Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

141 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Correction: Clinical utility of genetic testing in 201 preschool children with inherited eye disorders.
Lenassi E, Clayton-Smith J, Douzgou S, Ramsden SC, Ingram S, Hall G, Hardcastle CL, Fletcher TA, Taylor RL, Ellingford JM, Newman WD, Fenerty C, Sharma V, Lloyd IC, Biswas S, Ashworth JL, Black GC, Sergouniotis PI. Lenassi E, et al. Among authors: ramsden sc. Genet Med. 2020 Dec 22. doi: 10.1038/s41436-020-01068-8. Online ahead of print. Genet Med. 2020. PMID: 33353976 No abstract available.
Fisheries rely on threatened salt marshes.
Baker R, Taylor MD, Able KW, Beck MW, Cebrian J, Colombano DD, Connolly RM, Currin C, Deegan LA, Feller IC, Gilby BL, Kimball ME, Minello TJ, Rozas LP, Simenstad C, Turner RE, Waltham NJ, Weinstein MP, Ziegler SL, Zu Ermgassen PSE, Alcott C, Alford SB, Barbeau MA, Crosby SC, Dodds K, Frank A, Goeke J, Goodridge Gaines LA, Hardcastle FE, Henderson CJ, James WR, Kenworthy MD, Lesser J, Mallick D, Martin CW, McDonald AE, McLuckie C, Morrison BH, Nelson JA, Norris GS, Ollerhead J, Pahl JW, Ramsden S, Rehage JS, Reinhardt JF, Rezek RJ, Risse LM, Smith JAM, Sparks EL, Staver LW. Baker R, et al. Among authors: ramsden s. Science. 2020 Nov 6;370(6517):670-671. doi: 10.1126/science.abe9332. Science. 2020. PMID: 33154131 No abstract available.
Using an integrative machine learning approach utilising homology modelling to clinically interpret genetic variants: CACNA1F as an exemplar.
Sallah SR, Sergouniotis PI, Barton S, Ramsden S, Taylor RL, Safadi A, Kabir M, Ellingford JM, Lench N, Lovell SC, Black GCM. Sallah SR, et al. Among authors: ramsden s. Eur J Hum Genet. 2020 Sep;28(9):1274-1282. doi: 10.1038/s41431-020-0623-y. Epub 2020 Apr 20. Eur J Hum Genet. 2020. PMID: 32313206 Free PMC article.
Clinical utility of genetic testing in 201 preschool children with inherited eye disorders.
Lenassi E, Clayton-Smith J, Douzgou S, Ramsden SC, Ingram S, Hall G, Hardcastle CL, Fletcher TA, Taylor RL, Ellingford JM, Newman WD, Fenerty C, Sharma V, Lloyd IC, Biswas S, Ashworth JL, Black GC, Sergouniotis PI. Lenassi E, et al. Among authors: ramsden sc. Genet Med. 2020 Apr;22(4):745-751. doi: 10.1038/s41436-019-0722-8. Epub 2019 Dec 18. Genet Med. 2020. PMID: 31848469 Free PMC article.
Diagnostic yield of panel-based genetic testing in syndromic inherited retinal disease.
Jiman OA, Taylor RL, Lenassi E, Smith JC, Douzgou S, Ellingford JM, Barton S, Hardcastle C, Fletcher T, Campbell C, Ashworth J, Biswas S, Ramsden SC; UK Inherited Retinal Disease Consortium, Manson FD, Black GC. Jiman OA, et al. Among authors: ramsden sc. Eur J Hum Genet. 2020 May;28(5):576-586. doi: 10.1038/s41431-019-0548-5. Epub 2019 Dec 13. Eur J Hum Genet. 2020. PMID: 31836858 Free PMC article.
Clinical and genetic variability in children with partial albinism.
Campbell P, Ellingford JM, Parry NRA, Fletcher T, Ramsden SC, Gale T, Hall G, Smith K, Kasperaviciute D, Thomas E, Lloyd IC, Douzgou S, Clayton-Smith J, Biswas S, Ashworth JL, Black GCM, Sergouniotis PI. Campbell P, et al. Among authors: ramsden sc. Sci Rep. 2019 Nov 12;9(1):16576. doi: 10.1038/s41598-019-51768-8. Sci Rep. 2019. PMID: 31719542 Free PMC article.
141 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page