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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2006 2
2008 1
2009 2
2010 1
2011 3
2012 2
2013 3
2014 1
2015 4
2016 5
2017 17
2018 10
2019 5
2020 11
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58 results
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Page 1
Carrier testing in children and adolescents.
Vears DF, Metcalfe SA. Vears DF, et al. Eur J Med Genet. 2015 Dec;58(12):659-67. doi: 10.1016/j.ejmg.2015.11.006. Epub 2015 Nov 10. Eur J Med Genet. 2015. PMID: 26563495 Review.
Unsolved challenges in pediatric whole-exome sequencing: A literature analysis.
Bertier G, Sénécal K, Borry P, Vears DF. Bertier G, et al. Among authors: vears df. Crit Rev Clin Lab Sci. 2017 Mar;54(2):134-142. doi: 10.1080/10408363.2016.1275516. Epub 2017 Jan 28. Crit Rev Clin Lab Sci. 2017. PMID: 28132577 Review.
Key Implications of Data Sharing in Pediatric Genomics.
Rahimzadeh V, Schickhardt C, Knoppers BM, Sénécal K, Vears DF, Fernandez CV, Pfister S, Plon S, Terry S, Williams J, Williams MS, Cornel M, Friedman JM. Rahimzadeh V, et al. Among authors: vears df. JAMA Pediatr. 2018 May 1;172(5):476-481. doi: 10.1001/jamapediatrics.2017.5500. JAMA Pediatr. 2018. PMID: 29554172
Reply to C Harling.
Sénécal K, Thys K, Vears DF, Van Assche K, Knoppers BM, Borry P. Sénécal K, et al. Among authors: vears df. Eur J Hum Genet. 2017 Sep;25(9):1030. doi: 10.1038/ejhg.2017.89. Epub 2017 May 31. Eur J Hum Genet. 2017. PMID: 28561019 Free PMC article. No abstract available.
Reproductive autonomy in expanded carrier screening: more than meets the eye?
Chokoshvili D, Vears DF, Borry P. Chokoshvili D, et al. Among authors: vears df. Expert Rev Mol Diagn. 2018 Dec;18(12):993-994. doi: 10.1080/14737159.2018.1544496. Epub 2018 Nov 8. Expert Rev Mol Diagn. 2018. PMID: 30394810 No abstract available.
Growing complexity of (expanded) carrier screening: Direct-to-consumer, physician-mediated, and clinic-based offers.
Chokoshvili D, Vears DF, Borry P. Chokoshvili D, et al. Among authors: vears df. Best Pract Res Clin Obstet Gynaecol. 2017 Oct;44:57-67. doi: 10.1016/j.bpobgyn.2017.02.006. Epub 2017 Feb 16. Best Pract Res Clin Obstet Gynaecol. 2017. PMID: 28302443 Review.
Searching for secondary findings: considering actionability and preserving the right not to know.
Isidor B, Julia S, Saugier-Veber P, Weil-Dubuc PL, Bézieau S, Bieth E, Bonnefont JP, Munnich A, Bourdeaut F, Bourgain C, Chassaing N, Corradini N, Haye D, Plaisancie J, Dupin-Deguine D, Calvas P, Mignot C, Cogné B, Manouvrier S, Pasquier L, Héron D, Boycott KM, Turrini M, Vears DF, Nizon M, Vincent M. Isidor B, et al. Among authors: vears df. Eur J Hum Genet. 2019 Oct;27(10):1481-1484. doi: 10.1038/s41431-019-0438-x. Epub 2019 Jun 11. Eur J Hum Genet. 2019. PMID: 31186543 Free PMC article. No abstract available.
Exploration of genetic health professional - laboratory specialist interactions in diagnostic genomic sequencing.
Vears DF, Sénécal K, Borry P. Vears DF, et al. Eur J Med Genet. 2020 Mar;63(3):103749. doi: 10.1016/j.ejmg.2019.103749. Epub 2019 Aug 28. Eur J Med Genet. 2020. PMID: 31472303
Genetic health professionals' experiences returning results from diagnostic genomic sequencing to patients.
Vears DF, Sénécal K, Borry P. Vears DF, et al. J Genet Couns. 2020 Oct;29(5):807-815. doi: 10.1002/jgc4.1209. Epub 2019 Dec 19. J Genet Couns. 2020. PMID: 31856387
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features.
Berkovic SF, Oliver KL, Canafoglia L, Krieger P, Damiano JA, Hildebrand MS, Morbin M, Vears DF, Sofia V, Giuliano L, Garavaglia B, Simonati A, Santorelli FM, Gambardella A, Labate A, Belcastro V, Castellotti B, Ozkara C, Zeman A, Rankin J, Mole SE, Aguglia U, Farrell M, Rajagopalan S, McDougall A, Brammah S, Andermann F, Andermann E, Dahl HM, Franceschetti S, Carpenter S. Berkovic SF, et al. Among authors: vears df. Brain. 2019 Jan 1;142(1):59-69. doi: 10.1093/brain/awy297. Brain. 2019. PMID: 30561534
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