Jutta Schönling

867 total citations
12 papers, 722 citations indexed

About

Jutta Schönling is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Jutta Schönling has authored 12 papers receiving a total of 722 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Genetics. Recurrent topics in Jutta Schönling's work include Neurogenetic and Muscular Disorders Research (6 papers), RNA modifications and cancer (4 papers) and RNA Research and Splicing (4 papers). Jutta Schönling is often cited by papers focused on Neurogenetic and Muscular Disorders Research (6 papers), RNA modifications and cancer (4 papers) and RNA Research and Splicing (4 papers). Jutta Schönling collaborates with scholars based in Germany, United States and Poland. Jutta Schönling's co-authors include Brunhilde Wirth, Klaus Zerres, Sabine Rudnik‐Schöneborn, Eric Hahnen, Randolf Forkert, Thorsten Schmidt, Michael Krawczak, Andreas Podbielski, Klaus Warnatz and Gerhard Haase and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Genomics.

In The Last Decade

Jutta Schönling

12 papers receiving 703 citations

Peers

Countries citing papers authored by Jutta Schönling

Since Specialization

Citations

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

Fields of papers citing papers by Jutta Schönling

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jutta Schönling

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

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Effect of autolytic by-products on PCR-detection of beer spoilers in yeast slurry. 2019 ·Jutta Schönling, Edgar Pick, (unknown), (unknown)	1
2	Evaluation of a triplex real-time PCR system to detect the plant-pathogenic molds Alternaria spp., Fusarium spp. and C. purpurea 2015 ·Journal of Microbiological Methods ·(unknown), Jutta Schönling, Alexander Prange	8
3	Comparison of different methods for the recovery of DNA from spores of mycotoxin-producing moulds in spiked food samples 2015 ·Letters in Applied Microbiology ·(unknown), Jutta Schönling, Alexander Prange	5
4	Development of deoxynivalenol contents in relation to the PCR detection of potentially trichothecene producingFusarium spp. during storage of wheat 2000 ·Mycotoxin Research ·Barbara Birzele, Alexander Prange, Jutta Schönling, (unknown)	2
5	Missense Mutations in Exon 6 of the Survival Motor Neuron Gene in Patients with Spinal Muscular Atrophy (SMA) 1997 ·Human Molecular Genetics ·Eric Hahnen, Jutta Schönling, Sabine Rudnik‐Schöneborn, (unknown), Klaus Zerres, Brunhilde Wirth	89
6	De Novo Rearrangements Found in 2% of Index Patients with Spinal Muscular Atrophy: Mutational Mechanisms, Parental Origin, Mutation Rate, and Implications for Genetic Counseling 1997 ·The American Journal of Human Genetics ·Brunhilde Wirth, Thorsten Schmidt, Eric Hahnen, Sabine Rudnik‐Schöneborn, Michael Krawczak, (unknown), Jutta Schönling, Klaus Zerres	136
7	Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: new insights into molecular mechanisms responsible for the disease. 1996 ·PubMed ·Eric Hahnen, Jutta Schönling, Sabine Rudnik‐Schöneborn, Klaus Zerres, Brunhilde Wirth	122
8	Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals 1995 ·Human Molecular Genetics ·Eric Hahnen, Randolf Forkert, (unknown), Sabine Rudnik‐Schöneborn, Jutta Schönling, Klaus Zerres, (unknown), Brunhilde Wirth	237
9	Mapping of the Spinal MuscularAtrophy (SMA) Gene to a 750-kbInterval Flanked by Two NewMicrosatellites 1995 ·European Journal of Human Genetics ·Brunhilde Wirth, (unknown), A. Baasner, Arthur H.M. Burghes, Andreas Koch, (unknown), (unknown), (unknown), Klaus Zerres, Jutta Schönling	20
10	Large Linkage Analysis in 100 Families with Autosomal Recessive Spinal Muscular Atrophy (SMA) and 11 CEPH Families Using 15 Polymorphic Loci in the Region 5q11.2-q13.3 1994 ·Genomics ·Brunhilde Wirth, (unknown), (unknown), (unknown), (unknown), Michael Knapp, (unknown), Sabine Rudnik‐Schöneborn, Jutta Schönling, (unknown), N.K. Spurr, Klaus Zerres	38
11	Different promoters of SHV-2 and SHV-2a -lactamase lead to diverse levels of cefotaxime resistance in their bacterial producers 1991 ·Journal of General Microbiology ·Andreas Podbielski, Jutta Schönling, (unknown), Gerhard Haase	22
12	Molecular characterization of a new plasmid-encoded SHV-type -lactamase (SHV-2 variant) conferring high-level cefotaxime resistance upon Klebsiella pneumoniae 1991 ·Journal of General Microbiology ·Andreas Podbielski, Jutta Schönling, (unknown), Klaus Warnatz, (unknown)	42

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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