Found: 54
Select item for more details and to access through your institution.
Genetic variant rs1205 is associated with COVID-19 outcomes: The Strong Heart Study and Strong Heart Family Study.
- Published in:
- PLoS ONE, 2024, v. 19, n. 4, p. 1, doi. 10.1371/journal.pone.0302464
- By:
- Publication type:
- Article
Congenital Leptin Deficiency and Leptin Gene Missense Mutation Found in Two Colombian Sisters with Severe Obesity.
- Published in:
- Genes, 2019, v. 10, n. 5, p. 342, doi. 10.3390/genes10050342
- By:
- Publication type:
- Article
Genetic Variants Related to Cardiometabolic Traits Are Associated to B Cell Function, Insulin Resistance, and Diabetes Among AmeriCan Indians: The Strong Heart Family Study.
- Published in:
- Frontiers in Genetics, 2018, p. N.PAG, doi. 10.3389/fgene.2018.00466
- By:
- Publication type:
- Article
Engineering brown fat into skeletal muscle using ultrasound-targeted microbubble destruction gene delivery in obese Zucker rats: Proof of concept design.
- Published in:
- IUBMB Life, 2017, v. 69, n. 9, p. 745, doi. 10.1002/iub.1658
- By:
- Publication type:
- Article
Exome sequencing reveals novel genetic loci influencing obesity-related traits in Hispanic children.
- Published in:
- 2017
- By:
- Publication type:
- journal article
The genetic basis of the comorbidity between cannabis use and major depression.
- Published in:
- Addiction, 2017, v. 112, n. 1, p. 113, doi. 10.1111/add.13558
- By:
- Publication type:
- Article
Toward Precision Medicine: TBC1D4 Disruption Is Common Among the Inuit and Leads to Underdiagnosis of Type 2 Diabetes.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19.
- Published in:
- BMC Proceedings, 2016, v. 10, p. 71, doi. 10.1186/s12919-016-0008-y
- By:
- Publication type:
- Article
Association of TMTC2 With Human Nonsyndromic Sensorineural Hearing Loss.
- Published in:
- 2016
- By:
- Publication type:
- journal article
GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans.
- Published in:
- BMC Genomics, 2016, v. 17, p. 1, doi. 10.1186/s12864-016-2594-5
- By:
- Publication type:
- Article
Pathway-based analyses.
- Published in:
- BMC Genetics, 2016, v. 17, p. 42, doi. 10.1186/s12863-015-0314-9
- By:
- Publication type:
- Article
Genome- and epigenome-wide association study of hypertriglyceridemic waist in Mexican American families.
- Published in:
- Clinical Epigenetics, 2016, v. 8, p. 1, doi. 10.1186/s13148-016-0173-x
- By:
- Publication type:
- Article
Recurrent Major Depression and Right Hippocampal Volume: A Bivariate Linkage and Association Study.
- Published in:
- Human Brain Mapping, 2016, v. 37, n. 1, p. 191, doi. 10.1002/hbm.23025
- By:
- Publication type:
- Article
Genome-wide significant linkage of schizophrenia-related neuroanatomical trait to 12q24.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 8, p. 678, doi. 10.1002/ajmg.b.32360
- By:
- Publication type:
- Article
Novel epigenetic determinants of type 2 diabetes in Mexican-American families.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 18, p. 5330, doi. 10.1093/hmg/ddv232
- By:
- Publication type:
- Article
New insights from monogenic diabetes for "common" type 2 diabetes.
- Published in:
- Frontiers in Genetics, 2015, p. 1, doi. 10.3389/fgene.2015.00251
- By:
- Publication type:
- Article
Successful pharmaceutical-grade streptozotocin ( STZ)-induced hyperglycemia in a conscious tethered baboon ( Papio hamadryas) model.
- Published in:
- Journal of Medical Primatology, 2015, v. 44, n. 4, p. 202, doi. 10.1111/jmp.12182
- By:
- Publication type:
- Article
Shared Genetic Factors Influence Amygdala Volumes and Risk for Alcoholism.
- Published in:
- Neuropsychopharmacology, 2015, v. 40, n. 2, p. 412, doi. 10.1038/npp.2014.187
- By:
- Publication type:
- Article
Replication of obesity and diabetes-related SNP associations in individuals from Yucatán, México.
- Published in:
- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00380
- By:
- Publication type:
- Article
Genome-Wide Genetic and Transcriptomic Investigation of Variation in Antibody Response to Dietary Antigens.
- Published in:
- Genetic Epidemiology, 2014, v. 38, n. 5, p. 439, doi. 10.1002/gepi.21817
- By:
- Publication type:
- Article
A variance component-based gene burden test.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S49
- By:
- Publication type:
- Article
Evaluation of estimated genetic values and their application to genome-wide investigation of systolic blood pressure.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S66
- By:
- Publication type:
- Article
Novel QTL at chromosome 6p22 for alcohol consumption: Implications for the genetic liability of alcohol use disorders.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 4, p. 294, doi. 10.1002/ajmg.b.32231
- By:
- Publication type:
- Article
Gene-by-age effects on BMI from birth to adulthood: The fels longitudinal study.
- Published in:
- Obesity (19307381), 2014, v. 22, n. 3, p. 875, doi. 10.1002/oby.20517
- By:
- Publication type:
- Article
Genome-wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 84, doi. 10.1002/ajmg.b.32211
- By:
- Publication type:
- Article
Sulcal Depth-Position Profile Is a Genetically Mediated Neuroscientific Trait: Description and Characterization in the Central Sulcus.
