Repeated sequence (DNA) (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Repeated sequence (DNA)" in English language version.

refsWebsite

Global rank English rank

57nih.gov

4^th place

35doi.org

2^nd place

10semanticscholar.org

11^th place

8^th place

3harvard.edu

18^th place

17^th place

2genome.gov

9,308^th place

8,899^th place

1sciencedirect.com

149^th place

178^th place

1escholarship.org

1,523^rd place

976^th place

1nature.com

234^th place

397^th place

1worldcat.org

5^th place

doi.org

de Koning AP, Gu W, Castoe TA, Batzer MA, Pollock DD (December 2011). "Repetitive elements may comprise over two-thirds of the human genome". PLOS Genetics. 7 (12): e1002384. doi:10.1371/journal.pgen.1002384. PMC 3228813. PMID 22144907.
Lower SE, Dion-Côté AM, Clark AG, Barbash DA (November 2019). "Special Issue: Repetitive DNA Sequences". Genes. 10 (11): 896. doi:10.3390/genes10110896. PMC 6895920. PMID 31698818.
McCLINTOCK B (1951-01-01). "Chromosome organization and genic expression". Cold Spring Harbor Symposia on Quantitative Biology. 16: 13–47. doi:10.1101/sqb.1951.016.01.004. PMID 14942727.
Britten RJ, Kohne DE (August 1968). "Repeated sequences in DNA. Hundreds of thousands of copies of DNA sequences have been incorporated into the genomes of higher organisms". Science. 161 (3841): 529–540. doi:10.1126/science.161.3841.529. PMID 4874239.
Shapiro JA, von Sternberg R (May 2005). "Why repetitive DNA is essential to genome function". Biological Reviews of the Cambridge Philosophical Society. 80 (2): 227–250. doi:10.1017/s1464793104006657. PMID 15921050. S2CID 18866824.
Orgel LE, Crick FH, Sapienza C (December 1980). "Selfish DNA". Nature. 288 (5792): 645–646. Bibcode:1980Natur.288..645O. doi:10.1038/288645a0. PMID 7453798. S2CID 4370178.
Palazzo AF, Gregory TR (May 2014). "The case for junk DNA". PLOS Genetics. 10 (5): e1004351. doi:10.1371/journal.pgen.1004351. PMC 4014423. PMID 24809441.
Joly-Lopez Z, Bureau TE (April 2018). "Exaptation of transposable element coding sequences". Current Opinion in Genetics & Development. 49: 34–42. doi:10.1016/j.gde.2018.02.011. PMID 29525543.
Sznajder ŁJ, Swanson MS (July 2019). "Short Tandem Repeat Expansions and RNA-Mediated Pathogenesis in Myotonic Dystrophy". International Journal of Molecular Sciences. 20 (13): 3365. doi:10.3390/ijms20133365. PMC 6651174. PMID 31323950.
Wahls WP (1998). "Meiotic recombination hotspots: shaping the genome and insights into hypervariable minisatellite DNA change". Current Topics in Developmental Biology. 37: 37–75. doi:10.1016/s0070-2153(08)60171-4. ISBN 9780121531379. PMC 3151733. PMID 9352183.
Janssen A, Colmenares SU, Karpen GH (October 2018). "Heterochromatin: Guardian of the Genome". Annual Review of Cell and Developmental Biology. 34 (1): 265–288. doi:10.1146/annurev-cellbio-100617-062653. PMID 30044650. S2CID 51718804.
Qi J, Shafer RH (2005-06-02). "Covalent ligation studies on the human telomere quadruplex". Nucleic Acids Research. 33 (10): 3185–3192. doi:10.1093/nar/gki632. PMC 1142406. PMID 15933211.
Miga KH (September 2015). "Completing the human genome: the progress and challenge of satellite DNA assembly". Chromosome Research. 23 (3): 421–426. doi:10.1007/s10577-015-9488-2. PMID 26363799. S2CID 15229421.
Miga KH (September 2015). "Completing the human genome: the progress and challenge of satellite DNA assembly". Chromosome Research. 23 (3): 421–426. doi:10.1007/s004390050508. PMID 26363799. S2CID 615040.
Padeken J, Zeller P, Gasser SM (April 2015). "Repeat DNA in genome organization and stability". Current Opinion in Genetics & Development. Genome architecture and expression. 31: 12–19. doi:10.1016/j.gde.2015.03.009. PMID 25917896.
Wicker T, Sabot F, Hua-Van A, Bennetzen JL, Capy P, Chalhoub B, et al. (December 2007). "A unified classification system for eukaryotic transposable elements". Nature Reviews. Genetics. 8 (12): 973–982. doi:10.1038/nrg2165. PMID 17984973. S2CID 32132898.
Nicolau M, Picault N, Moissiard G (October 2021). "The Evolutionary Volte-Face of Transposable Elements: From Harmful Jumping Genes to Major Drivers of Genetic Innovation". Cells. 10 (11): 2952. doi:10.3390/cells10112952. PMC 8616336. PMID 34831175.
