Kerstin Kutsche

8.6k total citations
118 papers, 3.6k citations indexed

About

Kerstin Kutsche is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Kerstin Kutsche has authored 118 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 81 papers in Molecular Biology, 63 papers in Genetics and 29 papers in Cell Biology. Recurrent topics in Kerstin Kutsche's work include Genetics and Neurodevelopmental Disorders (21 papers), Connective tissue disorders research (17 papers) and Hedgehog Signaling Pathway Studies (12 papers). Kerstin Kutsche is often cited by papers focused on Genetics and Neurodevelopmental Disorders (21 papers), Connective tissue disorders research (17 papers) and Hedgehog Signaling Pathway Studies (12 papers). Kerstin Kutsche collaborates with scholars based in Germany, United States and India. Kerstin Kutsche's co-authors include Georg Rosenberger, Andreas Gal, Hans Gerd Nothwang, Denise Horn, Fanny Kortüm, Hanno J. Bolz, Ulrike Orth, Isabella Wimplinger, Alfredo Ramı́rez and Elizabeth C. Bryda and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Molecular and Cellular Biology.

In The Last Decade

Kerstin Kutsche

114 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kerstin Kutsche Germany 32 2.3k 1.3k 685 358 297 118 3.6k
Bernd Wollnik Germany 36 2.8k 1.2× 1.6k 1.2× 304 0.4× 306 0.9× 395 1.3× 138 4.3k
Gudrun Nürnberg Germany 44 2.9k 1.3× 1.6k 1.2× 895 1.3× 451 1.3× 424 1.4× 93 5.1k
Helger G. Yntema Netherlands 35 2.7k 1.2× 2.6k 2.0× 399 0.6× 372 1.0× 233 0.8× 100 4.9k
Anna‐Elina Lehesjoki Finland 39 2.1k 0.9× 1.6k 1.2× 943 1.4× 435 1.2× 216 0.7× 126 4.9k
Jean M. Hébert United States 34 3.8k 1.7× 1.1k 0.8× 598 0.9× 1.0k 2.8× 376 1.3× 83 5.5k
E. Bryan Crenshaw United States 32 4.0k 1.8× 1.3k 1.0× 445 0.6× 544 1.5× 346 1.2× 51 5.9k
Qiuxia Guo United States 22 2.3k 1.0× 535 0.4× 376 0.5× 381 1.1× 119 0.4× 33 3.5k
Bart P. Leroy Belgium 37 3.6k 1.6× 1.5k 1.1× 661 1.0× 484 1.4× 179 0.6× 157 4.8k
G. Giacomo Consalez Italy 35 2.0k 0.9× 667 0.5× 371 0.5× 723 2.0× 165 0.6× 93 3.3k
Stéphane Schurmans Belgium 32 2.3k 1.0× 912 0.7× 632 0.9× 983 2.7× 541 1.8× 94 4.1k

