Lucas Herissant
Dudelange, ES, Luxembourg
Last Updated: 09/26/2026
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Found 10 publications
Novel Variants in PUS7 Associated With Intellectual Disability and Growth Retardation: Expanding the Clinical Spectrum in 13 Patients.
Journal: Clinical genetics
Published: February 26, 2026
Novel Variants in PUS7 Associated With Intellectual Disability and Growth Retardation: Expanding the Clinical Spectrum in 13 Patients.
Journal: Clinical genetics
Published: February 26, 2026
Pathogenic XPO1 variants cause a dominant neurodevelopmental disorder.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 13, 2025
AUTS2-related syndrome: Insights from a large European cohort.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 28, 2024
1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients.
Journal: American journal of medical genetics. Part A
Published: December 15, 2021
Epileptic encephalopathy caused by ARV1 deficiency: Refinement of the genotype-phenotype spectrum and functional impact on GPI-anchored proteins.
Journal: Clinical genetics
Published: May 07, 2021
The ubiquitin-selective chaperone Cdc48/p97 associates with Ubx3 to modulate monoubiquitylation of histone H2B.
Journal: Nucleic acids research
Published: September 04, 2014
H2B ubiquitylation modulates spliceosome assembly and function in budding yeast.
Journal: Biology of the cell
Published: January 17, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026