Katrin Kausch

419 total citations
8 papers, 199 citations indexed

About

Katrin Kausch is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Katrin Kausch has authored 8 papers receiving a total of 199 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Katrin Kausch's work include Genomic variations and chromosomal abnormalities (3 papers), Chromosomal and Genetic Variations (2 papers) and Prenatal Screening and Diagnostics (2 papers). Katrin Kausch is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Chromosomal and Genetic Variations (2 papers) and Prenatal Screening and Diagnostics (2 papers). Katrin Kausch collaborates with scholars based in Germany, Netherlands and Italy. Katrin Kausch's co-authors include Julia R. Köhler, Thomas Haaf, T. Grimm, Giovanni Neri, Michael Schmid, James F. Reynolds, C. R. Müller, F. Lehmann‐Horn, M. Janka and Bé Wieringa and has published in prestigious journals such as Genomics, Human Genetics and Current topics in microbiology and immunology.

In The Last Decade

Katrin Kausch

8 papers receiving 184 citations

Peers

Katrin Kausch
Imma Rost Germany
L.G. Shaffer United States
Patricia A. Eng United States
Molly B. Sheridan United States
Gordon S. Stephen United Kingdom
Laura Davis‐Keppen United States
Katrin Kausch
Citations per year, relative to Katrin Kausch Katrin Kausch (= 1×) peers Marija Guć‐Šćekić

Countries citing papers authored by Katrin Kausch

Since Specialization
Citations

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

Fields of papers citing papers by Katrin Kausch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katrin Kausch

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

All Works

8 of 8 papers shown
1.
Cheng, Pan, et al.. (2000). B-Lymphocyte Signaling Receptors and the Control of Class-II Antigen Processing. Current topics in microbiology and immunology. 245(2). 101–126. 15 indexed citations
2.
Kausch, Katrin, Frank Kullmann, M.L. Mostacciuolo, et al.. (1992). Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene. Neuromuscular Disorders. 2(2). 111–115. 7 indexed citations
3.
Kausch, Katrin, T. Grimm, K. Ricker, et al.. (1991). No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers. Human Genetics. 86(3). 317–8. 17 indexed citations
4.
Kausch, Katrin, F. Lehmann‐Horn, M. Janka, et al.. (1991). Evidence for linkage of the central core disease locus to the proximal long arm of human chromosome 19. Genomics. 10(3). 765–769. 59 indexed citations
5.
Poot, Martin, Katrin Kausch, Julia R. Köhler, Thomas Haaf, & Holger Hoehn. (1990). The minor-groove binding DNA-ligands netropsin, distamycin A and berenil cause polyploidisation via impairment of the G2 phase of the cell cycle.. Cell Structure and Function. 15(3). 151–157. 22 indexed citations
6.
Kausch, Katrin, Thomas Haaf, Julia R. Köhler, et al.. (1988). Complex chromosomal rearrangement in a woman with multiple miscarriages. American Journal of Medical Genetics. 31(2). 415–420. 70 indexed citations
7.
Kausch, Katrin, Thomas Haaf, Michael Schmid, Giovanni Neri, & James F. Reynolds. (1988). Duplication 8q24.2→qter and 15q14→pter resulting from a 3:1 meiotic segregation of a maternal reciprocal translocation. American Journal of Medical Genetics. 31(4). 981–985. 4 indexed citations
8.
Kausch, Katrin, Julia R. Köhler, & Michael Schmid. (1988). Deletion 1q42.3----qter in a girl with psychomotoric retardation and multiple dysmorphisms.. PubMed. 31(3). 193–4. 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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