Homoplasmy (English Wikipedia)

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

refsWebsite

Global rank English rank

16nih.gov

4^th place

12doi.org

2^nd place

5semanticscholar.org

11^th place

8^th place

5worldcat.org

5^th place

3harvard.edu

18^th place

17^th place

2jstor.org

26^th place

20^th place

1miami.edu

4,511^th place

2,800^th place

1els-cdn.com

low place

1rupress.org

low place

doi.org

Dimauro, Salvatore; Davidzon, Guido (2005). "Mitochondrial DNA and disease". Annals of Medicine. 37 (3): 222–232. doi:10.1080/07853890510007368. PMID 16019721. S2CID 11114978.
Ballana, E.; Govea, N.; de Cid, R.; Garcia, C.; Arribas, C.; Rosell, J.; Estivill, X. (2008). "Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations". Hum. Mutat. 29 (2): 248–257. doi:10.1002/humu.20639. PMID 17999439. S2CID 25493822.
Coller, HA; Khrapko, K; Bodyak, ND; Nekhaeva, E; Herrero-Jimenez, P; Thilly, WG (2001). "High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection". Nature Genetics. 28 (2): 147–50. doi:10.1038/88859. PMID 11381261. S2CID 11929018.
Hoeh, Walter R.; Blakley, Karen H.; Brown, Wesley M. (1 January 1991). "Heteroplasmy Suggests Limited Biparental Inheritance of Mytilus Mitochondrial DNA". Science. 251 (5000): 1488–1490. Bibcode:1991Sci...251.1488H. doi:10.1126/science.1672472. JSTOR 2875830. PMID 1672472.
Gasparre, Giuseppe; Iommarini, Luisa; Porcelli, Anna Maria; Lang, Martin; Ferri, Gian Gaetano; Kurelac, Ivana; Zuntini, Roberta; Mariani, Elisa; Pennisi, Lucia Fiammetta (1 March 2009). "An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells". Human Mutation. 30 (3): 391–396. doi:10.1002/humu.20870. ISSN 1098-1004. PMID 19086058. S2CID 33063313.
Wallace, Douglas C.; Singh, Gurparkash; Lott, Marie T.; Hodge, Judy A.; Schurr, Theodore G.; Lezza, Angela M. S.; Elsas, Louis J.; Nikoskelainen, Eeva K. (1988). "Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy". Science. 242 (4884): 1427–1430. Bibcode:1988Sci...242.1427W. doi:10.1126/science.3201231. JSTOR 1702331. PMID 3201231.
Lightowlers, Robert N.; Chinnery, Patrick F.; Turnbull, Douglass M.; Howell, Neil (1997). "Mammalian mitochondrial genetics: heredity, heteroplasmy and disease" (PDF). Trends in Genetics. 13 (11): 450–455. doi:10.1016/S0168-9525(97)01266-3. PMID 9385842. Retrieved 8 February 2016.
Gasparre, Giuseppe; Porcelli, Anna Maria; Bonora, Elena; Pennisi, Lucia Fiammetta; Toller, Matteo; Iommarini, Luisa; Ghelli, Anna; Moretti, Massimo; Betts, Christine M. (22 May 2007). "Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors". Proceedings of the National Academy of Sciences. 104 (21): 9001–9006. Bibcode:2007PNAS..104.9001G. doi:10.1073/pnas.0703056104. ISSN 0027-8424. PMC 1885617. PMID 17517629.
Gilkerson, Robert W.; Schon, Eric A.; Hernandez, Evelyn; Davidson, Mercy M. (30 June 2008). "Mitochondrial nucleoids maintain genetic autonomy but allow for functional complementation". The Journal of Cell Biology. 181 (7): 1117–1128. doi:10.1083/jcb.200712101. ISSN 0021-9525. PMC 2442202. PMID 18573913.
Giordano (2015). "Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways". Cell Death and Disease. 6 (12): e2021. doi:10.1038/cddis.2015.364. PMC 4720897. PMID 26673666.
Pegoraro, Elena; Vettori, Andrea; Valentino, Maria L.; Molon, Annamaria; Mostacciuolo, Maria L.; Howell, Neil; Carelli, Valerio (15 May 2003). "X-inactivation pattern in multiple tissues from two leber's hereditary optic neuropathy (LHON) patients". American Journal of Medical Genetics Part A. 119A (1): 37–40. doi:10.1002/ajmg.a.10211. ISSN 1552-4833. PMID 12707956. S2CID 19349243.
Handoko, H. Y.; Wirapati, P. J.; Sudoyo, H. A.; Sitepu, M.; Marzuki, S. (1 August 1998). "Meiotic breakpoint mapping of a proposed X linked visual loss susceptibility locus in Leber's hereditary optic neuropathy". Journal of Medical Genetics. 35 (8): 668–671. doi:10.1136/jmg.35.8.668. ISSN 1468-6244. PMC 1051394. PMID 9719375.

