T. Tønnesen

2.2k total citations · 1 hit paper
43 papers, 1.5k citations indexed

About

T. Tønnesen is a scholar working on Molecular Biology, Nutrition and Dietetics and Physiology. According to data from OpenAlex, T. Tønnesen has authored 43 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 12 papers in Nutrition and Dietetics and 10 papers in Physiology. Recurrent topics in T. Tønnesen's work include Trace Elements in Health (11 papers), Lysosomal Storage Disorders Research (9 papers) and RNA and protein synthesis mechanisms (7 papers). T. Tønnesen is often cited by papers focused on Trace Elements in Health (11 papers), Lysosomal Storage Disorders Research (9 papers) and RNA and protein synthesis mechanisms (7 papers). T. Tønnesen collaborates with scholars based in Denmark, Germany and United Kingdom. T. Tønnesen's co-authors include Nina Horn, Zeynep Tümer, Anthony P. Monaco, Niels Tommerup, Jamel Chelly, Yumiko Ishikawa-Brush, James D. Friesen, Wim J. Kleijer, Niklas Dahl and Ulf Pettersson and has published in prestigious journals such as Nature Genetics, Journal of Bacteriology and Human Molecular Genetics.

In The Last Decade

T. Tønnesen

43 papers receiving 1.4k 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.

Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein

1993 557 citations Jamel Chelly, Zeynep Tümer et al. Nature Genetics profile →

Peers

Countries citing papers authored by T. Tønnesen

Since Specialization

Citations

This map shows the geographic impact of T. Tønnesen'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 T. Tønnesen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Tønnesen more than expected).

Fields of papers citing papers by T. Tønnesen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T. Tønnesen

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Identification of 9 novel IDS gene mutations in 19 unrelated Hunter syndrome (Mucopolysaccharidosis type II) patients 1998 ·Human Mutation ·Stanislav L. Karsten, (unknown), (unknown), Wim J. Kleijer, T. Tønnesen, Ulf Pettersson, Marie-Louise Bondeson	4
2	Inversion of the IDS gene resulting from recombination with IDS-related sequences in a common cause of the Hunter syndrome 1995 ·Human Molecular Genetics ·(unknown), Niklas Dahl, Helena Malmgren, Wim J. Kleijer, T. Tønnesen, (unknown), Ulf Pettersson	120
3	Characterization of the exon structure of the Menkes disease gene using vectorette PCR 1995 ·Genomics ·Zeynep Tümer, Burçak Vural, T. Tønnesen, Jamel Chelly, Anthony P. Monaco, Nina Horn	67
4	First trimester prenatal diagnosis of Menkes disease by DNA analysis. 1994 ·Journal of Medical Genetics ·Zeynep Tümer, T. Tønnesen, Jonathan Bohmann, W. Marg, Nina Horn	22
5	A cytogenetic survey in Menkes disease: implications for the detection of chromosomal rearrangements in X linked disorders. 1993 ·Journal of Medical Genetics ·Niels Tommerup, Zeynep Tümer, T. Tønnesen, Nina Horn	6
6	Clinical and biochemical consequences of copper-histidine therapy in Menkes disease 1993 ·European Journal of Pediatrics ·Joachim Kreuder, A. Otten, H. Fuder, Zeynep Tümer, T. Tønnesen, Nina Horn, D. Dralle	55
7	Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein breakdown → 1993 ·Nature Genetics ·Jamel Chelly, Zeynep Tümer, T. Tønnesen, (unknown), Yumiko Ishikawa-Brush, Niels Tommerup, Nina Horn, Anthony P. Monaco	557
8	Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS gene 1992 ·Human Molecular Genetics ·(unknown), Niklas Dahl, T. Tønnesen, Wim J. Kleijer, (unknown), K.‐H. Gustavson, Peter J. Wilson, C. Phillip Morris, John J. Hopwood, U. Pettersson	26
9	Characterization of a 1.0 Mb YAC contig spannning two chromosome breakpoints related to Menkes disease 1992 ·Human Molecular Genetics ·Zeynep Tümer, Jamel Chelly, Niels Tommerup, Yumiko Ishikawa-Brush, T. Tønnesen, Anthony P. Monaco, Nina Horn	25
10	Menkes Disease: An X‐Linked Neurological Disorder of the Copper Metabolism 1992 ·Brain Pathology ·Nina Horn, T. Tønnesen, (unknown)	50
11	Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2 1992 ·Human Genetics ·Zeynep Tümer, Niels Tommerup, T. Tønnesen, Joachim Kreuder, Ian Craig, Nina Horn	49
12	Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblings 1990 ·American Journal of Medical Genetics ·Serge Przedborski, Alina Ferster, Serge Goldman, (unknown), (unknown), T. Tønnesen, R. J. Pollitt, Esther Vamos	18
13	Clinical expression of Menkes syndrome in females 1990 ·Clinical Genetics ·Anne‐Marie Gerdes, T. Tønnesen, Nina Horn, Thierry Grisar, W. Marg, (unknown), (unknown), Norman W. Barton, Pascale Guiraud, A Joannard, M. J. Richard, F. Güttler	23
14	Postmortem Menkes diagnosis from carrier testing of female relatives 1987 ·Clinical Genetics ·T. Tønnesen, (unknown), Anne‐Marie Gerdes, Jakob Hansen, Edith Reske‐Nielsen, (unknown), Nina Horn	1
15	Experience with first trimester prenatal diagnosis of Menkes disease 1987 ·Prenatal Diagnosis ·T. Tønnesen, Nina Horn, (unknown), O. A. Jensen, Anne‐Marie Gerdes, Sylvie Girard, Else Marie Skjøde Damsgaard	9
16	Copper‐measurement in a muscle‐biopsy. A possible method for postmortem diagnosis of Menkes disease 1986 ·Clinical Genetics ·T. Tønnesen, (unknown), Else Marie Skjøde Damsgaard, Nina Horn	4
17	Paternal non‐disjunction in a 46, XY/ 47, XXY individual with a fragile 17p12 in the mother 1986 ·Clinical Genetics ·Niels Tommerup, T. Tønnesen, K. H. Gustavson	1
18	First trimester biopsies of chorionic villi for prenatal diagnosis: experience of two laboratories 1984 ·Clinical Genetics ·Margareta Mikkelsen, (unknown), T. Tønnesen, L. Marsk, J. Lindsten	4
19	Inhibitors of Ribonucleic Acid Synthesis in Saccharomyces cerevisiae : Decay Rate of Messenger Ribonucleic Acid 1973 ·Journal of Bacteriology ·T. Tønnesen, James D. Friesen	45
20	Isolation of two small molecular weight RNA components by MAK column chromatography 1971 ·Archives of Biochemistry and Biophysics ·Sune Frederiksen, T. Tønnesen, Per Hellung‐Larsen	10

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.

Explore authors with similar magnitude of impact