Svenja Alter

624 total citations
19 papers, 380 citations indexed

About

Svenja Alter is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Svenja Alter has authored 19 papers receiving a total of 380 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Cell Biology and 6 papers in Genetics. Recurrent topics in Svenja Alter's work include Skin and Cellular Biology Research (7 papers), Wnt/β-catenin signaling in development and cancer (4 papers) and Plant Reproductive Biology (3 papers). Svenja Alter is often cited by papers focused on Skin and Cellular Biology Research (7 papers), Wnt/β-catenin signaling in development and cancer (4 papers) and Plant Reproductive Biology (3 papers). Svenja Alter collaborates with scholars based in Germany, United States and France. Svenja Alter's co-authors include Thomas Dresselhaus, Andrea Bleckmann, Peggy Blattner, Uta Francke, Alfred J. Spiro, John F. Harper, Basil T. Darras, Yu Wang, Kai Christian Bader and Chris‐Carolin Schön and has published in prestigious journals such as PLANT PHYSIOLOGY, Clinical Infectious Diseases and Frontiers in Immunology.

In The Last Decade

Svenja Alter

18 papers receiving 379 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Svenja Alter Germany	9	250	117	68	45	43	19	380
Alexandra S. Weisman United States	7	440 1.8×	44 0.4×	39 0.6×	29 0.6×	20 0.5×	8	586
Shen Song China	12	387 1.5×	59 0.5×	200 2.9×	122 2.7×	31 0.7×	30	660
Huira C. Kopera United States	8	610 2.4×	388 3.3×	115 1.7×	26 0.6×	50 1.2×	10	762
Shuichi Matsuda Japan	12	164 0.7×	68 0.6×	27 0.4×	11 0.2×	27 0.6×	37	493
Eva Dehlin Sweden	10	546 2.2×	24 0.2×	43 0.6×	29 0.6×	27 0.6×	14	715
Arnoud C. Fijnvandraat Netherlands	6	340 1.4×	30 0.3×	35 0.5×	50 1.1×	24 0.6×	9	460
Gemma L. Curie United States	2	751 3.0×	73 0.6×	168 2.5×	31 0.7×	32 0.7×	3	787
Tiago Campos Pereira Brazil	13	262 1.0×	54 0.5×	35 0.5×	41 0.9×	19 0.4×	36	442
Maaike Welling Netherlands	11	551 2.2×	74 0.6×	121 1.8×	28 0.6×	7 0.2×	14	651
Joonsun Lee South Korea	7	496 2.0×	55 0.5×	90 1.3×	17 0.4×	47 1.1×	8	526

Countries citing papers authored by Svenja Alter

Since Specialization

Citations

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

Fields of papers citing papers by Svenja Alter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Svenja Alter

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

All Works

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19 of 19 papers shown

Giehl, Kathrin, Svenja Alter, Iliana Tantcheva‐Poór, et al.. (2024). Epidermolytic ichthyosis: Clinical spectrum and burden of disease in a large German cohort. Journal of the European Academy of Dermatology and Venereology. 39(5). 1028–1037. 1 indexed citations

Hotz, Alrun, Regina Fölster‐Holst, Vinzenz Oji, et al.. (2024). Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying ABCA12 Mutations. Genes. 15(3). 288–288. 2 indexed citations

Komlósi, Katalin, Cristina Glocker, Svenja Alter, et al.. (2024). Autosomal Dominant Lamellar Ichthyosis Due to a Missense Variant in the Gene NKPD1. Journal of Investigative Dermatology. 144(12). 2754–2763.e6. 2 indexed citations

Fischer, Judith, et al.. (2022). Lipoid proteinosis: Novel ECM1 pathogenic variants and intrafamilial variability in four unrelated Arab families. Pediatric Dermatology. 40(1). 113–119.

Schauer, Franziska, Alexander Nyström, Manfred Kunz, et al.. (2022). Case Report: Diagnostic and Therapeutic Challenges in Severe Mechanobullous Epidermolysis Bullosa Acquisita. Frontiers in Immunology. 13. 883967–883967. 1 indexed citations

Feige, Bernd, Kimon Runge, Kathrin Nickel, et al.. (2022). Obsessive–compulsive symptoms in ACTG1-associated Baraitser-Winter cerebrofrontofacial syndrome. Journal of Neural Transmission. 129(11). 1387–1391. 3 indexed citations

Zimmer, Andreas, et al.. (2022). Pathogenic variants in the SPTLC1 gene cause hyperkeratosis lenticularis perstans. British Journal of Dermatology. 188(1). 94–99. 4 indexed citations

Hotz, Alrun, Andreas Zimmer, Katalin Komlósi, et al.. (2021). The Importance of Extended Analysis Using Current Molecular Genetic Methods Based on the Example of a Cohort of 228 Patients with Hereditary Breast and Ovarian Cancer Syndrome. Genes. 12(10). 1483–1483. 1 indexed citations

Komlósi, Katalin, Alrun Hotz, Svenja Alter, et al.. (2020). Neonatal presentation of COG6‐CDG with prominent skin phenotype. JIMD Reports. 55(1). 51–58. 9 indexed citations

10.

Alter, Svenja, Andreas Zimmer, Misun Park, et al.. (2020). Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in protein kinase D1. Journal of Medical Genetics. 58(6). 415–421. 8 indexed citations

11.

Alter, Svenja, Alrun Hotz, Arne Jahn, et al.. (2018). Novel VPS33B mutation in a patient with autosomal recessive keratoderma‐ichthyosis‐deafness syndrome. American Journal of Medical Genetics Part A. 176(12). 2862–2866. 8 indexed citations

12.

Steinfurt, Johannes, Gerlind Franke, Anselm Hoppmann, et al.. (2018). A novel LMNA nonsense mutation causes two distinct phenotypes of cardiomyopathy with high risk of sudden cardiac death in a large five-generation family. EP Europace. 20(12). 2003–2013. 13 indexed citations

13.

Bourrat, E., P. Vabres, Julien Thévenon, et al.. (2018). Mosaicism due to postzygotic mutations in women with focal dermal hypoplasia. British Journal of Dermatology. 180(3). 657–661. 1 indexed citations

14.

Hotz, Alrun, E. Bourrat, Vinzenz Oji, et al.. (2018). Mutation update for CYP4F22 variants associated with autosomal recessive congenital ichthyosis. Human Mutation. 39(10). 1305–1313. 17 indexed citations

15.

Resentini, Francesca, Philipp Cyprys, Joshua G. Steffen, et al.. (2016). SUPPRESSOR OF FRIGIDA (SUF4) Supports Gamete Fusion via Regulating Arabidopsis EC1 Gene Expression. PLANT PHYSIOLOGY. 173(1). 155–166. 20 indexed citations

16.

Alter, Svenja, Kai Christian Bader, M. Spannagl, et al.. (2015). DroughtDB: an expert-curated compilation of plant drought stress genes and their homologs in nine species. Database. 2015. bav046–bav046. 47 indexed citations

17.

Bleckmann, Andrea, Svenja Alter, & Thomas Dresselhaus. (2014). The beginning of a seed: regulatory mechanisms of double fertilization. Frontiers in Plant Science. 5. 452–452. 72 indexed citations

18.

Stanberry, Lawrence R., et al.. (1994). Herpes Simplex Viremia: Report of Eight Pediatric Cases and Review of the Literature. Clinical Infectious Diseases. 18(3). 401–407. 40 indexed citations

19.

Darras, Basil T., Peggy Blattner, John F. Harper, et al.. (1988). Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.. PubMed. 43(5). 620–9. 131 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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