Trine Bjørg Hammer

789 total citations
14 papers, 215 citations indexed

About

Trine Bjørg Hammer is a scholar working on Genetics, Psychiatry and Mental health and Organic Chemistry. According to data from OpenAlex, Trine Bjørg Hammer has authored 14 papers receiving a total of 215 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 4 papers in Psychiatry and Mental health and 3 papers in Organic Chemistry. Recurrent topics in Trine Bjørg Hammer's work include Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers) and Carbohydrate Chemistry and Synthesis (3 papers). Trine Bjørg Hammer is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers) and Carbohydrate Chemistry and Synthesis (3 papers). Trine Bjørg Hammer collaborates with scholars based in Denmark, United Kingdom and Netherlands. Trine Bjørg Hammer's co-authors include Rikke S. Møller, Bob Oranje, Birte Glenthøj, Guido Rubboli, Katrine M. Johannesen, Johannes R. Lemke, Birgitte Fagerlund, William F.C. Baaré, Christina Fenger and Arnold Skimminge and has published in prestigious journals such as Epilepsia, Acta Paediatrica and The International Journal of Neuropsychopharmacology.

In The Last Decade

Trine Bjørg Hammer

12 papers receiving 215 citations

Peers

Trine Bjørg Hammer

GENET

PMH

PPCH

E. Veneselli Italy

Alya Qari Saudi Arabia

Cheuk Wing Fung China

Sorina Mihaela Papuc Romania

Laura L. Klitten Denmark

Thuy Le United States

Carlotta Stipa Italy

Shiqi Guang China

Silvia Masnada Italy

E. Veneselli Italy

Trine Bjørg Hammer

132 ×1.6

GENET

101 ×1.3

57 ×1.1

PMH

57 ×1.5

20 ×0.8

PPCH

Citations per year, relative to Trine Bjørg Hammer Trine Bjørg Hammer (= 1×) peers E. Veneselli

Countries citing papers authored by Trine Bjørg Hammer

Since Specialization

Citations

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

Fields of papers citing papers by Trine Bjørg Hammer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Trine Bjørg Hammer. 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 Trine Bjørg Hammer. The network helps show where Trine Bjørg Hammer may publish in the future.

Co-authorship network of co-authors of Trine Bjørg Hammer

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

All Works

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14 of 14 papers shown

Khinchi, Marianne Søndergaard, María J. Miranda, Trine Bjørg Hammer, et al.. (2024). Seizure and movement disorder in CACNA1E developmental and epileptic encephalopathy: Two sides of the same coin or same side of two different coins?. Epileptic Disorders. 26(4). 520–526.

Fenger, Christina, Trine Bjørg Hammer, Veronica M. Pravatà, et al.. (2023). An O-GlcNAc transferase pathogenic variant linked to intellectual disability affects pluripotent stem cell self-renewal. Disease Models & Mechanisms. 16(6). 10 indexed citations

Lildballe, Dorte L., Anja Lisbeth Frederiksen, Bitten Schönewolf‐Greulich, et al.. (2023). National clinical Genetic Networks - GENets - Establishment of expert collaborations in Denmark. European Journal of Medical Genetics. 66(12). 104872–104872.

Gardella, Elena, Roberto Michelucci, Christina Fenger, et al.. (2023). IRF2BPL as a novel causative gene for progressive myoclonus epilepsy. Epilepsia. 64(8). e170–e176. 5 indexed citations

Petersen, Esben Thade, Christina Fenger, Mette Cathrine Ørngreen, et al.. (2023). X-linked creatine transporter (SLC6A8) deficiency in females: Difficult to recognize, but a potentially treatable disease. Molecular Genetics and Metabolism. 140(3). 107694–107694. 5 indexed citations

Rasmussen, Maria, Naja Becher, Brian Nauheimer Andersen, et al.. (2021). Phenotypic heterogeneity and mosaicism in Xia-Gibbs syndrome: Five Danish patients with novel variants in AHDC1. European Journal of Medical Genetics. 64(9). 104280–104280. 5 indexed citations

Møller, Rikke S., et al.. (2021). Expansion of the CCDC22 associated Ritscher-Schinzel/3C syndrome and review of the literature: Should the minimal diagnostic criteria be revised?. European Journal of Medical Genetics. 64(7). 104246–104246. 12 indexed citations

Matricardi, Sara, Paola De Liso, Elena Freri, et al.. (2020). Neonatal developmental and epileptic encephalopathy due to autosomal recessive variants in SLC13A5 gene. Epilepsia. 61(11). 2474–2485. 33 indexed citations

Møller, Rikke S., Trine Bjørg Hammer, Guido Rubboli, Johannes R. Lemke, & Katrine M. Johannesen. (2019). From next-generation sequencing to targeted treatment of non-acquired epilepsies. Expert Review of Molecular Diagnostics. 19(3). 217–228. 36 indexed citations

10.

Suri, Mohnish, Archana Desurkar, Gaëtan Lesca, et al.. (2018). SLC35A2-related congenital disorder of glycosylation: Defining the phenotype. European Journal of Paediatric Neurology. 22(6). 1095–1102. 23 indexed citations

11.

Diness, Birgitte Rode, Gritt Overbeck, Tina Duelund Hjortshøj, et al.. (2017). Translation and Adaptation of the Genetic Counselling Outcome Scale (GCOS‐24) for Use in Denmark. Journal of Genetic Counseling. 26(5). 1080–1089. 23 indexed citations

12.

Madsen, Kathrine Skak, William F.C. Baaré, Trine Bjørg Hammer, et al.. (2015). Children and adolescents previously treated with glucocorticoids display lower verbal intellectual abilities. Acta Paediatrica. 104(8). 784–791. 9 indexed citations

13.

Hammer, Trine Bjørg, Bob Oranje, Arnold Skimminge, et al.. (2012). Structural brain correlates of sensorimotor gating in antipsychotic-naive men with first-episode schizophrenia. Journal of Psychiatry and Neuroscience. 38(1). 34–42. 26 indexed citations

14.

Hammer, Trine Bjørg, et al.. (2011). Stability of prepulse inhibition and habituation of the startle reflex in schizophrenia: a 6-year follow-up study of initially antipsychotic-naive, first-episode schizophrenia patients. The International Journal of Neuropsychopharmacology. 14(7). 913–925. 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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