Hilde Peeters

Hilde Peeters

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Hilde Peeters

Hilde Peeters

Publications by authors named "Hilde Peeters"

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The East Flanders Prospective Twin Survey (EFPTS): 55 Years Later.

Twin Res Hum Genet 2019 Sep 9:1-6. Epub 2019 Sep 9.

Department of Obstetrics and Gynaecology, Ghent University Hospital, Ghent University, Ghent, Belgium.

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http://dx.doi.org/10.1017/thg.2019.64DOI Listing
September 2019

Usefulness of fragile X checklist and CGG distribution in specialized institutions in Kinshasa, DR Congo.

J Community Genet 2019 Jan 4;10(1):153-159. Epub 2018 Jul 4.

Centre for Human Genetics, University Hospitals, University of Leuven, Herestraat 49, Bus 602, 3000, Leuven, Belgium.

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http://dx.doi.org/10.1007/s12687-018-0374-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325043PMC
January 2019

Olfactory function in patients with nonsyndromic orofacial clefts and their unaffected relatives.

Am J Med Genet A 2018 11 22;176(11):2375-2381. Epub 2018 Oct 22.

Department of Otorhinolaryngology, Head and Neck Surgery, University Hospitals Leuven, Leuven, Belgium.

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http://doi.wiley.com/10.1002/ajmg.a.40348
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http://dx.doi.org/10.1002/ajmg.a.40348DOI Listing
November 2018

ZNF462 and KLF12 are disrupted by a de novo translocation in a patient with syndromic intellectual disability and autism spectrum disorder.

Eur J Med Genet 2018 Jul 7;61(7):376-383. Epub 2018 Feb 7.

Center for Human Genetics, University Hospital Leuven, KU Leuven, Leuven, Belgium; Leuven Autism Research (LAuRes), Leuven, Belgium. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S17697212173063
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http://dx.doi.org/10.1016/j.ejmg.2018.02.002DOI Listing
July 2018

The ethics of patenting autism genes.

Nat Rev Genet 2018 05 26;19(5):247-248. Epub 2018 Mar 26.

Leuven Autism Research (LAuRes), KU Leuven.

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http://dx.doi.org/10.1038/nrg.2018.17DOI Listing
May 2018

Noise-robust assessment of SNP array based CNV calls through local noise estimation of log R ratios.

Stat Appl Genet Mol Biol 2018 04 28;17(2). Epub 2018 Apr 28.

Center for Human Genetics, University Hospital Leuven, KU Leuven, Leuven, Belgium.

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http://www.degruyter.com/view/j/sagmb.2018.17.issue-2/sagmb-
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http://dx.doi.org/10.1515/sagmb-2017-0026DOI Listing
April 2018

Testing the face shape hypothesis in twins discordant for nonsyndromic orofacial clefting.

Am J Med Genet A 2017 Nov 8;173(11):2886-2892. Epub 2017 Sep 8.

Center for Craniofacial and Dental Genetics, Department of Oral Biology, University of Pittsburgh, Pittsburgh, Pennsylvania.

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http://dx.doi.org/10.1002/ajmg.a.38471DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725745PMC
November 2017

Executive functioning and local-global visual processing: candidate endophenotypes for autism spectrum disorder?

J Child Psychol Psychiatry 2017 03 2;58(3):258-269. Epub 2016 Nov 2.

Parenting and Special Education Research Unit, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1111/jcpp.12637DOI Listing
March 2017

Genetic testing and counseling in the case of an autism diagnosis: A caregivers perspective.

Eur J Med Genet 2016 Sep 17;59(9):452-8. Epub 2016 Aug 17.

Centre for Biomedical Ethics and Law, KU Leuven, Belgium.

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http://dx.doi.org/10.1016/j.ejmg.2016.08.007DOI Listing
September 2016

The ethics of complexity. Genetics and autism, a literature review.

Am J Med Genet B Neuropsychiatr Genet 2016 Apr 12;171B(3):305-16. Epub 2016 Feb 12.

Centre for Biomedical Ethics and Law, KU Leuven, Leuven, Belgium.

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http://doi.wiley.com/10.1002/ajmg.b.32432
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http://dx.doi.org/10.1002/ajmg.b.32432DOI Listing
April 2016

Shooting a moving target. Researching autism genes: An interview study with professionals.

Eur J Med Genet 2016 Jan 23;59(1):32-8. Epub 2015 Dec 23.

Centre for Biomedical Ethics and Law, KU Leuven, Belgium.

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http://dx.doi.org/10.1016/j.ejmg.2015.12.009DOI Listing
January 2016

The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.