- Published in:
- Journal of Neuroscience, 2013, v. 33, n. 39, p. 15618, doi. 10.1523/JNEUROSCI.1616-13.2013
- By:
- Publication type:
- Article
Identification of Pleiotropic Genetic Effects on Obesity and Brain Anatomy.
- Published in:
- Human Heredity, 2013, v. 75, n. 2-4, p. 136, doi. 10.1159/000353953
- By:
- Publication type:
- Article
A comprehensive analysis of adiponectin QTLs using SNP association, SNP cis-effects on peripheral blood gene expression and gene expression correlation identified novel metabolic syndrome (MetS) genes with potential role in carcinogenesis and systemic inflammation
- Published in:
- BMC Medical Genomics, 2013, v. 6, n. 1, p. 1, doi. 10.1186/1755-8794-6-14
- By:
- Publication type:
- Article
Fatty acid binding protein 3 (fabp3) is associated with insulin, lipids and cardiovascular phenotypes of the metabolic syndrome through epigenetic modifications in a northern european family population.
- Published in:
- BMC Medical Genomics, 2013, v. 6, n. 1, p. 1, doi. 10.1186/1755-8794-6-9
- By:
- Publication type:
- Article
A Genome-Wide Integrative Genomic Study Localizes Genetic Factors Influencing Antibodies against Epstein-Barr Virus Nuclear Antigen 1 (EBNA-1)
- Published in:
- PLoS Genetics, 2013, v. 9, n. 1, p. 1, doi. 10.1371/journal.pgen.1003147
- By:
- Publication type:
- Article
Genome-Wide Association Scan Identifies a Risk Locus for Preeclampsia on 2q14, Near the Inhibin, Beta B Gene.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0033666
- By:
- Publication type:
- Article
Rare variants, common markers: synthetic association and beyond.
- Published in:
- Genetic Epidemiology, 2011, v. 35, p. S80, doi. 10.1002/gepi.20655
- By:
- Publication type:
- Article
Short Report : Evidence for Genetic Susceptibility to Developing Early Childhood Diarrhea among Shantytown Children Living in Northeastern Brazil.
- Published in:
- American Journal of Tropical Medicine & Hygiene, 2011, v. 85, n. 5, p. 893, doi. 10.4269/ajtmh.2011.11-0159
- By:
- Publication type:
- Article
Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.
- Published in:
- Nature Genetics, 2011, v. 43, n. 6, p. 539, doi. 10.1038/ng.838
- By:
- Publication type:
- Article
Genetic Analysis Workshop 17 mini-exome simulation.
- Published in:
- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S2
- By:
- Publication type:
- Article
Do rare variant genotypes predict common variant genotypes?
- Published in:
- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S87
- By:
- Publication type:
- Article
Genetic signal maximization using environmental regression.
- Published in:
- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S72
- By:
- Publication type:
- Article
Bivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family Study.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 18, p. 3662, doi. 10.1093/hmg/ddq274
- By:
- Publication type:
- Article
Transcriptomic epidemiology of smoking: the effect of smoking on gene expression in lymphocytes.
- Published in:
- BMC Medical Genomics, 2010, v. 3, p. 29, doi. 10.1186/1755-8794-3-29
- By:
- Publication type:
- Article
Quantitative Trait Nucleotide Analysis Using Bayesian Model Selection.
- Published in:
- Human Biology, 2009, v. 81, n. 5/6, p. 829, doi. 10.3378/027.081.0625
- By:
- Publication type:
- Article
Genetic Analysis Workshop 16: Strategies for genome-wide association study analyses.
- Published in:
- BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S1
- By:
- Publication type:
- Article
Genome-wide discovery of maternal effect variants.
- Published in:
- BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S19
- By:
- Publication type:
- Article
Analysis of multiple phenotypes.
- Published in:
- Genetic Epidemiology, 2009, v. 33, n. S1, p. S33, doi. 10.1002/gepi.20470
- By:
- Publication type:
- Article
Prevalence and Heritability of Clusters for Diagnostic Components of Metabolic Syndrome: The Oman Family Study.
- Published in:
- Metabolic Syndrome & Related Disorders, 2008, v. 6, n. 2, p. 129, doi. 10.1089/met.2007.0039
- By:
- Publication type:
- Article
Genetic determinants of mitochondrial content.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 12, p. 1504, doi. 10.1093/hmg/ddm101
- By:
- Publication type:
- Article
Do We Have to Increase Sensibility of Metabolic Syndrome Components? The Oman Family Study.
- Published in:
- Diabetes, 2007, v. 56, p. A266
- By:
- Publication type:
- Article
Type I error rates in association versus joint linkage/association tests in related individuals.
- Published in:
- Genetic Epidemiology, 2007, v. 31, n. 2, p. 173, doi. 10.1002/gepi.20200
- By:
- Publication type:
- Article
Heritability and Genetic Correlations of Metabolic Disease-Related Phenotypes in Mexico: Preliminary Report from the GEMM Family Study.
- Published in:
- Human Biology, 2007, v. 79, n. 1, p. 121, doi. 10.1353/hub.2007.0021
- By:
- Publication type:
- Article
Estimating the additive genetic effect of the X chromosome.
- Published in:
- Genetic Epidemiology, 2005, v. 29, n. 4, p. 377, doi. 10.1002/gepi.20093
- By:
- Publication type:
- Article
Quantitative Trait Nucleotide Analysis Using Bayesian Model Selection.
- Published in:
- Human Biology, 2005, v. 77, n. 5, p. 541, doi. 10.1353/hub.2006.0003
- By:
- Publication type:
- Article