Monica Jansson

492 total citations
6 papers, 374 citations indexed

About

Monica Jansson is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Monica Jansson has authored 6 papers receiving a total of 374 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Clinical Biochemistry and 1 paper in Genetics. Recurrent topics in Monica Jansson's work include Mitochondrial Function and Pathology (3 papers), ATP Synthase and ATPases Research (2 papers) and Metabolism and Genetic Disorders (2 papers). Monica Jansson is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), ATP Synthase and ATPases Research (2 papers) and Metabolism and Genetic Disorders (2 papers). Monica Jansson collaborates with scholars based in Sweden, Bangladesh and France. Monica Jansson's co-authors include Anders Oldfors, Damien Sternberg, Michel Fardeau, Anne Lombès, G. Fayet, Nils‐Göran Larsson, Anja Rantanen, Per‐Erik Jansson, Göran Widmalm and Kjell Hultenby and has published in prestigious journals such as Acta Neuropathologica, Genomics and European Journal of Human Genetics.

In The Last Decade

Monica Jansson

6 papers receiving 366 citations

Peers

Monica Jansson

MB

CB

ENDOC

EPIDE

PHYSI

Hisao Fukushima Japan

Begoña Ugarte‐Uribe Spain

Aaron B. Sullivan United States

Michelyne Breton France

Nathália Rocco-Machado Brazil

Constance J. Clancey United States

Qizong Lao United States

Pei-Chi Chiang Taiwan

Yolanda Auchli Switzerland

Hisao Fukushima Japan

Monica Jansson

177 ×0.7

MB

26 ×0.3

CB

73 ×1.4

ENDOC

65 ×1.3

EPIDE

207 ×4.1

PHYSI

Citations per year, relative to Monica Jansson Monica Jansson (= 1×) peers Hisao Fukushima

Countries citing papers authored by Monica Jansson

Since Specialization

Citations

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

Fields of papers citing papers by Monica Jansson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monica Jansson

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

All Works

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6 of 6 papers shown

1.

Kollberg, Gittan, Monica Jansson, Åsa Pérez-Bercoff, et al.. (2005). Low frequency of mtDNA point mutations in patients with PEO associated with POLG1 mutations. European Journal of Human Genetics. 13(4). 463–469. 28 indexed citations

2.

Fayet, G., Monica Jansson, Damien Sternberg, et al.. (2002). Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function. Neuromuscular Disorders. 12(5). 484–493. 156 indexed citations

3.

Rantanen, Anja, Monica Jansson, Anders Oldfors, & Nils‐Göran Larsson. (2001). Downregulation of Tfam and mtDNA copy number during mammalian spermatogenesis. Mammalian Genome. 12(10). 787–792. 58 indexed citations

4.

Jansson, Monica, Niklas Darín, Mårten Kyllerman, et al.. (2000). Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy. Acta Neuropathologica. 100(1). 23–28. 15 indexed citations

5.

Gåfvels, Mats, Maria Olin, Terje Raudsepp, et al.. (1999). Structure and Chromosomal Assignment of the Sterol 12α-Hydroxylase Gene (CYP8B1) in Human and Mouse: Eukaryotic Cytochrome P-450 Gene Devoid of Introns. Genomics. 56(2). 184–196. 57 indexed citations

6.

Weintraub, Andrej, Göran Widmalm, Per‐Erik Jansson, et al.. (1994). Vibrio cholerae O139 Bengal possesses a capsular polysaccharide which may confer increased virulence. Microbial Pathogenesis. 16(3). 235–241. 60 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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