els-cdn.com

ac.els-cdn.com

Lightowlers, Robert N.; Chinnery, Patrick F.; Turnbull, Douglass M.; Howell, Neil (1997). "Mammalian mitochondrial genetics: heredity, heteroplasmy and disease" (PDF). Trends in Genetics. 13 (11): 450–455. doi:10.1016/S0168-9525(97)01266-3. PMID 9385842. Retrieved 8 February 2016.

harvard.edu

ui.adsabs.harvard.edu

Hoeh, Walter R.; Blakley, Karen H.; Brown, Wesley M. (1 January 1991). "Heteroplasmy Suggests Limited Biparental Inheritance of Mytilus Mitochondrial DNA". Science. 251 (5000): 1488–1490. Bibcode:1991Sci...251.1488H. doi:10.1126/science.1672472. JSTOR 2875830. PMID 1672472.
Wallace, Douglas C.; Singh, Gurparkash; Lott, Marie T.; Hodge, Judy A.; Schurr, Theodore G.; Lezza, Angela M. S.; Elsas, Louis J.; Nikoskelainen, Eeva K. (1988). "Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy". Science. 242 (4884): 1427–1430. Bibcode:1988Sci...242.1427W. doi:10.1126/science.3201231. JSTOR 1702331. PMID 3201231.
Gasparre, Giuseppe; Porcelli, Anna Maria; Bonora, Elena; Pennisi, Lucia Fiammetta; Toller, Matteo; Iommarini, Luisa; Ghelli, Anna; Moretti, Massimo; Betts, Christine M. (22 May 2007). "Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors". Proceedings of the National Academy of Sciences. 104 (21): 9001–9006. Bibcode:2007PNAS..104.9001G. doi:10.1073/pnas.0703056104. ISSN 0027-8424. PMC 1885617. PMID 17517629.

jstor.org

Hoeh, Walter R.; Blakley, Karen H.; Brown, Wesley M. (1 January 1991). "Heteroplasmy Suggests Limited Biparental Inheritance of Mytilus Mitochondrial DNA". Science. 251 (5000): 1488–1490. Bibcode:1991Sci...251.1488H. doi:10.1126/science.1672472. JSTOR 2875830. PMID 1672472.
Wallace, Douglas C.; Singh, Gurparkash; Lott, Marie T.; Hodge, Judy A.; Schurr, Theodore G.; Lezza, Angela M. S.; Elsas, Louis J.; Nikoskelainen, Eeva K. (1988). "Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy". Science. 242 (4884): 1427–1430. Bibcode:1988Sci...242.1427W. doi:10.1126/science.3201231. JSTOR 1702331. PMID 3201231.

miami.edu

hihg.med.miami.edu

Heteroplasmy vs. Homoplasmy. University of Miami Faculty of Medicine. Accessed 21 October 2012.

