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Author Details
Full Name
Hugues Sicotte
Affiliation
Mayo Clinic
ORCID
Career Start Year
1999
Papers
59
H Index
29
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35331649
Implementation of preemptive DNA sequence-based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study.
Genet Med
2022
36135372
Molecular Profile Changes in Patients with Castrate-Resistant Prostate Cancer Pre- and Post-Abiraterone/Prednisone Treatment.
Mol Cancer Res
2022
32623598
Next-Generation Sequencing of CYP2C19 in Stent Thrombosis: Implications for Clopidogrel Pharmacogenomics.
Cardiovasc Drugs Ther
2021
33823155
A rare germline CDKN2A variant (47T>G; p16-L16R) predisposes carriers to pancreatic cancer by reducing cell cycle inhibition.
J Biol Chem
2021
33187969
Shorter Treatment-Naïve Leukocyte Telomere Length is Associated with Poorer Overall Survival of Patients with Pancreatic Ductal Adenocarcinoma.
Cancer Epidemiol Biomarkers Prev
2021
32312758
Leukocyte Telomere Length and Its Interaction with Germline Variation in Telomere-Related Genes in Relation to Pancreatic Adenocarcinoma Risk.
Cancer Epidemiol Biomarkers Prev
2020
31346613
Molecular profiling of long-term IDH-wildtype glioblastoma survivors.
Neuro Oncol
2019
28926134
Early genetic aberrations in patients with sporadic colorectal cancer.
Mol Carcinog
2018
30038052
<i>CDKN2A</i> Germline Rare Coding Variants and Risk of Pancreatic Cancer in Minority Populations.
Cancer Epidemiol Biomarkers Prev
2018
29391396
Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8.
Transl Psychiatry
2018
29069303
A prospective genome-wide study of prostate cancer metastases reveals association of wnt pathway activation and increased cell cycle proliferation with primary resistance to abiraterone acetate-prednisone.
Ann Oncol
2018
27436494
Elevated Levels of Adhesion Proteins Are Associated With Low Ankle-Brachial Index.
Angiology
2017
28255664
Adult infiltrating gliomas with WHO 2016 integrated diagnosis: additional prognostic roles of ATRX and TERT.
Acta Neuropathol
2017
28376176
Tumor Sequencing and Patient-Derived Xenografts in the Neoadjuvant Treatment of Breast Cancer.
J Natl Cancer Inst
2017
28473535
Androgen Receptor Variant AR-V9 Is Coexpressed with AR-V7 in Prostate Cancer Metastases and Predicts Abiraterone Resistance.
Clin Cancer Res
2017
28346443
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.
Nat Genet
2017
28203683
Identification of unique venous thromboembolism-susceptibility variants in African-Americans.
Thromb Haemost
2017
28572400
Hepatocyte growth factor demonstrates racial heterogeneity as a biomarker for coronary heart disease.
Heart
2017
27502248
Radiogenomics to characterize regional genetic heterogeneity in glioblastoma.
Neuro Oncol
2017
26892517
Circulating level of hepatocyte growth factor predicts incidence of type 2 diabetes mellitus: The Multi-Ethnic Study of Atherosclerosis (MESA).
Metabolism
2016
26638193
Impact of adiposity on cellular adhesion: The Multi-Ethnic Study of atherosclerosis (MESA).
Obesity (Silver Spring)
2016
27084275
Determining the frequency of pathogenic germline variants from exome sequencing in patients with castrate-resistant prostate cancer.
BMJ Open
2016
26848776
A targeted genetic association study of epithelial ovarian cancer susceptibility.
Oncotarget
2016
26842848
Measure transcript integrity using RNA-seq data.
BMC Bioinformatics
2016
25371537
Case-only exome sequencing and complex disease susceptibility gene discovery: study design considerations.
J Med Genet
2015
26296701
Exome sequencing reveals frequent deleterious germline variants in cancer susceptibility genes in women with invasive breast cancer undergoing neoadjuvant chemotherapy.
