Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
7 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.
Nat Genet. 2017 Oct;49(10):1529-1538. doi: 10.1038/ng.3933. Epub 2017 Aug 14.
Nat Genet. 2017.
PMID: 28805828
Free PMC article.
BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment.
Boel A, Steyaert W, De Rocker N, Menten B, Callewaert B, De Paepe A, Coucke P, Willaert A.
Boel A, et al. Among authors: de rocker n.
Sci Rep. 2016 Jul 27;6:30330. doi: 10.1038/srep30330.
Sci Rep. 2016.
PMID: 27461955
Free PMC article.
Item in Clipboard
Publisher Correction: BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment.
Boel A, Steyaert W, De Rocker N, Menten B, Callewaert B, De Paepe A, Coucke P, Willaert A.
Boel A, et al. Among authors: de rocker n.
Sci Rep. 2018 Oct 29;8(1):15845. doi: 10.1038/s41598-018-33869-y.
Sci Rep. 2018.
PMID: 30374100
Free PMC article.
Item in Clipboard
Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problems.
Vulto-van Silfhout AT, Rajamanickam S, Jensik PJ, Vergult S, de Rocker N, Newhall KJ, Raghavan R, Reardon SN, Jarrett K, McIntyre T, Bulinski J, Ownby SL, Huggenvik JI, McKnight GS, Rose GM, Cai X, Willaert A, Zweier C, Endele S, de Ligt J, van Bon BW, Lugtenberg D, de Vries PF, Veltman JA, van Bokhoven H, Brunner HG, Rauch A, de Brouwer AP, Carvill GL, Hoischen A, Mefford HC, Eichler EE, Vissers LE, Menten B, Collard MW, de Vries BB.
Vulto-van Silfhout AT, et al. Among authors: de rocker n.
Am J Hum Genet. 2014 May 1;94(5):649-61. doi: 10.1016/j.ajhg.2014.03.013. Epub 2014 Apr 10.
Am J Hum Genet. 2014.
PMID: 24726472
Free PMC article.
Item in Clipboard
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity.
De Rocker N, Vergult S, Koolen D, Jacobs E, Hoischen A, Zeesman S, Bang B, Béna F, Bockaert N, Bongers EM, de Ravel T, Devriendt K, Giglio S, Faivre L, Joss S, Maas S, Marle N, Novara F, Nowaczyk MJ, Peeters H, Polstra A, Roelens F, Rosenberg C, Thevenon J, Tümer Z, Vanhauwaert S, Varvagiannis K, Willaert A, Willemsen M, Willems M, Zuffardi O, Coucke P, Speleman F, Eichler EE, Kleefstra T, Menten B.
De Rocker N, et al.
Genet Med. 2015 Jun;17(6):460-6. doi: 10.1038/gim.2014.124. Epub 2014 Sep 18.
Genet Med. 2015.
PMID: 25232846
Free article.
Item in Clipboard
Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis.
Coppieters F, De Wilde B, Lefever S, De Meester E, De Rocker N, Van Cauwenbergh C, Pattyn F, Meire F, Leroy BP, Hellemans J, Vandesompele J, De Baere E.
Coppieters F, et al. Among authors: de rocker n.
Genet Med. 2012 Jun;14(6):576-85. doi: 10.1038/gim.2011.51. Epub 2012 Jan 26.
Genet Med. 2012.
PMID: 22261762
Free article.
Item in Clipboard
Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin.
Gistelinck C, Gioia R, Gagliardi A, Tonelli F, Marchese L, Bianchi L, Landi C, Bini L, Huysseune A, Witten PE, Staes A, Gevaert K, De Rocker N, Menten B, Malfait F, Leikin S, Carra S, Tenni R, Rossi A, De Paepe A, Coucke P, Willaert A, Forlino A.
Gistelinck C, et al. Among authors: de rocker n.
Sci Rep. 2016 Feb 15;6:21540. doi: 10.1038/srep21540.
Sci Rep. 2016.
PMID: 26876635
Free PMC article.
Item in Clipboard
Cite
Cite