Jenny Blechingberg

529 total citations
18 papers, 388 citations indexed

About

Jenny Blechingberg is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Jenny Blechingberg has authored 18 papers receiving a total of 388 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 4 papers in Genetics and 4 papers in Genetics. Recurrent topics in Jenny Blechingberg's work include RNA regulation and disease (4 papers), Cancer-related gene regulation (4 papers) and RNA Research and Splicing (4 papers). Jenny Blechingberg is often cited by papers focused on RNA regulation and disease (4 papers), Cancer-related gene regulation (4 papers) and RNA Research and Splicing (4 papers). Jenny Blechingberg collaborates with scholars based in Denmark, United States and United Kingdom. Jenny Blechingberg's co-authors include Anders Lade Nielsen, Rune Thomsen, Ida E. Holm, Arne Lund Jørgensen, Torben Heick Jensen, Anders D. Børglum, Karsten Nielsen, Yonglun Luo, Lars Bolund and Christian Kroun Damgaard and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Brain Research.

In The Last Decade

Jenny Blechingberg

16 papers receiving 387 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jenny Blechingberg Denmark 10 294 67 41 34 32 18 388
Frank Wessely United Kingdom 9 217 0.7× 52 0.8× 30 0.7× 33 1.0× 27 0.8× 10 322
И. В. Честков Russia 8 292 1.0× 64 1.0× 33 0.8× 97 2.9× 28 0.9× 11 367
Ewa Liszewska Poland 13 345 1.2× 74 1.1× 17 0.4× 51 1.5× 10 0.3× 23 543
Emmanuelle Ranza Switzerland 12 137 0.5× 103 1.5× 18 0.4× 36 1.1× 27 0.8× 22 295
Satoru Kobayashi Japan 9 156 0.5× 64 1.0× 31 0.8× 93 2.7× 15 0.5× 17 366
Mridu Kapur United States 10 355 1.2× 31 0.5× 26 0.6× 50 1.5× 15 0.5× 13 414
André Saraiva Leão Marcelo Antunes Brazil 9 140 0.5× 27 0.4× 31 0.8× 30 0.9× 51 1.6× 19 277
Nathalie Escande‐Beillard Singapore 10 130 0.4× 37 0.6× 23 0.6× 56 1.6× 14 0.4× 16 272
Antonella Sferra Italy 8 151 0.5× 43 0.6× 19 0.5× 47 1.4× 18 0.6× 12 246
Lucie Vizor United Kingdom 8 190 0.6× 53 0.8× 12 0.3× 80 2.4× 17 0.5× 15 336

Countries citing papers authored by Jenny Blechingberg

Since Specialization
Citations

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

Fields of papers citing papers by Jenny Blechingberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jenny Blechingberg. 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 Jenny Blechingberg. The network helps show where Jenny Blechingberg may publish in the future.