Breast Cancer Res Treat
2015
26695660
Mutational Landscapes of Sequential Prostate Metastases and Matched Patient Derived Xenografts during Enzalutamide Therapy.
PLoS One
2015
26061753
Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors.
N Engl J Med
2015
25916844
TP53 mutations, tetraploidy and homologous recombination repair defects in early stage high-grade serous ovarian cancer.
Nucleic Acids Res
2015
25900876
Zinc transporter genes and urological cancers: integrated analysis suggests a role for ZIP11 in bladder cancer.
Tumour Biol
2015
25998175
Trans-ethnic meta-analysis identifies common and rare variants associated with hepatocyte growth factor levels in the Multi-Ethnic Study of Atherosclerosis (MESA).
Ann Hum Genet
2015
25744700
P-selectin and subclinical and clinical atherosclerosis: the Multi-Ethnic Study of Atherosclerosis (MESA).
Atherosclerosis
2015
25576479
Multi-ethnic analysis reveals soluble L-selectin may be post-transcriptionally regulated by 3'UTR polymorphism: the Multi-Ethnic Study of Atherosclerosis (MESA).
Hum Genet
2015
24325915
Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer.
Carcinogenesis
2014
24972667
MAP-RSeq: Mayo Analysis Pipeline for RNA sequencing.
BMC Bioinformatics
2014
24908248
Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk.
Nat Genet
2014
24876377
PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data.
Bioinformatics
2014
24631064
Plasma and serum L-selectin and clinical and subclinical cardiovascular disease: the Multi-Ethnic Study of Atherosclerosis (MESA).
Transl Res
2014
23280628
Analysis of 60 reported glioma risk SNPs replicates published GWAS findings but fails to replicate associations from published candidate-gene studies.
Genet Epidemiol
2013
24154874
APOBEC3B upregulation and genomic mutation patterns in serous ovarian carcinoma.
Cancer Res
2013
23733245
Genetic variants in telomerase-related genes are associated with an older age at diagnosis in glioma patients: evidence for distinct pathways of gliomagenesis.
Neuro Oncol
2013
23382860
Inherited variants in regulatory T cell genes and outcome of ovarian cancer.
PLoS One
2013
23361564
Inherited variant on chromosome 11q23 increases susceptibility to IDH-mutated but not IDH-normal gliomas regardless of grade or histology.
Neuro Oncol
2013
22922872
A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutation.
Nat Genet
2012
23029201
IP-FCM measures physiologic protein-protein interactions modulated by signal transduction and small-molecule drug inhibition.
PLoS One
2012
21150883
Prevalence of CDKN2A mutations in pancreatic cancer patients: implications for genetic counseling.
Eur J Hum Genet
2011
21535878
SNPPicker: high quality tag SNP selection across multiple populations.
BMC Bioinformatics
2011
21646302
Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels.
Mayo Clin Proc
2011
21724856
Assessment of hepatocyte growth factor in ovarian cancer mortality.
Cancer Epidemiol Biomarkers Prev
2011
19517021
Genome-wide transcriptional profiling reveals microRNA-correlated genes and biological processes in human lymphoblastoid cell lines.
PLoS One
2009
1 - 50 of 59
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Mayo Clinic
Co-authored papers
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Richard M Weinshilboum
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Liewei Wang
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8
Gloria M Petersen
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Eric D Wieben
Mayo Clinic Rochester
Co-authored papers
8
Michael Y Tsai
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Michèle M Sale
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Christina L Wassel
Premier Inc.
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Alexander R Pico
Institute of Data Science and Biotechnology, Gladstone Institutes
Co-authored papers
6
Phillip S Kirsch
Mayo Clinic
Co-authored papers
6
Brooke L Fridley
H. Lee Moffitt Cancer Center and Research Institute
Co-authored papers
6
Mitchel S Berger
University of California san francisco
Co-authored papers
6
Ann L Oberg
Co-authored papers
6
Yan W Asmann
Mayo Clinic
Co-authored papers
5
Brian P O'Neill
Co-authored papers
5
Caterina Giannini
Mayo Clinic
Co-authored papers
5
Ellen L Goode
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Michael D Prados
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