Astrid Rasmussen

10.0k total citations · 2 hit papers
76 papers, 4.1k citations indexed

About

Astrid Rasmussen is a scholar working on Physiology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Astrid Rasmussen has authored 76 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Physiology, 28 papers in Molecular Biology and 27 papers in Cellular and Molecular Neuroscience. Recurrent topics in Astrid Rasmussen's work include Genetic Neurodegenerative Diseases (24 papers), Mitochondrial Function and Pathology (22 papers) and Salivary Gland Disorders and Functions (22 papers). Astrid Rasmussen is often cited by papers focused on Genetic Neurodegenerative Diseases (24 papers), Mitochondrial Function and Pathology (22 papers) and Salivary Gland Disorders and Functions (22 papers). Astrid Rasmussen collaborates with scholars based in United States, Mexico and Japan. Astrid Rasmussen's co-authors include R. Hal Scofield, Marc Labétoulle, Xavier Mariette, Simon Bowman, Raphaèle Séror, Lindsey A. Criswell, Caroline H. Shiboski, Thomas M. Lietman, Claudio Vitali and Stephen Shiboski and has published in prestigious journals such as Nature Genetics, The Journal of Immunology and PLoS ONE.

In The Last Decade

Astrid Rasmussen

71 papers receiving 4.1k 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.

2016 American College of Rheumatology/European League Against Rheumatism Classification Criteria for Primary Sjögren's Syndrome: A Consensus and Data‐Driven Methodology Involving Three International Patient Cohorts

2016 1.1k citations Astrid Rasmussen, R. Hal Scofield et al. profile →
2016 American College of Rheumatology/European League Against Rheumatism classification criteria for primary Sjögren's syndrome

2016 928 citations Astrid Rasmussen, R. Hal Scofield et al. Annals of the Rheumatic Diseases profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Astrid Rasmussen United States	27	2.0k	1.4k	1.1k	832	778	76	4.1k
Sonye K. Danoff United States	44	1.2k 0.6×	1.7k 1.2×	468 0.4×	491 0.6×	1.4k 1.8×	115	6.7k
Sakamuri V. Reddy United States	32	698 0.3×	1.3k 0.9×	337 0.3×	448 0.5×	393 0.5×	58	2.9k
Thierry Maisonobe France	47	555 0.3×	1.3k 1.0×	1.9k 1.8×	555 0.7×	1.2k 1.5×	195	5.9k
Akihiro Yasoda Japan	32	429 0.2×	1.4k 1.0×	125 0.1×	362 0.4×	390 0.5×	114	3.6k
Julie Wheway Australia	14	573 0.3×	352 0.3×	206 0.2×	223 0.3×	436 0.6×	15	2.5k
Steven Mumm United States	35	343 0.2×	2.2k 1.6×	246 0.2×	345 0.4×	1.3k 1.7×	126	5.2k
K C Flanders United States	27	566 0.3×	1.7k 1.2×	344 0.3×	264 0.3×	257 0.3×	33	3.8k
Anna Spada Italy	46	323 0.2×	2.6k 1.9×	445 0.4×	1.2k 1.4×	337 0.4×	172	7.0k
Y Ohsugi Japan	20	374 0.2×	1.1k 0.8×	138 0.1×	138 0.2×	555 0.7×	38	3.1k
Laurent Magy France	31	479 0.2×	587 0.4×	1.4k 1.3×	135 0.2×	236 0.3×	165	3.8k

Countries citing papers authored by Astrid Rasmussen

Since Specialization

Citations

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

Fields of papers citing papers by Astrid Rasmussen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Astrid Rasmussen

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

Kurien, Biji T., John A. Ice, Rebecca Wood, et al.. (2025). Mitochondrial dysfunction and fatigue in Sjögren’s disease. RMD Open. 11(2). e005046–e005046.

Espinosa‐Gongora, Carmen, Henrik Hasman, Joana Mourão, et al.. (2025). Evaluation of four DNA extraction kits for implementation of nanopore sequencing in routine surveillance of antimicrobial resistance in low-resource settings. Frontiers in Microbiology. 16. 1715467–1715467.

