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Author Details
Full Name
Sean McGrath
Affiliation
Harvard T.H. Chan School of Public Health
ORCID
Career Start Year
1996
Papers
54
H Index
27
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35305813
Effectiveness and safety of intrauterine insemination vs. assisted reproductive technology: emulating a target trial using an observational database of administrative claims.
Fertil Steril
2022
35687047
Detection of brain somatic variation in epilepsy-associated developmental lesions.
Epilepsia
2022
36191838
Pacific Biosciences Fusion and Long Isoform Pipeline for Cancer Transcriptome-Based Resolution of Isoform Complexity.
J Mol Diagn
2022
35045382
A deletion in the N gene of SARS-CoV-2 may reduce test sensitivity for detection of SARS-CoV-2.
Diagn Microbiol Infect Dis
2022
34859533
Long-read whole genome sequencing reveals HOXD13 alterations in synpolydactyly.
Hum Mutat
2022
35149534
Expanding the clinical phenotype of <i>FGFR1</i> internal tandem duplication.
Cold Spring Harb Mol Case Stud
2022
33428897
A switch in mechanism of action prevents doxorubicin-mediated cardiac damage.
Biochem Pharmacol
2021
33827698
Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastoma.
Acta Neuropathol Commun
2021
33893698
Novel morphologic findings in PLAG1-rearranged soft tissue tumors.
Genes Chromosomes Cancer
2021
34863095
Discovery of clinically relevant fusions in pediatric cancer.
BMC Genomics
2021
34041825
Gastroblastoma with a novel EWSR1-CTBP1 fusion presenting in adolescence.
Genes Chromosomes Cancer
2021
34048549
PTEN somatic mutations contribute to spectrum of cerebral overgrowth.
Brain
2021
33465168
A novel sialic acid-binding adhesin present in multiple species contributes to the pathogenesis of Infective endocarditis.
PLoS Pathog
2021
33028644
Infantile fibrosarcoma-like tumor driven by novel <i>RBPMS-MET</i> fusion consolidated with cabozantinib.
Cold Spring Harb Mol Case Stud
2020
30661756
Characterizing the Major Structural Variant Alleles of the Human Genome.
Cell
2019
31308084
Streptococcus oralis subsp. <i>dentisani</i> Produces Monolateral Serine-Rich Repeat Protein Fibrils, One of Which Contributes to Saliva Binding via Sialic Acid.
Infect Immun
2019
29495964
Improving eukaryotic genome annotation using single molecule mRNA sequencing.
BMC Genomics
2018
27364878
Assessing the performance of multiplexed tandem PCR for the diagnosis of pathogenic genotypes of Theileria orientalis using pooled blood samples from cattle.
Mol Cell Probes
2017
28396521
Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly.
Genome Res
2017
28523107
Encapsulation of Mitoxantrone within Cucurbit[8]uril Decreases Toxicity and Enhances Survival in a Mouse Model of Cancer.
ACS Med Chem Lett
2017
28760689
Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomes.
Exp Hematol
2017
27029710
A genomic case study of mixed fibrolamellar hepatocellular carcinoma.
Ann Oncol
2016
26499396
Identification of a novel fusion transcript between human relaxin-1 (RLN1) and human relaxin-2 (RLN2) in prostate cancer.
Mol Cell Endocrinol
2016
27181063
Comprehensive genomic analysis reveals FLT3 activation and a therapeutic strategy for a patient with relapsed adult B-lymphoblastic leukemia.
Exp Hematol
2016
25985720
Investigating the first outbreak of oriental theileriosis in cattle in South Australia using multiplexed tandem PCR (MT-PCR).
Ticks Tick Borne Dis
2015
26456686
Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects.
Cell Stem Cell
2015
26645048
Optimizing cancer genome sequencing and analysis.
Cell Syst
2015
25965570
Mutant U2AF1 Expression Alters Hematopoiesis and Pre-mRNA Splicing In Vivo.
