Paper Details

Paper Title

Rare deleterious germline variants and risk of lung cancer.

Paper Journal Title

NPJ Precis Oncol

Paper Citation Count

Paper Publication Year

2021

Bio Mention

Mesh Descriptor

Author Name	Affiliation
Xiangjun Xiao	Institute for Clinical and Translational Research, Baylor College of Medicine
Chao Cheng	Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine
Chao Cheng	Institute for Clinical and Translational Research, Baylor College of Medicine
Chao Cheng	Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine
Chao Cheng	Institute for Clinical and Translational Research, Baylor College of Medicine
Jinyoung Byun	Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine
Jinyoung Byun	Institute for Clinical and Translational Research, Baylor College of Medicine
Yafang Li	Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine
Yafang Li	Institute for Clinical and Translational Research, Baylor College of Medicine
Dakai Zhu	Institute for Clinical and Translational Research, Baylor College of Medicine
Michael E Scheurer	Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine
Michael E Scheurer	Baylor College of Medicine
Michael H Cho	Brigham and Women's Hospital and Harvard Medical School
Michael H Cho	Brigham and Women's Hospital and Harvard Medical School
Edwin K Silverman	Brigham and Women's Hospital and Harvard Medical School
Edwin K Silverman	Brigham and Women's Hospital and Harvard Medical School
Susan M Pinney	University of Cincinnati College of Medicine
Mariza de Andrade	Mayo Clinic College of Medicine
Mariza de Andrade	Mayo Clinic College of Medicine
Ping Yang	Mayo Clinic College of Medicine
Jolanta Lissowska	M. Sklodowska-Curie National Research Institute of Oncology
Jolanta Lissowska	M. Sklodowska-Curie National Research Institute of Oncology
Geoffrey Liu	Princess Margaret Cancer Center
John K Field	The University of Liverpool, Department of Molecular and Clinical Cancer Medicine
Rayjean J Hung	Lunenfeld-Tanenbaum Research Institute
Christopher I Amos	Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine
Christopher I Amos	Institute for Clinical and Translational Research, Baylor College of Medicine
Christopher I Amos	Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine
Christopher I Amos	Institute for Clinical and Translational Research, Baylor College of Medicine

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Dataset	Description	Source Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link

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