Find an Expert Across the RDCRN
Browse researchers, clinicians, and experts across the RDCRN consortia.
Inmaculada Aban, PhD
Myasthenia Gravis Rare Disease Network (MGNET)
University of Alabama at Birmingham
Expertise:
Clinical trials, Statistical research methodology
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Denise Martin Adams, MD
Advancing Rare Disorders: Vascular mAlformation Research Network with CaNVAS (ARDVARC)
Children's Hospital of Philadelphia
Expertise:
Vascular anomalies, Rare vascular tumors, Rare tumors, Education
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Laura A. Adang, MD, PhD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Children's Hospital of Philadelphia
Expertise:
Pediatric neurology, Leukodystrophy, Metachromatic leukodystrophy (MLD), Multiple sulfatase deficiency (MSD), x-linked adrenoleukodystrophy (ALD), Aicardi-Goutières syndrome (AGS)
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Nicholas Ah-Mew, MD
Rare Organic Acidemias Research Consortium (ROAR)
Children’s National Hospital
Expertise:
Organic acidemias, Inborn errors of metabolism, Pediatric inherited metabolic disorders
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Nicholas Ashton, PhD
Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium
Banner Health
Expertise:
Neurochemistry, Biomarker development
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Erika Augustine, MD, MS
Batten Disease Clinical Research Consortium (BDCRC)
Kennedy Krieger Institute
Expertise:
Neuronal ceroid lipofuscinoses (NCLs), Clinical trial design and operations
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Peter Baker, MD
Rare Organic Acidemias Research Consortium (ROAR)
University of Colorado Anschutz
Expertise:
Organic acidemias, Inborn errors of metabolism, Pediatric metabolic disorders
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Tara Bamat, MD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Children's Hospital of Philadelphia
Expertise:
Palliative care, Patient-physician communication, Trauma responsive care, Vicarious trauma, Physician well-being
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Peter Barker, PhD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Johns Hopkins University
Expertise:
Magnetic resonance imaging, Magnetic resonance spectroscopy, Quantitative imaging methods
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Martina Bebin, MD, MPA
Developmental Synaptopathies Consortium (DSC)
University of Alabama at Birmingham
Expertise:
Tuberous sclerosis complex (TSC)
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Michael Benatar, MD
Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium
Myasthenia Gravis Rare Disease Network (MGNET)
University of Miami
Expertise:
Amyotrophic lateral sclerosis (ALS), Myasthenia gravis, Biomarkers, Clinical trials, Pre-symptomatic disease
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Susan Berry, MD
Rare Organic Acidemias Research Consortium (ROAR)
University of Minnesota
Expertise:
Organic acidemias, Inborn errors of metabolism, Genetics, Metabolic disorders, Newborn screening and natural history studies
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Craig Blackstone, MD, PhD
Spastic Paraplegia Centers of Excellence Research Network (SP-CERN)
Massachusetts General Hospital
Expertise:
Molecular mechanisms of hereditary spastic paraplegia, Membrane trafficking, Endoplasmic reticulum biology
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Joshua L. Bonkowsky, MD, PhD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
University of Utah Health
Expertise:
Pediatric neurology, Leukodystrophy, x-linked adrenoleukodystrophy (ALD), Vanishing white matter disease (VWMD)
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Alexandra Borst, MD
Advancing Rare Disorders: Vascular mAlformation Research Network with CaNVAS (ARDVARC)
University of North Carolina
Expertise:
Vascular anomalies, Rare vascular tumors, Hematologic abnormalities in vascular anomalies, Hereditary hemorrhagic telangiectasia (HHT), Hemostasis thrombosis
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Richard Boucher, MD
Rare Bronchiectatic Diseases Consortium (RBDC)
UNC Health
Expertise:
Airway surface liquids, Epitheleal ion transport in human airway disease, Gene therapy, Novel therapy development for human lung disease
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Robert A. Brodsky, MD
Initiation of a cohort to define pathogenic Mechanisms, Precision diagnosis And Complications of Thrombotic Microangiopathies
Johns Hopkins Medicine
Expertise:
Hematology, Complement-mediated hemolytic anemias, Bone marrow failure, Bone marrow transplantation
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Joshua Burns, PhD
Spastic Paraplegia Centers of Excellence Research Network (SP-CERN)
St. Jude Children's Research Hospital
Expertise:
Neuromuscular diseases, Hereditary spastic paraplegia (HSP), Wearable sensors, Rehabilitation science
