Associated Papers
Variability in proliferative and migratory defects in Hirschsprung disease-associated RET pathogenic variants.
Fries LE et al.
American Journal of Human Genetics, 2025
Variability in proliferative and migratory defects in Hirschsprung disease-associated RET pathogenic variants.
Fries LE et al.
Biorxiv : the Preprint Server for Biology, 2024
Cell-Free DNA Sequencing Reveals Gene Variants in DNA Damage Repair Genes Associated with Prognosis of Prostate Cancer Patients.
Lieb V et al.
Cells, 2022
An integrative pan cancer analysis of RET aberrations and their potential clinical implications.
Zhou L et al.
Scientific Reports, 2022
Cell-Free DNA Variant Sequencing Using Plasma and AR-V7 Testing of Circulating Tumor Cells in Prostate Cancer Patients.
Lieb V et al.
Cells, 2021
Sequence characterization of RET in 117 Chinese Hirschsprung disease families identifies a large burden of de novo and parental mosaic mutations.
Jiang Q et al.
Orphanet Journal of Rare Diseases, 2019
Resectable lung lesions malignancy assessment and cancer detection by ultra-deep sequencing of targeted gene mutations in plasma cell-free DNA.
Peng M et al.
Journal of Medical Genetics, 2019
Functional Studies on Novel RET Mutations and Their Implications for Genetic Counseling for Hirschsprung Disease.
Wang H et al.
Frontiers in Genetics, 2019
The advances of genetics research on Hirschsprung's disease.
Ke J et al.
Pediatric Investigation, 2018
RET somatic mutations are underrecognized in Hirschsprung disease.
Jiang Q et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2018
Sporadic Hirschsprung Disease: Mutational Spectrum and Novel Candidate Genes Revealed by Next-generation Sequencing.
Zhang Z et al.
Scientific Reports, 2017
Targeted next generation sequencing of parotid gland cancer uncovers genetic heterogeneity.
Grünewald I et al.
Oncotarget, 2015
Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility.
Toledo RA et al.
Endocrine-related Cancer, 2015
Genotyping analysis of 3 RET polymorphisms demonstrates low somatic mutation rate in Chinese Hirschsprung disease patients.
Zhang Z et al.
International Journal of Clinical and Experimental Pathology, 2015
Beyond KRAS: Practical Molecular Targets in Pancreatic Adenocarcinoma.
Grinshpun A et al.
Case Reports in Oncology, 0
NGS-based profiling of key cancer genes in Indian triple-negative breast cancer patients reinforces molecular heterogeneity of the disease.
Sahasrabuddhe NA et al.
Indian Journal of Cancer, 0