Jessica Becker

3.8k total citations
24 papers, 729 citations indexed

About

Jessica Becker is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Jessica Becker has authored 24 papers receiving a total of 729 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Surgery and 6 papers in Molecular Biology. Recurrent topics in Jessica Becker's work include Reading and Literacy Development (4 papers), Gastroesophageal reflux and treatments (3 papers) and Cognitive and developmental aspects of mathematical skills (3 papers). Jessica Becker is often cited by papers focused on Reading and Literacy Development (4 papers), Gastroesophageal reflux and treatments (3 papers) and Cognitive and developmental aspects of mathematical skills (3 papers). Jessica Becker collaborates with scholars based in Germany, United Kingdom and United States. Jessica Becker's co-authors include Petra Knaus, Markus M. Nöthen, Bertram Müller‐Myhsok, Johannes Grünhagen, Claus‐Eric Ott, Peter N. Robinson, Raghu Bhushan, Kerstin U. Ludwig, Per Hoffmann and Gerd Schulte‐Körne and has published in prestigious journals such as Nature Communications, PLoS ONE and Scientific Reports.

In The Last Decade

Jessica Becker

23 papers receiving 719 citations

Peers

Jessica Becker

GENET

DEP

RHEUM

Iben Bache Denmark

Martha Hughes Canada

Veronica J. Peschansky United States

Katariina Hannula‐Jouppi Finland

Allison Adams United States

Miroslav Dumić Croatia

J.J.M. Engelen Netherlands

Lynn Ploughman United States

L. Leigh Field Canada

Keith L. Sternes United States

Iben Bache Denmark

Jessica Becker

254 ×0.8

341 ×1.4

GENET

40 ×0.4

47 ×0.4

DEP

24 ×0.3

RHEUM

Citations per year, relative to Jessica Becker Jessica Becker (= 1×) peers Iben Bache

Countries citing papers authored by Jessica Becker

Since Specialization

Citations

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

Fields of papers citing papers by Jessica Becker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jessica Becker

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

All Works

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20 of 20 papers shown

Trautmann, Marcel, Heidrun Gevensleben, Jessica Becker, et al.. (2020). Novel pathogenic alterations in pediatric and adult desmoid-type fibromatosis – A systematic analysis of 204 cases. Scientific Reports. 10(1). 3368–3368. 28 indexed citations

Trautmann, Marcel, Arne Krüger, Inga Grünewald, et al.. (2019). Phosphatidylinositol-3-kinase (PI3K)/Akt Signaling is Functionally Essential in Myxoid Liposarcoma. Molecular Cancer Therapeutics. 18(4). 834–844. 28 indexed citations

Haase, Tobias, Benjamin Kohl, Carola Meier, et al.. (2019). Discerning the spatio-temporal disease patterns of surgically induced OA mouse models. PLoS ONE. 14(4). e0213734–e0213734. 13 indexed citations

Vacková, Zuzana, Stefan Niebisch, Tania Triantafyllou, et al.. (2018). First genotype‐phenotype study reveals HLA‐DQβ1 insertion heterogeneity in high‐resolution manometry achalasia subtypes. United European Gastroenterology Journal. 7(1). 45–51. 9 indexed citations

Döhla, Manuel, Ines Gockel, Stefan Niebisch, et al.. (2018). Characterization of esophageal inflammation in patients with achalasia. A retrospective immunohistochemical study. Human Pathology. 85. 228–234. 8 indexed citations

Kuechler, Alma, Mona Grimmel, Jessica Becker, et al.. (2018). De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies. Human Genetics. 137(5). 401–411. 16 indexed citations

Forstner, Andreas J., Kerstin U. Ludwig, Anne C. Böhmer, et al.. (2017). Further evidence for genetic variation at the serotonin transporter gene SLC6A4 contributing toward anxiety. Psychiatric Genetics. 27(3). 96–102. 24 indexed citations

Kim-Hellmuth, Sarah, Benno Pütz, Pejman Mohammadi, et al.. (2017). Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations. Nature Communications. 8(1). 266–266. 106 indexed citations

Gockel, Ines, Stefan Niebisch, Jessica Becker, Johannes Schumacher, & Michaela Müller. (2016). So erkennen Sie die Achalasie. MMW - Fortschritte der Medizin. 158(21-22). 80–83.

10.

Engels, Hartmut, Kirsten Cremer, Jessica Becker, et al.. (2016). De novo microdeletions and point mutations affecting SOX2 in three individuals with intellectual disability but without major eye malformations. American Journal of Medical Genetics Part A. 173(2). 435–443. 13 indexed citations

11.

Cremer, Kirsten, Jessica Becker, Thomas Wieland, et al.. (2016). De novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth. European Journal of Human Genetics. 24(12). 1739–1745. 23 indexed citations

12.

Ludwig, Kerstin U., Philipp G. Sämann, Michael P. Alexander, et al.. (2013). A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults. Translational Psychiatry. 3(2). e229–e229. 24 indexed citations

13.

Becker, Jessica, Darina Czamara, Per Hoffmann, et al.. (2012). Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling. Translational Psychiatry. 2(7). e136–e136. 17 indexed citations

14.

Bhushan, Raghu, Johannes Grünhagen, Jessica Becker, et al.. (2012). miR-181a promotes osteoblastic differentiation through repression of TGF-β signaling molecules. The International Journal of Biochemistry & Cell Biology. 45(3). 696–705. 118 indexed citations

15.

Ruschke, Karen, Christian Hiepen, Jessica Becker, & Petra Knaus. (2012). BMPs are mediators in tissue crosstalk of the regenerating musculoskeletal system. Cell and Tissue Research. 347(3). 521–544. 48 indexed citations

16.

Becker, Jessica, Jens R. Wendland, Britta Haenisch, Markus M. Nöthen, & Johannes Schumacher. (2011). A systematic eQTL study of cis–trans epistasis in 210 HapMap individuals. European Journal of Human Genetics. 20(1). 97–101. 22 indexed citations

17.

Czamara, Darina, Jennifer Bruder, Jessica Becker, et al.. (2010). Association of a Rare Variant with Mismatch Negativity in a Region Between KIAA0319 and DCDC2 in Dyslexia. Behavior Genetics. 41(1). 110–119. 44 indexed citations

18.

Rojas-Martı́nez, Augusto, Heiko Reutter, Oscar F. Chacón‐Camacho, et al.. (2010). Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25. Birth Defects Research Part A Clinical and Molecular Teratology. 88(7). 535–537. 43 indexed citations

19.

Roeske, Darina, Kerstin U. Ludwig, Nina Neuhoff, et al.. (2009). First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. Molecular Psychiatry. 16(1). 97–107. 77 indexed citations

20.

Becker, Jessica, et al.. (1997). Personality and depression: a validation study of the depressive experiences questionnaire.. PubMed. 68(1). 197–210. 8 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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