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

Year Number of Results
1949 1
1950 1
1952 1
1964 2
1966 1
1973 1
1975 2
1976 1
1978 1
1990 1
1992 1
1993 1
1997 1
1999 1
2001 2
2002 3
2003 2
2004 2
2005 4
2006 1
2007 7
2008 5
2009 6
2010 5
2011 3
2012 4
2013 4
2014 2
2015 2
2016 3
2017 10
2018 4
2019 4
2020 1
2021 2
2022 1
2023 1
2024 1

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86 results

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Oliver AJ, Goldfrad CH, Tomkins SA, Grigg J. Oliver AJ, et al. Among authors: tomkins sa. J Pediatr. 2017 Jul;186:213-214. doi: 10.1016/j.jpeds.2017.02.058. Epub 2017 Mar 13. J Pediatr. 2017. PMID: 28302327 No abstract available.
Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD.
Andrews KA, Ascher DB, Pires DEV, Barnes DR, Vialard L, Casey RT, Bradshaw N, Adlard J, Aylwin S, Brennan P, Brewer C, Cole T, Cook JA, Davidson R, Donaldson A, Fryer A, Greenhalgh L, Hodgson SV, Irving R, Lalloo F, McConachie M, McConnell VPM, Morrison PJ, Murday V, Park SM, Simpson HL, Snape K, Stewart S, Tomkins SE, Wallis Y, Izatt L, Goudie D, Lindsay RS, Perry CG, Woodward ER, Antoniou AC, Maher ER. Andrews KA, et al. Among authors: tomkins se. J Med Genet. 2018 Jun;55(6):384-394. doi: 10.1136/jmedgenet-2017-105127. Epub 2018 Jan 31. J Med Genet. 2018. PMID: 29386252 Free PMC article.
INTERHEART.
McKee M, Leon DA, Tomkins S, Shkolnikov VM, Andreev E. McKee M, et al. Among authors: tomkins s. Lancet. 2005 Jan 8-14;365(9454):117-8; author reply 118. doi: 10.1016/S0140-6736(05)17691-0. Lancet. 2005. PMID: 15639282 No abstract available.
The Tomkins-Horn picture-arrangement test.
TOMKINS SS. TOMKINS SS. Trans N Y Acad Sci. 1952 Dec;15(2):46-50. doi: 10.1111/j.2164-0947.1952.tb01151.x. Trans N Y Acad Sci. 1952. PMID: 13029129 No abstract available.
Clinical and Molecular Features of Renal and Pheochromocytoma/Paraganglioma Tumor Association Syndrome (RAPTAS): Case Series and Literature Review.
Casey RT, Warren AY, Martin JE, Challis BG, Rattenberry E, Whitworth J, Andrews KA, Roberts T, Clark GR, West H, Smith PS, Docquier FM, Rodger F, Murray V, Simpson HL, Wallis Y, Giger O, Tran M, Tomkins S, Stewart GD, Park SM, Woodward ER, Maher ER. Casey RT, et al. Among authors: tomkins s. J Clin Endocrinol Metab. 2017 Nov 1;102(11):4013-4022. doi: 10.1210/jc.2017-00562. J Clin Endocrinol Metab. 2017. PMID: 28973655 Free PMC article. Review.
Delineating the phenotypic spectrum of Bainbridge-Ropers syndrome: 12 new patients with de novo, heterozygous, loss-of-function mutations in ASXL3 and review of published literature.
Balasubramanian M, Willoughby J, Fry AE, Weber A, Firth HV, Deshpande C, Berg JN, Chandler K, Metcalfe KA, Lam W, Pilz DT, Tomkins S. Balasubramanian M, et al. Among authors: tomkins s. J Med Genet. 2017 Aug;54(8):537-543. doi: 10.1136/jmedgenet-2016-104360. Epub 2017 Jan 18. J Med Genet. 2017. PMID: 28100473 Free article. Review.
De novo variants in CNOT3 cause a variable neurodevelopmental disorder.
Martin R, Splitt M, Genevieve D, Aten E, Collins A, de Bie CI, Faivre L, Foulds N, Giltay J, Ibitoye R, Joss S, Kennedy J, Kerr B, Kivuva E, Koopmans M, Newbury-Ecob R, Jean-Marçais N, Peeters EAJ, Smithson S, Tomkins S, Tranmauthem F, Piton A, van Haeringen A. Martin R, et al. Among authors: tomkins s. Eur J Hum Genet. 2019 Nov;27(11):1677-1682. doi: 10.1038/s41431-019-0413-6. Epub 2019 Jun 14. Eur J Hum Genet. 2019. PMID: 31201375 Free PMC article.
86 results