Kramerov DA, Vassetzky NS (2011). "SINEs". Wiley Interdisciplinary Reviews. RNA. 2 (6): 772–786. doi:10.1002/wrna.91. PMID 21976282. S2CID 222199613.
Lee HE, Ayarpadikannan S, Kim HS (2015). "Role of transposable elements in genomic rearrangement, evolution, gene regulation and epigenetics in primates". Genes & Genetic Systems. 90 (5): 245–257. doi:10.1266/ggs.15-00016. PMID 26781081.
Mangiavacchi A, Liu P, Della Valle F, Orlando V (July 2021). "New insights into the functional role of retrotransposon dynamics in mammalian somatic cells". Cellular and Molecular Life Sciences. 78 (13): 5245–5256. doi:10.1007/s00018-021-03851-5. PMC 8257530. PMID 33990851.
Ichiyanagi K (2013). "Epigenetic regulation of transcription and possible functions of mammalian short interspersed elements, SINEs". Genes & Genetic Systems. 88 (1): 19–29. doi:10.1266/ggs.88.19. PMID 23676707.
Pearson CE, Zorbas H, Price GB, Zannis-Hadjopoulos M (October 1996). "Inverted repeats, stem-loops, and cruciforms: significance for initiation of DNA replication". Journal of Cellular Biochemistry. 63 (1): 1–22. doi:10.1002/(SICI)1097-4644(199610)63:1<1::AID-JCB1>3.0.CO;2-3. eISSN 1097-4644. PMID 8891900. S2CID 22204780.
Usdin K, House NC, Freudenreich CH (22 January 2015). "Repeat instability during DNA repair: Insights from model systems". Critical Reviews in Biochemistry and Molecular Biology. 50 (2): 142–167. doi:10.3109/10409238.2014.999192. PMC 4454471. PMID 25608779.
Massey TH, Jones L (January 2018). "The central role of DNA damage and repair in CAG repeat diseases". Disease Models & Mechanisms. 11 (1): dmm031930. doi:10.1242/dmm.031930. PMC 5818082. PMID 29419417.
Cattaneo E, Zuccato C, Tartari M (December 2005). "Normal huntingtin function: an alternative approach to Huntington's disease". Nature Reviews. Neuroscience. 6 (12): 919–930. doi:10.1038/nrn1806. PMID 16288298. S2CID 10119487.
Maiuri T, Mocle AJ, Hung CL, Xia J, van Roon-Mom WM, Truant R (January 2017). "Huntingtin is a scaffolding protein in the ATM oxidative DNA damage response complex". Human Molecular Genetics. 26 (2): 395–406. doi:10.1093/hmg/ddw395. PMID 28017939.
Penagarikano O, Mulle JG, Warren ST (2007-09-01). "The pathophysiology of fragile x syndrome". Annual Review of Genomics and Human Genetics. 8 (1): 109–129. doi:10.1146/annurev.genom.8.080706.092249. PMID 17477822.
Hagerman RJ, Berry-Kravis E, Hazlett HC, Bailey DB, Moine H, Kooy RF, et al. (September 2017). "Fragile X syndrome". Nature Reviews. Disease Primers. 3 (1): 17065. doi:10.1038/nrdp.2017.65. PMID 28960184. S2CID 583204.
Abugable AA, Morris JL, Palminha NM, Zaksauskaite R, Ray S, El-Khamisy SF (September 2019). "DNA repair and neurological disease: From molecular understanding to the development of diagnostics and model organisms". DNA Repair. 81: 102669. doi:10.1016/j.dnarep.2019.102669. PMID 31331820.
Honti V, Vécsei L (June 2005). "Genetic and molecular aspects of spinocerebellar ataxias". Neuropsychiatric Disease and Treatment. 1 (2): 125–133. doi:10.2147/nedt.1.2.125.61044. PMC 2413192. PMID 18568057.
Bürk K (2017). "Friedreich Ataxia: current status and future prospects". Cerebellum & Ataxias. 4 (1): 4. doi:10.1186/s40673-017-0062-x. PMC 5383992. PMID 28405347.
Mazzara PG, Muggeo S, Luoni M, Massimino L, Zaghi M, Valverde PT, et al. (August 2020). "Frataxin gene editing rescues Friedreich's ataxia pathology in dorsal root ganglia organoid-derived sensory neurons". Nature Communications. 11 (1): 4178. Bibcode:2020NatCo..11.4178M. doi:10.1038/s41467-020-17954-3. PMC 7442818. PMID 32826895.
van Blitterswijk M, DeJesus-Hernandez M, Rademakers R (December 2012). "How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia: can we learn from other noncoding repeat expansion disorders?". Current Opinion in Neurology. 25 (6): 689–700. doi:10.1097/WCO.0b013e32835a3efb. PMC 3923493. PMID 23160421.
De Bustos A, Cuadrado A, Jouve N (November 2016). "Sequencing of long stretches of repetitive DNA". Scientific Reports. 6 (1): 36665. Bibcode:2016NatSR...636665D. doi:10.1038/srep36665. PMC 5098217. PMID 27819354.
Slotkin RK (1 May 2018). "The case for not masking away repetitive DNA". Mobile DNA. 9 (1): 15. doi:10.1186/s13100-018-0120-9. PMC 5930866. PMID 29743957.

