Rachel Soemedi

2.0k total citations
11 papers, 523 citations indexed

About

Rachel Soemedi is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Rachel Soemedi has authored 11 papers receiving a total of 523 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 3 papers in Genetics and 3 papers in Immunology. Recurrent topics in Rachel Soemedi's work include RNA Research and Splicing (6 papers), RNA modifications and cancer (5 papers) and RNA and protein synthesis mechanisms (4 papers). Rachel Soemedi is often cited by papers focused on RNA Research and Splicing (6 papers), RNA modifications and cancer (5 papers) and RNA and protein synthesis mechanisms (4 papers). Rachel Soemedi collaborates with scholars based in United States, United Kingdom and Norway. Rachel Soemedi's co-authors include William G. Fairbrother, Christy L. Rhine, Kamil J. Cygan, Pınar Bayrak‐Toydemir, John Yang, Jamie McDonald, Jing Wang, Susan T. Iannaccone, Pankaj B. Agrawal and Elizabeth T. DeChene and has published in prestigious journals such as Nature Communications, Nature Genetics and PLoS ONE.

In The Last Decade

Rachel Soemedi

11 papers receiving 517 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rachel Soemedi United States 9 405 116 108 61 55 11 523
Pauline A.M. Roest Netherlands 8 281 0.7× 75 0.6× 111 1.0× 25 0.4× 55 1.0× 8 461
Alfons Meindl Germany 11 332 0.8× 41 0.4× 121 1.1× 65 1.1× 27 0.5× 14 490
Suna Önengüt United States 11 396 1.0× 31 0.3× 120 1.1× 47 0.8× 26 0.5× 11 551
Filippo Beleggia Germany 12 243 0.6× 28 0.2× 111 1.0× 16 0.3× 45 0.8× 16 382
Elise R. Pfaltzgraff United States 12 278 0.7× 61 0.5× 42 0.4× 14 0.2× 32 0.6× 17 435
Annemieke H. van der Hout Netherlands 8 227 0.6× 110 0.9× 223 2.1× 29 0.5× 14 0.3× 13 451
Akatsuki Kubota Japan 11 215 0.5× 35 0.3× 26 0.2× 46 0.8× 70 1.3× 35 442
María Roqué Argentina 12 333 0.8× 23 0.2× 66 0.6× 23 0.4× 60 1.1× 37 483
Michelle Nguyen-McCarty United States 7 283 0.7× 21 0.2× 38 0.4× 59 1.0× 31 0.6× 8 398
Nicolas Sylvius United Kingdom 16 522 1.3× 265 2.3× 45 0.4× 30 0.5× 25 0.5× 30 796

Countries citing papers authored by Rachel Soemedi

Since Specialization
Citations

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

Fields of papers citing papers by Rachel Soemedi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rachel Soemedi

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

All Works

11 of 11 papers shown
1.
Clark, Nathaniel E., Chaorui Duan, Allison J. Taggart, et al.. (2024). The debranching enzyme Dbr1 regulates lariat turnover and intron splicing. Nature Communications. 15(1). 4617–4617. 8 indexed citations
2.
Rhine, Christy L., Kamil J. Cygan, Rachel Soemedi, et al.. (2018). Hereditary cancer genes are highly susceptible to splicing mutations. PLoS Genetics. 14(3). e1007231–e1007231. 37 indexed citations
3.
Soemedi, Rachel, Kamil J. Cygan, Christy L. Rhine, et al.. (2017). Pathogenic variants that alter protein code often disrupt splicing. Nature Genetics. 49(6). 848–855. 151 indexed citations
4.
Cygan, Kamil J., Rachel Soemedi, Christy L. Rhine, et al.. (2017). Defective splicing of the RB1 transcript is the dominant cause of retinoblastomas. Human Genetics. 136(9). 1303–1312. 5 indexed citations
5.
Soemedi, Rachel, Kamil J. Cygan, Christy L. Rhine, et al.. (2017). The effects of structure on pre-mRNA processing and stability. Methods. 125. 36–44. 36 indexed citations
6.
Soemedi, Rachel, Hugo Vega, Judson Belmont, Sohini Ramachandran, & William G. Fairbrother. (2014). Genetic Variation and RNA Binding Proteins: Tools and Techniques to Detect Functional Polymorphisms. Advances in experimental medicine and biology. 825. 227–266. 10 indexed citations
7.
Töpf, Ana, Helen Griffin, Elise Glen, et al.. (2014). Functionally Significant, Rare Transcription Factor Variants in Tetralogy of Fallot. PLoS ONE. 9(8). e95453–e95453. 46 indexed citations
8.
Soemedi, Rachel, Jonathan M. Levine, Sarah Geisler, et al.. (2014). Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development. Congenital Heart Disease. 10(3). 193–208. 21 indexed citations
9.
Ceyhan‐Birsoy, Ozge, Pankaj B. Agrawal, Carlos Hidalgo, et al.. (2013). Recessive truncating titin gene, TTN , mutations presenting as centronuclear myopathy. Neurology. 81(14). 1205–1214. 147 indexed citations
10.
Mitchell, Anna L., Heather J. Cordell, Rachel Soemedi, et al.. (2009). Programmed Death Ligand 1 (PD-L1) Gene Variants Contribute to Autoimmune Addison’s Disease and Graves’ Disease Susceptibility. Molecular Endocrinology. 23(11). 1935–1935. 3 indexed citations
11.
Mitchell, Anna L., Heather J. Cordell, Rachel Soemedi, et al.. (2009). Programmed Death Ligand 1 (PD-L1) Gene Variants Contribute to Autoimmune Addison’s Disease and Graves’ Disease Susceptibility. The Journal of Clinical Endocrinology & Metabolism. 94(12). 5139–5145. 59 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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