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

Year Number of Results
1933 2
1934 3
1935 2
1936 2
1938 2
1939 1
1941 1
1950 1
1974 1
1975 2
1976 1
1983 2
1984 1
1985 1
1986 6
1987 4
1988 7
1989 5
1990 8
1991 10
1992 7
1993 3
1994 2
1995 5
1996 4
1997 5
1998 8
1999 4
2000 2
2001 3
2002 6
2003 3
2004 2
2005 2
2006 4
2007 2
2008 3
2009 4
2010 7
2011 4
2012 4
2013 10
2014 8
2015 7
2016 5
2017 7
2018 1
2019 1
2022 0
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Article attribute
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Publication date

Search Results

173 results
Results by year
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Page 1
Whole-genome sequencing of quartet families with autism spectrum disorder.
Yuen RK, Thiruvahindrapuram B, Merico D, Walker S, Tammimies K, Hoang N, Chrysler C, Nalpathamkalam T, Pellecchia G, Liu Y, Gazzellone MJ, D'Abate L, Deneault E, Howe JL, Liu RS, Thompson A, Zarrei M, Uddin M, Marshall CR, Ring RH, Zwaigenbaum L, Ray PN, Weksberg R, Carter MT, Fernandez BA, Roberts W, Szatmari P, Scherer SW. Yuen RK, et al. Among authors: ray pn. Nat Med. 2015 Feb;21(2):185-91. doi: 10.1038/nm.3792. Epub 2015 Jan 26. Nat Med. 2015. PMID: 25621899
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.
Lionel AC, Costain G, Monfared N, Walker S, Reuter MS, Hosseini SM, Thiruvahindrapuram B, Merico D, Jobling R, Nalpathamkalam T, Pellecchia G, Sung WWL, Wang Z, Bikangaga P, Boelman C, Carter MT, Cordeiro D, Cytrynbaum C, Dell SD, Dhir P, Dowling JJ, Heon E, Hewson S, Hiraki L, Inbar-Feigenberg M, Klatt R, Kronick J, Laxer RM, Licht C, MacDonald H, Mercimek-Andrews S, Mendoza-Londono R, Piscione T, Schneider R, Schulze A, Silverman E, Siriwardena K, Snead OC, Sondheimer N, Sutherland J, Vincent A, Wasserman JD, Weksberg R, Shuman C, Carew C, Szego MJ, Hayeems RZ, Basran R, Stavropoulos DJ, Ray PN, Bowdin S, Meyn MS, Cohn RD, Scherer SW, Marshall CR. Lionel AC, et al. Among authors: ray pn. Genet Med. 2018 Apr;20(4):435-443. doi: 10.1038/gim.2017.119. Epub 2017 Aug 3. Genet Med. 2018. PMID: 28771251 Free PMC article.
The problem of Duchenne muscular dystrophy.
Worton RG, Ray PN, Bodrug S, Burghes AH, Hu X, Thompson MW. Worton RG, et al. Among authors: ray pn. Philos Trans R Soc Lond B Biol Sci. 1988 Jun 15;319(1194):275-84. doi: 10.1098/rstb.1988.0049. Philos Trans R Soc Lond B Biol Sci. 1988. PMID: 2900521 Review.
Myogenic regulation of dystrophin gene expression.
Klamut HJ, Zubrzycka-Gaarn EE, Bulman DE, Malhotra SB, Bodrug SE, Worton RG, Ray PN. Klamut HJ, et al. Among authors: ray pn. Br Med Bull. 1989 Jul;45(3):681-702. doi: 10.1093/oxfordjournals.bmb.a072352. Br Med Bull. 1989. PMID: 2688823 Review.
Chronic Ulcerative Colitis.
Chopra RN, Ray PN. Chopra RN, et al. Among authors: ray pn. Ind Med Gaz. 1939 Feb;74(2):65-74. Ind Med Gaz. 1939. PMID: 29011769 Free PMC article. No abstract available.
RNAseq analysis for the diagnosis of muscular dystrophy.
Gonorazky H, Liang M, Cummings B, Lek M, Micallef J, Hawkins C, Basran R, Cohn R, Wilson MD, MacArthur D, Marshall CR, Ray PN, Dowling JJ. Gonorazky H, et al. Among authors: ray pn. Ann Clin Transl Neurol. 2015 Dec 8;3(1):55-60. doi: 10.1002/acn3.267. eCollection 2016 Jan. Ann Clin Transl Neurol. 2015. PMID: 26783550 Free PMC article.
Clinical and genetic study of hereditary spastic paraplegia in Canada.
Chrestian N, Dupré N, Gan-Or Z, Szuto A, Chen S, Venkitachalam A, Brisson JD, Warman-Chardon J, Ahmed S, Ashtiani S, MacDonald H, Mohsin N, Mourabit-Amari K, Provencher P, Boycott KM, Stavropoulos DJ, Dion PA, Ray PN, Suchowersky O, Rouleau GA, Yoon G. Chrestian N, et al. Among authors: ray pn. Neurol Genet. 2016 Dec 5;3(1):e122. doi: 10.1212/NXG.0000000000000122. eCollection 2017 Feb. Neurol Genet. 2016. PMID: 27957547 Free PMC article.
173 results