标题
Rare germline deleterious variants increase susceptibility for lung cancer
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume -, Issue -, Pages -
出版商
Oxford University Press (OUP)
发表日期
2022-06-19
DOI
10.1093/hmg/ddac123
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Cancer Statistics, 2021
- (2021) Rebecca L. Siegel et al. CA-A CANCER JOURNAL FOR CLINICIANS
- Characterization of rare germline variants in familial multiple myeloma
- (2021) Calogerina Catalano et al. Blood Cancer Journal
- Rare deleterious germline variants and risk of lung cancer
- (2021) Yanhong Liu et al. npj Precision Oncology
- Rare variant contribution to human disease in 281,104 UK Biobank exomes
- (2021) Quanli Wang et al. NATURE
- Rare Germline Variants in Chordoma-Related Genes and Chordoma Susceptibility
- (2021) Sally Yepes et al. Cancers
- Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes
- (2020) Deepak N. Subramanian et al. Nature Communications
- Exploring human genomic diversity with gnomAD
- (2020) Linda Koch NATURE REVIEWS GENETICS
- Germline sequencing DNA repair genes in 5,545 men with aggressive and non-aggressive prostate cancer
- (2020) Burcu F Darst et al. JNCI-Journal of the National Cancer Institute
- Inherited Rare, Deleterious Variants in ATM Increase Lung Adenocarcinoma Risk
- (2020) Myvizhi Esai Selvan et al. Journal of Thoracic Oncology
- Using whole-exome sequencing and protein interaction networks to prioritize candidate genes for germline cutaneous melanoma susceptibility
- (2020) Sally Yepes et al. Scientific Reports
- Exome sequencing of Finnish isolates enhances rare-variant association power
- (2019) Adam E. Locke et al. NATURE
- Association of BRCA2 K3326* With Small Cell Lung Cancer and Squamous Cell Cancer of the Skin
- (2018) Thorunn Rafnar et al. JNCI-Journal of the National Cancer Institute
- Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer
- (2018) Yanhong Liu et al. Journal of Thoracic Oncology
- Association of BRCA2 K3326* With Small Cell Lung Cancer and Squamous Cell Cancer of the Skin
- (2018) Thorunn Rafnar et al. JNCI-Journal of the National Cancer Institute
- Rare, pathogenic germline variants in Fanconi Anemia genes increase risk for squamous lung cancer
- (2018) Myvizhi Esai Selvan et al. CLINICAL CANCER RESEARCH
- Mechanisms of DNA damage, repair, and mutagenesis
- (2017) Nimrat Chatterjee et al. ENVIRONMENTAL AND MOLECULAR MUTAGENESIS
- Rare germline variants in known melanoma susceptibility genes in familial melanoma
- (2017) Alisa M Goldstein et al. HUMAN MOLECULAR GENETICS
- Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
- (2017) James D McKay et al. NATURE GENETICS
- Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations
- (2016) Xiaohong R. Yang et al. HUMAN GENETICS
- Focused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung Cancer
- (2016) Yanhong Liu et al. Journal of Thoracic Oncology
- PathCards: multi-source consolidation of human biological pathways
- (2015) Frida Belinky et al. Database-The Journal of Biological Databases and Curation
- Trimmomatic: a flexible trimmer for Illumina sequence data
- (2014) Anthony M. Bolger et al. BIOINFORMATICS
- Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
- (2014) Yufei Wang et al. NATURE GENETICS
- Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma
- (2014) Jianxin Shi et al. NATURE GENETICS
- Causal analysis approaches in Ingenuity Pathway Analysis
- (2013) Andreas Krämer et al. BIOINFORMATICS
- Optimal Unified Approach for Rare-Variant Association Testing with Application to Small-Sample Case-Control Whole-Exome Sequencing Studies
- (2012) Seunggeun Lee et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff
- (2012) Pablo Cingolani et al. FLY
- Human Tribbles 3 Protects Nuclear DNA from Cytidine Deamination by APOBEC3A
- (2012) Marie-Ming Aynaud et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Tribbles in disease: Signaling pathways important for cellular function and neoplastic transformation
- (2011) Takashi Yokoyama et al. CANCER SCIENCE
- Sec16B is involved in the endoplasmic reticulum export of the peroxisomal membrane biogenesis factor peroxin 16 (Pex16) in mammalian cells
- (2011) S. Yonekawa et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
- (2010) A. McKenna et al. GENOME RESEARCH
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma
- (2009) Maria Teresa Landi et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Environment And Genetics in Lung cancer Etiology (EAGLE) study: An integrative population-based case-control study of lung cancer
- (2008) Maria Teresa Landi et al. BMC PUBLIC HEALTH
- Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
- (2008) Julius Gudmundsson et al. NATURE GENETICS
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