Andreas Zankl

5.7k total citations
82 papers, 1.9k citations indexed

About

Andreas Zankl is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Andreas Zankl has authored 82 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Genetics, 38 papers in Molecular Biology and 12 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Andreas Zankl's work include Connective tissue disorders research (28 papers), Genomics and Rare Diseases (11 papers) and Biomedical Text Mining and Ontologies (11 papers). Andreas Zankl is often cited by papers focused on Connective tissue disorders research (28 papers), Genomics and Rare Diseases (11 papers) and Biomedical Text Mining and Ontologies (11 papers). Andreas Zankl collaborates with scholars based in Australia, Switzerland and United Kingdom. Andreas Zankl's co-authors include Luisa Bonafé, Andrea Superti‐Furga, Emma L. Duncan, Matthew A. Brown, Tudor Groza, Luciano Molinari, Ravi Savarirayan, Belinda Campos‐Xavier, Albert Schinzel and Verity Pacey and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Andreas Zankl

77 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andreas Zankl Australia 25 1.1k 881 216 216 174 82 1.9k
Karen E. Heath Spain 28 1.1k 0.9× 1.3k 1.4× 273 1.3× 404 1.9× 116 0.7× 106 2.6k
David Ng United States 22 550 0.5× 924 1.0× 340 1.6× 196 0.9× 216 1.2× 45 1.9k
Claus‐Eric Ott Germany 20 698 0.6× 1.1k 1.2× 319 1.5× 123 0.6× 66 0.4× 51 1.7k
Helen Stewart United Kingdom 26 1.4k 1.3× 1.3k 1.4× 118 0.5× 232 1.1× 113 0.6× 57 2.5k
Ahmet Nayır Türkiye 17 810 0.7× 1.3k 1.5× 167 0.8× 180 0.8× 141 0.8× 49 2.4k
Jean McGowan‐Jordan Canada 15 675 0.6× 690 0.8× 208 1.0× 103 0.5× 68 0.4× 31 1.6k
Patrick Tarpey United Kingdom 23 496 0.4× 1.0k 1.2× 336 1.6× 133 0.6× 217 1.2× 55 2.0k
Tiong Yang Tan Australia 25 1.4k 1.2× 1.1k 1.3× 204 0.9× 203 0.9× 50 0.3× 69 2.3k
Abdelaziz Sefiani Morocco 21 526 0.5× 964 1.1× 86 0.4× 125 0.6× 141 0.8× 123 1.8k
Eul‐Ju Seo South Korea 24 417 0.4× 796 0.9× 106 0.5× 170 0.8× 98 0.6× 116 1.9k

Countries citing papers authored by Andreas Zankl

Since Specialization
Citations

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

Fields of papers citing papers by Andreas Zankl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Zankl

