Genetics of Chronic Kidney Disease in Low-Resource Settings.
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A. Sinha | R. Gbadegesin | A. Solarin | T. Ilori | K. Ng | Andréia Watanabe
[1] A. Köttgen,et al. Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. , 2022, Kidney international.
[2] Alicia R. Martin,et al. Diversity in Genomic Studies: A Roadmap to Address the Imbalance , 2022, Nature Medicine.
[3] P. Tan,et al. Multicenter study on the genetics of glomerular diseases among southeast and south Asians: Deciphering Diversities ‐ Renal Asian Genetics Network (DRAGoN) , 2022, Clinical genetics.
[4] M. Woodward,et al. Prevalence of chronic kidney disease in Asia: a systematic review and analysis , 2022, BMJ Global Health.
[5] Max W. Y. Lam,et al. Improving Polygenic Prediction in Ancestrally Diverse Populations , 2021, Nature Genetics.
[6] P. Yenchitsomanus,et al. Association between intelectin-1 variation and human kidney stone disease in northeastern Thai population , 2021, Urolithiasis.
[7] A. Sinha,et al. Next-Generation Sequencing for Congenital Nephrotic Syndrome: A Multi-Center Cross-Sectional Study from India , 2021, Indian Pediatrics.
[8] L. Onuchic,et al. APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal segmental glomerulosclerosis and other diagnoses , 2021, Pediatric Nephrology.
[9] N. Powe,et al. Race and Genetic Ancestry in Medicine - A Time for Reckoning with Racism. , 2021, The New England journal of medicine.
[10] D. Adu,et al. Overview of The Human Heredity and Health in Africa Kidney Disease Research Network (H3A-KDRN). , 2020, Kidney360.
[11] C. Khor,et al. Genome-Wide Meta-Analysis Identifies Three Novel Susceptibility Loci and Reveals Ethnic Heterogeneity of Genetic Susceptibility for IgA Nephropathy. , 2020, Journal of the American Society of Nephrology : JASN.
[12] S. Sengupta,et al. Frequency spectrum of rare and clinically relevant markers in multiethnic Indian populations (ClinIndb): A resource for genomic medicine in India , 2020, Human mutation.
[13] D. Goldstein,et al. Rare genetic causes of complex kidney and urological diseases , 2020, Nature Reviews Nephrology.
[14] Deepa Bhat,et al. Comprehensive Rare Disease Care model for screening and diagnosis of rare genetic diseases - an experience of private medical college and hospital, South India. , 2020, Intractable & rare diseases research.
[15] A. Morris,et al. Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans , 2020, bioRxiv.
[16] L. A. Teixeira,et al. New problems of a new health system: the creation of a national public policy of rare diseases care in Brazil (1990s-2010s). , 2020, Salud colectiva.
[17] L. G. Vu,et al. Global, regional, and national burden of chronic kidney disease, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017 , 2020, The Lancet.
[18] S. Marie,et al. Brazilian Network of Pediatric Nephrotic Syndrome (REBRASNI) , 2019, Kidney international reports.
[19] Ryan L. Collins,et al. The mutational constraint spectrum quantified from variation in 141,456 humans , 2020, Nature.
[20] Markus S. Schröder,et al. The GenomeAsia 100K Project enables genetic discoveries across Asia , 2019, Nature.
[21] C. Langefeld,et al. Effect of a Single Apolipoprotein L1 Gene Nephropathy Variant on the Risk of Advanced Lupus Nephritis in Brazilians , 2019, The Journal of Rheumatology.
[22] Max W. Y. Lam,et al. Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations , 2019, Cell.
[23] V. R. Rajendran,et al. Genomics of rare genetic diseases—experiences from India , 2019, Human Genomics.
[24] Karsten B. Sieber,et al. A catalog of genetic loci associated with kidney function from analyses of a million individuals , 2019, Nature Genetics.
[25] C. Jayasumana. Chronic Interstitial Nephritis in Agricultural Communities (CINAC) in Sri Lanka. , 2019, Seminars in nephrology.
[26] Alicia R. Martin,et al. Clinical use of current polygenic risk scores may exacerbate health disparities , 2019, Nature Genetics.
[27] Cristian Riella,et al. APOL1-Associated Kidney Disease in Brazil , 2019, Kidney international reports.
[28] Jitender Saini,et al. INDEX-db: The Indian Exome Reference Database (Phase I) , 2019, J. Comput. Biol..
[29] L. Hindorff,et al. Defining and Achieving Health Equity in Genomic Medicine. , 2019, Ethnicity & disease.
[30] M. Mills,et al. A scientometric review of genome-wide association studies , 2019, Communications Biology.
[31] James M. Eales,et al. Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies , 2019, Nature Communications.
[32] A. Kengne,et al. An African perspective on the genetic risk of chronic kidney disease: a systematic review , 2018, BMC Medical Genetics.
[33] Ankit Verma,et al. SAGE: a comprehensive resource of genetic variants integrating South Asian whole genomes and exomes , 2018, Database J. Biol. Databases Curation.
[34] A. Mokdad,et al. Analysis of the Global Burden of Disease study highlights the global, regional, and national trends of chronic kidney disease epidemiology from 1990 to 2016. , 2018, Kidney international.
[35] F. Schaefer,et al. Exploring the Clinical and Genetic Spectrum of Steroid Resistant Nephrotic Syndrome: The PodoNet Registry , 2018, Front. Pediatr..
