Skip to Main Content

Author Details

Sean McGrath
Harvard T.H. Chan School of Public Health
1996
54
27
PMIDPaper TitleJournal TitlePublished Year
35305813Effectiveness and safety of intrauterine insemination vs. assisted reproductive technology: emulating a target trial using an observational database of administrative claims.Fertil Steril2022
35687047Detection of brain somatic variation in epilepsy-associated developmental lesions.Epilepsia2022
36191838Pacific Biosciences Fusion and Long Isoform Pipeline for Cancer Transcriptome-Based Resolution of Isoform Complexity.J Mol Diagn2022
35045382A deletion in the N gene of SARS-CoV-2 may reduce test sensitivity for detection of SARS-CoV-2.Diagn Microbiol Infect Dis2022
34859533Long-read whole genome sequencing reveals HOXD13 alterations in synpolydactyly.Hum Mutat2022
35149534Expanding the clinical phenotype of <i>FGFR1</i> internal tandem duplication.Cold Spring Harb Mol Case Stud2022
33428897A switch in mechanism of action prevents doxorubicin-mediated cardiac damage.Biochem Pharmacol2021
33827698Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastoma.Acta Neuropathol Commun2021
33893698Novel morphologic findings in PLAG1-rearranged soft tissue tumors.Genes Chromosomes Cancer2021
34863095Discovery of clinically relevant fusions in pediatric cancer.BMC Genomics2021
34041825Gastroblastoma with a novel EWSR1-CTBP1 fusion presenting in adolescence.Genes Chromosomes Cancer2021
34048549PTEN somatic mutations contribute to spectrum of cerebral overgrowth.Brain2021
33465168A novel sialic acid-binding adhesin present in multiple species contributes to the pathogenesis of Infective endocarditis.PLoS Pathog2021
33028644Infantile fibrosarcoma-like tumor driven by novel <i>RBPMS-MET</i> fusion consolidated with cabozantinib.Cold Spring Harb Mol Case Stud2020
30661756Characterizing the Major Structural Variant Alleles of the Human Genome.Cell2019
31308084Streptococcus oralis subsp. <i>dentisani</i> Produces Monolateral Serine-Rich Repeat Protein Fibrils, One of Which Contributes to Saliva Binding via Sialic Acid.Infect Immun2019
29495964Improving eukaryotic genome annotation using single molecule mRNA sequencing.BMC Genomics2018
27364878Assessing the performance of multiplexed tandem PCR for the diagnosis of pathogenic genotypes of Theileria orientalis using pooled blood samples from cattle.Mol Cell Probes2017
28396521Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly.Genome Res2017
28523107Encapsulation of Mitoxantrone within Cucurbit[8]uril Decreases Toxicity and Enhances Survival in a Mouse Model of Cancer.ACS Med Chem Lett2017
28760689Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomes.Exp Hematol2017
27029710A genomic case study of mixed fibrolamellar hepatocellular carcinoma.Ann Oncol2016
26499396Identification of a novel fusion transcript between human relaxin-1 (RLN1) and human relaxin-2 (RLN2) in prostate cancer.Mol Cell Endocrinol2016
27181063Comprehensive genomic analysis reveals FLT3 activation and a therapeutic strategy for a patient with relapsed adult B-lymphoblastic leukemia.Exp Hematol2016
25985720Investigating the first outbreak of oriental theileriosis in cattle in South Australia using multiplexed tandem PCR (MT-PCR).Ticks Tick Borne Dis2015
26456686Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects.Cell Stem Cell2015
26645048Optimizing cancer genome sequencing and analysis.Cell Syst2015
25965570Mutant U2AF1 Expression Alters Hematopoiesis and Pre-mRNA Splicing In Vivo.Cancer Cell2015
24814956cDNA hybrid capture improves transcriptome analysis on low-input and archived samples.J Mol Diagn2014
23382650The Oxytricha trifallax macronuclear genome: a complex eukaryotic genome with 16,000 tiny chromosomes.PLoS Biol2013
22237025Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing.Nature2012
22817890The origin and evolution of mutations in acute myeloid leukemia.Cell2012
21436584Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression.J Clin Invest2011
20072128Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene content.Nature2010
21067377DNMT3A mutations in acute myeloid leukemia.N Engl J Med2010
20393555Genome remodelling in a basal-like breast cancer metastasis and xenograft.Nature2010
19668202BreakDancer: an algorithm for high-resolution mapping of genomic structural variation.Nat Methods2009
19657110Recurring mutations found by sequencing an acute myeloid leukemia genome.N Engl J Med2009
19607652The value of avian genomics to the conservation of wildlife.BMC Genomics2009
17933775Gallus GBrowse: a unified genomic database for the chicken.Nucleic Acids Res2008
18724933A sequence motif within chromatin entry sites directs MSL establishment on the Drosophila X chromosome.Cell2008
19052635Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain.PLoS One2008
18987736DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome.Nature2008
16702545Hotspots for copy number variation in chimpanzees and humans.Proc Natl Acad Sci U S A2006
16826518Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.Am J Hum Genet2006
15737067Lineage-specific expansions of retroviral insertions within the genomes of African great apes but not humans and orangutans.PLoS Biol2005
16169929A genome-wide survey of structural variation between human and chimpanzee.Genome Res2005
15918152Segmental duplications and copy-number variation in the human genome.Am J Hum Genet2005
11893129The frequency and effects of cytochrome P450 (CYP) 2C9 polymorphisms in patients receiving warfarin.J Am Coll Surg2002
12411588Template-directed dye-terminator incorporation with fluorescence polarization detection for analysis of single nucleotide polymorphisms implicated in sepsis.J Mol Diagn2002
  • 1 - 50 of 54

