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

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

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46 results

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Page 1
Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway.
Wright JT, Fete M, Schneider H, Zinser M, Koster MI, Clarke AJ, Hadj-Rabia S, Tadini G, Pagnan N, Visinoni AF, Bergendal B, Abbott B, Fete T, Stanford C, Butcher C, D'Souza RN, Sybert VP, Morasso MI. Wright JT, et al. Among authors: clarke aj. Am J Med Genet A. 2019 Mar;179(3):442-447. doi: 10.1002/ajmg.a.61045. Epub 2019 Jan 31. Am J Med Genet A. 2019. PMID: 30703280 Free PMC article. Review.
Rett syndrome: revised diagnostic criteria and nomenclature.
Neul JL, Kaufmann WE, Glaze DG, Christodoulou J, Clarke AJ, Bahi-Buisson N, Leonard H, Bailey ME, Schanen NC, Zappella M, Renieri A, Huppke P, Percy AK; RettSearch Consortium. Neul JL, et al. Among authors: clarke aj. Ann Neurol. 2010 Dec;68(6):944-50. doi: 10.1002/ana.22124. Ann Neurol. 2010. PMID: 21154482 Free PMC article.
Ethics in genetic counselling.
Clarke AJ, Wallgren-Pettersson C. Clarke AJ, et al. J Community Genet. 2019 Jan;10(1):3-33. doi: 10.1007/s12687-018-0371-7. Epub 2018 Jun 14. J Community Genet. 2019. PMID: 29949066 Free PMC article. Review.
Response to Beretich and Beretich.
Vockley J, Brunetti-Pierri N, Chung WK, Clarke AJ, Gold N, Green RC, Kagan S, Moroz T, Schaaf CP, Schulz M, De Baere E. Vockley J, et al. Among authors: clarke aj. Genet Med. 2023 Oct;25(10):100903. doi: 10.1016/j.gim.2023.100903. Epub 2023 May 25. Genet Med. 2023. PMID: 37245089 No abstract available.
Börjeson-Forssman-Lehmann syndrome: delineating the clinical and allelic spectrum in 14 new families.
Jain V, Foo SH, Chooi S, Moss C, Goodwin R, Berland S, Clarke AJ, Davies SJ, Corrin S, Murch O, Doyle S, Graham GE, Greenhalgh L, Holder SE, Johnson D, Kumar A, Ladda RL, Sell S, Begtrup A, Lynch SA, McCann E, Østern R, Pottinger C, Splitt M, Fry AE. Jain V, et al. Among authors: clarke aj. Eur J Hum Genet. 2023 Dec;31(12):1421-1429. doi: 10.1038/s41431-023-01447-0. Epub 2023 Sep 14. Eur J Hum Genet. 2023. PMID: 37704779 Free PMC article.
International Consensus Recommendations for the Assessment and Management of Individuals With CDKL5 Deficiency Disorder.
Amin S, Monaghan M, Aledo-Serrano A, Bahi-Buisson N, Chin RF, Clarke AJ, Cross JH, Demarest S, Devinsky O, Downs J, Pestana Knight EM, Olson H, Partridge CA, Stuart G, Trivisano M, Zuberi S, Benke TA. Amin S, et al. Among authors: clarke aj. Front Neurol. 2022 Jun 20;13:874695. doi: 10.3389/fneur.2022.874695. eCollection 2022. Front Neurol. 2022. PMID: 35795799 Free PMC article.
Reply to Bombard and Mighton.
Carrieri D, Howard HC, Clarke AJ, Stefansdottir V, Cornel MC, van El CG, Forzano F. Carrieri D, et al. Among authors: clarke aj. Eur J Hum Genet. 2019 Apr;27(4):507-508. doi: 10.1038/s41431-018-0315-z. Epub 2019 Jan 18. Eur J Hum Genet. 2019. PMID: 30659262 Free PMC article. No abstract available.
A perspective on "cure" for Rett syndrome.
Clarke AJ, Abdala Sheikh AP. Clarke AJ, et al. Orphanet J Rare Dis. 2018 Apr 2;13(1):44. doi: 10.1186/s13023-018-0786-6. Orphanet J Rare Dis. 2018. PMID: 29609636 Free PMC article.
A case-note review of continued pregnancies found to be at a high risk of Huntington's disease: considerations for clinical practice.
Wadrup F, Holden S, MacLeod R, Miedzybrodzka Z, Németh AH, Owens S, Pasalodos S, Quarrell O, Clarke AJ; UK Huntington’s Disease Predictive Testing Consortium. Wadrup F, et al. Among authors: clarke aj. Eur J Hum Genet. 2019 Aug;27(8):1215-1224. doi: 10.1038/s41431-019-0375-8. Epub 2019 Mar 19. Eur J Hum Genet. 2019. PMID: 30890781 Free PMC article. Review.
46 results