Berg JS - Search Results

1

Increasing the diagnostic yield of exome sequencing by copy number variant analysis.

Marchuk DS, Crooks K, Strande N, Kaiser-Rogers K, Milko LV, Brandt A, Arreola A, Tilley CR, Bizon C, Vora NL, Wilhelmsen KC, Evans JP, Berg JS. Marchuk DS, et al. Among authors: berg js. PLoS One. 2018 Dec 17;13(12):e0209185. doi: 10.1371/journal.pone.0209185. eCollection 2018. PLoS One. 2018. PMID: 30557390 Free PMC article.

2

Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: implications for application to clinical testing.

Berg JS, Evans JP, Leigh MW, Omran H, Bizon C, Mane K, Knowles MR, Weck KE, Zariwala MA. Berg JS, et al. Genet Med. 2011 Mar;13(3):218-29. doi: 10.1097/GIM.0b013e318203cff2. Genet Med. 2011. PMID: 21270641 Free PMC article.

3

Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time.

Berg JS, Khoury MJ, Evans JP. Berg JS, et al. Genet Med. 2011 Jun;13(6):499-504. doi: 10.1097/GIM.0b013e318220aaba. Genet Med. 2011. PMID: 21558861 Free article. No abstract available.

4

Next-generation DNA sequencing, regulation, and the limits of paternalism: the next challenge.

Evans JP, Berg JS. Evans JP, et al. Among authors: berg js. JAMA. 2011 Dec 7;306(21):2376-7. doi: 10.1001/jama.2011.1788. JAMA. 2011. PMID: 22147382 No abstract available.

5

An informatics approach to analyzing the incidentalome.

Berg JS, Adams M, Nassar N, Bizon C, Lee K, Schmitt CP, Wilhelmsen KC, Evans JP. Berg JS, et al. Genet Med. 2013 Jan;15(1):36-44. doi: 10.1038/gim.2012.112. Epub 2012 Sep 20. Genet Med. 2013. PMID: 22995991 Free PMC article.

6

We screen newborns, don't we?: realizing the promise of public health genomics.

Evans JP, Berg JS, Olshan AF, Magnuson T, Rimer BK. Evans JP, et al. Among authors: berg js. Genet Med. 2013 May;15(5):332-4. doi: 10.1038/gim.2013.11. Epub 2013 Mar 7. Genet Med. 2013. PMID: 23470837 Free PMC article. Review. No abstract available.

7

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.

Berg JS, Amendola LM, Eng C, Van Allen E, Gray SW, Wagle N, Rehm HL, DeChene ET, Dulik MC, Hisama FM, Burke W, Spinner NB, Garraway L, Green RC, Plon S, Evans JP, Jarvik GP; Members of the CSER Actionability and Return of Results Working Group. Berg JS, et al. Genet Med. 2013 Nov;15(11):860-7. doi: 10.1038/gim.2013.133. Epub 2013 Oct 24. Genet Med. 2013. PMID: 24195999 Free PMC article. Review.

8

GCH1 heterozygous mutation identified by whole-exome sequencing as a treatable condition in a patient presenting with progressive spastic paraplegia.

Fan Z, Greenwood R, Felix AC, Shiloh-Malawsky Y, Tennison M, Roche M, Crooks K, Weck K, Wilhelmsen K, Berg J, Evans J. Fan Z, et al. J Neurol. 2014 Mar;261(3):622-4. doi: 10.1007/s00415-014-7265-3. Epub 2014 Feb 8. J Neurol. 2014. PMID: 24509643 Free PMC article. No abstract available.

9

Genomic screening of the general adult population: key concepts for assessing net benefit with systematic evidence reviews.

Prince AE, Berg JS, Evans JP, Jonas DE, Henderson G. Prince AE, et al. Among authors: berg js. Genet Med. 2015 Jun;17(6):441-3. doi: 10.1038/gim.2014.129. Epub 2014 Sep 18. Genet Med. 2015. PMID: 25232850 Free PMC article. Review. No abstract available.

10

How can psychological science inform research about genetic counseling for clinical genomic sequencing?

Khan CM, Rini C, Bernhardt BA, Roberts JS, Christensen KD, Evans JP, Brothers KB, Roche MI, Berg JS, Henderson GE. Khan CM, et al. Among authors: berg js. J Genet Couns. 2015 Apr;24(2):193-204. doi: 10.1007/s10897-014-9804-6. Epub 2014 Dec 9. J Genet Couns. 2015. PMID: 25488723 Free PMC article.

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