Dr. Hilary Vernon is a Professor of Genetic Medicine and pediatrics at the Johns Hopkins University School of Medicine. She is also an attending physician at Kennedy Krieger Institute. Hilary Vernon has expertise in treating inborn errors of metabolism and mitochondrial disorders. She is the director of the Mitochondrial Care Center at The Johns Hopkins Hospital and the Barth Syndrome Interdisciplinary Clinic at the Kennedy Krieger Institute. Her research interests include understanding intermediary metabolism in Barth syndrome and in disorders of branch chain amino acid metabolism. Dr. Vernon also co-directs the Department of Genetic Medicine Clinical Trials Unit, and is the principal investigator on multiple clinical trials for rare diseases. Dr. Vernon received her medical degree and doctorate from Rutgers University, New Brunswick, New Jersey. She completed residencies in genetics and pediatrics at The Johns Hopkins University, and a fellowship in clinical laboratory biochemical genetics at The Johns Hopkins University. Dr. Vernon was recognized with the 2010 Francis F. Schwentker Award for Excellence in Research at Johns Hopkins University and the 2011 James B. Sidbury Jr. Fellowship in Biochemical Genetics at Johns Hopkins University. Dr. Vernon is rated as an Advanced provider by MediFind in the treatment of Infantile Neutropenia. Her top areas of expertise are Methylmalonic Acidemia, Propionic Acidemia, Infantile Neutropenia, Progressive External Ophthalmoplegia, and Gastrostomy.

Dr. Bonifant is a pediatric oncologist on the blood and marrow transplantation team at the Sidney Kimmel Comprehensive Cancer Center and an Assistant Professor of Pediatric Oncology at the Johns Hopkins University School of Medicine. She is also a member of the Bloomberg-Kimmel Institute for Immunotherapy. Her clinical specialty is stem cell transplantation for high-risk leukemias. Her research interests are in the areas of immunotherapy of cancer and malignant hematology. Currently, her research focuses on design and development of immune therapies as a treatment for poor-prognosis cancers, including development of engineered cellular immunotherapies for the treatment of Acute Myeloid Leukemia. Dr. Bonifant is a graduate of Wake Forest University and Georgetown University. She completed her Pediatric and Hematology/Oncology training at Johns Hopkins and at Baylor College of Medicine. Prior to her appointment at Johns Hopkins, she was an Assistant Professor in Pediatrics-Hematology/Oncology at the University of Michigan. Dr. Bonifant is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. Her top areas of expertise are Leukemia, Infantile Neutropenia, Acute Lymphoblastic Leukemia (ALL), and Childhood Acute Myeloid Leukemia.

Alexis Thompson is a Pediatrics specialist and an Intensive Care Medicine provider in Baltimore, Maryland. Dr. Thompson is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. Her top areas of expertise are Anemia, Infantile Neutropenia, Exocrine Pancreatic Insufficiency, Immune Thrombocytopenic Purpura (ITP), and Splenectomy.

Dr. Cohen is Director of Pediatric Neuro-Oncology and Clinical Director of the Division of Pediatric Oncology at the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins. He received his undergraduate degree at Brown University and earned his MD at the Upstate Medical University, in Syracuse, NY. He did his general Pediatric Residency and Chief Residency at the University of Colorado and completed his Pediatric Hematology/Oncology Fellowship at Johns Hopkins. He has served on the faculty since 1994. His research centers on clinical trials of novel therapeutics for children with brain tumors. Dr. Cohen is co-chair of the High-Grade Glioma committee for the Children's Oncology Group and in that capacity has a particular research interest in the development of therapeutics for the treatment of infiltrating gliomas. He serves on the scientific advisory board for a number of organizations including St. Baldricks and the Childhood Brain Tumor Foundation. He is on the editorial board for PDQ with responsibility for authorship of the pediatric CNS brain tumor summaries. The Pediatric Neuro-Oncology program conducts a broad range of research centered primarily around the development and testing of novel therapeutics for children with brain tumors. The multidisciplinary nature of this work translates into continual collaboration with specialists in pediatric neurosurgery, radiation oncology, neuropathology, neuroradiology, neurology, neuro-ophthalmology, neuropsychology, and other related disciplines. Dr. Cohen is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. His top areas of expertise are Glioma, Brain Stem Cancer, Medulloblastoma, Embryonal Tumor with Multilayered Rosettes, and Bone Marrow Aspiration.

