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

Year Number of Results
2004 2
2008 1
2011 3
2012 2
2013 5
2014 1
2015 6
2016 4
2017 1
2018 9
2019 7
2020 13
2021 8
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57 results
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Page 1
Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability.
Santos-Cortez RLP, Khan V, Khan FS, Mughal ZU, Chakchouk I, Lee K, Rasheed M, Hamza R, Acharya A, Ullah E, Saqib MAN, Abbe I, Ali G, Hassan MJ, Khan S, Azeem Z, Ullah I, Bamshad MJ, Nickerson DA, Schrauwen I, Ahmad W, Ansar M, Leal SM. Santos-Cortez RLP, et al. Among authors: ullah e. Hum Genet. 2018 Sep;137(9):735-752. doi: 10.1007/s00439-018-1928-6. Epub 2018 Aug 22. Hum Genet. 2018. PMID: 30167849 Free PMC article.
Towards scaling elementary flux mode computation.
Ullah E, Yosafshahi M, Hassoun S. Ullah E, et al. Brief Bioinform. 2020 Dec 1;21(6):1875-1885. doi: 10.1093/bib/bbz094. Brief Bioinform. 2020. PMID: 31745550 Free PMC article.
Predicting Patients at Risk of 30-Day Unplanned Hospital Readmission.
Baig M, Hua N, Zhang E, Robinson R, Armstrong D, Whittaker R, Robinson T, Mirza F, Ullah E. Baig M, et al. Among authors: ullah e. Stud Health Technol Inform. 2019 Aug 8;266:20-24. doi: 10.3233/SHTI190767. Stud Health Technol Inform. 2019. PMID: 31397296
Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohort.
Prasov L, Guan B, Ullah E, Archer SM, Ayres BM, Besirli CG, Wiinikka-Buesser L, Comer GM, Del Monte MA, Elner SG, Garnai SJ, Huryn LA, Johnson K, Kamat SS, Lieu P, Mian SI, Rygiel CA, Serpen JY, Pawar HS, Brooks BP, Moroi SE, Richards JE, Hufnagel RB. Prasov L, et al. Among authors: ullah e. Sci Rep. 2020 Nov 17;10(1):19986. doi: 10.1038/s41598-020-76725-8. Sci Rep. 2020. PMID: 33203948 Free PMC article.
57 results