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

Year Number of Results
2005 1
2007 1
2011 2
2012 1
2013 7
2014 3
2015 8
2016 9
2017 6
2018 4
2019 8
2020 8
2021 1
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56 results
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Page 1
A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease.
Smedley D, Schubach M, Jacobsen JOB, Köhler S, Zemojtel T, Spielmann M, Jäger M, Hochheiser H, Washington NL, McMurry JA, Haendel MA, Mungall CJ, Lewis SE, Groza T, Valentini G, Robinson PN. Smedley D, et al. Among authors: hochheiser h. Am J Hum Genet. 2016 Sep 1;99(3):595-606. doi: 10.1016/j.ajhg.2016.07.005. Epub 2016 Aug 25. Am J Hum Genet. 2016. PMID: 27569544 Free PMC article.
Using machine learning to selectively highlight patient information.
King AJ, Cooper GF, Clermont G, Hochheiser H, Hauskrecht M, Sittig DF, Visweswaran S. King AJ, et al. Among authors: hochheiser h. J Biomed Inform. 2019 Dec;100:103327. doi: 10.1016/j.jbi.2019.103327. Epub 2019 Oct 29. J Biomed Inform. 2019. PMID: 31676461 Free PMC article.
Disease insights through cross-species phenotype comparisons.
Haendel MA, Vasilevsky N, Brush M, Hochheiser HS, Jacobsen J, Oellrich A, Mungall CJ, Washington N, Köhler S, Lewis SE, Robinson PN, Smedley D. Haendel MA, et al. Among authors: hochheiser hs. Mamm Genome. 2015 Oct;26(9-10):548-55. doi: 10.1007/s00335-015-9577-8. Epub 2015 Jun 20. Mamm Genome. 2015. PMID: 26092691 Free PMC article. Review.
Gene coexpression networks reveal novel molecular endotypes in alpha-1 antitrypsin deficiency.
Chu JH, Zang W, Vukmirovic M, Yan X, Adams T, DeIuliis G, Hu B, Mihaljinec A, Schupp JC, Becich MJ, Hochheiser H, Gibson KF, Chen ES, Morris A, Leader JK, Wisniewski SR, Zhang Y, Sciurba FC, Collman RG, Sandhaus R, Herzog EL, Patterson KC, Sauler M, Strange C, Kaminski N; GRADS Investigators. Chu JH, et al. Among authors: hochheiser h. Thorax. 2020 Dec 10:thoraxjnl-2019-214301. doi: 10.1136/thoraxjnl-2019-214301. Online ahead of print. Thorax. 2020. PMID: 33303696
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