Lars Allan Larsen - The Wilhelm Johannsen Centre for Functional Genome Research, University of Copenhagen

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论文共 154 篇作者统计合作学者相似作者

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Loss of GFAP causes optico-retinal dysplasia and vision impairment

Menachem Viktor Khamo Sarusie,Cecilia Rönnbäck,Cathrine Jespersgaard, Sif Baungaard,Yeasmeen Ali,Line Kessel,Søren Tvorup Christensen,Karen Brøndum- Nielsen,Kjeld Møllgård,Thomas Rosenberg,Lars Allan Larsen,Karen Grønskov

medrxiv（2024）

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Discovery of a Novel Mutation F184S (c.551t>c) in GATA4 Gene Causing Congenital Heart Disease in a Consanguineous Saudi Family

Mahmood Rasool, Peter Natesan Pushparaj,Absarul Haque, Ayat Mohammed Shorbaji, Loubna Siraj Mira,Sherin Bakhashab,Mohamed Nabil Alama,Muhammad Farooq,Sajjad Karim,Lars Allan Larsen

HELIYONno. 17 (2024)

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

Canan Doganli, Daniel A. Baird,Yeasmeen Ali, Oskar Kaaber Thomsen,Enrique Audain, Line Jessen, Pauline Munck Truelsen,Johanne Bay Mogensen, Maria Schrøder Holm, Kateřina Apolínová, Lorenzo Buttò, Maria Diamanti,Jindřiška Leischner Fialová,Emma M. Wade,Stephen P. Robertson,Lotte Bang Pedersen,Laurent Argiro,Fabienne Lescroart,Marc-Phillip Hitz,Søren Tvorup Christensen,Lars Allan Larsen

biorxiv（2024）

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TBX5 Variants and Cardiac Phenotype: A Systematic Review of the Literature and a Novel Variant

Anne Kathrine Møller Nielsen,Anna Maria Dehn,Vibeke Hjortdal,Lars Allan Larsen

European journal of medical genetics（2024）

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Human Genetics of Atrial Septal Defect

Lars A Larsen,Marc-Phillip Hitz

Advances in experimental medicine and biology (2024): 467-480

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Rare Homozygous Cilia Gene Variants Identified in Consanguineous Congenital Heart Disease Patients

Daniel A. Baird,Hira Mubeen,Canan Doganli, Jasmijn B. Miltenburg, Oskar Kaaber Thomsen,Zafar Ali, Tahir Naveed,Asif ur Rehman,Shahid Mahmood Baig,Søren Tvorup Christensen,Muhammad Farooq,Lars Allan Larsen

Human geneticsno. 11 (2024): 1323-1339

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Pericardial Delta Like Non‐canonical NOTCH Ligand 1 (dlk1) Augments Fibrosis in the Heart Through Epithelial to Mesenchymal Transition

Charlotte Harken Jensen, Rikke Helin Johnsen,Tilde Eskildsen,Christina Baun,Ditte Gry Ellman,Shu Fang,Sara Thornby Bak,Svend Hvidsten,Lars Allan Larsen,Ann Mari Rosager,Lars Peter Riber,Mikael Schneider,Jo De Mey,Mads Thomassen,Mark Burton,Shizuka Uchida,Jorge Laborda,Ditte Caroline Andersen

CLINICAL AND TRANSLATIONAL MEDICINEno. 2 (2024)

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Mutations in the microcephaly gene,RRP7A, converge on defective TGFB/BMP signaling and associated trafficking events at the primary cilium

J. L. Fialova, J. Stensbol, S. Antony, E. Dyke,L. B. Pedersen,N. N. Kasri,K. Boldt,L. A. Larsen,S. T. Christensen

MOLECULAR BIOLOGY OF THE CELLno. 2 (2023): 933-933

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