Germline mutation (English Wikipedia)

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

refsWebsite

Global rank English rank

35nih.gov

4^th place

19doi.org

2^nd place

5harvard.edu

18^th place

17^th place

3semanticscholar.org

11^th place

8^th place

2cancer.gov

1,684^th place

1,350^th place

1berkeley.edu

580^th place

462^nd place

1web.archive.org

1^st place

1thetech.org

low place

1cancer.net

low place

1mayoclinic.org

1,610^th place

1,279^th place

1cysticfibrosis.ca

low place

1hopkinscf.org

low place

1geneticsandsociety.org

low place

berkeley.edu

evolution.berkeley.edu

"The causes of mutations". evolution.berkeley.edu. Retrieved 2017-11-30.

cancer.gov

"NCI Dictionary of Cancer Terms". National Cancer Institute. 2011-02-02. Retrieved 2017-11-30.
"The Genetics of Cancer". National Cancer Institute. NIH. 2015-04-22. Retrieved 23 September 2018.

cancer.net

"The Genetics of Cancer". Cancer.Net. 2012-03-26. Retrieved 2017-12-01.

cysticfibrosis.ca

"Cystic Fibrosis Canada". www.cysticfibrosis.ca. Retrieved 2017-11-30.

doi.org

Foulkes WD, Real FX (April 2013). "Many mosaic mutations". Current Oncology. 20 (2): 85–7. doi:10.3747/co.20.1449. PMC 3615857. PMID 23559869.
Samuels ME, Friedman JM (April 2015). "Genetic mosaics and the germ line lineage". Genes. 6 (2): 216–37. doi:10.3390/genes6020216. PMC 4488662. PMID 25898403.
Crow JF (October 2000). "The origins, patterns and implications of human spontaneous mutation". Nature Reviews Genetics. 1 (1): 40–7. doi:10.1038/35049558. PMID 11262873. S2CID 22279735.
Wong WS, Solomon BD, Bodian DL, Kothiyal P, Eley G, Huddleston KC, Baker R, Thach DC, Iyer RK, Vockley JG, Niederhuber JE (January 2016). "New observations on maternal age effect on germline de novo mutations". Nature Communications. 7: 10486. Bibcode:2016NatCo...710486W. doi:10.1038/ncomms10486. PMC 4735694. PMID 26781218.
Hassold T, Hunt P (December 2009). "Maternal age and chromosomally abnormal pregnancies: what we know and what we wish we knew". Current Opinion in Pediatrics. 21 (6): 703–8. doi:10.1097/MOP.0b013e328332c6ab. PMC 2894811. PMID 19881348.
Chen Q, Vazquez EJ, Moghaddas S, Hoppel CL, Lesnefsky EJ (September 2003). "Production of reactive oxygen species by mitochondria: central role of complex III". The Journal of Biological Chemistry. 278 (38): 36027–31. doi:10.1074/jbc.M304854200. PMID 12840017.
Ohno M, Sakumi K, Fukumura R, Furuichi M, Iwasaki Y, Hokama M, Ikemura T, Tsuzuki T, Gondo Y, Nakabeppu Y (April 2014). "8-oxoguanine causes spontaneous de novo germline mutations in mice". Scientific Reports. 4: 4689. Bibcode:2014NatSR...4E4689O. doi:10.1038/srep04689. PMC 3986730. PMID 24732879.
Rahbari R, Wuster A, Lindsay SJ, Hardwick RJ, Alexandrov LB, Turki SA, Dominiczak A, Morris A, Porteous D, Smith B, Stratton MR, Hurles ME (February 2016). "Timing, rates and spectra of human germline mutation". Nature Genetics. 48 (2): 126–133. doi:10.1038/ng.3469. PMC 4731925. PMID 26656846.
