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Expanding opportunities and emerging challenges: broadening the scope of genetic testing in nephrology
Author(s) -
Emily Groopman,
Ali G. Gharavi
Publication year - 2019
Publication title -
kidney international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.499
H-Index - 276
eISSN - 1523-1755
pISSN - 0085-2538
DOI - 10.1016/j.kint.2018.12.032
Subject(s) - exome sequencing , medicine , nephrology , genetic testing , exome , kidney disease , massive parallel sequencing , human genetics , bioinformatics , genetics , dna sequencing , biology , mutation , dna , gene
Massively parallel sequencing technologies such as exome sequencing are increasingly applied across medicine. Connaughton et al. report a high diagnostic yield of exome sequencing among adults with hereditary nephropathy or nephropathy of unknown cause. Their findings support broader use of genomic sequencing in nephrology and highlight key associated questions, including how to identify those patients for whom testing is indicated, pinpoint pathogenic variants, and balance the resultant health care benefits and clinical follow-up burden.

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