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Employment (1)

AbbVie: North Chicago, IL, US

2017-03-13 to present | Principal Research Scientist (Genomics Research Center)
Employment
Source: Self-asserted source
Fedik Rahimov

Education and qualifications (1)

The University of Iowa: Iowa City, IA, US

2003-09-01 to 2008-05-16 | PhD (Genetics)
Education
Source: Self-asserted source
Fedik Rahimov

Works (30)

High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene

Nature Communications
2024-11-06 | Journal article
DOI: 10.1038/s41467-024-53634-2
Contributors: Fedik Rahimov; Pekka Nieminen; Priyanka Kumari; Emma Juuri; Tiit Nikopensius; Kitt Paraiso; Jakob German; Antti Karvanen; Mart Kals; Abdelrahman G. Elnahas et al.
Source: check_circle
Crossref

High incidence and geographic distribution of cleft palate cases in Finland are associated with a regulatory variant inIRF6

2024-07-10 | Preprint
DOI: 10.1101/2024.07.09.24310146
Contributors: Fedik Rahimov; Pekka Nieminen; Priyanka Kumari; Emma Juuri; Tiit Nikopensius; Kitt Paraiso; Jakob German; Antti Karvanen; Mart Kals; Abdelrahman G. Elnahas et al.
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Crossref

Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequences.

Genome medicine
2024-03-21 | Journal article
DOI: 10.1186/s13073-024-01316-5
PMID: 38515211
PMC: PMC10956269
Contributors: Ideozu JE; Liu M; Riley-Gillis BM; Paladugu SR; Rahimov F; Krishnan P; Tripathi R; Dorr P; Levy H; Singh A et al.
Source: Self-asserted source
Fedik Rahimov

A genome-wide CRISPR screen supported by human genetics identifies theTNRC18gene locus as a novel regulator of inflammatory signaling

2023-10-04 | Preprint
DOI: 10.1101/2023.10.04.560902
Contributors: Fedik Rahimov; Sujana Ghosh; Sakina Petiwala; Mary Schmidt; Eugene Nyamugenda; Jason Tam; Daniel Verduzco; Sanjana Singh; Victor Avram; Apexa Modi et al.
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Crossref

A meta-analysis of genome-wide association studies in 614,243 individuals identifies 59 novel susceptibility loci underlying Dupuytren’s contracture

2022-06-09 | Preprint
DOI: 10.1101/2022.06.07.22276119
Contributors: Fedik Rahimov; Jacob F. Degner; John S. Lee; Xiuwen Zheng; Jozsef Karman; Howard J. Jacob; Jeffrey F. Waring
Source: check_circle
Crossref

High incidence and regional distribution of cleft palate in Finns are associated with a functional variant in an IRF6 enhancer

[]
2021-10-18 | Preprint
DOI: 10.21203/rs.3.rs-941741/v1
Source: Self-asserted source
Fedik Rahimov
grade
Preferred source (of 2)‎

Concordance between gene expression in peripheral whole blood and colonic tissue in children with inflammatory bowel disease.

PloS one
2019-10-16 | Journal article
DOI: 10.1371/journal.pone.0222952
PMID: 31618209
PMC: PMC6795427
Source: Self-asserted source
Fedik Rahimov

Transgenic zebrafish model of DUX4 misexpression reveals a developmental role in FSHD pathogenesis.

Human molecular genetics
2019-01-01 | Journal article
DOI: 10.1093/hmg/ddy348
PMID: 30307508
PMC: PMC6489409
Source: Self-asserted source
Fedik Rahimov

Normalizing hepcidin predicts <i>TMPRSS6</i> mutation status in patients with chronic iron deficiency.

Blood
2018-06-12 | Journal article
DOI: 10.1182/blood-2017-03-773028
PMID: 29895660
PMC: PMC6071554
Source: Self-asserted source
Fedik Rahimov

CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular Dystrophies.

Cell stem cell
2016-09-15 | Journal article
DOI: 10.1016/j.stem.2016.08.006
PMID: 27641304
PMC: PMC5135584
Source: Self-asserted source
Fedik Rahimov

A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency.

Nature genetics
2015-12-07 | Journal article
DOI: 10.1038/ng.3465
PMID: 26642240
PMC: PMC4696875
Source: Self-asserted source
Fedik Rahimov

Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9.

Blood
2015-10-21 | Journal article
DOI: 10.1182/blood-2015-09-659854
PMID: 26491070
PMC: PMC4683334
Source: Self-asserted source
Fedik Rahimov

Emerging preclinical animal models for FSHD.

