Lars Allan Larsen

Professor of Developmental Genetics

University of Copenhagen

Denmark

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Professor Lars Allan Larsen is a faculty member in the Department of Developmental Genetics at the University of Copenhagen, Denmark. His research focuses on the genetic basis of congenital heart diseases, genetic variants associated with vision impairment, and the implications of ciliary involvement in various disorders. Recent articles include significant findings on GFAP variants related to optico-retinal dysplasia and the discovery of mutations in genes such as GATA4 and TBX5 affecting cardiac phenotypes.

Articles (13)

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2024

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2024

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2024

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2024

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2024

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2024

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2023

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2022

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2022

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2021

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2021

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2020

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2020

Collaborators (9)

Ditte Caroline Andersen

University of Southern Denmark

DENMARK

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Lotte Pedersen

Københavns Universitet

DENMARK

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Alejandro Sifrim

Tenure Track Assistant Professor

Katholieke Universiteit Leuven

BELGIUM

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Alexandre Stewart

University of Ottawa Heart Institute

CANADA

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Lars Riber

University of Southern Denmark

DENMARK

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mads melbye

Norwegian University of Science and Technology

NORWAY

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Natasja Spring Ehlers

Københavns Universitet

DENMARK

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Line Kessel

Consultant, associate professor

Copenhagen University Hospital

DENMARK

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Vibeke E. Hjortdal

DENMARK

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Lars Allan Larsen

Research Interests

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About

Articles (13)

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

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

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

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

TBX5 variants and cardiac phenotype: A systematic review of the literature and a novel variant.

Human Genetics of Atrial Septal Defect.

The genetic background of hydrocephalus in a population-based cohort

Comparison of Outcome in Patients With Familial Versus Spontaneous Atrial Septal Defect

MCPH1: A Novel Case Report and a Review of the Literature

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

Mutation burden in patients with small unrepaired atrial septal defects

Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease.

RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesis.

Collaborators (9)

Ditte Caroline Andersen

Lotte Pedersen

Alejandro Sifrim

Alexandre Stewart

Lars Riber

mads melbye

Natasja Spring Ehlers

Line Kessel

Vibeke E. Hjortdal

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