Birgitte Bertelsen

1.0k total citations · 1 hit paper
26 papers, 525 citations indexed

About

Birgitte Bertelsen is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Birgitte Bertelsen has authored 26 papers receiving a total of 525 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Birgitte Bertelsen's work include Obsessive-Compulsive Spectrum Disorders (6 papers), Genetic factors in colorectal cancer (6 papers) and Cancer Genomics and Diagnostics (4 papers). Birgitte Bertelsen is often cited by papers focused on Obsessive-Compulsive Spectrum Disorders (6 papers), Genetic factors in colorectal cancer (6 papers) and Cancer Genomics and Diagnostics (4 papers). Birgitte Bertelsen collaborates with scholars based in Denmark, United States and United Kingdom. Birgitte Bertelsen's co-authors include Zeynep Tümer, Karen Brøndum‐Nielsen, Finn Cilius Nielsen, Kirstine Ravn, Nanette Mol Debes, Lusine Nazaryan‐Petersen, Liselotte Skov, Miyako Kodama, Frederik Otzen Bagger and Line Borgwardt and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Neurobiology of Aging.

In The Last Decade

Birgitte Bertelsen

26 papers receiving 510 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.

Whole genome sequencing in clinical practice

2024 56 citations Frederik Otzen Bagger, Line Borgwardt et al. BMC Medical Genomics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Birgitte Bertelsen Denmark	13	244	195	73	67	63	26	525
Angélica Oviedo United States	13	273 1.1×	133 0.7×	39 0.5×	33 0.5×	78 1.2×	27	923
Samira Ismail Egypt	13	363 1.5×	252 1.3×	72 1.0×	50 0.7×	31 0.5×	46	600
Immaculada Ponsa Spain	9	156 0.6×	161 0.8×	73 1.0×	56 0.8×	50 0.8×	16	380
James Colley United Kingdom	8	241 1.0×	383 2.0×	48 0.7×	79 1.2×	61 1.0×	13	539
Maria Descartes United States	16	399 1.6×	431 2.2×	37 0.5×	19 0.3×	32 0.5×	34	720
Oana Caluseriu Canada	14	583 2.4×	389 2.0×	74 1.0×	48 0.7×	87 1.4×	37	876
Sue Holder United Kingdom	7	318 1.3×	228 1.2×	27 0.4×	45 0.7×	21 0.3×	12	573
C.T. Falk United States	11	320 1.3×	547 2.8×	25 0.3×	74 1.1×	49 0.8×	21	859
Wang Ch Taiwan	9	420 1.7×	308 1.6×	22 0.3×	45 0.7×	27 0.4×	41	767
Patricia I. Bader United States	18	619 2.5×	584 3.0×	38 0.5×	18 0.3×	27 0.4×	32	1.1k

Countries citing papers authored by Birgitte Bertelsen

Since Specialization

Citations

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

Fields of papers citing papers by Birgitte Bertelsen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Birgitte Bertelsen

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

Borregaard, Britt, et al.. (2024). Challenges and benefits of using the HeartDiet food frequency questionnaire in cardiac rehabilitation practice. Nutrition Metabolism and Cardiovascular Diseases. 34(8). 1968–1975. 1 indexed citations

Bagger, Frederik Otzen, et al.. (2024). Whole genome sequencing in clinical practice. BMC Medical Genomics. 17(1). 39–39. 56 indexed citations breakdown →

Jelsig, Anne Marie, Thomas van Overeem Hansen, Niels Qvist, et al.. (2023). Survival, surveillance, and genetics in patients with Peutz–Jeghers syndrome: A nationwide study. Clinical Genetics. 104(1). 81–89. 7 indexed citations

Bertelsen, Birgitte, Karin Wadt, Iben Spanggaard, et al.. (2023). New pathogenic germline variants identified in mesothelioma. Lung Cancer. 179. 107172–107172. 3 indexed citations

Jelsig, Anne Marie, Thomas van Overeem Hansen, Niels Qvist, et al.. (2023). Whole genome sequencing and disease pattern in patients with juvenile polyposis syndrome: a nationwide study. Familial Cancer. 22(4). 429–436. 5 indexed citations

