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

Year Number of Results
1967 2
1969 1
1971 1
1978 1
1980 1
1981 1
1984 1
1986 1
1987 1
1988 6
1990 2
1991 1
1992 4
1993 6
1994 6
1995 4
1996 3
1998 8
1999 2
2001 2
2002 1
2003 4
2004 2
2005 6
2006 6
2007 1
2008 5
2009 9
2010 8
2011 11
2012 8
2013 8
2014 9
2015 11
2016 11
2017 9
2018 9
2019 14
2020 11
2021 12
2022 10
2023 6
2024 1

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194 results

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Page 1
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.
Snijders Blok L, Madsen E, Juusola J, Gilissen C, Baralle D, Reijnders MR, Venselaar H, Helsmoortel C, Cho MT, Hoischen A, Vissers LE, Koemans TS, Wissink-Lindhout W, Eichler EE, Romano C, Van Esch H, Stumpel C, Vreeburg M, Smeets E, Oberndorff K, van Bon BW, Shaw M, Gecz J, Haan E, Bienek M, Jensen C, Loeys BL, Van Dijck A, Innes AM, Racher H, Vermeer S, Di Donato N, Rump A, Tatton-Brown K, Parker MJ, Henderson A, Lynch SA, Fryer A, Ross A, Vasudevan P, Kini U, Newbury-Ecob R, Chandler K, Male A; DDD Study; Dijkstra S, Schieving J, Giltay J, van Gassen KL, Schuurs-Hoeijmakers J, Tan PL, Pediaditakis I, Haas SA, Retterer K, Reed P, Monaghan KG, Haverfield E, Natowicz M, Myers A, Kruer MC, Stein Q, Strauss KA, Brigatti KW, Keating K, Burton BK, Kim KH, Charrow J, Norman J, Foster-Barber A, Kline AD, Kimball A, Zackai E, Harr M, Fox J, McLaughlin J, Lindstrom K, Haude KM, van Roozendaal K, Brunner H, Chung WK, Kooy RF, Pfundt R, Kalscheuer V, Mehta SG, Katsanis N, Kleefstra T. Snijders Blok L, et al. Among authors: smeets e. Am J Hum Genet. 2015 Aug 6;97(2):343-52. doi: 10.1016/j.ajhg.2015.07.004. Epub 2015 Jul 30. Am J Hum Genet. 2015. PMID: 26235985 Free PMC article.
Rett Syndrome.
Smeets EE, Pelc K, Dan B. Smeets EE, et al. Mol Syndromol. 2012 Apr;2(3-5):113-127. doi: 10.1159/000337637. Epub 2012 Apr 16. Mol Syndromol. 2012. PMID: 22670134 Free PMC article.
[Rett syndrome].
van Urk PR, van den Berg MP, van Royen BJ, Smeets EE, Curfs LM. van Urk PR, et al. Among authors: smeets ee. Ned Tijdschr Geneeskd. 2014;158(3):A6686. Ned Tijdschr Geneeskd. 2014. PMID: 24423488 Dutch.
The role of TET-mediated DNA hydroxymethylation in prostate cancer.
Smeets E, Lynch AG, Prekovic S, Van den Broeck T, Moris L, Helsen C, Joniau S, Claessens F, Massie CE. Smeets E, et al. Mol Cell Endocrinol. 2018 Feb 15;462(Pt A):41-55. doi: 10.1016/j.mce.2017.08.021. Epub 2017 Sep 1. Mol Cell Endocrinol. 2018. PMID: 28870782 Review.
Progranulin mediates immune evasion of pancreatic ductal adenocarcinoma through regulation of MHCI expression.
Cheung PF, Yang J, Fang R, Borgers A, Krengel K, Stoffel A, Althoff K, Yip CW, Siu EHL, Ng LWC, Lang KS, Cham LB, Engel DR, Soun C, Cima I, Scheffler B, Striefler JK, Sinn M, Bahra M, Pelzer U, Oettle H, Markus P, Smeets EMM, Aarntzen EHJG, Savvatakis K, Liffers ST, Lueong SS, Neander C, Bazarna A, Zhang X, Paschen A, Crawford HC, Chan AWH, Cheung ST, Siveke JT. Cheung PF, et al. Among authors: smeets emm. Nat Commun. 2022 Jan 10;13(1):156. doi: 10.1038/s41467-021-27088-9. Nat Commun. 2022. PMID: 35013174 Free PMC article.
Functional noninvasive detection of glycolytic pancreatic ductal adenocarcinoma.
Heid I, Münch C, Karakaya S, Lueong SS, Winkelkotte AM, Liffers ST, Godfrey L, Cheung PFY, Savvatakis K, Topping GJ, Englert F, Kritzner L, Grashei M, Tannapfel A, Viebahn R, Wolters H, Uhl W, Vangala D, Smeets EMM, Aarntzen EHJG, Rauh D, Weichert W, Hoheisel JD, Hahn SA, Schilling F, Braren R, Trajkovic-Arsic M, Siveke JT. Heid I, et al. Among authors: smeets emm. Cancer Metab. 2022 Dec 9;10(1):24. doi: 10.1186/s40170-022-00298-5. Cancer Metab. 2022. PMID: 36494842 Free PMC article.
Rett syndrome and developmental regression.
Smeets EE, Townend GS, Curfs LMG. Smeets EE, et al. Neurosci Biobehav Rev. 2019 Sep;104:100-101. doi: 10.1016/j.neubiorev.2019.06.038. Epub 2019 Jul 5. Neurosci Biobehav Rev. 2019. PMID: 31283952 No abstract available.
Von Willebrand factor deficiency and atherosclerosis.
van Galen KP, Tuinenburg A, Smeets EM, Schutgens RE. van Galen KP, et al. Among authors: smeets em. Blood Rev. 2012 Sep;26(5):189-96. doi: 10.1016/j.blre.2012.05.002. Epub 2012 Jun 19. Blood Rev. 2012. PMID: 22721874 Review.
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature.
Reijnders MRF, Janowski R, Alvi M, Self JE, van Essen TJ, Vreeburg M, Rouhl RPW, Stevens SJC, Stegmann APA, Schieving J, Pfundt R, van Dijk K, Smeets E, Stumpel CTRM, Bok LA, Cobben JM, Engelen M, Mansour S, Whiteford M, Chandler KE, Douzgou S, Cooper NS, Tan EC, Foo R, Lai AHM, Rankin J, Green A, Lönnqvist T, Isohanni P, Williams S, Ruhoy I, Carvalho KS, Dowling JJ, Lev DL, Sterbova K, Lassuthova P, Neupauerová J, Waugh JL, Keros S, Clayton-Smith J, Smithson SF, Brunner HG, van Hoeckel C, Anderson M, Clowes VE, Siu VM, Ddd Study T, Selber P, Leventer RJ, Nellaker C, Niessing D, Hunt D, Baralle D. Reijnders MRF, et al. Among authors: smeets e. J Med Genet. 2018 Feb;55(2):104-113. doi: 10.1136/jmedgenet-2017-104946. Epub 2017 Nov 2. J Med Genet. 2018. PMID: 29097605 Free PMC article. Review.
194 results