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

Year Number of Results
2009 1
2010 5
2011 3
2012 7
2013 7
2014 9
2015 13
2016 21
2017 9
2018 7
2019 8
2020 8
2021 3
2022 5
2023 2
2024 1

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93 results

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Page 1
Clinical implementation of RNA sequencing for Mendelian disease diagnostics.
Yépez VA, Gusic M, Kopajtich R, Mertes C, Smith NH, Alston CL, Ban R, Beblo S, Berutti R, Blessing H, Ciara E, Distelmaier F, Freisinger P, Häberle J, Hayflick SJ, Hempel M, Itkis YS, Kishita Y, Klopstock T, Krylova TD, Lamperti C, Lenz D, Makowski C, Mosegaard S, Müller MF, Muñoz-Pujol G, Nadel A, Ohtake A, Okazaki Y, Procopio E, Schwarzmayr T, Smet J, Staufner C, Stenton SL, Strom TM, Terrile C, Tort F, Van Coster R, Vanlander A, Wagner M, Xu M, Fang F, Ghezzi D, Mayr JA, Piekutowska-Abramczuk D, Ribes A, Rötig A, Taylor RW, Wortmann SB, Murayama K, Meitinger T, Gagneur J, Prokisch H. Yépez VA, et al. Among authors: alston cl. Genome Med. 2022 Apr 5;14(1):38. doi: 10.1186/s13073-022-01019-9. Genome Med. 2022. PMID: 35379322 Free PMC article.
Recent Advances in Mitochondrial Disease.
Craven L, Alston CL, Taylor RW, Turnbull DM. Craven L, et al. Among authors: alston cl. Annu Rev Genomics Hum Genet. 2017 Aug 31;18:257-275. doi: 10.1146/annurev-genom-091416-035426. Epub 2017 Apr 17. Annu Rev Genomics Hum Genet. 2017. PMID: 28415858 Free article. Review.
Genomic Strategies in Mitochondrial Diagnostics.
Deen D, Alston CL, Hudson G, Taylor RW, Pyle A. Deen D, et al. Among authors: alston cl. Methods Mol Biol. 2023;2615:397-425. doi: 10.1007/978-1-0716-2922-2_27. Methods Mol Biol. 2023. PMID: 36807806
The genetics and pathology of mitochondrial disease.
Alston CL, Rocha MC, Lax NZ, Turnbull DM, Taylor RW. Alston CL, et al. J Pathol. 2017 Jan;241(2):236-250. doi: 10.1002/path.4809. Epub 2016 Nov 2. J Pathol. 2017. PMID: 27659608 Free PMC article. Review.
The genetic basis of isolated mitochondrial complex II deficiency.
Fullerton M, McFarland R, Taylor RW, Alston CL. Fullerton M, et al. Among authors: alston cl. Mol Genet Metab. 2020 Sep-Oct;131(1-2):53-65. doi: 10.1016/j.ymgme.2020.09.009. Epub 2020 Oct 3. Mol Genet Metab. 2020. PMID: 33162331 Free PMC article. Review.
Recent advances in understanding the molecular genetic basis of mitochondrial disease.
Thompson K, Collier JJ, Glasgow RIC, Robertson FM, Pyle A, Blakely EL, Alston CL, Oláhová M, McFarland R, Taylor RW. Thompson K, et al. Among authors: alston cl. J Inherit Metab Dis. 2020 Jan;43(1):36-50. doi: 10.1002/jimd.12104. Epub 2019 May 10. J Inherit Metab Dis. 2020. PMID: 31021000 Free PMC article. Review.
Dysferlin mutations and mitochondrial dysfunction.
Vincent AE, Rosa HS, Alston CL, Grady JP, Rygiel KA, Rocha MC, Barresi R, Taylor RW, Turnbull DM. Vincent AE, et al. Among authors: alston cl. Neuromuscul Disord. 2016 Nov;26(11):782-788. doi: 10.1016/j.nmd.2016.08.008. Epub 2016 Aug 29. Neuromuscul Disord. 2016. PMID: 27666772 Free PMC article.
93 results