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Results by year

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

Year Number of Results
1958 1
1961 1
1962 1
1965 1
1966 2
1967 1
1968 1
1969 1
1972 3
1973 2
1974 2
1975 2
1976 2
1977 1
1979 3
1980 3
1981 2
1982 1
1983 1
1984 2
1986 2
1987 6
1988 3
1989 2
1990 2
1991 2
1992 4
1993 6
1994 2
1995 5
1996 2
1997 2
1998 3
1999 9
2000 2
2001 9
2002 4
2003 9
2004 6
2005 7
2006 5
2007 6
2008 8
2009 6
2010 5
2011 10
2012 10
2013 14
2014 15
2015 9
2016 16
2017 9
2018 15
2019 9
2020 9
2021 10
2022 15
2023 8
2024 4

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282 results

Results by year

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Page 1
Whole-genome sequencing of patients with rare diseases in a national health system.
Turro E, Astle WJ, Megy K, Gräf S, Greene D, Shamardina O, Allen HL, Sanchis-Juan A, Frontini M, Thys C, Stephens J, Mapeta R, Burren OS, Downes K, Haimel M, Tuna S, Deevi SVV, Aitman TJ, Bennett DL, Calleja P, Carss K, Caulfield MJ, Chinnery PF, Dixon PH, Gale DP, James R, Koziell A, Laffan MA, Levine AP, Maher ER, Markus HS, Morales J, Morrell NW, Mumford AD, Ormondroyd E, Rankin S, Rendon A, Richardson S, Roberts I, Roy NBA, Saleem MA, Smith KGC, Stark H, Tan RYY, Themistocleous AC, Thrasher AJ, Watkins H, Webster AR, Wilkins MR, Williamson C, Whitworth J, Humphray S, Bentley DR; NIHR BioResource for the 100,000 Genomes Project; Kingston N, Walker N, Bradley JR, Ashford S, Penkett CJ, Freson K, Stirrups KE, Raymond FL, Ouwehand WH. Turro E, et al. Nature. 2020 Jul;583(7814):96-102. doi: 10.1038/s41586-020-2434-2. Epub 2020 Jun 24. Nature. 2020. PMID: 32581362 Free PMC article.
Whole-genome sequencing of a sporadic primary immunodeficiency cohort.
Thaventhiran JED, Lango Allen H, Burren OS, Rae W, Greene D, Staples E, Zhang Z, Farmery JHR, Simeoni I, Rivers E, Maimaris J, Penkett CJ, Stephens J, Deevi SVV, Sanchis-Juan A, Gleadall NS, Thomas MJ, Sargur RB, Gordins P, Baxendale HE, Brown M, Tuijnenburg P, Worth A, Hanson S, Linger RJ, Buckland MS, Rayner-Matthews PJ, Gilmour KC, Samarghitean C, Seneviratne SL, Sansom DM, Lynch AG, Megy K, Ellinghaus E, Ellinghaus D, Jorgensen SF, Karlsen TH, Stirrups KE, Cutler AJ, Kumararatne DS, Chandra A, Edgar JDM, Herwadkar A, Cooper N, Grigoriadou S, Huissoon AP, Goddard S, Jolles S, Schuetz C, Boschann F; Primary Immunodeficiency Consortium for the NIHR Bioresource; Lyons PA, Hurles ME, Savic S, Burns SO, Kuijpers TW, Turro E, Ouwehand WH, Thrasher AJ, Smith KGC. Thaventhiran JED, et al. Nature. 2020 Jul;583(7814):90-95. doi: 10.1038/s41586-020-2265-1. Epub 2020 May 6. Nature. 2020. PMID: 32499645 Free PMC article.
Evidence-based prosthodontics: 25 years later.
Jacob RF, Goldstein GR, Layton DM. Jacob RF, et al. Among authors: layton dm. J Prosthet Dent. 2018 Jan;119(1):1-3. doi: 10.1016/j.prosdent.2017.12.001. J Prosthet Dent. 2018. PMID: 29290239 No abstract available.
Mitapivat versus Placebo for Pyruvate Kinase Deficiency.
Al-Samkari H, Galactéros F, Glenthøj A, Rothman JA, Andres O, Grace RF, Morado-Arias M, Layton DM, Onodera K, Verhovsek M, Barcellini W, Chonat S, Judge MP, Zagadailov E, Xu R, Hawkins P, Beynon V, Gheuens S, van Beers EJ; ACTIVATE Investigators. Al-Samkari H, et al. Among authors: layton dm. N Engl J Med. 2022 Apr 14;386(15):1432-1442. doi: 10.1056/NEJMoa2116634. N Engl J Med. 2022. PMID: 35417638 Clinical Trial.
Dehydrated hereditary stomatocytosis.
Layton DM, Bain BJ. Layton DM, et al. Am J Hematol. 2016 Feb;91(2):266. doi: 10.1002/ajh.24212. Epub 2015 Nov 17. Am J Hematol. 2016. PMID: 26440377 Free article. No abstract available.
Voxelotor in sickle cell disease.
Bain BJ, Myburgh J, Hann A, Layton DM. Bain BJ, et al. Among authors: layton dm. Am J Hematol. 2022 Jun 1;97(6):830-832. doi: 10.1002/ajh.26549. Epub 2022 Apr 8. Am J Hematol. 2022. PMID: 35349729 Free article. No abstract available.
Hereditary red cell enzymopathies.
Arya R, Layton DM, Bellingham AJ. Arya R, et al. Among authors: layton dm. Blood Rev. 1995 Sep;9(3):165-75. doi: 10.1016/0268-960x(95)90022-5. Blood Rev. 1995. PMID: 8563518 Review.
282 results