Jón J. Jónsson

3.8k total citations
47 papers, 1.0k citations indexed

About

Jón J. Jónsson is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Jón J. Jónsson has authored 47 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 21 papers in Genetics and 6 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Jón J. Jónsson's work include BRCA gene mutations in cancer (6 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Jón J. Jónsson is often cited by papers focused on BRCA gene mutations in cancer (6 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Jón J. Jónsson collaborates with scholars based in Iceland, United States and United Kingdom. Jón J. Jónsson's co-authors include Ines Thiele, Swagatika Sahoo, Martin I. Sigurðsson, Hans T. Björnsson, Maike K. Aurich, Albert V. Smith, Monica Piccini, Francesca Vitelli, Alessandra Renieri and Barbara R. Pober and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Analytical Biochemistry.

In The Last Decade

Jón J. Jónsson

45 papers receiving 979 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jón J. Jónsson Iceland 18 618 370 121 99 82 47 1.0k
Tatsuo Yamamoto Japan 22 363 0.6× 226 0.6× 90 0.7× 264 2.7× 135 1.6× 80 1.5k
Katrien Van Beneden Belgium 26 513 0.8× 191 0.5× 86 0.7× 49 0.5× 145 1.8× 57 1.8k
Isabelle Pellerin France 21 780 1.3× 246 0.7× 62 0.5× 154 1.6× 37 0.5× 38 1.4k
Pascale Fanen France 26 764 1.2× 218 0.6× 167 1.4× 65 0.7× 101 1.2× 93 2.1k
Nilufar M. Inamdar United States 10 527 0.9× 131 0.4× 78 0.6× 42 0.4× 109 1.3× 11 989
Kelwyn Thomas United States 17 830 1.3× 260 0.7× 77 0.6× 42 0.4× 45 0.5× 28 1.2k
Chung‐Hsing Wang Taiwan 16 341 0.6× 156 0.4× 89 0.7× 98 1.0× 49 0.6× 56 837
Fred Mermelstein United States 18 1.1k 1.7× 190 0.5× 81 0.7× 58 0.6× 50 0.6× 27 1.6k
C.S. Chu United States 12 321 0.5× 184 0.5× 115 1.0× 40 0.4× 104 1.3× 13 1.2k
Nikolaos Tountas Greece 14 414 0.7× 150 0.4× 132 1.1× 58 0.6× 127 1.5× 27 1.2k

Countries citing papers authored by Jón J. Jónsson

Since Specialization
Citations

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

Fields of papers citing papers by Jón J. Jónsson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jón J. Jónsson. 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 Jón J. Jónsson. The network helps show where Jón J. Jónsson may publish in the future.

