Scott D Boyd

Summary

Affiliation: Stanford University
Country: USA

Publications

  1. pmc Deep sequencing and human antibody repertoire analysis
    Scott D Boyd
    Department of Pathology, Stanford University, Stanford, CA 94305, United States Electronic address
    Curr Opin Immunol 40:103-9. 2016
  2. pmc A Balanced Look at the Implications of Genomic (and Other "Omics") Testing for Disease Diagnosis and Clinical Care
    Scott D Boyd
    Department of Pathology, Stanford University, Stanford, CA 94305, USA
    Genes (Basel) 5:748-66. 2014
  3. doi request reprint Predicting vaccine responsiveness
    Scott D Boyd
    Department of Pathology, Stanford University, Stanford, CA 94305 Electronic address
    Cell Host Microbe 17:301-7. 2015
  4. pmc Human lymphocyte repertoires in ageing
    Scott D Boyd
    Department of Pathology, Stanford University, Stanford, CA, USA Electronic address
    Curr Opin Immunol 25:511-5. 2013
  5. pmc Selective immunophenotyping for diagnosis of B-cell neoplasms: immunohistochemistry and flow cytometry strategies and results
    Scott D Boyd
    Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA
    Appl Immunohistochem Mol Morphol 21:116-31. 2013
  6. doi request reprint Diagnostic applications of high-throughput DNA sequencing
    Scott D Boyd
    Department of Pathology, Stanford University, Stanford, CA 94305, USA
    Annu Rev Pathol 8:381-410. 2013
  7. doi request reprint Features of hemolysis due to Clostridium perfringens infection
    S D Boyd
    Department of Pathology, Stanford University, Stanford, CA 94305, USA
    Int J Lab Hematol 31:364-7. 2009
  8. doi request reprint Everything you wanted to know about small RNA but were afraid to ask
    Scott D Boyd
    Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305 2297, USA
    Lab Invest 88:569-78. 2008
  9. pmc Single B-cell deconvolution of peanut-specific antibody responses in allergic patients
    Ramona A Hoh
    Department of Pathology, Stanford University, Stanford, Calif
    J Allergy Clin Immunol 137:157-67. 2016
  10. pmc Human B-cell isotype switching origins of IgE
    Timothy J Looney
    Department of Pathology, Transplantation and Infection, Stanford University, Stanford, Calif
    J Allergy Clin Immunol 137:579-586.e7. 2016

