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Author Details

Sonal Brahmbhatt
University of British Columbia
2001
17
16
PMIDPaper TitleJournal TitlePublished Year
33441310Multiomics Characterization of Low-Grade Serous Ovarian Carcinoma Identifies Potential Biomarkers of MEK Inhibitor Sensitivity and Therapeutic Vulnerability.Cancer Res2021
29757368The long noncoding RNA landscape of neuroendocrine prostate cancer and its clinical implications.Gigascience2018
28330676Stromal Gene Expression is Predictive for Metastatic Primary Prostate Cancer.Eur Urol2018
28760909Circulating Tumor DNA Reveals Clinically Actionable Somatic Genome of Metastatic Bladder Cancer.Clin Cancer Res2017
27148695Genomic Alterations in Cell-Free DNA and Enzalutamide Resistance in Castration-Resistant Prostate Cancer.JAMA Oncol2016
25544761Identification of DEK as a potential therapeutic target for neuroendocrine prostate cancer.Oncotarget2015
26235627The Placental Gene PEG10 Promotes Progression of Neuroendocrine Prostate Cancer.Cell Rep2015
24356420High fidelity patient-derived xenografts for accelerating prostate cancer discovery and drug development.Cancer Res2014
25036877Systematic identification and characterization of RNA editing in prostate tumors.PLoS One2014
25155515Heterogeneity in the inter-tumor transcriptome of high risk prostate cancer.Genome Biol2014
22294438Integrated genome and transcriptome sequencing identifies a novel form of hybrid and aggressive prostate cancer.J Pathol2012
22553170From sequence to molecular pathology, and a mechanism driving the neuroendocrine phenotype in prostate cancer.J Pathol2012
22252602Next generation sequencing of prostate cancer from a patient identifies a deficiency of methylthioadenosine phosphorylase, an exploitable tumor target.Mol Cancer Ther2012
19014685A salmonid EST genomic study: genes, duplications, phylogeny and microarrays.BMC Genomics2008
12207934Exclusion of serine palmitoyltransferase long chain base subunit 2 (SPTLC2) as a common cause for hereditary sensory neuropathy.Neuromuscul Disord2002
11479835Hereditary sensory neuropathy type I: haplotype analysis shows founders in southern England and Europe.Am J Hum Genet2001
11242114Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I.Nat Genet2001
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Collaborators

Colin C Collins
University of British Columbia
Co-authored papers 13
Martin E Gleave
University of British Columbia
Co-authored papers 11
Stanislav V Volik
University of British Columbia
Co-authored papers 11
Alexander W Wyatt
University of British Columbia
Co-authored papers 10
Anne Haegert
University of British Columbia
Co-authored papers 10
Yuzhuo Wang
University of British Columbia
Co-authored papers 9
Robert H Bell
University of British Columbia
Co-authored papers 9
Fan Mo
Institute of Stem Cell and Regeneration, Chinese Academy of Sciences
Co-authored papers 9
Ladan Fazli
University of British Columbia
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Shawn Anderson
University of British Columbia
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Antonio Hurtado-Coll
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Brian McConeghy
University of British Columbia
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Dong Lin
Fujian Medical University Cancer Hospital and Fujian Cancer Hospital
Co-authored papers 6
Robert Shukin
University of British Columbia
Co-authored papers 5
Himisha Beltran
Dana-Farber Cancer Institute
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Mark A Rubin
University of Bern
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Hui Xue
Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences
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Chunxiao Wu
Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University
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Arul M Chinnaiyan
University of Michigan Medical School.
Co-authored papers 4
Suleyman Cenk Sahinalp
National Cancer Institute, National Institutes of Health
Co-authored papers 4
Anna Lapuk
Contextual Genomics Inc.
Co-authored papers 4
Amina Zoubeidi
University of British Columbia
Co-authored papers 3
Andrew McPherson
Memorial Sloan Kettering Cancer Center
Co-authored papers 3
Christopher A Maher
Washington University in St Louis
Co-authored papers 3
Marco A Marra
University of British Columbia
Co-authored papers 3
Martin Hirst
University of British Columbia
Co-authored papers 2
Kim N Chi
University of British Columbia
Co-authored papers 2
Raunak Shrestha
University of California San Francisco
Co-authored papers 2
Varune R Ramnarine
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Fereydoun Hormozdiari
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