The Autosomal Short Tandem Repeat Polymorphisms Are Potentially Associated with Cardiovascular Disease Predisposition in the Latin American Population: A Mini Review
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P. Guevara-Ramírez | Santiago Cadena-Ullauri | V. Ruiz-Pozo | Rafael Tamayo-Trujillo | E. Paz-Cruz | Adriana Alexandra Ibarra-Rodríguez | A. Zambrano | Nieves Doménech | Aníbal Gaviria
[1] N. Domenech,et al. Genomic analysis of a novel pathogenic variant in the gene LMNA associated with cardiac laminopathies found in Ecuadorian siblings: A case report , 2023, Frontiers in Cardiovascular Medicine.
[2] N. Domenech,et al. Case report: Genomic screening for inherited cardiac conditions in Ecuadorian mestizo relatives: Improving familial diagnose , 2022, Frontiers in Cardiovascular Medicine.
[3] Suli Huang,et al. Epigenetic regulation in cardiovascular disease: mechanisms and advances in clinical trials , 2022, Signal Transduction and Targeted Therapy.
[4] A. Wielgosz,et al. Equity and Prevention of Cardiovascular Diseases in Latin America and the Caribbean , 2022, Global heart.
[5] T. Romgaew,et al. Allele frequencies of 15 autosomal STR loci among 540 Myanmarese individuals in Thailand , 2022, Forensic Science International: Reports.
[6] D. Mäusezahl,et al. Cardiovascular Disease in the Peruvian Andes: Local Perceptions, Barriers, and Paths to Preventing Chronic Diseases in the Cajamarca Region , 2021, International Journal of Public Health.
[7] M. O’Flaherty,et al. Coronary heart disease and stroke mortality trends in Brazil 2000–2018 , 2021, PloS one.
[8] M. Zieger,et al. Expanding the Swiss autosomal marker set to 32 STRs , 2021, International Journal of Legal Medicine.
[9] D. Rodriguez,et al. Understanding inequities in health and health systems in Latin America and the Caribbean: a thematic series , 2021, International Journal for Equity in Health.
[10] J. Hubacek,et al. Genetics of Cardiovascular Disease: How Far Are We from Personalized CVD Risk Prediction and Management? , 2021, International journal of molecular sciences.
[11] M. Barash,et al. Forensic Autosomal Short Tandem Repeats and Their Potential Association With Phenotype , 2020, Frontiers in Genetics.
[12] D. Panagiotakos,et al. Diet and Cardiovascular Disease Risk Among Individuals with Familial Hypercholesterolemia: Systematic Review and Meta-Analysis , 2020, Nutrients.
[13] G. Chambers,et al. Population dataset for 21 simple tandem repeat loci in the Akan population of Ghana , 2020, Data in brief.
[14] C. Dávila-Cervantes. Cardiovascular disease in Mexico 1990–2017: secondary data analysis from the global burden of disease study , 2020, International Journal of Public Health.
[15] R. Brook,et al. Environmental determinants of cardiovascular disease: lessons learned from air pollution , 2020, Nature Reviews Cardiology.
[16] GART Gene , 2020, Definitions.
[17] W. Cui,et al. Population genetic data from 23 autosomal STR loci of Huaxia Platinum system in the Jining Han population , 2020, Molecular genetics & genomic medicine.
[18] C. Aguilar-Salinas,et al. Reducing the Clinical and Public Health Burden of Familial Hypercholesterolemia: A Global Call to Action. , 2020, JAMA cardiology.
[19] J. Danesh,et al. Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases , 2019, Nature Metabolism.
[20] Michael S. Yu,et al. Model System Identification of Novel Congenital Heart Disease Gene Candidates: focus on RPL13. , 2019, Human molecular genetics.
[21] R. Diaz,et al. Current Status and Future Strategies for Cardiovascular Disease in Argentina. , 2019, Circulation.
[22] R. Nieto-Martínez,et al. Cardiovascular Health in a National Sample of Venezuelan Subjects Assessed According to the AHA Score: The EVESCAM. , 2019, Global heart.
[23] C. Aguilar-Salinas,et al. Attributable Burden and Expenditure of Cardiovascular Diseases and Associated Risk Factors in Mexico and other Selected Mega-Countries , 2019, International journal of environmental research and public health.
[24] Carlos D. Neyra,et al. Allele frequencies of 21 autosomal STR markers in a mixed race Peruvian population applied to forensic practice , 2019, Spanish Journal of Legal Medicine.