Cancer Cell
2015
24814956
cDNA hybrid capture improves transcriptome analysis on low-input and archived samples.
J Mol Diagn
2014
23382650
The Oxytricha trifallax macronuclear genome: a complex eukaryotic genome with 16,000 tiny chromosomes.
PLoS Biol
2013
22237025
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing.
Nature
2012
22817890
The origin and evolution of mutations in acute myeloid leukemia.
Cell
2012
21436584
Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression.
J Clin Invest
2011
20072128
Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene content.
Nature
2010
21067377
DNMT3A mutations in acute myeloid leukemia.
N Engl J Med
2010
20393555
Genome remodelling in a basal-like breast cancer metastasis and xenograft.
Nature
2010
19668202
BreakDancer: an algorithm for high-resolution mapping of genomic structural variation.
Nat Methods
2009
19657110
Recurring mutations found by sequencing an acute myeloid leukemia genome.
N Engl J Med
2009
19607652
The value of avian genomics to the conservation of wildlife.
BMC Genomics
2009
17933775
Gallus GBrowse: a unified genomic database for the chicken.
Nucleic Acids Res
2008
18724933
A sequence motif within chromatin entry sites directs MSL establishment on the Drosophila X chromosome.
Cell
2008
19052635
Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain.
PLoS One
2008
18987736
DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome.
Nature
2008
16702545
Hotspots for copy number variation in chimpanzees and humans.
Proc Natl Acad Sci U S A
2006
16826518
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.
Am J Hum Genet
2006
15737067
Lineage-specific expansions of retroviral insertions within the genomes of African great apes but not humans and orangutans.
PLoS Biol
2005
16169929
A genome-wide survey of structural variation between human and chimpanzee.
Genome Res
2005
15918152
Segmental duplications and copy-number variation in the human genome.
Am J Hum Genet
2005
11893129
The frequency and effects of cytochrome P450 (CYP) 2C9 polymorphisms in patients receiving warfarin.
J Am Coll Surg
2002
12411588
Template-directed dye-terminator incorporation with fluorescence polarization detection for analysis of single nucleotide polymorphisms implicated in sepsis.
J Mol Diagn
2002
1 - 50 of 54
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Kelly A Frazer
University of California, USA Institute for Genomic Medicine
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row(s) 1 - 30 of 30
Collaborators
Vincent Magrini
The Ohio State University
Co-authored papers
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Richard K Wilson
The Ohio State University
Co-authored papers
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Elaine R Mardis
The Ohio State University
Co-authored papers
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Robert S Fulton
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Co-authored papers
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David E Larson
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers
12
Daniel C Koboldt
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Co-authored papers
12
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Washington University School of Medicine
Co-authored papers
11
Anthony R Miller
Institute for Genomic Medicine, Nationwide Children's Hospital
Co-authored papers
9
Li Ding
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers
9
Jason Walker
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers
8
Kathleen M Schieffer
Nationwide Children's Hospital
Co-authored papers
8
Timothy A Graubert
Massachusetts General Hospital
Co-authored papers
8
Michael D McLellan
McDonnell Genome Institute, Washington University in St. Louis
Co-authored papers
8
Catherine E Cottrell
Nationwide Children's Hospital
Co-authored papers
8
Peter White
The Ohio State University
Co-authored papers
8
Ken Chen
University of Texas MD Anderson Cancer Center
Co-authored papers
7
Jacqueline E Payton
Washington University School of Medicine.
Co-authored papers
7
Matthew J Walter
Washington University School of Medicine in St. Louis
Co-authored papers
7
Daniel C Link
Washington University School of Medicine
Co-authored papers
7
Evan E Eichler
University of Washington
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Malachi Griffith
Washington University
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Sharon E Heath
Washington University School of Medicine.
Co-authored papers
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Katherine E Miller
College of Medicine, The Ohio State University
Co-authored papers
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Joshua F McMichael
Washington University
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