Literature DB >> 29700468

Sizing up whole-genome sequencing studies of common diseases.

Naomi R Wray1,2, Jacob Gratten3.   

Abstract

Mesh：

Year:  2018        PMID： 29700468     DOI： 10.1038/s41588-018-0113-0

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  4 in total

1.  Family-based quantitative trait meta-analysis implicates rare noncoding variants in DENND1A in polycystic ovary syndrome.

Authors:  Matthew Dapas; Ryan Sisk; Richard S Legro; Margrit Urbanek; Andrea Dunaif; M Geoffrey Hayes
Journal:  J Clin Endocrinol Metab       Date:  2019-04-30       Impact factor: 5.958

Review 2.  Genetic testing for kidney disease of unknown etiology.

Authors:  Thomas Hays; Emily E Groopman; Ali G Gharavi
Journal:  Kidney Int       Date:  2020-04-24       Impact factor: 10.612

Review 3.  The Role of De Novo Noncoding Regulatory Mutations in Neurodevelopmental Disorders.

Authors:  Tychele N Turner; Evan E Eichler
Journal:  Trends Neurosci       Date:  2018-12-15       Impact factor: 13.837

Review 4.  Genetic testing for unexplained perinatal disorders.

Authors:  Thomas Hays; Ronald J Wapner
Journal:  Curr Opin Pediatr       Date:  2021-04-01       Impact factor: 2.856
  4 in total

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