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

Year Number of Results
1998 2
1999 1
2003 1
2008 1
2009 1
2010 1
2012 1
2013 1
2014 1
2015 2
2017 1
2023 0
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12 results
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Page 1
Knowing the patient's name.
Vardy C. Vardy C. Am J Nurs. 2012 Oct;112(10):12. doi: 10.1097/01.NAJ.0000421004.01512.d5. Am J Nurs. 2012. PMID: 23013679 No abstract available.
Homocystinuria: Challenges in diagnosis and management.
Garland J, Prasad A, Vardy C, Prasad C. Garland J, et al. Among authors: vardy c. Paediatr Child Health. 1999 Nov;4(8):557-62. doi: 10.1093/pch/4.8.557. Paediatr Child Health. 1999. PMID: 20213008 Free PMC article.
Social paediatrics: From 'lip service' to the health and well-being of Canada's children and youth.
Daneman D, Kellner J, Bernstein M, Dow K, Dugas MA, Duffy C, Eddy A, Filler G, Frappier JY, Gilmour S, Givelichian L, Huang L, Rockman-Greenberg C, Shevell M, Vardy C, Walti H, Orrbine E, Williams M. Daneman D, et al. Among authors: vardy c. Paediatr Child Health. 2013 Aug;18(7):351-2. Paediatr Child Health. 2013. PMID: 24421706 Free PMC article. No abstract available.
Structural variation of chromosomes in autism spectrum disorder.
Marshall CR, Noor A, Vincent JB, Lionel AC, Feuk L, Skaug J, Shago M, Moessner R, Pinto D, Ren Y, Thiruvahindrapduram B, Fiebig A, Schreiber S, Friedman J, Ketelaars CE, Vos YJ, Ficicioglu C, Kirkpatrick S, Nicolson R, Sloman L, Summers A, Gibbons CA, Teebi A, Chitayat D, Weksberg R, Thompson A, Vardy C, Crosbie V, Luscombe S, Baatjes R, Zwaigenbaum L, Roberts W, Fernandez B, Szatmari P, Scherer SW. Marshall CR, et al. Among authors: vardy c. Am J Hum Genet. 2008 Feb;82(2):477-88. doi: 10.1016/j.ajhg.2007.12.009. Epub 2008 Jan 17. Am J Hum Genet. 2008. PMID: 18252227 Free PMC article.
Straight talk about nursing.
Vardy CL. Vardy CL. Am J Nurs. 2014 May;114(5):13. doi: 10.1097/01.NAJ.0000446758.10718.f0. Am J Nurs. 2014. PMID: 24759460 No abstract available.
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder.
Tammimies K, Marshall CR, Walker S, Kaur G, Thiruvahindrapuram B, Lionel AC, Yuen RK, Uddin M, Roberts W, Weksberg R, Woodbury-Smith M, Zwaigenbaum L, Anagnostou E, Wang Z, Wei J, Howe JL, Gazzellone MJ, Lau L, Sung WW, Whitten K, Vardy C, Crosbie V, Tsang B, D'Abate L, Tong WW, Luscombe S, Doyle T, Carter MT, Szatmari P, Stuckless S, Merico D, Stavropoulos DJ, Scherer SW, Fernandez BA. Tammimies K, et al. Among authors: vardy c. JAMA. 2015 Sep 1;314(9):895-903. doi: 10.1001/jama.2015.10078. JAMA. 2015. PMID: 26325558
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
Fernandez BA, Roberts W, Chung B, Weksberg R, Meyn S, Szatmari P, Joseph-George AM, Mackay S, Whitten K, Noble B, Vardy C, Crosbie V, Luscombe S, Tucker E, Turner L, Marshall CR, Scherer SW. Fernandez BA, et al. Among authors: vardy c. J Med Genet. 2010 Mar;47(3):195-203. doi: 10.1136/jmg.2009.069369. Epub 2009 Sep 15. J Med Genet. 2010. PMID: 19755429
12 results