Literature DB >> 32733075

Bringing monogenic disease screening to the clinic.

Michael F Murray1, Monica A Giovanni2.   

Abstract

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Year:  2020        PMID： 32733075     DOI： 10.1038/s41591-020-1017-y

Source DB:  PubMed          Journal:  Nat Med        ISSN： 1078-8956            Impact factor:   53.440


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  3 in total

Review 1.  Addressing the routine failure to clinically identify monogenic cases of common disease.

Authors:  Michael F Murray; Muin J Khoury; Noura S Abul-Husn
Journal:  Genome Med       Date:  2022-06-07       Impact factor: 15.266

2.  Genomic Screening Identifies Individuals at High Risk for Hereditary Transthyretin Amyloidosis.

Authors:  Emily R Soper; Sabrina A Suckiel; Giovanna T Braganza; Amy R Kontorovich; Eimear E Kenny; Noura S Abul-Husn
Journal:  J Pers Med       Date:  2021-01-15

3.  From genes to public health: are we ready for DNA-based population screening?

Authors:  Muin J Khoury; W David Dotson
Journal:  Genet Med       Date:  2021-03-31       Impact factor: 8.864
  3 in total

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