escholarship.org

Janssen A, Colmenares SU, Karpen GH (October 2018). "Heterochromatin: Guardian of the Genome". Annual Review of Cell and Developmental Biology. 34 (1): 265–288. doi:10.1146/annurev-cellbio-100617-062653. PMID 30044650. S2CID 51718804.

genome.gov

"Tandem Repeat". Genome.gov. Retrieved 2022-09-30.
"Centromere". Genome.gov. Retrieved 2022-09-30.

harvard.edu

ui.adsabs.harvard.edu

Orgel LE, Crick FH, Sapienza C (December 1980). "Selfish DNA". Nature. 288 (5792): 645–646. Bibcode:1980Natur.288..645O. doi:10.1038/288645a0. PMID 7453798. S2CID 4370178.
Mazzara PG, Muggeo S, Luoni M, Massimino L, Zaghi M, Valverde PT, et al. (August 2020). "Frataxin gene editing rescues Friedreich's ataxia pathology in dorsal root ganglia organoid-derived sensory neurons". Nature Communications. 11 (1): 4178. Bibcode:2020NatCo..11.4178M. doi:10.1038/s41467-020-17954-3. PMC 7442818. PMID 32826895.
De Bustos A, Cuadrado A, Jouve N (November 2016). "Sequencing of long stretches of repetitive DNA". Scientific Reports. 6 (1): 36665. Bibcode:2016NatSR...636665D. doi:10.1038/srep36665. PMC 5098217. PMID 27819354.

nature.com

"Interspersed repetitive sequences - Latest research and news | Nature". www.nature.com. Retrieved 2022-09-30.