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Lindsay Burrage, MD, PhD
Rare Organic Acidemias Research Consortium (ROAR)
Baylor College of Medicine
Expertise:
Organic acidemias, Inborn errors of metabolism, Biochemical genetics, Translational research
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Daniel Calame, MD, PhD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Spastic Paraplegia Centers of Excellence Research Network (SP-CERN)
Baylor College of Medicine
Expertise:
Pediatric neurology, Hereditary spastic paraplegia (HSP), Cerebral palsy (CP), Clinical genetics, Pediatric genetics, Neurogenetics, Gene discovery
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Spero R. Cataland, MD
Initiation of a cohort to define pathogenic Mechanisms, Precision diagnosis And Complications of Thrombotic Microangiopathies
The Arthur G. James Cancer Hospital
Expertise:
Hematology, Clinical and translational research in thrombotic microangiopathies
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Shruti Chaturvedi, MBBS, MS
Initiation of a cohort to define pathogenic Mechanisms, Precision diagnosis And Complications of Thrombotic Microangiopathies
Johns Hopkins Medicine
Expertise:
Clinical and translational research, Epidemiology, Strombo microangiopathy, Thrombotic thrombocytopenic purpura, Complement
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Gang Chen, PhD
Rare Bronchiectatic Diseases Consortium (RBDC)
UNC Health
Expertise:
Lung stem/progenitor cells, Airway mucins, Inflammation in health and diseases
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Michelle R. Christie, MD
Spastic Paraplegia Centers of Excellence Research Network (SP-CERN)
Scottish Rite for Children
Expertise:
Neuromuscular disorders, Hereditary spastic paraplegia (HSP)
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Stacey Clardy, MD, PhD
Autoimmunity, Rasmussen’s, Inflammation & Status Epilepticus Research Network (ARISEN)
University of Utah Health
Expertise:
Autoimmune neurology
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Gary Cutter, PhD
Myasthenia Gravis Rare Disease Network (MGNET)
University of Alabama at Birmingham
Expertise:
Clinical trial design, Analysis and interpretation, Epidemiological studies and evaluation research
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Hong Dang, PhD
Rare Bronchiectatic Diseases Consortium (RBDC)
UNC Health
Expertise:
Bioinformatics, Genetics, Molecular biology, High-throughput data analysis, Biological databases and data mining, Biostatistics, Computer system administration
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An N. Dang Do, MD, PhD
Batten Disease Clinical Research Consortium (BDCRC)
Eunice Kennedy Shriver National Institute of Child Health and Human Development
Expertise:
Cellular stress in development and diseases
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Stephanie Davis, MD
Rare Bronchiectatic Diseases Consortium (RBDC)
UNC Health
Expertise:
Cystic fibrosis, Primary ciliary dyskinesia (PCD), Impact of preterm birth on lung disease
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Marie Y. Davis, MD, PhD
Spastic Paraplegia Centers of Excellence Research Network (SP-CERN)
University of Washington Medical School
Expertise:
Movement disorders, Hereditary spastic paraplegia (HSP), Neurogenetics
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Shanlee Davis, MD, PhD
Network for Advancing Sex Chromosome Aneuploidy Research Readiness (NASCARR)
University of Colorado Anschutz Medical Campus
Expertise:
Cardiometabolic health and gonadal function in infants, children and adolescents with X and Y chromosome variations, including Klinefelter and Turner syndromes
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Katherine (Alex) Despotes, MD
Rare Bronchiectatic Diseases Consortium (RBDC)
UNC Health
Expertise:
Cystic fibrosis, Non-cystic fibrosis bronchiectasis, Modulator therapy
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Darius Ebrahimi-Fakhari, MD, PhD
Spastic Paraplegia Centers of Excellence Research Network (SP-CERN)
Boston Children's Hospital
Expertise:
Hereditary spastic paraplegia (HSP), Neurodegeneration, Pediatric neurology, Movement disorders, Neurogenetics
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Florian Eichler, MD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Massachusetts General Hospital
Expertise:
Pediatric neurology, Leukodystrophy, x-linked adrenoleukodystrophy (ALD), Adrenomyeloneuropathy (AMN), Canavan disease (CD), CSF1R-related leukoencephalopathy (ALSP)
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Lisa T. Emrick, MD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Texas Children's Hospital
Expertise:
Pediatric neurology, Leukodystrophy, Neurogenetics, Neurometabolics, Mitochondrial encephalomyopathy, Lacticacidosis, Strokelike episodes (MELAS)
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Charles Esther, MD, PhD
