Katja Grohmann

969 total citations
8 papers, 530 citations indexed

About

Katja Grohmann is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Katja Grohmann has authored 8 papers receiving a total of 530 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Katja Grohmann's work include Neurogenetic and Muscular Disorders Research (8 papers), RNA modifications and cancer (6 papers) and RNA Research and Splicing (2 papers). Katja Grohmann is often cited by papers focused on Neurogenetic and Muscular Disorders Research (8 papers), RNA modifications and cancer (6 papers) and RNA Research and Splicing (2 papers). Katja Grohmann collaborates with scholars based in Germany, Poland and United Kingdom. Katja Grohmann's co-authors include Christoph Hübner, Klaus Zerres, Michael Sendtner, Alexander Diers, Sabine Rudnik‐Schöneborn, Markus Schuelke, Enrico Bertini, Francesco Muntoni, Rainer Rossi and Lionel Van Maldergem and has published in prestigious journals such as Nature Genetics, Journal of Neuroscience and Human Molecular Genetics.

In The Last Decade

Katja Grohmann

8 papers receiving 518 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Katja Grohmann Germany	8	388	349	134	132	88	8	530
Laura Torres‐Benito Germany	14	507 1.3×	578 1.7×	73 0.5×	151 1.1×	59 0.7×	15	679
Eric Villalón United States	12	243 0.6×	274 0.8×	72 0.5×	58 0.4×	69 0.8×	24	380
Marcos Valadares Brazil	11	161 0.4×	215 0.6×	46 0.3×	132 1.0×	27 0.3×	14	354
Antonio Vallarola Italy	10	197 0.5×	136 0.4×	62 0.5×	57 0.4×	152 1.7×	11	387
Paola Rinchetti Italy	11	167 0.4×	234 0.7×	68 0.5×	47 0.4×	77 0.9×	16	339
Hannah K. Shorrock United Kingdom	13	353 0.9×	416 1.2×	99 0.7×	111 0.8×	71 0.8×	22	543
Mou-xuan Du China	11	153 0.4×	136 0.4×	54 0.4×	58 0.4×	96 1.1×	18	398
Fernanda Gubert Brazil	13	136 0.4×	235 0.7×	153 1.1×	52 0.4×	64 0.7×	28	493
Lindsay M. Wallace United States	12	147 0.4×	573 1.6×	100 0.7×	34 0.3×	24 0.3×	21	665
Xavier Gaeta United States	7	187 0.5×	393 1.1×	85 0.6×	64 0.5×	26 0.3×	9	646

Countries citing papers authored by Katja Grohmann

Since Specialization

Citations

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

Fields of papers citing papers by Katja Grohmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katja Grohmann

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

All Works

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8 of 8 papers shown

Holtmann, Bettina, Stefan Wiese, Mohtashem Samsam, et al.. (2005). Triple Knock-Out ofCNTF,LIF, andCT-1Defines Cooperative and Distinct Roles of these Neurotrophic Factors for Motoneuron Maintenance and Function. Journal of Neuroscience. 25(7). 1778–1787. 57 indexed citations

Diers, Alexander, et al.. (2005). The ultrastructure of peripheral nerve, motor end-plate and skeletal muscle in patients suffering from spinal muscular atrophy with respiratory distress type 1 (SMARD1). Acta Neuropathologica. 110(3). 289–297. 27 indexed citations

Guenther, Ulf P., Markus Schuelke, Enrico Bertini, et al.. (2004). Genomic rearrangements at the IGHMBP2 gene locus in two patients with SMARD1. Human Genetics. 115(4). 319–326. 33 indexed citations

Rudnik‐Schöneborn, Sabine, Raymonda Varon, Katja Grohmann, et al.. (2004). Long-Term Observations of Patients with Infantile Spinal Muscular Atrophy with Respiratory Distress Type 1 (SMARD1). Neuropediatrics. 35(3). 174–182. 50 indexed citations

Grohmann, Katja. (2004). Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1). Human Molecular Genetics. 13(18). 2031–2042. 75 indexed citations

Appleton, Richard, Christoph Hübner, Katja Grohmann, & Raymonda Varon. (2004). ‘Congenital peripheral neuropathy presenting as apnoea and respiratory insufficiency: spinal muscular atrophy with respiratory distress type 1 (SMARD1)’. Developmental Medicine & Child Neurology. 46(8). 576–576. 11 indexed citations

Felderhoff‐Mueser, Ursula, Katja Grohmann, Anja Harder, et al.. (2002). Severe Spinal Muscular Atrophy Variant Associated With Congenital Bone Fractures. Journal of Child Neurology. 17(9). 718–721. 33 indexed citations

Grohmann, Katja, Markus Schuelke, Alexander Diers, et al.. (2001). Mutations in the gene encoding immunoglobulin μ-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1. Nature Genetics. 29(1). 75–77. 244 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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