nih.gov

pubmed.ncbi.nlm.nih.gov

de Koning AP, Gu W, Castoe TA, Batzer MA, Pollock DD (December 2011). "Repetitive elements may comprise over two-thirds of the human genome". PLOS Genetics. 7 (12): e1002384. doi:10.1371/journal.pgen.1002384. PMC 3228813. PMID 22144907.
Lower SE, Dion-Côté AM, Clark AG, Barbash DA (November 2019). "Special Issue: Repetitive DNA Sequences". Genes. 10 (11): 896. doi:10.3390/genes10110896. PMC 6895920. PMID 31698818.
McCLINTOCK B (1951-01-01). "Chromosome organization and genic expression". Cold Spring Harbor Symposia on Quantitative Biology. 16: 13–47. doi:10.1101/sqb.1951.016.01.004. PMID 14942727.
Britten RJ, Kohne DE (August 1968). "Repeated sequences in DNA. Hundreds of thousands of copies of DNA sequences have been incorporated into the genomes of higher organisms". Science. 161 (3841): 529–540. doi:10.1126/science.161.3841.529. PMID 4874239.
Shapiro JA, von Sternberg R (May 2005). "Why repetitive DNA is essential to genome function". Biological Reviews of the Cambridge Philosophical Society. 80 (2): 227–250. doi:10.1017/s1464793104006657. PMID 15921050. S2CID 18866824.
Ohno S (1972). "So much "junk" DNA in our genome". Brookhaven Symposia in Biology. 23: 366–370. PMID 5065367.
Orgel LE, Crick FH, Sapienza C (December 1980). "Selfish DNA". Nature. 288 (5792): 645–646. Bibcode:1980Natur.288..645O. doi:10.1038/288645a0. PMID 7453798. S2CID 4370178.
Palazzo AF, Gregory TR (May 2014). "The case for junk DNA". PLOS Genetics. 10 (5): e1004351. doi:10.1371/journal.pgen.1004351. PMC 4014423. PMID 24809441.
Joly-Lopez Z, Bureau TE (April 2018). "Exaptation of transposable element coding sequences". Current Opinion in Genetics & Development. 49: 34–42. doi:10.1016/j.gde.2018.02.011. PMID 29525543.
Sznajder ŁJ, Swanson MS (July 2019). "Short Tandem Repeat Expansions and RNA-Mediated Pathogenesis in Myotonic Dystrophy". International Journal of Molecular Sciences. 20 (13): 3365. doi:10.3390/ijms20133365. PMC 6651174. PMID 31323950.
Wahls WP (1998). "Meiotic recombination hotspots: shaping the genome and insights into hypervariable minisatellite DNA change". Current Topics in Developmental Biology. 37: 37–75. doi:10.1016/s0070-2153(08)60171-4. ISBN 9780121531379. PMC 3151733. PMID 9352183.
Janssen A, Colmenares SU, Karpen GH (October 2018). "Heterochromatin: Guardian of the Genome". Annual Review of Cell and Developmental Biology. 34 (1): 265–288. doi:10.1146/annurev-cellbio-100617-062653. PMID 30044650. S2CID 51718804.
Qi J, Shafer RH (2005-06-02). "Covalent ligation studies on the human telomere quadruplex". Nucleic Acids Research. 33 (10): 3185–3192. doi:10.1093/nar/gki632. PMC 1142406. PMID 15933211.
Miga KH (September 2015). "Completing the human genome: the progress and challenge of satellite DNA assembly". Chromosome Research. 23 (3): 421–426. doi:10.1007/s10577-015-9488-2. PMID 26363799. S2CID 15229421.
Miga KH (September 2015). "Completing the human genome: the progress and challenge of satellite DNA assembly". Chromosome Research. 23 (3): 421–426. doi:10.1007/s004390050508. PMID 26363799. S2CID 615040.
Padeken J, Zeller P, Gasser SM (April 2015). "Repeat DNA in genome organization and stability". Current Opinion in Genetics & Development. Genome architecture and expression. 31: 12–19. doi:10.1016/j.gde.2015.03.009. PMID 25917896.
Wicker T, Sabot F, Hua-Van A, Bennetzen JL, Capy P, Chalhoub B, et al. (December 2007). "A unified classification system for eukaryotic transposable elements". Nature Reviews. Genetics. 8 (12): 973–982. doi:10.1038/nrg2165. PMID 17984973. S2CID 32132898.
Nicolau M, Picault N, Moissiard G (October 2021). "The Evolutionary Volte-Face of Transposable Elements: From Harmful Jumping Genes to Major Drivers of Genetic Innovation". Cells. 10 (11): 2952. doi:10.3390/cells10112952. PMC 8616336. PMID 34831175.
Kramerov DA, Vassetzky NS (2011). "SINEs". Wiley Interdisciplinary Reviews. RNA. 2 (6): 772–786. doi:10.1002/wrna.91. PMID 21976282. S2CID 222199613.
Lee HE, Ayarpadikannan S, Kim HS (2015). "Role of transposable elements in genomic rearrangement, evolution, gene regulation and epigenetics in primates". Genes & Genetic Systems. 90 (5): 245–257. doi:10.1266/ggs.15-00016. PMID 26781081.
