Hanne Poulsen

1.6k total citations
31 papers, 1.2k citations indexed

About

Hanne Poulsen is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hanne Poulsen has authored 31 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 14 papers in Genetics and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hanne Poulsen's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Hanne Poulsen is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Hanne Poulsen collaborates with scholars based in Denmark, France and United Kingdom. Hanne Poulsen's co-authors include Margareta Mikkelsen, Niels Tommerup, Jan Egebjerg, Jørgen Kjems, Christian Kroun Damgaard, Jakob Nilsson, Karen Brøndum‐Nielsen, Aksel Lange, Bente Vilsen and Karen Brøndum Nielsen and has published in prestigious journals such as Molecular and Cellular Biology, Biochemistry and The Lancet Neurology.

In The Last Decade

Hanne Poulsen

31 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Hanne Poulsen Denmark 19 634 482 252 148 113 31 1.2k
Nikos C. Vamvakopoulos Greece 19 566 0.9× 431 0.9× 133 0.5× 31 0.2× 233 2.1× 39 1.9k
Richard F. Wintle Canada 14 415 0.7× 763 1.6× 136 0.5× 99 0.7× 56 0.5× 24 1.5k
Valeriya Gaysinskaya United States 17 479 0.8× 132 0.3× 206 0.8× 83 0.6× 129 1.1× 19 1.8k
Brenda Richards United States 16 498 0.8× 415 0.9× 58 0.2× 37 0.3× 46 0.4× 29 1.2k
D. M. de Kretser Australia 27 799 1.3× 627 1.3× 114 0.5× 62 0.4× 692 6.1× 54 2.4k
Ono H Japan 22 389 0.6× 261 0.5× 38 0.2× 68 0.5× 525 4.6× 62 1.5k
Amy C. Lossie United States 17 836 1.3× 717 1.5× 288 1.1× 28 0.2× 53 0.5× 40 1.2k
Huguette Brocas Belgium 20 739 1.2× 520 1.1× 55 0.2× 161 1.1× 19 0.2× 39 1.5k
Edmund C. Jenkins United States 20 431 0.7× 534 1.1× 73 0.3× 65 0.4× 38 0.3× 61 1.4k
Karen Plaut United States 21 459 0.7× 421 0.9× 142 0.6× 45 0.3× 45 0.4× 65 1.5k

Countries citing papers authored by Hanne Poulsen

Since Specialization
Citations

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

Fields of papers citing papers by Hanne Poulsen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hanne Poulsen

This figure shows the co-authorship network connecting the top 25 collaborators of Hanne Poulsen. A scholar is included among the top collaborators of Hanne Poulsen 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 Hanne Poulsen. Hanne Poulsen 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.
Poulsen, Hanne, et al.. (2020). The C‐terminal domains of the NMDA receptor: How intrinsically disordered tails affect signalling, plasticity and disease. European Journal of Neuroscience. 54(8). 6713–6739. 36 indexed citations
2.
Clausen, Michael V., et al.. (2016). Reappraising the effects of artemisinin on the ATPase activity of PfATP6 and SERCA1a E255L expressed in Xenopus laevis oocytes. Nature Structural & Molecular Biology. 23(1). 1–2. 8 indexed citations
3.
Heinzen, Erin L., Alexis Arzimanoglou, Allison Brashear, et al.. (2014). Distinct neurological disorders with ATP1A3 mutations. The Lancet Neurology. 13(5). 503–514. 178 indexed citations
4.
Kopeć, Wojciech, et al.. (2014). Molecular Mechanism of Na+,K+-ATPase Malfunction in Mutations Characteristic of Adrenal Hypertension. Biochemistry. 53(4). 746–754. 23 indexed citations
5.
Poulsen, Nina Aagaard, Iga Rybicka, Hanne Poulsen, et al.. (2014). Seasonal variation in content of riboflavin and major minerals in bulk milk from three Danish dairies. International Dairy Journal. 42. 6–11. 40 indexed citations
6.
Raarup, Merete K., Anja W. Fjorback, Stig M. R. Jensen, et al.. (2009). Enhanced yellow fluorescent protein photoconversion to a cyan fluorescent protein-like species is sensitive to thermal and diffusion conditions. Journal of Biomedical Optics. 14(3). 34039–34039. 11 indexed citations
7.
Morth, Jens Preben, Hanne Poulsen, Mads S. Toustrup-Jensen, et al.. (2008). The structure of the Na+,K+-ATPase and mapping of isoform differences and disease-related mutations. Philosophical Transactions of the Royal Society B Biological Sciences. 364(1514). 217–227. 73 indexed citations
8.
Poulsen, Hanne, Rasmus Jørgensen, Anders Heding, et al.. (2006). Dimerization of ADAR2 is mediated by the double-stranded RNA binding domain. RNA. 12(7). 1350–1360. 54 indexed citations
9.
Mikkelsen, Margareta, Hanne Poulsen, & Kim G. Nielsen. (2005). Incidence, survival, and mortality in Down syndrome in Denmark. American Journal of Medical Genetics. 37(S7). 75–78. 27 indexed citations
10.
Poulsen, Hanne, Jakob Nilsson, Christian Kroun Damgaard, Jan Egebjerg, & Jørgen Kjems. (2001). CRM1 Mediates the Export of ADAR1 through a Nuclear Export Signal within the Z-DNA Binding Domain. Molecular and Cellular Biology. 21(22). 7862–7871. 143 indexed citations
11.
Bartsch, Oliver, Michael B. Petersen, Hanne Poulsen, et al.. (1993). Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome. Human Genetics. 92(2). 127–32. 19 indexed citations
12.
Petersen, Michael B., Stylianos E. Antonarakis, Andrew C. Warren, et al.. (1992). Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.. PubMed. 51(3). 516–25. 49 indexed citations
13.
Mikkelsen, Margareta, Hanne Poulsen, & Niels Tommerup. (1989). Genetic risk factors in human trisomy 21.. PubMed. 311. 183–97. 7 indexed citations
14.
Poulsen, Hanne, et al.. (1982). MARTIN‐BELL SYNDROME fra(X) (q28) IN A SRI LANKAN FAMILY. Journal of Intellectual Disability Research. 26(4). 251–257. 4 indexed citations
15.
Poulsen, Hanne, Margareta Mikkelsen, & Gösta Holmgren. (1981). Peri‐ and paracentric inversions in chromosome 12: Prenatal diagnosis and family study. Prenatal Diagnosis. 1(1). 35–42. 18 indexed citations
16.
Nielsen, Karen Brøndum, Niels Tommerup, Hanne Poulsen, & Margareta Mikkelsen. (1981). X-Linked mental retardation with fragile X. a pedigree showing transmission by apparently unaffected males and partial expression in female carriers. Human Genetics. 59(1). 23–25. 59 indexed citations
17.
Tommerup, Niels, Hanne Poulsen, & Karen Brøndum‐Nielsen. (1981). 5-Fluoro-2'-deoxyuridine induction of the fragile site on Xq28 associated with X linked mental retardation.. Journal of Medical Genetics. 18(5). 374–376. 81 indexed citations
18.
Poulsen, Hanne, et al.. (1977). Inhibition of the development of Q-bands on human chromosomes by netropsin. Human Genetics. 39(3). 309–313. 10 indexed citations
19.
Hauge, M., et al.. (1975). The value of fluorescence markers in the distinction between maternal and fetal chromosomes. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 26(3). 187–191. 43 indexed citations
20.
Mikkelsen, Margareta, et al.. (1973). Unbalanced X/autosomal translocation with inactivation of the normal X chromosome. Cytogenetic and Genome Research. 12(5). 357–366. 28 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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