Found: 34
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Metabolomics insights into early type 2 diabetes pathogenesis and detection in individuals with normal fasting glucose.
- Published in:
- Diabetologia, 2018, v. 61, n. 6, p. 1315, doi. 10.1007/s00125-018-4599-x
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- Article
Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37691-7
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- Publication type:
- Article
The Musculoskeletal Knowledge Portal: Making Omics Data Useful to the Broader Scientific Community.
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- Journal of Bone & Mineral Research, 2020, v. 35, n. 9, p. 1626, doi. 10.1002/jbmr.4147
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- Article
A null mutation in does not ANGPTL8 associate with either plasma glucose or type 2 diabetes in humans.
- Published in:
- BMC Endocrine Disorders, 2016, v. 16, p. 1, doi. 10.1186/s12902-016-0088-8
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- Publication type:
- Article
Integrating evolutionary and regulatory information with multispecies approach implicates genes and pathways in obsessive-compulsive disorder.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00831-x
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- Publication type:
- Article
Association of a Low-Frequency Variant in HNF1A With Type 2 Diabetes in a Latino Population.
- Published in:
- JAMA: Journal of the American Medical Association, 2014, v. 311, n. 22, p. 2305, doi. 10.1001/jama.2014.6511
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- Article
Erratum. The First Genome-Wide Association Study for Type 2 Diabetes in Youth: The Progress in Diabetes Genetics in Youth (ProDiGY) Consortium. Diabetes 2021;70:996-1005.
- Published in:
- 2022
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- Publication type:
- journal article
23-OR: ADA Presidents' Select Abstract: Genetic Architecture and Novel Genes Implicated in Youth-Onset Type 2 Diabetes.
- Published in:
- Diabetes, 2021, v. 70, p. N.PAG, doi. 10.2337/db21-23-OR
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- Publication type:
- Article
The First Genome-Wide Association Study for Type 2 Diabetes in Youth: The Progress in Diabetes Genetics in Youth (ProDiGY) Consortium.
- Published in:
- 2021
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- Publication type:
- journal article
241-OR: Causal Gene Candidates for Type 2 Diabetes Based on Protein-Coding Variants in 127,676 Individuals.
- Published in:
- Diabetes, 2020, v. 69, p. N.PAG, doi. 10.2337/db20-241-OR
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- Publication type:
- Article
177-OR: Genome-Wide Association Study of Lipid Traits in Youth with Type 2 Diabetes: The ProDiGY (Progress in Diabetes Genetics in Youth) Consortium.
- Published in:
- Diabetes, 2019, v. 68, p. N.PAG, doi. 10.2337/db19-177-OR
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- Publication type:
- Article
A Low-Frequency Inactivating Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.
- Published in:
- 2017
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- Publication type:
- journal article
Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population.
- Published in:
- 2017
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- Publication type:
- journal article
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.
- Published in:
- Nature Genetics, 2014, v. 46, n. 4, p. 357, doi. 10.1038/ng.2915
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- Article
Evaluating empirical bounds on complex disease genetic architecture.
- Published in:
- Nature Genetics, 2013, v. 45, n. 12, p. 1418, doi. 10.1038/ng.2804
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- Publication type:
- Article
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes.
- Published in:
- Nature Genetics, 2013, v. 45, n. 11, p. 1380, doi. 10.1038/ng.2794
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- Publication type:
- Article
The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease.
- Published in:
- PLoS Genetics, 2015, v. 11, n. 4, p. 1, doi. 10.1371/journal.pgen.1005165
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- Publication type:
- Article
Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus.
- Published in:
- PLoS Genetics, 2015, v. 11, n. 1, p. 1, doi. 10.1371/journal.pgen.1004876
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- Publication type:
- Article
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 7, p. 1, doi. 10.1371/journal.pgen.1004494
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- Publication type:
- Article
Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls.
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- PLoS Genetics, 2013, v. 9, n. 4, p. 1, doi. 10.1371/journal.pgen.1003443
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- Publication type:
- Article
Genetic and Computational Identification of a Conserved Bacterial Metabolic Module.
- Published in:
- PLoS Genetics, 2008, v. 4, n. 12, p. 1, doi. 10.1371/journal.pgen.1000310
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- Publication type:
- Article
Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: A soft clustering analysis.
- Published in:
- 2018
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- Publication type:
- journal article
Current progress in network research: toward reference networks for key model organisms.
- Published in:
- Briefings in Bioinformatics, 2007, v. 8, n. 5, p. 318, doi. 10.1093/bib/bbm038
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- Publication type:
- Article
Efficiency and Power as a Function of Sequence Coverage, SNP Array Density, and Imputation.
- Published in:
- PLoS Computational Biology, 2012, v. 8, n. 7, p. 1, doi. 10.1371/journal.pcbi.1002604
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- Publication type:
- Article
A universal carrier test for the long tail of Mendelian disease.
- Published in:
- Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2010, v. 21, n. 4, p. 537, doi. 10.1016/j.rbmo.2010.05.012
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- Publication type:
- Article
An effector index to predict target genes at GWAS loci.
- Published in:
- Human Genetics, 2022, v. 141, n. 8, p. 1431, doi. 10.1007/s00439-022-02434-z
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- Publication type:
- Article
Rare loss of function variants in the hepatokine gene INHBE protect from abdominal obesity.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31757-8
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- Publication type:
- Article
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease.
- Published in:
- Science Translational Medicine, 2015, v. 7, n. 270, p. 1, doi. 10.1126/scitranslmed.3010134
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- Article
The Contribution of Low-Frequency and Rare Coding Variation to Susceptibility to Type 2 Diabetes.
- Published in:
- 2019
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- Publication type:
- journal article
Leveraging type 1 diabetes human genetic and genomic data in the T1D knowledge portal.
- Published in:
- PLoS Biology, 2023, v. 21, n. 9, p. 1, doi. 10.1371/journal.pbio.3002233
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- Publication type:
- Article
Genome-wide Association Study of Lipid Traits in Youth With Type 2 Diabetes.
- Published in:
- Journal of the Endocrine Society, 2021, v. 5, n. 11, p. 1, doi. 10.1210/jendso/bvab139
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- Article
Using multiple alignments to improve seeded local alignment algorithms.
- Published in:
- Nucleic Acids Research, 2005, v. 33, n. 14, p. 4563, doi. 10.1093/nar/gki767
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- Publication type:
- Article
Ancestry-specific high-risk gene variant profiling unmasks diabetes-associated genes.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 8, p. 655, doi. 10.1093/hmg/ddac255
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- Publication type:
- Article
Monogenic Diabetes in Youth With Presumed Type 2 Diabetes: Results From the Progress in Diabetes Genetics in Youth (ProDiGY) Collaboration.
- Published in:
- 2021
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- Publication type:
- journal article