Lars Allan Larsen

3.9k citations

91 papers · 2.7k indexed · h-index 29

Molecular Biology top 5%
Genetics top 2%
Cardiology and Cardiovascular Medicine top 2%
Epidemiology top 10%
Pulmonary and Respiratory Medicine top 10%

Co-authors: Paal Skytt Andersen Michael Christiansen Jens Vuust Søren T. Christensen Niels Tommerup Lotte B. Pedersen Kjeld Møllgård Troels Andersen
Topics: Congenital heart defects research (22 papers)Congenital Heart Disease Studies (15 papers)Genomic variations and chromosomal abnormalities (14 papers)
Cited by: Cardiology and Cardiovascular Medicine Genetics Molecular Biology
Journals: Proceedings of the National Academy of SciencesSHILAP Revista de lepidopterologíaThe Journal of Cell Biology
Partner nations: Denmark United States Germany

In The Last Decade

Lars Allan Larsen

88 papers receiving 2.6k citations

Peers

Countries citing papers authored by Lars Allan Larsen

Since Specialization

Citations

This map shows the geographic impact of Lars Allan Larsen's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Lars Allan Larsen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lars Allan Larsen more than expected).

Fields of papers citing papers by Lars Allan Larsen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lars Allan Larsen. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Lars Allan Larsen. The network helps show where Lars Allan Larsen may publish in the future.

