Danique Beijer

1.1k total citations
15 papers, 231 citations indexed

About

Danique Beijer is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Danique Beijer has authored 15 papers receiving a total of 231 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 4 papers in Neurology. Recurrent topics in Danique Beijer's work include Hereditary Neurological Disorders (6 papers), Neurological diseases and metabolism (4 papers) and Genetic Neurodegenerative Diseases (3 papers). Danique Beijer is often cited by papers focused on Hereditary Neurological Disorders (6 papers), Neurological diseases and metabolism (4 papers) and Genetic Neurodegenerative Diseases (3 papers). Danique Beijer collaborates with scholars based in United States, Germany and Belgium. Danique Beijer's co-authors include Jonathan Baets, Peter De Jonghe, Jonas Van Lent, Maike F. Dohrn, Ivan Ahel, Evgeniia Prokhorova, Stephan Züchner, Tine Deconinck, Thomas Agnew and Vincent Timmerman and has published in prestigious journals such as Nature Communications, Molecular Cell and Brain.

In The Last Decade

Danique Beijer

13 papers receiving 231 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Danique Beijer United States	9	124	75	72	33	31	15	231
William M. McKillop United States	9	105 0.8×	21 0.3×	63 0.9×	23 0.7×	35 1.1×	20	254
Meifan Chen United States	8	203 1.6×	50 0.7×	77 1.1×	14 0.4×	68 2.2×	14	321
Matthew Riolo United States	4	202 1.6×	71 0.9×	45 0.6×	33 1.0×	13 0.4×	6	278
Allison Knupp United States	8	153 1.2×	20 0.3×	55 0.8×	34 1.0×	71 2.3×	11	350
Beatrix A. Olofsson United States	5	331 2.7×	62 0.8×	64 0.9×	18 0.5×	25 0.8×	7	390
Vedrana Milić Rašić Serbia	8	151 1.2×	13 0.2×	70 1.0×	17 0.5×	29 0.9×	12	211
Cornelia E. Zorca Canada	10	236 1.9×	38 0.5×	23 0.3×	49 1.5×	35 1.1×	15	356
V Holcombe United States	5	314 2.5×	52 0.7×	79 1.1×	27 0.8×	23 0.7×	7	380
Camilla B. Mitchell Australia	10	164 1.3×	42 0.6×	104 1.4×	7 0.2×	79 2.5×	13	296
Liling Niu China	9	150 1.2×	66 0.9×	38 0.5×	72 2.2×	70 2.3×	12	296

Countries citing papers authored by Danique Beijer

Since Specialization

Citations

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

Fields of papers citing papers by Danique Beijer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Danique Beijer

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

All Works

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15 of 15 papers shown

Lauffer, Marlen C., Kimberly Amburgey, Danique Beijer, et al.. (2025). Screening rare genetic diagnoses for amenability to bespoke antisense oligonucleotide therapy development: A retrospective cohort study. Genetics in Medicine. 28(1). 101597–101597.

Dohrn, Maike F., Güney Bademci, Adriana Rebelo, et al.. (2024). Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism. Annals of Clinical and Translational Neurology. 11(4). 1075–1079. 1 indexed citations

Beijer, Danique, Willem De Ridder, Abigail L. D. Tadenev, et al.. (2024). Dominant NARS1 mutations causing axonal Charcot–Marie–Tooth disease expand NARS1-associated diseases. Brain Communications. 6(2). fcae070–fcae070. 7 indexed citations

Mohassel, Payam, Maike F. Dohrn, Museer A. Lone, et al.. (2023). P169 Childhood onset amyotrophic lateral sclerosis associated with SPTLC2 gain-of-function pathogenic variants: clinical, genetic, and biochemical insights. Neuromuscular Disorders. 33. S107–S107.

Dohrn, Maike F., Danique Beijer, Museer A. Lone, et al.. (2023). Recurrentde-novo gain-of-functionmutation inSPTLC2confirms dysregulated sphingolipid production to cause juvenile amyotrophic lateral sclerosis. Journal of Neurology Neurosurgery & Psychiatry. 95(3). 201–205. 6 indexed citations

Danzi, Matt C., Maike F. Dohrn, Sarah Fazal, et al.. (2023). Deep structured learning for variant prioritization in Mendelian diseases. Nature Communications. 14(1). 4167–4167. 22 indexed citations

Rebelo, Adriana, Maike F. Dohrn, Amjad Farooq, et al.. (2022). BiP inactivation due to loss of the deAMPylation function of FICD causes a motor neuron disease. Genetics in Medicine. 24(12). 2487–2500. 15 indexed citations

Beijer, Danique, Maike F. Dohrn, Sarah Fazal, et al.. (2022). RFC1 repeat expansions: A recurrent cause of sensory and autonomic neuropathy with cough and ataxia. European Journal of Neurology. 29(7). 2156–2161. 14 indexed citations

Beijer, Danique, Thomas Agnew, J.G.M. Rack, et al.. (2021). Biallelic ADPRHL2 mutations in complex neuropathy affect ADP ribosylation and DNA damage response. Life Science Alliance. 4(11). e202101057–e202101057. 16 indexed citations

10.

Prokhorova, Evgeniia, Thomas Agnew, Anne R. Wondisford, et al.. (2021). Unrestrained poly-ADP-ribosylation provides insights into chromatin regulation and human disease. Molecular Cell. 81(12). 2640–2655.e8. 71 indexed citations

11.

Beijer, Danique, Kiran Polavarapu, Veeramani Preethish‐Kumar, et al.. (2021). Homozygous N-terminal missense variant in PLEKHG5 associated with intermediate CMT: A case report. Journal of Neuromuscular Diseases. 9(2). 347–351. 1 indexed citations

12.

Beijer, Danique & Jonathan Baets. (2020). The expanding genetic landscape of hereditary motor neuropathies. Brain. 143(12). 3540–3563. 10 indexed citations

13.

Beijer, Danique, Tine Deconinck, Jan De Bleecker, et al.. (2019). Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy. Brain. 142(9). 2605–2616. 24 indexed citations

14.

Beijer, Danique, et al.. (2019). Defects in Axonal Transport in Inherited Neuropathies. Journal of Neuromuscular Diseases. 6(4). 401–419. 23 indexed citations

15.

Salter, Claire, Danique Beijer, Katy Barwick, et al.. (2018). Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies. Neurology Genetics. 4(2). e222–e222. 21 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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