Jutta Becker

3.2k citations
35 papers · 1.5k · h-index 16

Impact in

  • Genetics top 2%
    • Connective tissue disorders research
    • Genetic and Kidney Cyst Diseases
    • Genetic Syndromes and Imprinting
  • Rheumatology top 5%
    • Bone and Dental Protein Studies

Papers in

  • Molecular Biology 16
    • Renal and related cancers 9
    • RNA modifications and cancer 3
  • Genetics 16
    • Genetic and Kidney Cyst Diseases 11
    • Connective tissue disorders research 4
    • Neurogenetic and Muscular Disorders Research 4
    • Genetic Syndromes and Imprinting 4
Co-authors
Klaus Zerres (11 shared papers)Eckhard Schöenau (4 shared papers)Oliver Semler (4 shared papers)Gabi Mücher (7 shared papers)Christian Netzer (4 shared papers)Lisa M. Guay‐Woodford (9 shared papers)Bernd Wollnik (4 shared papers)C. Steinkamm (5 shared papers)
Journals
The American Journal of Human Genetics (3 papers)Human Molecular Genetics (2 papers)Frontiers in Aging Neuroscience (2 papers)The Journal of Urology (2 papers)Genomics (2 papers)
Partner nations
GermanyUnited StatesAustria

In The Last Decade

Jutta Becker

30 papers receiving 1.5k citations

Peers

Jutta Becker
Comparison fields: 5 of 108
  • Genetics 873
  • Rheumatology 228
  • Genetics 93
  • Molecular Biology 593
  • Cancer Research 91
Replace Małgorzata Wiench with:
Małgorzata Wiench Poland
Akitaka Tsujikawa Japan
Anne E. Eyler United States
Claus‐Eric Ott Germany
Rajeev Gupta United Kingdom
Maurízio Battaglia Parodi Italy
Cynthia Sandor United Kingdom
Catherine S. Lee United States
Ludovic Martin France
G. Coscas France
Jutta Becker relative to Małgorzata Wiench Poland Małgorzata Wiench's profile →
Citations per field
00.5×2×3×4×
Małgorzata Wiench · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Jutta Becker, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jutta Becker Line = papers co-authored together Jutta Becker links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 35 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta
The American Journal of Human Genetics ·Jutta Becker, Oliver Semler, Christian Gilissen, Yun Li, Hanno J. Bolz, Cecilia Giunta, Carsten Bergmann, Marianne Rohrbach, Friederike Koerber, Katharina Zimmermann, Petra de Vries, (unknown), Eckhard Schöenau, Bernd Wollnik, Joris A. Veltman, Alexander Hoischen, Christian Netzer
2011252
2
Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2β
Genes & Development ·Markus Moser, Armin Pscherer, Christina Roth, Jutta Becker, Gabi Mücher, Klaus Zerres, Christa Dixkens, Joachim Weis, Lisa M. Guay‐Woodford, Reinhard Buettner, Reinhard Fässler
1997226
3
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 ·Oliver Semler, Lutz Garbes, Katharina Keupp, Daniel Swan, Katharina Zimmermann, Jutta Becker, Sandra Iden, Brunhilde Wirth, Peer Eysel, Friederike Koerber, Eckhard Schöenau, Stefan K. Bohlander, Bernd Wollnik, Christian Netzer
2012187
4
Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology
American Journal of Medical Genetics ·Klaus Zerres, Gabi M�cher, Jutta Becker, C. Steinkamm, Sabine Rudnik-Sch�neborn, P�ivi Heikkil�, Juhani Rapola, Riitta Salonen, Gregory G. Germino, Luiz F. Onuchic, Stefan Somlo, Ellis D. Avner, L. Harman, John M. Stockwin, Lisa M. Guay‐Woodford
1998166
5
Autosomal recessive polycystic kidney disease
Journal of Molecular Medicine ·Klaus Zerres, Sabine Rudnik‐Schöneborn, C. Steinkamm, Jutta Becker, Gabi Mücher
1998103
6
First use of the RANKL antibody denosumab in osteogenesis imperfecta type VI.
PubMed ·Oliver Semler, Christian Netzer, Heike Hoyer‐Kuhn, Jutta Becker, Peer Eysel, Eckhard Schöenau
201290
7
The InfoSky visual explorer: Exploiting Hierarchical Structure and Document Similarities
Information Visualization ·Keith Andrews, Wolfgang Kienreich, Vedran Sabol, Jutta Becker, Georg Droschl, Frank Kappe, Michael Granitzer, Peter Auer, Klaus Tochtermann
200278
8
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 ·Julia Rahe, Jutta Becker, Gereon R. Fink, Josef Kessler, Juraj Kukolja, Andreas Rahn, Jan Rosén, Florian Szabados, Brunhilde Wirth, Elke Kalbe
201570
9
CHARGE and Kabuki syndromes: a phenotypic and molecular link
Human Molecular Genetics ·Yvonne Schulz, Luisa Freese, Johanna Mänz, Barbara Zoll, Christiane Völter, Knut Brockmann, Nina Bögershausen, Jutta Becker, Bernd Wollnik, Silke Pauli
201450
10
Discrepancy in redetermination of SMN2 copy numbers in children with SMA