Mangiavacchi A, Liu P, Della Valle F, Orlando V (July 2021). "New insights into the functional role of retrotransposon dynamics in mammalian somatic cells". Cellular and Molecular Life Sciences. 78 (13): 5245–5256. doi:10.1007/s00018-021-03851-5. PMC 8257530. PMID 33990851.
Ichiyanagi K (2013). "Epigenetic regulation of transcription and possible functions of mammalian short interspersed elements, SINEs". Genes & Genetic Systems. 88 (1): 19–29. doi:10.1266/ggs.88.19. PMID 23676707.
Pearson CE, Zorbas H, Price GB, Zannis-Hadjopoulos M (October 1996). "Inverted repeats, stem-loops, and cruciforms: significance for initiation of DNA replication". Journal of Cellular Biochemistry. 63 (1): 1–22. doi:10.1002/(SICI)1097-4644(199610)63:1<1::AID-JCB1>3.0.CO;2-3. eISSN 1097-4644. PMID 8891900. S2CID 22204780.
Usdin K, House NC, Freudenreich CH (22 January 2015). "Repeat instability during DNA repair: Insights from model systems". Critical Reviews in Biochemistry and Molecular Biology. 50 (2): 142–167. doi:10.3109/10409238.2014.999192. PMC 4454471. PMID 25608779.
Massey TH, Jones L (January 2018). "The central role of DNA damage and repair in CAG repeat diseases". Disease Models & Mechanisms. 11 (1): dmm031930. doi:10.1242/dmm.031930. PMC 5818082. PMID 29419417.
Cattaneo E, Zuccato C, Tartari M (December 2005). "Normal huntingtin function: an alternative approach to Huntington's disease". Nature Reviews. Neuroscience. 6 (12): 919–930. doi:10.1038/nrn1806. PMID 16288298. S2CID 10119487.
Maiuri T, Mocle AJ, Hung CL, Xia J, van Roon-Mom WM, Truant R (January 2017). "Huntingtin is a scaffolding protein in the ATM oxidative DNA damage response complex". Human Molecular Genetics. 26 (2): 395–406. doi:10.1093/hmg/ddw395. PMID 28017939.
Schulte J, Littleton JT (January 2011). "The biological function of the Huntingtin protein and its relevance to Huntington's Disease pathology". Current Trends in Neurology. 5: 65–78. PMC 3237673. PMID 22180703.
Penagarikano O, Mulle JG, Warren ST (2007-09-01). "The pathophysiology of fragile x syndrome". Annual Review of Genomics and Human Genetics. 8 (1): 109–129. doi:10.1146/annurev.genom.8.080706.092249. PMID 17477822.
Hagerman RJ, Berry-Kravis E, Hazlett HC, Bailey DB, Moine H, Kooy RF, et al. (September 2017). "Fragile X syndrome". Nature Reviews. Disease Primers. 3 (1): 17065. doi:10.1038/nrdp.2017.65. PMID 28960184. S2CID 583204.
Abugable AA, Morris JL, Palminha NM, Zaksauskaite R, Ray S, El-Khamisy SF (September 2019). "DNA repair and neurological disease: From molecular understanding to the development of diagnostics and model organisms". DNA Repair. 81: 102669. doi:10.1016/j.dnarep.2019.102669. PMID 31331820.
Honti V, Vécsei L (June 2005). "Genetic and molecular aspects of spinocerebellar ataxias". Neuropsychiatric Disease and Treatment. 1 (2): 125–133. doi:10.2147/nedt.1.2.125.61044. PMC 2413192. PMID 18568057.
Bürk K (2017). "Friedreich Ataxia: current status and future prospects". Cerebellum & Ataxias. 4 (1): 4. doi:10.1186/s40673-017-0062-x. PMC 5383992. PMID 28405347.
Mazzara PG, Muggeo S, Luoni M, Massimino L, Zaghi M, Valverde PT, et al. (August 2020). "Frataxin gene editing rescues Friedreich's ataxia pathology in dorsal root ganglia organoid-derived sensory neurons". Nature Communications. 11 (1): 4178. Bibcode:2020NatCo..11.4178M. doi:10.1038/s41467-020-17954-3. PMC 7442818. PMID 32826895.
Hahn C, Salajegheh MK (January 2016). "Myotonic disorders: A review article". Iranian Journal of Neurology. 15 (1): 46–53. PMC 4852070. PMID 27141276.
van Blitterswijk M, DeJesus-Hernandez M, Rademakers R (December 2012). "How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia: can we learn from other noncoding repeat expansion disorders?". Current Opinion in Neurology. 25 (6): 689–700. doi:10.1097/WCO.0b013e32835a3efb. PMC 3923493. PMID 23160421.
De Bustos A, Cuadrado A, Jouve N (November 2016). "Sequencing of long stretches of repetitive DNA". Scientific Reports. 6 (1): 36665. Bibcode:2016NatSR...636665D. doi:10.1038/srep36665. PMC 5098217. PMID 27819354.
Slotkin RK (1 May 2018). "The case for not masking away repetitive DNA". Mobile DNA. 9 (1): 15. doi:10.1186/s13100-018-0120-9. PMC 5930866. PMID 29743957.

