Literature DB >> 23166345

Applying deep DNA sequencing to common, complex pediatric traits.

John M Dagle1, Jeffrey C Murray.   

Abstract

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Year:  2012        PMID： 23166345      PMCID： PMC3507258          DOI： 10.1542/peds.2012-2870

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  11 in total

Review 1.  The human microbiome and its potential importance to pediatrics.

Authors:  Coreen L Johnson; James Versalovic
Journal:  Pediatrics       Date:  2012-04-02       Impact factor: 7.124

2.  Clan genomics and the complex architecture of human disease.

Authors:  James R Lupski; John W Belmont; Eric Boerwinkle; Richard A Gibbs
Journal:  Cell       Date:  2011-09-30       Impact factor: 41.582

3.  Noninvasive whole-genome sequencing of a human fetus.

Authors:  Jacob O Kitzman; Matthew W Snyder; Mario Ventura; Alexandra P Lewis; Ruolan Qiu; Lavone E Simmons; Hilary S Gammill; Craig E Rubens; Donna A Santillan; Jeffrey C Murray; Holly K Tabor; Michael J Bamshad; Evan E Eichler; Jay Shendure
Journal:  Sci Transl Med       Date:  2012-06-06       Impact factor: 17.956

Review 4.  The impact of genomics on pediatric research and medicine.

Authors:  John J Connolly; Hakon Hakonarson
Journal:  Pediatrics       Date:  2012-05-07       Impact factor: 7.124

5.  The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditions.

Authors:  Michael J Bamshad; Jay A Shendure; David Valle; Ada Hamosh; James R Lupski; Richard A Gibbs; Eric Boerwinkle; Richard P Lifton; Mark Gerstein; Murat Gunel; Shrikant Mane; Deborah A Nickerson
Journal:  Am J Med Genet A       Date:  2012-05-24       Impact factor: 2.802

6.  Assessing public attitudes on the retention and use of residual newborn screening blood samples: a focus group study.

Authors:  Erin Rothwell; Rebecca Anderson; Aaron Goldenberg; Michelle H Lewis; Louisa Stark; Matthew Burbank; Bob Wong; Jeffrey R Botkin
Journal:  Soc Sci Med       Date:  2012-02-18       Impact factor: 4.634

7.  Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.

Authors:  Jennifer A Wambach; Daniel J Wegner; Kelcey Depass; Hillary Heins; Todd E Druley; Robi D Mitra; Ping An; Qunyuan Zhang; Lawrence M Nogee; F Sessions Cole; Aaron Hamvas
Journal:  Pediatrics       Date:  2012-11-19       Impact factor: 7.124

8.  Non-invasive fetal genome sequencing: opportunities and challenges.

Authors:  Holly K Tabor; Jeffrey C Murray; Hilary S Gammill; Jacob O Kitzman; Matthew W Snyder; Mario Ventura; Alexandra P Lewis; Ruolan Qiu; LaVone E Simmons; Craig E Rubens; Mark K Santillan; Evan E Eichler; Edith Y Cheng; Michael J Bamshad; Jay Shendure
Journal:  Am J Med Genet A       Date:  2012-08-10       Impact factor: 2.802

9.  Incidental medical information in whole-exome sequencing.

Authors:  Benjamin D Solomon; Donald W Hadley; Daniel E Pineda-Alvarez; Aparna Kamat; Jamie K Teer; Praveen F Cherukuri; Nancy F Hansen; Pedro Cruz; Alice C Young; Benjamin E Berkman; Settara C Chandrasekharappa; James C Mullikin
Journal:  Pediatrics       Date:  2012-05-14       Impact factor: 7.124

10.  Non-invasive prenatal measurement of the fetal genome.

Authors:  H Christina Fan; Wei Gu; Jianbin Wang; Yair J Blumenfeld; Yasser Y El-Sayed; Stephen R Quake
Journal:  Nature       Date:  2012-07-19       Impact factor: 49.962
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