Lars A. Larsen

Copenhagen, Denmark

Last Updated: 09/26/2026

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Found 42 publications

TAK1 operates at the primary cilium in non-canonical TGFB/BMP signaling to control heart development.

TAK1 operates at the primary cilium in non-canonical TGFB/BMP signaling to control heart development.

Journal: PLoS biology

Published: May 01, 2026

ZDHHC5 interacts physically and functionally with DLG1 at primary cilia and regulates ciliary length and kidney morphology.

ZDHHC5 interacts physically and functionally with DLG1 at primary cilia and regulates ciliary length and kidney morphology.

Journal: Frontiers in cell and developmental biology

Published: February 06, 2026

The primary cilium at the helm: gatekeeper of TGF-β superfamily signaling in development, homeostasis, and disease.

The primary cilium at the helm: gatekeeper of TGF-β superfamily signaling in development, homeostasis, and disease.

Journal: Biochemical Society transactions

Published: July 14, 2025

DDIAS shields single-stranded DNA in mitosis and promotes vertebrate brain development.

DDIAS shields single-stranded DNA in mitosis and promotes vertebrate brain development.

Journal: Cell

Published: June 30, 2025

Primary cilia as architects of the neocortex: Roles in brain development, function, and microcephaly.

Primary cilia as architects of the neocortex: Roles in brain development, function, and microcephaly.

Journal: Developmental cell

Published: April 24, 2025

Oculocutaneous albinism variants in 28 consanguineous families and functional classification of a pathogenic deep intron variant in TYR.

Oculocutaneous albinism variants in 28 consanguineous families and functional classification of a pathogenic deep intron variant in TYR.

Journal: European journal of human genetics : EJHG

Published: March 18, 2025

Assessing the contribution of rare variants to congenital heart disease through a large-scale case-control exome study.

Assessing the contribution of rare variants to congenital heart disease through a large-scale case-control exome study.

Journal: NPJ genomic medicine

Published: March 03, 2025

Human Genetics of Atrial Septal Defect.

Human Genetics of Atrial Septal Defect.

Journal: Advances in experimental medicine and biology

Published: June 17, 2024

A novel GFAP frameshift variant identified in a family with optico-retinal dysplasia and vision impairment.

A novel GFAP frameshift variant identified in a family with optico-retinal dysplasia and vision impairment.

Journal: Human molecular genetics

Published: May 02, 2024

Rare homozygous cilia gene variants identified in consanguineous congenital heart disease patients.

Rare homozygous cilia gene variants identified in consanguineous congenital heart disease patients.

Journal: Human genetics

Published: March 07, 2024

Discovery of a novel mutation F184S (c.551T>C) in GATA4 gene causing congenital heart disease in a consanguineous Saudi family.

Discovery of a novel mutation F184S (c.551T>C) in GATA4 gene causing congenital heart disease in a consanguineous Saudi family.

Journal: Heliyon

Published: November 27, 2023

Pericardial delta like non-canonical NOTCH ligand 1 (Dlk1) augments fibrosis in the heart through epithelial to mesenchymal transition.

Pericardial delta like non-canonical NOTCH ligand 1 (Dlk1) augments fibrosis in the heart through epithelial to mesenchymal transition.

Journal: Clinical and translational medicine

Published: August 01, 2023

Showing 1-12 of 42

Last Updated: 09/26/2026