Jacqueline Rimmler

4.1k total citations · 1 hit paper
17 papers, 2.3k citations indexed

About

Jacqueline Rimmler is a scholar working on Molecular Biology, Physiology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Jacqueline Rimmler has authored 17 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Physiology and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Jacqueline Rimmler's work include Alzheimer's disease research and treatments (5 papers), Glaucoma and retinal disorders (3 papers) and Corneal surgery and disorders (3 papers). Jacqueline Rimmler is often cited by papers focused on Alzheimer's disease research and treatments (5 papers), Glaucoma and retinal disorders (3 papers) and Corneal surgery and disorders (3 papers). Jacqueline Rimmler collaborates with scholars based in United States, France and Saudi Arabia. Jacqueline Rimmler's co-authors include Jonathan L. Haines, Ann M. Saunders, Allen D. Roses, Jeffery M. Vance, Elizabeth H. Corder, Warren J. Strittmatter, G. W. Small, P. M. Conneally, P. A. Locke and Ken Schmader and has published in prestigious journals such as Nature Genetics, PLoS ONE and Brain.

In The Last Decade

Jacqueline Rimmler

17 papers receiving 2.2k citations

Hit Papers

Protective effect of apolipoprotein E type 2 allele for l... 1994 2026 2004 2015 1994 400 800 1.2k
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.

  1. Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease
    1994 1.4k citations Elizabeth H. Corder, Ann M. Saunders et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jacqueline Rimmler United States 14 1.2k 709 476 307 272 17 2.3k
Corinne Lendon United Kingdom 31 1.6k 1.3× 993 1.4× 523 1.1× 420 1.4× 427 1.6× 67 3.1k
Eloy Rodríguez‐Rodríguez Spain 27 670 0.6× 700 1.0× 290 0.6× 201 0.7× 138 0.5× 99 1.9k
Ignacio Mateo Spain 25 508 0.4× 619 0.9× 214 0.4× 238 0.8× 111 0.4× 59 1.5k
F. Coria Spain 25 852 0.7× 625 0.9× 347 0.7× 332 1.1× 115 0.4× 61 1.8k
Bhumsoo Kim United States 25 1.0k 0.9× 1.0k 1.4× 106 0.2× 423 1.4× 103 0.4× 37 2.6k
Sadao Takase Japan 19 353 0.3× 466 0.7× 214 0.4× 229 0.7× 50 0.2× 67 1.4k
Jon Infante Spain 34 748 0.6× 1.1k 1.5× 162 0.3× 970 3.2× 175 0.6× 156 3.0k
Cinzia Ferri Italy 20 630 0.5× 576 0.8× 109 0.2× 392 1.3× 61 0.2× 32 1.6k
Giulia Bellini Italy 29 356 0.3× 720 1.0× 240 0.5× 531 1.7× 185 0.7× 56 2.0k
Émilie Faivre France 18 715 0.6× 603 0.9× 104 0.2× 574 1.9× 147 0.5× 29 2.1k

Countries citing papers authored by Jacqueline Rimmler

Since Specialization
Citations

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

Fields of papers citing papers by Jacqueline Rimmler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacqueline Rimmler

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

All Works

17 of 17 papers shown
1.
Li, Yi‐Ju, Mollie Minear, Xuejun Qin, et al.. (2014). Mitochondrial Polymorphism A10398G and Haplogroup I Are Associated With Fuchs' Endothelial Corneal Dystrophy. Investigative Ophthalmology & Visual Science. 55(7). 4577–4577. 16 indexed citations
2.
LaPointe, Nancy M. Allen, Yuliya Lokhnygina, Jacqueline Rimmler, et al.. (2014). Use Of Rate And Rhythm Control Drugs In Patients Younger Than 65 Years With Atrial Fibrillation.. PubMed. 7(1). 1062–1062. 7 indexed citations
3.
Minear, Mollie, Yi‐Ju Li, Jacqueline Rimmler, et al.. (2013). Genetic screen of African Americans with Fuchs endothelial corneal dystrophy.. PubMed. 19. 2508–16. 24 indexed citations
4.
Li, Yi‐Ju, Mollie Minear, Jacqueline Rimmler, et al.. (2011). Replication of TCF4 through Association and Linkage Studies in Late-Onset Fuchs Endothelial Corneal Dystrophy. PLoS ONE. 6(4). e18044–e18044. 64 indexed citations
5.
Ashley‐Koch, Allison E., Yujun Shao, Jacqueline Rimmler, et al.. (2005). An autosomal genomic screen for dementia in an extended Amish family. Neuroscience Letters. 379(3). 199–204. 24 indexed citations
6.
Kenealy, S J, Marie‐Claude Babron, Yvonne M. Bradford, et al.. (2004). A Second-Generation Genomic Screen for Multiple Sclerosis. The American Journal of Human Genetics. 75(6). 1070–1078. 40 indexed citations
7.
Barcellos, Lisa F., Jorge R. Oksenberg, Patricia Bucher, et al.. (2002). Genetic basis for clinical expression in multiple sclerosis. Brain. 125(1). 150–158. 117 indexed citations
8.
Schmidt, Silke, Lisa F. Barcellos, K DeSombre, et al.. (2002). Association of Polymorphisms in the Apolipoprotein E Region with Susceptibility to and Progression of Multiple Sclerosis. The American Journal of Human Genetics. 70(3). 708–717. 104 indexed citations
9.
Siddique, Teepu, Afif Hentati, Guo‐Xiong Deng, et al.. (2002). A molecular genetic approach to amyotrophic lateral sclerosis.. PubMed. 25-26. 60–9. 1 indexed citations
10.
Haines, J. L., Lisa F. Barcellos, Margaret A. Pericak‐Vance, et al.. (2001). Linkage and association analysis of chromosome 19q13 in multiple sclerosis. Neurogenetics. 3(4). 195–201. 28 indexed citations
11.
Green, A. J., Lisa F. Barcellos, Jacqueline Rimmler, et al.. (2001). Sequence variation in the transforming growth factor-β1 (TGFB1) gene and multiple sclerosis susceptibility. Journal of Neuroimmunology. 116(1). 116–124. 26 indexed citations
12.
Barcellos, Lisa F., Anna Maria Schito, Jacqueline Rimmler, et al.. (2000). CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Immunogenetics. 51(4-5). 281–288. 107 indexed citations
13.
Xia, Yu, B.L. Rosi, Larry H. Yamaoka, et al.. (1996). Genetic studies in Alzheimer's disease with an NACP/α‐synuclein polymorphism. Annals of Neurology. 40(2). 207–215. 91 indexed citations
14.
Pericak‐Vance, Margaret A., Christine Cole Johnson, Jacqueline Rimmler, et al.. (1996). Alzheimer's disease and apolipoprotein e‐4 allele in an amish population. Annals of Neurology. 39(6). 700–704. 43 indexed citations
15.
Corder, Elizabeth H., Ann M. Saunders, Warren J. Strittmatter, et al.. (1995). Apolipoprotein E, survival in Alzheimer's disease patients, and the competing risks of death and Alzheimer's disease. Neurology. 45(7). 1323–1328. 138 indexed citations
16.
Corder, Elizabeth H., Ann M. Saunders, Neil Risch, et al.. (1994). Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease. Nature Genetics. 7(2). 180–184. 1414 indexed citations breakdown →
17.
Vance, Jeffery M., Emily Whisenant, Deborah B. Loeb, et al.. (1993). Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26.. Journal of Medical Genetics. 30(6). 487–491. 11 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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