nih.gov

pubmed.ncbi.nlm.nih.gov

Dimauro, Salvatore; Davidzon, Guido (2005). "Mitochondrial DNA and disease". Annals of Medicine. 37 (3): 222–232. doi:10.1080/07853890510007368. PMID 16019721. S2CID 11114978.
Ballana, E.; Govea, N.; de Cid, R.; Garcia, C.; Arribas, C.; Rosell, J.; Estivill, X. (2008). "Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations". Hum. Mutat. 29 (2): 248–257. doi:10.1002/humu.20639. PMID 17999439. S2CID 25493822.
Coller, HA; Khrapko, K; Bodyak, ND; Nekhaeva, E; Herrero-Jimenez, P; Thilly, WG (2001). "High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection". Nature Genetics. 28 (2): 147–50. doi:10.1038/88859. PMID 11381261. S2CID 11929018.
Hoeh, Walter R.; Blakley, Karen H.; Brown, Wesley M. (1 January 1991). "Heteroplasmy Suggests Limited Biparental Inheritance of Mytilus Mitochondrial DNA". Science. 251 (5000): 1488–1490. Bibcode:1991Sci...251.1488H. doi:10.1126/science.1672472. JSTOR 2875830. PMID 1672472.
Gasparre, Giuseppe; Iommarini, Luisa; Porcelli, Anna Maria; Lang, Martin; Ferri, Gian Gaetano; Kurelac, Ivana; Zuntini, Roberta; Mariani, Elisa; Pennisi, Lucia Fiammetta (1 March 2009). "An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells". Human Mutation. 30 (3): 391–396. doi:10.1002/humu.20870. ISSN 1098-1004. PMID 19086058. S2CID 33063313.
Wallace, Douglas C.; Singh, Gurparkash; Lott, Marie T.; Hodge, Judy A.; Schurr, Theodore G.; Lezza, Angela M. S.; Elsas, Louis J.; Nikoskelainen, Eeva K. (1988). "Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy". Science. 242 (4884): 1427–1430. Bibcode:1988Sci...242.1427W. doi:10.1126/science.3201231. JSTOR 1702331. PMID 3201231.
Lightowlers, Robert N.; Chinnery, Patrick F.; Turnbull, Douglass M.; Howell, Neil (1997). "Mammalian mitochondrial genetics: heredity, heteroplasmy and disease" (PDF). Trends in Genetics. 13 (11): 450–455. doi:10.1016/S0168-9525(97)01266-3. PMID 9385842. Retrieved 8 February 2016.
Gasparre, Giuseppe; Porcelli, Anna Maria; Bonora, Elena; Pennisi, Lucia Fiammetta; Toller, Matteo; Iommarini, Luisa; Ghelli, Anna; Moretti, Massimo; Betts, Christine M. (22 May 2007). "Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors". Proceedings of the National Academy of Sciences. 104 (21): 9001–9006. Bibcode:2007PNAS..104.9001G. doi:10.1073/pnas.0703056104. ISSN 0027-8424. PMC 1885617. PMID 17517629.
Gilkerson, Robert W.; Schon, Eric A.; Hernandez, Evelyn; Davidson, Mercy M. (30 June 2008). "Mitochondrial nucleoids maintain genetic autonomy but allow for functional complementation". The Journal of Cell Biology. 181 (7): 1117–1128. doi:10.1083/jcb.200712101. ISSN 0021-9525. PMC 2442202. PMID 18573913.
Giordano (2015). "Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways". Cell Death and Disease. 6 (12): e2021. doi:10.1038/cddis.2015.364. PMC 4720897. PMID 26673666.
Pegoraro, Elena; Vettori, Andrea; Valentino, Maria L.; Molon, Annamaria; Mostacciuolo, Maria L.; Howell, Neil; Carelli, Valerio (15 May 2003). "X-inactivation pattern in multiple tissues from two leber's hereditary optic neuropathy (LHON) patients". American Journal of Medical Genetics Part A. 119A (1): 37–40. doi:10.1002/ajmg.a.10211. ISSN 1552-4833. PMID 12707956. S2CID 19349243.
Handoko, H. Y.; Wirapati, P. J.; Sudoyo, H. A.; Sitepu, M.; Marzuki, S. (1 August 1998). "Meiotic breakpoint mapping of a proposed X linked visual loss susceptibility locus in Leber's hereditary optic neuropathy". Journal of Medical Genetics. 35 (8): 668–671. doi:10.1136/jmg.35.8.668. ISSN 1468-6244. PMC 1051394. PMID 9719375.

ncbi.nlm.nih.gov

Gasparre, Giuseppe; Porcelli, Anna Maria; Bonora, Elena; Pennisi, Lucia Fiammetta; Toller, Matteo; Iommarini, Luisa; Ghelli, Anna; Moretti, Massimo; Betts, Christine M. (22 May 2007). "Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors". Proceedings of the National Academy of Sciences. 104 (21): 9001–9006. Bibcode:2007PNAS..104.9001G. doi:10.1073/pnas.0703056104. ISSN 0027-8424. PMC 1885617. PMID 17517629.
Gilkerson, Robert W.; Schon, Eric A.; Hernandez, Evelyn; Davidson, Mercy M. (30 June 2008). "Mitochondrial nucleoids maintain genetic autonomy but allow for functional complementation". The Journal of Cell Biology. 181 (7): 1117–1128. doi:10.1083/jcb.200712101. ISSN 0021-9525. PMC 2442202. PMID 18573913.
Giordano (2015). "Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways". Cell Death and Disease. 6 (12): e2021. doi:10.1038/cddis.2015.364. PMC 4720897. PMID 26673666.
Handoko, H. Y.; Wirapati, P. J.; Sudoyo, H. A.; Sitepu, M.; Marzuki, S. (1 August 1998). "Meiotic breakpoint mapping of a proposed X linked visual loss susceptibility locus in Leber's hereditary optic neuropathy". Journal of Medical Genetics. 35 (8): 668–671. doi:10.1136/jmg.35.8.668. ISSN 1468-6244. PMC 1051394. PMID 9719375.