Rare Bronchiectatic Diseases Consortium (RBDC)
UNC Health
Expertise:
Cystic fibrosis, Primary ciliary dyskinesia (PCD), Non-cystic fibrosis bronchiectasis
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S. Ali Fatemi, MD, MBA
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Kennedy Krieger Institute
Expertise:
Pediatric neurology, Leukodystrophy, x-linked adrenoleukodystrophy (ALD), Adrenomyeloneuropathy (AMN), Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL)
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Richard S. Finkel, MD
Spastic Paraplegia Centers of Excellence Research Network (SP-CERN)
St. Jude Children's Research Hospital
Expertise:
Neuromuscular disorders, Hereditary spastic paraplegia (HSP), Clinical trial design
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Kristen Fisher, DO
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Baylor College of Medicine
Expertise:
Pediatric neurology, Leukodystrophy, Neuroinflammatory disorders, Aicardi-Goutières syndrome (AGS)
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Brian T. Fisher, DO, MPH, MSCE
Pediatric Fungal Network STudy of Rare Invasive Fungal DisEases in Immunocompromised Pediatric Patients (PFN-STRIDE)
Children's Hospital of Philadelphia
Expertise:
Infections in immunocompromised children
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Jeanne M. Franzone, MD
Brittle Bone Disorders Consortium (BBDC)
Nemours Children's Hospital
Expertise:
Clubfoot, Fracture management, Limb length discrepancy, Osteogenesis imperfecta
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Jamie L. Fraser, MD, PhD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Children’s National Medical Center
Expertise:
Pediatric neurology, Leukodystrophy, Biochemical genetics, Medical genetics, Leukoencephalopathy with calcifications and cysts (LCC)
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Alexandra Freeman, MD
Rare Bronchiectatic Diseases Consortium (RBDC)
National Institutes of Health
Expertise:
Primary immunodeficiencies, STAT3-Hyper IgE syndrome, Inborn errors of immunity
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Francesco Gavazzi, MD, PhD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Children's Hospital of Philadelphia
Expertise:
Pediatric neurology, Leukodystrophy, Outcome measure design and validation, Metachromatic leukodystrophy (MLD), TUBB4A-related Leukodystrophy, Pol III-related leukodystrophy, Pelizaeus-Merzbacher disease (PMD), Multiple sulfatase deficiency (MSD), Aicardi-Goutières syndrome (AGS), WDR45-related disorders
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Michael Gelb, PhD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
University of Washington
Expertise:
Clinical enzymology, Phospholipases, Protein prenylation, Anti-parasite therapeutics, Mass spectrometry, Newborn screening assay development
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Lindsey George, MD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Children's Hospital of Philadelphia
Expertise:
Hemostasis and thrombosis disorders, Hemophilia gene therapy, Hemophilia
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Donald L. Gilbert, MD, MS
Spastic Paraplegia Centers of Excellence Research Network (SP-CERN)
Cincinnati Children's Hospital Medical Center
Expertise:
Pediatric neurology, Movement disorders, Hereditary spastic paraplegia (HSP)
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Allan Glanzman, DPT
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Children's Hospital of Philadelphia
Expertise:
Neuromuscular disorders, Rehabilitation
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Grace Gombolay, MD
Autoimmunity, Rasmussen’s, Inflammation & Status Epilepticus Research Network (ARISEN)
Children's Healthcare of Atlanta
Expertise:
Multiple sulfatase deficiency (MSD), ADEM, MOGAD, Neuromyelitis optica spectrum disorder
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Danielle Gomez Reynolds, MD
Brittle Bone Disorders Consortium (BBDC)
University South Florida
Expertise:
Pediatric endocrinology
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Robert Grundmeier, MD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Children's Hospital of Philadelphia
Expertise:
General pediatrics, Clinical informatics
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Adrienne Hammill, MD, PhD
Advancing Rare Disorders: Vascular mAlformation Research Network with CaNVAS (ARDVARC)
Cincinnati Children's Hospital Medical Center
Expertise:
Vascular anomalies, Hereditary hemorrhagic telangiectasia (HHT), Sturge-Weber syndrome
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Lawrence Hirsch, MD
Autoimmunity, Rasmussen’s, Inflammation & Status Epilepticus Research Network (ARISEN)
Yale School of Medicine
Expertise:
Adult epilepsy, NORSE/FIRES, Status epilepticus, Seizures, EEG monitoring
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Robyn Howarth, PhD, ABPP
