SMAD4 mutations and cross-talk between TGF-β/IFNγ signaling accelerate rates of DNA damage and cellular senescence, resulting in a segmental progeroid syndrome—the Myhre syndrome - Renuka Kandhaya-Pillai; Deyin Hou; Jiaming Zhang; Xiaomeng Yang; Goli Compoginis; Takayasu Mori; Tamara Tchkonia; George M. Martin; Fuki M. Hisama; James L. Kirkland; Junko Oshima (GeroScience, 2021)

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations - Katrin Friedrich; Lin Lee; Dru F. Leistritz; Gudrun Nürnberg; Bidisha Saha; Fuki M. Hisama; Daniel K. Eyman; Davor Lessel; Peter Nürnberg; Chumei Li; María J. Garcia-F-Villalta; Carolien M. Kets; et al. (Human Genetics, 2010)