Jon Jonasson

3.8k total citations
100 papers, 2.6k citations indexed

About

Jon Jonasson is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jon Jonasson has authored 100 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 28 papers in Genetics and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jon Jonasson's work include Prenatal Screening and Diagnostics (14 papers), Genomic variations and chromosomal abnormalities (10 papers) and DNA Repair Mechanisms (9 papers). Jon Jonasson is often cited by papers focused on Prenatal Screening and Diagnostics (14 papers), Genomic variations and chromosomal abnormalities (10 papers) and DNA Repair Mechanisms (9 papers). Jon Jonasson collaborates with scholars based in Sweden, United Kingdom and Denmark. Jon Jonasson's co-authors include H. Harris, Hans‐Jürg Monstein, S. Povey, Alf A. Lindberg, Maj Hultén, Erik Iwarsson, J. Lindsten, J O McGee, Pedro Luís da Costa Aguiar Alves and Ferenc Karpati and has published in prestigious journals such as Nature, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Jon Jonasson

96 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jon Jonasson Sweden 32 1.1k 565 413 309 277 100 2.6k
Nicklas Strömberg Sweden 34 1.8k 1.6× 353 0.6× 448 1.1× 230 0.7× 59 0.2× 71 3.6k
Isabel Bandı́n Spain 29 796 0.7× 385 0.7× 202 0.5× 267 0.9× 281 1.0× 106 3.0k
Robert Daniels United States 27 1.3k 1.2× 379 0.7× 841 2.0× 104 0.3× 102 0.4× 72 3.0k
Takashi Kawana Japan 25 640 0.6× 223 0.4× 1.6k 3.8× 437 1.4× 66 0.2× 135 3.0k
Jean‐Pierre Y. Scheerlinck Australia 33 1.0k 0.9× 191 0.3× 667 1.6× 167 0.5× 248 0.9× 88 3.5k
Thewarach Laha Thailand 35 861 0.8× 101 0.2× 267 0.6× 779 2.5× 420 1.5× 119 4.9k
M. La Plaça Italy 35 831 0.8× 406 0.7× 1.3k 3.2× 155 0.5× 146 0.5× 268 4.4k
Jean‐Pierre Vaerman Belgium 34 1.0k 0.9× 281 0.5× 460 1.1× 386 1.2× 50 0.2× 90 3.4k
Barbara I. Kazmierczak United States 33 2.5k 2.3× 857 1.5× 262 0.6× 175 0.6× 33 0.1× 61 3.6k
Nobuo Okahashi Japan 40 2.2k 2.0× 312 0.6× 686 1.7× 204 0.7× 42 0.2× 106 5.3k

Countries citing papers authored by Jon Jonasson

Since Specialization
Citations

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

Fields of papers citing papers by Jon Jonasson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jon Jonasson

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

All Works

20 of 20 papers shown
1.
Fredriksson, Nils Johan, et al.. (2024). Familial hypercholesterolemia – Targeted whole gene sequencing as a diagnostic approach. SHILAP Revista de lepidopterología. 59. 1–9.
2.
Gréen, Henrik, et al.. (2021). Technical in-depth comparison of two massive parallel DNA-sequencing methods for formalin-fixed paraffin-embedded tissue from victims of sudden cardiac death. Forensic Science International Genetics. 53. 102522–102522. 2 indexed citations
3.
Jonasson, Jon, et al.. (2020). Genome-wide analyses disclose the distinctive HLA architecture and the pharmacogenetic landscape of the Somali population. Scientific Reports. 10(1). 5652–5652. 9 indexed citations
4.
Jonasson, Jon, et al.. (2019). Commentary: "The Etiology of Down Syndrome". 3–5. 1 indexed citations
5.
Sahlin, Ellika, Anna Gréen, Peter Gustavsson, et al.. (2019). Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirth. PLoS ONE. 14(1). e0210017–e0210017. 19 indexed citations
6.
Gréen, Anna, Jon Jonasson, Hartmut Vogt, et al.. (2018). Could Dissimilar Phenotypic Effects of ACTB Missense Mutations Reflect the Actin Conformational Change Two Novel Mutations and Literature Review. Molecular Syndromology. 9(5). 259–265. 11 indexed citations
7.
8.
Samuelsson, Annika, Barbro Isaksson, Jon Jonasson, et al.. (2012). Changes in the aerobic faecal flora of patients treated with antibiotics for acute intra-abdominal infection. Scandinavian Journal of Infectious Diseases. 44(11). 820–827. 8 indexed citations
9.
Caspersson, Torbjörn, et al.. (2009). Translocations causing non-fluorescent Y chromosomes in human XO/XY mosaics. Hereditas. 68(2). 317–324.
10.
Jonasson, Jon, et al.. (2009). Distribution of mitomycin C induced breaks on human chromosomes. Hereditas. 74(2). 273–282. 7 indexed citations
11.
Jonasson, Jon & M. Holmberg. (2009). Evidence for an inverse relationship between X-ray induced chromatid and chromosome breakage in human chromosomes. Hereditas. 75(2). 259–266. 3 indexed citations
12.
Jonasson, Jon, Pedro Luís da Costa Aguiar Alves, & Amy R. Strom. (2009). Polymorphisms in the centromeric region of the chromosomes of the laboratory mouse. Hereditas. 90(1). 111–117.
13.
Holmberg, M. & Jon Jonasson. (2009). Preferential location of X-ray induced chromosome breakage in the R-bands of human chromosomes. Hereditas. 74(1). 57–68. 13 indexed citations
14.
Santesson, Berta, Jon Jonasson, Kenneth Nilsson, & Kerstin Lindahl‐Kiessling. (2008). Modulation of SCE frequencies in cell lines derived from human B and T lymphocytes. Hereditas. 98(2). 175–180.
15.
Hällgren, Anita, et al.. (2004). Genetic Relatedness of Enterococcus Faecalis Isolates with High-level Gentamicin Resistance from Patients with Bacteraemia in the South East of Sweden 1994–2001. Scandinavian Journal of Infectious Diseases. 36(6-7). 405–409. 5 indexed citations
16.
17.
Jonasson, Jon, et al.. (2001). Rapid molecular identification and subtyping of Helicobacter pylori by pyrosequencing of the 16S rDNA variable V1 and V3 regions. FEMS Microbiology Letters. 199(1). 103–107. 62 indexed citations
18.
Karpati, Ferenc & Jon Jonasson. (1996). Polymerase chain reaction for the detection ofPseudomonas aeruginosa,Stenotrophomonas maltophiliaandBurkholderia cepaciain sputum of patients with cystic fibrosis. Molecular and Cellular Probes. 10(6). 397–403. 41 indexed citations
19.
Nicholls, Robert D., Jon Jonasson, J O McGee, et al.. (1987). High resolution gene mapping of the human alpha globin locus.. Journal of Medical Genetics. 24(1). 39–46. 38 indexed citations
20.
Holmberg, M. & Jon Jonasson. (1974). Synergistic effect of X-ray and UV irradation on the frequency of chromosome breakage in human lymphocytes. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 23(2). 213–221. 12 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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