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• Variation in DNA Base Excision Repair Genes in Fuchs Endothelial Corneal Dystrophy.

  Wójcik KA, Synowiec E, Polakowski P, Błasiak J, Szaflik J, Szaflik JP. Wójcik KA, et al. Med Sci Monit. 2015 Sep 21;21:2809-27. doi: 10.12659/MSM.894273. Med Sci Monit. 2015. PMID: 26388025 Free PMC article.
• Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.

  Stolk L, Perry JR, Chasman DI, He C, Mangino M, Sulem P, Barbalic M, Broer L, Byrne EM, Ernst F, Esko T, Franceschini N, Gudbjartsson DF, Hottenga JJ, Kraft P, McArdle PF, Porcu E, Shin SY, Smith AV, van Wingerden S, Zhai G, Zhuang WV, Albrecht E, Alizadeh BZ, Aspelund T, Bandinelli S, Lauc LB, Beckmann JS, Boban M, Boerwinkle E, Broekmans FJ, Burri A, Campbell H, Chanock SJ, Chen C, Cornelis MC, Corre T, Coviello AD, d'Adamo P, Davies G, de Faire U, de Geus EJ, Deary IJ, Dedoussis GV, Deloukas P, Ebrahim S, Eiriksdottir G, Emilsson V, Eriksson JG, Fauser BC, Ferreli L, Ferrucci L, Fischer K, Folsom AR, Garcia ME, Gasparini P, Gieger C, Glazer N, Grobbee DE, Hall P, Haller T, Hankinson SE, Hass M, Hayward C, Heath AC, Hofman A, Ingelsson E, Janssens AC, Johnson AD, Karasik D, Kardia SL, Keyzer J, Kiel DP, Kolcic I, Kutalik Z, Lahti J, Lai S, Laisk T, Laven JS, Lawlor DA, Liu J, Lopez LM, Louwers YV, Magnusson PK, Marongiu M, Martin NG, Klaric IM, Masciullo C, McKnight B, Medland SE, Melzer D, Mooser V, Navarro P, Newman AB, Nyholt DR, Onland-Moret NC, Palotie A, Paré G, Parker AN, Pedersen NL, Peeters PH, Pistis G, Plump AS, Polasek O, Pop VJ, Psaty BM, Räikkönen K, Rehnberg E, Ro… See abstract for full author list ➔ Stolk L, et al. Nat Genet. 2012 Jan 22;44(3):260-8. doi: 10.1038/ng.1051. Nat Genet. 2012. PMID: 22267201 Free PMC article.
• Nucleotide incorporation by human DNA polymerase gamma opposite benzo[a]pyrene and benzo[c]phenanthrene diol epoxide adducts of deoxyguanosine and deoxyadenosine.

  Graziewicz MA, Sayer JM, Jerina DM, Copeland WC. Graziewicz MA, et al. Nucleic Acids Res. 2004 Jan 16;32(1):397-405. doi: 10.1093/nar/gkh213. Print 2004. Nucleic Acids Res. 2004. PMID: 14729924 Free PMC article.
• Mitochondria and Parkinson's Disease: Clinical, Molecular, and Translational Aspects.

  Borsche M, Pereira SL, Klein C, Grünewald A. Borsche M, et al. J Parkinsons Dis. 2021;11(1):45-60. doi: 10.3233/JPD-201981. J Parkinsons Dis. 2021. PMID: 33074190 Free PMC article. Review.
• Mitochondrial single-stranded DNA binding protein novel de novo SSBP1 mutation in a child with single large-scale mtDNA deletion (SLSMD) clinically manifesting as Pearson, Kearns-Sayre, and Leigh syndromes.

  Gustafson MA, McCormick EM, Perera L, Longley MJ, Bai R, Kong J, Dulik M, Shen L, Goldstein AC, McCormack SE, Laskin BL, Leroy BP, Ortiz-Gonzalez XR, Ellington MG, Copeland WC, Falk MJ. Gustafson MA, et al. PLoS One. 2019 Sep 3;14(9):e0221829. doi: 10.1371/journal.pone.0221829. eCollection 2019. PLoS One. 2019. PMID: 31479473 Free PMC article.