Jan Pedersen

862 total citations
26 papers, 605 citations indexed

About

Jan Pedersen is a scholar working on Genetics, Epidemiology and Infectious Diseases. According to data from OpenAlex, Jan Pedersen has authored 26 papers receiving a total of 605 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 5 papers in Epidemiology and 4 papers in Infectious Diseases. Recurrent topics in Jan Pedersen's work include Genomic variations and chromosomal abnormalities (4 papers), Viral gastroenteritis research and epidemiology (3 papers) and Respiratory viral infections research (2 papers). Jan Pedersen is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Viral gastroenteritis research and epidemiology (3 papers) and Respiratory viral infections research (2 papers). Jan Pedersen collaborates with scholars based in Norway, United States and Belgium. Jan Pedersen's co-authors include Dale F. Hay, Alison Nash, Kåre Berg, Dennis A. Senne, Kåre Berg, Amaresh Das, Erica Spackman, David L. Suarez, Herman Van den Berghe and Lovise Mæhle and has published in prestigious journals such as Child Development, Journal of Clinical Microbiology and The Journal of Pediatrics.

In The Last Decade

Jan Pedersen

26 papers receiving 572 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jan Pedersen Norway 16 164 125 106 99 87 26 605
William J. Jordan United States 18 79 0.5× 122 1.0× 199 1.9× 27 0.3× 46 0.5× 64 1.3k
Yu-Yu Wu China 15 87 0.5× 157 1.3× 184 1.7× 352 3.6× 187 2.1× 44 1.2k
Hans Jakob Ingerslev Denmark 34 161 1.0× 164 1.3× 611 5.8× 89 0.9× 39 0.4× 102 3.7k
Brigitte Assouline France 18 134 0.8× 200 1.6× 201 1.9× 161 1.6× 58 0.7× 27 1.3k
Hélène Paradis Canada 17 115 0.7× 115 0.9× 382 3.6× 23 0.2× 25 0.3× 53 926
Amber Johnson United States 14 124 0.8× 97 0.8× 359 3.4× 131 1.3× 154 1.8× 27 1.2k
Christine Cameron United States 21 72 0.4× 104 0.8× 221 2.1× 120 1.2× 26 0.3× 35 1.8k
Elizabeth Kim United States 15 58 0.4× 62 0.5× 111 1.0× 44 0.4× 34 0.4× 33 641
Rachel Lefebvre France 13 146 0.9× 43 0.3× 43 0.4× 44 0.4× 11 0.1× 24 416
William A. Reid United Kingdom 15 36 0.2× 40 0.3× 139 1.3× 20 0.2× 17 0.2× 82 1.0k

Countries citing papers authored by Jan Pedersen

Since Specialization
Citations

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

Fields of papers citing papers by Jan Pedersen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jan Pedersen

This figure shows the co-authorship network connecting the top 25 collaborators of Jan Pedersen. A scholar is included among the top collaborators of Jan Pedersen 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 Jan Pedersen. Jan Pedersen 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.
Rohlin, Anna, Ulf Lundstam, Theofanis Zagoras, et al.. (2015). GREM1 and POLE variants in hereditary colorectal cancer syndromes. Genes Chromosomes and Cancer. 55(1). 95–106. 29 indexed citations
2.
Heimdal, Ketil, Lovise Mæhle, Jaran Apold, Jan Pedersen, & Pål Møller. (2003). The Norwegian founder mutations in BRCA1: high penetrance confirmed in an incident cancer series and differences observed in the risk of ovarian cancer. European Journal of Cancer. 39(15). 2205–2213. 33 indexed citations
3.
Pedersen, Jan, et al.. (2002). Vitamins A and E in Serum in Relation to Weight and Lung Function in Patients with Advanced Pulmonary Disease. International Journal for Vitamin and Nutrition Research. 72(6). 360–368. 6 indexed citations
5.
Retterstøl, Lars, Peter Kierulf, Jan Pedersen, et al.. (2001). Plasma fibrinogen level and long‐term prognosis in Norwegian middle‐aged patients with previous myocardial infarction. A 10 year follow‐up study. Journal of Internal Medicine. 249(6). 511–518. 15 indexed citations
6.
Møller, Pål, Ketil Heimdal, Jaran Apold, et al.. (2001). Genetic epidemiology of BRCA1 mutations in Norway. European Journal of Cancer. 37(18). 2428–2434. 36 indexed citations
7.
Pedersen, Jan, Dennis A. Senne, B. Panigrahy, & Donald L. Reynolds. (2001). Detection of Avian Pneumovirus in Tissues and Swab Specimens from Infected Turkeys. Avian Diseases. 45(3). 581–581. 5 indexed citations
8.
Dar, Arshud, Sagar M. Goyal, Jan Pedersen, et al.. (2000). A Modified Enzyme-Linked Immunosorbent Assay for the Detection of Avian Pneumovirus Antibodies. Journal of Veterinary Diagnostic Investigation. 12(4). 381–384. 43 indexed citations
9.
Liestøl, Knut, E. A. Kvittingen, Helge Rootwelt, et al.. (2000). Association between apolipoprotein E genotypes and cancer risk in patients with acquired immunodeficiency syndrome.. PubMed. 24(5). 496–9. 6 indexed citations
10.
Braathen, Geir J., et al.. (2000). [Genetic counseling in presymptomatic testing for Huntington disease].. PubMed. 120(20). 2412–6. 1 indexed citations
11.
Pedersen, Jan, et al.. (1993). Campomelic dysplasia — an underdiagnosed condition?. European Journal of Pediatrics. 152(4). 331–333. 17 indexed citations
12.
Eiklid, Kristin, Lisbeth Tranebjærg, Hans Geir Eiken, et al.. (1993). Frequency of the ΔF508 and exon 11 mutations in Norwegian cystic fibrosis patients. Clinical Genetics. 44(1). 12–14. 4 indexed citations
13.
Pedersen, Jan & Kåre Berg. (1989). Interaction between low density lipoprotein receptor (LDLR) and apolipoprotein E (apoE) alleles contributes to normal variation in lipid level. Clinical Genetics. 35(5). 331–337. 54 indexed citations
14.
Mills, Rosemary S. L., Jan Pedersen, & Joan E. Grusec. (1989). Sex differences in reasoning and emotion about altruism. Sex Roles. 20(11-12). 603–621. 22 indexed citations
15.
Pedersen, Jan & Kåre Berg. (1988). Normal DNA polymorphism at the low density lipoprotein receptor (LDLR) locus associated with serum cholesterol level. Clinical Genetics. 34(5). 306–312. 37 indexed citations
16.
Hay, Dale F., Alison Nash, & Jan Pedersen. (1983). Interaction between Six-Month-Old Peers. Child Development. 54(3). 557–557. 28 indexed citations
17.
Hay, Dale F., Alison Nash, & Jan Pedersen. (1983). Interaction between Six-Month-Old Peers. Child Development. 54(3). 557–562. 28 indexed citations
18.
Hay, Dale F., Alison Nash, & Jan Pedersen. (1981). Responses of Six-Month-Olds to the Distress of Their Peers. Child Development. 52(3). 1071–1071. 52 indexed citations
19.
Fryns, J. P., et al.. (1980). Deletion of the short arm of chromosome 9. European Journal of Pediatrics. 134(3). 201–204. 10 indexed citations
20.
Pedersen, Jan, et al.. (1980). Multiple synostosis syndrome. European Journal of Pediatrics. 134(3). 273–275. 4 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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