McFarland, Karen N., Anjana Tiwari, Vera I. Hashem, et al.. (2024). Extended haplotype with rs41524547-G defines the ancestral origin of SCA10. Human Molecular Genetics. 33(18). 1567–1574. 3 indexed citations

Khatri, Bhuwan, Constantin Georgescu, Christina Lawrence, et al.. (2023). Autoantibodies identify primary Sjögren's syndrome in patients lacking serum IgG specific for Ro/SS-A and La/SS-B. Annals of the Rheumatic Diseases. 82(9). 1181–1190. 10 indexed citations

Rasmussen, Astrid, Chuang Li, Nathan Pezant, et al.. (2023). Multiple Correspondence Analysis and HLA-Associations of Organ Involvement in a Large Cohort of African-American and European-American Patients with Sarcoidosis. Lung. 201(3). 297–302. 4 indexed citations

Scofield, R. Hal, Rohan Sharma, Teresa Aberle, et al.. (2023). Impact of race and ethnicity on family participation in systemic lupus erythematosus genetic studies. 1. 3 indexed citations

Garman, Lori, Nathan Pezant, Astrid Rasmussen, et al.. (2022). Novel HLA associations with outcomes of Mycobacterium tuberculosis exposure and sarcoidosis in individuals of African ancestry using nearest‐neighbor feature selection. Genetic Epidemiology. 46(7). 463–474. 7 indexed citations

Hernandez‐Castillo, Carlos R., Rosalinda Díaz, Aurelio Campos‐Romo, et al.. (2019). Extensive cerebellar and thalamic degeneration in spinocerebellar ataxia type 10. Parkinsonism & Related Disorders. 66. 182–188. 17 indexed citations

Szczerba, Barbara M., Paulina Kapłonek, Nina Wolska, et al.. (2015). Interaction between innate immunity and Ro52-induced antibody causes Sjögren's syndrome-like disorder in mice. Annals of the Rheumatic Diseases. 75(3). 617–622. 44 indexed citations

10.

Chacón‐Camacho, Oscar F., et al.. (2010). Clinical and molecular features of familial and sporadic cases of von Hippel‐Lindau disease from Mexico. Clinical and Experimental Ophthalmology. 38(3). 277–283. 6 indexed citations

11.

Alonso, María Elisa, Adriana Ochoa, Ana Luisa Sosa, et al.. (2009). Presymptomatic Diagnosis in Huntington's Disease: The Mexican Experience. Genetic Testing and Molecular Biomarkers. 13(6). 717–720. 19 indexed citations

12.

Bai, Dongsheng, Julia N. Bailey, Reyna M. Durón, et al.. (2008). DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy. Epilepsia. 50(5). 1184–1190. 11 indexed citations

13.

López, Marisol, Jorge Guerrero, Petra Yescas, et al.. (2007). Apolipoprotein E ε4 allele is associated with Parkinson disease risk in a Mexican Mestizo population. Movement Disorders. 22(3). 417–420. 19 indexed citations

14.

Suzuki, Toshimitsu, Antonio V. Delgado‐Escueta, María Elisa Alonso, et al.. (2006). Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy. Neuroscience Letters. 405(1-2). 126–131. 11 indexed citations

15.

Matsuura, Tohru, Ping Fang, Xi Lin, et al.. (2004). Somatic and Germline Instability of the ATTCT Repeat in Spinocerebellar Ataxia Type 10. The American Journal of Human Genetics. 74(6). 1216–1224. 47 indexed citations

16.

Fernández-Ruíz, Juan, Rosalinda Díaz, Patricia Vergara Aragón, et al.. (2003). Olfactory dysfunction in hereditary ataxia and basal ganglia disorders. Neuroreport. 14(10). 1339–1341. 33 indexed citations

17.

Suzuki, Toshimitsu, Ryoji Morita, Yoshihisa Sugimoto, et al.. (2002). Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11–p12: LRRC1, GCLC, KIAA0057 and CLIC5. Epilepsy Research. 50(3). 265–275. 10 indexed citations

18.

Rasmussen, Astrid & Elisa Alonso. (2002). El diagnóstico predictivo genético y sus implicaciones. Redalyc (Universidad Autónoma del Estado de México). 25(1). 9–13. 3 indexed citations

19.

Matsuura, Tohru, Takanori Yamagata, Daniel L. Burgess, et al.. (2000). Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nature Genetics. 26(2). 191–194. 370 indexed citations

20.

Rasmussen, Astrid, et al.. (2000). Huntington Disease in Children: Genotype-Phenotype Correlation. Neuropediatrics. 31(4). 190–194. 58 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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