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Page 1
Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study.
Butler MG, Hartin SN, Hossain WA, Manzardo AM, Kimonis V, Dykens E, Gold JA, Kim SJ, Weisensel N, Tamura R, Miller JL, Driscoll DJ. Butler MG, et al. Among authors: weisensel n. J Med Genet. 2019 Mar;56(3):149-153. doi: 10.1136/jmedgenet-2018-105301. Epub 2018 May 5. J Med Genet. 2019. PMID: 29730598 Free PMC article.
UGT2B10 genotype influences nicotine glucuronidation, oxidation, and consumption.
Berg JZ, von Weymarn LB, Thompson EA, Wickham KM, Weisensel NA, Hatsukami DK, Murphy SE. Berg JZ, et al. Among authors: weisensel na. Cancer Epidemiol Biomarkers Prev. 2010 Jun;19(6):1423-31. doi: 10.1158/1055-9965.EPI-09-0959. Epub 2010 May 25. Cancer Epidemiol Biomarkers Prev. 2010. PMID: 20501767 Free PMC article.
A role for XLF in DNA repair and recombination in human somatic cells.
Fattah FJ, Kweon J, Wang Y, Lee EH, Kan Y, Lichter N, Weisensel N, Hendrickson EA. Fattah FJ, et al. Among authors: weisensel n. DNA Repair (Amst). 2014 Mar;15:39-53. doi: 10.1016/j.dnarep.2013.12.006. Epub 2014 Jan 21. DNA Repair (Amst). 2014. PMID: 24461734 Free PMC article.