Autoimmunity, Rasmussen’s, Inflammation & Status Epilepticus Research Network (ARISEN)
Children's Healthcare of Atlanta
Expertise:
Pediatric autoimmune encephalitis
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Charles Howe, PhD
Autoimmunity, Rasmussen’s, Inflammation & Status Epilepticus Research Network (ARISEN)
Mayo Clinic Rochester
Expertise:
Pediatric seizure disorders, CNS autoimmunity, Novel human model systems, Neuroimmunology, Neuroinflammation
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Jing Huang, PhD
Advancing Craniosynostosis Treatment Rare Diseases Consortium (ACT)
Perelman School of Medicine, University of Pennsylvania
Expertise:
Biostatistics, Epidemiology
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Anna Huppler, MD
Pediatric Fungal Network STudy of Rare Invasive Fungal DisEases in Immunocompromised Pediatric Patients (PFN-STRIDE)
Medical College of Wisconsin
Expertise:
Infections in immunocompromised children and adults
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Jennifer Hwang, MD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Children's Hospital of Philadelphia
Expertise:
Palliative care, Patient-physician communication, Medical education
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Anuja Java, MD
Initiation of a cohort to define pathogenic Mechanisms, Precision diagnosis And Complications of Thrombotic Microangiopathies
Washington University St. Louis
Expertise:
Genetics and treatment of complement mediated kidney diseases including thrombotic microangiopathies, atypical hemolytic uremic syndrome, Atypical hemolytic uremic syndrome, C3 glomerulopathy, Management of recurrent glomerular diseases after kidney transplant
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Michael R. Jeng, MD
Advancing Rare Disorders: Vascular mAlformation Research Network with CaNVAS (ARDVARC)
Stanford Medicine
Expertise:
Pediatric hematology, Vascular anomalies, Histiocytic disorders
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Shafali Jeste, MD
Developmental Synaptopathies Consortium (DSC)
University of California at Los Angeles
Expertise:
Autism and related neurodevelopmental disorders
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Henry J. Kaminski, MD
Myasthenia Gravis Rare Disease Network (MGNET)
George Washington University
Expertise:
Myasthenia gravis
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John Kane Fink, MD
Spastic Paraplegia Centers of Excellence Research Network (SP-CERN)
University of Michigan Medical School
Expertise:
Hereditary spastic paraplegia (HSP), Neurogenetics
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Mary Karalius, MD
Autoimmunity, Rasmussen’s, Inflammation & Status Epilepticus Research Network (ARISEN)
USCF Health
Expertise:
Autoimmune and infectious encephalitis, MOGAD, NMO, ADEM, Transverse myelitis, Optic neuritis
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Stephanie Keller, MD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Emory University
Expertise:
Pediatric neurology, Leukodystrophy
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Anna Kerr, PhD
Advancing Rare Disorders: Vascular mAlformation Research Network with CaNVAS (ARDVARC)
Washington University St. Louis
Expertise:
Healthcare communication, Family-centered care, Qualitative research, Medical education
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Mehmet Kesimer, PhD
Rare Bronchiectatic Diseases Consortium (RBDC)
UNC Health
Expertise:
Airway mucins, Mucus biochemistry, Proteomics, Chronic lung disease
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Alexander Kolevzon, MD
Developmental Synaptopathies Consortium (DSC)
Icahn School of Medicine at Mount Sinai
Expertise:
Autism, Phelan-McDermid syndrome, FOXP1 syndrome, ADNP syndrome
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Deborah Krakow, MD
Brittle Bone Disorders Consortium (BBDC)
University of California Los Angeles
Expertise:
Osteogenesis imperfecta
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Darcy Krueger, MD, PhD
Developmental Synaptopathies Consortium (DSC)
Cincinnati Children's Hospital Medical Center
Expertise:
Tuberous sclerosis complex (TSC)
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Linda L. Kusner, PhD
Myasthenia Gravis Rare Disease Network (MGNET)
George Washington University
Expertise:
Pathophysiology of myasthenia gravis
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Brendan Lee, MD, PhD
Brittle Bone Disorders Consortium (BBDC)
Baylor College of Medicine
Expertise:
Developmental, translational and clinical studies of skeletal dysplasias and inborn errors of metabolism
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Janice Lee, DDS, MD, MS
Brittle Bone Disorders Consortium (BBDC)
National Institute of Dental and Craniofacial Research
Expertise:
Craniofacial and oral anomalies
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Eric Chien-Wei Liao, MD, PhD
Advancing Craniosynostosis Treatment Rare Diseases Consortium (ACT)