rupress.org

jcb.rupress.org

Gilkerson, Robert W.; Schon, Eric A.; Hernandez, Evelyn; Davidson, Mercy M. (30 June 2008). "Mitochondrial nucleoids maintain genetic autonomy but allow for functional complementation". The Journal of Cell Biology. 181 (7): 1117–1128. doi:10.1083/jcb.200712101. ISSN 0021-9525. PMC 2442202. PMID 18573913.

semanticscholar.org

api.semanticscholar.org

Dimauro, Salvatore; Davidzon, Guido (2005). "Mitochondrial DNA and disease". Annals of Medicine. 37 (3): 222–232. doi:10.1080/07853890510007368. PMID 16019721. S2CID 11114978.
Ballana, E.; Govea, N.; de Cid, R.; Garcia, C.; Arribas, C.; Rosell, J.; Estivill, X. (2008). "Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations". Hum. Mutat. 29 (2): 248–257. doi:10.1002/humu.20639. PMID 17999439. S2CID 25493822.
Coller, HA; Khrapko, K; Bodyak, ND; Nekhaeva, E; Herrero-Jimenez, P; Thilly, WG (2001). "High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection". Nature Genetics. 28 (2): 147–50. doi:10.1038/88859. PMID 11381261. S2CID 11929018.
Gasparre, Giuseppe; Iommarini, Luisa; Porcelli, Anna Maria; Lang, Martin; Ferri, Gian Gaetano; Kurelac, Ivana; Zuntini, Roberta; Mariani, Elisa; Pennisi, Lucia Fiammetta (1 March 2009). "An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells". Human Mutation. 30 (3): 391–396. doi:10.1002/humu.20870. ISSN 1098-1004. PMID 19086058. S2CID 33063313.
Pegoraro, Elena; Vettori, Andrea; Valentino, Maria L.; Molon, Annamaria; Mostacciuolo, Maria L.; Howell, Neil; Carelli, Valerio (15 May 2003). "X-inactivation pattern in multiple tissues from two leber's hereditary optic neuropathy (LHON) patients". American Journal of Medical Genetics Part A. 119A (1): 37–40. doi:10.1002/ajmg.a.10211. ISSN 1552-4833. PMID 12707956. S2CID 19349243.

worldcat.org

search.worldcat.org

Gasparre, Giuseppe; Iommarini, Luisa; Porcelli, Anna Maria; Lang, Martin; Ferri, Gian Gaetano; Kurelac, Ivana; Zuntini, Roberta; Mariani, Elisa; Pennisi, Lucia Fiammetta (1 March 2009). "An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells". Human Mutation. 30 (3): 391–396. doi:10.1002/humu.20870. ISSN 1098-1004. PMID 19086058. S2CID 33063313.
Gasparre, Giuseppe; Porcelli, Anna Maria; Bonora, Elena; Pennisi, Lucia Fiammetta; Toller, Matteo; Iommarini, Luisa; Ghelli, Anna; Moretti, Massimo; Betts, Christine M. (22 May 2007). "Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors". Proceedings of the National Academy of Sciences. 104 (21): 9001–9006. Bibcode:2007PNAS..104.9001G. doi:10.1073/pnas.0703056104. ISSN 0027-8424. PMC 1885617. PMID 17517629.
Gilkerson, Robert W.; Schon, Eric A.; Hernandez, Evelyn; Davidson, Mercy M. (30 June 2008). "Mitochondrial nucleoids maintain genetic autonomy but allow for functional complementation". The Journal of Cell Biology. 181 (7): 1117–1128. doi:10.1083/jcb.200712101. ISSN 0021-9525. PMC 2442202. PMID 18573913.
Pegoraro, Elena; Vettori, Andrea; Valentino, Maria L.; Molon, Annamaria; Mostacciuolo, Maria L.; Howell, Neil; Carelli, Valerio (15 May 2003). "X-inactivation pattern in multiple tissues from two leber's hereditary optic neuropathy (LHON) patients". American Journal of Medical Genetics Part A. 119A (1): 37–40. doi:10.1002/ajmg.a.10211. ISSN 1552-4833. PMID 12707956. S2CID 19349243.
Handoko, H. Y.; Wirapati, P. J.; Sudoyo, H. A.; Sitepu, M.; Marzuki, S. (1 August 1998). "Meiotic breakpoint mapping of a proposed X linked visual loss susceptibility locus in Leber's hereditary optic neuropathy". Journal of Medical Genetics. 35 (8): 668–671. doi:10.1136/jmg.35.8.668. ISSN 1468-6244. PMC 1051394. PMID 9719375.