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

Year Number of Results
1886 1
1946 5
1947 1
1948 1
1952 1
1953 1
1954 1
1963 1
1965 2
1967 1
1968 2
1969 1
1974 1
1975 3
1978 1
1980 1
1985 1
1987 1
1993 4
1994 2
1995 1
1996 7
1997 1
1998 2
2000 1
2001 1
2002 1
2003 2
2004 1
2005 2
2006 1
2007 5
2008 7
2009 6
2010 11
2011 5
2012 7
2013 12
2014 8
2015 7
2016 13
2017 18
2018 12
2019 7
2020 11
2021 13
2022 19
2023 9
2024 5

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199 results

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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.
Evaluation of Daily Low-Dose Prednisolone During Upper Respiratory Tract Infection to Prevent Relapse in Children With Relapsing Steroid-Sensitive Nephrotic Syndrome: The PREDNOS 2 Randomized Clinical Trial.
Christian MT, Webb NJA, Mehta S, Woolley RL, Afentou N, Frew E, Brettell EA, Khan AR, Milford DV, Bockenhauer D, Saleem MA, Hall AS, Koziell A, Maxwell H, Hegde S, Prajapati H, Gilbert RD, Jones C, McKeever K, Cook W, Ives N. Christian MT, et al. Among authors: maxwell h. JAMA Pediatr. 2022 Mar 1;176(3):236-243. doi: 10.1001/jamapediatrics.2021.5189. JAMA Pediatr. 2022. PMID: 34928294 Free PMC article. Clinical Trial.
C3 Glomerulopathy and Related Disorders in Children: Etiology-Phenotype Correlation and Outcomes.
Wong EKS, Marchbank KJ, Lomax-Browne H, Pappworth IY, Denton H, Cooke K, Ward S, McLoughlin AC, Richardson G, Wilson V, Harris CL, Morgan BP, Hakobyan S, McAlinden P, Gale DP, Maxwell H, Christian M, Malcomson R, Goodship THJ, Marks SD, Pickering MC, Kavanagh D, Cook HT, Johnson SA; MPGN/DDD/C3 Glomerulopathy Rare Disease Group and National Study of MPGN/DDD/C3 Glomerulopathy Investigators. Wong EKS, et al. Among authors: maxwell h. Clin J Am Soc Nephrol. 2021 Nov;16(11):1639-1651. doi: 10.2215/CJN.00320121. Epub 2021 Sep 22. Clin J Am Soc Nephrol. 2021. PMID: 34551983 Free PMC article.
GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements.
Dixon PH, Levine AP, Cebola I, Chan MMY, Amin AS, Aich A, Mozere M, Maude H, Mitchell AL, Zhang J; NIHR BioResource; Genomics England Research Consortium Collaborators; Chambers J, Syngelaki A, Donnelly J, Cooley S, Geary M, Nicolaides K, Thorsell M, Hague WM, Estiu MC, Marschall HU, Gale DP, Williamson C. Dixon PH, et al. Nat Commun. 2022 Aug 17;13(1):4840. doi: 10.1038/s41467-022-29931-z. Nat Commun. 2022. PMID: 35977952 Free PMC article.
Priapism.
Brown RS, Mazansky H, Maxwell HM. Brown RS, et al. Among authors: maxwell hm. S Afr Med J. 1968 Sep 7;42(34):886-9. S Afr Med J. 1968. PMID: 5706630 No abstract available.
Theriogenology Question of the Month.
Cowley JD, Maxwell HS. Cowley JD, et al. Among authors: maxwell hs. J Am Vet Med Assoc. 2022 Apr 6;260(9):1003-1005. doi: 10.2460/javma.22.02.0067. J Am Vet Med Assoc. 2022. PMID: 35389878 Free article. No abstract available.
Clinical approaches to infertility in the bitch.
Wilborn RR, Maxwell HS. Wilborn RR, et al. Among authors: maxwell hs. Vet Clin North Am Small Anim Pract. 2012 May;42(3):457-68, v. doi: 10.1016/j.cvsm.2012.01.016. Vet Clin North Am Small Anim Pract. 2012. PMID: 22482812 Review.
Padma 28 for intermittent claudication.
Stewart M, Morling JR, Maxwell H. Stewart M, et al. Among authors: maxwell h. Cochrane Database Syst Rev. 2016 Mar 29;3(3):CD007371. doi: 10.1002/14651858.CD007371.pub3. Cochrane Database Syst Rev. 2016. PMID: 27021597 Free PMC article. Review.
Sclerotherapy for lower limb telangiectasias.
Schwartz L, Maxwell H. Schwartz L, et al. Among authors: maxwell h. Cochrane Database Syst Rev. 2011 Dec 7;2011(12):CD008826. doi: 10.1002/14651858.CD008826.pub2. Cochrane Database Syst Rev. 2011. PMID: 22161437 Free PMC article. Review.
199 results