Fedik Rahimov

10.2k total citations
24 papers, 1.7k citations indexed

About

Fedik Rahimov is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Fedik Rahimov has authored 24 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Surgery. Recurrent topics in Fedik Rahimov's work include Muscle Physiology and Disorders (11 papers), Craniofacial Disorders and Treatments (6 papers) and RNA modifications and cancer (5 papers). Fedik Rahimov is often cited by papers focused on Muscle Physiology and Disorders (11 papers), Craniofacial Disorders and Treatments (6 papers) and RNA modifications and cancer (5 papers). Fedik Rahimov collaborates with scholars based in United States, Brazil and United Kingdom. Fedik Rahimov's co-authors include Louis M. Kunkel, Jeffrey C. Murray, Astanand Jugessur, Charles P. Emerson, Kathryn R. Wagner, Oliver D. King, Carrie Aldrich, Inna Chervoneva, Heather Gray and Carole Ober and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Fedik Rahimov

23 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fedik Rahimov United States 19 1.1k 627 278 211 189 24 1.7k
Anthonie J. van Essen Netherlands 27 1.4k 1.2× 920 1.5× 156 0.6× 221 1.0× 56 0.3× 49 2.3k
Louise Brueton United Kingdom 24 908 0.8× 604 1.0× 198 0.7× 154 0.7× 91 0.5× 34 1.5k
Michel van Geel Netherlands 26 1.5k 1.3× 616 1.0× 105 0.4× 89 0.4× 77 0.4× 93 2.1k
Stephen B. Ting Australia 22 1.3k 1.2× 256 0.4× 174 0.6× 173 0.8× 335 1.8× 56 2.1k
Caroline Rooryck France 25 1.0k 0.9× 668 1.1× 156 0.6× 164 0.8× 61 0.3× 75 1.9k
Luigi Warren United States 8 2.3k 2.0× 330 0.5× 178 0.6× 372 1.8× 149 0.8× 10 2.6k
Kirsten S. Sigrist United States 14 1.9k 1.7× 495 0.8× 52 0.2× 399 1.9× 201 1.1× 17 2.4k
Holger Kulessa United States 13 1.2k 1.0× 190 0.3× 117 0.4× 144 0.7× 282 1.5× 13 1.7k
Marilyn Travis United States 19 920 0.8× 320 0.5× 234 0.8× 195 0.9× 843 4.5× 20 2.2k
Gérard Tachdjian France 28 1.5k 1.3× 973 1.6× 483 1.7× 780 3.7× 107 0.6× 113 3.4k

Countries citing papers authored by Fedik Rahimov

Since Specialization
Citations

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

Fields of papers citing papers by Fedik Rahimov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fedik Rahimov

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

All Works

20 of 20 papers shown
1.
Ideozu, Justin E., Mengzhen Liu, Bridget Riley‐Gillis, et al.. (2024). Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequences. Genome Medicine. 16(1). 43–43. 10 indexed citations
2.
Stolzenburg, Lindsay R., Sahar Esmaeeli, Ameya Kulkarni, et al.. (2023). Functional characterization of a single nucleotide polymorphism associated with Alzheimer’s disease in a hiPSC-based neuron model. PLoS ONE. 18(9). e0291029–e0291029. 1 indexed citations
3.
Palmer, Nathan, Jocelyn A. Silvester, Jessica J. Lee, et al.. (2019). Concordance between gene expression in peripheral whole blood and colonic tissue in children with inflammatory bowel disease. PLoS ONE. 14(10). e0222952–e0222952. 33 indexed citations
4.
Lek, Angela, Jeffrey J. Widrick, Hiroaki Mitsuhashi, et al.. (2018). Transgenic zebrafish model of DUX4 misexpression reveals a developmental role in FSHD pathogenesis. Human Molecular Genetics. 28(2). 320–331. 12 indexed citations
5.
Alexander, Matthew S., Anete Rozkalne, Alessandro Colletta, et al.. (2016). CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular Dystrophies. Cell stem cell. 19(6). 800–807. 83 indexed citations
6.
Lek, Angela, Fedik Rahimov, Peter L. Jones, & Louis M. Kunkel. (2015). Emerging preclinical animal models for FSHD. Trends in Molecular Medicine. 21(5). 295–306. 34 indexed citations
7.
Alexander, Matthew S., Juan Carlos Casar, Norio Motohashi, et al.. (2014). MicroRNA-486–dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy–associated symptoms. Journal of Clinical Investigation. 124(6). 2651–2667. 119 indexed citations
8.
Zhang, Tracy, Oliver D. King, Fedik Rahimov, et al.. (2014). Human skeletal muscle xenograft as a new preclinical model for muscle disorders. Human Molecular Genetics. 23(12). 3180–3188. 43 indexed citations
9.
Fakhouri, Walid D., Fedik Rahimov, Catia Attanasio, et al.. (2014). An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects. Human Molecular Genetics. 23(10). 2711–2720. 41 indexed citations
10.
Stadler, Guido, Fedik Rahimov, Oliver D. King, et al.. (2013). Telomere position effect regulates DUX4 in human facioscapulohumeral muscular dystrophy. Nature Structural & Molecular Biology. 20(6). 671–678. 82 indexed citations
11.
Mitsuhashi, Satomi, Steven E. Boyden, Elicia Estrella, et al.. (2013). Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2. Neuromuscular Disorders. 23(12). 975–980. 31 indexed citations
12.
Jones, Takako I., Jennifer C. J. Chen, Fedik Rahimov, et al.. (2012). Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis. Human Molecular Genetics. 21(20). 4419–4430. 139 indexed citations
13.
Eran, Alal, Jin Billy Li, Jillian McCarthy, et al.. (2012). Comparative RNA editing in autistic and neurotypical cerebella. Molecular Psychiatry. 18(9). 1041–1048. 56 indexed citations
14.
Homma, Sachiko, Jennifer C. J. Chen, Fedik Rahimov, et al.. (2011). A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function. European Journal of Human Genetics. 20(4). 404–410. 55 indexed citations
15.
Rahimov, Fedik, et al.. (2011). Gene expression profiling of skeletal muscles treated with a soluble activin type IIB receptor. Physiological Genomics. 43(8). 398–407. 45 indexed citations
16.
Jugessur, Astanand, Fedik Rahimov, Rolv T. Lie, et al.. (2008). Genetic variants in IRF6 and the risk of facial clefts: single‐marker and haplotype‐based analyses in a population‐based case‐control study of facial clefts in Norway. Genetic Epidemiology. 32(5). 413–424. 80 indexed citations
17.
Rahimov, Fedik, et al.. (2006). GLI2 mutations in four Brazilian patients: How wide is the phenotypic spectrum?. American Journal of Medical Genetics Part A. 140A(23). 2571–2576. 47 indexed citations
18.
Vieira, Alexandre R., Sandra Daack‐Hirsch, Têmis Maria Félix, et al.. (2005). Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate. PLoS Genetics. 1(6). e64–e64. 200 indexed citations
19.
Vieira, Alexandre R., Sandra Daack‐Hirsch, Têmis Maria Félix, et al.. (2005). Direct Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate. PLoS Genetics. preprint(2005). e64–e64. 1 indexed citations
20.
Ober, Carole, Carrie Aldrich, Inna Chervoneva, et al.. (2003). Variation in the HLA-G Promoter Region Influences Miscarriage Rates. The American Journal of Human Genetics. 72(6). 1425–1435. 183 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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