Who Should Have Multigene Germline Testing for Hereditary Cancer?

Dyskeratosis congenita and telomere biology disorders.

Next-generation sequencing errors due to genetic variation in WRAP53 encoding TCAB1 on chromosome 17.

Shwachman Diamond syndrome: narrow genotypic spectrum and variable clinical features.

Germline-somatic JAK2 interactions are associated with clonal expansion in myelofibrosis.

Spectrum and Incidence of Skin Cancer among Individuals with Li-Fraumeni Syndrome.

Genetic testing in severe aplastic anemia is required for optimal hematopoietic cell transplant outcomes.

Uncovering the Genetic Etiology of the (Posttherapy) Broken Heart.

Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries.

Utility of interim blood tests for cancer screening in Li-Fraumeni syndrome.

Fundamental immune-oncogenicity trade-offs define driver mutation fitness.

Author Correction: Fundamental immune-oncogenicity trade-offs define driver mutation fitness.

Telomere length and epigenetic clocks as markers of cellular aging: a comparative study.

The TP53 Database: transition from the International Agency for Research on Cancer to the US National Cancer Institute.

Clinical outcomes in transient epileptic amnesia: A 10-year follow-up cohort study of 47 cases.