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Author Details

Petar Stojanov
1984
58
27
PMIDPaper TitleJournal TitlePublished Year
33070196Unpaired data empowers association tests.Bioinformatics2021
31497776Low-Dimensional Density Ratio Estimation for Covariate Shift Correction.2019
31497777Data-Driven Approach to Multiple-Source Domain Adaptation.2019
28658208Recurrent and functional regulatory mutations in breast cancer.Nature2017
29017547Reconstructing cancer drug response networks using multitask learning.BMC Syst Biol2017
26806129Mutational Strand Asymmetries in Cancer Genomes Reveal Mechanisms of DNA Damage and Repair.Cell2016
25056374Integrative and comparative genomic analysis of HPV-positive and HPV-negative head and neck squamous cell carcinomas.Clin Cancer Res2015
25916570Low incidence of complications after cephalic vein cutdown for pacemaker lead implantation in children weighing less than 10 kilograms: A single-center experience with long-term follow-up.Heart Rhythm2015
26192918Paired exome analysis of Barrett's esophagus and adenocarcinoma.Nat Genet2015
24778153Somatic mutation as a mechanism of Wnt/β-catenin pathway activation in CLL.Blood2014
24390350Discovery and saturation analysis of cancer genes across 21 tumour types.Nature2014
24336318Reduced local mutation density in regulatory DNA of cancer genomes is linked to DNA repair.Nat Biotechnol2014
24434212Widespread genetic heterogeneity in multiple myeloma: implications for targeted therapy.Cancer Cell2014
24323028Integrative and comparative genomic analysis of lung squamous cell carcinomas in East Asian patients.J Clin Oncol2014
25186949The genomic landscape of pediatric Ewing sarcoma.Cancer Discov2014
25013076Cancer therapy. Ex vivo culture of circulating breast tumor cells for individualized testing of drug susceptibility.Science2014
24836576Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine.Nat Med2014
25224413TET2 mutations predict response to hypomethylating agents in myelodysplastic syndrome patients.Blood2014
25092778Somatic mutations predict poor outcome in patients with myelodysplastic syndrome after hematopoietic stem-cell transplantation.J Clin Oncol2014
23415222Evolution and impact of subclonal mutations in chronic lymphocytic leukemia.Cell2013
23770567Mutational heterogeneity in cancer and the search for new cancer-associated genes.Nature2013
23852170An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancers.Nat Genet2013
23525077Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity.Nat Genet2013
22980975Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing.Cell2012
22343534Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing.Proc Natl Acad Sci U S A2012
22622578Melanoma genome sequencing reveals frequent PREX2 mutations.Nature2012
22820256Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations.Nature2012
22610119Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer.Nat Genet2012
22150006SF3B1 and other novel cancer genes in chronic lymphocytic leukemia.N Engl J Med2011
21798893The mutational landscape of head and neck squamous cell carcinoma.Science2011
22069992[Long-term follow-up after catheter-ablation of atrioventricular junction and pacemaker implantation in patients with uncontrolled atrial fibrillation and heart failure].Srpski Arhiv Za Celokupno Lekarstvo2011
18834459Permanent endovenous pediatric pacing: absence of lead failure--20 years follow-up study.PACE - Pacing and Clinical Electrophysiology2008
17227810Age-related role of ambulatory electrocardiographic monitoring in risk stratification of patients with complete congenital atrioventricular block.Europace2007
15869665Prevalence of venous obstruction in permanent endovenous pacing in newborns and infants: follow-up study.Pacing Clin Electrophysiol2005
12453686Aorto-caval fistulas.2002
11137813Permanent endocardial pacing by cephalic vein access in new-borns and infants--surgical techniques.2001
11534283[Analysis of programmed pacing rate levels in patients with the carotid sinus hypersensitivity syndrome and implanted Clarity pacemakers].Srpski Arhiv Za Celokupno Lekarstvo2001
11208495Sudden rate drop intervention rate level in patients with new 'clarity' pacemakers and carotid sinus syndrome.Medical Science Monitor2001
11089428[Metabolic parameters in the evaluation of frequency-adaptive sensors in pacemakers].Srpski Arhiv Za Celokupno Lekarstvo2000
9474649Absorbable suture technique: solution to the growth problem in pediatric pacing with endocardial leads.PACE - Pacing and Clinical Electrophysiology1998
10951815[The popliteal artery entrapment syndrome].Acta chirurgica Iugoslavica1997
17974352[Factors determining late patency of aortobifemoral bypass graft].Srpski Arhiv Za Celokupno Lekarstvo1997
9340799[Carotid body tumor].Srpski Arhiv Za Celokupno Lekarstvo1997
9265235[Aneurysms of the carotid arteries].Srpski Arhiv Za Celokupno Lekarstvo1997
8774824Evaluation of asynchronous left ventricular relaxation by Doppler echocardiography during ventricular pacing with AV synchrony (VDD): comparison with atrial pacing (AAI).PACE - Pacing and Clinical Electrophysiology1996
10951761[Ruptured abdominal aortic aneurysms].Acta chirurgica Iugoslavica1995
7785376[Comparative analysis of vascular injuries during times of peace and war].Acta chirurgica Iugoslavica1994
7838792Transvenous permanent pacing in a one-day-old infant.PACE - Pacing and Clinical Electrophysiology1994
1383950Assessment of long-term stability of chronic ventricular pacing thresholds in steroid-eluting electrodes.PACE - Pacing and Clinical Electrophysiology1992
1806993[Femoro-popliteal bypass in situ].Srpski Arhiv Za Celokupno Lekarstvo1991
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Broad Institute of MIT and Harvard
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The Broad Institute of Harvard and MIT
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Princess Margaret Cancer Centre, University Health Network
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The Broad Institute of Harvard and MIT
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Novartis Institutes for BioMedical Research
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