Paul Brennan

发表

WA: The Scale of Change Demands We Work Together

Paul Brennan, Peter Beatty, Jonathan Smith, 2008 .

All Praise The Creator

Paul Brennan, 2000 .

Towards LarKC: A Platform for Web-Scale Reasoning

Dieter Fensel, Frank van Harmelen, Lael J. Schooler, 2008, 2008 IEEE International Conference on Semantic Computing.

Incorporating Touch-Screen Technology into Minimal-Access Simulation

Paul Brennan, Mark Hughes, Roland Partridge, 2013 .

Duplication: most cases on database are innocent.

Paul Brennan, 2008, Nature.

Needlestack: an ultra-sensitive variant caller for multi-sample next generation sequencing data

Paul Brennan, Elisabeth Brambilla, Matthieu Foll, 2019, bioRxiv.

Should we or shouldn't we use spoken commands in voice interfaces?

Marita Franzke, Gerhard Deffner, Paul Brennan, 1991, CHI '91.

drawProteins: a Bioconductor/R package for reproducible and programmatic generation of protein schematics

Paul Brennan, P. Brennan, 2018, F1000Research.

UWB power propagation for bio-medical implanted devices

Mohammad Ghavami, Paul Brennan, Mehran Ghafari, 2015, 2015 17th International Conference on E-health Networking, Application & Services (HealthCom).

Pleiotropic Associations of Risk Variants Identified for Other Cancers With Lung Cancer Risk: The PAGE and TRICL Consortia

Wei Chen, Dana C. Crawford, Ewa Deelman, 2014, Journal of the National Cancer Institute.

Prediction of acute myeloid leukaemia risk in healthy individuals

Paolo Vineis, Zhen Zhao, Amos Tanay, 2018, Nature.

Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types.

Jian Su, Wen Tan, Paolo Vineis, 2015, Journal of the National Cancer Institute.

Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls

Yang Zhao, Andres Metspalu, Paul Brennan, 2012, Human molecular genetics.

Comparison of Pathway Analysis Approaches Using Lung Cancer GWAS Data Sets

Paul Brennan, Christopher I. Amos, Laurent Briollais, 2012, PloS one.

Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations.

Steven Gallinger, Peter Kraft, Nazneen Rahman, 2016, Cancer research.

Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.

William Wheeler, Hideo Tanaka, Jianxin Shi, 2014, Human molecular genetics.

Whole genome sequencing of a sporadic primary immunodeficiency cohort

Antonis Pantazis, Keith W. Muir, David J. Williams, 2020, Nature.

Genome-wide association study of familial lung cancer

Paul Brennan, Mariza de Andrade, Maria Teresa Landi, 2018, Carcinogenesis.

Genetic variants on 15q25.1, smoking, and lung cancer: an assessment of mediation and interaction.

Eric J Tchetgen Tchetgen, Paul Brennan, Tyler J VanderWeele, 2012, American journal of epidemiology.

Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types

Alison P. Klein, William Wheeler, Li Jin, 2015 .

Genome‐wide association study of INDELs identified four novel susceptibility loci associated with lung cancer risk

Paul Brennan, John K Field, David C Christiani, 2020, International journal of cancer.

Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers

Alison P. Klein, Yan Zhang, Peter Kraft, 2019, bioRxiv.

Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium.

Paul Brennan, Yun-Chul Hong, Kari Stefansson, 2010, Journal of the National Cancer Institute.

Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population

Paul Brennan, John K Field, Xiangjun Xiao, 2018, Carcinogenesis.