Stefanie Weber

2.1k total citations
31 papers, 1.5k citations indexed

About

Stefanie Weber is a scholar working on Molecular Biology, Genetics and Pollution. According to data from OpenAlex, Stefanie Weber has authored 31 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Pollution. Recurrent topics in Stefanie Weber's work include Renal and related cancers (8 papers), Pediatric Urology and Nephrology Studies (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Stefanie Weber is often cited by papers focused on Renal and related cancers (8 papers), Pediatric Urology and Nephrology Studies (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Stefanie Weber collaborates with scholars based in Germany, United States and Switzerland. Stefanie Weber's co-authors include Juliane Hollender, W. Dott, E. Huertas, Stuart J. Khan, Hans H. Richnow, Franz Schaefer, Corinne Antignac, M. Salgot, Otto Mehls and Walter Doerfler and has published in prestigious journals such as Environmental Science & Technology, The Science of The Total Environment and Water Research.

In The Last Decade

Stefanie Weber

30 papers receiving 1.4k citations

Peers

Stefanie Weber

POLLU

PPCH

IME

HTM

Imran Hussain United States

Weifeng Ruan China

Pan Yang China

Ida Damgaard Denmark

Carsten K. Schmidt Germany

Lizhi Wu China

Shengde Wu China

Vanessa Cristina de Oliveira Souza Brazil

Kan Wang China

Uwe Heinrich Germany

Imran Hussain United States

Stefanie Weber

825 ×1.2

460 ×1.4

POLLU

30 ×0.1

PPCH

117 ×0.5

IME

328 ×1.4

HTM

Citations per year, relative to Stefanie Weber Stefanie Weber (= 1×) peers Imran Hussain

Countries citing papers authored by Stefanie Weber

Since Specialization

Citations

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

Fields of papers citing papers by Stefanie Weber

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefanie Weber

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

All Works

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20 of 20 papers shown

Jansen, Andreas, Jens Sommer, Robert S. Krauss, et al.. (2025). Test–retest reliability of functional near infrared spectroscopy during tasks of inhibitory control and working memory. Psychiatry Research Neuroimaging. 350. 111993–111993.

König, Jens, et al.. (2023). Review of neurodevelopmental disorders in patients with HNF1B gene variations. Frontiers in Pediatrics. 11. 1149875–1149875. 6 indexed citations

Doerfler, Walter, et al.. (2018). Inheritable epigenetic response towards foreign DNA entry by mammalian host cells: a guardian of genomic stability. Epigenetics. 13(12). 1141–1153. 5 indexed citations

Epting, Jannis, Peter Huggenberger, Michael D. Besmer, et al.. (2017). Variabilität der grundwasserqualität. Einflussfaktoren für die Grundwasserqualität Flussnaher Trinkwasserfassungen. DORA Eawag (Swiss Federal Institute of Aquatic Science and Technology (Eawag)). 97(2). 30–39. 1 indexed citations

Weber, Stefanie, et al.. (2015). DNA Methylation and Transcription in HERV (K, W, E) and LINE Sequences Remain Unchanged Upon Foreign DNA Insertions. Epigenomics. 8(2). 157–165. 5 indexed citations

Weber, Stefanie. (2012). Novel genetic aspects of congenital anomalies of kidney and urinary tract. Current Opinion in Pediatrics. 24(2). 212–218. 43 indexed citations

Schild, Ralf L., Tanja Knüppel, Moira Konrad, et al.. (2012). Double homozygous missense mutations in DACH1 and BMP4 in a patient with bilateral cystic renal dysplasia. Nephrology Dialysis Transplantation. 28(1). 227–232. 18 indexed citations

Brockschmidt, Antje, Byung Ha Chung, Stefanie Weber, et al.. (2011). CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT). Nephrology Dialysis Transplantation. 27(6). 2355–2364. 28 indexed citations

Renkema, Kirsten Y., Paul J.D. Winyard, Ilya Skovorodkin, et al.. (2011). Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT). Nephrology Dialysis Transplantation. 26(12). 3843–3851. 62 indexed citations

10.

Weber, Stefanie, Christina Landwehr, Alexander Hoischen, et al.. (2010). Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization. Nephrology Dialysis Transplantation. 26(1). 136–143. 48 indexed citations

11.

Fischer, Anko, et al.. (2010). Carbon and hydrogen isotope fractionation during anaerobic quinoline degradation. Chemosphere. 81(3). 400–407. 17 indexed citations

12.

Weber, Stefanie, et al.. (2010). A Distinct DNA-Methylation Boundary in the 5′- Upstream Sequence of the FMR1 Promoter Binds Nuclear Proteins and Is Lost in Fragile X Syndrome. The American Journal of Human Genetics. 86(1). 98–100. 2 indexed citations

13.

Nijenhuis, Ivonne, Paula Martínez, Howard Junca, et al.. (2009). In situ investigation of microbial diversity and anaerobic chlorobenzene degradation along a vertical gradient. Geochimica et Cosmochimica Acta Supplement. 73. 1 indexed citations

14.

Weber, Stefanie, et al.. (2009). A Distinct DNA-Methylation Boundary in the 5′- Upstream Sequence of the FMR1 Promoter Binds Nuclear Proteins and Is Lost in Fragile X Syndrome. The American Journal of Human Genetics. 85(5). 606–616. 74 indexed citations

15.

Weber, Stefanie, Paul J.D. Winyard, Jessica Sullivan-Brown, et al.. (2008). SIX2 and BMP4 Mutations Associate With Anomalous Kidney Development. Journal of the American Society of Nephrology. 19(5). 891–903. 150 indexed citations

16.

Braeckevelt, Mareike, Gwenaël Imfeld, Nicole Stelzer, et al.. (2007). Assessment of in situ biodegradation of monochlorobenzene in contaminated groundwater treated in a constructed wetland. Environmental Pollution. 148(2). 428–437. 57 indexed citations

17.

Imfeld, Gwenaël, Ivonne Nijenhuis, Marcell Nikolausz, et al.. (2007). Assessment of in situ degradation of chlorinated ethenes and bacterial community structure in a complex contaminated groundwater system. Water Research. 42(4-5). 871–882. 53 indexed citations

18.

Weber, Stefanie, Vincent Morinière, Tanja Knüppel, et al.. (2006). Prevalence of Mutations in Renal Developmental Genes in Children with Renal Hypodysplasia. Journal of the American Society of Nephrology. 17(10). 2864–2870. 226 indexed citations

19.

Weber, Stefanie, et al.. (2004). Degradation of estradiol and ethinyl estradiol by activated sludge and by a defined mixed culture. Applied Microbiology and Biotechnology. 67(1). 106–112. 102 indexed citations

20.

Weber, Stefanie, Karl P. Schlingmann, Melanie Peters, et al.. (2001). Primary Gene Structure and Expression Studies of Rodent Paracellin-1. Journal of the American Society of Nephrology. 12(12). 2664–2672. 41 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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