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

Year Number of Results
1935 1
1936 2
1938 1
1965 1
1968 1
1972 1
1979 1
1981 1
1988 1
1991 1
1993 1
1994 1
1995 1
1996 2
1997 4
1999 1
2000 3
2001 3
2002 2
2003 3
2004 5
2005 5
2006 3
2007 1
2008 4
2009 2
2010 3
2011 3
2012 4
2013 7
2014 3
2015 6
2016 6
2017 6
2018 5
2019 5
2020 12
2021 14
2022 10
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Article type
Publication date

Search Results

116 results
Results by year
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Page 1
Mitochondrial Diseases: A Diagnostic Revolution.
Schon KR, Ratnaike T, van den Ameele J, Horvath R, Chinnery PF. Schon KR, et al. Trends Genet. 2020 Sep;36(9):702-717. doi: 10.1016/j.tig.2020.06.009. Epub 2020 Jul 13. Trends Genet. 2020. PMID: 32674947 Review.
Congenital Insensitivity to Pain Overview.
Schon KR, Parker APJ, Woods CG. Schon KR, et al. 2018 Feb 8 [updated 2020 Jun 11]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2018 Feb 8 [updated 2020 Jun 11]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 29419974 Free Books & Documents. Review.
Single-cell BCR and transcriptome analysis after influenza infection reveals spatiotemporal dynamics of antigen-specific B cells.
Mathew NR, Jayanthan JK, Smirnov IV, Robinson JL, Axelsson H, Nakka SS, Emmanouilidi A, Czarnewski P, Yewdell WT, Schön K, Lebrero-Fernández C, Bernasconi V, Rodin W, Harandi AM, Lycke N, Borcherding N, Yewdell JW, Greiff V, Bemark M, Angeletti D. Mathew NR, et al. Among authors: schon k. Cell Rep. 2021 Jun 22;35(12):109286. doi: 10.1016/j.celrep.2021.109286. Cell Rep. 2021. PMID: 34161770 Free PMC article.
Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study.
Schon KR, Horvath R, Wei W, Calabrese C, Tucci A, Ibañez K, Ratnaike T, Pitceathly RDS, Bugiardini E, Quinlivan R, Hanna MG, Clement E, Ashton E, Sayer JA, Brennan P, Josifova D, Izatt L, Fratter C, Nesbitt V, Barrett T, McMullen DJ, Smith A, Deshpande C, Smithson SF, Festenstein R, Canham N, Caulfield M, Houlden H, Rahman S, Chinnery PF; Genomics England Research Consortium. Schon KR, et al. BMJ. 2021 Nov 3;375:e066288. doi: 10.1136/bmj-2021-066288. BMJ. 2021. PMID: 34732400 Free PMC article. Clinical Trial.
Genotype, extrapyramidal features, and severity of variant ataxia-telangiectasia.
Schon K, van Os NJH, Oscroft N, Baxendale H, Scoffings D, Ray J, Suri M, Whitehouse WP, Mehta PR, Everett N, Bottolo L, van de Warrenburg BP, Byrd PJ, Weemaes C, Willemsen MA, Tischkowitz M, Taylor AM, Hensiek AE. Schon K, et al. Ann Neurol. 2019 Feb;85(2):170-180. doi: 10.1002/ana.25394. Ann Neurol. 2019. PMID: 30549301 Free PMC article.
116 results