Anja Wulf

628 total citations
14 papers, 445 citations indexed

About

Anja Wulf is a scholar working on Molecular Biology, Genetics and Artificial Intelligence. According to data from OpenAlex, Anja Wulf has authored 14 papers receiving a total of 445 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Genetics and 3 papers in Artificial Intelligence. Recurrent topics in Anja Wulf's work include Biomedical Text Mining and Ontologies (7 papers), Genomics and Rare Diseases (6 papers) and Genetic Associations and Epidemiology (6 papers). Anja Wulf is often cited by papers focused on Biomedical Text Mining and Ontologies (7 papers), Genomics and Rare Diseases (6 papers) and Genetic Associations and Epidemiology (6 papers). Anja Wulf collaborates with scholars based in United States. Anja Wulf's co-authors include Marta Gwinn, Muin J. Khoury, Wei Yu, Mindy Clyne, Muin J. Khoury, W. David Dotson, Ajay Yesupriya, Tiebin Liu, Katherine Kolor and Michael Bowen and has published in prestigious journals such as BMC Bioinformatics, Clinical Pharmacology & Therapeutics and Genetics in Medicine.

In The Last Decade

Anja Wulf

14 papers receiving 431 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 Wulf United States 12 213 187 75 60 37 14 445
Mark Kroese United Kingdom 14 241 1.1× 94 0.5× 109 1.5× 52 0.9× 77 2.1× 28 633
David Glazer Canada 4 187 0.9× 91 0.5× 127 1.7× 51 0.8× 41 1.1× 7 343
Peter Goodhand Canada 6 206 1.0× 99 0.5× 166 2.2× 55 0.9× 44 1.2× 8 400
Magdalena Zwierzyna United Kingdom 8 144 0.7× 176 0.9× 54 0.7× 28 0.5× 36 1.0× 11 522
Teresa Kruisselbrink United States 11 214 1.0× 252 1.3× 51 0.7× 47 0.8× 34 0.9× 23 744
Wendy A. Wolf United States 14 299 1.4× 229 1.2× 139 1.9× 40 0.7× 29 0.8× 35 813
Christine M. Cutillo United States 7 202 0.9× 118 0.6× 60 0.8× 26 0.4× 54 1.5× 7 504
Anneliene Hechtelt Jonker France 13 256 1.2× 184 1.0× 72 1.0× 41 0.7× 83 2.2× 28 515
Latrice Landry United States 7 185 0.9× 61 0.3× 110 1.5× 62 1.0× 19 0.5× 15 344
David Westergaard Denmark 13 103 0.5× 184 1.0× 128 1.7× 33 0.6× 16 0.4× 36 699

Countries citing papers authored by Anja Wulf

Since Specialization
Citations

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

Fields of papers citing papers by Anja Wulf

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anja Wulf

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

All Works

14 of 14 papers shown
1.
Khoury, Muin J., Michael Bowen, Mindy Clyne, et al.. (2017). From public health genomics to precision public health: a 20-year journey. Genetics in Medicine. 20(6). 574–582. 98 indexed citations
2.
Yu, Wei, Marta Gwinn, W. David Dotson, et al.. (2016). A knowledge base for tracking the impact of genomics on population health. Genetics in Medicine. 18(12). 1312–1314. 16 indexed citations
3.
Clyne, Mindy, Sheri D. Schully, W. David Dotson, et al.. (2014). Horizon scanning for translational genomic research beyond bench to bedside. Genetics in Medicine. 16(7). 535–538. 22 indexed citations
4.
Dotson, W. David, Michael P. Douglas, Katherine Kolor, et al.. (2013). Prioritizing Genomic Applications for Action by Level of Evidence: A Horizon-Scanning Method. Clinical Pharmacology & Therapeutics. 95(4). 394–402. 46 indexed citations
5.
Yesupriya, Ajay, Camilla B. Pimentel, Mindy Clyne, et al.. (2013). A systematic review of cancer GWAS and candidate gene meta-analyses reveals limited overlap but similar effect sizes. European Journal of Human Genetics. 22(3). 402–408. 42 indexed citations
6.
Gwinn, Marta, Daurice A. Grossniklaus, Wei Yu, et al.. (2011). Horizon scanning for new genomic tests. Genetics in Medicine. 13(2). 161–165. 32 indexed citations
7.
Yu, Wei, Ajay Yesupriya, Anja Wulf, et al.. (2011). GWAS Integrator: a bioinformatics tool to explore human genetic associations reported in published genome-wide association studies. European Journal of Human Genetics. 19(10). 1095–1099. 28 indexed citations
8.
Schully, Sheri D., Wei Yu, Linda M. Dong, et al.. (2011). Cancer GAMAdb: database of cancer genetic associations from meta-analyses and genome-wide association studies. European Journal of Human Genetics. 19(8). 928–930. 16 indexed citations
9.
Yu, Wei, Renée M. Ned, Anja Wulf, et al.. (2009). The need for genetic variant naming standards in published abstracts of human genetic association studies. BMC Research Notes. 2(1). 56–56. 9 indexed citations
10.
Yu, Wei, Mindy Clyne, Siobhan M. Dolan, et al.. (2008). GAPscreener: An automatic tool for screening human genetic association literature in PubMed using the support vector machine technique. BMC Bioinformatics. 9(1). 205–205. 45 indexed citations
11.
Yu, Wei, Anja Wulf, Tiebin Liu, Muin J. Khoury, & Marta Gwinn. (2008). Gene Prospector: An evidence gateway for evaluating potential susceptibility genes and interacting risk factors for human diseases. BMC Bioinformatics. 9(1). 528–528. 58 indexed citations
12.
Yu, Wei, Anja Wulf, Ajay Yesupriya, et al.. (2008). HuGE Watch: tracking trends and patterns of published studies of genetic association and human genome epidemiology in near-real time. European Journal of Human Genetics. 16(9). 1155–1158. 11 indexed citations
13.
Yu, Wei, et al.. (2007). An automatic method to generate domain-specific investigator networks using PubMed abstracts. BMC Medical Informatics and Decision Making. 7(1). 17–17. 13 indexed citations
14.

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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