Cai L, Wang P (March 1995). "Induction of a cytogenetic adaptive response in germ cells of irradiated mice with very low-dose rate of chronic gamma-irradiation and its biological influence on radiation-induced DNA or chromosomal damage and cell killing in their male offspring". Mutagenesis. 10 (2): 95–100. doi:10.1093/mutage/10.2.95. PMID 7603336.
Chandley AC (April 1991). "On the parental origin of de novo mutation in man". Journal of Medical Genetics. 28 (4): 217–23. doi:10.1136/jmg.28.4.217. PMC 1016821. PMID 1677423.
Hook, EB (September 1981). "Rates of chromosome abnormalities at different maternal ages". Obstetrics and Gynecology. 27 (1): 282–5. doi:10.1016/0091-2182(82)90145-8. PMID 6455611.
Ghanta, Sujana (October 2010). "Non-Invasive Prenatal Detection of Trisomy 21 Using Tandem Single Nucleotide Polymorphisms". PLOS ONE. 5 (10): e13184. Bibcode:2010PLoSO...513184G. doi:10.1371/journal.pone.0013184. PMC 2951898. PMID 20949031.
O'Sullivan BP, Freedman SD (May 2009). "Cystic fibrosis". Lancet. 373 (9678): 1891–904. doi:10.1016/S0140-6736(09)60327-5. PMID 19403164. S2CID 46011502.
Sander JD, Joung JK (April 2014). "CRISPR-Cas systems for editing, regulating and targeting genomes". Nature Biotechnology. 32 (4): 347–55. doi:10.1038/nbt.2842. PMC 4022601. PMID 24584096.
Shalem O, Sanjana NE, Hartenian E, Shi X, Scott DA, Mikkelson T, Heckl D, Ebert BL, Root DE, Doench JG, Zhang F (January 2014). "Genome-scale CRISPR-Cas9 knockout screening in human cells". Science. 343 (6166): 84–87. Bibcode:2014Sci...343...84S. doi:10.1126/science.1247005. PMC 4089965. PMID 24336571.
Smith C, Gore A, Yan W, Abalde-Atristain L, Li Z, He C, Wang Y, Brodsky RA, Zhang K, Cheng L, Ye Z (July 2014). "Whole-genome sequencing analysis reveals high specificity of CRISPR/Cas9 and TALEN-based genome editing in human iPSCs". Cell Stem Cell. 15 (1): 12–3. doi:10.1016/j.stem.2014.06.011. PMC 4338993. PMID 24996165.
Bedell VM, Wang Y, Campbell JM, Poshusta TL, Starker CG, Krug RG, Tan W, Penheiter SG, Ma AC, Leung AY, Fahrenkrug SC, Carlson DF, Voytas DF, Clark KJ, Essner JJ, Ekker SC (November 2012). "In vivo genome editing using a high-efficiency TALEN system". Nature. 491 (7422): 114–8. Bibcode:2012Natur.491..114B. doi:10.1038/nature11537. PMC 3491146. PMID 23000899.
Nemudryi AA, Valetdinova KR, Medvedev SP, Zakian SM (July 2014). "TALEN and CRISPR/Cas Genome Editing Systems: Tools of Discovery". Acta Naturae. 6 (3): 19–40. doi:10.32607/20758251-2014-6-3-19-40. PMC 4207558. PMID 25349712.
Urnov FD, Rebar EJ, Holmes MC, Zhang HS, Gregory PD (September 2010). "Genome editing with engineered zinc finger nucleases". Nature Reviews Genetics. 11 (9): 636–46. doi:10.1038/nrg2842. PMID 20717154. S2CID 205484701.

