Susanne Gerit Kircher

910 total citations
48 papers, 420 citations indexed

About

Susanne Gerit Kircher is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Susanne Gerit Kircher has authored 48 papers receiving a total of 420 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 17 papers in Molecular Biology and 12 papers in Physiology. Recurrent topics in Susanne Gerit Kircher's work include Connective tissue disorders research (13 papers), Lysosomal Storage Disorders Research (9 papers) and Neurogenetic and Muscular Disorders Research (8 papers). Susanne Gerit Kircher is often cited by papers focused on Connective tissue disorders research (13 papers), Lysosomal Storage Disorders Research (9 papers) and Neurogenetic and Muscular Disorders Research (8 papers). Susanne Gerit Kircher collaborates with scholars based in Austria, Russia and Tunisia. Susanne Gerit Kircher's co-authors include Eduard Paschke, Olaf A. Bodamer, Andreas Gal, Karin Tuschl, Ali Al Kaissi, Franz Grill, Rudolf Ganger, Vladimir Kenis, Gert Lübec and Kenneth I. Berger and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Neurochemistry and Medicine.

In The Last Decade

Susanne Gerit Kircher

40 papers receiving 412 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Susanne Gerit Kircher Austria 12 214 115 108 81 73 48 420
Judy Qiang Canada 10 109 0.5× 149 1.3× 81 0.8× 101 1.2× 39 0.5× 21 540
Alexander Broomfield United Kingdom 14 358 1.7× 124 1.1× 137 1.3× 205 2.5× 63 0.9× 54 613
Mislen Bauer United States 10 269 1.3× 107 0.9× 208 1.9× 143 1.8× 84 1.2× 19 561
Eugênia Ribeiro Valadares Brazil 12 159 0.7× 93 0.8× 90 0.8× 149 1.8× 148 2.0× 38 433
Jason S. Weisstein United States 9 191 0.9× 66 0.6× 105 1.0× 117 1.4× 36 0.5× 10 424
Patrick A. Lundquist United States 8 238 1.1× 50 0.4× 40 0.4× 130 1.6× 55 0.8× 16 440
Esmée Oussoren Netherlands 15 383 1.8× 169 1.5× 166 1.5× 245 3.0× 106 1.5× 32 768
Hernán Amartino Argentina 15 400 1.9× 139 1.2× 195 1.8× 102 1.3× 103 1.4× 47 596
Françoise Bouhour France 9 173 0.8× 75 0.7× 115 1.1× 239 3.0× 32 0.4× 18 463
Gilles Morin France 9 226 1.1× 58 0.5× 156 1.4× 158 2.0× 74 1.0× 22 463

Countries citing papers authored by Susanne Gerit Kircher

Since Specialization
Citations

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

Fields of papers citing papers by Susanne Gerit Kircher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Susanne Gerit Kircher. 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 Susanne Gerit Kircher. The network helps show where Susanne Gerit Kircher may publish in the future.

