Jutta Becker

3.0k citations

27 papers · 1.4k indexed · h-index 16

Genetics top 2%
- Genetic and Kidney Cyst Diseases 11
- Genetic Syndromes and Imprinting 4
- Connective tissue disorders research 4
- Neurogenetic and Muscular Disorders Research 3
Rheumatology top 5%
Molecular Biology top 10%
- Renal and related cancers 9
- RNA modifications and cancer 3
Genetics top 10%
- Genetic and Kidney Cyst Diseases 11
- Genetic Syndromes and Imprinting 4
- Connective tissue disorders research 4
- Neurogenetic and Muscular Disorders Research 3
Cancer Research
Pediatrics, Perinatology and Child Health
- Pediatric Urology and Nephrology Studies 3
Oncology
- Bone health and treatments 2

Co-authors: Klaus Zerres Gabi Mücher Eckhard Schöenau Christian Netzer Oliver Semler Brunhilde Wirth Lisa M. Guay‐Woodford Bernd Wollnik
Cited by: Genetics Rheumatology Molecular Biology
Journals: Frontiers in Aging Neuroscience (2 papers)Human Molecular Genetics (2 papers)The American Journal of Human Genetics (2 papers)
Partner nations: Germany United States Switzerland

In The Last Decade

Jutta Becker

24 papers receiving 1.4k citations

Peers

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

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

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20 of 20 papers shown

#	Work
1	Isogenic patient-derived organoids reveal early neurodevelopmental defects in spinal muscular atrophy initiation Cell Reports Medicine ·光司武市,Ivan Comings Weld,Leon Li,Sneha Kumari,B. Da S. Hanny,Antonio Caldarelli,杨熠岑,Jutta Becker,Fabian Rost,Michele Marass,Brunhilde Wirth,Marc Beyer,Lorenzo Bonaguro,Natalia Rodríguez‐Muela	2024	9
2	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,Gary A. Ethridge,Julia Meyer,Jutta Becker,Gereon R. Fink,Juraj Kukolja,Р. А. Зайнуллин,Florian Szabados,Brunhilde Wirth,Josef Kessler	2018	30
3	Systematic assessment of urinary hydroxy-oxo-glutarate for diagnosis and follow-up of primary hyperoxaluria type III Pediatric Nephrology ·Dominik Hammer,Markus Feldkötter,Shiang-Wei Li,Jutta Becker,Bodo B. Beck,Bernd Höppe	2017	22
4	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	2017	15
5	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 ·A Gajewska,Jutta Becker,Gereon R. Fink,Josef Kessler,Juraj Kukolja,Р. А. Зайнуллин,準也林,Florian Szabados,Brunhilde Wirth,Elke Kalbe	2015	70
6	CHARGE and Kabuki syndromes: a phenotypic and molecular link Human Molecular Genetics ·チコ,Nathaniel Rutman,Christos Zacheilas,Barbara Zoll,Christiane Völter,Knut Brockmann,Nina Bögershausen,Jutta Becker,Bernd Wollnik,Silke Pauli	2014	50
7	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	2013	27
8	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	2012	184
9	7 Mb de novo deletion within 8q21 in a patient with distal arthrogryposis type 2B (DA2B) European Journal of Medical Genetics ·Timothy Rugh,Jutta Becker,Raoul Heller,Odile Boute,Joris Andrieux,Juliane Hoyer,Arif B. Ekici,André Reis,Anita Rauch	2011	7
10	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,Brunhilde Wirth,Eckhard Schöenau,Bernd Wollnik,Joris A. Veltman,Alexander Hoischen,Christian Netzer	2011	250
11	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 ·Yvonne Hofmann,Jutta Becker,A Debreczeni,Ellis D. Avner,Michal Mrug,Lisa M. Guay‐Woodford,Stefan Somlo,Klaus Zerres,Gregory G. Germino,Luiz F. Onuchic	2000	6
12	Digitale Unterschrift - Sichere Rechtsgeschäfte im Internet (Teil 1). Jutta Becker,John Lamberty	1999	0
13	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 ·Luiz F. Onuchic,Michal Mrug,謙二小林,Hande Zapsu,Jutta Becker,Klaus Zerres,Ellis D. Avner,Mehul Dixit,Stefan Somlo,Gregory G. Germino,Lisa M. Guay‐Woodford	1999	6
14	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,В. В. Легкий,A. Subaric-Leitis,Juhani Rapola,Riitta Salonen,Gregory G. Germino,Luiz F. Onuchic,Stefan Somlo,Ellis D. Avner,L. Harman,Deng Hong-chao,Lisa M. Guay‐Woodford	1999	11
15	Autosomal recessive polycystic kidney disease Journal of Molecular Medicine ·Klaus Zerres,Sabine Rudnik‐Schöneborn,C. Steinkamm,Jutta Becker,Gabi Mücher	1998	103
16	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	1998	34
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,Deng Hong-chao,Lisa M. Guay‐Woodford	1998	16
18	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	1997	226
19	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,W. Hirte,Toshio Mochizuki,Brian T. Beeson,Deng Hong-chao,Gabi Mücher,Jutta Becker,M J Christie,Ellis D. Avner,Lisa M. Guay‐Woodford,Klaus Zerres,Stefan Somlo,Gregory G. Germino	1997	21
20	Autosomal Recessive Polycystic Kidney Disease Contributions to nephrology ·Klaus Zerres,Jutta Becker,Fernando Torres-Vega,Sabine Rudnik-Sch�neborn	1997	2

About Jutta Becker

Jutta Becker is a scholar working on Genetics, Genetics and Molecular Biology, having authored 27 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (11 papers), Renal and related cancers (9 papers), Genetic Syndromes and Imprinting (4 papers), Connective tissue disorders research (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), Pediatric Urology and Nephrology Studies (3 papers), RNA modifications and cancer (3 papers) and Bone health and treatments (2 papers). The work is most often cited by research in Genetics (895 citations), Rheumatology (281 citations) and Molecular Biology (699 citations). Jutta Becker has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Klaus Zerres, Gabi Mücher, Eckhard Schöenau, Christian Netzer, Oliver Semler, Brunhilde Wirth, Lisa M. Guay‐Woodford, Bernd Wollnik, C. Steinkamm and Katharina Zimmermann. Their work appears in journals such as Frontiers in Aging Neuroscience, Human Molecular Genetics, The American Journal of Human Genetics, 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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