Alexandra Topa

439 total citations
13 papers, 239 citations indexed

About

Alexandra Topa is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Alexandra Topa has authored 13 papers receiving a total of 239 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Alexandra Topa's work include Craniofacial Disorders and Treatments (3 papers), Ocular Disorders and Treatments (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Alexandra Topa is often cited by papers focused on Craniofacial Disorders and Treatments (3 papers), Ocular Disorders and Treatments (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Alexandra Topa collaborates with scholars based in Sweden, Finland and France. Alexandra Topa's co-authors include Emmanuelle Plaisier, Laure‐Hélène Noël, Marie-Claire Gübler, Vincent Morinière, Saïd Lebbah, Patrick Nitschké, Marie‐Alice Macher, Corinne Antignac, Pascale Hilbert and Solenn Pruvost and has published in prestigious journals such as Journal of the American Society of Nephrology, Journal of Medical Genetics and Frontiers in Genetics.

In The Last Decade

Alexandra Topa

13 papers receiving 237 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexandra Topa Sweden 7 141 117 67 45 38 13 239
Ruiji Jiang United States 4 107 0.8× 49 0.4× 74 1.1× 177 3.9× 34 0.9× 4 252
Lev Shagam Russia 3 80 0.6× 46 0.4× 106 1.6× 66 1.5× 46 1.2× 8 180
Lynn Pais United States 7 96 0.7× 52 0.4× 11 0.2× 6 0.1× 5 0.1× 19 168
Margrethe Kjeldsen Denmark 9 254 1.8× 45 0.4× 29 0.4× 2 0.0× 13 0.3× 13 339
Ramiro Nández United States 5 158 1.1× 48 0.4× 10 0.1× 96 2.1× 3 0.1× 6 301
Ellen L. van Agtmaal Netherlands 7 200 1.4× 15 0.1× 17 0.3× 17 0.4× 79 2.1× 7 317
Alka V. Ekbote India 7 136 1.0× 102 0.9× 6 0.1× 3 0.1× 10 0.3× 13 216
Emiel Baten Belgium 8 133 0.9× 147 1.3× 3 0.0× 9 0.2× 12 0.3× 8 234
Erik Disteldorf Germany 5 32 0.2× 49 0.4× 13 0.2× 42 0.9× 4 0.1× 5 254
Juliane Eckhold Germany 8 116 0.8× 66 0.6× 3 0.0× 6 0.1× 12 0.3× 10 202

Countries citing papers authored by Alexandra Topa

Since Specialization
Citations

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

Fields of papers citing papers by Alexandra Topa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexandra Topa

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

All Works

13 of 13 papers shown
1.
Topa, Alexandra, Anna Rohlin, André Fehr, et al.. (2024). The value of genome-wide analysis in craniosynostosis. Frontiers in Genetics. 14. 1322462–1322462. 3 indexed citations
2.
Topa, Alexandra, Anna Rohlin, Mattias K. Andersson, et al.. (2022). The outcome of targeted NGS screening in patients with syndromic forms of sagittal and pansynostosis - IL11RA is an emerging core-gene for pansynostosis. European Journal of Medical Genetics. 65(5). 104476–104476. 4 indexed citations
3.
Topa, Alexandra, et al.. (2020). Visual function and quality of life in children and adolescents with anophthalmia and microphthalmia treated with ocular prosthesis. Acta Ophthalmologica. 98(7). 662–670. 6 indexed citations
4.
Topa, Alexandra, et al.. (2020). Children and young adults with anophthalmia and microphthalmia: Diagnosis and Management. Acta Ophthalmologica. 98(8). 848–858. 8 indexed citations
5.
Topa, Alexandra, Anna Rohlin, Mattias K. Andersson, et al.. (2019). NGS targeted screening of 100 Scandinavian patients with coronal synostosis. American Journal of Medical Genetics Part A. 182(2). 348–356. 13 indexed citations
6.
Hedberg‐Oldfors, Carola, et al.. (2017). Grand paternal inheritance of X-linked myotubular myopathy due to mosaicism, and identification of necklace fibers in an asymptomatic male. Neuromuscular Disorders. 27(9). 843–847. 4 indexed citations
7.
Topa, Alexandra, Lena Samuelsson, Lovisa Lovmar, Göran Stenman, & Lars Kölby. (2017). On the significance of craniosynostosis in a case of Kabuki syndrome with a concomitant KMT2D mutation and 3.2 Mbp de novo 10q22.3q23.1 deletion. American Journal of Medical Genetics Part A. 173(8). 2219–2225. 13 indexed citations
8.
Topa, Alexandra, M. Tulinius, Anders Oldfors, & Carola Hedberg‐Oldfors. (2016). Novel myopathy in a newborn with Shwachman–Diamond syndrome and review of neonatal presentation. American Journal of Medical Genetics Part A. 170(5). 1155–1164. 7 indexed citations
9.
Topa, Alexandra, et al.. (2015). [Anophthalmia and microphthalmia requires multidisciplinary care. Many of the children also have other medical problems].. PubMed. 112. 1 indexed citations
10.
Morinière, Vincent, Karin Dahan, Pascale Hilbert, et al.. (2014). Improving Mutation Screening in Familial Hematuric Nephropathies through Next Generation Sequencing. Journal of the American Society of Nephrology. 25(12). 2740–2751. 102 indexed citations
11.
Hofmeister, Wolfgang, Daniel Nilsson, Alexandra Topa, et al.. (2014). CTNND2—a candidate gene for reading problems and mild intellectual disability. Journal of Medical Genetics. 52(2). 111–122. 29 indexed citations
12.
Lindstrand, Anna, Giedré Grigelioniené, Daniel Nilsson, et al.. (2013). Different mutations in PDE4D associated with developmental disorders with mirror phenotypes. Journal of Medical Genetics. 51(1). 45–54. 44 indexed citations
13.
Topa, Alexandra, et al.. (2011). 11.2.2 Reducing the Gap Between Formal and Informal Worlds in Automotive Safety‐Critical Systems. INCOSE International Symposium. 21(1). 1306–1320. 5 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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