Celine Helsmoortel

Gent, VLG, Belgium

Last Updated: 09/26/2026

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Found 16 publications

Performance Evaluation of Three DNA Sample Tracking Tools in a Whole Exome Sequencing Workflow.

Performance Evaluation of Three DNA Sample Tracking Tools in a Whole Exome Sequencing Workflow.

Journal: Molecular diagnosis & therapy

Published: March 20, 2022

Osmotic stress inhibits leaf growth of Arabidopsis thaliana by enhancing ARF-mediated auxin responses.

Osmotic stress inhibits leaf growth of Arabidopsis thaliana by enhancing ARF-mediated auxin responses.

Journal: The New phytologist

Published: November 07, 2019

Decentralization of Next-Generation RNA Sequencing-Based MammaPrint® and BluePrint® Kit at University Hospitals Leuven and Curie Institute Paris.

Decentralization of Next-Generation RNA Sequencing-Based MammaPrint® and BluePrint® Kit at University Hospitals Leuven and Curie Institute Paris.

Journal: Translational oncology

Published: June 27, 2019

Correction to: The Compassionate Side of Neuroscience: Tony Sermone's Undiagnosed Genetic Journey-ADNP Mutation.

Correction to: The Compassionate Side of Neuroscience: Tony Sermone's Undiagnosed Genetic Journey-ADNP Mutation.

Journal: Journal of molecular neuroscience : MN

Published: January 22, 2018

Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability.

Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability.

Journal: Gene

Published: October 14, 2016

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.

Journal: Nature genetics

Published: September 23, 2016

Erratum to: The Compassionate Side of Neuroscience: Tony Sermone's Undiagnosed Genetic Journey--ADNP Mutation.

Erratum to: The Compassionate Side of Neuroscience: Tony Sermone's Undiagnosed Genetic Journey--ADNP Mutation.

Journal: Journal of molecular neuroscience : MN

Published: March 30, 2016

Whole genome sequencing of a dizygotic twin suggests a role for the serotonin receptor HTR7 in autism spectrum disorder.

Whole genome sequencing of a dizygotic twin suggests a role for the serotonin receptor HTR7 in autism spectrum disorder.

Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

Published: February 14, 2016

The Compassionate Side of Neuroscience: Tony Sermone's Undiagnosed Genetic Journey--ADNP Mutation.

The Compassionate Side of Neuroscience: Tony Sermone's Undiagnosed Genetic Journey--ADNP Mutation.

Journal: Journal of molecular neuroscience : MN

Published: July 15, 2015

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Journal: American journal of human genetics

Published: June 04, 2015

Multiplexed High Resolution Melting Assay for Versatile Sample Tracking in a Diagnostic and Research Setting.

Multiplexed High Resolution Melting Assay for Versatile Sample Tracking in a Diagnostic and Research Setting.

Journal: The Journal of molecular diagnostics : JMD

Published: April 23, 2015

The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism.

The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism.

Journal: American journal of medical genetics. Part C, Seminars in medical genetics

Published: August 30, 2014

Showing 1-12 of 16

Last Updated: 09/26/2026