Children's Hospital of Philadelphia
Expertise:
Craniofacial genetics and biology, Cleft lip and palate repair, Complex pediatric reconstruction
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Feng-Chang Lin, PhD
Rare Bronchiectatic Diseases Consortium (RBDC)
UNC Health
Expertise:
Development of novel statistical methods for modeling recurrent events
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Alessandra Livraghi-Butrico, PhD
Rare Bronchiectatic Diseases Consortium (RBDC)
UNC Health
Expertise:
Animal models of inflammatory and obstructive lung diseases, Lung mucosal immunology, Mucus biology, Ex vivo phenotyping of human muco-inflammatory lung diseases
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Joana Mack, MD
Advancing Rare Disorders: Vascular mAlformation Research Network with CaNVAS (ARDVARC)
Arkansas Children's
Expertise:
Vascular anomalies
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Eric Macklin, PhD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Massachusetts General Hospital
Expertise:
Neurodegenerative and neurodevelopmental diseases, Clinical trial design, Parkinson's disease, Amyotrophic lateral sclerosis (ALS)
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Micah T. McClain, MD, PhD
Pediatric Fungal Network STudy of Rare Invasive Fungal DisEases in Immunocompromised Pediatric Patients (PFN-STRIDE)
Duke University School of Medicine
Expertise:
Biomarker based diagnostics and severity prediction tools
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Gerry McElvaney, MBBCh, FRCPI, DSc
Rare Bronchiectatic Diseases Consortium (RBDC)
Royal College of Surgeons in Ireland
Expertise:
Alpha-1 antitrypsin deficiency (AATD), Cystic fibrosis, Proteases, Anti-proteases, Lung inflammation
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Corey McMillan, PhD
Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium
University of Pennsylvania Perlman School of Medicine
Expertise:
Neurodegeneration, Neuroimaging, Frontotemporal degeneration (FTD), Alzheimer's disease (AD), Amyotrophic lateral sclerosis (ALS)
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Dararat Mingbunjerdsuk, MD
Spastic Paraplegia Centers of Excellence Research Network (SP-CERN)
Seattle Children's Hospital
Expertise:
Pediatric neurology, Hereditary spastic paraplegia (HSP), Neurogenetics
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Ahmed Moustafa, PhD
Pediatric Fungal Network STudy of Rare Invasive Fungal DisEases in Immunocompromised Pediatric Patients (PFN-STRIDE)
Children's Hospital of Philadelphia
Expertise:
Infectious disease genomics
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Tahseen Mozafar, MD
Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium
University of California Irvine
Expertise:
Inclusion body myositis, Muscle disease, Multi-system proteinopathy, Neuromuscular pathology
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Kristy Murray, DVM, PhD
Autoimmunity, Rasmussen’s, Inflammation & Status Epilepticus Research Network (ARISEN)
Children's Healthcare of Atlanta
Expertise:
Neuroimmunological diseases, Neuroinfectious diseases, Epidemiology
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Sandesh Nagamani, MBBS, MD, FACMG
Brittle Bone Disorders Consortium (BBDC)
Baylor College of Medicine
Expertise:
Genetic disorders
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Amanda Nagy, MD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Massachusetts General Hospital
Expertise:
Pediatric neurology, Leukodystrophy, Canavan disease (CD)
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Hope Northrup, MD
Developmental Synaptopathies Consortium (DSC)
The University of Texas Health Science Center at Houston
Expertise:
Lysosomal storage diseases (LSDs), Tuberous sclerosis complex (TSC)
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Wanda O'Neal, PhD
Rare Bronchiectatic Diseases Consortium (RBDC)
UNC Health
Expertise:
Molecular genetics, Molecular biology, Animal models of muco-obstructive lung disease, Cystic fibrosis, COPD, Primary ciliary dyskinesia (PCD), Bronchiectasis, Airway epithelial cell biology, Pulmonary disease
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Kenneth N. Olivier, MD, MPH
Rare Bronchiectatic Diseases Consortium (RBDC)
UNC Health
Expertise:
Bronchiectasis, Nontuberculous mycobacteria, Primary ciliary dyskinesia (PCD)
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Eric Orwoll, MD
Brittle Bone Disorders Consortium (BBDC)
Oregon Health and Science University
Expertise:
Endocrinology, Diabetes
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Kevin O’Connor, PhD
Myasthenia Gravis Rare Disease Network (MGNET)
Yale School of Medicine
Expertise:
Neuroimmunology of myasthenia gravis
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Pratik Patel, MD
Pediatric Fungal Network STudy of Rare Invasive Fungal DisEases in Immunocompromised Pediatric Patients (PFN-STRIDE)