Co-authorship network of co-authors of Lars Allan Larsen

This figure shows the co-authorship network connecting the top 25 collaborators of Lars Allan Larsen. A scholar is included among the top collaborators of Lars Allan Larsen based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Lars Allan Larsen. Lars Allan Larsen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	A novel GFAP frameshift variant identified in a family with optico-retinal dysplasia and vision impairment 2024 ·Human Molecular Genetics ·(unknown),Cecilia Rönnbäck,Cathrine Jespersgaard,(unknown),(unknown),Line Kessel,Søren T. Christensen,Karen Brøndum‐Nielsen,Kjeld Møllgård,Thomas Rosenberg,Lars Allan Larsen,Karen Grønskov	1
2	Rare homozygous cilia gene variants identified in consanguineous congenital heart disease patients 2024 ·Human Genetics ·(unknown),(unknown),(unknown),(unknown),(unknown),Zafar Ali,(unknown),(unknown),Shahid Mahmood Baig,Søren T. Christensen,Muhammad Bilal Farooq,Lars Allan Larsen	2
3	The genetic background of hydrocephalus in a population-based cohort: implication of ciliary involvement 2022 ·Brain Communications ·Tina Nørgaard Munch,Paula L. Hedley,Christian M. Hagen,Marie Bækvad‐Hansen,Frank Geller,Jonas Bybjerg‐Grauholm,Merete Nordentoft,Anders D. Børglum,Thomas Werge,Mads Melbye,David M. Hougaard,Lars Allan Larsen,Søren T. Christensen,Michael Christiansen	3
4	Mutation burden in patients with small unrepaired atrial septal defects 2021 ·SHILAP Revista de lepidopterología ·(unknown),Camilla Nyboe,(unknown),Sebastian Udholm,(unknown),Vibeke E. Hjortdal,Lars Allan Larsen	6
5	Haploinsufficiency of ARHGAP42 is associated with hypertension 2019 ·European Journal of Human Genetics ·(unknown),Malene Bøgehus Rasmussen,Mana M. Mehrjouy,Lusine Nazaryan‐Petersen,Claus Hansen,Mads Bak,Niels Grarup,Anne Nørremølle,Lars Allan Larsen,Henrik Vestergaard,Torben Hansen,Niels Tommerup,Iben Bache	12
6	The E3 ubiquitin ligase SMURF1 regulates cell-fate specification and outflow tract septation during mammalian heart development 2018 ·Scientific Reports ·Klaus Koefoed,(unknown),Peter Andersen,(unknown),Melanie Pye,Troels Andersen,(unknown),Eske Bendsen,Masahiro Narimatsu,Frederik Vilhardt,Lotte B. Pedersen,Jeffrey L. Wrana,Robert H. Anderson,Kjeld Møllgård,Søren T. Christensen,Lars Allan Larsen	21
7	IFT20 modulates ciliary PDGFRα signaling by regulating the stability of Cbl E3 ubiquitin ligases 2017 ·The Journal of Cell Biology ·F Schmid,(unknown),(unknown),(unknown),(unknown),Pietro Farinelli,Lars Allan Larsen,Jens Andersen,Lotte B. Pedersen,Søren T. Christensen	52
8	Detecting 22q11.2 Deletions by Use of Multiplex Ligation-Dependent Probe Amplification on DNA from Neonatal Dried Blood Spot Samples 2010 ·Journal of Molecular Diagnostics ·Karina M. Sørensen,Peter Agergaard,Charlotte Olesen,Paal Skytt Andersen,Lars Allan Larsen,John R. Østergaard,Jan P. Schouten,Michael Christiansen	30
9	Using Nucleofection of siRNA Constructs for Knockdown of Primary Cilia in P19.CL6 Cancer Stem Cell Differentiation into Cardiomyocytes 2009 ·Methods in cell biology ·Christian Clément,Lars Allan Larsen,Søren T. Christensen	14
10	GLI1 Is Involved in Cell Cycle Regulation and Proliferation of NT2 Embryonal Carcinoma Stem Cells 2008 ·DNA and Cell Biology ·(unknown),Allan Lind-Thomsen,Mikkel W. Pedersen,Hanne Jarmer,Mads Bak,Lis Hasholt,Niels Tommerup,Zeynep Tümer,Lars Allan Larsen	9
11	A Homogeneous Assay for Analysis of FMR1 Promoter Methylation in Patients with Fragile X Syndrome 2007 ·Clinical Chemistry ·Christina Dahl,Karen Grønskov,Lars Allan Larsen,Per Guldberg,Karen Brøndum‐Nielsen	27
12	Screening of 99 Danish Patients with Congenital Heart Disease for GATA4 Mutations 2006 ·Genetic Testing ·Litu Zhang,Zeynep Tümer,(unknown),Paal Skytt Andersen,Niels Tommerup,Lars Allan Larsen	18
13	Hedgehog signaling in small-cell lung cancer: Frequent in vivo but a rare event in vitro 2006 ·Lung Cancer ·(unknown),Mikkel W. Pedersen,Nina Marie Pedersen,Christian Ensinger,Zeynep Tümer,Niels Tommerup,Hans Skovgaard Poulsen,Lars Allan Larsen	64
14	Potassium Must Be Considered in Congenital Long QT Syndrome 2005 ·Michael Christiansen,Keld Kjeldsen,Göran Wettrell,Lars Allan Larsen,L Lundkvist,Paal Skytt Andersen,(unknown),Jørgen K. Kanters,Jens Vuust	5
15	Identification of a Novel EYA1 Splice-Site Mutation in a Danish Branchio-Oto-Renal Syndrome Family 2004 ·Genetic Testing ·(unknown),Zeynep Tümer,Niels Tommerup,Lisbeth Tranebjærg,Lars Allan Larsen	7
16	GJB2 and GJB6 Mutations in 165 Danish Patients Showing Non-Syndromic Hearing Impairment 2004 ·Genetic Testing ·Karen Grønskov,Lars Allan Larsen,Nanna Dahl Rendtorff,Agnete Parving,Bent Nørgaard‐Pedersen,Karen Brøndum‐Nielsen	10
17	Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency 2004 ·European Journal of Human Genetics ·Paal Skytt Andersen,Ole Havndrup,Henning Bundgaard,Lars Allan Larsen,Jens Vuust,Anders Kirstein Pedersen,Keld Kjeldsen,Michael Christiansen	58
18	High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method 2003 ·Human Mutation ·Paal Skytt Andersen,Cathrine Jespersgaard,Jens Vuust,Michael Christiansen,Lars Allan Larsen	47
19	High Throughput Mutation Screening by Automated Capillary Electrophoresis 2000 ·Combinatorial Chemistry & High Throughput Screening ·Lars Allan Larsen,Michael Christiansen,Jens Vuust,Paal Skytt Andersen	22
20	High-throughput analysis of Fragile X (CGG) n alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis 1997 ·Human Genetics ·Lars Allan Larsen,Karen Grønskov,Bent Nørgaard‐Pedersen,Karen Brøndum‐Nielsen,Lis Hasholt,Jens Vuust	42

About Lars Allan Larsen

Lars Allan Larsen is a scholar working on Genetics, Cardiology and Cardiovascular Medicine and Molecular Biology, having authored 91 papers that have together received 2.7k indexed citations. Recurring topics across this work include Congenital heart defects research (22 papers), Congenital Heart Disease Studies (15 papers) and Genomic variations and chromosomal abnormalities (14 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (728 citations), Genetics (827 citations) and Molecular Biology (2.0k citations). Lars Allan Larsen has collaborated with scholars based in Denmark, United States and Germany. Frequent co-authors include Paal Skytt Andersen, Michael Christiansen, Jens Vuust, Søren T. Christensen, Niels Tommerup, Lotte B. Pedersen, Kjeld Møllgård, Troels Andersen, Jørgen K. Kanters and Christian Clément. Their work appears in journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and The Journal of Cell Biology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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