Publications by authors named "An Crepel"

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A complex Xp11.22 deletion in a patient with syndromic autism: exploration of FAM120C as a positional candidate gene for autism.
Veerle De Wolf, An Crepel, Frans Schuit, Leentje van Lommel, Berten Ceulemans

Am J Med Genet A· December 2014

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Association of CDH11 with non-syndromic ASD.
An Crepel, Veerle De Wolf, Nathalie Brison, Berten Ceulemans, Didier Walleghem

Am J Med Genet B Neuropsychiatr Genet· July 2014

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Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12.
Christophe Goubau, Koen Devriendt, Nathalie Van der Aa, An Crepel, Dagmar Wieczorek

Eur J Hum Genet· December 2013

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Narrowing the critical deletion region for autism spectrum disorders on 16p11.2.
An Crepel, Jean Steyaert, Wouter De la Marche, Veerle De Wolf, Jean-Pierre Fryns

Am J Med Genet B Neuropsychiatr Genet· March 2011

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Human plasma glycome in attention-deficit hyperactivity disorder and autism spectrum disorders.
Nela Pivac, Ana Knezević, Olga Gornik, Maja Pucić, Wilmar Igl, An Crepel

Mol Cell Proteomics· January 2011

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SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles.
Dries Castermans, Karolien Volders, An Crepel, Liesbeth Backx, Rita De Vos

Hum Mol Genet· April 2010

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Position effect leading to haploinsufficiency in a mosaic ring chromosome 14 in a boy with autism.
Dries Castermans, Bernard Thienpont, Karolien Volders, An Crepel, Joris R Vermeesch

Eur J Hum Genet· October 2008

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