geneticsandsociety.org

"About Human Germline Gene Editing | Center for Genetics and Society". www.geneticsandsociety.org. Retrieved 2017-12-01.

harvard.edu

ui.adsabs.harvard.edu

Wong WS, Solomon BD, Bodian DL, Kothiyal P, Eley G, Huddleston KC, Baker R, Thach DC, Iyer RK, Vockley JG, Niederhuber JE (January 2016). "New observations on maternal age effect on germline de novo mutations". Nature Communications. 7: 10486. Bibcode:2016NatCo...710486W. doi:10.1038/ncomms10486. PMC 4735694. PMID 26781218.
Ohno M, Sakumi K, Fukumura R, Furuichi M, Iwasaki Y, Hokama M, Ikemura T, Tsuzuki T, Gondo Y, Nakabeppu Y (April 2014). "8-oxoguanine causes spontaneous de novo germline mutations in mice". Scientific Reports. 4: 4689. Bibcode:2014NatSR...4E4689O. doi:10.1038/srep04689. PMC 3986730. PMID 24732879.
Ghanta, Sujana (October 2010). "Non-Invasive Prenatal Detection of Trisomy 21 Using Tandem Single Nucleotide Polymorphisms". PLOS ONE. 5 (10): e13184. Bibcode:2010PLoSO...513184G. doi:10.1371/journal.pone.0013184. PMC 2951898. PMID 20949031.
Shalem O, Sanjana NE, Hartenian E, Shi X, Scott DA, Mikkelson T, Heckl D, Ebert BL, Root DE, Doench JG, Zhang F (January 2014). "Genome-scale CRISPR-Cas9 knockout screening in human cells". Science. 343 (6166): 84–87. Bibcode:2014Sci...343...84S. doi:10.1126/science.1247005. PMC 4089965. PMID 24336571.
Bedell VM, Wang Y, Campbell JM, Poshusta TL, Starker CG, Krug RG, Tan W, Penheiter SG, Ma AC, Leung AY, Fahrenkrug SC, Carlson DF, Voytas DF, Clark KJ, Essner JJ, Ekker SC (November 2012). "In vivo genome editing using a high-efficiency TALEN system". Nature. 491 (7422): 114–8. Bibcode:2012Natur.491..114B. doi:10.1038/nature11537. PMC 3491146. PMID 23000899.