[36] B. Jaar,et al. Burden of chronic kidney disease on the African continent: a systematic review and meta-analysis , 2018, BMC Nephrology.
[37] S. Mane,et al. Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome. , 2018, Clinical journal of the American Society of Nephrology : CJASN.
[38] J. Pesquero,et al. Targeted Next-Generation Sequencing in Brazilian Children With Nephrotic Syndrome Submitted to Renal Transplant , 2017, Transplantation.
[39] K. Girisha,et al. India Allele Finder: a web-based annotation tool for identifying common alleles in next-generation sequencing data of Indian origin , 2017, BMC Research Notes.
[40] Christopher R. Gignoux,et al. Human demographic history impacts genetic risk prediction across diverse populations , 2016, bioRxiv.
[41] Kathleen F. Kerr,et al. African Ancestry-Specific Alleles and Kidney Disease Risk in Hispanics/Latinos. , 2017, Journal of the American Society of Nephrology : JASN.
[42] P. Kimmel,et al. Genomic approaches to the burden of kidney disease in Sub-Saharan Africa: the Human Heredity and Health in Africa (H3Africa) Kidney Disease Research Network. , 2016, Kidney international.
[43] D. Friedman,et al. Apolipoprotein L1 and Kidney Disease in African Americans , 2016, Trends in Endocrinology & Metabolism.
[44] P. Kimmel,et al. Human Heredity and Health (H3) in Africa Kidney Disease Research Network: A Focus on Methods in Sub-Saharan Africa. , 2015, Clinical journal of the American Society of Nephrology : CJASN.
[45] A. Adeyemo,et al. HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome. , 2015, Journal of the American Society of Nephrology : JASN.
[46] S. Chew,et al. Identification of new susceptibility loci for IgA nephropathy in Han Chinese , 2015, Nature Communications.
[47] Andrew D. Moran. South Asia. , 2021, Global heart.
[48] Tesfaye B Mersha,et al. Self-reported race/ethnicity in the age of genomic research: its potential impact on understanding health disparities , 2015, Human Genomics.
[49] Murim Choi,et al. Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens , 2014, Nature Genetics.
[50] M. McCarthy,et al. Research Capacity: Enabling African Scientists to Engage Fully in the Genomic Revolution , 2014 .
[51] C. Rotimi,et al. Evolution of the primate trypanolytic factor APOL1 , 2014, Proceedings of the National Academy of Sciences.
[52] S. Naicker,et al. The epidemiology of chronic kidney disease in sub-Saharan Africa: a systematic review and meta-analysis. , 2014, The Lancet. Global health.
[53] R. Yamada,et al. An Integrative Study of the Genetic, Social and Environmental Determinants of Chronic Kidney Disease Characterized by Tubulointerstitial Damages in the North Central Region of Sri Lanka , 2014, Journal of occupational health.
[54] F. Salzano,et al. Interethnic admixture and the evolution of Latin American populations , 2013, Genetics and molecular biology.
[55] D. Friedman,et al. Genetics of kidney failure and the evolving story of APOL1. , 2011, The Journal of clinical investigation.
[56] Francisco M. De La Vega,et al. Genomics for the world , 2011, Nature.
[57] M. Hutz,et al. The Genomic Ancestry of Individuals from Different Geographical Regions of Brazil Is More Uniform Than Expected , 2011, PloS one.
[58] Anirban Dutta,et al. Indian genetic disease database , 2010, Nucleic Acids Res..
[59] Debasis Dash,et al. IGVBrowser–a genomic variation resource from diverse Indian populations , 2010, Database J. Biol. Databases Curation.
[60] C. Winkler,et al. The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans. , 2010, Journal of the American Society of Nephrology : JASN.
[61] C. Winkler,et al. Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans , 2010, Science.
[62] F. Hildebrandt. Genetic kidney diseases , 2010, The Lancet.
[63] P. Majumder. The Human Genetic History of South Asia , 2010, Current Biology.
[64] Jin Ok Yang,et al. Mapping Human Genetic Diversity in Asia , 2009, Science.
[65] Eduardo Barrientos,et al. Analysis of genomic diversity in Mexican Mestizo populations to develop genomic medicine in Mexico , 2009, Proceedings of the National Academy of Sciences.
[66] C. Chan,et al. Parallel genotyping of 10,204 single nucleotide polymorphisms to screen for susceptible genes for IgA nephropathy. , 2000, Annals of the Academy of Medicine, Singapore.
[67] D. Vlahov,et al. MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis , 2008, Nature Genetics.
[68] D. Reich,et al. MYH9 is associated with nondiabetic end-stage renal disease in African Americans , 2008, Nature Genetics.
[69] R. Brasseur,et al. Apolipoprotein L-I is the trypanosome lytic factor of human serum , 2003, Nature.
[70] M. Tanner,et al. Band 3 mutations, distal renal tubular acidosis, and Southeast Asian ovalocytosis. , 2002, Kidney international.
[71] B. Kiberd,et al. Cumulative risk for developing end-stage renal disease in the US population. , 2002, Journal of the American Society of Nephrology : JASN.
[72] International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome , 2001, Nature.
[73] L. Vanhamme,et al. A VSG Expression Site–Associated Gene Confers Resistance to Human Serum in Trypanosoma rhodesiense , 1998, Cell.
[74] P. Jarolim,et al. Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosis. , 1991, Proceedings of the National Academy of Sciences of the United States of America.