Trends in molecular medicine
2015-03-20 | Journal article
DOI: 10.1016/j.molmed.2015.02.011
PMID: 25801126
PMC: PMC4424175
Source: Self-asserted source
Fedik Rahimov

MicroRNA-486-dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy-associated symptoms.

The Journal of clinical investigation
2014-05-01 | Journal article
DOI: 10.1172/jci73579
PMID: 24789910
PMC: PMC4038577
Source: Self-asserted source
Fedik Rahimov

Human skeletal muscle xenograft as a new preclinical model for muscle disorders.

Human molecular genetics
2014-01-22 | Journal article
DOI: 10.1093/hmg/ddu028
PMID: 24452336
PMC: PMC4030773
Source: Self-asserted source
Fedik Rahimov

An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects.

Human molecular genetics
2014-01-16 | Journal article
DOI: 10.1093/hmg/ddt664
PMID: 24442519
PMC: PMC3990169
Source: Self-asserted source
Fedik Rahimov

Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2.

Neuromuscular disorders : NMD
2013-08-31 | Journal article
DOI: 10.1016/j.nmd.2013.08.009
PMID: 24128691
PMC: PMC3851942
Source: Self-asserted source
Fedik Rahimov

Telomere position effect regulates DUX4 in human facioscapulohumeral muscular dystrophy.

Nature structural & molecular biology
2013-05-05 | Journal article
DOI: 10.1038/nsmb.2571
PMID: 23644600
PMC: PMC3711615
Source: Self-asserted source
Fedik Rahimov

The cell biology of disease: cellular and molecular mechanisms underlying muscular dystrophy.

The Journal of cell biology
2013-05-01 | Journal article
DOI: 10.1083/jcb.201212142
PMID: 23671309
PMC: PMC3653356
Source: Self-asserted source
Fedik Rahimov

Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers.

Proceedings of the National Academy of Sciences of the United States of America
2012-09-17 | Journal article
DOI: 10.1073/pnas.1209508109
PMID: 22988124
PMC: PMC3479603
Source: Self-asserted source
Fedik Rahimov

Comparative RNA editing in autistic and neurotypical cerebella.

Molecular psychiatry
2012-08-07 | Journal article
DOI: 10.1038/mp.2012.118
PMID: 22869036
PMC: PMC3494744
Source: Self-asserted source
Fedik Rahimov

Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis.

Human molecular genetics
2012-07-13 | Journal article
DOI: 10.1093/hmg/dds284
PMID: 22798623
PMC: PMC3459465
Source: Self-asserted source
Fedik Rahimov

A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function.

European journal of human genetics : EJHG
2011-11-23 | Journal article
DOI: 10.1038/ejhg.2011.213
PMID: 22108603
PMC: PMC3306860
Source: Self-asserted source
Fedik Rahimov

Genetics of nonsyndromic orofacial clefts.

The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
2011-05-05 | Journal article
DOI: 10.1597/10-178
PMID: 21545302
PMC: PMC3437188
Source: Self-asserted source
Fedik Rahimov

Gene expression profiling of skeletal muscles treated with a soluble activin type IIB receptor.

Physiological genomics
2011-01-25 | Journal article
DOI: 10.1152/physiolgenomics.00223.2010
PMID: 21266502
PMC: PMC3092338
Source: Self-asserted source
Fedik Rahimov

Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip.

Nature genetics
2008-10-05 | Journal article
DOI: 10.1038/ng.242
PMID: 18836445
PMC: PMC2691688
Source: Self-asserted source
Fedik Rahimov

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
2008-07-01 | Journal article
DOI: 10.1002/gepi.20314
PMID: 18278815
PMC: PMC2680842
Source: Self-asserted source
Fedik Rahimov

GLI2 mutations in four Brazilian patients: how wide is the phenotypic spectrum?

American journal of medical genetics. Part A
2006-12-01 | Journal article
DOI: 10.1002/ajmg.a.31370
PMID: 17096318
Source: Self-asserted source
Fedik Rahimov

Medical sequencing of candidate genes for nonsyndromic cleft lip and palate.

PLoS genetics
2005-12-02 | Journal article
DOI: 10.1371/journal.pgen.0010064
PMID: 16327884
PMC: PMC1298935
Source: Self-asserted source
Fedik Rahimov

Variation in the HLA-G promoter region influences miscarriage rates.

American journal of human genetics
2003-04-29 | Journal article
DOI: 10.1086/375501
PMID: 12721954
PMC: PMC1180303
Source: Self-asserted source
Fedik Rahimov
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