hopkinscf.org

"Prenatal Diagnosis". Johns Hopkins Cystic Fibrosis Center. Retrieved 23 September 2018.

mayoclinic.org

"Huntington's disease". Mayo Clinic. Retrieved 23 September 2018.

nih.gov

pubmed.ncbi.nlm.nih.gov

Foulkes WD, Real FX (April 2013). "Many mosaic mutations". Current Oncology. 20 (2): 85–7. doi:10.3747/co.20.1449. PMC 3615857. PMID 23559869.
Samuels ME, Friedman JM (April 2015). "Genetic mosaics and the germ line lineage". Genes. 6 (2): 216–37. doi:10.3390/genes6020216. PMC 4488662. PMID 25898403.
Crow JF (October 2000). "The origins, patterns and implications of human spontaneous mutation". Nature Reviews Genetics. 1 (1): 40–7. doi:10.1038/35049558. PMID 11262873. S2CID 22279735.
Wong WS, Solomon BD, Bodian DL, Kothiyal P, Eley G, Huddleston KC, Baker R, Thach DC, Iyer RK, Vockley JG, Niederhuber JE (January 2016). "New observations on maternal age effect on germline de novo mutations". Nature Communications. 7: 10486. Bibcode:2016NatCo...710486W. doi:10.1038/ncomms10486. PMC 4735694. PMID 26781218.
Hassold T, Hunt P (December 2009). "Maternal age and chromosomally abnormal pregnancies: what we know and what we wish we knew". Current Opinion in Pediatrics. 21 (6): 703–8. doi:10.1097/MOP.0b013e328332c6ab. PMC 2894811. PMID 19881348.
Chen Q, Vazquez EJ, Moghaddas S, Hoppel CL, Lesnefsky EJ (September 2003). "Production of reactive oxygen species by mitochondria: central role of complex III". The Journal of Biological Chemistry. 278 (38): 36027–31. doi:10.1074/jbc.M304854200. PMID 12840017.
Ohno M, Sakumi K, Fukumura R, Furuichi M, Iwasaki Y, Hokama M, Ikemura T, Tsuzuki T, Gondo Y, Nakabeppu Y (April 2014). "8-oxoguanine causes spontaneous de novo germline mutations in mice". Scientific Reports. 4: 4689. Bibcode:2014NatSR...4E4689O. doi:10.1038/srep04689. PMC 3986730. PMID 24732879.
Rahbari R, Wuster A, Lindsay SJ, Hardwick RJ, Alexandrov LB, Turki SA, Dominiczak A, Morris A, Porteous D, Smith B, Stratton MR, Hurles ME (February 2016). "Timing, rates and spectra of human germline mutation". Nature Genetics. 48 (2): 126–133. doi:10.1038/ng.3469. PMC 4731925. PMID 26656846.
Cai L, Wang P (March 1995). "Induction of a cytogenetic adaptive response in germ cells of irradiated mice with very low-dose rate of chronic gamma-irradiation and its biological influence on radiation-induced DNA or chromosomal damage and cell killing in their male offspring". Mutagenesis. 10 (2): 95–100. doi:10.1093/mutage/10.2.95. PMID 7603336.
Chandley AC (April 1991). "On the parental origin of de novo mutation in man". Journal of Medical Genetics. 28 (4): 217–23. doi:10.1136/jmg.28.4.217. PMC 1016821. PMID 1677423.
Hook, EB (September 1981). "Rates of chromosome abnormalities at different maternal ages". Obstetrics and Gynecology. 27 (1): 282–5. doi:10.1016/0091-2182(82)90145-8. PMID 6455611.
Ghanta, Sujana (October 2010). "Non-Invasive Prenatal Detection of Trisomy 21 Using Tandem Single Nucleotide Polymorphisms". PLOS ONE. 5 (10): e13184. Bibcode:2010PLoSO...513184G. doi:10.1371/journal.pone.0013184. PMC 2951898. PMID 20949031.
O'Sullivan BP, Freedman SD (May 2009). "Cystic fibrosis". Lancet. 373 (9678): 1891–904. doi:10.1016/S0140-6736(09)60327-5. PMID 19403164. S2CID 46011502.
Sander JD, Joung JK (April 2014). "CRISPR-Cas systems for editing, regulating and targeting genomes". Nature Biotechnology. 32 (4): 347–55. doi:10.1038/nbt.2842. PMC 4022601. PMID 24584096.
Shalem O, Sanjana NE, Hartenian E, Shi X, Scott DA, Mikkelson T, Heckl D, Ebert BL, Root DE, Doench JG, Zhang F (January 2014). "Genome-scale CRISPR-Cas9 knockout screening in human cells". Science. 343 (6166): 84–87. Bibcode:2014Sci...343...84S. doi:10.1126/science.1247005. PMC 4089965. PMID 24336571.
Smith C, Gore A, Yan W, Abalde-Atristain L, Li Z, He C, Wang Y, Brodsky RA, Zhang K, Cheng L, Ye Z (July 2014). "Whole-genome sequencing analysis reveals high specificity of CRISPR/Cas9 and TALEN-based genome editing in human iPSCs". Cell Stem Cell. 15 (1): 12–3. doi:10.1016/j.stem.2014.06.011. PMC 4338993. PMID 24996165.
Bedell VM, Wang Y, Campbell JM, Poshusta TL, Starker CG, Krug RG, Tan W, Penheiter SG, Ma AC, Leung AY, Fahrenkrug SC, Carlson DF, Voytas DF, Clark KJ, Essner JJ, Ekker SC (November 2012). "In vivo genome editing using a high-efficiency TALEN system". Nature. 491 (7422): 114–8. Bibcode:2012Natur.491..114B. doi:10.1038/nature11537. PMC 3491146. PMID 23000899.
Nemudryi AA, Valetdinova KR, Medvedev SP, Zakian SM (July 2014). "TALEN and CRISPR/Cas Genome Editing Systems: Tools of Discovery". Acta Naturae. 6 (3): 19–40. doi:10.32607/20758251-2014-6-3-19-40. PMC 4207558. PMID 25349712.
Urnov FD, Rebar EJ, Holmes MC, Zhang HS, Gregory PD (September 2010). "Genome editing with engineered zinc finger nucleases". Nature Reviews Genetics. 11 (9): 636–46. doi:10.1038/nrg2842. PMID 20717154. S2CID 205484701.