Neurology ·David Schorling, Jutta Becker, Astrid Pechmann, Thorsten Langer, Brunhilde Wirth, Janbernd Kirschner
201936
11
Fine Mapping of the Autosomal Recessive Polycystic Kidney Disease Locus (PKHD1) and the Genes MUT, RDS, CSNK2β, and GSTA1 at 6p21.1–p12
Genomics ·Gabi Mücher, Jutta Becker, Michael Knapp, Reinhard Büttner, Markus Moser, Sabine Rudnik‐Schöneborn, Stefan Somlo, Gregory G. Germino, Luiz F. Onuchic, Ellis D. Avner, Lisa M. Guay‐Woodford, Klaus Zerres
199834
12
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 ·Elke Kalbe, Mandy Roheger, Kay Paluszak, Julia Meyer, Jutta Becker, Gereon R. Fink, Juraj Kukolja, Andreas Rahn, Florian Szabados, Brunhilde Wirth, Josef Kessler
201830
13
A Nonclassical IFITM5 Mutation Located in the Coding Region Causes Severe Osteogenesis Imperfecta With Prenatal Onset
Journal of Bone and Mineral Research ·Heike Hoyer‐Kuhn, Oliver Semler, Lutz Garbes, Katharina Zimmermann, Jutta Becker, Bernd Wollnik, Eckhard Schöenau, Christian Netzer
201328
14
Systematic assessment of urinary hydroxy-oxo-glutarate for diagnosis and follow-up of primary hyperoxaluria type III
Pediatric Nephrology ·Ada Ventzke, Markus Feldkötter, Andrew Zu-Sern Wei, Jutta Becker, Bodo B. Beck, Bernd Höppe
201722
15
An Integrated Genetic and Physical Map of the Autosomal Recessive Polycystic Kidney Disease Region
Genomics ·Xosé M. Lens, Luiz F. Onuchic, Guanqing Wu, Tomohito Hayashi, Martin Daoust, Toshio Mochizuki, Lorenzo B. Santarina, John M. Stockwin, Gabi Mücher, Jutta Becker, William E. Sweeny, Ellis D. Avner, Lisa M. Guay‐Woodford, Klaus Zerres, Stefan Somlo, Gregory G. Germino
199721
16
A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction
Human Molecular Genetics ·Walid Fazeli, Peter Herkenrath, Barbara Stiller, Antje Neugebauer, Julia Fricke, Ruth Lang‐Roth, Gudrun Nürnberg, Michaela Thoenes, Jutta Becker, Janine Altmüller, Alexander E. Volk, Christian Kubisch, Raoul Heller
201715
17
Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology
American Journal of Medical Genetics ·Klaus Zerres, Gabi Mücher, Jutta Becker, C. Steinkamm, Sabine Rudnik‐Schöneborn, Päivi Heikkilä, Juhani Rapola, Riitta Salonen, Gregory G. Germino, Luiz F. Onuchic, Stefan Somlo, Ellis D. Avner, L. Harman, John M. Stockwin, Lisa M. Guay‐Woodford
199815
18
Isogenic patient-derived organoids reveal early neurodevelopmental defects in spinal muscular atrophy initiation
Cell Reports Medicine ·Tobias Graß, Zeynep Dokuzluoglu, Felix Buchner, Ines Rosignol, J Thomas, Antonio Caldarelli, Anna Dalinskaya, Jutta Becker, Fabian Rost, Michele Marass, (unknown), Marc Beyer, Lorenzo Bonaguro, Natalia Rodríguez‐Muela
202410
19
Prenatal Diagnosis of Autosomal Recessive Polycystic Kidney Disease (ARPKD): Molecular Genetics, Clinical Experience, and Fetal Morphology
The Journal of Urology ·Klaus Zerres, Gabi Mücher, Jutta Becker, C. Steinkamm, S. Rudnik-Schnewborn, P. Heikkil, Juhani Rapola, Riitta Salonen, Gregory G. Germino, Luiz F. Onuchic, Stefan Somlo, Ellis D. Avner, L. Harman, John M. Stockwin, Lisa M. Guay‐Woodford
199910
20
Semantic Annotation and Retrieval of Digital Photos
Mathias Lux, Jutta Becker, Harald Krottmaier
20038

About Jutta Becker

Jutta Becker is a scholar working on Molecular Biology, Genetics, Genetics, Surgery and Pediatrics, Perinatology and Child Health, having authored 35 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (11 papers), Renal and related cancers (9 papers), Connective tissue disorders research (4 papers), Neurogenetic and Muscular Disorders Research (4 papers), Genetic Syndromes and Imprinting (4 papers), Pediatric Urology and Nephrology Studies (3 papers), RNA modifications and cancer (3 papers) and Bone and Dental Protein Studies (2 papers). The work is most often cited by research in Genetics (873 citations), Rheumatology (228 citations), Genetics (93 citations), Molecular Biology (593 citations) and Cancer Research (91 citations). Jutta Becker has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include Klaus Zerres, Eckhard Schöenau, Oliver Semler, Gabi Mücher, Christian Netzer, Lisa M. Guay‐Woodford, Bernd Wollnik, C. Steinkamm, Katharina Zimmermann and Brunhilde Wirth. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics, Frontiers in Aging Neuroscience, The Journal of Urology and Genomics.

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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