Nina Horn

4.4k total citations · 1 hit paper
88 papers, 3.1k citations indexed

About

Nina Horn is a scholar working on Nutrition and Dietetics, Molecular Biology and Hematology. According to data from OpenAlex, Nina Horn has authored 88 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Nutrition and Dietetics, 50 papers in Molecular Biology and 12 papers in Hematology. Recurrent topics in Nina Horn's work include Trace Elements in Health (61 papers), RNA regulation and disease (27 papers) and Iron Metabolism and Disorders (11 papers). Nina Horn is often cited by papers focused on Trace Elements in Health (61 papers), RNA regulation and disease (27 papers) and Iron Metabolism and Disorders (11 papers). Nina Horn collaborates with scholars based in Denmark, Germany and United Kingdom. Nina Horn's co-authors include Zeynep Tümer, T. Tønnesen, Lisbeth Birk Møller, Anthony P. Monaco, Niels Tommerup, Jamel Chelly, Yumiko Ishikawa-Brush, Connie Lund, K Baerlocher and Flemming Wibrand and has published in prestigious journals such as The Lancet, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Nina Horn

87 papers receiving 3.0k 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 Zeynep Tümer, T. Tønnesen et al. profile →

Peers

Countries citing papers authored by Nina Horn

Since Specialization

Citations

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

Fields of papers citing papers by Nina Horn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nina Horn

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

#	Work	Indexed citations
1	Ethics in pre-ART genetics: a missed X-linked Menkes disease case 2023 ·Journal of Assisted Reproduction and Genetics ·Anne‐Marie Gerdes, Lisbeth Birk Møller, Nina Horn	2
2	ATP7A-Regulated Enzyme Metalation and Trafficking in the Menkes Disease Puzzle 2021 ·Biomedicines ·Nina Horn, Pernilla Wittung‐Stafshede	60
3	Orchestration of dynamic copper navigation – new and missing pieces 2017 ·Metallomics ·Helena Öhrvik, Jan Aaseth, Nina Horn	52
4	Experience with First Trimester Prenatal Diagnosis of Menkes Disease1 2015 ·Current problems in dermatology ·(unknown), Nina Horn, (unknown), O. A. Jensen	0
5	Clinical expression of Menkes disease in females with normal karyotype 2012 ·Orphanet Journal of Rare Diseases ·Lisbeth Birk Møller, Małgorzata Lenartowicz, M. T. Zabot, Josiane Arnaud, Lydie Bürglen, Chris Bennett, (unknown), Richard Fisher, Sandra Janssens, Shehla Mohammed, Margreet G.E.M. Ausems, Zeynep Tümer, Nina Horn, Thomas G. Jensen	36
6	Evidence That Translation Reinitiation Leads to a Partially Functional Menkes Protein Containing Two Copper-Binding Sites 2006 ·The American Journal of Human Genetics ·(unknown), Connie Lund, (unknown), Jakob R. Winther, Nina Horn, Lisbeth Birk Møller	51
7	Identification and analysis of 21 novel disease-causing amino acid substitutions in the conserved part of ATP7A 2005 ·Human Mutation ·Lisbeth Birk Møller, Jens T. Bukrinsky, Anne Mølgaard, (unknown), Connie Lund, Zeynep Tümer, Sine Larsen, Nina Horn	43
8	X-Linked Menkes Disease: First Documented Report of Germ-Line Mosaicism 2004 ·Genetic Testing ·(unknown), Lisbeth Birk Møller, Katie Plunkett, John W. Belmont, Zeynep Tümer, Nina Horn	6
9	Similar Splice-Site Mutations of the ATP7A Gene Lead to Different Phenotypes: Classical Menkes Disease or Occipital Horn Syndrome 2000 ·The American Journal of Human Genetics ·Lisbeth Birk Møller, Zeynep Tümer, Connie Lund, Carsten Tilbæk Petersen, Trevor Cole, (unknown), (unknown), Lars Riff Jensen, Nina Horn	84
10	Accumulated experience with prenatal diagnosis of menkes disease by neutron activation analysis of chorionic villi specimens 1999 ·Biological Trace Element Research ·K. Heydorn, Else Marie Skjøde Damsgaard, Nina Horn	6
11	Investigation of the copper binding sites in the Menkes disease protein, ATP7A 1998 ·Journal of Inherited Metabolic Disease ·(unknown), Nicklas Bonander, Göran Karlsson, Nina Horn, Zeynep Tümer, Ole Farver	5
12	Menkes disease: recent advances and new aspects. 1997 ·Journal of Medical Genetics ·Zeynep Tümer, Nina Horn	61
13	Pyruvate dehydrogenase deficiency caused by a 33 base pair duplication in the PDH E1α subunit 1994 ·Human Molecular Genetics ·Lise Lotte Hansen, Nina Horn, Hans‐Henrik M. Dahl, Torben A. Kruse	12
14	Analysis of Mnk, the Murine Homologue of the Locus for Menkes Disease, in Normal and Mottled (Mo) Mice 1994 ·Genomics ·(unknown), (unknown), P. H. Glenister, Jamel Chelly, Zeynep Tümer, Nina Horn, Anthony P. Monaco, Yvonne Boyd	19
15	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
16	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
17	The binding of mouse hybridoma and human IgE antibodies to the major fecal allergen, Der p I, of Dermatophagoides pteronyssinus . Relative binding site location and species specificity studied by solid-phase inhibition assays with radiolabeled antigen. 1988 ·The Journal of Immunology ·Peter Lind, Ole C. Hansen, Nina Horn	62
18	Variability in clinical expression of Menkes syndrome 1988 ·European Journal of Pediatrics ·Anne‐Marie Gerdes, (unknown), Eugene Pergament, (unknown), K Baerlocher, (unknown), F. G�ttler, Nina Horn	37
19	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
20	Menkes X linked disease: two clonal cell populations in heterozygotes. 1980 ·Journal of Medical Genetics ·Nina Horn, (unknown), Valerie McGuire	21

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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