Dr. Aaron M. Milstone is a professor of pediatrics at the Johns Hopkins University School of Medicine. He holds a joint appointments in Epidemiology and Health Policy and Management at the Bloomberg School of Public Health. A pediatric epidemiologist, Dr. Milstone specializes in treating infectious diseases in children. He serves as an associate hospital epidemiologist at The Johns Hopkins Hospital and the pediatric lead for infection prevention for the Johns Hopkins Health System. Dr. Milstone earned his medical degree from Yale University School of Medicine. He completed both a pediatrics residency and a research fellowship in pediatric infectious diseases at Children's Hospital of Philadelphia. He also completed a pediatric infectious diseases fellowship at Johns Hopkins. He holds a M.H.S. (Graduate Training Program in Clinical Investigation) from the Johns Hopkins Bloomberg School of Public Health and Johns Hopkins University School of Medicine. Dr. Milstone joined the Johns Hopkins faculty in 2007. His research interests focus on antibiotic resistance and prevention of healthcare-associated infections. He had led numerous clinical trials including the Pediatric SCRUB Trial and TREAT PARENTS Trial testing strategies to prevent organism transmission and healthcare-associated infections. He is principal investigator of the BrighT STAR Collaborative, guiding hospitals nationwide to reduce over-testing as a strategy to reduce antibiotic use and resistance. Dr. Milstone is a fellow of the American Academy of Pediatrics, the Infectious Diseases Society of America, the Pediatric Infectious Diseases Society, and the Society for Healthcare Epidemiology of America. His many other professional honors include the Pediatric Infectious Diseases Society’s 2014 Young Investigator Award, the inaugural 2013 Caroline B. Hall Clinical Innovation Award, and the Society for Healthcare Epidemiology of America 2018 Mentor Scholar Award, and 2023 Johns Hopkins Medicine Armstrong Award for Excellence in Quality & Safety. Dr. Milstone is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. His top areas of expertise are Sepsis, Methicillin-Resistant Staphylococcus Aureus (MRSA), Severe Acute Respiratory Syndrome (SARS), and Neonatal Sepsis.

Daniel Rhee, M.D., M.P.H., joins the Johns Hopkins Department of Surgery as Assistant Professor of Surgery and Director of the Pediatric Surgical Oncology Program. Dr. Rhee’s areas of clinical expertise include pediatric surgical oncology as well as neonatal and general pediatric surgery. Dr. Rhee received his undergraduate degree from the University of Michigan and earned his medical degree from The Ohio State University College of Medicine. He completed his residency in general surgery at St. Joseph Mercy Hospital before completing fellowships at Johns Hopkins Hospital in Pediatric Surgery and Memorial Sloan Kettering Cancer Center in Pediatric Surgical Oncology. Dr. Rhee is a member of several professional societies, including the American College of Surgeons, American Pediatric Surgical Association, the Association of Academic Surgeons, the Children’s Oncology Group, and The International Society of Paediatric Surgical Oncology. Dr. Rhee’s research interests involve childhood tumors including neuroblastoma, sarcoma, Wilms tumor, hepatoblastoma, pancreatoblastoma, reconstruction for chest wall tumors, germ cell tumors, and desmoplastic small round cell tumors. His research interests also include use of 3D printing for simulation for surgical training, improving surgical outcomes in pediatric surgery and improving access to surgical care in low and middle-income countries. Dr. Rhee is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. His top areas of expertise are Adult Soft Tissue Sarcoma, Appendicitis, Tracheoesophageal Fistula, Appendectomy, and Pancreaticoduodenectomy.

Dr. Maureen M. Gilmore is an assistant professor of pediatrics at the Johns Hopkins University School of Medicine. Her areas of clinical expertise include Neonatal-Perinatal Medicine. At Johns Hopkins Children's Center, Dr. Gilmore serves as Medical director of the Level IV Neonatal Intensive Care Unit. She previously was the NICU Medical Director at Johns Hopkins Bayview Medical Center, and her early career was in Neonatology at Penn State University Dr. Gilmore earned her M.D. from the State University of New York Health Science Center at Brooklyn. She completed her Pediatrics residency at the University of Rochester/Strong Memorial Hospital and performed a fellowship in Neonatal -Perinatal Medicine at Johns Hopkins. Her research interests include neuromonitoring and neonatal autoregulation, neonatal abstinenece syndrome, and patient safety. Dr. Gilmore serves on the Perinatal Advisory Committee for the Maryland Institute for Emergency Medical Services Systems. She is a fellow of the American Academy of Pediatrics (AAP) and a member of the Maryland chapter of the AAP. Dr. Gilmore is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. Her top areas of expertise are High Blood Pressure in Infants, Hypothermia, Premature Infant, and Necrotizing Enterocolitis.

