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
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 2 |
2021 | 1 |
2022 | 1 |
2024 | 1 |
Search Results
5 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
The 22q11.2 Low Copy Repeats.
Genes (Basel). 2022 Nov 11;13(11):2101. doi: 10.3390/genes13112101.
Genes (Basel). 2022.
PMID: 36421776
Free PMC article.
Review.
22q11.2 Low Copy Repeats Expanded in the Human Lineage.
Vervoort L, Dierckxsens N, Pereboom Z, Capozzi O, Rocchi M, Shaikh TH, Vermeesch JR.
Vervoort L, et al.
Front Genet. 2021 Jul 15;12:706641. doi: 10.3389/fgene.2021.706641. eCollection 2021.
Front Genet. 2021.
PMID: 34335701
Free PMC article.
Item in Clipboard
Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins.
Vervoort L, Demaerel W, Rengifo LY, Odrzywolski A, Vergaelen E, Hestand MS, Breckpot J, Devriendt K, Swillen A, McDonald-McGinn DM, Fiksinski AM, Zinkstok JR, Morrow BE, Heung T, Vorstman JAS, Bassett AS, Chow EWC, Shashi V; International 22q11.2 Brain; Behavior Consortium; Vermeesch JR.
Vervoort L, et al.
Hum Mol Genet. 2019 Nov 15;28(22):3724-3733. doi: 10.1093/hmg/ddz166.
Hum Mol Genet. 2019.
PMID: 31884517
Free PMC article.
Item in Clipboard
The 22q11 low copy repeats are characterized by unprecedented size and structural variability.
Demaerel W, Mostovoy Y, Yilmaz F, Vervoort L, Pastor S, Hestand MS, Swillen A, Vergaelen E, Geiger EA, Coughlin CR, Chow SK, McDonald-McGinn D, Morrow B, Kwok PY, Xiao M, Emanuel BS, Shaikh TH, Vermeesch JR.
Demaerel W, et al. Among authors: vervoort l.
Genome Res. 2019 Sep;29(9):1389-1401. doi: 10.1101/gr.248682.119.
Genome Res. 2019.
PMID: 31481461
Free PMC article.
Item in Clipboard
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome.
Vervoort L, Dierckxsens N, Santos MS, Meynants S, Souche E, Cools R, Heung T, Devriendt K, Peeters H, McDonald-McGinn DM, Swillen A, Breckpot J, Emanuel BS, Van Esch H, Bassett AS, Vermeesch JR.
Vervoort L, et al.
bioRxiv [Preprint]. 2024 Mar 18:2024.03.14.585046. doi: 10.1101/2024.03.14.585046.
bioRxiv. 2024.
PMID: 38562770
Free PMC article.
Preprint.
Item in Clipboard
Cite
Cite