Anna Schossig

861 total citations
15 papers, 259 citations indexed

About

Anna Schossig is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Anna Schossig has authored 15 papers receiving a total of 259 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Cell Biology and 6 papers in Genetics. Recurrent topics in Anna Schossig's work include Skin and Cellular Biology Research (4 papers), Hair Growth and Disorders (4 papers) and Bone and Dental Protein Studies (3 papers). Anna Schossig is often cited by papers focused on Skin and Cellular Biology Research (4 papers), Hair Growth and Disorders (4 papers) and Bone and Dental Protein Studies (3 papers). Anna Schossig collaborates with scholars based in Austria, Germany and Netherlands. Anna Schossig's co-authors include Johannes Zschocke, Christine Fauth, Robert Gruber, Matthias Schmuth, Andreas Janecke, Nicole I. Wolf, Maria Fischer, Stephan Pabinger, Gernot Stocker and Andreas Dander and has published in prestigious journals such as PLoS ONE, Neurology and Gene.

In The Last Decade

Anna Schossig

15 papers receiving 253 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anna Schossig Austria	10	153	92	74	41	24	15	259
Xuanzhu Liu China	11	224 1.5×	56 0.6×	123 1.7×	14 0.3×	17 0.7×	14	333
Maria Rosaria Piemontese Italy	12	248 1.6×	141 1.5×	111 1.5×	17 0.4×	17 0.7×	23	393
Arturo Incao United States	12	176 1.2×	73 0.8×	126 1.7×	7 0.2×	34 1.4×	15	355
Yukiko Kuroda Japan	11	127 0.8×	178 1.9×	25 0.3×	17 0.4×	11 0.5×	40	271
Abdul Wali Pakistan	12	170 1.1×	58 0.6×	131 1.8×	13 0.3×	7 0.3×	34	268
Bo Hou China	10	195 1.3×	134 1.5×	33 0.4×	15 0.4×	31 1.3×	27	308
Echaieb Anis France	2	137 0.9×	41 0.4×	81 1.1×	6 0.1×	29 1.2×	3	232
Daniela Torres United States	6	131 0.9×	23 0.3×	50 0.7×	12 0.3×	20 0.8×	22	240
Catherine Rhéaume United States	9	271 1.8×	66 0.7×	21 0.3×	5 0.1×	21 0.9×	13	394
Anne Blomhoff Norway	10	119 0.8×	204 2.2×	90 1.2×	27 0.7×	3 0.1×	11	453

Countries citing papers authored by Anna Schossig

Since Specialization

Citations

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

Fields of papers citing papers by Anna Schossig

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Schossig

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Eckl, Katja‐Martina, Robert Gruber, Andrew S. Marriott, et al.. (2021). Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V. Frontiers in Genetics. 12. 689940–689940. 5 indexed citations

Doğan, Özlem Akgün, Pelin Özlem Şimşek‐Kiper, Ekim Z. Taşkıran, et al.. (2021). Kohlschütter-Tönz Syndrome With a Novel ROGD1 Variant in 3 Individuals: A Rare Clinical Entity. Journal of Child Neurology. 36(10). 816–822. 8 indexed citations

Schatz, Ulrich A., Verena Moosbrugger‐Martinz, Stefan Blunder, et al.. (2020). Spektrum der Ichthyosen in einer österreichischen Ichthyosekohorte von 2004–2007. JDDG Journal der Deutschen Dermatologischen Gesellschaft. 18(1). 17–26. 4 indexed citations

Schatz, Ulrich A., Verena Moosbrugger‐Martinz, Stefan Blunder, et al.. (2019). Spectrum of ichthyoses in an Austrian ichthyosis cohort from 2004 to 2017. JDDG Journal der Deutschen Dermatologischen Gesellschaft. 18(1). 17–25. 10 indexed citations

Schossig, Anna, et al.. (2018). Cleft lip/palate and hereditary diffuse gastric cancer: report of a family harboring a CDH1 c.687 + 1G > A germline mutation and review of the literature. Familial Cancer. 18(2). 253–260. 19 indexed citations

Indelicato, Elisabetta, Wolfgang Nachbauer, Christine Fauth, et al.. (2018). SYNE1-ataxia: Novel genotypic and phenotypic findings. Parkinsonism & Related Disorders. 62. 210–214. 17 indexed citations

Zschocke, Johannes, et al.. (2018). High risk of peri‐implant disease in periodontal Ehlers–Danlos Syndrome. A case series. Clinical Oral Implants Research. 29(11). 1101–1106. 7 indexed citations

Schatz, Ulrich A., Stephan Wenninger, Benedikt Schoser, et al.. (2018). Evidence of mild founder LMOD3 mutations causing nemaline myopathy 10 in Germany and Austria. Neurology. 91(18). e1690–e1694. 11 indexed citations

Zschocke, Johannes, Anna Schossig, Dieter D. Bosshardt, et al.. (2017). Variable expressivity of TCTEX1D2 mutations and a possible pathogenic link of molar-incisor malformation to ciliary dysfunction. Archives of Oral Biology. 80. 222–228. 10 indexed citations

10.

Schossig, Anna, Agnès Bloch‐Zupan, Adrian Lussi, et al.. (2016). SLC13A5 is the second gene associated with Kohlschütter–Tönz syndrome. Journal of Medical Genetics. 54(1). 54–62. 40 indexed citations

11.

Deutschmann, Andrea, et al.. (2014). Genotype-based databases for variants causing rare diseases. Gene. 550(1). 136–140. 10 indexed citations

12.

Fischer, Maria, René Snajder, Stephan Pabinger, et al.. (2012). SIMPLEX: Cloud-Enabled Pipeline for the Comprehensive Analysis of Exome Sequencing Data. PLoS ONE. 7(8). e41948–e41948. 37 indexed citations

13.

Schmuth, Matthias, Andreas Janecke, Christine Fauth, et al.. (2012). Inherited ichthyoses/generalized Mendelian disorders of cornification. European Journal of Human Genetics. 21(2). 123–133. 62 indexed citations

14.

Schossig, Anna, Nicole I. Wolf, Ines Kapferer, Alfried Kohlschütter, & Johannes Zschocke. (2012). Epileptic encephalopathy and amelogenesis imperfecta: Kohlschütter–Tönz syndrome. European Journal of Medical Genetics. 55(5). 319–322. 17 indexed citations

15.

Schossig, Anna, Nicole I. Wolf, Martin Jean Koch, et al.. (2007). Epileptische Enzephalopathie und Zahnschmelzdefekt (Kohlschütter-Tönz-Syndrom). Medizinische Genetik. 19(4). 422–426. 2 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.

Explore authors with similar magnitude of impact