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Zankl. A scholar is included among the top collaborators of Andreas Zankl 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 Andreas Zankl. Andreas Zankl 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.
Zankl, Andreas, et al.. (2024). Impeccable Keccak. IACR Transactions on Cryptographic Hardware and Embedded Systems. 2024(2). 154–189. 1 indexed citations
2.
Moh, Edward S. X., Andreas Zankl, & Nicolle H. Packer. (2023). Phenotyping CHST3 skeletal dysplasia from freezer-induced urine sediments. Australian Journal of Chemistry. 76(8). 476–481. 1 indexed citations
3.
Smet, M., et al.. (2022). Bruck Syndrome: Beyond the Obvious. Fetal Diagnosis and Therapy. 49(11-12). 479–485. 1 indexed citations
4.
Minoche, André E., Ben Lundie, Greg B. Peters, et al.. (2021). ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data. Genome Medicine. 13(1). 32–32. 38 indexed citations
5.
Esch, Hilde Van, Rita Colnaghi, Kathleen Freson, et al.. (2019). Defective DNA Polymerase α-Primase Leads to X-Linked Intellectual Disability Associated with Severe Growth Retardation, Microcephaly, and Hypogonadism. The American Journal of Human Genetics. 104(5). 957–967. 26 indexed citations
6.
McInerney‐Leo, Aideen, Carine Le Goff, Paul Leo, et al.. (2016). Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasia. Queensland's institutional digital repository (The University of Queensland). 3 indexed citations
7.
Zankl, Andreas, Emma L. Duncan, Paul Leo, et al.. (2014). Multicentric Carpotarsal Osteolysis Is Caused by Mutations Clustering in the Amino-Terminal Transcriptional Activation Domain of MAFB. The American Journal of Human Genetics. 94(4). 643–643. 3 indexed citations
8.
Ekbote, Alka V., et al.. (2014). Patient with Mutation in the Matrix Metalloproteinase 2 (MMP2) Gene - A Case Report and Review of the Literature. Journal of Clinical Research in Pediatric Endocrinology. 6(1). 40–46. 15 indexed citations
9.
McInerney‐Leo, Aideen, Gareth Baynam, Craig F. Munns, et al.. (2014). The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type V. BMC Musculoskeletal Disorders. 15(1). 107–107. 20 indexed citations
10.
Groza, Tudor, et al.. (2013). Inferring characteristic phenotypes via class association rule mining in the bone dysplasia domain. Journal of Biomedical Informatics. 48. 73–83. 11 indexed citations
11.
Groza, Tudor, Andreas Zankl, & Jane Hunter. (2012). Experiences with modeling composite phenotypes in the SKELETOME project. Lecture notes in computer science. 7650. 82–97. 1 indexed citations
12.
McInerney‐Leo, Aideen, et al.. (2012). Next generation sequencing identifies mutations clustering in the amino-terminal transcriptional activation domain of Mafb in multicentric carpotarsal osteolysis. Internal Medicine Journal. 42. 2–2. 2 indexed citations
13.
McGill, James, Andreas Zankl, Robert S. Ware, et al.. (2011). Functional performance in young Australian children with achondroplasia. Developmental Medicine & Child Neurology. 53(10). 944–950. 52 indexed citations
14.
Conwell, Louise S., Pia Hermanns, & Andreas Zankl. (2008). Short Stature and Metaphyeal Dysplasia Due to Cartilage-Hair Hypoplasia. Journal of Pediatric Endocrinology and Metabolism. 21(3). 209–11. 5 indexed citations
15.
Zankl, Andreas, Étienne Mornet, & Shell Fean Wong. (2008). Specific ultrasonographic features of perinatal lethal hypophosphatasia. American Journal of Medical Genetics Part A. 146A(9). 1200–1204. 16 indexed citations
16.
Zankl, Andreas, et al.. (2007). Right-Sided Diaphragmatic Eventration: A Rare Cause of Non-Immune Hydrops Fetalis. Neonatology. 92(1). 14–18. 7 indexed citations
17.
Zankl, Andreas, et al.. (2004). Novel mutation in the tyrosine kinase domain of FGFR2 in a patient with Pfeiffer syndrome. American Journal of Medical Genetics Part A. 131A(3). 299–300. 15 indexed citations
18.
Zankl, Andreas, Tayfun Güngör, & Albert Schinzel. (2003). Cranio‐cerebello‐cardiac (3C) syndrome: Follow‐up study of the original patient. American Journal of Medical Genetics Part A. 118A(1). 55–59. 5 indexed citations
19.
Zankl, Andreas & Luciano Molinari. (2003). ABase—A tool for the rapid assessment of anthropometric measurements on handheld computers. American Journal of Medical Genetics Part A. 121A(2). 146–150. 22 indexed citations
20.
Ulrich, Rainer G., Diana Koletzki, Sylvie Lachmann, et al.. (1999). New chimaeric hepatitis B virus core particles carrying hantavirus (serotype Puumala) epitopes: immunogenicity and protection against virus challenge. Journal of Biotechnology. 73(2-3). 141–153. 36 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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