Mutant (Danish Wikipedia)

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

Last modified: 08:27:08, 3 July 2025 (UTC)

Ref.Un. Ref.Website

Global rank Danish rank

77nih.gov

5^th place

16^th place

44doi.org

2^nd place

9^th place

22nature.com

207^th place

192^nd place

11nytimes.com

7^th place

21^st place

11blogspot.dk

low place

379^th place

11springer.com

182^nd place

523^rd place

blogspot.dk (Global: low place; Danish: 379^th place)

sandwalk.blogspot.dk

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

doi.org (Global: 2^nd place; Danish: 9^th place)

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 (Global: 207^th place; Danish: 192^nd place)

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

nih.gov (Global: 5^th place; Danish: 16^th place)

ncbi.nlm.nih.gov

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.
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.
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
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.
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
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
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.

nytimes.com (Global: 7^th place; Danish: 21^st place)

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

springer.com (Global: 182^nd place; Danish: 523^rd place)

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.

Mutant (Danish Wikipedia)

blogspot.dk (Global: low place; Danish: 379th place)

sandwalk.blogspot.dk

doi.org (Global: 2nd place; Danish: 9th place)

nature.com (Global: 207th place; Danish: 192nd place)

nih.gov (Global: 5th place; Danish: 16th place)