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Author Details
Full Name
Brandy Klotzle
Affiliation
Departments of Bioinformatics and Clinical Genomics, Illumina Inc.
ORCID
Career Start Year
2009
Papers
36
H Index
25
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
26902887
DNA methylation profiles in African American prostate cancer patients in relation to disease progression.
Genomics
2019
30304370
Pisces: an accurate and versatile variant caller for somatic and germline next-generation sequencing data.
Bioinformatics
2019
30007336
COL18A1 is a candidate eye iridocorneal angle-closure gene in humans.
Hum Mol Genet
2018
27358489
Epigenome-Wide Tumor DNA Methylation Profiling Identifies Novel Prognostic Biomarkers of Metastatic-Lethal Progression in Men Diagnosed with Clinically Localized Prostate Cancer.
Clin Cancer Res
2017
29137428
<i>PTEN</i> loss is associated with prostate cancer recurrence and alterations in tumor DNA methylation profiles.
Oncotarget
2017
27134041
Mutation in ADORA1 identified as likely cause of early-onset parkinsonism and cognitive dysfunction.
Mov Disord
2016
26612861
Substantial DNA methylation differences between two major neuronal subtypes in human brain.
Nucleic Acids Res
2016
26675814
Identification of mutation in GTPBP2 in patients of a family with neurodegeneration accompanied by iron deposition in the brain.
Neurobiol Aging
2016
27651837
Epigenetic signature of Gleason score and prostate cancer recurrence after radical prostatectomy.
Clin Epigenetics
2016
27142338
Prostate tumor DNA methylation is associated with cigarette smoking and adverse prostate cancer outcomes.
Cancer
2016
25725944
HMSN-P caused by p.Pro285Leu mutation in TFG is not confined to patients with Far East ancestry.
Neurobiol Aging
2015
26305677
Targeted or whole genome sequencing of formalin fixed tissue samples: potential applications in cancer genomics.
Oncotarget
2015
26383847
Epigenomic profiling of DNA methylation in paired prostate cancer versus adjacent benign tissue.
Prostate
2015
26692910
Epigenomic profiling of prostate cancer identifies differentially methylated genes in TMPRSS2:ERG fusion-positive versus fusion-negative tumors.
Clin Epigenetics
2015
24057217
Differences in DNA methylation between human neuronal and glial cells are concentrated in enhancers and non-CpG sites.
Nucleic Acids Res
2014
25455305
Diagnosis of cystathionine beta-synthase deficiency by genetic analysis.
J Neurol Sci
2014
25179373
Application of a low cost array-based technique - TAB-Array - for quantifying and mapping both 5mC and 5hmC at single base resolution in human pluripotent stem cells.
Genomics
2014
24844137
Clinical investigational studies for validation of a next-generation sequencing in vitro diagnostic device for cystic fibrosis testing.
Expert Rev Mol Diagn
2014
24949580
Identification of p.Gln858* in ATP13A2 in two EOPD patients and presentation of their clinical features.
Neurosci Lett
2014
24718283
Validation study of genes with hypermethylated promoter regions associated with prostate cancer recurrence.
Cancer Epidemiol Biomarkers Prev
2014
23295441
Integrative molecular analysis of intrahepatic cholangiocarcinoma reveals 2 classes that have different outcomes.
Gastroenterology
2013
23759946
The novel mutation p.Asp251Asn in the β-subunit of succinate-CoA ligase causes encephalomyopathy and elevated succinylcarnitine.
J Hum Genet
2013
23509297
Whole-genome haplotyping by dilution, amplification, and sequencing.
Proc Natl Acad Sci U S A
2013
23550148
Succinate dehydrogenase mutation underlies global epigenomic divergence in gastrointestinal stromal tumor.
Cancer Discov
2013
23571109
Epigenome-wide ovarian cancer analysis identifies a methylation profile differentiating clear-cell histology with epigenetic silencing of the HERG K+ channel.
Hum Mol Genet
2013
23177740
Genome-wide methylation profiles reveal quantitative views of human aging rates.
Mol Cell
2013
23166001
PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation.
Mov Disord
2013
22098531
Manifestation of diffuse yellowish keratoderma on the palms and soles in autosomal recessive congenital ichthyosis patients may be indicative of mutations in NIPAL4.
J Dermatol
2012
23064414
Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia.
Nat Genet
2012
22539340
LTBP2 mutations cause Weill-Marchesani and Weill-Marchesani-like syndrome and affect disruptions in the extracellular matrix.
Hum Mutat
2012
22347404
Highly parallel genome-wide expression analysis of single mammalian cells.
PLoS One
2012
21843359
Gene expression profiling of human whole blood samples with the Illumina WG-DASL assay.
BMC Genomics
2011
21839163
High density DNA methylation array with single CpG site resolution.
Genomics
2011
21865163
Genetic and genomic analyses of RNA polymerase II-pausing factor in regulation of mammalian transcription and cell growth.
J Biol Chem
2011
19410283
Analysis of gene expression in stage I serous tumors identifies critical pathways altered in ovarian cancer.
Gynecol Oncol
2009
19997620
Whole-genome gene expression profiling of formalin-fixed, paraffin-embedded tissue samples.
PLoS One
2009
1 - 36 of 36
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Dean A Troyer
Eastern Virginia Medical School
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Sun Yat-sen University
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