Dr. Gerald Raymond is a clinical geneticist and neurologist at Johns Hopkins where he is also a professor of genetic medicine and neurology. He obtained his MD at the University of Connecticut and was trained in Pediatrics at Johns Hopkins Hospital and Neurology at the Mass. General Hospital. He received additional training in developmental neuropathology at the Universite Catholique de Louvain in Belgium and clinical genetics at the Harvard Program. Dr. Raymond’s research has been at the overlap of genetics and neurology with specific focus on peroxisomal disorders including adrenoleukodystrophy. He has been actively involved in newborn screening for ALD and in developing clinical follow-up programs. He has extensive experience in clinical management of neurogenetic issues including peroxisomal and lysosomal disorders. He presently serves as the Director of the Lysosomal Storage Disease program in the department of Genetic Medicine. Dr. Raymond is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. His top areas of expertise are Adrenoleukodystrophy (ALD), CACH Syndrome, Zellweger Syndrome, and Leukodystrophy.

Dr. Howard Lederman is a professor of pediatrics at the Johns Hopkins University School of Medicine. He is the director of the Immunodeficiency Clinic, the Pediatric Immunology Laboratory, and the Ataxia-Telangiectasia (A-T) Clinical Center. Dr. Lederman specializes in the evaluation, diagnostic testing and long-term management of patients of all ages who have known or suspected primary immunodeficiency diseases. He is an expert on the use of gamma globulin therapy for a wide variety of disorders. After receiving his M.D. and Ph.D. from the University of Michigan, Dr. Lederman came to Johns Hopkins Children’s Center for a residency in pediatrics, followed by a fellowship in immunology at the Hospital for Sick Children in Toronto. Dr. Lederman’s current research laboratory and clinical research focuses on better understanding and treating patients with ataxia-telangiectasia, a devastating neurological disorder for which there is no cure. He is a member of numerous professional societies, including American Association of Immunologists, the American Society for Microbiology and the Clinical Immunology Society. Dr. Lederman is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. His top areas of expertise are Common Variable Immune Deficiency, X-Linked Agammaglobulinemia, Immunodeficiency with Hyper IgM Type 1, and Hyper IgE Syndrome.

Brenda Banwell is the director of the Department of Pediatrics, as well as pediatrician-in-chief and co-director of Johns Hopkins Children’s Center, where she helps manage the hospital’s many clinical and research centers. Dr. Banwell is a renowned expert in the research and treatment of pediatric multiple sclerosis (MS) and other neuroimmune disorders. She specializes in and studies the use of neuroimaging to assess the clinical and cognitive impact of the conditions, as well as the function of the immune system in children with these disorders. She also created a standardized clinical care algorithm and clinical database in order to evaluate the clinical impact of MS. Dr. Banwell has published more than 250 manuscripts in high-impact journals, along with over 25 book chapters. In addition, she has over 200 national and international invited lectureships and visiting professorships. An advocate for pediatric multiple sclerosis needs and research, Dr. Banwell serves as chair of the International Medical and Scientific Board of the Multiple Sclerosis International Federation, and the Myelin Oligodendrocyte Glycoprotein Antibody–Associated Disease (MOGAD) International Research Consortium. She is also chair of the pediatric committee of the National Institutes of Health NeuroNEXT program, which conducts studies on treatments for neurological diseases through academic, private, and industry collaborations. Dr. Banwell currently serves as past-chair of the International Pediatric Multiple Sclerosis Study Group, Dr. Banwell earned her medical degree from the University of Western Ontario. She later completed a residency in pediatrics at the University of Western Ontario-Children's Hospital of Western Ontario and a second residency in pediatric neurology at University of Toronto – The Hospital for Sick Children. Her residencies were followed by a fellowship in neuromuscular research at Mayo Clinic. Dr. Banwell is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. Her top areas of expertise are Multiple Sclerosis (MS), CACH Syndrome, Optic Neuritis, and Transverse Myelitis.

