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

Year Number of Results
2000 1
2011 1
2012 5
2013 4
2014 6
2015 2
2016 1
2018 2
2020 3
2021 3
2022 0
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24 results
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Page 1
Translational endpoints in fragile X syndrome.
de Esch CE, Zeidler S, Willemsen R. de Esch CE, et al. Neurosci Biobehav Rev. 2014 Oct;46 Pt 2:256-69. doi: 10.1016/j.neubiorev.2013.10.012. Epub 2013 Oct 30. Neurosci Biobehav Rev. 2014. PMID: 24184744 Review.
Risk factors and pattern of weight gain in youths using antipsychotic drugs.
van der Esch CCL, Kloosterboer SM, van der Ende J, Reichart CG, Kouijzer MEJ, de Kroon MMJ, van Daalen E, Ester WA, Rieken R, Dieleman GC, Hillegers MHJ, van Gelder T, Koch BCP, Dierckx B. van der Esch CCL, et al. Eur Child Adolesc Psychiatry. 2021 Aug;30(8):1263-1271. doi: 10.1007/s00787-020-01614-4. Epub 2020 Aug 24. Eur Child Adolesc Psychiatry. 2021. PMID: 32839872 Free PMC article.
Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons.
Seabra CM, Aneichyk T, Erdin S, Tai DJC, De Esch CEF, Razaz P, An Y, Manavalan P, Ragavendran A, Stortchevoi A, Abad C, Young JI, Maciel P, Talkowski ME, Gusella JF. Seabra CM, et al. Among authors: de esch cef. Mol Autism. 2020 Jun 5;11(1):45. doi: 10.1186/s13229-020-00354-1. Mol Autism. 2020. PMID: 32503625 Free PMC article.
Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production.
Chen H, Victor AK, Klein J, Tacer KF, Tai DJ, de Esch C, Nuttle A, Temirov J, Burnett LC, Rosenbaum M, Zhang Y, Ding L, Moresco JJ, Diedrich JK, Yates JR 3rd, Tillman HS, Leibel RL, Talkowski ME, Billadeau DD, Reiter LT, Potts PR. Chen H, et al. Among authors: de esch c. JCI Insight. 2020 Sep 3;5(17):e138576. doi: 10.1172/jci.insight.138576. JCI Insight. 2020. PMID: 32879135 Free PMC article.
CXorf56, a dendritic neuronal protein, identified as a new candidate gene for X-linked intellectual disability.
Verkerk AJMH, Zeidler S, Breedveld G, Overbeek L, Huigh D, Koster L, van der Linde H, de Esch C, Severijnen LA, de Vries BBA, Swagemakers SMA, Willemsen R, Hoogeboom AJM, van der Spek PJ, Oostra BA. Verkerk AJMH, et al. Among authors: de esch c. Eur J Hum Genet. 2018 Apr;26(4):552-560. doi: 10.1038/s41431-017-0051-9. Epub 2018 Jan 26. Eur J Hum Genet. 2018. PMID: 29374277 Free PMC article.
24 results