Lars K. Hansen

Odense Universitetshospital, Sdr. Boulevard 29
Odense, 5000, Denmark

Last Updated: 09/26/2026

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Found 39 publications

Erratum: Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology.

Erratum: Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology.

Journal: HGG advances

Published: December 30, 2022

CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.

CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.

Journal: European journal of human genetics : EJHG

Published: December 21, 2022

Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology.

Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology.

Journal: HGG advances

Published: December 14, 2021

Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis, and ventriculomegaly in humans.

Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis, and ventriculomegaly in humans.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 25, 2021

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.

Journal: Genome medicine

Published: September 04, 2020

Automatic sleep stage classification based on subcutaneous EEG in patients with epilepsy.

Automatic sleep stage classification based on subcutaneous EEG in patients with epilepsy.

Journal: Biomedical engineering online

Published: June 13, 2019

Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinism.

Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinism.

Journal: European journal of medical genetics

Published: December 17, 2018

Gait analysis for individually tailored interdisciplinary interventions in children with cerebral palsy: a randomized controlled trial.

Gait analysis for individually tailored interdisciplinary interventions in children with cerebral palsy: a randomized controlled trial.

Journal: Developmental medicine and child neurology

Published: December 15, 2018

Mosaic MECP2 variants in males with classical Rett syndrome features, including stereotypical hand movements.

Mosaic MECP2 variants in males with classical Rett syndrome features, including stereotypical hand movements.

Journal: Clinical genetics

Published: August 29, 2018

Efficacy and Safety of Dapagliflozin in Patients With Inadequately Controlled Type 1 Diabetes (the DEPICT-2 Study): 24-Week Results From a Randomized Controlled Trial.

Efficacy and Safety of Dapagliflozin in Patients With Inadequately Controlled Type 1 Diabetes (the DEPICT-2 Study): 24-Week Results From a Randomized Controlled Trial.

Journal: Diabetes care

Published: March 21, 2018

Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease.

Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease.

Journal: Neurology

Published: January 12, 2018

De Novo Variants in GRIA4 Lead to Intellectual Disability with or without Seizures and Gait Abnormalities.

De Novo Variants in GRIA4 Lead to Intellectual Disability with or without Seizures and Gait Abnormalities.

Journal: American journal of human genetics

Published: August 10, 2017

Showing 1-12 of 39

Last Updated: 09/26/2026