[25] Edgardo Delgado,et al. Frecuencias alélicas de 21 marcadores STR autosómicos en una población mestiza peruana aplicado a la práctica forense , 2019, Revista Española de Medicina Legal.
[26] A. López-Cortés,et al. The three-hybrid genetic composition of an Ecuadorian population using AIMs-InDels compared with autosomes, mitochondrial DNA and Y chromosome data , 2019, Scientific Reports.
[27] Andrew B. Conley,et al. Genetic ancestry, admixture and health determinants in Latin America , 2018, BMC Genomics.
[28] L. Monserrat,et al. Differential diagnosis of thickened myocardium: an illustrative MRI review , 2018, Insights into Imaging.
[29] Li Jin,et al. Application of Causal Inference to Genomic Analysis: Advances in Methodology , 2018, Front. Genet..
[30] P. Rastogi,et al. Hypothyroidism-induced reversible dilated cardiomyopathy , 2018, Journal of postgraduate medicine.
[31] Jeroen J. Bax,et al. European Society of Cardiology: Cardiovascular Disease Statistics 2017. , 2018, European heart journal.
[32] David Heckerman,et al. Profiling of Short-Tandem-Repeat Disease Alleles in 12,632 Human Whole Genomes , 2017, American journal of human genetics.
[33] G. Limongelli,et al. The Role of von Willebrand Factor in Vascular Inflammation: From Pathogenesis to Targeted Therapy , 2017, Mediators of inflammation.
[34] Jifeng Cai,et al. Genetic polymorphism of 29 STR loci in the Hunan Han population from China , 2017, Forensic sciences research.
[35] Benedicto Cuervo Alvarez. LA CONQUISTA Y COLONIZACIÓN ESPAÑOLA DE AMÉRICA. , 2016 .
[36] A. Rodday,et al. Prevalence of Familial Hypercholesterolemia in the 1999 to 2012 United States National Health and Nutrition Examination Surveys (NHANES) , 2016, Circulation.
[37] R. Ofori-Asenso,et al. Cardiovascular diseases in Ghana within the context of globalization. , 2016, Cardiovascular diagnosis and therapy.
[38] Edna M Gamboa Delgado,et al. Cardiovascular Risk and Its Associated Factors in Health Care Workers in Colombia: A Study Protocol , 2015, JMIR research protocols.
[39] Paul Medvedev,et al. Accurate typing of short tandem repeats from genome-wide sequencing data and its applications , 2015, Genome research.
[40] C. Haas,et al. Tyrosine Hydroxylase TH01 9.3 Allele in the Occurrence of Sudden Infant Death Syndrome in Swiss Caucasians , 2014, Journal of forensic sciences.
[41] Lanas Fernando,et al. Cardiovascular disease in Latin America: the growing epidemic. , 2014, Progress in cardiovascular diseases.
[42] A. Majluf-Cruz,et al. Association of vWA and TPOX Polymorphisms with Venous Thrombosis in Mexican Mestizos , 2014, BioMed research international.
[43] Yaniv Erlich,et al. The landscape of human STR variation , 2014, bioRxiv.
[44] C. Gehrig,et al. Allelic proportions of 16 STR loci—including the new European Standard Set (ESS) loci—in a Swiss population sample , 2014, International Journal of Legal Medicine.
[45] E. Boerwinkle,et al. Possible Race and Gender Divergence in Association of Genetic Variations with Plasma von Willebrand Factor: A Study of ARIC and 1000 Genome Cohorts , 2014, PloS one.
[46] D. Srivastava,et al. Genetics of Human Cardiovascular Disease , 2012, Cell.
[47] W. Manning,et al. Hypothyroid cardiomyopathy: a reversible form of systolic heart failure. , 2011, The American journal of medicine.
[48] C. Stefanadis,et al. Fibrinogen and cardiovascular disease: genetics and biomarkers. , 2011, Blood reviews.
[49] D. Davalos,et al. Fibrinogen as a key regulator of inflammation in disease , 2011, Seminars in Immunopathology.
[50] L. Hui,et al. Novel association analysis between 9 short tandem repeat loci polymorphisms and coronary heart disease based on a cross-validation design. , 2011, Atherosclerosis.
[51] R. Deka,et al. Autosomal short tandem repeat genetic variation of the Basques in Spain , 2011, Croatian medical journal.
[52] C. Courts,et al. Significant Association of TH01 Allele 9.3 and SIDS , 2011, Journal of forensic sciences.
