SETX (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "SETX" in English language version.

Last modified: 12:18:09, 11 August 2026 (UTC)

Ref.Un. Ref.Website

Global rank English rank

5^th place

5^th place

2^nd place

2^nd place

630^th place

326^th place

22adsabs.harvard.edu

14^th place

9^th place

11archives-ouvertes.fr

1,143^rd place

973^rd place

adsabs.harvard.edu (Global: 14^th place; English: 9^th place)

ui.adsabs.harvard.edu

Cohen S, Puget N, Lin YL, Clouaire T, Aguirrebengoa M, Rocher V, et al. (February 2018). "Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations". Nature Communications. 9 (1): 533. Bibcode:2018NatCo...9..533C. doi:10.1038/s41467-018-02894-w. PMC 5803260. PMID 29416069.
Cohen S, Puget N, Lin YL, Clouaire T, Aguirrebengoa M, Rocher V, et al. (February 2018). "Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations". Nature Communications. 9 (1): 533. Bibcode:2018NatCo...9..533C. doi:10.1038/s41467-018-02894-w. PMC 5803260. PMID 29416069.

archives-ouvertes.fr (Global: 1,143^rd place; English: 973^rd place)

hal.archives-ouvertes.fr

Richard P, Feng S, Tsai YL, Li W, Rinchetti P, Muhith U, et al. (August 2020). "SETX (senataxin), the helicase mutated in AOA2 and ALS4, functions in autophagy regulation" (PDF). Autophagy. 17 (8): 1889–1906. doi:10.1080/15548627.2020.1796292. PMC 8386630. PMID 32686621.

doi.org (Global: 2^nd place; English: 2^nd place)

