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

Year Number of Results
1994 2
1999 2
2000 2
2001 3
2002 2
2003 5
2004 2
2005 2
2006 5
2007 7
2008 4
2009 5
2010 11
2011 4
2012 10
2013 11
2014 7
2015 4
2016 3
2017 2
2018 9
2019 3
2020 3
2021 5
2022 3
2023 3
2024 1

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105 results

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Page 1
Next-generation sequencing. Preface.
Rees MI. Rees MI. Adv Protein Chem Struct Biol. 2012;89:vii-ix. doi: 10.1016/B978-0-12-394287-6.09990-0. Adv Protein Chem Struct Biol. 2012. PMID: 23046885 No abstract available.
Tubulin genes and malformations of cortical development.
Romaniello R, Arrigoni F, Fry AE, Bassi MT, Rees MI, Borgatti R, Pilz DT, Cushion TD. Romaniello R, et al. Among authors: rees mi. Eur J Med Genet. 2018 Dec;61(12):744-754. doi: 10.1016/j.ejmg.2018.07.012. Epub 2018 Jul 17. Eur J Med Genet. 2018. PMID: 30016746 Review.
Epilepsy mortality in Wales during COVID-19.
Daniels H, Lacey AS, Mikadze D, Akbari A, Fonferko-Shadrach B, Hollinghurst J, Lyons RA, Rees MI, Sawhney IM, Powell RH, Kerr MP, Pickrell WO. Daniels H, et al. Among authors: rees mi. Seizure. 2022 Jan;94:39-42. doi: 10.1016/j.seizure.2021.11.017. Epub 2021 Nov 27. Seizure. 2022. PMID: 34864250 Free PMC article.
Trait impulsivity in Juvenile Myoclonic Epilepsy.
Shakeshaft A, Panjwani N, McDowall R, Crudgington H, Peña Ceballos J, Andrade DM, Beier CP, Fong CY, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Orsini A, Rees MI, Rubboli G, Selmer KK, Smith AB, Striano P, Syvertsen M, Talvik I, Thomas RH, Zarubova J, Richardson MP, Strug LJ, Pal DK; BIOJUME Consortium. Shakeshaft A, et al. Among authors: rees mi. Ann Clin Transl Neurol. 2021 Jan;8(1):138-152. doi: 10.1002/acn3.51255. Epub 2020 Dec 2. Ann Clin Transl Neurol. 2021. PMID: 33264519 Free PMC article.
Next generation sequencing methodologies--an overview.
Pickrell WO, Rees MI, Chung SK. Pickrell WO, et al. Among authors: rees mi. Adv Protein Chem Struct Biol. 2012;89:1-26. doi: 10.1016/B978-0-12-394287-6.00001-X. Adv Protein Chem Struct Biol. 2012. PMID: 23046880 Review.
The genetics of hyperekplexia: more than startle!
Harvey RJ, Topf M, Harvey K, Rees MI. Harvey RJ, et al. Among authors: rees mi. Trends Genet. 2008 Sep;24(9):439-47. doi: 10.1016/j.tig.2008.06.005. Epub 2008 Aug 15. Trends Genet. 2008. PMID: 18707791 Review.
Sex-specific disease modifiers in juvenile myoclonic epilepsy.
Shakeshaft A, Panjwani N, Collingwood A, Crudgington H, Hall A, Andrade DM, Beier CP, Fong CY, Gardella E, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Møller RS, Ng CC, Orsini A, Rees MI, Rubboli G, Selmer KK, Striano P, Syvertsen M, Thomas RH, Zarubova J, Richardson MP, Strug LJ, Pal DK. Shakeshaft A, et al. Among authors: rees mi. Sci Rep. 2022 Feb 21;12(1):2785. doi: 10.1038/s41598-022-06324-2. Sci Rep. 2022. PMID: 35190554 Free PMC article.
Clinical spectrum of STX1B-related epileptic disorders.
Wolking S, May P, Mei D, Møller RS, Balestrini S, Helbig KL, Altuzarra CD, Chatron N, Kaiwar C, Stöhr K, Widdess-Walsh P, Mendelsohn BA, Numis A, Cilio MR, Van Paesschen W, Svendsen LL, Oates S, Hughes E, Goyal S, Brown K, Sifuentes Saenz M, Dorn T, Muhle H, Pagnamenta AT, Vavoulis DV, Knight SJL, Taylor JC, Canevini MP, Darra F, Gavrilova RH, Powis Z, Tang S, Marquetand J, Armstrong M, McHale D, Klee EW, Kluger GJ, Lowenstein DH, Weckhuysen S, Pal DK, Helbig I, Guerrini R, Thomas RH, Rees MI, Lesca G, Sisodiya SM, Weber YG, Lal D, Marini C, Lerche H, Schubert J. Wolking S, et al. Among authors: rees mi. Neurology. 2019 Mar 12;92(11):e1238-e1249. doi: 10.1212/WNL.0000000000007089. Epub 2019 Feb 8. Neurology. 2019. PMID: 30737342 Free PMC article.
Validating epilepsy diagnoses in routinely collected data.
Fonferko-Shadrach B, Lacey AS, White CP, Powell HWR, Sawhney IMS, Lyons RA, Smith PEM, Kerr MP, Rees MI, Pickrell WO. Fonferko-Shadrach B, et al. Among authors: rees mi. Seizure. 2017 Nov;52:195-198. doi: 10.1016/j.seizure.2017.10.008. Epub 2017 Oct 13. Seizure. 2017. PMID: 29059611 Free PMC article.
105 results