Ute Grasshoff

2.5k total citations
29 papers, 791 citations indexed

About

Ute Grasshoff is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ute Grasshoff has authored 29 papers receiving a total of 791 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 15 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ute Grasshoff's work include Genomic variations and chromosomal abnormalities (12 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Genomics and Rare Diseases (4 papers). Ute Grasshoff is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Genomics and Rare Diseases (4 papers). Ute Grasshoff collaborates with scholars based in Germany, France and Netherlands. Ute Grasshoff's co-authors include Michael Bonin, Andreas Dufke, Andreas Tzschach, Dorothea Bornholdt, Bárbara Fritz, Arne König, Frank Oeffner, Rudolf Happle, María del Carmen Boente and Katja Höfling and has published in prestigious journals such as Nature Genetics, Genome Research and Neurobiology of Aging.

In The Last Decade

Ute Grasshoff

27 papers receiving 760 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ute Grasshoff Germany 12 477 463 100 91 74 29 791
David B. Everman United States 20 466 1.0× 657 1.4× 146 1.5× 41 0.5× 84 1.1× 39 1.1k
Kenji Naritomi Japan 17 463 1.0× 400 0.9× 133 1.3× 44 0.5× 65 0.9× 58 689
Anne Puech United States 15 351 0.7× 604 1.3× 90 0.9× 55 0.6× 109 1.5× 25 851
Dominique Martin‐Coignard France 14 424 0.9× 522 1.1× 78 0.8× 30 0.3× 53 0.7× 22 817
Simon Holden United Kingdom 12 219 0.5× 296 0.6× 37 0.4× 16 0.2× 50 0.7× 35 585
Eva Rossier Germany 13 392 0.8× 406 0.9× 73 0.7× 34 0.4× 20 0.3× 21 644
Julia Parrish United States 13 348 0.7× 414 0.9× 20 0.2× 41 0.5× 57 0.8× 19 695
Jiong Yan United States 15 487 1.0× 650 1.4× 35 0.3× 94 1.0× 76 1.0× 27 1.0k
Viola Alesi Italy 13 309 0.6× 263 0.6× 67 0.7× 37 0.4× 41 0.6× 59 558
Thomas Schwarzbraun Austria 14 252 0.5× 517 1.1× 38 0.4× 70 0.8× 184 2.5× 26 852

Countries citing papers authored by Ute Grasshoff

Since Specialization
Citations

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

Fields of papers citing papers by Ute Grasshoff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ute Grasshoff

This figure shows the co-authorship network connecting the top 25 collaborators of Ute Grasshoff. A scholar is included among the top collaborators of Ute Grasshoff 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 Ute Grasshoff. Ute Grasshoff 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.
Grasshoff, Ute & Stephanie Spranger. (2024). Humangenetische Diagnostik und Beratung - wer, wann und wie?. Pädiatrie. 36(1). 22–31.
2.
Kohl, Susanne, et al.. (2023). An early onset cone dystrophy due to CEP290 mutation: a case report. Documenta Ophthalmologica. 147(3). 203–209.
3.
Lipska‐Ziętkiewicz, Beata S., Vincent Michaud, James Lespinasse, et al.. (2022). Phenotypic characterization of seven individuals with Marbach–Schaaf neurodevelopmental syndrome. American Journal of Medical Genetics Part A. 188(9). 2627–2636. 3 indexed citations
4.
Horber, Veronka, Ute Grasshoff, Élodie Sellier, et al.. (2021). The Role of Neuroimaging and Genetic Analysis in the Diagnosis of Children With Cerebral Palsy. Frontiers in Neurology. 11. 628075–628075. 13 indexed citations
5.
König, A., Hemmen Sabir, Brigitte Strizek, et al.. (2021). Isolated cytokine‐enriched pericardial effusion: A likely key feature for Aymé‐Gripp syndrome. American Journal of Medical Genetics Part A. 188(2). 624–627. 3 indexed citations
6.
Bauer, Daniel, et al.. (2020). GlyT1 encephalopathy: Characterization of presumably disease causing GlyT1 mutations. Neurochemistry International. 139. 104813–104813. 5 indexed citations
7.
Park, Joohyun, Karin Schäferhoff, Luigi Janiri, et al.. (2019). Novel HIVEP2 Variants in Patients with Intellectual Disability. Molecular Syndromology. 10(4). 195–201. 7 indexed citations
8.
Park, Joohyun, Mari Rossi, Maren Rautenberg, et al.. (2019). De novo variants in SLC12A6 cause sporadic early-onset progressive sensorimotor neuropathy. Journal of Medical Genetics. 57(4). 283–288. 10 indexed citations
9.
Schroeder, Christopher, Arif B. Ekici, Ute Moog, et al.. (2014). Genome-wide UPD screening in patients with intellectual disability. European Journal of Human Genetics. 22(10). 1233–1235. 4 indexed citations
10.
Rieß, Angelika, Ute Grasshoff, Karin Schäferhoff, et al.. (2013). Xq22.3–q23 deletion including ACSL4 in a patient with intellectual disability. American Journal of Medical Genetics Part A. 161(4). 860–864. 32 indexed citations
11.
Synofzik, Matthis, Christoph Born, Axel Rominger, et al.. (2013). Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease. Neurobiology of Aging. 35(5). 1212.e1–1212.e5. 35 indexed citations
12.
Tzschach, Andreas, Ute Grasshoff, Karin Schäferhoff, et al.. (2012). Interstitial 9q34.11–q34.13 deletion in a patient with severe intellectual disability, hydrocephalus, and cleft lip/palate. American Journal of Medical Genetics Part A. 158A(7). 1709–1712. 6 indexed citations
13.
Rieß, Angelika, Ute Grasshoff, Karin Schäferhoff, et al.. (2012). Interstitial 3p25.3–p26.1 deletion in a patient with intellectual disability. American Journal of Medical Genetics Part A. 158A(10). 2587–2590. 11 indexed citations
14.
Grasshoff, Ute, Michael Bonin, Arif B. Ekici, et al.. (2011). De novo MECP2 duplication in two females with random X-inactivation and moderate mental retardation. European Journal of Human Genetics. 19(5). 507–512. 33 indexed citations
15.
Endris, Volker, Karl Hackmann, Teresa Neuhann, et al.. (2010). Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia. American Journal of Medical Genetics Part A. 152A(11). 2908–2911. 43 indexed citations
16.
Zweier, Markus, Anne Gregor, Christiane Zweier, et al.. (2010). Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression. Human Mutation. 31(6). 722–733. 114 indexed citations
17.
Boy, Jana, Thorsten Schmidt, Ute Grasshoff, et al.. (2009). A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeats. Neurobiology of Disease. 37(2). 284–293. 42 indexed citations
18.
Chen, Wei, Vera M. Kalscheuer, Andreas Tzschach, et al.. (2008). Mapping translocation breakpoints by next-generation sequencing. Genome Research. 18(7). 1143–1149. 102 indexed citations
19.
Grzeschik, Karl‐Heinz, Dorothea Bornholdt, Frank Oeffner, et al.. (2007). Deficiency of PORCN, a regulator of Wnt signaling, is associated with focal dermal hypoplasia. Nature Genetics. 39(7). 833–835. 181 indexed citations
20.
Grasshoff, Ute, Sylke Singer, Thomas Liehr, et al.. (2003). A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q24→1q22 and partial monosomy 4q27→q28. Cytogenetic and Genome Research. 103(1-2). 17–23. 26 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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