Jutta Becker

3.0k total citations
27 papers, 1.4k citations indexed

About

Jutta Becker is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Jutta Becker has authored 27 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 16 papers in Genetics and 4 papers in Genetics. Recurrent topics in Jutta Becker's work include Genetic and Kidney Cyst Diseases (11 papers), Renal and related cancers (9 papers) and Genetic Syndromes and Imprinting (4 papers). Jutta Becker is often cited by papers focused on Genetic and Kidney Cyst Diseases (11 papers), Renal and related cancers (9 papers) and Genetic Syndromes and Imprinting (4 papers). Jutta Becker collaborates with scholars based in Germany, United States and Switzerland. Jutta Becker's co-authors include Klaus Zerres, Gabi Mücher, Christian Netzer, Oliver Semler, Eckhard Schöenau, Brunhilde Wirth, Lisa M. Guay‐Woodford, Bernd Wollnik, C. Steinkamm and Katharina Zimmermann and has published in prestigious journals such as Genes & Development, Neurology and The American Journal of Human Genetics.

In The Last Decade

Jutta Becker

24 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jutta Becker Germany 16 895 699 281 134 123 27 1.4k
Zvi Borochowitz Israel 24 875 1.0× 1.0k 1.5× 224 0.8× 125 0.9× 68 0.6× 67 2.2k
Sheela Nampoothiri India 21 763 0.9× 917 1.3× 172 0.6× 94 0.7× 99 0.8× 125 1.7k
Yoshio Makita Japan 24 797 0.9× 916 1.3× 139 0.5× 181 1.4× 100 0.8× 77 1.8k
Nadia Sakati Saudi Arabia 22 546 0.6× 819 1.2× 123 0.4× 111 0.8× 123 1.0× 78 1.7k
Michael B. Bober United States 27 834 0.9× 761 1.1× 455 1.6× 128 1.0× 241 2.0× 99 2.0k
Mirja Somer Finland 25 816 0.9× 1.5k 2.1× 106 0.4× 128 1.0× 56 0.5× 49 2.4k
Christian Netzer Germany 19 804 0.9× 460 0.7× 401 1.4× 224 1.7× 180 1.5× 36 1.4k
Dieter Kotzot Austria 29 1.9k 2.1× 1.3k 1.9× 167 0.6× 123 0.9× 49 0.4× 100 2.9k
Maria Hoeltzenbein Germany 23 794 0.9× 899 1.3× 420 1.5× 51 0.4× 111 0.9× 54 2.8k
Gary A. Bellus United States 19 1.3k 1.5× 1.3k 1.9× 147 0.5× 148 1.1× 58 0.5× 30 2.0k

Countries citing papers authored by Jutta Becker

Since Specialization
Citations

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

Fields of papers citing papers by Jutta Becker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jutta Becker

