Literature DB >> 26050126

Diagnosing kidney disease in the genetic era.

Sindhuri Prakash1, Ali G Gharavi.   

Abstract

PURPOSE OF REVIEW: Recent technological improvements have increased the use of genetic testing in the clinic. This review serves to summarize the many practical benefits of genetic testing, discusses various methodologies that can be used clinically, and exemplifies ways in which genetics is propelling the field forward in nephrology. RECENT
FINDINGS: The advent of next-generation sequencing and microarray technologies has heralded an unprecedented number of discoveries in the field of nephrology, providing many opportunities for incorporating genomic diagnostics into clinical care. The use of genetic testing, particularly in pediatrics, can provide accurate diagnoses in puzzling cases, resolve misclassification of disease, and identify subsets of individuals with treatable conditions.
SUMMARY: Genetic testing may have broad benefits for patients and their families. Knowing the precise molecular etiology of disease can help clinicians determine the exact therapeutic course, and counsel patients and their families about prognosis. Genetic discoveries can also improve the classification of kidney disease and identify new targets for therapy.

Entities:  

Mesh:

Year:  2015        PMID: 26050126     DOI: 10.1097/MNH.0000000000000139

Source DB:  PubMed          Journal:  Curr Opin Nephrol Hypertens        ISSN: 1062-4821            Impact factor:   2.894


  7 in total

1.  NPHP1 (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRD.

Authors:  Rozemarijn Snoek; Jessica van Setten; Brendan J Keating; Ajay K Israni; Pamala A Jacobson; William S Oetting; Arthur J Matas; Roslyn B Mannon; Zhongyang Zhang; Weijia Zhang; Ke Hao; Barbara Murphy; Roman Reindl-Schwaighofer; Andreas Heinzl; Rainer Oberbauer; Ondrej Viklicky; Peter J Conlon; Caragh P Stapleton; Stephan J L Bakker; Harold Snieder; Edith D J Peters; Bert van der Zwaag; Nine V A M Knoers; Martin H de Borst; Albertien M van Eerde
Journal:  J Am Soc Nephrol       Date:  2018-04-13       Impact factor: 10.121

Review 2.  Towards precision nephrology: the opportunities and challenges of genomic medicine.

Authors:  Jordan G Nestor; Emily E Groopman; Ali G Gharavi
Journal:  J Nephrol       Date:  2017-10-17       Impact factor: 3.902

Review 3.  The expanding phenotypic spectra of kidney diseases: insights from genetic studies.

Authors:  Marijn F Stokman; Kirsten Y Renkema; Rachel H Giles; Franz Schaefer; Nine V A M Knoers; Albertien M van Eerde
Journal:  Nat Rev Nephrol       Date:  2016-07-04       Impact factor: 28.314

Review 4.  How Omics Data Can Be Used in Nephrology.

Authors:  Eugene P Rhee
Journal:  Am J Kidney Dis       Date:  2018-02-23       Impact factor: 8.860

5.  Routine use of clinical exome-based next-generation sequencing for evaluation of patients with thrombotic microangiopathies.

Authors:  Joseph P Gaut; Sanjay Jain; John D Pfeifer; Katinka A Vigh-Conrad; Meagan Corliss; Mukesh K Sharma; Jonathan W Heusel; Catherine E Cottrell
Journal:  Mod Pathol       Date:  2017-07-28       Impact factor: 7.842

Review 6.  Application of next-generation sequencing technology to diagnosis and treatment of focal segmental glomerulosclerosis.

Authors:  Yutaka Harita
Journal:  Clin Exp Nephrol       Date:  2017-07-27       Impact factor: 2.801

Review 7.  Diagnostic Yield of Next-Generation Sequencing in Patients With Chronic Kidney Disease of Unknown Etiology.

Authors:  Amber de Haan; Mark Eijgelsheim; Liffert Vogt; Nine V A M Knoers; Martin H de Borst
Journal:  Front Genet       Date:  2019-12-13       Impact factor: 4.599

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.