Anja Ernst

467 total citations
27 papers, 302 citations indexed

About

Anja Ernst is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Anja Ernst has authored 27 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in Anja Ernst's work include Prenatal Screening and Diagnostics (5 papers), Liver Disease Diagnosis and Treatment (3 papers) and Helicobacter pylori-related gastroenterology studies (3 papers). Anja Ernst is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Liver Disease Diagnosis and Treatment (3 papers) and Helicobacter pylori-related gastroenterology studies (3 papers). Anja Ernst collaborates with scholars based in Denmark, Germany and United Kingdom. Anja Ernst's co-authors include Henrik Krarup, Bent Ascanius Jacobsen, Vibeke Andersen, Inge Søkilde Pedersen, Mette Østergaard, Henrik Okkels, Michael B. Petersen, Ulla Vogel, Vang Quy Le and Jane Christensen and has published in prestigious journals such as Human Molecular Genetics, Journal of Hepatology and Human Reproduction.

In The Last Decade

Anja Ernst

25 papers receiving 300 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anja Ernst Denmark 11 121 93 88 61 57 27 302
Alexandre Aubourg France 7 166 1.4× 29 0.3× 125 1.4× 57 0.9× 119 2.1× 13 299
Arzu Akçay Türkiye 10 53 0.4× 69 0.7× 97 1.1× 34 0.6× 36 0.6× 46 348
Varsha Shridhar United States 8 92 0.8× 200 2.2× 29 0.3× 86 1.4× 44 0.8× 17 445
Shinji Tomikawa Japan 11 89 0.7× 72 0.8× 42 0.5× 69 1.1× 27 0.5× 57 342
L. Harman United States 6 184 1.5× 188 2.0× 27 0.3× 34 0.6× 26 0.5× 10 309
José María Huguet Spain 10 106 0.9× 52 0.6× 89 1.0× 86 1.4× 61 1.1× 30 276
Carole Saison France 9 57 0.5× 106 1.1× 39 0.4× 41 0.7× 43 0.8× 16 406
Lindsey Sattler United States 6 269 2.2× 33 0.4× 189 2.1× 61 1.0× 95 1.7× 7 365
Blanka Vidan‐Jeras Slovenia 10 98 0.8× 50 0.5× 56 0.6× 51 0.8× 136 2.4× 25 317
Zhihua Ran China 12 144 1.2× 54 0.6× 98 1.1× 69 1.1× 64 1.1× 27 278