Chance PF, Rabin BA, Ryan SG, Ding Y, Scavina M, Crain B, et al. (March 1998). "Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34". American Journal of Human Genetics. 62 (3): 633–40. doi:10.1086/301769. PMC 1376963. PMID 9497266.
Németh AH, Bochukova E, Dunne E, Huson SM, Elston J, Hannan MA, et al. (November 2000). "Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34". American Journal of Human Genetics. 67 (5): 1320–6. doi:10.1016/S0002-9297(07)62962-0. PMC 1288574. PMID 11022012.
Groh M, Albulescu LO, Cristini A, Gromak N (October 2017). "Senataxin: Genome Guardian at the Interface of Transcription and Neurodegeneration". Journal of Molecular Biology. 429 (21): 3181–3195. doi:10.1016/j.jmb.2016.10.021. PMID 27771483.
Hamperl S, Cimprich KA (July 2014). "The contribution of co-transcriptional RNA:DNA hybrid structures to DNA damage and genome instability". DNA Repair. 19: 84–94. doi:10.1016/j.dnarep.2014.03.023. PMC 4051866. PMID 24746923.
Skourti-Stathaki K, Proudfoot NJ (July 2014). "A double-edged sword: R loops as threats to genome integrity and powerful regulators of gene expression". Genes & Development. 28 (13): 1384–96. doi:10.1101/gad.242990.114. PMC 4083084. PMID 24990962.
Yüce Ö, West SC (January 2013). "Senataxin, defective in the neurodegenerative disorder ataxia with oculomotor apraxia 2, lies at the interface of transcription and the DNA damage response". Molecular and Cellular Biology. 33 (2): 406–17. doi:10.1128/MCB.01195-12. PMC 3554130. PMID 23149945.
Richard P, Manley JL (October 2017). "R Loops and Links to Human Disease". Journal of Molecular Biology. 429 (21): 3168–3180. doi:10.1016/j.jmb.2016.08.031. PMC 5478472. PMID 27600412.
Hamperl S, Cimprich KA (July 2014). "The contribution of co-transcriptional RNA:DNA hybrid structures to DNA damage and genome instability". DNA Repair. 19: 84–94. doi:10.1016/j.dnarep.2014.03.023. PMC 4051866. PMID 24746923.
Cohen S, Puget N, Lin YL, Clouaire T, Aguirrebengoa M, Rocher V, et al. (February 2018). "Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations". Nature Communications. 9 (1): 533. Bibcode:2018NatCo...9..533C. doi:10.1038/s41467-018-02894-w. PMC 5803260. PMID 29416069.
Crossley MP, Bocek M, Cimprich KA (February 2019). "R-Loops as Cellular Regulators and Genomic Threats". Molecular Cell. 73 (3): 398–411. doi:10.1016/j.molcel.2019.01.024. PMC 6402819. PMID 30735654.
Cohen S, Puget N, Lin YL, Clouaire T, Aguirrebengoa M, Rocher V, et al. (February 2018). "Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations". Nature Communications. 9 (1): 533. Bibcode:2018NatCo...9..533C. doi:10.1038/s41467-018-02894-w. PMC 5803260. PMID 29416069.
Skourti-Stathaki K, Proudfoot NJ, Gromak N (June 2011). "Human senataxin resolves RNA/DNA hybrids formed at transcriptional pause sites to promote Xrn2-dependent termination". Molecular Cell. 42 (6): 794–805. doi:10.1016/j.molcel.2011.04.026. PMC 3145960. PMID 21700224.
Richard P, Feng S, Tsai YL, Li W, Rinchetti P, Muhith U, et al. (August 2020). "SETX (senataxin), the helicase mutated in AOA2 and ALS4, functions in autophagy regulation" (PDF). Autophagy. 17 (8): 1889–1906. doi:10.1080/15548627.2020.1796292. PMC 8386630. PMID 32686621.
Grunseich C, Wang IX, Watts JA, Burdick JT, Guber RD, Zhu Z, et al. (February 2018). "Senataxin Mutation Reveals How R-Loops Promote Transcription by Blocking DNA Methylation at Gene Promoters". Molecular Cell. 69 (3): 426–437.e7. doi:10.1016/j.molcel.2017.12.030. PMC 5815878. PMID 29395064.
Crossley MP, Bocek M, Cimprich KA (February 2019). "R-Loops as Cellular Regulators and Genomic Threats". Molecular Cell. 73 (3): 398–411. doi:10.1016/j.molcel.2019.01.024. PMC 6402819. PMID 30735654.
Richard P, Rosonina E (October 2021). "Regulating autophagy: a novel role for SETX (Senataxin)". Neural Regeneration Research. 16 (10): 2008–2009. doi:10.4103/1673-5374.308091. PMC 8343329. PMID 33642381.

ensembl.org (Global: 630^th place; English: 326^th place)

may2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000107290 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000043535 – Ensembl, May 2017

nih.gov (Global: 5^th place; English: 5^th place)

