Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Edit custom filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

15 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
CRISPR/Cas9-mediated genome editing in naïve human embryonic stem cells.
Jacobs EZ, Warrier S, Volders PJ, D'haene E, Van Lombergen E, Vantomme L, Van der Jeught M, Heindryckx B, Menten B, Vergult S. Jacobs EZ, et al. Among authors: vantomme l. Sci Rep. 2017 Nov 30;7(1):16650. doi: 10.1038/s41598-017-16932-y. Sci Rep. 2017. PMID: 29192200 Free PMC article.
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability.
Pérez Baca MDR, Jacobs EZ, Vantomme L, Leblanc P, Bogaert E, Dheedene A, De Cock L, Haghshenas S, Foroutan A, Levy MA, Kerkhof J, McConkey H, Chen CA, Batzir NA, Wang X, Palomares M, Carels M; ZFHX3 consortium; Dermaut B, Sadikovic B, Menten B, Yuan B, Vergult S, Callewaert B. Pérez Baca MDR, et al. Among authors: vantomme l. Am J Hum Genet. 2024 Mar 7;111(3):509-528. doi: 10.1016/j.ajhg.2024.01.013. Epub 2024 Feb 26. Am J Hum Genet. 2024. PMID: 38412861 Free PMC article.
Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci.
D'haene E, López-Soriano V, Martínez-García PM, Kalayanamontri S, Rey AD, Sousa-Ortega A, Naranjo S, Van de Sompele S, Vantomme L, Mahieu Q, Vergult S, Neto A, Gómez-Skarmeta JL, Martínez-Morales JR, Bauwens M, Tena JJ, De Baere E. D'haene E, et al. Among authors: vantomme l. Genome Biol. 2024 May 17;25(1):123. doi: 10.1186/s13059-024-03250-6. Genome Biol. 2024. PMID: 38760655 Free PMC article.
Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder.
Pérez Baca MDR, Palomares-Bralo M, Vanhooydonck M, Hamerlinck L, D'haene E, Leimbacher S, Jacobs EZ, De Cock L, D'haenens E, Dheedene A, Malfait Z, Vantomme L, Silva A, Rooney K, Zhao X, Saeidian AH, Owen NM, Santos-Simarro F, Lleuger-Pujol R, García-Miñaúr S, Losantos-García I, Menten B, Gestri G, Ragge N; ZFHX4 consortium; Sadikovic B, Bogaert E, Vleminckx K, Naert T, Syx D, Callewaert B, Vergult S. Pérez Baca MDR, et al. Among authors: vantomme l. Am J Hum Genet. 2025 Jun 5;112(6):1388-1414. doi: 10.1016/j.ajhg.2025.04.008. Epub 2025 May 13. Am J Hum Genet. 2025. PMID: 40367947 Free PMC article.
Cracking rare disorders: a new minimally invasive RNA-seq protocol.
De Cock L, D'haenens E, Vantomme L, Backers L, Beyens A, Claes KB, De Clercq G, de Putter R, Kumps C, Schuermans N, Sourbron J, Syryn H, Tavernier S, Vanbelleghem E, Vanakker O, Vandekerckhove B, Van Damme T, Callewaert B, Dheedene A, Vergult S, Menten B. De Cock L, et al. Among authors: vantomme l. NPJ Genom Med. 2025 May 28;10(1):45. doi: 10.1038/s41525-025-00502-7. NPJ Genom Med. 2025. PMID: 40436861 Free PMC article.
De Novo CUL3 Variant in a Child Presenting With Hypertension and Kidney Failure.
Peremans L, Dendooven A, D'haenens E, Symoens S, Callewaert B, Decock L, Vantomme L, Vergult S, Dehoorne J, Dossche L, Prytula A, Raes A, Renson T, Snauwaert E, Van Damme T. Peremans L, et al. Among authors: vantomme l. Kidney Int Rep. 2025 Apr 21;10(7):2484-2487. doi: 10.1016/j.ekir.2025.04.032. eCollection 2025 Jul. Kidney Int Rep. 2025. PMID: 40677353 Free PMC article. No abstract available.
Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment.
Hamerlinck L, D'haene E, Vaughan MB, Van Loon N, Pérez Baca MDR, Leimbacher S, Kosicki M, Colombo L, Genbrugge L, Vantomme L, Daal E, Ramos LLP, Avdjieva-Tzavella DM, Goel H, Devriendt K, Jordanova A, Dheedene A, Visel A, Menten B, Callewaert B, Vergult S. Hamerlinck L, et al. Among authors: vantomme l. Nat Commun. 2026 Jun 3. doi: 10.1038/s41467-026-73770-1. Online ahead of print. Nat Commun. 2026. PMID: 42236689 Free article.
15 results