Kristin Kessler

513 total citations
6 papers, 182 citations indexed

About

Kristin Kessler is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Kristin Kessler has authored 6 papers receiving a total of 182 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Cell Biology. Recurrent topics in Kristin Kessler's work include Genetic and Kidney Cyst Diseases (5 papers), Microtubule and mitosis dynamics (3 papers) and Protist diversity and phylogeny (2 papers). Kristin Kessler is often cited by papers focused on Genetic and Kidney Cyst Diseases (5 papers), Microtubule and mitosis dynamics (3 papers) and Protist diversity and phylogeny (2 papers). Kristin Kessler collaborates with scholars based in Germany, Netherlands and Czechia. Kristin Kessler's co-authors include Andreas Gießl, Christian T. Thiel, Arif B. Ekici, André Reis, Johann Helmut Brandstätter, Stavit A. Shalev, Thomas Kirchner, H Stöß, Anita Rauch and Ernst Beinder and has published in prestigious journals such as Scientific Reports, Journal of Cell Science and The American Journal of Human Genetics.

In The Last Decade

Kristin Kessler

6 papers receiving 181 citations

Peers

Kristin Kessler

MB

GENET

CB

PPCH

NEURO

Gaurav V. Harlalka United Kingdom

Elisabeth E. Mlynarski United States

Amira Masri Jordan

Yannis Duffourd France

Eric Scott United States

Ange‐Line Bruel France

Arjan PM de Brouwer Netherlands

Marie‐Line Jacquemont France

Christeen Ramane J. Pedurupillay Norway

Bita Bozorgmehr Iran

Gaurav V. Harlalka United Kingdom

Kristin Kessler

184 ×1.3

MB

95 ×0.7

GENET

62 ×1.1

CB

19 ×1.1

PPCH

11 ×0.8

NEURO

Citations per year, relative to Kristin Kessler Kristin Kessler (= 1×) peers Gaurav V. Harlalka

Countries citing papers authored by Kristin Kessler

Since Specialization

Citations

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

Fields of papers citing papers by Kristin Kessler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kristin Kessler

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

All Works

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6 of 6 papers shown

1.

Falk, Nathalie, Kristin Kessler, Angelika A. Noegel, et al.. (2019). Lack of a Retinal Phenotype in a Syne-2/Nesprin-2 Knockout Mouse Model. Cells. 8(10). 1238–1238. 6 indexed citations

2.

Falk, Nathalie, Kristin Kessler, Karsten Boldt, et al.. (2018). Functional analyses of Pericentrin and Syne-2 interaction in ciliogenesis. Journal of Cell Science. 131(16). 8 indexed citations

3.

Kessler, Kristin, Steffen Uebe, Nathalie Falk, et al.. (2015). DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects. Scientific Reports. 5(1). 11649–11649. 26 indexed citations

4.

Kessler, Kristin, Nathalie Falk, Markham T. Frohlich, et al.. (2015). Identification of mutations in DYNC2LI1, a member of the mammalian cytoplasmic dynein 2 complex, expands the clinical spectrum of Jeune/ATD ciliopathies. Europe PMC (PubMed Central). 4(S1). 1 indexed citations

5.

Kessler, Kristin, Steffen Uebe, Stephan C. F. Neuhauss, et al.. (2014). MAP4-Dependent Regulation of Microtubule Formation Affects Centrosome, Cilia, and Golgi Architecture as a Central Mechanism in Growth Regulation. Human Mutation. 36(1). 87–97. 17 indexed citations

6.

Thiel, Christian T., Kristin Kessler, Andreas Gießl, et al.. (2011). NEK1 Mutations Cause Short-Rib Polydactyly Syndrome Type Majewski. The American Journal of Human Genetics. 88(1). 106–114. 124 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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