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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Rare Diseases
Last data update: Apr 18, 2024
. (Total: 63623 Documents since 2012)
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Genetic kidney diseases as an underrecognized cause of chronic kidney disease: the key role of international registry reports.
Torra Roser et al. Clinical kidney journal 2021 14(8) 1879-1885
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Positive renal familial history in IgA nephropathy is associated with worse renal outcomes: a single-center longitudinal study.
Sato Yoshinori et al. BMC nephrology 2021 22(1) 230
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Utility of Genomic Testing after Renal Biopsy.
Murray Susan L et al. American journal of nephrology 2019 Dec 51(1) 43-53
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Prospects of genetic testing for steroid-resistant nephrotic syndrome in Nigerian children: a narrative review of challenges and opportunities.
Anigilaje Emmanuel Ademola et al. International journal of nephrology and renovascular disease 2019 12119-136
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Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.
Mann Nina et al. Journal of the American Society of Nephrology : JASN 2019 Jan
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The genetics and molecular pathogenesis of systemic lupus erythematosus (SLE) in populations of different ancestry.
Goulielmos George N et al. Gene 2018 May
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Prevalence of Fabry disease in dialysis patients: Japan Fabry disease screening study (J-FAST).
Saito Osamu et al. Clin. Exp. Nephrol. 2015 Jul 22.
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The Irish Kidney Gene Project - Prevalence of Family History in Patients with Kidney Disease in Ireland.
Connaughton Dervla M et al. Nephron 2015 Jul 18.
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 18, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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