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

Year Number of Results
1998 2
2003 2
2004 2
2005 6
2006 6
2007 3
2008 2
2009 4
2010 2
2011 4
2012 4
2013 7
2014 8
2015 2
2016 10
2017 8
2018 9
2019 9
2020 6
2021 9
2022 12
2023 7
2024 1

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111 results

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Page 1
Management of frozen shoulder: a systematic review and cost-effectiveness analysis.
Maund E, Craig D, Suekarran S, Neilson A, Wright K, Brealey S, Dennis L, Goodchild L, Hanchard N, Rangan A, Richardson G, Robertson J, McDaid C. Maund E, et al. Among authors: hanchard n. Health Technol Assess. 2012;16(11):1-264. doi: 10.3310/hta16110. Health Technol Assess. 2012. PMID: 22405512 Free PMC article. Review.
CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity.
Ernst ME, Baugh EH, Thomas A, Bier L, Lippa N, Stong N, Mulhern MS, Kushary S, Akman CI, Heinzen EL, Yeh R, Bi W, Hanchard NA, Burrage LC, Leduc MS, Chong JSC, Bend R, Lyons MJ, Lee JA, Suwannarat P, Brilstra E, Simon M, Koopmans M, van Binsbergen E, Groepper D, Fleischer J, Nava C, Keren B, Mignot C, Mathieu S, Mancini GMS, Madan-Khetarpal S, Infante EM, Bluvstein J, Seeley A, Bachman K, Klee EW, Schultz-Rogers LE, Hasadsri L, Barnett S, Ellingson MS, Ferber MJ, Narayanan V, Ramsey K, Rauch A, Joset P, Steindl K, Sheehan T, Poduri A, Vasquez A, Ruivenkamp C, White SM, Pais L, Monaghan KG, Goldstein DB, Sands TT, Aggarwal V. Ernst ME, et al. Among authors: hanchard na. Epilepsia. 2021 Jul;62(7):e103-e109. doi: 10.1111/epi.16931. Epub 2021 May 26. Epilepsia. 2021. PMID: 34041744 Free PMC article.
Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing.
Murdock DR, Dai H, Burrage LC, Rosenfeld JA, Ketkar S, Müller MF, Yépez VA, Gagneur J, Liu P, Chen S, Jain M, Zapata G, Bacino CA, Chao HT, Moretti P, Craigen WJ, Hanchard NA; Undiagnosed Diseases Network; Lee B. Murdock DR, et al. Among authors: hanchard na. J Clin Invest. 2021 Jan 4;131(1):e141500. doi: 10.1172/JCI141500. J Clin Invest. 2021. PMID: 33001864 Free PMC article. Clinical Trial.
Editorial overview: Congenital cardiovascular disease.
Hanchard NA, Mefford HC. Hanchard NA, et al. Curr Opin Genet Dev. 2022 Dec;77:102006. doi: 10.1016/j.gde.2022.102006. Epub 2022 Nov 23. Curr Opin Genet Dev. 2022. PMID: 36434853 No abstract available.
Management of adults with primary frozen shoulder in secondary care (UK FROST): a multicentre, pragmatic, three-arm, superiority randomised clinical trial.
Rangan A, Brealey SD, Keding A, Corbacho B, Northgraves M, Kottam L, Goodchild L, Srikesavan C, Rex S, Charalambous CP, Hanchard N, Armstrong A, Brooksbank A, Carr A, Cooper C, Dias JJ, Donnelly I, Hewitt C, Lamb SE, McDaid C, Richardson G, Rodgers S, Sharp E, Spencer S, Torgerson D, Toye F; UK FROST Study Group. Rangan A, et al. Among authors: hanchard n. Lancet. 2020 Oct 3;396(10256):977-989. doi: 10.1016/S0140-6736(20)31965-6. Lancet. 2020. PMID: 33010843 Free article. Clinical Trial.
The neglect of kwashiorkor.
May T, Babirekere-Iriso E, Traoré M, Berbain E, Ahmed M, Amadi B, Briend A, Manary M, Shamit Koroma A, Hanchard N, Frahm Olsen M, Friis H, PrayGod G, Girma T, Moussa M, Mahamadou A, Hotez P, Seini Sabo H. May T, et al. Among authors: hanchard n. Lancet Child Adolesc Health. 2023 Nov;7(11):751-753. doi: 10.1016/S2352-4642(23)00214-6. Epub 2023 Aug 25. Lancet Child Adolesc Health. 2023. PMID: 37640033 No abstract available.
Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management.
Meng L, Pammi M, Saronwala A, Magoulas P, Ghazi AR, Vetrini F, Zhang J, He W, Dharmadhikari AV, Qu C, Ward P, Braxton A, Narayanan S, Ge X, Tokita MJ, Santiago-Sim T, Dai H, Chiang T, Smith H, Azamian MS, Robak L, Bostwick BL, Schaaf CP, Potocki L, Scaglia F, Bacino CA, Hanchard NA, Wangler MF, Scott D, Brown C, Hu J, Belmont JW, Burrage LC, Graham BH, Sutton VR, Craigen WJ, Plon SE, Lupski JR, Beaudet AL, Gibbs RA, Muzny DM, Miller MJ, Wang X, Leduc MS, Xiao R, Liu P, Shaw C, Walkiewicz M, Bi W, Xia F, Lee B, Eng CM, Yang Y, Lalani SR. Meng L, et al. Among authors: hanchard na. JAMA Pediatr. 2017 Dec 4;171(12):e173438. doi: 10.1001/jamapediatrics.2017.3438. Epub 2017 Dec 4. JAMA Pediatr. 2017. PMID: 28973083 Free PMC article.
Polygenic risk scores for CARDINAL study.
Adebamowo CA, Adeyemo A, Ashaye A, Akpa OM, Chikowore T, Choudhury A, Fakim YJ, Fatumo S, Hanchard N, Hauser M, Mitchell B, Mulder N, Ofori-Acquah SF, Owolabi M, Ramsay M, Tayo B, VasanthKumar AB, Zhang Y, Adebamowo SN. Adebamowo CA, et al. Among authors: hanchard n. Nat Genet. 2022 May;54(5):527-530. doi: 10.1038/s41588-022-01074-3. Nat Genet. 2022. PMID: 35513726 Free PMC article.
111 results