Andy Willaert

Andy Willaert

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Andy Willaert

Andy Willaert

Publications by authors named "Andy Willaert"

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33Publications

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BATCH-GE: Analysis of NGS Data for Genome Editing Assessment.

Methods Mol Biol 2018 ;1865:83-90

Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.

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http://link.springer.com/10.1007/978-1-4939-8784-9_6
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http://dx.doi.org/10.1007/978-1-4939-8784-9_6DOI Listing
May 2019

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

Sci Rep 2017 11 28;7(1):16518. Epub 2017 Nov 28.

Center for Medical Genetics Ghent, Ghent University Hospital, Ghent, Belgium.

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http://dx.doi.org/10.1038/s41598-017-16725-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705637PMC
November 2017

RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder.

Neurology 2015 Apr 3;84(17):1760-6. Epub 2015 Apr 3.

From the Department of Neurology (P.S., B.D.) and the Center for Medical Genetics (T.V.D., W.S., A.W., A.D.P., P.J.C., B.D.), Ghent University Hospital, Belgium; and Inserm U1172, Centre de Recherches J-P Aubert (B.S.), and Inserm U1167, Institut Pasteur de Lille (B.D.), Université de Lille, France.

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http://www.neurology.org/content/84/17/1760.full.pdf
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http://www.neurology.org/cgi/doi/10.1212/WNL.000000000000152
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http://dx.doi.org/10.1212/WNL.0000000000001521DOI Listing
April 2015

Zebrafish models for ectopic mineralization disorders: practical issues from morpholino design to post-injection observations.

Front Genet 2013 8;4:74. Epub 2013 May 8.

Center for Medical Genetics, Ghent University Hospital Ghent, Belgium ; Department of Genetic Engineering and Biotechnology, Shahjalal University of Science and Technology Sylhet, Bangladesh.

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http://dx.doi.org/10.3389/fgene.2013.00074DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669896PMC
June 2013

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

Eur J Hum Genet 2008 Aug 27;16(8):970-6. Epub 2008 Feb 27.

Department of Medical Genetics, Ghent University Hospital, Ghent, Belgium.

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http://www.nature.com/articles/ejhg200831
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http://dx.doi.org/10.1038/ejhg.2008.31DOI Listing
August 2008

Missense mutations in LRP5 are not a common cause of idiopathic osteoporosis in adult men.

J Bone Miner Res 2005 Nov 11;20(11):1951-9. Epub 2005 Jul 11.

Department of Endocrinology, Ghent University Hospital, Ghent, Belgium.

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http://dx.doi.org/10.1359/JBMR.050705DOI Listing
November 2005