- journal article
Putative Prostate Cancer Risk SNP in an Androgen Receptor-Binding Site of the Melanophilin Gene Illustrates Enrichment of Risk SNPs in Androgen Receptor Target Sites.
- Published in:
- Human Mutation, 2016, v. 37, n. 1, p. 52, doi. 10.1002/humu.22909
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- Publication type:
- Article
Comprehensive Analysis of Pathogenic Deletion Variants in Fanconi Anemia Genes.
- Published in:
- Human Mutation, 2014, v. 35, n. 11, p. 1342, doi. 10.1002/humu.22680
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- Publication type:
- Article
Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 3, p. 535, doi. 10.1093/hmg/ddp522
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- Publication type:
- Article
A Drosophila functional evaluation of candidates from human genome-wide association studies of type 2 diabetes and related metabolic traits identifies tissue-specific roles for dHHEX.
- Published in:
- BMC Genomics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2164-14-136
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- Publication type:
- Article
Bone dysplasia in Hutchinson‐Gilford progeria syndrome is associated with dysregulated differentiation and function of bone cell populations.
- Published in:
- Aging Cell, 2023, v. 22, n. 9, p. 1, doi. 10.1111/acel.13903
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- Publication type:
- Article
Analysis of somatic mutations identifies signs of selection during in vitro aging of primary dermal fibroblasts.
- Published in:
- Aging Cell, 2019, v. 18, n. 6, p. N.PAG, doi. 10.1111/acel.13010
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- Publication type:
- Article
Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18581-8
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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
A Transcription Start Site Map in Human Pancreatic Islets Reveals Functional Regulatory Signatures.
- Published in:
- 2021
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- Publication type:
- journal 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
A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family.
- Published in:
- BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2350-15-34
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- Publication type:
- Article