L G Jensen

421 total citations
24 papers, 363 citations indexed

About

L G Jensen is a scholar working on Surgery, Molecular Biology and Cancer Research. According to data from OpenAlex, L G Jensen has authored 24 papers receiving a total of 363 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Surgery, 10 papers in Molecular Biology and 7 papers in Cancer Research. Recurrent topics in L G Jensen's work include Lipoproteins and Cardiovascular Health (14 papers), RNA Research and Splicing (7 papers) and Cancer, Lipids, and Metabolism (5 papers). L G Jensen is often cited by papers focused on Lipoproteins and Cardiovascular Health (14 papers), RNA Research and Splicing (7 papers) and Cancer, Lipids, and Metabolism (5 papers). L G Jensen collaborates with scholars based in Denmark, Poland and United States. L G Jensen's co-authors include N. Gregersen, Henrik Kjærulf Jensen, Ole Færgeman, Peter S. Hansen, Hans Meinertz, Lars Bolund, J. Ellegaard, Lene Heickendorff, P. D. Jensen and T. Christensen and has published in prestigious journals such as Nature Methods, Clinical Chemistry and American Journal of Physiology-Cell Physiology.

In The Last Decade

L G Jensen

23 papers receiving 355 citations

Peers

L G Jensen

SURGE

PFM

GENET

Gwenda J. Graham United States

Thomas W. Apel Germany

Torng‐Sen Lin Taiwan

María-Mercé García-Barceló Hong Kong

Agnes Fresnoza Canada

Ning-Yuan Chen United States

Debbie A. Nickerson United States

Balázs Murnyák Hungary

Jagjit Singh United States

N Beauchamp United Kingdom

Gwenda J. Graham United States

L G Jensen

51 ×0.2

SURGE

64 ×0.6

20 ×0.2

18 ×0.4

PFM

23 ×0.5

GENET

Citations per year, relative to L G Jensen L G Jensen (= 1×) peers Gwenda J. Graham

Countries citing papers authored by L G Jensen

Since Specialization

Citations

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

Fields of papers citing papers by L G Jensen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L G Jensen

This figure shows the co-authorship network connecting the top 25 collaborators of L G Jensen. A scholar is included among the top collaborators of L G 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 L G Jensen. L G Jensen 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

Jensen, L G, David J. Williamson, Juliette Griffié, et al.. (2022). Correction of multiple-blinking artifacts in photoactivated localization microscopy. Nature Methods. 19(5). 594–602. 21 indexed citations

Jensen, L G, David J. Williamson, & Ute Hahn. (2022). Semiparametric point process modeling of blinking artifacts in PALM. The Annals of Applied Statistics. 16(3).

Jensen, L G, et al.. (2020). NodeDrop: A Method for Finding Sufficient Network Architecture Size. 1–9. 2 indexed citations

Jensen, P. D., F. T. Jensen, T. Christensen, et al.. (2001). Indirect evidence for the potential ability of magnetic resonance imaging to evaluate the myocardial iron content in patients with transfusional iron overload. Magnetic Resonance Materials in Physics Biology and Medicine. 12(2-3). 153–166. 32 indexed citations

Jensen, Henrik Kjærulf, L G Jensen, Hans Meinertz, et al.. (1999). Spectrum of LDL receptor gene mutations in Denmark: implications for molecular diagnostic strategy in heterozygous familial hypercholesterolemia. Atherosclerosis. 146(2). 337–344. 38 indexed citations

Jensen, L G, et al.. (1998). Pig epidermal growth factor precursor contains segments that are highly conserved among species. Scandinavian Journal of Clinical and Laboratory Investigation. 58(4). 287–298. 4 indexed citations

Jensen, Henrik Kjærulf, L G Jensen, Peter S. Hansen, Ole Færgeman, & N. Gregersen. (1996). An Iranian‐Armenian LDLR frameshift mutation causing familial hypercholesterolemia. Clinical Genetics. 49(2). 88–90. 4 indexed citations

Jensen, Henrik Kjærulf, et al.. (1996). A G^‐1‐to‐A acceptor splice site LDLR mutant allele leads to reduced relative transcript levels in patients with heterozygous familial hypercholesterolemia. Clinical Genetics. 49(4). 175–179. 9 indexed citations

Jensen, L G, Henrik Kjærulf Jensen, Henrik Nissen, et al.. (1996). An LDL receptor promoter mutation in a heterozygous FH patient with dramatically skewed ratio between the two allelic mRNA variants. Human Mutation. 7(1). 82–84. 11 indexed citations

10.