Countries citing papers authored by Kerstin Kutsche

Since Specialization
Citations

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

Fields of papers citing papers by Kerstin Kutsche

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kerstin Kutsche

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

All Works

20 of 20 papers shown
1.
Harms, Frederike L., Jessica E. Rexach, Stéphanie Efthymiou, et al.. (2024). Loss of TBC1D2B causes a progressive neurological disorder with gingival overgrowth. European Journal of Human Genetics. 32(5). 558–566. 1 indexed citations
2.
3.
Nishimura, Gen, Jakob Ek, Mads Bak, et al.. (2024). Novel biallelic PISD missense variants cause spondyloepimetaphyseal dysplasia with disproportionate short stature and fragmented mitochondrial morphology. Clinical Genetics. 106(3). 360–366. 3 indexed citations
4.
Mir, Thomas S., Gerhard Schön, Kerstin Kutsche, et al.. (2024). Late diagnosis of Marfan syndrome is associated with unplanned aortic surgery and cardiovascular death. Journal of Thoracic and Cardiovascular Surgery. 169(4). 1201–1209.e33.
5.
Kozlik‐Feldmann, Rainer, et al.. (2024). Intrinsic cardiomyopathy in pediatric Marfan syndrome: predictive factors and risk assessments. Pediatric Research. 98(4). 1467–1473.
6.
7.
Dahimène, Shehrazade, Davor Lessel, Kjara S Pilch, et al.. (2022). Biallelic CACNA2D1 loss-of-function variants cause early-onset developmental epileptic encephalopathy. Brain. 145(8). 2721–2729. 29 indexed citations
8.
Bierhals, Tatjana, Marta Campiglio, Jessika Johannsen, et al.. (2020). A homozygous missense variant in CACNB4 encoding the auxiliary calcium channel beta4 subunit causes a severe neurodevelopmental disorder and impairs channel and non-channel functions. PLoS Genetics. 16(3). e1008625–e1008625. 26 indexed citations
9.
Kortüm, Fanny, Rami Abou Jamra, Malik Alawi, et al.. (2018). Clinical and genetic spectrum of AMPD2-related pontocerebellar hypoplasia type 9. European Journal of Human Genetics. 26(5). 695–708. 23 indexed citations
10.
Harms, Frederike L., Sheela Nampoothiri, Shams Anazi, et al.. (2017). Elsahy–Waters syndrome is caused by biallelic mutations in CDH11. American Journal of Medical Genetics Part A. 176(2). 477–482. 9 indexed citations
11.
Vogel, Markus, Eunike Velleuer, Ertan Mayatepek, et al.. (2016). Homozygous HOXB1 loss‐of‐function mutation in a large family with hereditary congenital facial paresis. American Journal of Medical Genetics Part A. 170(7). 1813–1819. 21 indexed citations
12.
Fernández‐Vizarra, Erika, Malik Alawi, K. Gerhard Brand, et al.. (2015). Mutations in NDUFB11, Encoding a Complex I Component of the Mitochondrial Respiratory Chain, Cause Microphthalmia with Linear Skin Defects Syndrome. The American Journal of Human Genetics. 96(4). 640–650. 60 indexed citations
13.
Girisha, Katta M., Fanny Kortüm, Hitesh Shah, et al.. (2015). A novel multiple joint dislocation syndrome associated with a homozygous nonsense variant in the EXOC6B gene. European Journal of Human Genetics. 24(8). 1206–1210. 14 indexed citations
14.
Bayer, Janine, Gabriele M. Rune, Kerstin Kutsche, et al.. (2012). Estrogen and the male hippocampus: Genetic variation in the aromatase gene predicting serum estrogen is associated with hippocampal gray matter volume in men. Hippocampus. 23(2). 117–121. 9 indexed citations
15.
Gremer, Lothar, Alessandro De Luca, Torsten Merbitz-Zahradnik, et al.. (2009). Duplication of Glu37 in the switch I region of HRAS impairs effector/GAP binding and underlies Costello syndrome by promoting enhanced growth factor-dependent MAPK and AKT activation. Human Molecular Genetics. 19(5). 790–802. 32 indexed citations
16.
Najm, Juliane, Denise Horn, Isabella Wimplinger, et al.. (2008). Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum. Nature Genetics. 40(9). 1065–1067. 202 indexed citations
17.
Martínez‐Garay, Isabel, Miguel Tomás Vila, Silvestre Oltra, et al.. (2006). A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation. European Journal of Human Genetics. 15(1). 29–34. 28 indexed citations
18.
Martínez‐Garay, Isabel, Amin Rustom, Hans‐Hermann Gerdes, & Kerstin Kutsche. (2006). The novel centrosomal associated protein CEP55 is present in the spindle midzone and the midbody. Genomics. 87(2). 243–253. 68 indexed citations
19.
Meinecke, Peter, Andrew E. Czeizel, László Tı́már, et al.. (2003). Disruption of the PDGFB gene in a 1;22 translocation patient does not cause Costello syndrome. Genomics. 83(5). 883–892. 3 indexed citations
20.
Kutsche, Kerstin, Sascha Knauf, Martina Schmidt, et al.. (2000). Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium. Cytogenetic and Genome Research. 91(1-4). 141–147. 7 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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