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Clinical and analytical validation of FoundationOne®CDx, a comprehensive genomic profiling assay for solid tumors

PloS one, 2022-01, Vol.17 (3), p.e0264138

2022

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Rare variant analysis for family-based design

PloS one, 2013-01, Vol.8 (1), p.e48495-e48495

2013

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Handling the data management needs of high-throughput sequencing data: SpeedGene, a compression algorithm for the efficient storage of genetic data

BMC bioinformatics, 2012-05, Vol.13 (1), p.100-100, Article 100

2012

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A Novel Method for Detecting Association Between DNA Methylation and Diseases Using Spatial Information

Genetic epidemiology, 2014-12, Vol.38 (8), p.714-721

2014

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Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1

Journal of cachexia, sarcopenia and muscle, 2017-06, Vol.8 (3), p.428-436

2017

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Subpopulation Treatment Effect Pattern Plot (STEPP) Methods with R and Stata

Journal of Data Science, 2023-01, Vol.21 (1), p.106-126

2023

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On the analysis of sequence data: testing for disease susceptibility loci using patterns of linkage disequilibrium

Genetic epidemiology, 2011-12, Vol.35 (8), p.880-886

2011

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Evaluation of "IFITM3" rs12252 Association With Severe Pediatric Influenza Infection

The Journal of infectious diseases, 2017-07, Vol.216 (1), p.14-21

2017

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The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk

Neurology, 2014-10, Vol.83 (15), p.1353-1358

2014

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Subpopulation Treatment Effect Pattern Plot (STEPP) analysis for continuous, binary, and count outcomes

Clinical trials (London, England), 2016-08, Vol.13 (4), p.382-390

2016

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Identifying treatment effect heterogeneity in clinical trials using subpopulations of events: STEPP

Clinical trials (London, England), 2016-04, Vol.13 (2), p.169-179

2016

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Quantitative trait prediction based on genetic marker-array data, a simulation study

Bioinformatics, 2011-03, Vol.27 (6), p.745-748

2011

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Evaluation of Mannose Binding Lectin Gene Variants in Pediatric Influenza Virus-Related Critical Illness

Frontiers in immunology, 2019-05, Vol.10, p.1005-1005

2019

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A comparative analysis of family-based and population-based association tests using whole genome sequence data

BMC proceedings, 2014-06, Vol.8 (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo), p.S33-S33, Article S33

2014

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Abstract A028: Clinical and analytic validation of FoundationOne CDx™ for NTRK fusion-positive solid tumors in patients treated with entrectinib

Molecular cancer therapeutics, 2019-12, Vol.18 (12_Supplement), p.A028-A028

2019

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A phase 1 study of AGEN2373, a novel CD137 agonist antibody designed to avoid hepatoxicity, in patients with advanced solid tumors

Journal of clinical oncology, 2023-06, Vol.41 (16_suppl), p.2524-2524

2023

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Assessing the Genotyping Quality of Different SNP-Chips and Imputed Data Using Family-Data

2010 4th International Conference on Bioinformatics and Biomedical Engineering, 2010, p.1-3

2010

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A general semi-parametric approach to the analysis of genetic association studies in population-based designs

BMC genetics, 2013-02, Vol.14 (1), p.13

2013

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Clinical and analytical validation of FoundationOne.sup.®CDx, a comprehensive genomic profiling assay for solid tumors

PloS one, 2022-03, Vol.17 (3), p.e0264138

2022

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Subgroup Analyses and Information from Clinical Trials on Breast Cancer

Breast Cancer, 2017, p.891-903

2017

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41: ASSOCIATION OF MANNOSE-BINDING LECTIN WITH INFLUENZA CRITICAL ILLNESS IN CHILDREN

Critical care medicine, 2018-01, Vol.46 (1 Suppl 1), p.21-21

2018

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Quantitative trait prediction based on genetic marker-array data, a simulation studv

Bioinformatics (Oxford, England), 2011, Vol.27 (6), p.745-748

2011

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Gene expression profile alone is inadequate in predicting complete response in multiple myeloma

Leukemia, 2014-11, Vol.28 (11), p.2229-2234

2014

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Vitamin D-binding protein haplotype is associated with hospitalization for RSV bronchiolitis

Clinical and experimental allergy, 2014-02, Vol.44 (2), p.231-237

2014

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Abstract 1607: An ERBB2 follow-on companion diagnostic for clinical care of patients with breast cancer

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.1607-1607

2018

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Clinical and analytical validation of FoundationOne®CDx, a comprehensive genomic profiling assay for solid tumors

Rare variant analysis for family-based design

Handling the data management needs of high-throughput sequencing data: SpeedGene, a compression algorithm for the efficient storage of genetic data

A Novel Method for Detecting Association Between DNA Methylation and Diseases Using Spatial Information

Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1

Subpopulation Treatment Effect Pattern Plot (STEPP) Methods with R and Stata

On the analysis of sequence data: testing for disease susceptibility loci using patterns of linkage disequilibrium

Evaluation of "IFITM3" rs12252 Association With Severe Pediatric Influenza Infection

The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk

Subpopulation Treatment Effect Pattern Plot (STEPP) analysis for continuous, binary, and count outcomes

Identifying treatment effect heterogeneity in clinical trials using subpopulations of events: STEPP

Quantitative trait prediction based on genetic marker-array data, a simulation study

Evaluation of Mannose Binding Lectin Gene Variants in Pediatric Influenza Virus-Related Critical Illness

A comparative analysis of family-based and population-based association tests using whole genome sequence data

Abstract A028: Clinical and analytic validation of FoundationOne CDx™ for NTRK fusion-positive solid tumors in patients treated with entrectinib

A phase 1 study of AGEN2373, a novel CD137 agonist antibody designed to avoid hepatoxicity, in patients with advanced solid tumors

Assessing the Genotyping Quality of Different SNP-Chips and Imputed Data Using Family-Data

A general semi-parametric approach to the analysis of genetic association studies in population-based designs

Clinical and analytical validation of FoundationOne.sup.®CDx, a comprehensive genomic profiling assay for solid tumors

Subgroup Analyses and Information from Clinical Trials on Breast Cancer

41: ASSOCIATION OF MANNOSE-BINDING LECTIN WITH INFLUENZA CRITICAL ILLNESS IN CHILDREN

Quantitative trait prediction based on genetic marker-array data, a simulation studv

Gene expression profile alone is inadequate in predicting complete response in multiple myeloma

Vitamin D-binding protein haplotype is associated with hospitalization for RSV bronchiolitis

Abstract 1607: An ERBB2 follow-on companion diagnostic for clinical care of patients with breast cancer

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