Countries citing papers authored by Anja Ernst

Since Specialization
Citations

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

Fields of papers citing papers by Anja Ernst

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anja Ernst

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

All Works

20 of 20 papers shown
1.
Larsen, Martin J., Pernille Mathiesen Tørring, L. Sperling, et al.. (2025). Genetics in fetal medicine. Ugeskrift for Læger. 187(18). 1–9.
2.
Mapendano, Christophe K., Mads Sønderkær, Andreas Carus, et al.. (2025). Longer survival with precision medicine in late-stage cancer patients. ESMO Open. 10(1). 104089–104089. 2 indexed citations
3.
Thompson, Kyle, Emanuele Bellacchio, Courtney E. French, et al.. (2021). Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease. Human Molecular Genetics. 31(4). 523–534. 13 indexed citations
4.
Lund, Ida Charlotte Bay, Olav Bjørn Petersen, Naja Becher, et al.. (2020). National data on the early clinical use of non‐invasive prenatal testing in public and private healthcare in Denmark 2013–2017. Acta Obstetricia Et Gynecologica Scandinavica. 100(5). 884–892. 12 indexed citations
5.
Ingerslev, Hans Jakob, Ulrik Schiøler Kesmodel, Birte Degn, et al.. (2020). A systematic review on concurrent aneuploidy screening and preimplantation genetic testing for hereditary disorders: What is the prevalence of aneuploidy and is there a clinical effect from aneuploidy screening?. Acta Obstetricia Et Gynecologica Scandinavica. 99(6). 696–706. 8 indexed citations
6.
Andersen, Stine Linding, et al.. (2020). Use of genetic testing for hypolactasia trait in the North Denmark Region. Scandinavian Journal of Gastroenterology. 55(9). 1012–1018. 1 indexed citations
7.
Pedersen, Inge Søkilde, et al.. (2019). Mitochondrial Disease Caused by a Novel Homozygous Mutation (Gly106del) in the SCO1 Gene. Neonatology. 116(3). 290–294. 10 indexed citations
8.
9.
Madsen, Lone Wulff, Anne Øvrehus, Jan Gerstoft, et al.. (2019). THU-193-4 week treatment for hepatitis C: A randomized controlled trial (4RIBC). Journal of Hepatology. 70(1). e247–e248. 1 indexed citations
10.
Le, Vang Quy, et al.. (2016). De novo KAT6B Mutation Identified with Whole-Exome Sequencing in a Girl with Say-Barber/Biesecker/Young-Simpson Syndrome. Molecular Syndromology. 8(1). 24–29. 4 indexed citations
11.
Ernst, Anja, Vang Quy Le, Inge Søkilde Pedersen, et al.. (2015). The <b><i>PHF6</i></b> Mutation c.1A>G; pM1V Causes Börjeson-Forsman-Lehmann Syndrome in a Family with Four Affected Young Boys. Molecular Syndromology. 6(4). 181–186. 4 indexed citations
12.
Le, Vang Quy, Astrid Petersen, Inge Søkilde Pedersen, et al.. (2015). ECEL1 mutation causes fetal arthrogryposis multiplex congenita. American Journal of Medical Genetics Part A. 167(4). 731–743. 24 indexed citations
13.
Andersen, Vibeke, Anja Ernst, Jurgita Šventoraitytė, et al.. (2011). Assessment of heterogeneity between European Populations: a Baltic and Danish replication case-control study of SNPs from a recent European ulcerative colitis genome wide association study. BMC Medical Genetics. 12(1). 139–139. 6 indexed citations
14.
Ernst, Anja, Vibeke Andersen, Mette Østergaard, et al.. (2011). Common polymorphisms in the microsomal epoxide hydrolase and N-acetyltransferase 2 genes in association with inflammatory bowel disease in the Danish population. European Journal of Gastroenterology & Hepatology. 23(3). 269–274. 4 indexed citations
15.
Andersen, Vibeke, Anja Ernst, Jane Christensen, et al.. (2010). The polymorphism rs3024505 proximal to IL-10 is associated with risk of ulcerative colitis and Crohns disease in a Danish case-control study. BMC Medical Genetics. 11(1). 82–82. 49 indexed citations
16.
Andersen, Vibeke, Elaine R. Nimmo, Henrik Krarup, et al.. (2010). Cyclooxygenase-2 (COX-2) polymorphisms and risk of inflammatory bowel disease in a Scottish and Danish case–control study. Inflammatory Bowel Diseases. 17(4). 937–946. 22 indexed citations
17.
Ernst, Anja, Vibeke Andersen, Mette Østergaard, et al.. (2010). Genetic variants of glutathione S-transferases μ, θ, and π display no susceptibility to inflammatory bowel disease in the Danish population. Scandinavian Journal of Gastroenterology. 45(9). 1068–1075. 12 indexed citations
18.
Østergaard, Mette, Anja Ernst, Rodrigo Labouriau, et al.. (2008). Cyclooxygenase-2, multidrug resistance 1, and breast cancer resistance protein gene polymorphisms and inflammatory bowel disease in the Danish population. Scandinavian Journal of Gastroenterology. 44(1). 65–73. 32 indexed citations
19.
Ernst, Anja, Bent Ascanius Jacobsen, Mette Østergaard, et al.. (2007). Mutations in CARD15 and smoking confer susceptibility to Crohn's disease in the Danish population. Scandinavian Journal of Gastroenterology. 42(12). 1445–1451. 24 indexed citations
20.
Ernst, Anja, Henrik Okkels, Anne Grove, et al.. (2006). Telomerase activity determined by conventional telomeric repeat amplification protocol and reverse transcriptase‐polymerase chain reaction assay in ovarian lesions: A comparison of assays. Scandinavian Journal of Clinical and Laboratory Investigation. 66(4). 287–298. 2 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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