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Chance PF, Rabin BA, Ryan SG, Ding Y, Scavina M, Crain B, et al. (March 1998). "Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34". American Journal of Human Genetics. 62 (3): 633–40. doi:10.1086/301769. PMC 1376963. PMID 9497266.
Németh AH, Bochukova E, Dunne E, Huson SM, Elston J, Hannan MA, et al. (November 2000). "Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34". American Journal of Human Genetics. 67 (5): 1320–6. doi:10.1016/S0002-9297(07)62962-0. PMC 1288574. PMID 11022012.
"Entrez Gene: SETX senataxin".
Hamperl S, Cimprich KA (July 2014). "The contribution of co-transcriptional RNA:DNA hybrid structures to DNA damage and genome instability". DNA Repair. 19: 84–94. doi:10.1016/j.dnarep.2014.03.023. PMC 4051866. PMID 24746923.
Skourti-Stathaki K, Proudfoot NJ (July 2014). "A double-edged sword: R loops as threats to genome integrity and powerful regulators of gene expression". Genes & Development. 28 (13): 1384–96. doi:10.1101/gad.242990.114. PMC 4083084. PMID 24990962.
Yüce Ö, West SC (January 2013). "Senataxin, defective in the neurodegenerative disorder ataxia with oculomotor apraxia 2, lies at the interface of transcription and the DNA damage response". Molecular and Cellular Biology. 33 (2): 406–17. doi:10.1128/MCB.01195-12. PMC 3554130. PMID 23149945.
Richard P, Manley JL (October 2017). "R Loops and Links to Human Disease". Journal of Molecular Biology. 429 (21): 3168–3180. doi:10.1016/j.jmb.2016.08.031. PMC 5478472. PMID 27600412.
Hamperl S, Cimprich KA (July 2014). "The contribution of co-transcriptional RNA:DNA hybrid structures to DNA damage and genome instability". DNA Repair. 19: 84–94. doi:10.1016/j.dnarep.2014.03.023. PMC 4051866. PMID 24746923.
Cohen S, Puget N, Lin YL, Clouaire T, Aguirrebengoa M, Rocher V, et al. (February 2018). "Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations". Nature Communications. 9 (1): 533. Bibcode:2018NatCo...9..533C. doi:10.1038/s41467-018-02894-w. PMC 5803260. PMID 29416069.
Crossley MP, Bocek M, Cimprich KA (February 2019). "R-Loops as Cellular Regulators and Genomic Threats". Molecular Cell. 73 (3): 398–411. doi:10.1016/j.molcel.2019.01.024. PMC 6402819. PMID 30735654.
Cohen S, Puget N, Lin YL, Clouaire T, Aguirrebengoa M, Rocher V, et al. (February 2018). "Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations". Nature Communications. 9 (1): 533. Bibcode:2018NatCo...9..533C. doi:10.1038/s41467-018-02894-w. PMC 5803260. PMID 29416069.
Skourti-Stathaki K, Proudfoot NJ, Gromak N (June 2011). "Human senataxin resolves RNA/DNA hybrids formed at transcriptional pause sites to promote Xrn2-dependent termination". Molecular Cell. 42 (6): 794–805. doi:10.1016/j.molcel.2011.04.026. PMC 3145960. PMID 21700224.
Richard P, Feng S, Tsai YL, Li W, Rinchetti P, Muhith U, et al. (August 2020). "SETX (senataxin), the helicase mutated in AOA2 and ALS4, functions in autophagy regulation" (PDF). Autophagy. 17 (8): 1889–1906. doi:10.1080/15548627.2020.1796292. PMC 8386630. PMID 32686621.
Grunseich C, Wang IX, Watts JA, Burdick JT, Guber RD, Zhu Z, et al. (February 2018). "Senataxin Mutation Reveals How R-Loops Promote Transcription by Blocking DNA Methylation at Gene Promoters". Molecular Cell. 69 (3): 426–437.e7. doi:10.1016/j.molcel.2017.12.030. PMC 5815878. PMID 29395064.
Crossley MP, Bocek M, Cimprich KA (February 2019). "R-Loops as Cellular Regulators and Genomic Threats". Molecular Cell. 73 (3): 398–411. doi:10.1016/j.molcel.2019.01.024. PMC 6402819. PMID 30735654.
Richard P, Rosonina E (October 2021). "Regulating autophagy: a novel role for SETX (Senataxin)". Neural Regeneration Research. 16 (10): 2008–2009. doi:10.4103/1673-5374.308091. PMC 8343329. PMID 33642381.

