Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer

BACKGROUND: Genome-wide association studies (GWAS) are widely used to map genomic regions contributing to lung cancer (LC) susceptibility but they typically do not identify the precise disease-causing genes/variants. To unveil the inherited causal LC variants, we performed focused exome sequencing a...

সম্পূর্ণ বিবরণ

সংরক্ষণ করুন:
গ্রন্থ-পঞ্জীর বিবরন
প্রকাশিত:J Thorac Oncol
প্রধান লেখক: Liu, Yanhong, Lusk, Christine M., Cho, Michael H., Silverman, Edwin K., Qiao, Dandi, Zhang, Ruyang, Scheurer, Michael E., Kheradmand, Farrah, Wheeler, David A., Tsavachidis, Spiridon, Armstrong, Georgina, Zhu, Dakai, Wistuba, Ignacio I., Chow, Chi-Wan B., Behrens, Carmen, Pikielny, Claudio W., Neslund-Dudas, Christine, Pinney, Susan M., Anderson, Marshall, Kupert, Elena, Bailey-Wilson, Joan, Gaba, Colette, Mandal, Diptasri, You, Ming, de Andrade, Mariza, Yang, Ping, Field, John K., Liloglou, Triantafillos, Davies, Michael, Lissowska, Jolanta, Swiatkowska, Beata, Zaridze, David, Mukeriya, Anush, Janout, Vladimir, Holcatova, Ivana, Mates, Dana, Milosavljevic, Sasa, Scelo, Ghislaine, Brennan, Paul, McKay, James, Liu, Geoffrey, Hung, Rayjean J., Christiani, David C., Schwartz, Ann G., Amos, Christopher I, Spitz, Margaret R.
বিন্যাস: Artigo
ভাষা:Inglês
প্রকাশিত: 2018
বিষয়গুলি:
Article
অনলাইন ব্যবহার করুন:https://ncbi.nlm.nih.gov/pmc/articles/PMC6366341/
https://ncbi.nlm.nih.gov/pubmed/29981437
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jtho.2018.06.016
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