FSHD: a repeat contraction disease finally ready to expand (our understanding of its pathogenesis). by Christopher E Pearson

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De novo mutations, genetic mosaicism and human disease by Mohiuddin Mohiuddin, R. Frank Kooy, Christopher E. Pearson, Christopher E. Pearson

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Fragile sites, chromosomal lesions, tandem repeats, and disease by Mila Mirceta, Mila Mirceta, Natalie Shum, Natalie Shum, Monika H. M. Schmidt, Monika H. M. Schmidt, Christopher E. Pearson, Christopher E. Pearson

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ATRX proximal protein associations boast roles beyond histone deposition. by William A Scott, Erum Z Dhanji, Boris J A Dyakov, Ema S Dreseris, Jonathon S Asa, Laura J Grange, Mila Mirceta, Christopher E Pearson, Grant S Stewart, Anne-Claude Gingras, Eric I Campos

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CTCF cis-regulates trinucleotide repeat instability in an epigenetic manner: a novel basis for mutational hot spot determination. by Randell T Libby, Katharine A Hagerman, Victor V Pineda, Rachel Lau, Diane H Cho, Sandy L Baccam, Michelle M Axford, John D Cleary, James M Moore, Bryce L Sopher, Stephen J Tapscott, Galina N Filippova, Christopher E Pearson, Albert R La Spada

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Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches. by Ricardo Mouro Pinto, Ella Dragileva, Andrew Kirby, Alejandro Lloret, Edith Lopez, Jason St Claire, Gagan B Panigrahi, Caixia Hou, Kim Holloway, Tammy Gillis, Jolene R Guide, Paula E Cohen, Guo-Min Li, Christopher E Pearson, Mark J Daly, Vanessa C Wheeler

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