Children's Healthcare of Atlanta
Expertise:
Pediatric transplant and oncology infectious disease, Leukemia/lymphoma, Diagnostics
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Paul J. Planet, MD, PhD
Pediatric Fungal Network STudy of Rare Invasive Fungal DisEases in Immunocompromised Pediatric Patients (PFN-STRIDE)
Children's Hospital of Philadelphia
Expertise:
Microbial ecology and evolution, Bacterial pathogenesis and virulence, Microbiomics and genomics, Phylogenetics, Global spread of antimicrobial resistance, MRSA, Infection in cystic fibrosis
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Sam Pleasure, MD
Autoimmunity, Rasmussen’s, Inflammation & Status Epilepticus Research Network (ARISEN)
USCF Health
Expertise:
Autoimmune neurology, Neurological autoantibody-associated conditions
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Brenda Porter, MD, PhD
Developmental Synaptopathies Consortium (DSC)
Stanford University Medical Center
Expertise:
Tuberous sclerosis complex (TSC), Epilepsy, Epilepsy surgery, SLC13A5 epilepsy disorder
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Robert Potter, PhD
Pediatric Fungal Network STudy of Rare Invasive Fungal DisEases in Immunocompromised Pediatric Patients (PFN-STRIDE)
Children's Hospital of Philadelphia
Expertise:
Infectious disease genomics, Clinical microbiology
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Siddharth Prakash, MD, PhD
Network for Advancing Sex Chromosome Aneuploidy Research Readiness (NASCARR)
UT Health Houston
Expertise:
Turner syndrome, Congenital heart disease, Cardiovascular genetics
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Cathleen Raggio, MD
Brittle Bone Disorders Consortium (BBDC)
Hospital for Special Surgery
Expertise:
Skeletal dysplasia, Ehlers-Danlos, Scoliosis, Scoliosis research, Osteogenesis imperfecta
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Frank Rauch, MD
Brittle Bone Disorders Consortium (BBDC)
Shriners Hospital for Children
Expertise:
Bone diseases in children
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Armin Raznahan, MD, PhD
Network for Advancing Sex Chromosome Aneuploidy Research Readiness (NASCARR)
NIMH Intramural Research Program
Expertise:
Clinical psychiatric phenotyping, Neuroimaging, Genomics, Computational biology
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Michelle Rengarajan, MD, PhD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Massachusetts General Hospital
Expertise:
Autoimmune endocrine disease, Epithelial-immune interactions, Human immunology, Immune-related adverse events, Quantitative cell biology, Single cell genomics, Systems immunology
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Mustafa Sahin, MD, PhD
Developmental Synaptopathies Consortium (DSC)
Boston Children’s Hospital
Expertise:
Tuberous sclerosis complex (TSC)
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Nathan Schloemer, MD
Advancing Rare Disorders: Vascular mAlformation Research Network with CaNVAS (ARDVARC)
Children's Wisconsin
Expertise:
Vascular anomalies, Precision medicine, Rare vascular tumors, Curling, Solid malignancies
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Adam J. Shapiro, MD
Rare Bronchiectatic Diseases Consortium (RBDC)
McGill University
Expertise:
Primary ciliary dyskinesia (PCD), Non-cystic fibrosis bronchiectasis, Clinical phenotyping, Chronic respiratory disease in Indigenous populations
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Justine Shults, PhD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Children's Hospital of Philadelphia
Expertise:
Biostatistics, Clinical epidemiology
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Michael Shy, MD
Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium
Spastic Paraplegia Centers of Excellence Research Network (SP-CERN)
University of Iowa
Expertise:
Neuromuscular diseases, Neuropathies, Charcot-Marie-Tooth disease, Inherited neuropathies, Clinical trials
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Bryan Sisk, MD
Advancing Rare Disorders: Vascular mAlformation Research Network with CaNVAS (ARDVARC)
Washington University St. Louis
Expertise:
Vascular malformations, Vascular anomalies, Pediatric oncology, Histiocytoses, Qualitative research, Patient-reported outcomes
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Pamela SW. Smith, MD
Brittle Bone Disorders Consortium (BBDC)
Phoenix Children's Hospital
Expertise:
Pediatric bone disorders
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Peter Smith, MD
Brittle Bone Disorders Consortium (BBDC)
Shriners Hospital for Children / Marquette University
Expertise:
Orthopaedic surgery, Orthopedics
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Amena Smith Fine, MD, PhD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Kennedy Krieger Institute
Expertise:
Pediatric neurology, Leukodystrophy, x-linked adrenoleukodystrophy (ALD), Adrenomyeloneuropathy (AMN), Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL)