pubmed.ncbi.nlm.nih.gov

Chance PF, Rabin BA, Ryan SG, Ding Y, Scavina M, Crain B, et al. (March 1998). "Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34". American Journal of Human Genetics. 62 (3): 633–40. doi:10.1086/301769. PMC 1376963. PMID 9497266.
Németh AH, Bochukova E, Dunne E, Huson SM, Elston J, Hannan MA, et al. (November 2000). "Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34". American Journal of Human Genetics. 67 (5): 1320–6. doi:10.1016/S0002-9297(07)62962-0. PMC 1288574. PMID 11022012.
Groh M, Albulescu LO, Cristini A, Gromak N (October 2017). "Senataxin: Genome Guardian at the Interface of Transcription and Neurodegeneration". Journal of Molecular Biology. 429 (21): 3181–3195. doi:10.1016/j.jmb.2016.10.021. PMID 27771483.
Hamperl S, Cimprich KA (July 2014). "The contribution of co-transcriptional RNA:DNA hybrid structures to DNA damage and genome instability". DNA Repair. 19: 84–94. doi:10.1016/j.dnarep.2014.03.023. PMC 4051866. PMID 24746923.
Skourti-Stathaki K, Proudfoot NJ (July 2014). "A double-edged sword: R loops as threats to genome integrity and powerful regulators of gene expression". Genes & Development. 28 (13): 1384–96. doi:10.1101/gad.242990.114. PMC 4083084. PMID 24990962.
Yüce Ö, West SC (January 2013). "Senataxin, defective in the neurodegenerative disorder ataxia with oculomotor apraxia 2, lies at the interface of transcription and the DNA damage response". Molecular and Cellular Biology. 33 (2): 406–17. doi:10.1128/MCB.01195-12. PMC 3554130. PMID 23149945.
Richard P, Manley JL (October 2017). "R Loops and Links to Human Disease". Journal of Molecular Biology. 429 (21): 3168–3180. doi:10.1016/j.jmb.2016.08.031. PMC 5478472. PMID 27600412.
Hamperl S, Cimprich KA (July 2014). "The contribution of co-transcriptional RNA:DNA hybrid structures to DNA damage and genome instability". DNA Repair. 19: 84–94. doi:10.1016/j.dnarep.2014.03.023. PMC 4051866. PMID 24746923.
Cohen S, Puget N, Lin YL, Clouaire T, Aguirrebengoa M, Rocher V, et al. (February 2018). "Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations". Nature Communications. 9 (1): 533. Bibcode:2018NatCo...9..533C. doi:10.1038/s41467-018-02894-w. PMC 5803260. PMID 29416069.
Crossley MP, Bocek M, Cimprich KA (February 2019). "R-Loops as Cellular Regulators and Genomic Threats". Molecular Cell. 73 (3): 398–411. doi:10.1016/j.molcel.2019.01.024. PMC 6402819. PMID 30735654.
Cohen S, Puget N, Lin YL, Clouaire T, Aguirrebengoa M, Rocher V, et al. (February 2018). "Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations". Nature Communications. 9 (1): 533. Bibcode:2018NatCo...9..533C. doi:10.1038/s41467-018-02894-w. PMC 5803260. PMID 29416069.
Skourti-Stathaki K, Proudfoot NJ, Gromak N (June 2011). "Human senataxin resolves RNA/DNA hybrids formed at transcriptional pause sites to promote Xrn2-dependent termination". Molecular Cell. 42 (6): 794–805. doi:10.1016/j.molcel.2011.04.026. PMC 3145960. PMID 21700224.
Richard P, Feng S, Tsai YL, Li W, Rinchetti P, Muhith U, et al. (August 2020). "SETX (senataxin), the helicase mutated in AOA2 and ALS4, functions in autophagy regulation" (PDF). Autophagy. 17 (8): 1889–1906. doi:10.1080/15548627.2020.1796292. PMC 8386630. PMID 32686621.
Grunseich C, Wang IX, Watts JA, Burdick JT, Guber RD, Zhu Z, et al. (February 2018). "Senataxin Mutation Reveals How R-Loops Promote Transcription by Blocking DNA Methylation at Gene Promoters". Molecular Cell. 69 (3): 426–437.e7. doi:10.1016/j.molcel.2017.12.030. PMC 5815878. PMID 29395064.
Crossley MP, Bocek M, Cimprich KA (February 2019). "R-Loops as Cellular Regulators and Genomic Threats". Molecular Cell. 73 (3): 398–411. doi:10.1016/j.molcel.2019.01.024. PMC 6402819. PMID 30735654.
Richard P, Rosonina E (October 2021). "Regulating autophagy: a novel role for SETX (Senataxin)". Neural Regeneration Research. 16 (10): 2008–2009. doi:10.4103/1673-5374.308091. PMC 8343329. PMID 33642381.