Dr. W. Christopher Golden is an Associate Professor of Pediatrics at the Johns Hopkins University School of Medicine. His area of clinical expertise is neonatology. His research interests include congenital and neonatal infections, neonatal bilirubin metabolism, care of healthy newborns, and pediatric medical education (in particular, medical student education). Currently, he is the Director of the Pediatrics Core Clerkship in the School of Medicine. As Medical Director of the Newborn Nursery, he has been the site Principal Investigator (PI) or a collaborator on research involving improving safe sleep practices in newborns, screening babies for adrenoleukodystrophy and biliary atresia, employing functional MRI (fMRI) to study neonatal cerebral blood flow and oxygen metabolism, using investigational therapies to prevent vertical transmission of HIV, and studying acyclovir pharmacokinetics in neonates with confirmed or suspected herpes simplex virus (HSV) infection. Dr. Golden received his undergraduate degree in zoology from Duke University. He subsequently completed all of his medical training (medical degree, Pediatrics residency and Neonatal-Perinatal Medicine fellowship) at the Johns Hopkins University School of Medicine. Nationally, Dr. Golden is on the Editorial Advisory Board of The Journal of Pediatrics and Contemporary Pediatrics. He also served as Co-Leader of the Core Clerkship Collaborative of the Council on Medical Student Education in Pediatrics (COMSEP), the premier national organization for design, development, and formal academic study of methods in pediatric education in medical schools. Dr. Golden also is the Chair (2023-2025) of the Pediatric Section of the National Medical Association (NMA), the largest and oldest organization representing African American physicians (and their patients) in the United States. At Hopkins, he serves on the Department of Pediatrics Intern Selection Committee and as Core Faculty for the Department of Pediatrics for the Accreditation Council for Graduate Medical Education. Dr. Golden is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. His top areas of expertise are Congenital Syphilis, Transient Familial Hyperbilirubinemia, Polydactyly, and Newborn Low Blood Sugar.

Dr. John D. Coulson is an assistant professor of pediatrics at the Johns Hopkins University School of Medicine. His area of clinical expertise is pediatric cardiology. He earned his M.D. at University of Michigan Medical School. He completed his medical training and a pediatrics residency at Stanford University Medical Center before training in naval flight surgery at the Naval Aerospace Medical Institute. He then completed fellowships in pediatric cardiology and developmental biology at Stanford. He also served as a medical officer for the U.S. Navy for nine years. Dr. Coulson was an honorary member of the Russian Scientific Society of Interventional Radiology and Endovascular Surgery in 2001. He has published a number of journal articles and co-authored several book chapters related to pediatric cardiology. Dr. Coulson is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. His top areas of expertise are Pulmonary Hypertension, Pediatric Myocarditis, Hypertension, and Tetralogy of Fallot.

Carl E. Stafstrom is a pediatric neurologist, caring for children with epilepsy. Dr. Stafstrom received his medical degree from the University of Washington School of Medicine in Seattle, with residencies at the University of Washington Medical Center and Tufts New England Medical Center, as well as fellowships at Harvard for neurology research and Boston Children’s Hospital in clinical neurophysiology, electroencephalography, and epilepsy. Dr. Stafstrom previously served as Professor of Neurology and Pediatrics at the University of Wisconsin-Madison School of Medicine and Public Health and Chief of Pediatric Neurology at American Family Children’s Hospital at UW Madison. Dr. Stafstrom is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. His top areas of expertise are Epilepsy, Seizures, West Syndrome, Endovascular Embolization, and Deep Brain Stimulation.

As a physician scientist in the hematological malignancies and stem cell transplantation division with Sidney Kimmel Comprehensive Cancer Center at the Johns Hopkins, my focus is on the various aspects of cellular therapy in the treatment of hematological malignancies. My primary research focus is to develop strategies to prevent relapse of hematological malignancies following allogeneic stem cell transplantation. Additionally, I serve as the director of the adult CAR T program for hematological malignancies as we grow our CAR T program to help patients with advanced hematological malignancies. My academic interest in this space lies in studying the aspects of toxicity of CAR T cell therapy with an aim to improve long term outcomes in these patients. Among hematological malignancies, myeloproliferative disorders are my area of interest and I work to study newer drugs in early phase of development and also its treatment using allogeneic stem cell transplantation. Patient appointments: 410-955-8893. Dr. Jain is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. Her top areas of expertise are Myelofibrosis, Myeloproliferative Neoplasms (MPN), Splenomegaly, Bone Marrow Transplant, and Splenectomy.

