Fedik Rahimov

10.2k citations

24 papers · 1.7k indexed · h-index 19

Genetics top 5%
- Craniofacial Disorders and Treatments 6
- Cleft Lip and Palate Research 5
- Genomics and Rare Diseases 2
Genetics top 5%
- Craniofacial Disorders and Treatments 6
- Cleft Lip and Palate Research 5
- Genomics and Rare Diseases 2
Aging top 10%
Molecular Biology top 10%
- Muscle Physiology and Disorders 11
- RNA modifications and cancer 5
- RNA Research and Splicing 5
- dental development and anomalies 3
Immunology
Surgery
- Tissue Engineering and Regenerative Medicine 2

Co-authors: Louis M. Kunkel Jeffrey C. Murray Astanand Jugessur Charles P. Emerson Kathryn R. Wagner Oliver D. King Carrie Aldrich Inna Chervoneva
Cited by: Genetics Aging Molecular Biology
Journals: Human Molecular Genetics (4 papers)PLoS Genetics (2 papers)PLoS ONE (2 papers)
Partner nations: United States Brazil United Kingdom

In The Last Decade

Fedik Rahimov

23 papers receiving 1.7k citations

Peers

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

The 25 scholars most cited alongside Fedik Rahimov, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Fedik Rahimov Line = papers co-authored together Fedik Rahimov links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequences Genome Medicine ·Justin E. Ideozu,Mengzhen Liu,Bridget Riley‐Gillis,Sara Henein,Fedik Rahimov,Preethi Krishnan,Rakesh Tripathi,Patrick Dorr,Hara Levy,Ashvani K. Singh,Jeffrey F. Waring,Aparna Vasanthakumar	2024	10
2	Functional characterization of a single nucleotide polymorphism associated with Alzheimer’s disease in a hiPSC-based neuron model PLoS ONE ·Lindsay R. Stolzenburg,Sahar Esmaeeli,Ameya Kulkarni,Erin Murphy,Taekyung Kwon,WeiZhong ZHAO,Christopher Gillies,Joshua D. Stender,Sung Eun Kim,Peter Reinhardt,Fedik Rahimov,Jeffrey F. Waring,Cyril Y. Ramathal	2023	1
3	Concordance between gene expression in peripheral whole blood and colonic tissue in children with inflammatory bowel disease PLoS ONE ·Nathan Palmer,Jocelyn A. Silvester,Jessica J. Lee,Andrew L. Beam,Inbar Fried,Vladimir I. Valtchinov,Fedik Rahimov,Sek Won Kong,Saum Ghodoussipour,Cecilia Fonseca Rivera,Athos Bousvaros,Richard J. Grand,Louis M. Kunkel,Isaac S. Kohane	2019	33
4	Transgenic zebrafish model of DUX4 misexpression reveals a developmental role in FSHD pathogenesis Human Molecular Genetics ·Козлов Сергей Николаевич,Angela Lek,Jeffrey J. Widrick,Hiroaki Mitsuhashi,Camila Ferreira de Ascenção,Vandana Gupta,Fedik Rahimov,Md. Nurul Absar Chowdhury,Tracy Zhang,Devin Gibbs,Karen D. Antinyan,Jéssica Cristina Da Costa,shahrbanoo khoshkab,Louis M. Kunkel	2018	12
5	CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular Dystrophies Cell stem cell ·Matthew S. Alexander,Anete Rozkalne,Alessandro Colletta,Janelle M. Spinazzola,Samuel Johnson,Fedik Rahimov,Hui Meng,Michael W. Lawlor,Elicia Estrella,Louis M. Kunkel,Emanuela Gussoni	2016	83
6	Emerging preclinical animal models for FSHD Trends in Molecular Medicine ·Angela Lek,Fedik Rahimov,Peter L. Jones,Louis M. Kunkel	2015	34
7	MicroRNA-486–dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy–associated symptoms Journal of Clinical Investigation ·Matthew S. Alexander,Juan Carlos Casar,Norio Motohashi,Natássia M. Vieira,Iris Eisenberg,Jamie L. Marshall,Molly Gasperini,Angela Lek,Jennifer A. Myers,Elicia Estrella,Peter B. Kang,Frederic Shapiro,Fedik Rahimov,Genri Kawahara,Jeffrey J. Widrick,Louis M. Kunkel	2014	119
8	Human skeletal muscle xenograft as a new preclinical model for muscle disorders Human Molecular Genetics ·Tracy Zhang,Oliver D. King,Fedik Rahimov,Takako I. Jones,Christopher W. Ward,Jaclyn P. Kerr,Nan Liu,Charles P. Emerson,Louis M. Kunkel,Terence A. Partridge,Kathryn R. Wagner	2014	43
9	An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects Human Molecular Genetics ·Walid D. Fakhouri,Fedik Rahimov,Catia Attanasio,Evelyn N. Kouwenhoven,Caldarera R,Têmis Maria Félix,Larissa Nitschke,Marta Aparecida Ribeiro,Edith Côté,Youssef A. Kousa,直践河野,L Pennacchio,Hans van Bokhoven,Axel Visel,Huiqing Zhou,Jeffrey C. Murray,Brian C. Schutte	2014	41
