William J. Steinbach
Chair and Associate Dean
Also affiliated: Goethe University Frankfurt (2012–2017); University of Bern (2017); Leeds General Infirmary (2012); Arkansas Children's Hospital (2022); Nationwide Children's Hospital (2008–2012); Lucile Packard Children's Hospital (2000–2001); Children's Hospital of Philadelphia (2015–2017); University of Massachusetts Chan Medical School (2006); Duke University (2002–2025); Baylor College of Medicine (2012); University of Toronto (2008); Great Ormond Street Hospital (2012); University Hospital of Bern (2017); Hospital for Sick Children (2012–2017); London South Bank University (2012); University of Iowa Stead Family Children’s Hospital (2012); Duke Medical Center (2002–2025); Stanford Medicine (2001–2003); Texas Children's Hospital (2012); Duke University Hospital (2017); Arkansas Children's Research Institute (2022–2026); University of York (2012–2015); The Ohio State University (2008–2012); Stanford University (2000–2003); McMaster University (2015)
Pediatrics, College of Medicine
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
William J. Steinbach's research program focuses on the pathogenesis, diagnosis, and treatment of invasive fungal infections, particularly in immunosuppressed children. For over two decades, he has led an NIH-funded multidisciplinary clinical care and research program supporting this patient population. His work encompasses molecular, translational, and clinical investigations, with broader applications to all infections in immunocompromised patients.
Steinbach has significant experience as a principal investigator on federal grants, having led multiple R01 awards and T32 awards in molecular mycology and pediatric infectious diseases. He has also served on national scientific and research advisory panels. His scholarship is reflected in a high h-index of 68, over 280 publications, and more than 26,000 citations. He currently holds the Robert H. Fiser, Jr. MD Endowed Chair in Pediatrics and serves as Chair of Pediatrics and Associate Dean for Child Health at the University of Arkansas for Medical Sciences, in addition to being Pediatrician-in-Chief at Arkansas Children’s.
Metrics
- h-index: 68
- Publications: 287
- Citations: 27,716
Positions
-
Chair and Associate Dean 2022–presentUniversity of Arkansas for Medical Sciences Pediatrics, College of Medicine Institutional directory
-
Pediatrician-in-Chief 2022–presentArkansas Children's Hospital ORCID
Selected Publications
-
Drugs for Parasitic Infections (2025)
-
New Approaches and a Call to Action (2025)
-
Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi (2024)
-
Transition to Enteral Triazole Antifungal Therapy for Pediatric Invasive Candidiasis: Secondary Analysis of a Multicenter Cohort Study Conducted by the Pediatric Fungal Network (2024)
-
Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi (2024)
-
Fecal Microbiota Transplantation: Information for the Pediatrician (2023)
-
Tuning sterol extraction kinetics yields a renal-sparing polyene antifungal (2023)
-
Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22-modified FK520 analog against <i>C. neoformans</i> (2023)
-
Adjunctive Diagnostic Studies Completed Following Detection of Candidemia in Children: Secondary Analysis of Observed Practice From a Multicenter Cohort Study Conducted by the Pediatric Fungal Network (2023)
-
Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22 modified FK520 analog against <i>C. neoformans</i> (2023)
-
American Society for Transplantation and Cellular Therapy Series, #6: Management of Invasive Candidiasis in Hematopoietic Cell Transplantation Recipients (2023)
-
Calcineurin Inhibitor CN585 Exhibits Off-Target Effects in the Human Fungal Pathogen Aspergillus fumigatus (2022)
-
Prospective Evaluation of the Fungitell® (1→3) <scp>Beta‐D‐Glucan</scp> Assay as a Diagnostic Tool for Invasive Fungal Disease in Pediatric Allogeneic Hematopoietic Cell Transplantation: A Report from the Children's Oncology Group (2022)
Federal Grants 1 $269,148 total
Clinician Research Education and Scientific Training (CREST) Program
Collaboration Network
Top Collaborators
- Tuning sterol extraction kinetics yields a renal-sparing polyene antifungal
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22-modified FK520 analog against <i>C. neoformans</i>
- Calcineurin Inhibitor CN585 Exhibits Off-Target Effects in the Human Fungal Pathogen Aspergillus fumigatus
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22 modified FK520 analog against <i>C. neoformans</i>
Showing 5 of 6 shared publications
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22-modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22 modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22-modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22 modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22-modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22 modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22-modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22 modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22-modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22 modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22-modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22 modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22-modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22 modified FK520 analog against <i>C. neoformans</i>
- Structure-guided design and synthesis of C22- and C32-modified FK520 analogs with enhanced activity against human pathogenic fungi
- Prospective Evaluation of the Fungitell® (1→3) <scp>Beta‐D‐Glucan</scp> Assay as a Diagnostic Tool for Invasive Fungal Disease in Pediatric Allogeneic Hematopoietic Cell Transplantation: A Report from the Children's Oncology Group
- Adjunctive Diagnostic Studies Completed Following Detection of Candidemia in Children: Secondary Analysis of Observed Practice From a Multicenter Cohort Study Conducted by the Pediatric Fungal Network
- Transition to Enteral Triazole Antifungal Therapy for Pediatric Invasive Candidiasis: Secondary Analysis of a Multicenter Cohort Study Conducted by the Pediatric Fungal Network
- Prospective Evaluation of the Fungitell® (1→3) <scp>Beta‐D‐Glucan</scp> Assay as a Diagnostic Tool for Invasive Fungal Disease in Pediatric Allogeneic Hematopoietic Cell Transplantation: A Report from the Children's Oncology Group
- Adjunctive Diagnostic Studies Completed Following Detection of Candidemia in Children: Secondary Analysis of Observed Practice From a Multicenter Cohort Study Conducted by the Pediatric Fungal Network
- Transition to Enteral Triazole Antifungal Therapy for Pediatric Invasive Candidiasis: Secondary Analysis of a Multicenter Cohort Study Conducted by the Pediatric Fungal Network
- Fecal Microbiota Transplantation: Information for the Pediatrician
- Adjunctive Diagnostic Studies Completed Following Detection of Candidemia in Children: Secondary Analysis of Observed Practice From a Multicenter Cohort Study Conducted by the Pediatric Fungal Network
- Transition to Enteral Triazole Antifungal Therapy for Pediatric Invasive Candidiasis: Secondary Analysis of a Multicenter Cohort Study Conducted by the Pediatric Fungal Network
- Prospective Evaluation of the Fungitell® (1→3) <scp>Beta‐D‐Glucan</scp> Assay as a Diagnostic Tool for Invasive Fungal Disease in Pediatric Allogeneic Hematopoietic Cell Transplantation: A Report from the Children's Oncology Group
- Adjunctive Diagnostic Studies Completed Following Detection of Candidemia in Children: Secondary Analysis of Observed Practice From a Multicenter Cohort Study Conducted by the Pediatric Fungal Network
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22-modified FK520 analog against <i>C. neoformans</i>
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22 modified FK520 analog against <i>C. neoformans</i>
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22-modified FK520 analog against <i>C. neoformans</i>
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22 modified FK520 analog against <i>C. neoformans</i>
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22-modified FK520 analog against <i>C. neoformans</i>
- Enhanced fungal specificity and <i>in vivo</i> therapeutic efficacy of a C-22 modified FK520 analog against <i>C. neoformans</i>
Similar Researchers
Based on overlapping research topics