Associated Papers
Germline Cancer Predisposition Results From the National Cancer Institute-Children's Oncology Group Pediatric MATCH Trial.
Scollon S et al.
Jco Precision Oncology, 2025
41166674 (PubMed )
Supplement: po-9-e2500742-s001.pdf
Hallmarks of a genomically distinct subclass of head and neck cancer.
Muijlwijk T et al.
Nature Communications, 2024
39428388 (PubMed )
Supplement: 41467_2024_53390_MOESM4_ESM.xlsx › 3._List_of_all_somatic_variants
Next-generation sequencing uncovers crucial mutated genes and potential therapeutic targets in ovarian cancer patients.
Zhao T et al.
American Journal of Translational Research, 2024
Mosaicism in Tumor Suppressor Gene Syndromes: Prevalence, Diagnostic Strategies, and Transmission Risk.
Chen JL et al.
Annual Review of Genomics and Human Genetics, 2022
36044908 (PubMed )
Supplement: gg23-giannikou_suptable1.xlsx › PTEN
Systemic lupus erythematosus in a girl with PTEN variant and transaldolase deficiency: a novel phenotype.
Al-Mayouf SM et al.
Clinical Rheumatology, 2020
Comprehensive Genomic Profiling of Rare Tumors: Routes to Targeted Therapies.
Wang S et al.
Frontiers in Oncology, 2020
32373528 (PubMed )
Supplement: Table_6.xlsx › Sheet1
PTEN in Autism and Neurodevelopmental Disorders.
Rademacher S et al.
Cold Spring Harbor Perspectives in Medicine, 2019
De Novo PTEN Mutation in a Young Boy with Cutaneous Vasculitis.
Mauro A et al.
Case Reports in Pediatrics, 2017
Cowden's syndrome with immunodeficiency.
Browning MJ et al.
Journal of Medical Genetics, 2015
Systemic lupus erythematosus in a patient with PTEN hamartoma tumour syndrome.
Lee T et al.
The British Journal of Dermatology, 2014
Select a paper to view details