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Integrated Genomic Characterization of Pancreatic Ductal Adenocarcinoma

Cancer cell, 2017-08, Vol.32 (2), p.185-203.e13

2017

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Measure transcript integrity using RNA-seq data

BMC bioinformatics, 2016-02, Vol.17 (1), p.58-58, Article 58

2016

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Androgen Receptor Variant AR-V9 Is Coexpressed with AR-V7 in Prostate Cancer Metastases and Predicts Abiraterone Resistance

Clinical cancer research, 2017-08, Vol.23 (16), p.4704-4715

2017

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Radiogenomics to characterize regional genetic heterogeneity in glioblastoma

Neuro-oncology (Charlottesville, Va.), 2017-01, Vol.19 (1), p.128-137

2017

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Prevalence of CDKN2A mutations in pancreatic cancer patients: implications for genetic counseling

European journal of human genetics : EJHG, 2011-04, Vol.19 (4), p.472-478

2011

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P-selectin and subclinical and clinical atherosclerosis: The Multi-Ethnic Study of Atherosclerosis (MESA)

Atherosclerosis, 2015-05, Vol.240 (1), p.3-9

2015

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Next-Generation Sequencing of CYP2C19 in Stent Thrombosis: Implications for Clopidogrel Pharmacogenomics

Cardiovascular drugs and therapy, 2021-06, Vol.35 (3), p.549-559

2021

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Circulating level of hepatocyte growth factor predicts incidence of type 2 diabetes mellitus: The Multi-Ethnic Study of Atherosclerosis (MESA)

Metabolism, clinical and experimental, 2016-03, Vol.65 (3), p.64-72

2016

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Mutational Landscapes of Sequential Prostate Metastases and Matched Patient Derived Xenografts during Enzalutamide Therapy

PloS one, 2015-12, Vol.10 (12), p.e0145176

2015

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Zinc transporter genes and urological cancers: integrated analysis suggests a role for ZIP11 in bladder cancer

Tumor biology, 2015-09, Vol.36 (10), p.7431-7437

2015

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Genomic Association Analysis Suggests Chromosome 12 Locus Influencing Antihypertensive Response to Thiazide Diuretic

Hypertension (Dallas, Tex. 1979), 2008-08, Vol.52 (2), p.359-365

2008

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Genome-wide transcriptional profiling reveals microRNA-correlated genes and biological processes in human lymphoblastoid cell lines

PloS one, 2009-06, Vol.4 (6), p.e5878-e5878

2009

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IP-FCM measures physiologic protein-protein interactions modulated by signal transduction and small-molecule drug inhibition

PloS one, 2012-09, Vol.7 (9), p.e45722

2012

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Inherited variants in regulatory T cell genes and outcome of ovarian cancer

PloS one, 2013-01, Vol.8 (1), p.e53903-e53903

2013

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GLOSSI: a method to assess the association of genetic loci-sets with complex diseases

BMC bioinformatics, 2009-04, Vol.10 (1), p.102-102, Article 102

2009

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Introducing RefSeq and LocusLink: curated human genome resources at the NCBI

Trends in genetics, 2000, Vol.16 (1), p.44-47

2000

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SNPPicker: high quality tag SNP selection across multiple populations

BMC bioinformatics, 2011-05, Vol.12 (1), p.129-129, Article 129

2011

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Deep sequencing reveals that low level TP53 mutations are ubiquitous in ovarian cancer patients and controls: successes and challenges for early detection

Translational cancer research, 2016-08, Vol.5 (S2), p.S345-S348

Sicotte, Hugues

2016

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Molecular Profiling Reveals Biologically Discrete Subsets and Pathways of Progression in Diffuse Glioma

Cell, 2016-01, Vol.164 (3), p.550-563

2016

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Adult infiltrating gliomas with WHO 2016 integrated diagnosis: additional prognostic roles of ATRX and TERT

Acta neuropathologica, 2017-06, Vol.133 (6), p.1001-1016

2017

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Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors

Nature genetics, 2017-05, Vol.49 (5), p.789-794

2017

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MAP-RSeq: Mayo Analysis Pipeline for RNA sequencing

BMC bioinformatics, 2014-06, Vol.15 (1), p.224-224, Article 224

2014

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eP383: Mayo Clinic GeneGuide: A population-scale genetic interpretation software for reporting pathogenic and likely pathogenic variants impacting the CDC Tier1 genes

Genetics in medicine, 2022-03, Vol.24 (3), p.S241-S242

2022

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Integrated Genomic Characterization of Pancreatic Ductal Adenocarcinoma

Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors

Measure transcript integrity using RNA-seq data

Androgen Receptor Variant AR-V9 Is Coexpressed with AR-V7 in Prostate Cancer Metastases and Predicts Abiraterone Resistance

Radiogenomics to characterize regional genetic heterogeneity in glioblastoma

Prevalence of CDKN2A mutations in pancreatic cancer patients: implications for genetic counseling

P-selectin and subclinical and clinical atherosclerosis: The Multi-Ethnic Study of Atherosclerosis (MESA)

Next-Generation Sequencing of CYP2C19 in Stent Thrombosis: Implications for Clopidogrel Pharmacogenomics

Circulating level of hepatocyte growth factor predicts incidence of type 2 diabetes mellitus: The Multi-Ethnic Study of Atherosclerosis (MESA)

Mutational Landscapes of Sequential Prostate Metastases and Matched Patient Derived Xenografts during Enzalutamide Therapy

Zinc transporter genes and urological cancers: integrated analysis suggests a role for ZIP11 in bladder cancer

Genomic Association Analysis Suggests Chromosome 12 Locus Influencing Antihypertensive Response to Thiazide Diuretic

Mayo Genome Consortia: A Genotype-Phenotype Resource for Genome-Wide Association Studies With an Application to the Analysis of Circulating Bilirubin Levels

Genome-wide transcriptional profiling reveals microRNA-correlated genes and biological processes in human lymphoblastoid cell lines

IP-FCM measures physiologic protein-protein interactions modulated by signal transduction and small-molecule drug inhibition

Inherited variants in regulatory T cell genes and outcome of ovarian cancer

GLOSSI: a method to assess the association of genetic loci-sets with complex diseases

Introducing RefSeq and LocusLink: curated human genome resources at the NCBI

SNPPicker: high quality tag SNP selection across multiple populations

Deep sequencing reveals that low level TP53 mutations are ubiquitous in ovarian cancer patients and controls: successes and challenges for early detection

Molecular Profiling Reveals Biologically Discrete Subsets and Pathways of Progression in Diffuse Glioma

Adult infiltrating gliomas with WHO 2016 integrated diagnosis: additional prognostic roles of ATRX and TERT

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors

MAP-RSeq: Mayo Analysis Pipeline for RNA sequencing

eP383: Mayo Clinic GeneGuide: A population-scale genetic interpretation software for reporting pathogenic and likely pathogenic variants impacting the CDC Tier1 genes

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