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Page 1
Multiple paralogues and recombination mechanisms contribute to the high incidence of 22q11.2 Deletion Syndrome.
Vervoort L, Dierckxsens N, Sousa Santos M, Meynants S, Souche E, Cools R, Heung T, Devriendt K, Peeters H, McDonald-McGinn D, Swillen A, Breckpot J, Emanuel BS, Van Esch H, Bassett AS, Vermeesch JR. Vervoort L, et al. Among authors: dierckxsens n. Genome Res. 2024 Nov 13:gr.279331.124. doi: 10.1101/gr.279331.124. Online ahead of print. Genome Res. 2024. PMID: 39537358
Tracing Homopolymers in Oikopleura dioica's Mitogenome.
Dierckxsens N, Watanabe K, Tan Y, Masunaga A, Mansfield MJ, Miao J, Luscombe NM, Plessy C. Dierckxsens N, et al. Genome Biol Evol. 2024 Sep 3;16(9):evae182. doi: 10.1093/gbe/evae182. Genome Biol Evol. 2024. PMID: 39162185 Free PMC article.
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. Among authors: dierckxsens n. bioRxiv [Preprint]. 2024 Mar 18:2024.03.14.585046. doi: 10.1101/2024.03.14.585046. bioRxiv. 2024. Update in: Genome Res. 2024 Nov 13:gr.279331.124. doi: 10.1101/gr.279331.124 PMID: 38562770 Free PMC article. Updated. Preprint.
Parental genomes segregate into distinct blastomeres during multipolar zygotic divisions leading to mixoploid and chimeric blastocysts.
De Coster T, Masset H, Tšuiko O, Catteeuw M, Zhao Y, Dierckxsens N, Aparicio AL, Dimitriadou E, Debrock S, Peeraer K, de Ruijter-Villani M, Smits K, Van Soom A, Vermeesch JR. De Coster T, et al. Among authors: dierckxsens n. Genome Biol. 2022 Oct 3;23(1):201. doi: 10.1186/s13059-022-02763-2. Genome Biol. 2022. PMID: 36184650 Free PMC article.
Primary mediastinal large B-cell lymphoma is characterized by large-scale copy-neutral loss of heterozygosity.
Tuveri S, Debackere K, Marcelis L, Dierckxsens N, Demeulemeester J, Dimitriadou E, Dierickx D, Lefesvre P, Deraedt K, Graux C, Michaux L, Cools J, Tousseyn T, Vermeesch JR, Wlodarska I. Tuveri S, et al. Among authors: dierckxsens n. Genes Chromosomes Cancer. 2022 Oct;61(10):603-615. doi: 10.1002/gcc.23069. Epub 2022 Jul 9. Genes Chromosomes Cancer. 2022. PMID: 35611992
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. Among authors: dierckxsens n. Front Genet. 2021 Jul 15;12:706641. doi: 10.3389/fgene.2021.706641. eCollection 2021. Front Genet. 2021. PMID: 34335701 Free PMC article.
Unraveling heteroplasmy patterns with NOVOPlasty.
Dierckxsens N, Mardulyn P, Smits G. Dierckxsens N, et al. NAR Genom Bioinform. 2019 Oct 24;2(1):lqz011. doi: 10.1093/nargab/lqz011. eCollection 2020 Mar. NAR Genom Bioinform. 2019. PMID: 33575563 Free PMC article.
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