Publications by authors named "Nele Cosemans"

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8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder.
Nele Cosemans, Jarymke Maljaars, Annick Vogels, Maureen Holvoet, Koen Devriendt

Neurogenetics· July 2021

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Increased Ca signaling in neurons derived from ASD induced pluripotent stem cells.
Sahar Avazzadeh, Katya McDonagh, Jamie Reilly, Yanqin Wang, Stephanie D Boomkamp, Nele Cosemans

Mol Autism· June 2020

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The clinical relevance of intragenic deletions.
Nele Cosemans, Laura Vandenhove, Annick Vogels, Koenraad Devriendt, Hilde Van Esch

J Med Genet· May 2020

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Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencing.
Molka Kammoun, Erika Souche, Paul Brady, Jia Ding, Nele Cosemans

Prenat Diagn· August 2018

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ZNF462 and KLF12 are disrupted by a de novo translocation in a patient with syndromic intellectual disability and autism spectrum disorder.
Nele Cosemans, Laura Vandenhove, Jarymke Maljaars, Hilde Van Esch, Koenraad Devriendt

Eur J Med Genet· July 2018

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Noise-robust assessment of SNP array based CNV calls through local noise estimation of log R ratios.
Nele Cosemans, Peter Claes, Nathalie Brison, Joris Robert Vermeesch, Hilde Peeters

Stat Appl Genet Mol Biol· April 2018

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Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.
Holly A F Stessman, Bo Xiong, Bradley P Coe, Tianyun Wang, Kendra Hoekzema, Nele Cosemans

Nat Genet· April 2017

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Executive functioning and local-global visual processing: candidate endophenotypes for autism spectrum disorder?
Lien Van Eylen, Bart Boets, Nele Cosemans, Hilde Peeters, Jean Steyaert

J Child Psychol Psychiatry· March 2017

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