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

Year Number of Results
1996 1
1998 1
2001 1
2003 3
2004 2
2005 1
2006 2
2009 1
2010 1
2011 1
2012 2
2013 1
2014 1
2018 1
2019 1
2020 2
2021 1
2022 2
2023 1
2024 0

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23 results

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Page 1
Genetic diversity within leukemia-associated immunophenotype-defined subclones in AML.
Tiso F, Koorenhof-Scheele TN, Huys E, Martens JHA, de Graaf AO, van der Reijden BA, Langemeijer SMC, Preijers FWMB, Kroeze LI, Jansen JH. Tiso F, et al. Among authors: huys e. Ann Hematol. 2022 Mar;101(3):571-579. doi: 10.1007/s00277-021-04747-x. Epub 2022 Jan 13. Ann Hematol. 2022. PMID: 35024892 Free PMC article.
Reprogramming of bone marrow myeloid progenitor cells in patients with severe coronary artery disease.
Noz MP, Bekkering S, Groh L, Nielen TM, Lamfers EJ, Schlitzer A, El Messaoudi S, van Royen N, Huys EH, Preijers FW, Smeets EM, Aarntzen EH, Zhang B, Li Y, Bremmers ME, van der Velden WJ, Dolstra H, Joosten LA, Gomes ME, Netea MG, Riksen NP. Noz MP, et al. Among authors: huys eh. Elife. 2020 Nov 10;9:e60939. doi: 10.7554/eLife.60939. Elife. 2020. PMID: 33168134 Free PMC article.
Platelet CD34 expression in a patient with a partial deletion of transcription factor subunit CBFB.
van Bergen MGJM, Saes JL, Simons A, Hebeda KM, Henskens YMC, Barteling W, Huys E, Laros-van Gorkom BAP, Schols SEM, Preijers FW, Jongmans MCJ, Jansen JH, van der Reijden BA. van Bergen MGJM, et al. Among authors: huys e. Am J Hematol. 2020 Jun;95(6):E136-E139. doi: 10.1002/ajh.25770. Epub 2020 Apr 8. Am J Hematol. 2020. PMID: 32124467 Free PMC article. No abstract available.
Diagnostic genome profiling in mental retardation.
de Vries BB, Pfundt R, Leisink M, Koolen DA, Vissers LE, Janssen IM, Reijmersdal Sv, Nillesen WM, Huys EH, Leeuw Nd, Smeets D, Sistermans EA, Feuth T, van Ravenswaaij-Arts CM, van Kessel AG, Schoenmakers EF, Brunner HG, Veltman JA. de Vries BB, et al. Among authors: huys eh. Am J Hum Genet. 2005 Oct;77(4):606-16. doi: 10.1086/491719. Epub 2005 Aug 30. Am J Hum Genet. 2005. PMID: 16175506 Free PMC article.
Characterization of a recurrent t(1;2)(p36;p24) in human uterine leiomyoma.
van Rijk A, Sweers M, Huys E, Kersten M, Merkx G, van Kessel AG, Debiec-Rychter M, Schoenmakers EF. van Rijk A, et al. Among authors: huys e. Cancer Genet Cytogenet. 2009 Aug;193(1):54-62. doi: 10.1016/j.cancergencyto.2009.03.011. Cancer Genet Cytogenet. 2009. PMID: 19602464
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.
Vissers LE, van Ravenswaaij CM, Admiraal R, Hurst JA, de Vries BB, Janssen IM, van der Vliet WA, Huys EH, de Jong PJ, Hamel BC, Schoenmakers EF, Brunner HG, Veltman JA, van Kessel AG. Vissers LE, et al. Among authors: huys eh. Nat Genet. 2004 Sep;36(9):955-7. doi: 10.1038/ng1407. Epub 2004 Aug 8. Nat Genet. 2004. PMID: 15300250
23 results