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

Year Number of Results
1965 1
1993 1
1994 1
1995 4
1996 1
1997 1
1998 1
1999 1
2000 1
2002 1
2005 1
2006 2
2007 2
2010 2
2011 1
2012 5
2013 3
2014 1
2015 1
2016 4
2017 1
2018 1
2019 3
2020 1
2021 1
2022 2
2023 5
2024 3

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46 results

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Page 1
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
Walsh R, Thomson KL, Ware JS, Funke BH, Woodley J, McGuire KJ, Mazzarotto F, Blair E, Seller A, Taylor JC, Minikel EV, Exome Aggregation Consortium, MacArthur DG, Farrall M, Cook SA, Watkins H. Walsh R, et al. Among authors: seller a. Genet Med. 2017 Feb;19(2):192-203. doi: 10.1038/gim.2016.90. Epub 2016 Aug 17. Genet Med. 2017. PMID: 27532257 Free PMC article.
DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model.
Wordsworth S, Leal J, Blair E, Legood R, Thomson K, Seller A, Taylor J, Watkins H. Wordsworth S, et al. Among authors: seller a. Eur Heart J. 2010 Apr;31(8):926-35. doi: 10.1093/eurheartj/ehq067. Epub 2010 Mar 18. Eur Heart J. 2010. PMID: 20299350 Review.
The Clinical Relevance of the NATALEE Study: Application of the NATALEE Criteria to a Real-World Cohort from Two Large German Breast Cancer Centers.
Schäffler H, Mergel F, Pfister K, Lukac S, Fink A, Veselinovic K, Rack B, Fink V, Leinert E, Dimpfl M, Englisch A, Tegeler CM, Seller A, Grischke EM, Hahn M, Volmer LL, Engler T, Frevert ML, Taran FA, Janni W, Brucker SY, Hartkopf AD, Dannehl D. Schäffler H, et al. Among authors: seller a. Int J Mol Sci. 2023 Nov 15;24(22):16366. doi: 10.3390/ijms242216366. Int J Mol Sci. 2023. PMID: 38003555 Free PMC article.
Clinical dividends from the molecular genetic diagnosis of craniosynostosis.
Wilkie AO, Bochukova EG, Hansen RM, Taylor IB, Rannan-Eliya SV, Byren JC, Wall SA, Ramos L, Venâncio M, Hurst JA, O'Rourke AW, Williams LJ, Seller A, Lester T. Wilkie AO, et al. Among authors: seller a. Am J Med Genet A. 2006 Dec 1;140(23):2631-9. doi: 10.1002/ajmg.a.31366. Am J Med Genet A. 2006. PMID: 16838304 Review.
Clinical dividends from the molecular genetic diagnosis of craniosynostosis.
Wilkie AO, Bochukova EG, Hansen RM, Taylor IB, Rannan-Eliya SV, Byren JC, Wall SA, Ramos L, Venâncio M, Hurst JA, O'rourke AW, Williams LJ, Seller A, Lester T. Wilkie AO, et al. Among authors: seller a. Am J Med Genet A. 2007 Aug 15;143A(16):1941-9. doi: 10.1002/ajmg.a.31905. Am J Med Genet A. 2007. PMID: 17621648 Review.
46 results