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Results by year

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

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Search Results

193 results

Results by year

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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.
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.
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.
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.
Physiology of membrane lipid asymmetry.
Bevers EM, Smeets EF, Comfurius P, Zwaal RF. Bevers EM, et al. Among authors: smeets ef. Lupus. 1994 Aug;3(4):235-40. doi: 10.1177/096120339400300406. Lupus. 1994. PMID: 7804308 Review. No abstract available.
193 results