Einzelnukleotid-Polymorphismus (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Einzelnukleotid-Polymorphismus" in German language version.

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E Papaemmanuil, FJ Hosking, J Vijayakrishnan, A Price, B Olver, E Sheridan, SE Kinsey, T Lightfoot, E Roman, JA Irving, JM Allan, IP Tomlinson, M Taylor, M Greaves, RS Houlston: Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. In: Nat Genet., 2009, 41(9), S. 1006–1010, doi:10.1038/ng.430, PMID 19684604
DL Thomas, CL Thio, MP Martin, Y Qi, D Ge, C O’Huigin, J Kidd, K Kidd, SI Khakoo, G Alexander, JJ Goedert, GD Kirk, SM Donfield, HR Rosen, LH Tobler, MP Busch, JG McHutchison, DB Goldstein, M Carrington: Genetic variation in IL28B and spontaneous clearance of hepatitis C virus. In: Nature, 2009, 461(7265), S. 798–801. doi:10.1038/nature08463, PMID 19759533.
T. Bersaglieri, P. C. Sabeti u. a.: Genetic signatures of strong recent positive selection at the lactase gene. In: American Journal of Human Genetics. Band 74, Nummer 6, Juni 2004, S. 1111–1120, doi:10.1086/421051, PMID 15114531, PMC 1182075 (freier Volltext).
Friederike Flachsbart, Janina Dose, Liljana Gentschew, Claudia Geismann, weitere 29 Autoren sowie Almut Nebel: Identification and characterization of two functional variants in the human longevity gene FOXO3. In: Nature Communication 8/2017: 2063, 1–12. doi:10.1038/s41467-017-02183-y.

E Papaemmanuil, FJ Hosking, J Vijayakrishnan, A Price, B Olver, E Sheridan, SE Kinsey, T Lightfoot, E Roman, JA Irving, JM Allan, IP Tomlinson, M Taylor, M Greaves, RS Houlston: Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. In: Nat Genet., 2009, 41(9), S. 1006–1010, doi:10.1038/ng.430, PMID 19684604
Hugot et al.: Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn’s Disease. In: Nature, Band 411, Mai 2001, S. 599–603, PMID 11385576.
Ogura et al.: A frameshift mutation in NOD2 associated with susceptibility to Crohn’s disease. In: Nature, Band 411, Mai 2001, S. 603–606, PMID 11385577. (freier Volltext).
DL Thomas, CL Thio, MP Martin, Y Qi, D Ge, C O’Huigin, J Kidd, K Kidd, SI Khakoo, G Alexander, JJ Goedert, GD Kirk, SM Donfield, HR Rosen, LH Tobler, MP Busch, JG McHutchison, DB Goldstein, M Carrington: Genetic variation in IL28B and spontaneous clearance of hepatitis C virus. In: Nature, 2009, 461(7265), S. 798–801. doi:10.1038/nature08463, PMID 19759533.
T. Bersaglieri, P. C. Sabeti u. a.: Genetic signatures of strong recent positive selection at the lactase gene. In: American Journal of Human Genetics. Band 74, Nummer 6, Juni 2004, S. 1111–1120, doi:10.1086/421051, PMID 15114531, PMC 1182075 (freier Volltext).