Anne Hedemand

888 total citations
11 papers, 196 citations indexed

About

Anne Hedemand is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Anne Hedemand has authored 11 papers receiving a total of 196 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Cognitive Neuroscience. Recurrent topics in Anne Hedemand's work include Genetics and Neurodevelopmental Disorders (4 papers), Genetic Associations and Epidemiology (3 papers) and Glycosylation and Glycoproteins Research (2 papers). Anne Hedemand is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genetic Associations and Epidemiology (3 papers) and Glycosylation and Glycoproteins Research (2 papers). Anne Hedemand collaborates with scholars based in Denmark, United States and Faroe Islands. Anne Hedemand's co-authors include Anders D. Børglum, Mette Nyegaard, Ole Mors, Henriette N. Buttenschøn, Ditte Demontis, Jakob Grove, Thomas D. Als, Thomas Werge, Torben A. Kruse and Hans A. Dahl and has published in prestigious journals such as Psychoneuroendocrinology, Human Genetics and Translational Psychiatry.

In The Last Decade

Anne Hedemand

11 papers receiving 191 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne Hedemand Denmark 8 90 61 31 25 23 11 196
Helene Dukal Germany 7 82 0.9× 39 0.6× 17 0.5× 31 1.2× 15 0.7× 11 177
Chuan Jiao China 9 194 2.2× 55 0.9× 25 0.8× 25 1.0× 17 0.7× 14 286
Fiona Middle United Kingdom 8 76 0.8× 56 0.9× 67 2.2× 14 0.6× 14 0.6× 9 215
Fumichika Nishimura Japan 7 105 1.2× 64 1.0× 27 0.9× 29 1.2× 20 0.9× 9 193
Anisha Bhanot United States 4 82 0.9× 66 1.1× 41 1.3× 16 0.6× 17 0.7× 6 219
Mandy Parkinson-Bates Australia 7 199 2.2× 30 0.5× 18 0.6× 42 1.7× 23 1.0× 8 305
Lalit Kaurani Germany 10 207 2.3× 62 1.0× 55 1.8× 60 2.4× 34 1.5× 16 387
Aaron D. Besterman United States 10 110 1.2× 130 2.1× 45 1.5× 18 0.7× 16 0.7× 24 338
María de los Ángeles Robinson‐Agramonte Cuba 8 57 0.6× 67 1.1× 47 1.5× 26 1.0× 19 0.8× 21 293
Ivana Furač Croatia 10 91 1.0× 142 2.3× 60 1.9× 30 1.2× 33 1.4× 20 290

Countries citing papers authored by Anne Hedemand

Since Specialization
Citations

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

Fields of papers citing papers by Anne Hedemand

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Hedemand

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

All Works

11 of 11 papers shown
1.
Buttenschøn, Henriette N., Anne Hedemand, Marit N. Nielsen, et al.. (2016). Association between genes on chromosome 19p13.2 and panic disorder. Psychiatric Genetics. 26(6). 287–292. 7 indexed citations
2.
Starnawska, Anna, Ditte Demontis, Anne Hedemand, et al.. (2016). CACNA1C hypermethylation is associated with bipolar disorder. Translational Psychiatry. 6(6). e831–e831. 35 indexed citations
3.
Lescai, Francesco, Jieqin Liang, Qibin Li, et al.. (2016). Whole‐exome sequencing implicatesDGKHas a risk gene for panic disorder in the Faroese population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(8). 1013–1022. 10 indexed citations
4.
Debost, Jean-Christophe, Liselotte Petersen, Jakob Grove, et al.. (2015). Investigating interactions between early life stress and two single nucleotide polymorphisms in HSD11B2 on the risk of schizophrenia. Psychoneuroendocrinology. 60. 18–27. 7 indexed citations
5.
Buttenschøn, Henriette N., Anne Hedemand, Hans A. Dahl, et al.. (2013). Are TMEM genes potential candidate genes for panic disorder?. Psychiatric Genetics. 24(1). 37–41. 8 indexed citations
6.
Nyegaard, Mette, Ditte Demontis, Anne Hedemand, et al.. (2012). No association of polymorphisms in human endogenous retrovirus K18 and CD48 with schizophrenia. Psychiatric Genetics. 22(3). 146–148. 9 indexed citations
7.
Demontis, Ditte, Mette Nyegaard, Jane Christensen, et al.. (2011). The gene encoding the melanin-concentrating hormone receptor 1 is associated with schizophrenia in a Danish case–control sample. Psychiatric Genetics. 22(2). 62–69. 7 indexed citations
8.
Demontis, Ditte, Mette Nyegaard, Henriette N. Buttenschøn, et al.. (2011). Association of GRIN1 and GRIN2A‐D With schizophrenia and genetic interaction with maternal herpes simplex virus‐2 infection affecting disease risk. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(8). 913–922. 39 indexed citations
9.
Dahl, Hans A., Henriette N. Buttenschøn, Mette Nyegaard, et al.. (2011). A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene. European Journal of Human Genetics. 20(1). 84–90. 33 indexed citations
10.
Christensen, Ulla, Mette Nyegaard, Annette Haagerup, et al.. (2009). Linkage of atopic dermatitis to chromosomes 4q22, 3p24 and 3q21. Human Genetics. 126(4). 549–557. 12 indexed citations
11.
Nexø, Bjørn A., Ulla Vogel, Anja Olsen, et al.. (2008). Linkage disequilibrium mapping of a breast cancer susceptibility locus near RAI/PPP1R13L/iASPP. BMC Medical Genetics. 9(1). 56–56. 29 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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