Lars Riff Jensen

2.3k total citations
12 papers, 1.3k citations indexed

About

Lars Riff Jensen is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Lars Riff Jensen has authored 12 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 2 papers in Immunology. Recurrent topics in Lars Riff Jensen's work include Genetics and Neurodevelopmental Disorders (9 papers), Epigenetics and DNA Methylation (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Lars Riff Jensen is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Epigenetics and DNA Methylation (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Lars Riff Jensen collaborates with scholars based in Germany, France and Australia. Lars Riff Jensen's co-authors include Jean‐Pierre Fryns, Jozef Gécz, Martine Raynaud, Claude Moraine, Hilde Van Esch, Andreas Tzschach, Hans‐Hilger Ropers, Thierry Bienvenu, Karen Hollanders and Dorien Lugtenberg and has published in prestigious journals such as The American Journal of Human Genetics, Gene and Neuroscience Letters.

In The Last Decade

Lars Riff Jensen

12 papers receiving 1.3k citations

Peers

Lars Riff Jensen
Cheryl Shoubridge Australia
R. Curtis Rogers United States
Bhooma Thiruvahindrapuram Canada
Marianne Till France
Jean‐Baptiste Rivière Canada
Anthony Leotta United States
Jan E. Dumon Belgium
Jon Schoorlemmer Spain
Edwin J. Young Canada
Audrey Labalme France
Cheryl Shoubridge Australia
Lars Riff Jensen
Citations per year, relative to Lars Riff Jensen Lars Riff Jensen (= 1×) peers Cheryl Shoubridge

Countries citing papers authored by Lars Riff Jensen

Since Specialization
Citations

This map shows the geographic impact of Lars Riff Jensen'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 Riff Jensen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lars Riff Jensen more than expected).

Fields of papers citing papers by Lars Riff Jensen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lars Riff Jensen. 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 Riff Jensen. The network helps show where Lars Riff Jensen may publish in the future.

Co-authorship network of co-authors of Lars Riff Jensen

This figure shows the co-authorship network connecting the top 25 collaborators of Lars Riff Jensen. A scholar is included among the top collaborators of Lars Riff Jensen 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 Riff Jensen. Lars Riff Jensen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
2.
Santos-Rebouças, Cíntia Barros, Natalia Fintelman‐Rodrigues, Lars Riff Jensen, et al.. (2011). A novel nonsense mutation in KDM5C/JARID1C gene causing intellectual disability, short stature and speech delay. Neuroscience Letters. 498(1). 67–71. 45 indexed citations
3.
Jensen, Lars Riff, H. Bartenschlager, Sinitdhorn Rujirabanjerd, et al.. (2010). A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C. PubMed. 3(1). 2–2. 32 indexed citations
4.
Motazacker, Mohammad Mahdi, Benjamin R. Rost, Tim Hucho, et al.. (2007). A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation. The American Journal of Human Genetics. 81(4). 792–798. 112 indexed citations
5.
Budny, Bartłomiej, Wei Chen, Heymut Omran, et al.. (2006). A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral–facial–digital type I syndrome. Human Genetics. 120(2). 171–178. 122 indexed citations
6.
Jensen, Lars Riff, Steffen Lenzner, Bettina A. Moser, et al.. (2006). X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11. European Journal of Human Genetics. 15(1). 68–75. 12 indexed citations
7.
Chen, Wei, Lars Riff Jensen, Jozef Gécz, et al.. (2006). Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation. European Journal of Human Genetics. 15(3). 375–378. 19 indexed citations
8.
Tzschach, Andreas, Steffen Lenzner, Bettina A. Moser, et al.. (2006). NovelJARID1C/SMCX mutations in patients with X-linked mental retardation. Human Mutation. 27(4). 389–389. 87 indexed citations
9.
Jensen, Lars Riff, Ulf Gurok, Bettina A. Moser, et al.. (2005). Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation. The American Journal of Human Genetics. 76(2). 227–236. 285 indexed citations
10.
Esch, Hilde Van, Marijke Bauters, Jaakko Ignatius, et al.. (2005). Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males. The American Journal of Human Genetics. 77(3). 442–453. 473 indexed citations
11.
Tümer, Zeynep, Peter J.P. Croucher, Lars Riff Jensen, et al.. (2002). Genomic structure, chromosome mapping and expression analysis of the human AVIL gene, and its exclusion as a candidate for locus for inflammatory bowel disease at 12q13–14 (IBD2). Gene. 288(1-2). 179–185. 15 indexed citations
12.
Møller, Lisbeth Birk, Zeynep Tümer, Connie Lund, et al.. (2000). Similar Splice-Site Mutations of the ATP7A Gene Lead to Different Phenotypes: Classical Menkes Disease or Occipital Horn Syndrome. The American Journal of Human Genetics. 66(4). 1211–1220. 84 indexed citations

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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