J Child Neurol 2015 Dec 20;30(14):1947-53. Epub 2015 Sep 20.

Beyster Center for Genomics of Psychiatric Diseases, Department of Psychiatry, and Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA, USA

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http://dx.doi.org/10.1177/0883073815602066DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4739844PMC
December 2015

Platelet studies in autism spectrum disorder patients and first-degree relatives.

Mol Autism 2015 23;6:57. Epub 2015 Oct 23.

Department of Cardiovascular Sciences, Centre for Molecular and Vascular Biology, KU Leuven, Gasthuisberg Campus, O & N I, Herestraat 49-b911, 3000 Leuven, Belgium ; The LAuRes Consortium, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1186/s13229-015-0051-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619313PMC
October 2015

Homozygous missense mutation in STYXL1 associated with moderate intellectual disability, epilepsy and behavioural complexities.

Eur J Med Genet 2015 Apr 24;58(4):205-10. Epub 2015 Feb 24.

Center for Human Genetics, University Hospitals Leuven, KU Leuven, Leuven, Belgium; Laboratory for the Genetics of Cognition, KU Leuven, Leuven, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2015.02.006DOI Listing
April 2015

A complex Xp11.22 deletion in a patient with syndromic autism: exploration of FAM120C as a positional candidate gene for autism.

Am J Med Genet A 2014 Dec 24;164A(12):3035-41. Epub 2014 Sep 24.

Center for Human Genetics, University Hospitals Leuven, KU Leuven, Leuven, Belgium; Leuven Autism Research (LAuRes), KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1002/ajmg.a.36752DOI Listing
December 2014

Homozygous loss-of-function mutation in ALMS1 causes the lethal disorder mitogenic cardiomyopathy in two siblings.

Eur J Med Genet 2014 Sep 24;57(9):532-5. Epub 2014 Jun 24.

Center of Human Genetics, University Hospitals Leuven, Katholieke Universiteit Leuven, Belgium.

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http://dx.doi.org/10.1016/j.ejmg.2014.06.004DOI Listing
September 2014

Association of CDH11 with non-syndromic ASD.

Am J Med Genet B Neuropsychiatr Genet 2014 Jul 19;165B(5):391-8. Epub 2014 May 19.

Center for Human Genetics, University Hospitals Leuven, KU Leuven, Leuven, Belgium; Leuven Autism Research (LAuRes), Leuven, Belgium.

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http://dx.doi.org/10.1002/ajmg.b.32243DOI Listing
July 2014

Genetic counseling for susceptibility loci and neurodevelopmental disorders: the del15q11.2 as an example.

Am J Med Genet A 2013 Nov 10;161A(11):2846-54. Epub 2013 Oct 10.

Center for Human Genetics, University Hospitals Leuven, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1002/ajmg.a.36209DOI Listing
November 2013

Multiple pilomatricomas with somatic CTNNB1 mutations in children with constitutive mismatch repair deficiency.

Genes Chromosomes Cancer 2013 Jul 30;52(7):656-64. Epub 2013 Apr 30.

Department of Human Genetics, KU Leuven, University Hospitals Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1002/gcc.22061DOI Listing
July 2013

The East Flanders Prospective Twin Survey (EFPTS): an actual perception.

Twin Res Hum Genet 2013 Feb 29;16(1):58-63. Epub 2012 Oct 29.

Department of Human Genetics, University Hospitals, Leuven, Belgium.

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http://dx.doi.org/10.1017/thg.2012.75DOI Listing
February 2013

Time trends in the natural dizygotic twinning rate.

Hum Reprod 2011 Aug 13;26(8):2247-52. Epub 2011 Jun 13.

Department for Human Genetics, University Hospital Leuven, Herestraat 49, B-3000 Leuven, Belgium.

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http://dx.doi.org/10.1093/humrep/der180DOI Listing
August 2011

Focal preauricular dermal dysplasia: distinctive congenital lesions with a bilateral and symmetric distribution.

Eur J Med Genet 2006 Mar-Apr;49(2):135-9. Epub 2005 Aug 11.

Department of Medical Genetics, Rikshospitalet, Forskningsveien 2B, 0407 Oslo, Norway.

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http://dx.doi.org/10.1016/j.ejmg.2005.06.005DOI Listing
April 2009

Human laterality disorders.

Eur J Med Genet 2006 Sep-Oct;49(5):349-62. Epub 2006 Jan 3.

Department of Human Genetics, University Hospital Gasthuisberg, University of Leuven, Herestraat 49, B-3000 Leuven, Belgium.

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http://dx.doi.org/10.1016/j.ejmg.2005.12.003DOI Listing
November 2006