Maria Eriksson

7.4k total citations · 3 hit papers
95 papers, 5.5k citations indexed

About

Maria Eriksson is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Maria Eriksson has authored 95 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Molecular Biology, 13 papers in Surgery and 13 papers in Genetics. Recurrent topics in Maria Eriksson's work include Nuclear Structure and Function (32 papers), RNA Research and Splicing (27 papers) and DNA Repair Mechanisms (12 papers). Maria Eriksson is often cited by papers focused on Nuclear Structure and Function (32 papers), RNA Research and Splicing (27 papers) and DNA Repair Mechanisms (12 papers). Maria Eriksson collaborates with scholars based in Sweden, United States and Finland. Maria Eriksson's co-authors include Michael R. Erdos, Francis S. Collins, Leslie B. Gordon, Dale K. Shumaker, Robert D. Goldman, Anne E. Goldman, Satya Khuon, Amalia Dutra, Sandra G. Durkin and Michael Boehnke and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Maria Eriksson

91 papers receiving 5.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

2003 1.6k citations Maria Eriksson, Michael R. Erdos et al. profile →
Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson–Gilford progeria syndrome

2004 868 citations Robert D. Goldman, Dale K. Shumaker et al. Proceedings of the National Academy of Sciences profile →
Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging

2006 568 citations Dale K. Shumaker, Thomas Dechat et al. Proceedings of the National Academy of Sciences profile →

Peers

Maria Eriksson

PHYSI

GENET

CCM

Lynn A. Megeney Canada

Koichi Kokame Japan

Michelle Olive United States

Ernst‐Martin Füchtbauer Denmark

Josef Müller‐Höcker Germany

Kay‐Dietrich Wagner France

Kathryn White United Kingdom

Nicole Wagner France

Donal MacGrogan United States

Mathias Mericskay France

Lynn A. Megeney Canada

Maria Eriksson

3.6k ×0.8

684 ×1.1

PHYSI

677 ×1.5

308 ×0.7

GENET

430 ×1.6

CCM

Citations per year, relative to Maria Eriksson Maria Eriksson (= 1×) peers Lynn A. Megeney

Countries citing papers authored by Maria Eriksson

Since Specialization

Citations

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

Fields of papers citing papers by Maria Eriksson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Eriksson

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Eriksson. A scholar is included among the top collaborators of Maria Eriksson 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 Maria Eriksson. Maria Eriksson 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

Vrtačnik, Peter, Santhilal Subhash, Hafdís T. Helgadóttir, et al.. (2025). Induced somatic mutation accumulation during skeletal muscle regeneration reduces muscle strength. Nature Aging. 5(9). 1739–1749.

Revêchon, Gwladys, et al.. (2023). Somatic mutations in vascular wall function and age-associated disease. European Heart Journal. 44(40). 4208–4210. 6 indexed citations

Franco, Irene & Maria Eriksson. (2022). Reverting to old theories of ageing with new evidence for the role of somatic mutations. Nature Reviews Genetics. 23(11). 645–646. 3 indexed citations

Franco, Irene, Gwladys Revêchon, & Maria Eriksson. (2022). Challenges of proving a causal role of somatic mutations in the aging process. Aging Cell. 21(5). e13613–e13613. 13 indexed citations

Nord, Christoffer, et al.. (2021). 3D imaging of human organs with micrometer resolution - applied to the endocrine pancreas. Communications Biology. 4(1). 1063–1063. 9 indexed citations

Franco, Irene, Rodrigo Fernandez‐Gonzalo, Peter Vrtačnik, et al.. (2019). Healthy skeletal muscle aging: The role of satellite cells, somatic mutations and exercise. International review of cell and molecular biology. 346. 157–200. 13 indexed citations

Franco, Irene, Anna Johansson, Karl Olsson, et al.. (2018). Somatic mutagenesis in satellite cells associates with human skeletal muscle aging. Nature Communications. 9(1). 800–800. 93 indexed citations

Sola-Carvajal, Agustín, et al.. (2015). Skin Disease in Laminopathy-Associated Premature Aging. Journal of Investigative Dermatology. 135(11). 2577–2583. 8 indexed citations

Eriksson, Maria, et al.. (2011). Stem cell depletion in Hutchinson–Gilford progeria syndrome. Aging Cell. 10(6). 1011–1020. 69 indexed citations

10.

Hanif, Mubashir, et al.. (2008). Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease. Journal of Cell Science. 121(7). 969–978. 66 indexed citations

11.

Eriksson, Maria, Anna‐Lisa Osvalder, & Sven Dahlman. (2007). Ergonomisk utvärdering av spårövergångar och säkerhetsåtgärder.. Chalmers Research (Chalmers University of Technology).

12.

Bohman, Katarina, Ola Boström, Anna‐Lisa Osvalder, & Maria Eriksson. (2007). Rear Seat Frontal Impact Protection for Children Seated on Booster Cushions – An Attitude, Handling and Safety Approach. Chalmers Research (Chalmers University of Technology). 10 indexed citations

13.

Shumaker, Dale K., Thomas Dechat, Alexander Kohlmaier, et al.. (2006). Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging. Proceedings of the National Academy of Sciences. 103(23). 8703–8708. 568 indexed citations breakdown →

14.

Bohman, Katarina, Ola Boström, Maria Eriksson, & Anna‐Lisa Osvalder. (2006). Frontal Impact Protection of Children on Booster Cushions - an Attitude, Handling and Safety Approach. Chalmers Publication Library (Chalmers University of Technology). 1 indexed citations

15.

Eriksson, Maria, et al.. (2002). Biostimulation and bioaugmentation for on-site treatment of weathered diesel fuel in Arctic soil. Applied Microbiology and Biotechnology. 59(4-5). 551–556. 79 indexed citations

16.

Eriksson, Maria, Tor Ansved, Maria Anvret, & Nessa Carey. (2001). A Mammalian Radial Spokehead-Like Gene, RSHL1, at the Myotonic Dystrophy-1 Locus. Biochemical and Biophysical Research Communications. 281(4). 835–841. 14 indexed citations

17.

Zhang, Zhiping, Maria Eriksson, Gunnar Falk, et al.. (1998). Failure to Achieve Gene Conversion with Chimeric Circular Oligonucleotides: Potentially Misleading PCR Artifacts Observed. Antisense and Nucleic Acid Drug Development. 8(6). 531–536. 34 indexed citations

18.

Bergqvist, Ingela, et al.. (1998). Transgenic Cre recombinase expression in germ cells and early embryogenesis directs homogeneous and ubiquitous deletion of loxP‐flanked gene segments. FEBS Letters. 438(1-2). 76–80. 15 indexed citations

19.

Höglund, Stefan, Lennart Åkerblom, Muhsin Özel, et al.. (1990). Characterization of Immunostimulating Complexes (ISCOMS) of HIV-1. Viral Immunology. 3(3). 195–206. 9 indexed citations

20.

Lindén, Anders, Maria Eriksson, Steen Holger Hansen, & K. UVNÄS‐MOBERG. (1990). Suckling-induced release of cholecystokinin into plasma in the lactating rat: effects of abdominal vagotomy and lesions of central pathways concerned with milk ejection. Journal of Endocrinology. 127(2). 257–263. 26 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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