[53] S. E. D. dos Santos,et al. Allelic frequencies and statistical data obtained from 12 codis STR loci in an admixed population of the Brazilian Amazon , 2011, Genetics and molecular biology.
[54] M. Hutz,et al. The Genomic Ancestry of Individuals from Different Geographical Regions of Brazil Is More Uniform Than Expected , 2011, PloS one.
[55] E. Fliers,et al. Increasing levels of free thyroxine as a risk factor for a first venous thrombosis: a case-control study. , 2010, Blood.
[56] D. O'Connor,et al. Human Tyrosine Hydroxylase Natural Genetic Variation: Delineation of Functional Transcriptional Control Motifs Disrupted in the Proximal Promoter , 2010, Circulation. Cardiovascular genetics.
[57] P. Gregersen,et al. Accounting for ancestry: population substructure and genome-wide association studies. , 2008, Human molecular genetics.
[58] Ó. García,et al. Population genetic data for 15 STR loci (Identifiler kit) in Bolivia. , 2008, Legal medicine.
[59] C. Ladenvall,et al. Fibrinogen gene variation and ischemic stroke , 2008, Journal of thrombosis and haemostasis : JTH.
[60] J. Lau,et al. Angiotensin-converting enzyme insertion/deletion gene polymorphic variant as a marker of coronary artery disease: a meta-analysis. , 2008, Archives of internal medicine.
[61] T. Yasuda,et al. Allele frequencies for 15 STR loci in Ovambo population using AmpFlSTR Identifiler Kit. , 2008, Legal medicine.
[62] D. Grobbee,et al. Peroxisome proliferator-activated receptor gamma-2 P12A polymorphism and risk of acute myocardial infarction, coronary heart disease and ischemic stroke: A case-cohort study and meta-analyses , 2008, Vascular health and risk management.
[63] P. Schneider,et al. Forensic STRs as potential disease markers: a study of VWA and von Willebrand's Disease. , 2007, Forensic science international. Genetics.
[64] D. Corach,et al. Population genetic analysis of 15 autosomal STRs loci in the central region of Argentina. , 2006, Forensic science international.
[65] L. Borjas,et al. Genetic variation of 15 STR autosomal loci in the Maracaibo population from Venezuela. , 2006, Forensic science international.
[66] J. Butler,et al. Genetics and Genomics of Core Short Tandem Repeat Loci Used in Human Identity Testing , 2006, Journal of forensic sciences.
[67] L. Hsu,et al. Functional polymorphisms of FGA, encoding α fibrinogen, are associated with susceptibility to venous thromboembolism in a Taiwanese population , 2006, Human Genetics.
[68] H. Rangel-Villalobos,et al. STR data for 15 loci in a population sample from the central region of Mexico. , 2005, Forensic science international.
[69] R. Almarza,et al. Genetic data for six STR loci in Valparaiso population (Chile). , 2005, Journal of forensic sciences.
[70] M. Klintschar,et al. TH01, a Tetrameric Short Tandem Repeat Locus in the Tyrosine Hydroxylase Gene: Association with Myocardial Hypertrophy and Death from Myocardial Infarction? , 2005, Disease markers.
[71] Á. Carracedo,et al. Erratum to ¿Analysis of the CODIS autosomal STR loci in four main Colombian regions¿ [Forensic Sci. Int. 137 (2003) 67¿73] , 2004 .
[72] E. Nevo,et al. Microsatellites within genes: structure, function, and evolution. , 2004, Molecular biology and evolution.
[73] J. Gardin,et al. Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults. , 1995, Circulation.
[74] Tsippi Iny Stein,et al. The GeneCards Suite , 2021, Practical Guide to Life Science Databases.
[75] W. Ageno,et al. Increasing levels of free thyroxine as a risk factor for a first venous thrombosis : a case-control study , 2017 .
[76] J. Builes,et al. Twenty two autosomal microsatellite data from Ecuador (Powerplex Fusion) , 2013 .
[77] Islas Canarias. Allele frequency distribution of cofiler STRs in a Canary Islands population (Spain) , 2003 .
[78] John M. Butler,et al. STRBase: a short tandem repeat DNA database for the human identity testing community , 2001, Nucleic Acids Res..
[79] International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome , 2001, Nature.
[80] A. Sajantila,et al. Population Genetic Comparisons among Eight Populations using Allele Frequency and Sequence Data from Three Microsatellite Loci , 1996, European journal of human genetics : EJHG.
[81] G. Burch. [Cardiovascular diseases]. , 1956, Revista medica cubana.