ncbi.nlm.nih.gov

de Koning AP, Gu W, Castoe TA, Batzer MA, Pollock DD (December 2011). "Repetitive elements may comprise over two-thirds of the human genome". PLOS Genetics. 7 (12): e1002384. doi:10.1371/journal.pgen.1002384. PMC 3228813. PMID 22144907.
Lower SE, Dion-Côté AM, Clark AG, Barbash DA (November 2019). "Special Issue: Repetitive DNA Sequences". Genes. 10 (11): 896. doi:10.3390/genes10110896. PMC 6895920. PMID 31698818.
Palazzo AF, Gregory TR (May 2014). "The case for junk DNA". PLOS Genetics. 10 (5): e1004351. doi:10.1371/journal.pgen.1004351. PMC 4014423. PMID 24809441.
Sznajder ŁJ, Swanson MS (July 2019). "Short Tandem Repeat Expansions and RNA-Mediated Pathogenesis in Myotonic Dystrophy". International Journal of Molecular Sciences. 20 (13): 3365. doi:10.3390/ijms20133365. PMC 6651174. PMID 31323950.
Wahls WP (1998). "Meiotic recombination hotspots: shaping the genome and insights into hypervariable minisatellite DNA change". Current Topics in Developmental Biology. 37: 37–75. doi:10.1016/s0070-2153(08)60171-4. ISBN 9780121531379. PMC 3151733. PMID 9352183.
Qi J, Shafer RH (2005-06-02). "Covalent ligation studies on the human telomere quadruplex". Nucleic Acids Research. 33 (10): 3185–3192. doi:10.1093/nar/gki632. PMC 1142406. PMID 15933211.
Nicolau M, Picault N, Moissiard G (October 2021). "The Evolutionary Volte-Face of Transposable Elements: From Harmful Jumping Genes to Major Drivers of Genetic Innovation". Cells. 10 (11): 2952. doi:10.3390/cells10112952. PMC 8616336. PMID 34831175.
Mangiavacchi A, Liu P, Della Valle F, Orlando V (July 2021). "New insights into the functional role of retrotransposon dynamics in mammalian somatic cells". Cellular and Molecular Life Sciences. 78 (13): 5245–5256. doi:10.1007/s00018-021-03851-5. PMC 8257530. PMID 33990851.
Usdin K, House NC, Freudenreich CH (22 January 2015). "Repeat instability during DNA repair: Insights from model systems". Critical Reviews in Biochemistry and Molecular Biology. 50 (2): 142–167. doi:10.3109/10409238.2014.999192. PMC 4454471. PMID 25608779.
Massey TH, Jones L (January 2018). "The central role of DNA damage and repair in CAG repeat diseases". Disease Models & Mechanisms. 11 (1): dmm031930. doi:10.1242/dmm.031930. PMC 5818082. PMID 29419417.
Schulte J, Littleton JT (January 2011). "The biological function of the Huntingtin protein and its relevance to Huntington's Disease pathology". Current Trends in Neurology. 5: 65–78. PMC 3237673. PMID 22180703.
Honti V, Vécsei L (June 2005). "Genetic and molecular aspects of spinocerebellar ataxias". Neuropsychiatric Disease and Treatment. 1 (2): 125–133. doi:10.2147/nedt.1.2.125.61044. PMC 2413192. PMID 18568057.
Bürk K (2017). "Friedreich Ataxia: current status and future prospects". Cerebellum & Ataxias. 4 (1): 4. doi:10.1186/s40673-017-0062-x. PMC 5383992. PMID 28405347.
Mazzara PG, Muggeo S, Luoni M, Massimino L, Zaghi M, Valverde PT, et al. (August 2020). "Frataxin gene editing rescues Friedreich's ataxia pathology in dorsal root ganglia organoid-derived sensory neurons". Nature Communications. 11 (1): 4178. Bibcode:2020NatCo..11.4178M. doi:10.1038/s41467-020-17954-3. PMC 7442818. PMID 32826895.
Hahn C, Salajegheh MK (January 2016). "Myotonic disorders: A review article". Iranian Journal of Neurology. 15 (1): 46–53. PMC 4852070. PMID 27141276.
van Blitterswijk M, DeJesus-Hernandez M, Rademakers R (December 2012). "How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia: can we learn from other noncoding repeat expansion disorders?". Current Opinion in Neurology. 25 (6): 689–700. doi:10.1097/WCO.0b013e32835a3efb. PMC 3923493. PMID 23160421.
De Bustos A, Cuadrado A, Jouve N (November 2016). "Sequencing of long stretches of repetitive DNA". Scientific Reports. 6 (1): 36665. Bibcode:2016NatSR...636665D. doi:10.1038/srep36665. PMC 5098217. PMID 27819354.
Slotkin RK (1 May 2018). "The case for not masking away repetitive DNA". Mobile DNA. 9 (1): 15. doi:10.1186/s13100-018-0120-9. PMC 5930866. PMID 29743957.