Heydorn, Arne, et al.. (2023). Thyrotoxic periodic paralysis in a Caucasian man without identifiable genetic predisposition: a case report. Thyroid Research. 16(1). 10–10. 2 indexed citations

Jelsig, Anne Marie, Birgitte Bertelsen, Isabel Forss, & John Gásdal Karstensen. (2020). Two cases of somatic STK11 mosaicism in Danish patients with Peutz–Jeghers syndrome. Familial Cancer. 20(1). 55–59. 11 indexed citations

Higgs, Martin R., Maria Rossing, Birgitte Bertelsen, et al.. (2020). Germline RBBP8 variants associated with early-onset breast cancer compromise replication fork stability. Journal of Clinical Investigation. 130(8). 4069–4080. 20 indexed citations

Bertelsen, Birgitte, Christina W. Yde, Miglė Gabrielaitė, et al.. (2019). High frequency of pathogenic germline variants within homologous recombination repair in patients with advanced cancer. npj Genomic Medicine. 4(1). 13–13. 54 indexed citations

10.

Lei, Ulrikke, et al.. (2019). Novel SUFU Frameshift Variant Leading to Meningioma in Three Generations in a Family with Gorlin Syndrome. SHILAP Revista de lepidopterología. 2019(1). 9650184–9650184. 8 indexed citations

11.

Nazaryan‐Petersen, Lusine, Birgitte Bertelsen, Mads Bak, et al.. (2016). Germline Chromothripsis Driven by L1-Mediated Retrotransposition and Alu/Alu Homologous Recombination. Human Mutation. 37(4). 385–395. 42 indexed citations

12.

Padmanabhuni, Shanmukha Sampath, Ann-Louise Esserlind, Jes Olesen, et al.. (2016). Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort. Frontiers in Neuroscience. 10. 531–531. 5 indexed citations

13.

Bertelsen, Birgitte, Lusine Nazaryan‐Petersen, Wei Sun, et al.. (2015). A germline chromothripsis event stably segregating in 11 individuals through three generations. Genetics in Medicine. 18(5). 494–500. 54 indexed citations

14.

Roos, Laura, Birgitte Bertelsen, Pernille Harris, et al.. (2015). Case report: a novel KERA mutation associated with cornea plana and its predicted effect on protein function. BMC Medical Genetics. 16(1). 40–40. 8 indexed citations

15.

Bertelsen, Birgitte, Bob Oranje, Birgitte Fagerlund, et al.. (2015). Association Study of CHRNA7 Promoter Variants with Sensory and Sensorimotor Gating in Schizophrenia Patients and Healthy Controls: A Danish Case–Control Study. NeuroMolecular Medicine. 17(4). 423–430. 21 indexed citations

16.

Bertelsen, Birgitte, Linea Cecilie Melchior, Lars R. Jensen, et al.. (2014). A t(3;9)(q25.1;q34.3) translocation leading to OLFM1 fusion transcripts in Gilles de la Tourette syndrome, OCD and ADHD. Psychiatry Research. 225(3). 268–275. 13 indexed citations

17.

Bertelsen, Birgitte, Lars R. Jensen, Birte Glenthøj, et al.. (2014). Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome. European Journal of Human Genetics. 22(11). 1283–1289. 56 indexed citations

18.

Bertelsen, Birgitte, Nanette Mol Debes, Liselotte Skov, et al.. (2013). Microduplication of 15q13.3 and Xq21.31 in a family with tourette syndrome and comorbidities. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(8). 825–831. 26 indexed citations

19.

Bertelsen, Birgitte, Zeynep Tümer, & Kirstine Ravn. (2011). Three New Loci for Determining X Chromosome Inactivation Patterns. Journal of Molecular Diagnostics. 13(5). 537–540. 37 indexed citations

20.

Tümer, Zeynep, Birgitte Bertelsen, Ole Gredal, et al.. (2011). A novel heterozygous nonsense mutation of the OPTN gene segregating in a Danish family with ALS. Neurobiology of Aging. 33(1). 208.e1–208.e5. 46 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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