Nature Search

Challenges in expert ratings of marine habitat and species sensitivity to anthropogenic pressures

Niko Kallio
Jesper H. Andersen
Samuli Korpinen
ResearchOpen Access12 Apr 2025
Scientific Reports

Volume: 15, P: 1-11
Author Correction: Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease loci

Victor Lopez Soriano
Alfredo Dueñas Rey
Elfride De Baere
Amendments and CorrectionsOpen Access10 May 2024
Nature Communications

Volume: 15, P: 1
Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis

Jan Hellemans
Olena Preobrazhenska
Geert R Mortier
Research17 Oct 2004
Nature Genetics

Volume: 36, P: 1213-1218
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome

Paul J Coucke
Andy Willaert
Anne De Paepe
Research19 Mar 2006
Nature Genetics

Volume: 38, P: 452-457
Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease loci

Ultraconserved non-coding elements (UCNEs) can regulate developmental gene expression. Retinal multi-omics data integration revealed UCNEs to be candidate cis-regulatory elements during retinal development, which may be implicated in rare eye diseases.

Victor Lopez Soriano
Alfredo Dueñas Rey
Elfride De Baere
ResearchOpen Access21 Feb 2024
Nature Communications

Volume: 15, P: 1-14
A genome-wide linkage scan for low spinal bone mineral density in a single extended family confirms linkage to 1p36.3

Andy Willaert
Inge Van Pottelbergh
Paul Coucke
Research27 Feb 2008
European Journal of Human Genetics

Volume: 16, P: 970-976
Prime editing outperforms homology-directed repair as a tool for CRISPR-mediated variant knock-in in zebrafish

The authors evaluate multiple factors to improve knock-in rates using CRISPR-mediated homology-directed repair in zebrafish, before demonstrating that prime editing is a superior alternative.

Michiel Vanhooydonck
Elyne De Neef
Kathleen B. M. Claes
Research28 May 2025
Lab Animal

Volume: 54, P: 165-172
Publisher Correction: BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment

Annekatrien Boel
Wouter Steyaert
Andy Willaert
Amendments and CorrectionsOpen Access29 Oct 2018
Scientific Reports

Volume: 8, P: 1
Expressed repetitive elements are broadly applicable reference targets for normalization of reverse transcription-qPCR data in mice

Marjolijn Renard
Suzanne Vanhauwaert
Andy Willaert
ResearchOpen Access16 May 2018
Scientific Reports

Volume: 8, P: 1-9
BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment

Annekatrien Boel
Woutert Steyaert
Andy Willaert
ResearchOpen Access27 Jul 2016
Scientific Reports

Volume: 6, P: 1-10
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity

Nina De Rocker
Sarah Vergult
Björn Menten
Research18 Sept 2014
Genetics in Medicine

Volume: 17, P: 460-466
Maximizing CRISPR/Cas9 phenotype penetrance applying predictive modeling of editing outcomes in Xenopus and zebrafish embryos

Thomas Naert
Dieter Tulkens
Kris Vleminckx
ResearchOpen Access04 Sept 2020
Scientific Reports

Volume: 10, P: 1-12
Arterial tortuosity syndrome: 40 new families and literature review

Aude Beyens
Juliette Albuisson
Bert Callewaert
Research11 Jan 2018
Genetics in Medicine

Volume: 20, P: 1236-1245
Accurate quantification of homologous recombination in zebrafish: brca2 deficiency as a paradigm

Jeroen Vierstraete
Andy Willaert
Kathleen B. M. Claes
ResearchOpen Access28 Nov 2017
Scientific Reports

Volume: 7, P: 1-10
CRISPR/Cas9 mediated knockout of rb1 and rbl1 leads to rapid and penetrant retinoblastoma development in Xenopus tropicalis

Thomas Naert
Robin Colpaert
Kris Vleminckx
ResearchOpen Access14 Oct 2016
Scientific Reports

Volume: 6, P: 1-10
Correction: Arterial tortuosity syndrome: 40 new families and literature review

Aude Beyens
Juliette Albuisson
Bert Callewaert
Amendments and Corrections10 Sept 2018
Genetics in Medicine

Volume: 21, P: 1894-1895

Search

Challenges in expert ratings of marine habitat and species sensitivity to anthropogenic pressures

Author Correction: Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease loci

Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis

Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome

Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease loci

A genome-wide linkage scan for low spinal bone mineral density in a single extended family confirms linkage to 1p36.3

Prime editing outperforms homology-directed repair as a tool for CRISPR-mediated variant knock-in in zebrafish

Publisher Correction: BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment

Expressed repetitive elements are broadly applicable reference targets for normalization of reverse transcription-qPCR data in mice

BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment

Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity

Maximizing CRISPR/Cas9 phenotype penetrance applying predictive modeling of editing outcomes in Xenopus and zebrafish embryos

Arterial tortuosity syndrome: 40 new families and literature review

Accurate quantification of homologous recombination in zebrafish: brca2 deficiency as a paradigm

CRISPR/Cas9 mediated knockout of rb1 and rbl1 leads to rapid and penetrant retinoblastoma development in Xenopus tropicalis

Correction: Arterial tortuosity syndrome: 40 new families and literature review

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