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Hereditary Cancer in Clinical Practice|May 14, 2024
The risk of skin cancer in women who carry BRCA1 or BRCA2 mutationsSteven A Narod, Kelly Metcalfe, Amy Finch, et al.
Hereditary Cancer in Clinical Practice|October 20, 2023
Diagnosis of patients with Lynch syndrome lacking the Amsterdam II or Bethesda criteriaMiguel Angel Trujillo-Rojas, María de la Luz Ayala-Madrigal, Melva Gutiérrez-Angulo, et al.
Hereditary Cancer in Clinical Practice|October 12, 2023
The prevalence of lynch syndrome (DNA mismatch repair protein deficiency) in patients with primary localized prostate cancer using immunohistochemistry screeningSuguru Oka, Shinji Urakami, Kiichi Hagiwara, et al.
Hereditary Cancer in Clinical Practice|May 12, 2026
Renal cell carcinoma risk among individuals heterozygous for fumarate hydratase variants: further insights into genotype-phenotype correlationsTrevor L Hoffman, Sony Wirio, Vivek Sethumadhavan
Hereditary Cancer in Clinical Practice|June 11, 2026
Association analysis of germline variants in GEN1 with a susceptibility to prostate cancer in Polish menKatarzyna Gliniewicz, Klaudia Stempa, Dominika Wokołorczyk, et al.
Hereditary Cancer in Clinical Practice|May 16, 2018
Challenges in recruiting African-American women for a breast cancer genetics studyAmanda J Compadre, Melinda E Simonson, Katy Gray, et al.
Hereditary Cancer in Clinical Practice|July 16, 2026
The psychosocial impact of receiving a polygenic risk score informing risk of prostate cancerMatthew Hogben, Emma Hainsworth, Barbara Benton, et al.
Hereditary Cancer in Clinical Practice|January 21, 2020
Whole-body MRI within a surveillance program for carriers with clinically actionable germline TP53 variants - the Swedish constitutional TP53 study SWEP53Meis Omran, Lennart Blomqvist, Yvonne Brandberg, et al.
Hereditary Cancer in Clinical Practice|June 13, 2022
Clinical characteristics and genetic testing outcome of suspected hereditary peripheral nerve sheath tumours in a tertiary cancer institution in SingaporeJerold Loh, Pei Yi Ong, Denise Li Meng Goh, et al.
Hereditary Cancer in Clinical Practice|October 13, 2021
Germline mutations among Polish patients with acute myeloid leukemiaAneta Bąk, Katarzyna Skonieczka, Anna Jaśkowiec, et al.
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