10	Telomere position effect regulates DUX4 in human facioscapulohumeral muscular dystrophy Nature Structural & Molecular Biology ·Guido Stadler,Fedik Rahimov,Oliver D. King,Jennifer C. J. Chen,Jérôme D. Robin,Kathryn R. Wagner,Jerry W. Shay,Charles P. Emerson,Woodring E. Wright	2013	82
11	Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2 Neuromuscular Disorders ·Satomi Mitsuhashi,Steven E. Boyden,Elicia Estrella,Takako I. Jones,Fedik Rahimov,Timothy W. Yu,Basil T. Darras,Anthony A. Amato,Rebecca D. Folkerth,Peter L. Jones,Louis M. Kunkel,Peter B. Kang	2013	31
12	Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis Human Molecular Genetics ·Takako I. Jones,Jennifer C. J. Chen,Fedik Rahimov,Sachiko Homma,W. Lin,Mary Lou Beermann,Oliver D. King,Jeffrey B. Miller,Louis M. Kunkel,Charles P. Emerson,Kathryn R. Wagner,Peter L. Jones	2012	139
13	Comparative RNA editing in autistic and neurotypical cerebella Molecular Psychiatry ·Alal Eran,Jin Billy Li,Anna Löfgren Burström,Jillian McCarthy,Fedik Rahimov,Christin Collins,Kyriacos Markianos,David Margulies,Emery N. Brown,Sarah E. Calvo,Isaac S. Kohane,Louis M. Kunkel	2012	56
14	A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function European Journal of Human Genetics ·Sachiko Homma,Jennifer C. J. Chen,Fedik Rahimov,Mary Lou Beermann,Emil Dietz Fuglsang,Genila Bibat,Kathryn R. Wagner,Louis M. Kunkel,Charles P. Emerson,Jeffrey B. Miller	2011	55
15	Gene expression profiling of skeletal muscles treated with a soluble activin type IIB receptor Physiological Genomics ·Fedik Rahimov,Oliver D. King,Miquel Solé Inarejos,عباس اسفندیاری خالدی,Charles P. Emerson,Louis M. Kunkel,Kathryn R. Wagner	2011	45
16	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 ·Astanand Jugessur,Fedik Rahimov,Rolv T. Lie,Allen J. Wilcox,Håkon K. Gjessing,Roy M. Nilsen,Taghi Agha Hoseyni,Jeffrey C. Murray	2008	80
17	GLI2 mutations in four Brazilian patients: How wide is the phenotypic spectrum? American Journal of Medical Genetics Part A ·Fedik Rahimov,Lucilene Arilho Ribeiro,E. R. Waring,Antônio Richieri‐Costa,Jeffrey C. Murray	2006	47
18	Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate PLoS Genetics ·Alexandre R. Vieira,刘伟良,Sandra Daack‐Hirsch,Bárbara Marina da Silva Pinho,Têmis Maria Félix,Fedik Rahimov,박응렬,Pierre Gosselin,Yoriko Watanabe,Marla Johnson,Jennifer S. Fang,Sarah O’Brien,Iêda M. Orioli,Eduardo E. Castilla,David Fitzpatrick,Rulang Jiang,Mary L. Marazita,Jeffrey C. Murray	2005	200
19	Direct Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate PLoS Genetics ·Alexandre R. Vieira,刘伟良,Sandra Daack‐Hirsch,Bárbara Marina da Silva Pinho,Têmis Maria Félix,Fedik Rahimov,박응렬,Pierre Gosselin,Yoriko Watanabe,Marla Johnson,Jennifer S. Fang,Sarah O’Brien,Iêda M. Orioli,Eduardo E. Castilla,David Fitzpatrick,Rulang Jiang,Mary L. Marazita,Jeffrey C. Murray	2005	1
20	Variation in the HLA-G Promoter Region Influences Miscarriage Rates The American Journal of Human Genetics ·Carole Ober,Carrie Aldrich,Inna Chervoneva,Christine Billstrand,Fedik Rahimov,Heather Gray,Terry Hyslop	2003	183

About Fedik Rahimov

Fedik Rahimov is a scholar working on Aging, Genetics, Genetics, Molecular Biology and Cell Biology, having authored 24 papers that have together received 1.7k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (11 papers), Craniofacial Disorders and Treatments (6 papers), RNA modifications and cancer (5 papers), Cleft Lip and Palate Research (5 papers), RNA Research and Splicing (5 papers), dental development and anomalies (3 papers), Genomics and Rare Diseases (2 papers) and Tissue Engineering and Regenerative Medicine (2 papers). The work is most often cited by research in Genetics (278 citations), Genetics (627 citations), Aging (30 citations), Molecular Biology (1.1k citations) and Immunology (189 citations). Fedik Rahimov has collaborated with scholars based in United States, Brazil and United Kingdom. Frequent 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. Their work appears in journals such as Human Molecular Genetics, PLoS Genetics, PLoS ONE, The Journal of Cell Biology and Trends in Molecular Medicine.

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.

Explore authors with similar magnitude of impact