1. Mitochondrial DNA deletions are associated with non-B DNA conformations. Damas J, Carneiro J, Gonçalves J, Stewart JB, Samuels DC, Amorim A, Pereira F (2012) Nucleic Acids Res 40(16): 7606-21
    › Primary publication · 22661583 (PubMed) · PMC3439893 (PubMed Central)
  2. Epigenetics, epidemiology and mitochondrial DNA diseases. Chinnery PF, Elliott HR, Hudson G, Samuels DC, Relton CL (2012) Int J Epidemiol 41(1): 177-87
    › Primary publication · 22287136 (PubMed) · PMC3304530 (PubMed Central)
  3. Correlated tissue expression of genes of cytoplasmic and mitochondrial nucleotide metabolisms in normal tissues is disrupted in transformed tissues. Gandhi VV, Samuels DC (2012) Nucleosides Nucleotides Nucleic Acids 31(2): 112-29
    › Primary publication · 22303991 (PubMed) · PMC3464496 (PubMed Central)
  4. Adult-onset spinocerebellar ataxia syndromes due to MTATP6 mutations. Pfeffer G, Blakely EL, Alston CL, Hassani A, Boggild M, Horvath R, Samuels DC, Taylor RW, Chinnery PF (2012) J Neurol Neurosurg Psychiatry 83(9): 883-6
    › Primary publication · 22577227 (PubMed) · PMC4034166 (PubMed Central)
  5. The Bcl-2-associated death promoter (BAD) lowers the threshold at which the Bcl-2-interacting domain death agonist (BID) triggers mitochondria disintegration. Howells CC, Baumann WT, Samuels DC, Finkielstein CV (2011) J Theor Biol 271(1): 114-23
    › Primary publication · 21130780 (PubMed)
  6. Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system. Monnot S, Gigarel N, Samuels DC, Burlet P, Hesters L, Frydman N, Frydman R, Kerbrat V, Funalot B, Martinovic J, Benachi A, Feingold J, Munnich A, Bonnefont JP, Steffann J (2011) Hum Mutat 32(1): 116-25
    › Primary publication · 21120938 (PubMed) · PMC3058134 (PubMed Central)
  7. Replication pauses of the wild-type and mutant mitochondrial DNA polymerase gamma: a simulation study. Song Z, Cao Y, Samuels DC (2011) PLoS Comput Biol 7(11): e1002287
    › Primary publication · 22125488 (PubMed) · PMC3219627 (PubMed Central)
  8. Poor correlations in the levels of pathogenic mitochondrial DNA mutations in polar bodies versus oocytes and blastomeres in humans. Gigarel N, Hesters L, Samuels DC, Monnot S, Burlet P, Kerbrat V, Lamazou F, Benachi A, Frydman R, Feingold J, Rotig A, Munnich A, Bonnefont JP, Frydman N, Steffann J (2011) Am J Hum Genet 88(4): 494-8
    › Primary publication · 21473984 (PubMed) · PMC3071907 (PubMed Central)
  9. POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblasts. Stewart JD, Schoeler S, Sitarz KS, Horvath R, Hallmann K, Pyle A, Yu-Wai-Man P, Taylor RW, Samuels DC, Kunz WS, Chinnery PF (2011) Biochim Biophys Acta 1812(3): 321-5
    › Primary publication · 21138766 (PubMed)
  10. Mitochondrial genomics and CD4 T-cell count recovery after antiretroviral therapy initiation in AIDS clinical trials group study 384. Grady BJ, Samuels DC, Robbins GK, Selph D, Canter JA, Pollard RB, Haas DW, Shafer R, Kalams SA, Murdock DG, Ritchie MD, Hulgan T, ACTG 384 and DACS 250 Study Teams (2011) J Acquir Immune Defic Syndr 58(4): 363-70
    › Primary publication · 21792066 (PubMed) · PMC3204178 (PubMed Central)