Co-authorship network of co-authors of Susanne Gerit Kircher

This figure shows the co-authorship network connecting the top 25 collaborators of Susanne Gerit Kircher. A scholar is included among the top collaborators of Susanne Gerit Kircher 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 Susanne Gerit Kircher. Susanne Gerit Kircher 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.
Kaissi, Ali Al, et al.. (2023). Meticulous and Early Understanding of Congenital Cranial Defects Can Save Lives. Children. 10(7). 1240–1240.
2.
Rehder, Helga, Susanne Gerit Kircher, Katharina Schoner, et al.. (2023). Brain malformations in diprosopia observed in clinical cases, museum specimens and artistic representations. Orphanet Journal of Rare Diseases. 18(1). 57–57. 2 indexed citations
3.
Kircher, Susanne Gerit, Helga Rehder, Eduard Winter, et al.. (2023). History and highlights of the teratological collection in theNarrenturm, Vienna (Austria). American Journal of Medical Genetics Part A. 191(5). 1301–1324. 2 indexed citations
4.
Kaissi, Ali Al, Sergey Ryabykh, Vladimir Kenis, et al.. (2023). The articular and the craniocervical abnormalities are of confusing age of onset in patients with Maroteaux-Lamy disease (MPS VI). Minerva Pediatrics. 75(2). 1 indexed citations
5.
Kaissi, Ali Al, Sergey Ryabykh, Vladimir Kenis, et al.. (2023). Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia. Children. 10(10). 1715–1715.
6.
7.
8.
Kaissi, Ali Al, Sergey Ryabykh, Vladimir Kenis, et al.. (2020). Arthrogryposis is a descriptive term, not a specific disease entity: escobar syndrome is an Example. Minerva Pediatrics. 76(1). 30–36. 1 indexed citations
9.
Schoner, Katharina, Martina Witsch‐Baumgartner, R. Bald, et al.. (2019). Smith‐Lemli‐Opitz syndrome — Fetal phenotypes with special reference to the syndrome‐specific internal malformation pattern. Birth Defects Research. 112(2). 175–185. 14 indexed citations
10.
Rehder, Helga, Franco Laccone, Susanne Gerit Kircher, et al.. (2018). Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB‐related skeletal disorders in three fetuses and a 106‐year‐old exhibit. American Journal of Medical Genetics Part A. 176(7). 1559–1568. 2 indexed citations
11.
Kaissi, Ali Al, Maher Ben Ghachem, Vladimir Kenis, et al.. (2018). Schmid's Type of Metaphyseal Chondrodysplasia: Diagnosis and Management. Orthopaedic Surgery. 10(3). 241–246. 11 indexed citations
12.
Kaissi, Ali Al, et al.. (2017). Craniosynostosis, Scheuermann's disease, and intellectual disability resembling Shprintzen–Goldberg syndrome. Medicine. 96(12). e6199–e6199. 4 indexed citations
13.
Kaissi, Ali Al, Maher Ben Ghachem, Farid Ben Chehida, et al.. (2016). Can Multiple Hereditary Exostoses Overlap With Mesomelic Dysplasia?. Journal of Clinical Medicine Research. 8(8). 605–609. 1 indexed citations
14.
Kaissi, Ali Al, Vladimir Kenis, Maher Ben Ghachem, et al.. (2016). The Diversity of the Clinical Phenotypes in Patients With Fibrodysplasia Ossificans Progressiva. Journal of Clinical Medicine Research. 8(3). 246–253. 18 indexed citations
15.
Kaissi, Ali Al, Sergey Ryabykh, Vladimir Kenis, et al.. (2016). Spine malformation complex in 3 diverse syndromic entities. Medicine. 95(50). e5505–e5505. 7 indexed citations
16.
Kaissi, Ali Al, et al.. (2016). The constellation of skeletal deformities in a family with mixed types of mucopolysaccharidoses. Medicine. 95(32). e4561–e4561. 6 indexed citations
17.
Hendriksz, Christian J., Kenneth I. Berger, Christina Lampe, et al.. (2016). Health-related quality of life in mucopolysaccharidosis: looking beyond biomedical issues. Orphanet Journal of Rare Diseases. 11(1). 119–119. 39 indexed citations
18.
Susani, Martin, et al.. (2013). Comparative study of CO2- and Er:YAG laser ablation of multiple cutaneous neurofibromas in von Recklinghausen's disease. Lasers in Medical Science. 29(3). 1083–1091. 16 indexed citations
19.
Kirchner, Lieselotte, Susanne Gerit Kircher, Ulrike Salzer‐Muhar, et al.. (2003). Infantile sialic acid storage disease and protein-losing gastroenteropathy. Pediatric Neurology. 28(4). 313–317. 2 indexed citations
20.
Lübec, Gert, et al.. (1986). Noninvasive diagnosis of tubular damage by the use of the urinary chondroitin-4-sulfate/heparan sulfate ratio.. PubMed. 21(4). 357–61. 1 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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