meshb.nlm.nih.gov

"MeSH Browser". meshb.nlm.nih.gov. Retrieved 2022-09-30.

sciencedirect.com

"Repeated Sequence (DNA) - an overview | ScienceDirect Topics". www.sciencedirect.com. Retrieved 2022-10-04.

semanticscholar.org

api.semanticscholar.org

Shapiro JA, von Sternberg R (May 2005). "Why repetitive DNA is essential to genome function". Biological Reviews of the Cambridge Philosophical Society. 80 (2): 227–250. doi:10.1017/s1464793104006657. PMID 15921050. S2CID 18866824.
Orgel LE, Crick FH, Sapienza C (December 1980). "Selfish DNA". Nature. 288 (5792): 645–646. Bibcode:1980Natur.288..645O. doi:10.1038/288645a0. PMID 7453798. S2CID 4370178.
Janssen A, Colmenares SU, Karpen GH (October 2018). "Heterochromatin: Guardian of the Genome". Annual Review of Cell and Developmental Biology. 34 (1): 265–288. doi:10.1146/annurev-cellbio-100617-062653. PMID 30044650. S2CID 51718804.
Miga KH (September 2015). "Completing the human genome: the progress and challenge of satellite DNA assembly". Chromosome Research. 23 (3): 421–426. doi:10.1007/s10577-015-9488-2. PMID 26363799. S2CID 15229421.
Miga KH (September 2015). "Completing the human genome: the progress and challenge of satellite DNA assembly". Chromosome Research. 23 (3): 421–426. doi:10.1007/s004390050508. PMID 26363799. S2CID 615040.
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worldcat.org

Pearson CE, Zorbas H, Price GB, Zannis-Hadjopoulos M (October 1996). "Inverted repeats, stem-loops, and cruciforms: significance for initiation of DNA replication". Journal of Cellular Biochemistry. 63 (1): 1–22. doi:10.1002/(SICI)1097-4644(199610)63:1<1::AID-JCB1>3.0.CO;2-3. eISSN 1097-4644. PMID 8891900. S2CID 22204780.