Recommended Authors

Universitat de Barcelona (UB)
Career Start Year 2010
Number of shared co-authors 13
Huadong Hospital Affiliated to Fudan University
Career Start Year 2007
Number of shared co-authors 0
Adelaide Medical School, The University of Adelaide
Career Start Year 2007
Number of shared co-authors 5
Children's Cancer Institute, Lowy Cancer Research Centre
Career Start Year 2006
Number of shared co-authors 5
QIMR Berghofer Medical Research Institute
Career Start Year 2005
Number of shared co-authors 4
Children's Hospital of Philadelphia
Career Start Year 2004
Number of shared co-authors 2
Icahn School of Medicine at Mount Sinai
Career Start Year 2004
Number of shared co-authors 9
Mayo Clinic College of Medicine and Science
Career Start Year 2001
Number of shared co-authors 4
Broad Institute of MIT and Harvard
Career Start Year 2001
Number of shared co-authors 35
National Human Genome Research Institute, National Institutes of Health
Career Start Year 2000
Number of shared co-authors 18
Mayo Clinic
Career Start Year 2000
Number of shared co-authors 0
HudsonAlpha Institute for Biotechnology
Career Start Year 1999
Number of shared co-authors 3
University of Washington
Career Start Year 1997
Number of shared co-authors 12
University of Washington
Career Start Year 1996
Number of shared co-authors 18
University of British Columbia
Career Start Year 1995
Number of shared co-authors 57
The University of Texas MD Anderson Cancer Center
Career Start Year 1995
Number of shared co-authors 0
University of British Columbia
Career Start Year 1993
Number of shared co-authors 53
university of california los angeles
Career Start Year 1993
Number of shared co-authors 3
Baylor College of Medicine
Career Start Year 1992
Number of shared co-authors 37
Ontario Institute for Cancer Research
Career Start Year 1991
Number of shared co-authors 15
Baylor College of Medicine
Career Start Year 1991
Number of shared co-authors 35
Yale School of Medicine
Career Start Year 1989
Number of shared co-authors 2
Baylor College of Medicine
Career Start Year 1988
Number of shared co-authors 39
Baylor College of Medicine
Career Start Year 1987
Number of shared co-authors 43
Baylor College of Medicine
Career Start Year 1987
Number of shared co-authors 27
McGill University
Career Start Year 1986
Number of shared co-authors 3
National Human Genome Research Institute, National Institutes of Health
Career Start Year 1985
Number of shared co-authors 31
Baylor College of Medicine
Career Start Year 1984
Number of shared co-authors 40
CytoGnomix Inc.
Career Start Year 1981
Number of shared co-authors 3
University of California, USA Institute for Genomic Medicine
Career Start Year 1967
Number of shared co-authors 10

Collaborators

The Ohio State University
Co-authored papers 32
The Ohio State University
Co-authored papers 29
The Ohio State University
Co-authored papers 28
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 16
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 12
Institute for Genomic Medicine, Nationwide Children's Hospital
Co-authored papers 12
Washington University School of Medicine
Co-authored papers 11
Institute for Genomic Medicine, Nationwide Children's Hospital
Co-authored papers 9
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 9
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 8
Nationwide Children's Hospital
Co-authored papers 8
Massachusetts General Hospital
Co-authored papers 8
McDonnell Genome Institute, Washington University in St. Louis
Co-authored papers 8
Nationwide Children's Hospital
Co-authored papers 8
The Ohio State University
Co-authored papers 8
University of Texas MD Anderson Cancer Center
Co-authored papers 7
Washington University School of Medicine.
Co-authored papers 7
Washington University School of Medicine in St. Louis
Co-authored papers 7
Washington University School of Medicine
Co-authored papers 7
University of Washington
Co-authored papers 7
Washington University
Co-authored papers 6
Washington University School of Medicine.
Co-authored papers 6
College of Medicine, The Ohio State University
Co-authored papers 6
Washington University
Co-authored papers 6
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 6
Washington University School of Medicine
Co-authored papers 6
Washington University School of Medicine
Co-authored papers 6
The Institute for Genomic Medicine, Nationwide Children's Hospital
Co-authored papers 6
Washington University School of Medicine
Co-authored papers 6
The Institute for Genomic Medicine at Nationwide Children's Hospital
Co-authored papers 6