Mutant (Danish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Mutant" in Danish language version.

refsWebsite

Global rank Danish rank

2^nd place

13^th place

234^th place

176^th place

7^th place

28^th place

1sandwalk.blogspot.dk

low place

low place

274^th place

469^th place

doi.org

Tomita Y, Takeda A, Okinaga S, Tagami H, Shibahara S (1989) Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene. Biochemical and Biophysical Research Communications 164, 990-6. doi: 10.1016/0006-291x(89)91767-1. PMID: 2511845.
Duffy DL, Montgomery GW, Chen W, Zhao ZZ, Le L, James MR, Hayward NK, Martin NG, Sturm RA (2007) A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation. American Journal of Human Genetics 80, 241-52. doi: 10.1086/510885. Epub 2006 Dec 20. PMID: 17236130
Russell WL, Kelly EM (1982) Mutation frequencies in male mice and the estimation of genetic hazards of radiation in men. Proceedings of the National Academy of Sciences U. S. A. 79, 542-4. doi: 10.1073/pnas.79.2.542. PMID: 6952206
Bard D, Verger P, Hubert P (1997) Chernobyl, 10 years after: health consequences. Epidemiologic Reviews 19, 187-204. doi: 10.1093/oxfordjournals.epirev.a017952. PMID: 9494782.

nature.com

White D, Rabago-Smith M. Genotype-phenotype associations and human eye color. Journal of Human Genetics 2011 Jan;56(1):5-7. doi: 10.1038/jhg.2010.126. Epub 2010 Oct 14. PMID: 20944644.
Møller AP, Mousseau TA (2015) Strong effects of ionizing radiation from Chernobyl on mutation rates. Scientific Reports 5, 8363. doi: 10.1038/srep08363. PMID: 25666381

nytimes.com

Chang, K. (2005) Yes, It's a Lobster, and Yes, It's Blue. New York Times, 15. marts 2005, Hentet 29. november 2023.

sandwalk.blogspot.dk

Sandwalk: Human mutation rates - what's the right number?

springer.com

link.springer.com

Eiberg H, Troelsen J, Nielsen M, Mikkelsen A, Mengel-From J, Kjaer KW, Hansen L. Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression. Hum Genet. 2008 Mar;123(2):177-87. doi: 10.1007/s00439-007-0460-x. PMID: 18172690.