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Author Details
Full Name
Andrey Sivachenko
Affiliation
Cystic Fibrosis Foundation
ORCID
Career Start Year
2003
Papers
40
H Index
35
Expertise
CM4AI Collaborator
Jake Y. Chen (CM4AI)
PMID
Paper Title
Journal Title
Published Year
30563749
Isogenic cell models of cystic fibrosis-causing variants in natively expressing pulmonary epithelial cells.
J Cyst Fibros
2019
30563749
Isogenic cell models of cystic fibrosis-causing variants in natively expressing pulmonary epithelial cells.
J Cyst Fibros
2019
24498085
A pan-cancer analysis of transcriptome changes associated with somatic mutations in U2AF1 reveals commonly altered splicing events.
PLoS One
2014
25512523
Complementary genomic approaches highlight the PI3K/mTOR pathway as a common vulnerability in osteosarcoma.
Proc Natl Acad Sci U S A
2014
24323028
Integrative and comparative genomic analysis of lung squamous cell carcinomas in East Asian patients.
J Clin Oncol
2014
24498085
A pan-cancer analysis of transcriptome changes associated with somatic mutations in U2AF1 reveals commonly altered splicing events.
PLoS One
2014
24816817
Massively parallel sequencing of human urinary exosome/microvesicle RNA reveals a predominance of non-coding RNA.
PLoS One
2014
25186949
The genomic landscape of pediatric Ewing sarcoma.
Cancer Discov
2014
24836576
Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine.
Nat Med
2014
24695405
PRADA: pipeline for RNA sequencing data analysis.
Bioinformatics
2014
25512523
Complementary genomic approaches highlight the PI3K/mTOR pathway as a common vulnerability in osteosarcoma.
Proc Natl Acad Sci U S A
2014
25186949
The genomic landscape of pediatric Ewing sarcoma.
Cancer Discov
2014
24836576
Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine.
Nat Med
2014
24816817
Massively parallel sequencing of human urinary exosome/microvesicle RNA reveals a predominance of non-coding RNA.
PLoS One
2014
24695405
PRADA: pipeline for RNA sequencing data analysis.
Bioinformatics
2014
24323028
Integrative and comparative genomic analysis of lung squamous cell carcinomas in East Asian patients.
J Clin Oncol
2014
23334666
The genetic landscape of high-risk neuroblastoma.
Nat Genet
2013
23770567
Mutational heterogeneity in cancer and the search for new cancer-associated genes.
Nature
2013
24185511
Somatic mutation of CDKN1B in small intestine neuroendocrine tumors.
Nat Genet
2013
23786770
Inhibitor-sensitive FGFR2 and FGFR3 mutations in lung squamous cell carcinoma.
Cancer Res
2013
23685885
Comparative analysis of RNA sequencing methods for degraded or low-input samples.
Nat Methods
2013
23396013
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.
Nat Biotechnol
2013
23525077
Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity.
Nat Genet
2013
23622249
Punctuated evolution of prostate cancer genomes.
Cell
2013
23415222
Evolution and impact of subclonal mutations in chronic lymphocytic leukemia.
Cell
2013
23334666
The genetic landscape of high-risk neuroblastoma.
Nat Genet
2013
24185511
Somatic mutation of CDKN1B in small intestine neuroendocrine tumors.
Nat Genet
2013
23685885
Comparative analysis of RNA sequencing methods for degraded or low-input samples.
Nat Methods
2013
23622249
Punctuated evolution of prostate cancer genomes.
Cell
2013
23770567
Mutational heterogeneity in cancer and the search for new cancer-associated genes.
Nature
2013
23786770
Inhibitor-sensitive FGFR2 and FGFR3 mutations in lung squamous cell carcinoma.
Cancer Res
2013
23396013
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.
Nat Biotechnol
2013
23415222
Evolution and impact of subclonal mutations in chronic lymphocytic leukemia.
Cell
2013
23525077
Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity.
Nat Genet
2013
22610119
Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer.
Nat Genet
2012
22539670
RNA-SeQC: RNA-seq metrics for quality control and process optimization.
Bioinformatics
2012
22622578
Melanoma genome sequencing reveals frequent PREX2 mutations.
Nature
2012
22722202
Sequence analysis of mutations and translocations across breast cancer subtypes.
Nature
2012
22820256
Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations.
Nature
2012
22610119
Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer.
Nat Genet
2012
22817889
A landscape of driver mutations in melanoma.
Cell
2012
22980975
Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing.
Cell
2012
22980975
Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing.
Cell
2012
22722202
Sequence analysis of mutations and translocations across breast cancer subtypes.
Nature
2012
22820256
Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations.
Nature
2012
22817889
A landscape of driver mutations in melanoma.
Cell
2012
22539670
RNA-SeQC: RNA-seq metrics for quality control and process optimization.
Bioinformatics
2012
22622578
Melanoma genome sequencing reveals frequent PREX2 mutations.
Nature
2012
21478889
A framework for variation discovery and genotyping using next-generation DNA sequencing data.
Nat Genet
2011
21307934
The genomic complexity of primary human prostate cancer.
Nature
2011
1 - 50 of 80
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