This figure shows the co-authorship network connecting the top 25 collaborators of Jutta Becker. A scholar is included among the top collaborators of Jutta Becker 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 Jutta Becker. Jutta Becker 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.
Caldarelli, Antonio, Jutta Becker, Fabian Rost, et al.. (2024). Isogenic patient-derived organoids reveal early neurodevelopmental defects in spinal muscular atrophy initiation. Cell Reports Medicine. 5(8). 101659–101659. 9 indexed citations
2.
Kalbe, Elke, Mandy Roheger, Julia Meyer, et al.. (2018). Effects of a Cognitive Training With and Without Additional Physical Activity in Healthy Older Adults: A Follow-Up 1 Year After a Randomized Controlled Trial. Frontiers in Aging Neuroscience. 10. 407–407. 30 indexed citations
3.
Feldkötter, Markus, et al.. (2017). Systematic assessment of urinary hydroxy-oxo-glutarate for diagnosis and follow-up of primary hyperoxaluria type III. Pediatric Nephrology. 32(12). 2263–2271. 22 indexed citations
4.
Fazeli, Walid, Peter Herkenrath, Barbara Stiller, et al.. (2017). A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction. Human Molecular Genetics. 26(20). 4055–4066. 15 indexed citations
5.
Becker, Jutta, Gereon R. Fink, Josef Kessler, et al.. (2015). Cognitive training with and without additional physical activity in healthy older adults: cognitive effects, neurobiological mechanisms, and prediction of training success. Frontiers in Aging Neuroscience. 7. 187–187. 70 indexed citations
6.
Zoll, Barbara, Christiane Völter, Knut Brockmann, et al.. (2014). CHARGE and Kabuki syndromes: a phenotypic and molecular link. Human Molecular Genetics. 23(16). 4396–4405. 50 indexed citations
7.
Hoyer‐Kuhn, Heike, Oliver Semler, Lutz Garbes, et al.. (2013). A Nonclassical IFITM5 Mutation Located in the Coding Region Causes Severe Osteogenesis Imperfecta With Prenatal Onset. Journal of Bone and Mineral Research. 29(6). 1387–1391. 27 indexed citations
8.
Semler, Oliver, Lutz Garbes, Katharina Keupp, et al.. (2012). A Mutation in the 5′-UTR of IFITM5 Creates an In-Frame Start Codon and Causes Autosomal-Dominant Osteogenesis Imperfecta Type V with Hyperplastic Callus. The American Journal of Human Genetics. 91(2). 349–357. 184 indexed citations
9.
Becker, Jutta, Raoul Heller, Odile Boute, et al.. (2011). 7 Mb de novo deletion within 8q21 in a patient with distal arthrogryposis type 2B (DA2B). European Journal of Medical Genetics. 54(5). e495–e500. 7 indexed citations
10.
Becker, Jutta, Oliver Semler, Christian Gilissen, et al.. (2011). Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta. The American Journal of Human Genetics. 88(3). 362–371. 250 indexed citations
11.
Hofmann, Yvonne, Jutta Becker, Ellis D. Avner, et al.. (2000). Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for autosomal recessive polycystic kidney disease. European Journal of Human Genetics. 8(3). 163–166. 6 indexed citations
12.
Becker, Jutta, et al.. (1999). Digitale Unterschrift - Sichere Rechtsgeschäfte im Internet (Teil 1).. 19. 46.
13.
Onuchic, Luiz F., Michal Mrug, Jutta Becker, et al.. (1999). Genomic organization of the KIAA0057 gene that encodes a TRAM-like protein and its exclusion as a polycystic kidney and hepatic disease 1 (PKHD1) candidate gene. Mammalian Genome. 10(12). 1175–1178. 6 indexed citations
14.
Zerres, Klaus, Gabi Mücher, Jutta Becker, et al.. (1999). Prenatal Diagnosis of Autosomal Recessive Polycystic Kidney Disease (ARPKD): Molecular Genetics, Clinical Experience, and Fetal Morphology. The Journal of Urology. 161(1). 368–369. 11 indexed citations
15.
Zerres, Klaus, Sabine Rudnik‐Schöneborn, C. Steinkamm, Jutta Becker, & Gabi Mücher. (1998). Autosomal recessive polycystic kidney disease. Journal of Molecular Medicine. 76(5). 303–309. 103 indexed citations
16.
Mücher, Gabi, Jutta Becker, Michael Knapp, et al.. (1998). Fine Mapping of the Autosomal Recessive Polycystic Kidney Disease Locus (PKHD1) and the Genes MUT, RDS, CSNK2β, and GSTA1 at 6p21.1–p12. Genomics. 48(1). 40–45. 34 indexed citations
17.
Zerres, Klaus, Gabi Mücher, Jutta Becker, et al.. (1998). Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology. American Journal of Medical Genetics. 76(2). 137–144. 16 indexed citations
18.
Moser, Markus, Armin Pscherer, Christina Roth, et al.. (1997). Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2β. Genes & Development. 11(15). 1938–1948. 226 indexed citations
19.
Lens, Xosé M., Luiz F. Onuchic, Guanqing Wu, et al.. (1997). An Integrated Genetic and Physical Map of the Autosomal Recessive Polycystic Kidney Disease Region. Genomics. 41(3). 463–466. 21 indexed citations
20.
Zerres, Klaus, et al.. (1997). Autosomal Recessive Polycystic Kidney Disease. Contributions to nephrology. 122. 10–16. 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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