Cornelia Kraus

4.8k total citations
75 papers, 2.0k citations indexed

About

Cornelia Kraus is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Cornelia Kraus has authored 75 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 41 papers in Genetics and 10 papers in Pathology and Forensic Medicine. Recurrent topics in Cornelia Kraus's work include Genetics and Neurodevelopmental Disorders (16 papers), Genomic variations and chromosomal abnormalities (14 papers) and Genetic factors in colorectal cancer (9 papers). Cornelia Kraus is often cited by papers focused on Genetics and Neurodevelopmental Disorders (16 papers), Genomic variations and chromosomal abnormalities (14 papers) and Genetic factors in colorectal cancer (9 papers). Cornelia Kraus collaborates with scholars based in Germany, Switzerland and United States. Cornelia Kraus's co-authors include André Reis, Anita Rauch, Christian T. Thiel, Juliane Hoyer, Christiane Zweier, Wolfgang G. Ballhausen, Udo Trautmann, Martin Zenker, Arif B. Ekici and Ulrike Hüffmeier and has published in prestigious journals such as Journal of Molecular Biology, The Journal of Clinical Endocrinology & Metabolism and Scientific Reports.

In The Last Decade

Cornelia Kraus

72 papers receiving 1.9k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Cornelia Kraus 1.0k 967 216 212 188 75 2.0k
David Geneviève 1.3k 1.3× 1.1k 1.1× 136 0.6× 202 1.0× 143 0.8× 80 2.3k
Tayfun Özçelık 1.5k 1.4× 859 0.9× 138 0.6× 225 1.1× 325 1.7× 59 3.1k
Roberto Mendoza‐Londono 1.0k 1.0× 1.2k 1.2× 78 0.4× 151 0.7× 151 0.8× 85 2.1k
Armand Bottani 1.2k 1.2× 1.3k 1.4× 154 0.7× 302 1.4× 97 0.5× 62 2.2k
Bertrand Isidor 1.3k 1.2× 908 0.9× 116 0.5× 107 0.5× 165 0.9× 112 2.1k
Ana Cristina Victorino Krepischi 1.4k 1.3× 1.4k 1.5× 183 0.8× 295 1.4× 243 1.3× 146 2.7k
Mirja Somer 1.5k 1.4× 816 0.8× 113 0.5× 240 1.1× 128 0.7× 49 2.4k
Nurten Akarsu 1.4k 1.3× 817 0.8× 131 0.6× 196 0.9× 130 0.7× 67 2.8k
Francesca Mari 2.2k 2.1× 2.2k 2.3× 110 0.5× 145 0.7× 215 1.1× 103 3.8k
Kwame Anyane‐Yeboa 1.3k 1.2× 1.2k 1.3× 121 0.6× 361 1.7× 97 0.5× 66 2.3k

Countries citing papers authored by Cornelia Kraus

Since Specialization
Citations

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

Fields of papers citing papers by Cornelia Kraus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cornelia Kraus

