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Blood|July 1, 2022
Genetic testing in severe aplastic anemia is required for optimal hematopoietic cell transplant outcomesLisa J McReynolds, Maryam Rafati, Youjin Wang, et al.International Journal of Environmental Research and Public Health|June 27, 2024
Rehabilitation Services for Young-Onset Dementia: Examples from High- and Low-Middle-Income CountriesAida Suárez-González, Sharon A Savage, Suvarna Alladi, et al.Plos Genetics|September 7, 2013
A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndromeBari J Ballew, Vijai Joseph, Saurav De, et al.Nature Communications|August 26, 2025
Peripheral blood DNA methylation predicts the early onset of primary tumor in TP53 mutation carriersVallijah Subasri, Benjamin Brew, Brianne Laverty, et al.Nature Communications|February 16, 2025
Genetic regulation of TERT splicing affects cancer risk by altering cellular longevity and replicative potentialOscar Florez-Vargas, Michelle Ho, Maxwell H Hogshead, et al.Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
Genetic regulation of <i>TERT</i> splicing contributes to reduced or elevated cancer risk by altering cellular longevity and replicative potentialOscar Florez-Vargas, Michelle Ho, Maxwell Hogshead, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 30, 2024
Update on Recommendations for Surveillance for Children with Predisposition to Hematopoietic MalignancyLuke D Maese, Marcin W Wlodarski, Sun Young Kim, et al.Cancer Research Communications|June 28, 2023
Multiple Germline Events Contribute to Cancer Development in Patients with Li-Fraumeni SyndromeVallijah Subasri, Nicholas Light, Nisha Kanwar, et al.Medrxiv : the Preprint Server for Health Sciences|June 29, 2026
Fanconi Anemia as a Window into Premalignant Field Cancerization of the Oral MucosaTamar Berger, Frank X Donovan, Yu-Chien Lin, et al.Science Advances|April 11, 2025
Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenitaAdrián Sanz-Moreno, Lore Becker, Kan Xie, et al.Pageof 71