Associated Papers
Combining germline, tissue and liquid biopsy analysis by comprehensive genomic profiling to improve the yield of actionable variants in a real-world cancer cohort.
Vanni I et al.
Journal of Translational Medicine, 2024
Immunotherapy for colorectal cancer: insight from inherited genetics.
Tjader NP et al.
Trends in Cancer, 2024
Novel NARS2 variants in a patient with early-onset status epilepticus: case study and literature review.
Yang N et al.
Bmc Pediatrics, 2024
Genetic Risk Factors for Nontuberculous Mycobacterial Pulmonary Disease (Systematic Review).
Sviridov PS et al.
Sovremennye Tekhnologii V Meditsine, 2024
RB1 aberrations predict outcomes of immune checkpoint inhibitor combination therapy in NSCLC.
Wang Q et al.
Frontiers in Oncology, 2023
PDCD1 and IFNL4 genetic variants and risk of developing hepatitis C virus-related diseases.
De Re V et al.
Liver International : Official Journal of the International Association for the Study of the Liver, 2021
PDCD1 and PDCD1LG1 polymorphisms affect the susceptibility to multiple myeloma.
Kasamatsu T et al.
Clinical and Experimental Medicine, 2020
Analysis of 75 Candidate SNPs Associated With Acute Rejection in Kidney Transplant Recipients: Validation of rs2910164 in MicroRNA MIR146A.
Oetting WS et al.
Transplantation, 2019
Association between single-nucleotide polymorphisms and adverse events in nivolumab-treated non-small cell lung cancer patients.
Bins S et al.
British Journal of Cancer, 2018
Genetics of acute rejection after kidney transplantation.
Dorr CR et al.
Transplant International : Official Journal of the European Society for Organ Transplantation, 2018
PDCD1 gene polymorphisms as regulators of T-lymphocyte activity in cutaneous melanoma risk and prognosis.
Gomez GVB et al.
Pigment Cell & Melanoma Research, 2018
PDCD1 and CTLA4 polymorphisms affect the susceptibility to, and clinical features of, chronic immune thrombocytopenia.
Kasamatsu T et al.
British Journal of Haematology, 2018
PD-1 gene polymorphic variation is linked with first symptom of disease and severity of relapsing-remitting form of MS.
Pawlak-Adamska E et al.
Journal of Neuroimmunology, 2017
TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.
Ogata T et al.
Plos One, 2014
Genetic variations of immunoregulatory genes associated with Rasmussen syndrome.
Takahashi Y et al.
Epilepsy Research, 2013