Enrika Bartels

1.1k total citations
21 papers, 345 citations indexed

About

Enrika Bartels is a scholar working on Surgery, Urology and Genetics. According to data from OpenAlex, Enrika Bartels has authored 21 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Surgery, 8 papers in Urology and 8 papers in Genetics. Recurrent topics in Enrika Bartels's work include Congenital gastrointestinal and neural anomalies (9 papers), Urological Disorders and Treatments (8 papers) and Esophageal and GI Pathology (5 papers). Enrika Bartels is often cited by papers focused on Congenital gastrointestinal and neural anomalies (9 papers), Urological Disorders and Treatments (8 papers) and Esophageal and GI Pathology (5 papers). Enrika Bartels collaborates with scholars based in Germany, United Kingdom and United States. Enrika Bartels's co-authors include Heiko Reutter, Michael Ludwig, Markus M. Nöthen, Markus Draaken, Charlotte Schramm, Eberhard Schmiedeke, Thomas M. Boemers, Dominik Schmidt, Per Hoffmann and Stefan Holland‐Cunz and has published in prestigious journals such as Orphanet Journal of Rare Diseases, Cytogenetic and Genome Research and European Journal of Pediatrics.

In The Last Decade

Enrika Bartels

21 papers receiving 323 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Enrika Bartels Germany 11 220 81 80 79 76 21 345
Elizabeth A. Leeth United States 8 115 0.5× 103 1.3× 25 0.3× 46 0.6× 143 1.9× 11 287
Hidenori Nishio Japan 10 112 0.5× 96 1.2× 102 1.3× 36 0.5× 46 0.6× 46 276
G. Batcup United Kingdom 11 218 1.0× 46 0.6× 44 0.6× 49 0.6× 28 0.4× 20 340
Anne Truong United States 12 222 1.0× 106 1.3× 60 0.8× 20 0.3× 58 0.8× 12 689
C. Thuillier France 9 159 0.7× 42 0.5× 113 1.4× 44 0.6× 20 0.3× 40 264
M. Vitéz Hungary 10 127 0.6× 70 0.9× 42 0.5× 18 0.2× 62 0.8× 16 263
Patricia K. Donahoe United States 8 126 0.6× 239 3.0× 23 0.3× 93 1.2× 110 1.4× 8 425
Gilvydas Verkauskas Lithuania 13 178 0.8× 168 2.1× 86 1.1× 27 0.3× 72 0.9× 42 369
Irene M. Irving United Kingdom 8 172 0.8× 39 0.5× 22 0.3× 43 0.5× 54 0.7× 15 297
Arianna Lesma Italy 7 112 0.5× 113 1.4× 68 0.8× 38 0.5× 120 1.6× 14 309

Countries citing papers authored by Enrika Bartels

Since Specialization
Citations

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

Fields of papers citing papers by Enrika Bartels

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Enrika Bartels

This figure shows the co-authorship network connecting the top 25 collaborators of Enrika Bartels. A scholar is included among the top collaborators of Enrika Bartels 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 Enrika Bartels. Enrika Bartels 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.
Kohlschmidt, Nicolai, Andreas Hentschel, Enrika Bartels, et al.. (2022). Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects. Orphanet Journal of Rare Diseases. 17(1). 29–29. 5 indexed citations
2.
Mroczek, Magdalena, Dimitrios Zafeiriou, Andreas Roos, et al.. (2020). Three Individuals with PURA Syndrome in a Cohort of Patients with Neuromuscular Disease. Neuropediatrics. 52(5). 390–393. 8 indexed citations
3.
Spier, Isabel, Hartmut Engels, Heiko Reutter, et al.. (2019). Male infant with paternal uniparental diploidy mosaicism and a 46,XX/46,XY karyotype. American Journal of Medical Genetics Part A. 179(11). 2252–2256. 8 indexed citations
4.
Draaken, Markus, Sadaf S. Mughal, Tracie Pennimpede, et al.. (2013). Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12. Birth Defects Research Part A Clinical and Molecular Teratology. 97(3). 133–139. 15 indexed citations
5.
Draaken, Markus, Enrika Bartels, Eberhard Schmiedeke, et al.. (2013). CNV Analysis in Monozygotic Twin Pairs Discordant for Urorectal Malformations. Twin Research and Human Genetics. 16(4). 802–807. 7 indexed citations
6.
7.
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
8.
Bartels, Enrika, R Stressig, J Ritgen, et al.. (2012). Nine new twin pairs with esophageal atresia: A review of the literature and performance of a twin study of the disorder. Birth Defects Research Part A Clinical and Molecular Teratology. 94(3). 182–186. 15 indexed citations
9.
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
10.
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
11.
Hilger, Alina C., Charlotte Schramm, Markus Draaken, et al.. (2012). Familial occurrence of the VATER/VACTERL association. Pediatric Surgery International. 28(7). 725–729. 27 indexed citations
12.
Draaken, Markus, Claudia Zeidler, Alina C. Hilger, et al.. (2012). Involvement of the WNT and FGF signaling pathways in non-isolated anorectal malformations: Sequencing analysis of WNT3A, WNT5A, WNT11, DACT1, FGF10, FGFR2 and the T gene. International Journal of Molecular Medicine. 30(6). 1459–1464. 22 indexed citations
13.
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
14.
Bartels, Enrika, Markus Draaken, Bernd Kazmierczak, et al.. (2011). De novo Partial Trisomy 18p and Partial Monosomy 18q in a Patient with Anorectal Malformation. Cytogenetic and Genome Research. 134(3). 243–248. 9 indexed citations
15.
Draaken, Markus, Heiko Reutter, Charlotte Schramm, et al.. (2010). Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy. European Journal of Medical Genetics. 53(2). 55–60. 48 indexed citations
16.
Draaken, Markus, Charlotte Schramm, Lars Wittler, et al.. (2010). Embryonic expression of the cysteine rich protein 61 (CYR61) gene: A candidate for the development of human epispadias. Birth Defects Research Part A Clinical and Molecular Teratology. 88(7). 546–550. 5 indexed citations
17.
Reutter, Heiko, Franz Rüschendorf, Manuel Mattheisen, et al.. (2010). Evidence for linkage of the bladder exstrophy‐epispadias complex on chromosome 4q31.21‐22 and 19q13.31‐41 from a consanguineous iranian family. Birth Defects Research Part A Clinical and Molecular Teratology. 88(9). 757–761. 6 indexed citations
18.
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
19.
Schramm, Charlotte, Markus Draaken, Enrika Bartels, et al.. (2010). De novo microduplication at 22q11.21 in a patient with VACTERL association. European Journal of Medical Genetics. 54(1). 9–13. 46 indexed citations
20.
Rösch, Wolfgang, Markus Draaken, Michael Ludwig, et al.. (2010). Microduplications At 22q11.21 are Associated with Classic Bladder Exstrophy. Journal of Pediatric Urology. 6. S21–S21. 2 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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