Collaborators

Detail Information

Publications20

  1. pmc Deep sequencing and human antibody repertoire analysis
    Scott D Boyd
    Department of Pathology, Stanford University, Stanford, CA 94305, United States Electronic address
    Curr Opin Immunol 40:103-9. 2016
    ..Here, we highlight recent advances in this fast-moving field. ..
  2. pmc A Balanced Look at the Implications of Genomic (and Other "Omics") Testing for Disease Diagnosis and Clinical Care
    Scott D Boyd
    Department of Pathology, Stanford University, Stanford, CA 94305, USA
    Genes (Basel) 5:748-66. 2014
    ..Here, we present an overview of conceptual and practical issues to be considered in planning for the integration of genomic methods or, in principle, any other type of "omics" testing into clinical care. ..
  3. doi request reprint Predicting vaccine responsiveness
    Scott D Boyd
    Department of Pathology, Stanford University, Stanford, CA 94305 Electronic address
    Cell Host Microbe 17:301-7. 2015
    ....
  4. pmc Human lymphocyte repertoires in ageing
    Scott D Boyd
    Department of Pathology, Stanford University, Stanford, CA, USA Electronic address
    Curr Opin Immunol 25:511-5. 2013
    ....
  5. pmc Selective immunophenotyping for diagnosis of B-cell neoplasms: immunohistochemistry and flow cytometry strategies and results
    Scott D Boyd
    Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA
    Appl Immunohistochem Mol Morphol 21:116-31. 2013
    ..We present data from cases seen at our institution from 2004 through 2008 using this approach, to provide a practical reference for findings seen in daily diagnostic practice...
  6. doi request reprint Diagnostic applications of high-throughput DNA sequencing
    Scott D Boyd
    Department of Pathology, Stanford University, Stanford, CA 94305, USA
    Annu Rev Pathol 8:381-410. 2013
    ..Transition of new DNA sequencing methodologies to the clinical laboratory is under way and is likely to have a major impact on all areas of medicine...
  7. doi request reprint Features of hemolysis due to Clostridium perfringens infection
    S D Boyd
    Department of Pathology, Stanford University, Stanford, CA 94305, USA
    Int J Lab Hematol 31:364-7. 2009
    ..Blood cultures tested culture positive for C. perfringens. We present images demonstrating the salient features of the peripheral blood smear in cases of this uncommon but deadly cause of hemolysis...
  8. doi request reprint Everything you wanted to know about small RNA but were afraid to ask
    Scott D Boyd
    Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305 2297, USA
    Lab Invest 88:569-78. 2008
    ..A review of current evidence for the role of these molecules in human health and disease will be helpful to pathologists and medical researchers as the fascinating story of these small regulators continues to unfold...
  9. pmc Single B-cell deconvolution of peanut-specific antibody responses in allergic patients
    Ramona A Hoh
    Department of Pathology, Stanford University, Stanford, Calif
    J Allergy Clin Immunol 137:157-67. 2016
    ..The frequencies, cellular phenotypes, epitope specificity, and clonal diversity of allergen-specific B cells in patients with food allergy are not fully understood but are of major pathogenic and therapeutic significance...
  10. pmc Human B-cell isotype switching origins of IgE
    Timothy J Looney
    Department of Pathology, Transplantation and Infection, Stanford University, Stanford, Calif
    J Allergy Clin Immunol 137:579-586.e7. 2016
    ..Much of our knowledge of IgE lineage development derives from model studies in mice rather than from human subjects...
  11. pmc IgH sequences in common variable immune deficiency reveal altered B cell development and selection
    Krishna M Roskin
    Department of Pathology, Stanford University, Stanford, CA 94305, USA
    Sci Transl Med 7:302ra135. 2015
    ....
  12. doi request reprint Laboratory and Data Analysis Methods for Characterization of Human B Cell Repertoires by High-Throughput DNA Sequencing
    Chen Wang
    Department of Pathology, Stanford University, 300 Pasteur Drive, Stanford, CA, 94305, USA
    Methods Mol Biol 1343:219-33. 2015
    ..Here, we describe strategies for preparing and analyzing human antibody gene libraries for studying B cell repertoires. ..
  13. pmc Human responses to influenza vaccination show seroconversion signatures and convergent antibody rearrangements
    Katherine J L Jackson
    Department of Pathology, School of Medicine, Stanford University, Stanford, CA 94305, USA School of Biotechnology and Biomolecular Science, University of New South Wales, Sydney, NSW 2052, Australia
    Cell Host Microbe 16:105-14. 2014
    ..These results indicate that microbes can induce specific signatures of immunoglobulin gene rearrangements and that pathogen exposure can potentially be assessed from B cell repertoires. ..
  14. pmc Effects of aging, cytomegalovirus infection, and EBV infection on human B cell repertoires
    Chen Wang
    Department of Pathology, Stanford University, Stanford, CA 94305
    J Immunol 192:603-11. 2014
    ..These findings isolate effects of aging from those of chronic viral infection on B cell repertoires and provide a baseline for understanding human B cell responses to vaccination or infectious stimuli. ..
  15. pmc Molecular and cellular mechanisms of food allergy and food tolerance
    R Sharon Chinthrajah
    Department of Medicine, Stanford University School of Medicine, Stanford, Calif Department of Pediatrics, Stanford University School of Medicine, Stanford, Calif Sean N Parker Center for Allergy and Asthma Research, Stanford University School of Medicine, Stanford, Calif
    J Allergy Clin Immunol 137:984-97. 2016
    ....
  16. doi request reprint Integration of genomic medicine into pathology residency training: the stanford open curriculum
    Iris Schrijver
    Department of Pathology, Stanford University School of Medicine, Stanford, California 94305, USA
    J Mol Diagn 15:141-8. 2013
    ..This curriculum is freely accessible online...
  17. doi request reprint Broadening Horizons: New Antibodies Against Influenza
    Katherine J L Jackson
    Department of Pathology, Stanford University, CA 94305, USA
    Cell 166:532-3. 2016
    ..2016; Kallewaard et al., 2016). Antibodies with similar structural features are elicited in multiple subjects, suggesting that modified vaccine regimens could provide broad protection. ..
  18. pmc Diversification of the antigen-specific T cell receptor repertoire after varicella zoster vaccination
    Qian Qi
    Division of Immunology and Rheumatology, Department of Medicine, Stanford University, Stanford, CA 94305, USA Department of Medicine, VA Palo Alto Health Care System, Palo Alto, CA 94304, USA
    Sci Transl Med 8:332ra46. 2016
    ..Our results suggest that repertoire analysis of antigen-specific TCRs can be an important readout to assess whether a vaccination was able to generate memory cells in clonal sizes that are necessary for immune protection. ..
  19. pmc Successful immunotherapy induces previously unidentified allergen-specific CD4+ T-cell subsets
    John F Ryan
    Sean N Parker Center for Allergy and Asthma Research at Stanford University, Pulmonary and Critical Care Medicine, Institute of Immunity, Transplantation, and Infectious Diseases, Stanford University, Stanford, CA 94305
    Proc Natl Acad Sci U S A 113:E1286-95. 2016
    ....
  20. pmc New tools for classification and monitoring of autoimmune diseases
    Holden T Maecker
    Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA
    Nat Rev Rheumatol 8:317-28. 2012
    ..These analyses are revealing a more comprehensive and interconnected view of the immune system than ever before and should have an important role in directing future treatment approaches for autoimmune diseases...