Mette Hollensted

3.6k total citations
17 papers, 308 citations indexed

About

Mette Hollensted is a scholar working on Genetics, Surgery and Physiology. According to data from OpenAlex, Mette Hollensted has authored 17 papers receiving a total of 308 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Surgery and 7 papers in Physiology. Recurrent topics in Mette Hollensted's work include Pancreatic function and diabetes (6 papers), Regulation of Appetite and Obesity (5 papers) and Birth, Development, and Health (4 papers). Mette Hollensted is often cited by papers focused on Pancreatic function and diabetes (6 papers), Regulation of Appetite and Obesity (5 papers) and Birth, Development, and Health (4 papers). Mette Hollensted collaborates with scholars based in Denmark, China and Pakistan. Mette Hollensted's co-authors include Torben Hansen, Oluf Pedersen, Jens‐Christian Holm, Sten Madsbad, Jens J. Holst, Eva W. Iepsen, Jinyi Zhang, Anette P. Gjesing, Signe S. Torekov and Henrik S. Thomsen and has published in prestigious journals such as PLoS ONE, Cell Metabolism and Diabetologia.

In The Last Decade

Mette Hollensted

17 papers receiving 303 citations

Peers

Mette Hollensted
Mette Hollensted
Citations per year, relative to Mette Hollensted Mette Hollensted (= 1×) peers Saleem S. Qader

Countries citing papers authored by Mette Hollensted

Since Specialization
Citations

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

Fields of papers citing papers by Mette Hollensted

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mette Hollensted

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

All Works

17 of 17 papers shown
1.
Trier, Cæcilie, Mette Hollensted, Mathilde Svendstrup, et al.. (2021). Obesity treatment effect in danish children and adolescents carrying melanocortin-4 receptor mutations. Yearbook of pediatric endocrinology. 1 indexed citations
2.
Trier, Cæcilie, Mette Hollensted, Theresia M. Schnurr, et al.. (2020). Obesity treatment effect in Danish children and adolescents carrying Melanocortin-4 Receptor mutations. International Journal of Obesity. 45(1). 66–76. 25 indexed citations
3.
Niazi, Robina Khan, Jihua Sun, Henri Theil, et al.. (2019). Increased frequency of rare missense PPP1R3B variants among Danish patients with type 2 diabetes. PLoS ONE. 14(1). e0210114–e0210114. 5 indexed citations
4.
Niazi, Robina Khan, Anette P. Gjesing, Mette Hollensted, et al.. (2019). Screening of 31 genes involved in monogenic forms of obesity in 23 Pakistani probands with early-onset childhood obesity: a case report. BMC Medical Genetics. 20(1). 152–152. 5 indexed citations
5.
Sun, Jihua, Henri Theil, Mette Hollensted, et al.. (2019). Sequencing reveals protective and pathogenic effects on development of diabetes of rare GLIS3 variants. PLoS ONE. 14(8). e0220805–e0220805. 5 indexed citations
6.
Iepsen, Eva W., Jinyi Zhang, Mette Hollensted, et al.. (2019). Adults with pathogenic MC4R mutations have increased final height and thereby increased bone mass. Journal of Bone and Mineral Metabolism. 38(1). 117–125. 9 indexed citations
7.
Aasbrenn, Martin, Theresia M. Schnurr, Henri Theil, et al.. (2019). Genetic Determinants of Weight Loss After Bariatric Surgery. Obesity Surgery. 29(8). 2554–2561. 22 indexed citations
8.
Hollensted, Mette, Yuvaraj Mahendran, Theresia M. Schnurr, et al.. (2018). An adult-based insulin resistance genetic risk score associates with insulin resistance, metabolic traits and altered fat distribution in Danish children and adolescents who are overweight or obese. Diabetologia. 61(8). 1769–1779. 11 indexed citations
9.
Niazi, Robina Khan, Anette P. Gjesing, Mette Hollensted, et al.. (2018). Identification of novel LEPR mutations in Pakistani families with morbid childhood obesity. BMC Medical Genetics. 19(1). 199–199. 10 indexed citations
10.
Hollensted, Mette, Claus Thorn Ekstrøm, Oluf Pedersen, et al.. (2018). Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study. BMC Medical Genetics. 19(1). 207–207. 3 indexed citations
11.
Iepsen, Eva W., Jinyi Zhang, Henrik S. Thomsen, et al.. (2018). Patients with Obesity Caused by Melanocortin-4 Receptor Mutations Can Be Treated with a Glucagon-like Peptide-1 Receptor Agonist. Cell Metabolism. 28(1). 23–32.e3. 99 indexed citations
12.
Hollensted, Mette, Theresia M. Schnurr, Tenna Ruest Haarmark Nielsen, et al.. (2018). Genetic Susceptibility for Childhood BMI has no Impact on Weight Loss Following Lifestyle Intervention in Danish Children. Obesity. 26(12). 1915–1922. 10 indexed citations
13.
Nielsen, Tenna Ruest Haarmark, Emil V. R. Appel, Mathilde Svendstrup, et al.. (2017). A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents. PLoS ONE. 12(3). e0174204–e0174204. 11 indexed citations
14.
Gjesing, Anette P., Rui Gao, Jeannet Lauenborg, et al.. (2017). High Prevalence of Diabetes-Predisposing Variants in MODY Genes Among Danish Women With Gestational Diabetes Mellitus. Journal of the Endocrine Society. 1(6). 681–690. 30 indexed citations
15.
Hollensted, Mette, Tarunveer S. Ahluwalia, Henri Theil, et al.. (2015). Common variants in LEPR, IL6, AMD1, and NAMPT do not associate with risk of juvenile and childhood obesity in Danes: a case–control study. BMC Medical Genetics. 16(1). 105–105. 9 indexed citations
16.
Gao, Rui, Yanxia Liu, Anette P. Gjesing, et al.. (2014). Evaluation of a target region capture sequencing platform using monogenic diabetes as a study-model. BMC Genetics. 15(1). 13–13. 45 indexed citations
17.
Banasik, Karina, Mette Hollensted, Ehm A. Andersson, et al.. (2012). The effect of FOXA2rs1209523 on glucose-related phenotypes and risk of type 2 diabetes in Danish individuals. BMC Medical Genetics. 13(1). 10–10. 8 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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