Associated Papers
Comprehensive characterization of early-onset lung cancer, in Chinese young adults.
Tian Y et al.
Nature Communications, 2025
40000630 (PubMed )
Supplement: 41467_2025_57309_MOESM8_ESM.xlsx › DNA_results
A multiparameter liquid biopsy approach allows to track melanoma dynamics and identify early treatment resistance.
Scaini MC et al.
Npj Precision Oncology, 2024
Gene mutations in sporadic lymphangioleiomyomatosis and genotype-phenotype correlation analysis.
Huang J et al.
Bmc Pulmonary Medicine, 2022
36117164 (PubMed )
Supplement: 12890_2022_2154_MOESM4_ESM.xlsx › sheet1
Epigenetic modifier gene mutations in chronic myeloid leukemia (CML) at diagnosis are associated with risk of relapse upon treatment discontinuation.
Adnan Awad S et al.
Blood Cancer Journal, 2022
A genomic mutation spectrum of collecting duct carcinoma in the Chinese population.
Zhang H et al.
Bmc Medical Genomics, 2022
34980126 (PubMed )
Supplement: 12920_2021_1143_MOESM3_ESM.xlsx › Supplementary_Table_3
Genomic characterization of intracranial teratomas using whole genome sequencing.
Zhang C et al.
Frontiers in Oncology, 2022
36457486 (PubMed )
Supplement: DataSheet_1.xlsx › Table_S2
Calibration-free NGS quantitation of mutations below 0.01% VAF.
Dai P et al.
Nature Communications, 2021
34675197 (PubMed )
Supplement: 41467_2021_26308_MOESM1_ESM.pdf
Targeted exome sequencing identifies mutational landscape in a cohort of 1500 Chinese patients with non-small cell lung carcinoma (NSCLC).
Zhou YJ et al.
Human Genomics, 2021
Malignant transformation and genetic alterations are uncoupled in early colorectal cancer progression.
Mamlouk S et al.
Bmc Biology, 2020
32895052 (PubMed )
Supplement: 12915_2020_844_MOESM4_ESM.xlsx › AC31_Ad_private
Effect of GNAQ alteration on RANKL-induced osteoclastogenesis in human non-small-cell lung cancer.
Choi JY et al.
Bone & Joint Research, 2020
Genomic variation as a marker of response to neoadjuvant therapy in locally advanced rectal cancer.
Douglas JK et al.
Molecular & Cellular Oncology, 2020
Recurrent GNAQ mutation encoding T96S in natural killer/T cell lymphoma.
Li Z et al.
Nature Communications, 2019
A somatic activating NRAS variant associated with kaposiform lymphangiomatosis.
Barclay SF et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
Loss-of-function mutations in QRICH2 cause male infertility with multiple morphological abnormalities of the sperm flagella.
Shen Y et al.
Nature Communications, 2019
30683861 (PubMed )
Supplement: 41467_2018_8182_MOESM10_ESM.xls › PA
Somatic mutational profiles of stage II and III gastric cancer according to tumor microenvironment immune type.
Koh J et al.
Genes, Chromosomes & Cancer, 2019
Genetic Alterations in Primary Acral Melanoma and Acral Melanocytic Nevus in Korea: Common Mutated Genes Show Distinct Cytomorphological Features.
Moon KR et al.
The Journal of Investigative Dermatology, 2018
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