Co-authorship network of co-authors of Jón J. Jónsson

This figure shows the co-authorship network connecting the top 25 collaborators of Jón J. Jónsson. A scholar is included among the top collaborators of Jón J. Jónsson 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 Jón J. Jónsson. Jón J. Jónsson 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.
Arnadottir, Gudny A., Brynjar Ö. Jensson, Aðalbjörg Jónasdóttir, et al.. (2023). A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome. European Journal of Human Genetics. 32(1). 44–51. 4 indexed citations
2.
Stefánsdóttir, Vigdís, Christine Patch, Carla van El, et al.. (2020). Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland. European Journal of Human Genetics. 28(12). 1656–1661. 14 indexed citations
3.
Stefánsdóttir, Vigdís, Oskar T. Johannsson, Heather Skirton, & Jón J. Jónsson. (2016). Counsellee’s experience of cancer genetic counselling with pedigrees that automatically incorporate genealogical and cancer database information. Journal of Community Genetics. 7(3). 229–235. 1 indexed citations
4.
Bruns, David E., et al.. (2014). Variability of ethics education in laboratory medicine training programs: Results of an international survey. Clinica Chimica Acta. 442. 115–118. 13 indexed citations
5.
Sahoo, Swagatika, Leifur Franzson, Jón J. Jónsson, & Ines Thiele. (2012). A compendium of inborn errors of metabolism mapped onto the human metabolic network. Molecular BioSystems. 8(10). 2545–2558. 49 indexed citations
6.
Stefánsdóttir, Vigdís, Oskar T. Johannsson, Heather Skirton, et al.. (2012). The use of genealogy databases for risk assessment in genetic health service: a systematic review. Journal of Community Genetics. 4(1). 1–7. 13 indexed citations
7.
Sigurðsson, Martin I., Albert V. Smith, Hans T. Björnsson, & Jón J. Jónsson. (2012). The distribution of a germline methylation marker suggests a regional mechanism of LINE-1 silencing by the piRNA-PIWI system. BMC Genetics. 13(1). 31–31. 11 indexed citations
8.
Ásgeirsson, Hilmir, et al.. (2010). Bráðir kviðverkir af völdum slitróttrar bráðaporfýríu - sjúkratilfelli og yfirlit. Læknablaðið. 2010(6). 413–418.
9.
Stefánsdóttir, Vigdís, Heather Skirton, Kristján Jónasson, Hildur Harðardóttir, & Jón J. Jónsson. (2010). Effects of knowledge, education, and experience on acceptance of first trimester screening for chromosomal anomalies. Acta Obstetricia Et Gynecologica Scandinavica. 89(7). 931–938. 20 indexed citations
10.
Sigurðsson, Martin I., Albert V. Smith, Hans T. Björnsson, & Jón J. Jónsson. (2009). HapMap methylation-associated SNPs, markers of germline DNA methylation, positively correlate with regional levels of human meiotic recombination. Genome Research. 19(4). 581–589. 49 indexed citations
11.
Sigurðsson, Martin I., Neema Jamshidi, Jón J. Jónsson, & Bernhard Ø. Palsson. (2009). Genome-scale network analysis of imprinted human metabolic genes. Epigenetics. 4(1). 43–46. 17 indexed citations
12.
Jónsson, Jón J., Laufey Tryggvadóttír, Gudrún V. Skúladóttir, et al.. (2007). Positive Association Between DNA Strand Breaks in Peripheral Blood Mononuclear Cells and Polyunsaturated Fatty Acids in Red Blood Cells From Women. Nutrition and Cancer. 59(1). 21–28. 6 indexed citations
13.
14.
Benedikz, John, et al.. (2005). [Prevalence of myotonic dystrophy in Iceland].. PubMed. 91(11). 829–34. 4 indexed citations
15.
Jónsson, Jón J., et al.. (2003). Quantitative assays for maedi-visna virus genetic sequences and mRNA’s based on RT-PCR with real-time FRET measurements. Virology. 307(1). 135–142. 9 indexed citations
16.
Pan, Dao, Jón J. Jónsson, Stephen E. Braun, R. Scott McIvor, & Chester B. Whitley. (2000). “Supercharged Cells” for Delivery of Recombinant Human Iduronate-2-Sulfatase. Molecular Genetics and Metabolism. 70(3). 170–178. 6 indexed citations
17.
18.
Piccini, Monica, Francesca Vitelli, Mirella Bruttini, et al.. (1998). FACL4, a New Gene Encoding Long-Chain Acyl-CoA Synthetase 4, Is Deleted in a Family with Alport Syndrome, Elliptocytosis, and Mental Retardation. Genomics. 47(3). 350–358. 92 indexed citations
19.
Braun, Stephen E., Dao Pan, Elena L. Aronovich, et al.. (1996). Preclinical Studies of Lymphocyte Gene Therapy for Mild Hunter Syndrome (Mucopolysaccharidosis Type II). Human Gene Therapy. 7(3). 283–290. 35 indexed citations
20.
Jónsson, Jón J., et al.. (1992). Intron requirement for expression of the human purine nucleoside phosphorylase gene. Nucleic Acids Research. 20(12). 3191–3198. 64 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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