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Betty Soliven, MD
Myasthenia Gravis Rare Disease Network (MGNET)
University of Chicago
Expertise:
Myasthenia, CIDP, Amyotrophic lateral sclerosis (ALS), Myopathies
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Latha Soorya, PhD
Developmental Synaptopathies Consortium (DSC)
Rush University Medical Center
Expertise:
Pediatric and adolescent psychology
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Daniel Spielman, PhD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Stanford University
Expertise:
Magnetic resonance imaging, Magnetic resonance spectroscopy, Quantitative imaging methods
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Isha Srivastava, MD, PhD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Stanford University
Expertise:
Pediatric neurology, Leukodystrophy, x-linked adrenoleukodystrophy (ALD), Cerebral palsy (CP)
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Jeffrey M. Statland, MD
Myasthenia Gravis Rare Disease Network (MGNET)
University of Kansas Medical Center
Expertise:
Facioscapulohumeral muscular dystrophy (FSHD)
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William J. Steinbach, MD
Pediatric Fungal Network STudy of Rare Invasive Fungal DisEases in Immunocompromised Pediatric Patients (PFN-STRIDE)
Arkansas Children's
Expertise:
Infections in immunocompromised children
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Julie M. Steinbrink, MD, MHS
Pediatric Fungal Network STudy of Rare Invasive Fungal DisEases in Immunocompromised Pediatric Patients (PFN-STRIDE)
Duke University School of Medicine
Expertise:
Infections in immunocompromised adults, Fungal infections, Noninvasive host biomarkers of infection
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Eric Storch, PhD
Brittle Bone Disorders Consortium (BBDC)
Baylor College of Medicine
Expertise:
Assessment and treatment of children, adolescents and adults with obsessive-compulsive and related disorders (i.e., OCD, Tourette, hairpulling disorder, skinpicking, misophonia) and anxiety disorders
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John Strang, PsyD
Network for Advancing Sex Chromosome Aneuploidy Research Readiness (NASCARR)
Children's National
Expertise:
Gender-diverse youth health, Neurodivergence, Advocacy, Community-based research
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Coral Stredny, MD
Autoimmunity, Rasmussen’s, Inflammation & Status Epilepticus Research Network (ARISEN)
Boston Children's Hospital
Expertise:
Rasmussen syndrome, NORSE/FIRES, Autoimmune encephalitis, Pediatric epilepsy/seizures, Autoimmune neurology
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V. Reid Sutton, MD
Brittle Bone Disorders Consortium (BBDC)
Rare Organic Acidemias Research Consortium (ROAR)
Baylor College of Medicine
Expertise:
Diagnosis of genetic syndromes, Dysmorphology, Genetic mechanisms of disease, Inborn errors of metabolism, Skeletal dysplasia, Organic acidemias, Inherited metabolic disorders, NIH-sponsored clinical trials & natural history studies
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Nicole Tartaglia, MD
Network for Advancing Sex Chromosome Aneuploidy Research Readiness (NASCARR)
University of Colorado Anschutz Medical Campus
Expertise:
Developmental-behavioral pediatrics
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Jesse A. Taylor, MD
Advancing Craniosynostosis Treatment Rare Diseases Consortium (ACT)
Children's Hospital of Philadelphia
Expertise:
Cleft lip and palate repair, Congenital and acquired deformities of the skull and face, Craniosynostosis, Facial asymmetry, Jaw surgery, Ear deformities, Plastic surgery
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Laura Tosi, MD
Brittle Bone Disorders Consortium (BBDC)
Children’s National Medical Center
Expertise:
Rare bone disease, Bone health, Trauma
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Bela Turk, MD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Kennedy Krieger Institute
Expertise:
Pediatric neurology, Leukodystrophy, Outcome measure design and validation, x-linked adrenoleukodystrophy (ALD), Adrenomyeloneuropathy (AMN), Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL)
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Mark Urata, MD, DDS
Advancing Craniosynostosis Treatment Rare Diseases Consortium (ACT)
Children's Hospital of Los Angeles
Expertise:
Complex craniofacial anomalies, Craniosynostosis, Syndromic reconstruction, Jaw surgery, Jaw deformities
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Marka Van Blitterswijk, MD, PhD
Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium
Mayo Clinic
Expertise:
Amyotrophic lateral sclerosis (ALS), Frontotemporal degeneration (FTD), Neurogenetics
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Keith P. Van Haren, MD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Stanford Children's Health
Expertise:
Pediatric neurology, Leukodystrophy, Adrenoleukodystrophy (ALD), Acute flaccid myelitis (AFM)
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Adeline L. Vanderver, MD
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Children's Hospital of Philadelphia
Expertise:
Pediatric neurology, Leukodystrophy, Metachromatic leukodystrophy (MLD), TUBB4A-related Leukodystrophy, Pol III-related leukodystrophy, Pelizaeus-Merzbacher disease (PMD), Aicardi-Goutières syndrome (AGS), Adrenoleukodystrophy (ALD), Undiagnosed leukodystrophies, Next generation sequencing
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Danita Velasco, MD, FAAP, FACMG
Brittle Bone Disorders Consortium (BBDC)
University of Nebraska Medical Center
Expertise:
Pediatric genetics
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Jennifer Vermilion, MD
Batten Disease Clinical Research Consortium (BDCRC)
University of Rochester Medicine
Expertise:
Batten diseases, Tourette syndrome
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Donald Vinh, MD, FRCPC, FACP
Rare Bronchiectatic Diseases Consortium (RBDC)
McGill University
Expertise:
Primary immunodeficiencies/inborn errors of immunity (i.e. humoral immuno deficiencies/HID), Molecular genetics, Functional immunology, Novel therapies
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Gerard Vockley, MD, PhD
Rare Organic Acidemias Research Consortium (ROAR)
University of Pittsburgh, School of Medicine
Expertise:
Organic acidemias, Inborn errors of metabolism, Translational research, Industry sponsored clinical trials
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Amy T. Waldman, MD, MSCE
Global Leukodystrophy Initiative Clinical Trials Network (GLIA-CTN)
Children's Hospital of Philadelphia
Expertise:
Pediatric neurology, Leukodystrophy, Alexander disease, Krabbe disease (KD), Canavan disease (CD), Adrenoleukodystrophy (ALD), Vanishing white matter disease (VWMD)
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Rachel Wattier, MD, MHS
Pediatric Fungal Network STudy of Rare Invasive Fungal DisEases in Immunocompromised Pediatric Patients (PFN-STRIDE)
UCSF Benioff Children's Hospitals
Expertise:
Pediatric infectious diseases clinical epidemiology and health services research, Implementation science, Patient and family engagement, Qualitative and mixed methods research
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Conrad Chris Weihl, MD, PhD
Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium
Washington University
Expertise:
Inclusion body myositis, Muscular dystrophies, Myopathy, Multi-system proteinopathy
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Jill Weimer, PhD
Batten Disease Clinical Research Consortium (BDCRC)
Sanford Health
Expertise:
Rare neuropediatric diseases and neurodevelopment
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Nathan P. Wiederhold, PharmD
Pediatric Fungal Network STudy of Rare Invasive Fungal DisEases in Immunocompromised Pediatric Patients (PFN-STRIDE)
University of Texas, San Antonio
Expertise:
Antifungal susceptibility, Clinical diagnostics, Antifungal PK/PD, Investigational antifungals
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Michael Wilson, MD, MA
Autoimmunity, Rasmussen’s, Inflammation & Status Epilepticus Research Network (ARISEN)
USCF Health
Expertise:
Infectious and autoimmune syndromes of the central nervous system
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Matthew Wolfgang, PhD
Rare Bronchiectatic Diseases Consortium (RBDC)
UNC Health
Expertise:
Respiratory microbiome, Respiratory infection biology, Airway cell culture models of infection, Pseudomonas aeruginosa pathogenesis, Antibiotic treatment failure
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Melinda Wu, MD, MCR
Advancing Rare Disorders: Vascular mAlformation Research Network with CaNVAS (ARDVARC)
Brittle Bone Disorders Consortium (BBDC)
Oregon Health and Science University
Expertise:
Vascular anomalies, Pediatric hematology, Cancer and cellular therapy survivorship, Understanding skeletal fragility of children and young adults
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Gang Wu, PhD
Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium
St. Jude Children's Research Hospital
Expertise:
Amyotrophic lateral sclerosis (ALS), Frontotemporal degeneration (FTD), Neurogenetics
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Joseph P. Zackular, PhD
Pediatric Fungal Network STudy of Rare Invasive Fungal DisEases in Immunocompromised Pediatric Patients (PFN-STRIDE)
Children's Hospital of Philadelphia
Expertise:
Microbial ecology, Microbiome, Bacterial pathogenesis and virulence, Enteric infection, Clostridioides difficile infection, Genomics
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Stephan Züchner, MD, PhD
Spastic Paraplegia Centers of Excellence Research Network (SP-CERN)
University of Miami
Expertise:
Genomics, Neurogenetics, Gene discovery
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