Co-authorship network of co-authors of Jenny Blechingberg

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

All Works

18 of 18 papers shown
1.
2.
Herlin, Morten Krogh, et al.. (2024). Phenotypes, Genetics, and Estimated Prevalence of Focal Dermal Hypoplasia (Goltz Syndrome): A Single‐Center Report. Pediatric Dermatology. 41(6). 1106–1113.
3.
Sommerlund, Mette, Casper Kruse, Hans Gjørup, et al.. (2024). Hypohidrotic ectodermal dysplasia caused by an intragenic duplication in EDAR. European Journal of Medical Genetics. 72. 104982–104982. 2 indexed citations
4.
Herlin, Morten Krogh, Jenny Blechingberg, Sigrún Alba Jóhannesdóttir Schmidt, et al.. (2024). Clinical presentation and genetics of tricho-rhino-phalangeal syndrome (TRPS) type 1: A single-center case series of 15 patients and seven novel TRPS1 variants. European Journal of Medical Genetics. 69. 104937–104937. 2 indexed citations
5.
Blechingberg, Jenny, et al.. (2024). CRISPR activation to characterize splice-altering variants in easily accessible cells. The American Journal of Human Genetics. 111(2). 309–322. 8 indexed citations
6.
Schmidt, Sigrún Alba Jóhannesdóttir, Kirsten Rønholt, Anette Bygum, et al.. (2024). Prevalence and Patient Characteristics of Ectodermal Dysplasias in Denmark. JAMA Dermatology. 160(5). 502–502. 4 indexed citations
7.
Vogel, Ida, et al.. (2021). A novel homozygous variant in C1QBP causes severe IUGR, edema, and cardiomyopathy in two fetuses. JIMD Reports. 59(1). 20–25. 4 indexed citations
8.
Blechingberg, Jenny, Mads Kjølby, Giulia Monti, et al.. (2018). An alternative transcript of the Alzheimer's disease risk gene SORL1 encodes a truncated receptor. Neurobiology of Aging. 71. 266.e11–266.e24. 8 indexed citations
9.
Christensen, Jane, Jonatan Pallesen, Manuel Mattheisen, et al.. (2016). Identification of the BRD1 interaction network and its impact on mental disorder risk. Genome Medicine. 8(1). 53–53. 24 indexed citations
10.
Luo, Yonglun, Jenny Blechingberg, Shengting Li, et al.. (2015). EWS and FUS bind a subset of transcribed genes encoding proteins enriched in RNA regulatory functions. BMC Genomics. 16(1). 929–929. 17 indexed citations
11.
Blechingberg, Jenny, Yonglun Luo, Lars Bolund, Christian Kroun Damgaard, & Anders Lade Nielsen. (2012). Gene Expression Responses to FUS, EWS, and TAF15 Reduction and Stress Granule Sequestration Analyses Identifies FET-Protein Non-Redundant Functions. PLoS ONE. 7(9). e46251–e46251. 39 indexed citations
12.
Blechingberg, Jenny, Ida E. Holm, & Anders Lade Nielsen. (2011). Characterization and expression analysis in the developing embryonic brain of the porcine FET family: FUS, EWS, and TAF15. Gene. 493(1). 27–35. 10 indexed citations
13.
Thomsen, Rune, et al.. (2011). Analysis of HP1α regulation in human breast cancer cells. Molecular Carcinogenesis. 50(8). 601–613. 19 indexed citations
14.
Thomsen, Rune, et al.. (2010). ANALYSIS OF qPCR DATA BY CONVERTING EXPONENTIALLY RELATED Ct VALUES INTO LINEARLY RELATED X0 VALUES. Journal of Bioinformatics and Computational Biology. 8(5). 885–900. 87 indexed citations
15.
Blechingberg, Jenny, Ida E. Holm, Marianne Johansen, Anders D. Børglum, & Anders Lade Nielsen. (2009). Aromatic l-amino acid decarboxylase expression profiling and isoform detection in the developing porcine brain. Brain Research. 1308. 1–13. 13 indexed citations
16.
Blechingberg, Jenny, Søren Lykke‐Andersen, Torben Heick Jensen, Arne Lund Jørgensen, & Anders Lade Nielsen. (2007). Regulatory mechanisms for 3′-end alternative splicing and polyadenylation of the Glial Fibrillary Acidic Protein, GFAP, transcript. Nucleic Acids Research. 35(22). 7636–7650. 31 indexed citations
17.
Blechingberg, Jenny, Ida E. Holm, Karsten Nielsen, et al.. (2007). Identification and characterization of GFAPκ, a novel glial fibrillary acidic protein isoform. Glia. 55(5). 497–507. 60 indexed citations
18.
Bjarkam, Carsten Reidies, Inger M. Olsen, Morten Muhlig Nielsen, et al.. (2006). Evidence implicating BRD1 with brain development and susceptibility to both schizophrenia and bipolar affective disorder. Molecular Psychiatry. 11(12). 1126–1138. 60 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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2026