Dale J. Annear

Antwerpen, VLG, Belgium

Last Updated: 09/26/2026

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Found 19 publications

Correction: A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome.

Correction: A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome.

Journal: European journal of human genetics : EJHG

Published: March 31, 2026

Polymorphic CGG repeats in gene regulation and disease.

Polymorphic CGG repeats in gene regulation and disease.

Journal: American journal of human genetics

Published: October 14, 2025

CGG, CAG, and GAA: Genome-wide comparison of the disease linked trinucleotide short tandem repeats.

CGG, CAG, and GAA: Genome-wide comparison of the disease linked trinucleotide short tandem repeats.

Journal: BMC genomics

Published: July 29, 2025

An Adnp frameshift variant disrupts Wnt signalling inducing chromatocytoskeletal defects and autism-related behaviour in male mice.

An Adnp frameshift variant disrupts Wnt signalling inducing chromatocytoskeletal defects and autism-related behaviour in male mice.

Journal: EBioMedicine

Published: July 15, 2025

ADNP Exhibits Methyltransferase Activity in Overexpression Systems and Modulates DNA and Histone Methylation.

ADNP Exhibits Methyltransferase Activity in Overexpression Systems and Modulates DNA and Histone Methylation.

Journal: Autism research : official journal of the International Society for Autism Research

Published: July 01, 2025

Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes.

Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes.

Journal: Genome medicine

Published: April 12, 2025

A frameshift variant in activity-dependent neuroprotective protein (ADNP) causes nucleocytoskeletal alterations in a dizygotic male twin: a case study.

A frameshift variant in activity-dependent neuroprotective protein (ADNP) causes nucleocytoskeletal alterations in a dizygotic male twin: a case study.

Journal: Clinical epigenetics

Published: April 11, 2025

Whole-Genome Sequencing Reveals Individual and Cohort Level Insights into Chromosome 9p Syndromes.

Whole-Genome Sequencing Reveals Individual and Cohort Level Insights into Chromosome 9p Syndromes.

Journal: medRxiv : the preprint server for health sciences

Published: April 08, 2025

The Nutrigenomic Effect of Mela Rosa Marchigiana Callus Extract on Cellular Senescence: Insight From a Preliminary In Vitro Study.

The Nutrigenomic Effect of Mela Rosa Marchigiana Callus Extract on Cellular Senescence: Insight From a Preliminary In Vitro Study.

Journal: Molecular nutrition & food research

Published: March 18, 2025

A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome.

A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome.

Journal: European journal of human genetics : EJHG

Published: February 11, 2025

A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome.

A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome.

Journal: European journal of human genetics : EJHG

Published: February 11, 2025

Minimal repeats are ubiquitous sites of crossover and recombination across the human genome.

Minimal repeats are ubiquitous sites of crossover and recombination across the human genome.

Journal: BMC genomics

Published: February 03, 2025

Showing 1-12 of 19

Last Updated: 09/26/2026