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Author Details
Full Name
Michael Parfenov
Affiliation
Harvard Medical School, Brigham and Women's Hospital
ORCID
Career Start Year
2004
Papers
21
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35138907
A functional genomic approach to actionable gene fusions for precision oncology.
Sci Adv
2022
35138907
A functional genomic approach to actionable gene fusions for precision oncology.
Sci Adv
2022
34250035
Cardiomyocyte Proliferative Capacity Is Restricted in Mice With <i>Lmna</i> Mutation.
Front Cardiovasc Med
2021
34250035
Cardiomyocyte Proliferative Capacity Is Restricted in Mice With <i>Lmna</i> Mutation.
Front Cardiovasc Med
2021
32601476
Genomic analyses implicate noncoding de novo variants in congenital heart disease.
Nat Genet
2020
32601476
Genomic analyses implicate noncoding de novo variants in congenital heart disease.
Nat Genet
2020
29892087
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy.
Genet Med
2019
29892087
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy.
Genet Med
2019
29360822
ViroFind: A novel target-enrichment deep-sequencing platform reveals a complex JC virus population in the brain of PML patients.
PLoS One
2018
30040209
Droplet Digital PCR with EvaGreen Assay: Confirmational Analysis of Structural Variants.
Curr Protoc Hum Genet
2018
29527824
Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errors.
Hum Mutat
2018
29360822
ViroFind: A novel target-enrichment deep-sequencing platform reveals a complex JC virus population in the brain of PML patients.
PLoS One
2018
30040209
Droplet Digital PCR with EvaGreen Assay: Confirmational Analysis of Structural Variants.
Curr Protoc Hum Genet
2018
29527824
Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errors.
Hum Mutat
2018
27239561
Molecular profiling of dilated cardiomyopathy that progresses to heart failure.
JCI Insight
2016
27239561
Molecular profiling of dilated cardiomyopathy that progresses to heart failure.
JCI Insight
2016
26061751
Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
N Engl J Med
2015
26132004
Finding Pathogenic Nucleic Acid Sequences in Next Generation Sequencing Data.
Curr Protoc Hum Genet
2015
26061751
Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
N Engl J Med
2015
26132004
Finding Pathogenic Nucleic Acid Sequences in Next Generation Sequencing Data.
Curr Protoc Hum Genet
2015
23975679
Loss of FHL1 induces an age-dependent skeletal muscle myopathy associated with myofibrillar and intermyofibrillar disorganization in mice.
Hum Mol Genet
2014
25313082
Characterization of HPV and host genome interactions in primary head and neck cancers.
Proc Natl Acad Sci U S A
2014
23975679
Loss of FHL1 induces an age-dependent skeletal muscle myopathy associated with myofibrillar and intermyofibrillar disorganization in mice.
Hum Mol Genet
2014
24379297
Increased burden of cardiovascular disease in carriers of APOL1 genetic variants.
Circ Res
2014
25313082
Characterization of HPV and host genome interactions in primary head and neck cancers.
Proc Natl Acad Sci U S A
2014
24379297
Increased burden of cardiovascular disease in carriers of APOL1 genetic variants.
Circ Res
2014
23665959
De novo mutations in histone-modifying genes in congenital heart disease.
Nature
2013
23665959
De novo mutations in histone-modifying genes in congenital heart disease.
Nature
2013
22958901
Burden of rare sarcomere gene variants in the Framingham and Jackson Heart Study cohorts.
Am J Hum Genet
2012
22958901
Burden of rare sarcomere gene variants in the Framingham and Jackson Heart Study cohorts.
Am J Hum Genet
2012
19899640
[Complex analysis of genetic predisposition to ischemic stroke in Russians].
Mol Biol (Mosk)
2009
19899640
[Complex analysis of genetic predisposition to ischemic stroke in Russians].
Mol Biol (Mosk)
2009
18567199
[Fibrinogen genes polymorphism in patients with ischemic stroke].
Zh Nevrol Psikhiatr Im S S Korsakova
2008
19431272
[The beta-fibrinogen gene polymorphism, fibrinogen level and platelet aggregation in patients with ischemic stroke].
Zh Nevrol Psikhiatr Im S S Korsakova
2008
18567199
[Fibrinogen genes polymorphism in patients with ischemic stroke].
Zh Nevrol Psikhiatr Im S S Korsakova
2008
19431272
[The beta-fibrinogen gene polymorphism, fibrinogen level and platelet aggregation in patients with ischemic stroke].
Zh Nevrol Psikhiatr Im S S Korsakova
2008
17328917
Polymorphism of apolipoprotein E (APOE) and lipoprotein lipase (LPL) genes and ischaemic stroke in individuals of Yakut ethnicity.
J Neurol Sci
2007
17328917
Polymorphism of apolipoprotein E (APOE) and lipoprotein lipase (LPL) genes and ischaemic stroke in individuals of Yakut ethnicity.
J Neurol Sci
2007
17286114
Genetic risk factors of arterial hypertension: analysis of ischemic stroke patients from the Yakut ethnic group.
Dokl Biochem Biophys
2006
17286114
Genetic risk factors of arterial hypertension: analysis of ischemic stroke patients from the Yakut ethnic group.
Dokl Biochem Biophys
2006
15270848
Prevention of experimental autoimmune encephalomyelitis in DA rats by grafting primary skin fibroblasts engineered to express transforming growth factor-beta1.
Clin Exp Immunol
2004
15270848
Prevention of experimental autoimmune encephalomyelitis in DA rats by grafting primary skin fibroblasts engineered to express transforming growth factor-beta1.
Clin Exp Immunol
2004
1 - 42 of 42
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