Burr R, Leshchiner I, Costantino C, Blohmer M, Sundaresan T, Cha J
Nat Cancer. 2024; 5(11):1681-1696.
PMID: 39406916
PMC: 11584400.
DOI: 10.1038/s43018-024-00840-y.
Liu Y, Fang L, Wang Y, Fan T, Wang L, Xiao C
Cell Death Dis. 2024; 15(10):738.
PMID: 39389944
PMC: 11467305.
DOI: 10.1038/s41419-024-07129-z.
Serio V, Rosati D, Maffeo D, Rina A, Ghisalberti M, Bellan C
Cancers (Basel). 2024; 16(16).
PMID: 39199663
PMC: 11352340.
DOI: 10.3390/cancers16162887.
Liu M, Niu X, Liu H, Chen J
Oncol Lett. 2023; 26(1):282.
PMID: 37274482
PMC: 10236141.
DOI: 10.3892/ol.2023.13868.
Sagan O, Rothstein A, Jambunathan B, Hadziahmetovic M, Antoniolli A, Rashid M
Front Oncol. 2023; 13:1176868.
PMID: 37265791
PMC: 10230275.
DOI: 10.3389/fonc.2023.1176868.
Case report: identification of EGFR R776H and FANCE R381H germline mutations in a patient with multiple pulmonary nodules.
Wu Z, Wang Y, Jin L, Wei J, Han L, Su J
J Cancer Res Clin Oncol. 2022; 149(2):921-927.
PMID: 36163560
DOI: 10.1007/s00432-022-04290-w.
A Germline Mutation in ATR Is Associated With Lung Adenocarcinoma in Asian Patients.
Bao G, Guan X, Liang J, Yao Y, Xiang Y, Li T
Front Oncol. 2022; 12:855305.
PMID: 35712480
PMC: 9195140.
DOI: 10.3389/fonc.2022.855305.
A Case of Isolated Myeloid Sarcoma Associated With Germline T790M Variant: The Importance of Recognizing Potential Germline Variants on Somatic Tumor Sequencing Panels.
Walker M, Folstad M, Smith-Simmer K, Reinig E, Nadiminti K, Lovrien L
J Hematol. 2022; 11(2):71-76.
PMID: 35573754
PMC: 9076140.
DOI: 10.14740/jh983.
Cancer Predisposition Genes in Adolescents and Young Adults (AYAs): a Review Paper from the Italian AYA Working Group.
Toss A, Quarello P, Mascarin M, Banna G, Zecca M, Cinieri S
Curr Oncol Rep. 2022; 24(7):843-860.
PMID: 35320498
PMC: 9170630.
DOI: 10.1007/s11912-022-01213-3.
Identification of the Unique Clinical and Genetic Features of Chinese Lung Cancer Patients With Germline Mutations in a Large-Scale Retrospective Study.
Lin X, Peng M, Chen Q, Yuan M, Chen R, Deng H
Front Oncol. 2021; 11:774156.
PMID: 34869019
PMC: 8637204.
DOI: 10.3389/fonc.2021.774156.
Clinical Cohort Analysis of Germline T790M Demonstrates Penetrance Across Ethnicities and Races, Sexes, and Ages.
Berry D, Wang X, Michalski S, Kang H, Yang S, Creelan B
JCO Precis Oncol. 2021; 4.
PMID: 34164592
PMC: 8216676.
DOI: 10.1200/PO.19.00297.
Presentation of mutations in 162 family probands with multiple primary lung cancer.
Li C, Wang Y, Su K, Liu Y, Wang L, Zheng B
Transl Lung Cancer Res. 2021; 10(4):1734-1746.
PMID: 34012789
PMC: 8107753.
DOI: 10.21037/tlcr-20-1001.
Profiling Oncogenic Germline Mutations in Unselected Chinese Lung Cancer Patients.
Yang J, Li H, Li B, Li W, Guo Q, Ling Hu
Front Oncol. 2021; 11:647598.
PMID: 33898318
PMC: 8058453.
DOI: 10.3389/fonc.2021.647598.
Significant Benefits of Osimertinib Against Adenosquamous Carcinoma Harboring Germline T790M Mutation.
Huo R, Li J, Li X, Shi J, Wang K, Jiao J
Oncologist. 2020; 25(10):826-832.
PMID: 32367600
PMC: 7543298.
DOI: 10.1634/theoncologist.2019-0938.
Inherited lung cancer: a review.
de Alencar V, Formiga M, Cordeiro de Lima V
Ecancermedicalscience. 2020; 14:1008.
PMID: 32104210
PMC: 7039693.
DOI: 10.3332/ecancer.2020.1008.
Spectrum of Pathogenic Germline Mutations in Chinese Lung Cancer Patients through Next-Generation Sequencing.
Tian P, Cheng X, Zhao Z, Zhang Y, Bao C, Wang Y
Pathol Oncol Res. 2019; 26(1):109-114.
PMID: 31721094
DOI: 10.1007/s12253-019-00771-5.
Potential genetic modifiers for somatic EGFR mutation in lung cancer: a meta-analysis and literature review.
Cheng Y, Gan Y, Liu D, Davies M, Li W, Field J
BMC Cancer. 2019; 19(1):1068.
PMID: 31703574
PMC: 6842246.
DOI: 10.1186/s12885-019-6317-6.
Inherited lung cancer syndromes targeting never smokers.
Yamamoto H, Yatabe Y, Toyooka S
Transl Lung Cancer Res. 2018; 7(4):498-504.
PMID: 30225213
PMC: 6131180.
DOI: 10.21037/tlcr.2018.06.01.
Circulating Cell-Free Tumour DNA in the Management of Cancer.
Francis G, Stein S
Int J Mol Sci. 2015; 16(6):14122-42.
PMID: 26101870
PMC: 4490543.
DOI: 10.3390/ijms160614122.
Correlation between familial cancer history and epidermal growth factor receptor mutations in Taiwanese never smokers with non-small cell lung cancer: a case-control study.
Cheng P, Cheng Y
J Thorac Dis. 2015; 7(3):281-7.
PMID: 25922704
PMC: 4387390.
DOI: 10.3978/j.issn.2072-1439.2015.02.03.