Jensen, Henrik Kjærulf, L G Jensen, Finn Heath, et al.. (1996). Phenotypic characterization of a patient homozygous for the D558N LDL receptor gene mutation. Clinical Genetics. 50(5). 388–392. 1 indexed citations

11.

Jensen, Henrik Kjærulf, L G Jensen, Peter S. Hansen, Ole Færgeman, & N. Gregersen. (1996). Two point mutations (313 + 1G→A and 313 + 1G→T) in the splice donor site of intron 3 of the low-density lipoprotein receptor gene are associated with familial hypercholesterolemia. Human Mutation. 7(3). 269–271. 15 indexed citations

12.

Jensen, Henrik Kjærulf, L G Jensen, Peter S. Hansen, Ole Færgeman, & N. Gregersen. (1996). The Trp23-Stop and Trp66-Gly mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in Denmark. Atherosclerosis. 120(1-2). 57–65. 24 indexed citations

13.

Jensen, Thøger Gorm, Brage Storstein Andresen, Henrik Kjærulf Jensen, et al.. (1996). Rapid characterization of disease-causing mutations in the low density lipoprotein receptor (LDL-R) gene by overexpression in COS cells.. PubMed. 34 Suppl 3. 9–11. 6 indexed citations

14.

Jensen, Henrik Kjærulf, L G Jensen, Peter S. Hansen, Ole Færgeman, & N. Gregersen. (1996). High sensitivity of the single-strand conformation polymorphism method for detecting sequence variations in the low-density lipoprotein receptor gene validated by DNA sequencing. Clinical Chemistry. 42(8). 1140–1146. 62 indexed citations

15.

Jensen, Henrik Kjærulf, L G Jensen, Peter S. Hansen, Ole Færgeman, & Niels Gregersen. (1996). Two point mutations (313 + 1G→A and 313 + 1G→T) in the splice donor site of intron 3 of the low‐density lipoprotein receptor gene are associated with familial hypercholesterolemia. Human Mutation. 7(3). 269–271. 1 indexed citations

16.

Jensen, Henrik Kjærulf, Peter S. Hansen, L G Jensen, et al.. (1995). Complexity of molecular genetics of dyslipidemia in a family highly susceptible to ischemic heart disease. Clinical Genetics. 48(1). 23–28. 3 indexed citations

17.

Jensen, L G, Henrik Kjærulf Jensen, Finn Heath, et al.. (1995). Allele-specific quantitation of low density lipoprotein receptor gene transcripts. Atherosclerosis. 115. S9–S9. 1 indexed citations

18.

Petersen, Niels Erik, Leif K. Larsen, Henrik Nissen, et al.. (1995). Improved RNase protection assay for quantifying LDL-receptor mRNA; estimation of analytical imprecision and biological variance in peripheral blood mononuclear cells. Clinical Chemistry. 41(11). 1605–1613. 18 indexed citations

19.

Jensen, Henrik Kjærulf, et al.. (1994). An alanine²⁹‐serine variant in exon 2 of the low density lipoprotein receptor gene: no association with hypercholesterolemia. Clinical Genetics. 46(2). 214–215. 7 indexed citations

20.

Jensen, L G, Henrik Kjærulf Jensen, Lars Ulrik Gerdes, et al.. (1994). A new, highly informative Smal polymorphism in intron 7 of the low density lipoprotein receptor (LDLR) gene. Clinical Genetics. 45(1). 52–53. 14 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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