This figure shows the co-authorship network connecting the top 25 collaborators of Cornelia Kraus. A scholar is included among the top collaborators of Cornelia Kraus 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 Cornelia Kraus. Cornelia Kraus 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.
Krumbiegel, Mandy, Thomas Rupprecht, Cornelia Kraus, et al.. (2024). Severe manifestation of Rauch‐Azzarello syndrome associated with biallelic deletion of CTNND2 . Clinical Genetics. 106(2). 180–186.
2.
Vasileiou, Georgia, Juliane Hoyer, Christian T. Thiel, et al.. (2019). Prenatal diagnosis of HNF1B ‐associated renal cysts: Is there a need to differentiate intragenic variants from 17q12 microdeletion syndrome?. Prenatal Diagnosis. 39(12). 1136–1147. 19 indexed citations
3.
Wiesener, Antje, Karl X. Knaup, Maike Büttner‐Herold, et al.. (2019). Molecular diagnosis of kidney transplant failure based on urine. American Journal of Transplantation. 20(5). 1410–1416. 2 indexed citations
4.
Hüffmeier, Ulrike, Regina Trollmann, Ute Hehr, et al.. (2019). The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy. Orphanet Journal of Rare Diseases. 14(1). 38–38. 42 indexed citations
5.
Menzel-Severing, Johannes, et al.. (2018). Brittle-Cornea-Syndrom Typ 1 durch Compound-Heterozygotie zweier Mutationen im ZNF469-Gen. Der Ophthalmologe. 116(8). 780–784. 6 indexed citations
6.
Popp, Bernt, Arif B. Ekici, Christian T. Thiel, et al.. (2017). Exome Pool-Seq in neurodevelopmental disorders. European Journal of Human Genetics. 25(12). 1364–1376. 59 indexed citations
7.
Donato, Nataliya Di, C. Le Caignec, Barbara Klink, et al.. (2014). Distinct phenotype of PHF6 deletions in females. European Journal of Medical Genetics. 57(2-3). 85–89. 15 indexed citations
8.
Kraus, Cornelia, et al.. (2014). Stable DNA Methylation Boundaries and Expanded Trinucleotide Repeats: Role of DNA Insertions. Journal of Molecular Biology. 426(14). 2554–2566. 15 indexed citations
9.
Kraus, Cornelia, Tilman T. Rau, Katharina Erlenbach‐Wünsch, et al.. (2014). Comprehensive screening for mutations associated with colorectal cancer in unselected cases reveals penetrant and nonpenetrant mutations. International Journal of Cancer. 136(6). E559–68. 21 indexed citations
10.
Zweier, Christiane, Cornelia Kraus, Louise Brueton, et al.. (2013). A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype. Journal of Medical Genetics. 50(12). 838–847. 32 indexed citations
11.
Isidor, Bertrand, Olivier Pichon, Richard Redon, et al.. (2010). Mesomelia-Synostoses Syndrome Results from Deletion of SULF1 and SLCO5A1 Genes at 8q13. The American Journal of Human Genetics. 87(1). 95–100. 31 indexed citations
12.
13.
Kraus, Cornelia, et al.. (2007). Effect of Cardioactive Drugs on Action Potential Generation and Propagation in Embryonic Stem Cell-Derived Cardiomyocytes. Cellular Physiology and Biochemistry. 19(5_6). 239–248. 3 indexed citations
14.
Rauch, Anita, Juliane Hoyer, Sabine Guth, et al.. (2006). Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation. American Journal of Medical Genetics Part A. 140A(19). 2063–2074. 288 indexed citations
15.
Melichar, Volker O., Sabine Guth, Heide Hellebrand, et al.. (2006). A male infant with a 9.6 Mb terminal Xp deletion including the OA1 locus: Limit of viability of Xp deletions in males. American Journal of Medical Genetics Part A. 143A(2). 135–141. 28 indexed citations
16.
Zenker, Martin, Anita Rauch, Andreas Winterpacht, et al.. (2004). A Dual Phenotype of Periventricular Nodular Heterotopia and Frontometaphyseal Dysplasia in One Patient Caused by a Single FLNA Mutation Leading to Two Functionally Different Aberrant Transcripts. The American Journal of Human Genetics. 74(4). 731–737. 50 indexed citations
17.
Zenker, Martin, Bendicht Wermuth, Udo Trautmann, et al.. (2004). Severe, neonatal‐onset OTC deficiency in twin sisters with a de novo balanced reciprocal translocation t(X;5)(p21.1;q11). American Journal of Medical Genetics Part A. 132A(2). 185–188. 16 indexed citations
18.
Kraus, Cornelia, et al.. (2000). RNA-based mutation screening in German families with Sjögren-Larsson syndrome. European Journal of Human Genetics. 8(4). 299–306. 17 indexed citations
19.
Sillén, Anna, I. Anton‐Lamprecht, Cornelia Kraus, et al.. (1998). Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndrome. Human Mutation. 12(6). 377–384. 38 indexed citations
20.
Bala, Shashi, Cornelia Kraus, Juul Wijnen, P. Meera Khan, & Wolfgang G. Ballhausen. (1996). Multiple products in the protein truncation test due to alternative splicing in the adenomatous polyposis coli (APC) gene. Human Genetics. 98(5). 528–533. 24 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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