Maria Rasmussen

1.3k total citations
44 papers, 930 citations indexed

About

Maria Rasmussen is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Maria Rasmussen has authored 44 papers receiving a total of 930 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 12 papers in Genetics and 10 papers in Physiology. Recurrent topics in Maria Rasmussen's work include Simulation-Based Education in Healthcare (9 papers), Renal and related cancers (8 papers) and Innovations in Medical Education (6 papers). Maria Rasmussen is often cited by papers focused on Simulation-Based Education in Healthcare (9 papers), Renal and related cancers (8 papers) and Innovations in Medical Education (6 papers). Maria Rasmussen collaborates with scholars based in Denmark, United States and Canada. Maria Rasmussen's co-authors include Charlotte Ringsted, Martin G. Tolsgaard, Amandus Gustafsson, Michael B. Petersen, Bjørn Richelsen, Jens Meldgaard Bruun, Aina S. Lihn, Mads Rasmussen, Steen B. Pedersen and Birgitta Trolle and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Genetics.

In The Last Decade

Maria Rasmussen

39 papers receiving 908 citations

Peers

Maria Rasmussen
Jennifer Conn Australia
R Hall United Kingdom
MaryAnn O’Riordan United States
Dara Brodsky United States
Isam W. Nasr United States
Délio Marques Conde Brazil
José L. Gonzalez United States
Jaden R. Kohn United States
P. Manzoni Italy
Dulaney A. Wilson United States
Jennifer Conn Australia
Maria Rasmussen
Citations per year, relative to Maria Rasmussen Maria Rasmussen (= 1×) peers Jennifer Conn

Countries citing papers authored by Maria Rasmussen

Since Specialization
Citations

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

Fields of papers citing papers by Maria Rasmussen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Rasmussen

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Rasmussen. A scholar is included among the top collaborators of Maria Rasmussen 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 Rasmussen. Maria Rasmussen 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.
Pedersen, Katja Venborg, Mads Malik Aagaard, Jesper Graakjær, et al.. (2024). The role of genomic disorders in chronic kidney failure of undetermined aetiology ≤50 years. Clinical Kidney Journal. 17(7). sfae166–sfae166.
2.
Rasmussen, Maria, et al.. (2024). Reverse Phenotypes of Patients with Genetically Confirmed Liddle Syndrome. Clinical Journal of the American Society of Nephrology. 19(5). 610–619. 2 indexed citations
3.
Lildballe, Dorte L., Anja Lisbeth Frederiksen, Bitten Schönewolf‐Greulich, et al.. (2023). National clinical Genetic Networks - GENets - Establishment of expert collaborations in Denmark. European Journal of Medical Genetics. 66(12). 104872–104872.
4.
Andersen, Eline Sandvig, Maria Rasmussen, & Claus Lohman Brasen. (2022). Hypophosphatasia as a plausible cause of vitamin B6 associated mouth pain: a case-report. Scandinavian Journal of Pain. 23(2). 416–418. 1 indexed citations
5.
Rasmussen, Maria, Naja Becher, Brian Nauheimer Andersen, et al.. (2021). Phenotypic heterogeneity and mosaicism in Xia-Gibbs syndrome: Five Danish patients with novel variants in AHDC1. European Journal of Medical Genetics. 64(9). 104280–104280. 5 indexed citations
6.
Lildballe, Dorte L., et al.. (2021). Clinical genetic diagnostics in Danish autosomal dominant polycystic kidney disease patients reveal possible founder variants. European Journal of Medical Genetics. 64(4). 104183–104183. 4 indexed citations
7.
Lildballe, Dorte L., Maria Rasmussen, Lone Sunde, et al.. (2021). Functional megalin is expressed in renal cysts in a mouse model of adult polycystic kidney disease. Clinical Kidney Journal. 14(11). 2420–2427. 3 indexed citations
8.
Lildballe, Dorte L., et al.. (2021). Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion. SHILAP Revista de lepidopterología. 2021. 1–5.
9.
Lildballe, Dorte L., et al.. (2021). Family History is Important to Identify Patients with Monogenic Causes of Adult-Onset Chronic Kidney Disease. ˜The œNephron journals/Nephron journals. 146(1). 49–57. 5 indexed citations
10.
Rasmussen, Maria, et al.. (2020). PAX2 variant associated with bilateral kidney agenesis and broad intrafamilial disease variability. Clinical Kidney Journal. 14(2). 704–706. 5 indexed citations
11.
Andersen, Betina Ristorp, Maria Rasmussen, Karl Bang Christensen, et al.. (2020). Making the best of the worst: Care quality during emergency cesarean sections. PLoS ONE. 15(2). e0227988–e0227988. 1 indexed citations
12.
Rasmussen, Maria, Lone Sunde, Mette Ramsing, et al.. (2017). Targeted gene sequencing and whole‐exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies. Clinical Genetics. 93(4). 860–869. 40 indexed citations
13.
Rasmussen, Maria, Lone Sunde, René Frydensbjerg Andersen, Olav Bjørn Petersen, & Morten Smærup Olsen. (2017). Infants with prenatally diagnosed kidney anomalies have an increased risk of urinary tract infections. Acta Paediatrica. 106(11). 1875–1881. 1 indexed citations
14.
Rasmussen, Maria, Else Marie Vestergaard, Jesper Graakjær, et al.. (2016). 17q12 deletion and duplication syndrome in Denmark—A clinical cohort of 38 patients and review of the literature. American Journal of Medical Genetics Part A. 170(11). 2934–2942. 50 indexed citations
15.
Herlin, Morten Krogh, Anne‐Mette Bay Bjørn, Maria Rasmussen, Birgitta Trolle, & Michael B. Petersen. (2016). Prevalence and patient characteristics of Mayer–Rokitansky–Küster–Hauser syndrome: a nationwide registry-based study. Human Reproduction. 31(10). 2384–2390. 99 indexed citations
16.
Rasmussen, Maria, Steen Pedersen, Lone Sunde, et al.. (2014). A novel FBN1 variant in a large Marfan family with high penetrance of aortic dissection or rupture.. PubMed. 61(11). A4949–A4949. 1 indexed citations
17.
Tolsgaard, Martin G., et al.. (2013). Improving Efficiency of Clinical Skills Training: A Randomized Trial. Journal of General Internal Medicine. 28(8). 1072–1077. 43 indexed citations
18.
Rasmussen, Maria, Peter Dieckmann, S. Barry Issenberg, et al.. (2012). Long-term intended and unintended experiences after Advanced Life Support training. Resuscitation. 84(3). 373–377. 29 indexed citations
19.
Jensen, Morten Lind, Rasmus Hesselfeldt, Maria Rasmussen, et al.. (2008). Newly graduated doctors’ competence in managing cardiopulmonary arrests assessed using a standardized Advanced Life Support (ALS) assessment. Resuscitation. 77(1). 63–68. 27 indexed citations
20.
Rasmussen, Maria, Aina S. Lihn, Steen B. Pedersen, et al.. (2006). Adiponectin Receptors in Human Adipose Tissue: Effects of Obesity, Weight Loss, and Fat Depots. Obesity. 14(1). 28–35. 127 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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