ncbi.nlm.nih.gov

Griffiths AJ, Miller JH, Suzuki DT, Lewontin RC, Gelbart WM (2000). "Somatic versus germinal mutation". An Introduction to Genetic Analysis (7th ed.).
Foulkes WD, Real FX (April 2013). "Many mosaic mutations". Current Oncology. 20 (2): 85–7. doi:10.3747/co.20.1449. PMC 3615857. PMID 23559869.
Samuels ME, Friedman JM (April 2015). "Genetic mosaics and the germ line lineage". Genes. 6 (2): 216–37. doi:10.3390/genes6020216. PMC 4488662. PMID 25898403.
Wong WS, Solomon BD, Bodian DL, Kothiyal P, Eley G, Huddleston KC, Baker R, Thach DC, Iyer RK, Vockley JG, Niederhuber JE (January 2016). "New observations on maternal age effect on germline de novo mutations". Nature Communications. 7: 10486. Bibcode:2016NatCo...710486W. doi:10.1038/ncomms10486. PMC 4735694. PMID 26781218.
Hassold T, Hunt P (December 2009). "Maternal age and chromosomally abnormal pregnancies: what we know and what we wish we knew". Current Opinion in Pediatrics. 21 (6): 703–8. doi:10.1097/MOP.0b013e328332c6ab. PMC 2894811. PMID 19881348.
Ohno M, Sakumi K, Fukumura R, Furuichi M, Iwasaki Y, Hokama M, Ikemura T, Tsuzuki T, Gondo Y, Nakabeppu Y (April 2014). "8-oxoguanine causes spontaneous de novo germline mutations in mice". Scientific Reports. 4: 4689. Bibcode:2014NatSR...4E4689O. doi:10.1038/srep04689. PMC 3986730. PMID 24732879.
Rahbari R, Wuster A, Lindsay SJ, Hardwick RJ, Alexandrov LB, Turki SA, Dominiczak A, Morris A, Porteous D, Smith B, Stratton MR, Hurles ME (February 2016). "Timing, rates and spectra of human germline mutation". Nature Genetics. 48 (2): 126–133. doi:10.1038/ng.3469. PMC 4731925. PMID 26656846.
Chandley AC (April 1991). "On the parental origin of de novo mutation in man". Journal of Medical Genetics. 28 (4): 217–23. doi:10.1136/jmg.28.4.217. PMC 1016821. PMID 1677423.
Ghanta, Sujana (October 2010). "Non-Invasive Prenatal Detection of Trisomy 21 Using Tandem Single Nucleotide Polymorphisms". PLOS ONE. 5 (10): e13184. Bibcode:2010PLoSO...513184G. doi:10.1371/journal.pone.0013184. PMC 2951898. PMID 20949031.
Sander JD, Joung JK (April 2014). "CRISPR-Cas systems for editing, regulating and targeting genomes". Nature Biotechnology. 32 (4): 347–55. doi:10.1038/nbt.2842. PMC 4022601. PMID 24584096.
Shalem O, Sanjana NE, Hartenian E, Shi X, Scott DA, Mikkelson T, Heckl D, Ebert BL, Root DE, Doench JG, Zhang F (January 2014). "Genome-scale CRISPR-Cas9 knockout screening in human cells". Science. 343 (6166): 84–87. Bibcode:2014Sci...343...84S. doi:10.1126/science.1247005. PMC 4089965. PMID 24336571.
Smith C, Gore A, Yan W, Abalde-Atristain L, Li Z, He C, Wang Y, Brodsky RA, Zhang K, Cheng L, Ye Z (July 2014). "Whole-genome sequencing analysis reveals high specificity of CRISPR/Cas9 and TALEN-based genome editing in human iPSCs". Cell Stem Cell. 15 (1): 12–3. doi:10.1016/j.stem.2014.06.011. PMC 4338993. PMID 24996165.
Bedell VM, Wang Y, Campbell JM, Poshusta TL, Starker CG, Krug RG, Tan W, Penheiter SG, Ma AC, Leung AY, Fahrenkrug SC, Carlson DF, Voytas DF, Clark KJ, Essner JJ, Ekker SC (November 2012). "In vivo genome editing using a high-efficiency TALEN system". Nature. 491 (7422): 114–8. Bibcode:2012Natur.491..114B. doi:10.1038/nature11537. PMC 3491146. PMID 23000899.
Nemudryi AA, Valetdinova KR, Medvedev SP, Zakian SM (July 2014). "TALEN and CRISPR/Cas Genome Editing Systems: Tools of Discovery". Acta Naturae. 6 (3): 19–40. doi:10.32607/20758251-2014-6-3-19-40. PMC 4207558. PMID 25349712.

ghr.nlm.nih.gov

"Huntington disease". Genetics Home Reference. NIH. Retrieved 23 September 2018.
Reference, Genetics Home. "CFTR gene". Genetics Home Reference. Retrieved 2017-11-30.

semanticscholar.org

api.semanticscholar.org

Crow JF (October 2000). "The origins, patterns and implications of human spontaneous mutation". Nature Reviews Genetics. 1 (1): 40–7. doi:10.1038/35049558. PMID 11262873. S2CID 22279735.
O'Sullivan BP, Freedman SD (May 2009). "Cystic fibrosis". Lancet. 373 (9678): 1891–904. doi:10.1016/S0140-6736(09)60327-5. PMID 19403164. S2CID 46011502.
Urnov FD, Rebar EJ, Holmes MC, Zhang HS, Gregory PD (September 2010). "Genome editing with engineered zinc finger nucleases". Nature Reviews Genetics. 11 (9): 636–46. doi:10.1038/nrg2842. PMID 20717154. S2CID 205484701.

thetech.org

genetics.thetech.org

"Mutations and Disease | Understanding Genetics". The Tech Interactive. Archived from the original on 2021-09-14.

web.archive.org

"Mutations and Disease | Understanding Genetics". The Tech Interactive. Archived from the original on 2021-09-14.