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Year Number of Results
1991 1
2002 2
2004 4
2005 2
2006 1
2007 2
2008 4
2009 6
2010 1
2011 1
2012 2
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2014 2
2015 7
2016 3
2017 8
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2020 5
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2024 2

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Page 1
Guidelines for Genetic Testing and Management of Alport Syndrome.
Savige J, Lipska-Zietkiewicz BS, Watson E, Hertz JM, Deltas C, Mari F, Hilbert P, Plevova P, Byers P, Cerkauskaite A, Gregory M, Cerkauskiene R, Ljubanovic DG, Becherucci F, Errichiello C, Massella L, Aiello V, Lennon R, Hopkinson L, Koziell A, Lungu A, Rothe HM, Hoefele J, Zacchia M, Martic TN, Gupta A, van Eerde A, Gear S, Landini S, Palazzo V, Al-Rabadi L, Claes K, Corveleyn A, Van Hoof E, van Geel M, Williams M, Ashton E, Belge H, Ars E, Bierzynska A, Gangemi C, Renieri A, Storey H, Flinter F. Savige J, et al. Among authors: watson e. Clin J Am Soc Nephrol. 2022 Jan;17(1):143-154. doi: 10.2215/CJN.04230321. Epub 2021 Dec 20. Clin J Am Soc Nephrol. 2022. PMID: 34930753 Free PMC article.
Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria.
Savige J, Storey H, Watson E, Hertz JM, Deltas C, Renieri A, Mari F, Hilbert P, Plevova P, Byers P, Cerkauskaite A, Gregory M, Cerkauskiene R, Ljubanovic DG, Becherucci F, Errichiello C, Massella L, Aiello V, Lennon R, Hopkinson L, Koziell A, Lungu A, Rothe HM, Hoefele J, Zacchia M, Martic TN, Gupta A, van Eerde A, Gear S, Landini S, Palazzo V, Al-Rabadi L, Claes K, Corveleyn A, Van Hoof E, van Geel M, Williams M, Ashton E, Belge H, Ars E, Bierzynska A, Gangemi C, Lipska-Ziętkiewicz BS. Savige J, et al. Among authors: watson e. Eur J Hum Genet. 2021 Aug;29(8):1186-1197. doi: 10.1038/s41431-021-00858-1. Epub 2021 Apr 15. Eur J Hum Genet. 2021. PMID: 33854215 Free PMC article.
Letter From the Guest Editors.
Vijayaraghavan G, Watson E. Vijayaraghavan G, et al. Among authors: watson e. Semin Ultrasound CT MR. 2023 Feb;44(1):1. doi: 10.1053/j.sult.2022.12.001. Epub 2022 Dec 20. Semin Ultrasound CT MR. 2023. PMID: 36792267 No abstract available.
Ascertaining pathogenicity of genetic variants: caution required.
Arslan Z, Watson E, Bockenhauer D. Arslan Z, et al. Among authors: watson e. Pediatr Nephrol. 2023 May;38(5):1695-1696. doi: 10.1007/s00467-023-05909-x. Epub 2023 Feb 21. Pediatr Nephrol. 2023. PMID: 36809442 No abstract available.
Basement membrane defects in CD151-associated glomerular disease.
Naylor RW, Watson E, Williamson S, Preston R, Davenport JB, Thornton N, Lowe M, Williams M, Lennon R. Naylor RW, et al. Among authors: watson e. Pediatr Nephrol. 2022 Dec;37(12):3105-3115. doi: 10.1007/s00467-022-05447-y. Epub 2022 Mar 12. Pediatr Nephrol. 2022. PMID: 35278129 Free PMC article.
Runnels mitigate marsh drowning in microtidal salt marshes.
Watson EB, Ferguson W, Champlin LK, White JD, Ernst N, Sylla HA, Wilburn BP, Wigand C. Watson EB, et al. Front Environ Sci. 2022 Nov 3;10:1-17. doi: 10.3389/fenvs.2022.987246. Front Environ Sci. 2022. PMID: 36507472 Free PMC article.
Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria.
Savige J, Storey H, Watson E, Hertz JM, Deltas C, Renieri A, Mari F, Hilbert P, Plevova P, Byers P, Cerkauskaite A, Gregory M, Cerkauskiene R, Ljubanovic DG, Becherucci F, Errichiello C, Massella L, Aiello V, Lennon R, Hopkinson L, Koziell A, Lungu A, Rothe HM, Hoefele J, Zacchia M, Martic TN, Gupta A, van Eerde A, Gear S, Landini S, Palazzo V, Al-Rabadi L, Claes K, Corveleyn A, Van Hoof E, van Geel M, Williams M, Ashton E, Belge H, Ars E, Bierzynska A, Gangemi C, Lipska-Ziętkiewicz BS. Savige J, et al. Among authors: watson e. Eur J Hum Genet. 2024 Jan;32(1):132. doi: 10.1038/s41431-023-01288-x. Eur J Hum Genet. 2024. PMID: 36721056 Free PMC article. No abstract available.
80 results