Sabine Grasshoff‐Derr

828 total citations
11 papers, 178 citations indexed

About

Sabine Grasshoff‐Derr is a scholar working on Surgery, Rheumatology and Urology. According to data from OpenAlex, Sabine Grasshoff‐Derr has authored 11 papers receiving a total of 178 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Surgery, 4 papers in Rheumatology and 2 papers in Urology. Recurrent topics in Sabine Grasshoff‐Derr's work include Congenital gastrointestinal and neural anomalies (10 papers), Gastrointestinal disorders and treatments (6 papers) and Intestinal Malrotation and Obstruction Disorders (3 papers). Sabine Grasshoff‐Derr is often cited by papers focused on Congenital gastrointestinal and neural anomalies (10 papers), Gastrointestinal disorders and treatments (6 papers) and Intestinal Malrotation and Obstruction Disorders (3 papers). Sabine Grasshoff‐Derr collaborates with scholars based in Germany, United States and Netherlands. Sabine Grasshoff‐Derr's co-authors include Eberhard Schmiedeke, Heiko Reutter, Stefan Holland‐Cunz, Ekkehart Jenetzky, Nicole Schwarzer, Enrika Bartels, Nadine Zwink, Dominik Schmidt, Stuart Hosie and Stefanie Märzheuser and has published in prestigious journals such as Journal of Pediatric Surgery, Orphanet Journal of Rare Diseases and European Journal of Pediatrics.

In The Last Decade

Sabine Grasshoff‐Derr

11 papers receiving 168 citations

Peers

Sabine Grasshoff‐Derr

SURGE

UROLO

RHEUM

PRM

GENET

Jeremy Robertson Australia

Yuzuo Bai China

Nicoleta Panait France

Simone Pötzsch Germany

W.N.P. Willemsen Netherlands

Helen Garrott United Kingdom

B. Sjollema Netherlands

Yunli Bi China

Kathy Vander Eeckt Belgium

Valerio Mais Italy

Jeremy Robertson Australia

Sabine Grasshoff‐Derr

43 ×0.3

SURGE

20 ×0.5

UROLO

14 ×0.5

RHEUM

19 ×0.8

PRM

25 ×1.7

GENET

Citations per year, relative to Sabine Grasshoff‐Derr Sabine Grasshoff‐Derr (= 1×) peers Jeremy Robertson

Countries citing papers authored by Sabine Grasshoff‐Derr

Since Specialization

Citations

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

Fields of papers citing papers by Sabine Grasshoff‐Derr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabine Grasshoff‐Derr

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

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

Hilger, Alina C., Eberhard Schmiedeke, Frank‐Mattias Schäfer, et al.. (2022). Re‐sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL‐like association, and isolated anorectal malformation. Birth Defects Research. 114(10). 478–486. 9 indexed citations

Midrio, Paola, Iris A.L.M. van Rooij, Giulia Brisighelli, et al.. (2020). Inter- and Intraobserver Variation in the Assessment of Preoperative Colostograms in Male Anorectal Malformations: An ARM-Net Consortium Survey. Frontiers in Pediatrics. 8. 571–571. 3 indexed citations

Dworschak, Gabriel C., Markus Draaken, Alina C. Hilger, et al.. (2014). Genome‐wide mapping of copy number variations in patients with both anorectal malformations and central nervous system abnormalities. Birth Defects Research Part A Clinical and Molecular Teratology. 103(4). 235–242. 16 indexed citations

Blaauw, Ivo de, Charlotte H. W. Wijers, Eberhard Schmiedeke, et al.. (2013). First results of a European multi-center registry of patients with anorectal malformations. Journal of Pediatric Surgery. 48(12). 2530–2535. 45 indexed citations

Schmiedeke, Eberhard, Nadine Zwink, Nicole Schwarzer, et al.. (2012). Unexpected results of a nationwide, treatment-independent assessment of fecal incontinence in patients with anorectal anomalies. Pediatric Surgery International. 28(8). 825–830. 29 indexed citations

Zwink, Nadine, Ekkehart Jenetzky, Eberhard Schmiedeke, et al.. (2012). Assisted reproductive techniques and the risk of anorectal malformations: a German case-control study. Orphanet Journal of Rare Diseases. 7(1). 65–65. 19 indexed citations

Bartels, Enrika, Ekkehart Jenetzky, Benjamin D. Solomon, et al.. (2012). Inheritance of the VATER/VACTERL association. Pediatric Surgery International. 28(7). 681–685. 26 indexed citations

Grasshoff‐Derr, Sabine, et al.. (2012). 1,5-jähriger Junge mit stark zunehmendem, deutlich vorgewölbtem Abdomen. Der Chirurg. 83(9). 815–818. 1 indexed citations

Jenetzky, Ekkehart, Nadine Zwink, Heiko Reutter, et al.. (2011). German Network for Congenital Uro-REctal Malformations: first evaluation and interpretation of postoperative urological complications in anorectal malformations. Pediatric Surgery International. 27(10). 1085–1089. 7 indexed citations

10.

Grasshoff‐Derr, Sabine, et al.. (2011). A successful treatment strategy in infants and adolescents with anorectal malformation and incontinence with combined hydrocolonic ultrasound and bowel management. Pediatric Surgery International. 27(10). 1099–1103. 8 indexed citations

11.

Schramm, Charlotte, Markus Draaken, Enrika Bartels, et al.. (2010). Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature. European Journal of Pediatrics. 170(6). 741–746. 15 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.

Explore authors with similar magnitude of impact