Dr. David Valle is a professor of pediatrics and ophthalmology at the Johns Hopkins School of Medicine and former director of the Johns Hopkins Department of Genetic Medicine. He also serves as a geneticist for the Johns Hopkins Children’s Center. Dr. Valle holds a bachelor’s degree and medical degree from Duke University. He completed a pediatric residency at Johns Hopkins University before joining the Johns Hopkins faculty. He is interested in the genetic contributions to health and disease. He is the founding director of the Johns Hopkins Center for Inherited Disease Research. Over the years, his laboratory has discovered the genetic causation for more than 20 diseases, including those responsible for inborn errors of metabolism, inherited retinal degeneration, disorders of cellular organelle biogenesis and genetic variations that contribute risk for common disorders such as schizophrenia. Dr. Valle also serves as director of the Predoctoral Training Program in Human Genetics, as well as co-director of the Genes to Society program. He was a 2014 recipient of the annual Victor A. McKusick Leadership Award from the American Society of Human Genetics, which recognizes individuals whose professional achievements have fostered and enriched the development of human genetics as well as its assimilation into the broader context of science, medicine and health. Dr. Valle is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. His top areas of expertise are Spondyloepimetaphyseal Dysplasia Strudwick Type, Micrognathia, Urea Cycle Disorders (UCD), and Spondyloepiphyseal Dysplasia Congenita.

Alexander Testino is a Pediatric Neurologist in Baltimore, Maryland. Dr. Testino is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. His top area of expertise is Infantile Neutropenia.

Erica Prochaska is an assistant professor of pediatrics in the Division of Infectious Diseases at the Johns Hopkins University School of Medicine. She obtained her medical degree from the University of Michigan Medical School and completed a residency in pediatrics at the Children’s Hospital of Pittsburgh. She began her career as a pediatric hospitalist before going to Johns Hopkins for a pediatric infectious disease fellowship, after which she joined the Johns Hopkins faculty. Dr. Prochaska is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. Her top area of expertise is Infantile Neutropenia.

Valerie Curren is a Pediatric Cardiologist in Baltimore, Maryland. Dr. Curren is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. Her top area of expertise is Infantile Neutropenia.

Dr. Deborah Persaud is a professor of pediatrics at the Johns Hopkins University School of Medicine, and the director of the Division of Pediatric Infectious Diseases at Johns Hopkins Children's Center. She holds joint appointments in international health and molecular microbiology and immunology at the Johns Hopkins Bloomberg School of Public Health. A clinician and researcher specializing in the study and treatment of HIV-1 infection in children, she directs the pediatric infectious diseases fellowship program at the Johns Hopkins Children’s Center. Dr. Persaud received her B.S. in chemistry from York College in New York. A 1985 graduate of the New York University School of Medicine, she trained in pediatrics at Babies Hospital/Columbia Presbyterian Medical Center in New York, where she was chief resident. She was an infectious disease fellow, an Aaron Diamond postdoctoral research fellow and a faculty member at New York University. She joined the Johns Hopkins faculty in 1997, following a visiting lectureship at the Moi University in Eldoret, Kenya. Her research interests include HIV/AIDS drug development and mother-to-child HIV transmission. Dr. Persaud is the scientific chair of the HIV CURE Scientific Committee of the International Maternal, Pediatric Adolescent AIDS Clinical Trials (IMPAACT) group. She was awarded the prestigious Elizabeth Glaser Scientist Award for her HIV research and was recognized by Nature magazine in 2013 as one of “Ten People Who Mattered This Year.” She was recognized by Time magazine as among the “100 Most Influential People of 2013” for her pediatric HIV treatment research. Dr. Persaud is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. Her top areas of expertise are HIV/AIDS, Sepsis, Multisystem Inflammatory Syndrome in Children (MIS-C), and Pneumocystis Jiroveci Pneumonia.

Dr. Nara Lygia De Macena Sobreira is an assistant professor at the McKusick-Nathans Department of Genetic Medicine at Johns Hopkins University School of Medicine. Her area of expertise is rare Mendelian phenotypes, analysis of next-generation sequencing, and functional testing of candidate causative variants. She earned her M.D. at the University of Pernambuco in Brazil. She finished her Ph.D. in Human Genetics at Johns Hopkins followed by a one-year postdoc also at Johns Hopkins School of Medicine. During her Ph.D., she worked with Dr. David Valle using next-generation sequencing to elucidate the molecular basis of rare Mendelian phenotypes and in 2010 she discovered PTPN11 as the gene responsible for metachondromatosis by using whole-genome sequencing. She completed residencies in clinical genetics at both Universidade Federal de Sao Paulo and Johns Hopkins. Her main clinical and research focus is on identifying the genetic bases of rare phenotypes, mainly, phenotypes associated with cartilage tumors and vascular anomalies (including Ollier disease and Maffucci syndrome), and on understanding the physiopathology of these phenotypes to identify pharmacological strategies to treat them. She has worked extensively on developing strategies to better analyze the variants identified by next-generation sequencing and on novel strategies for data sharing. She participated on the development of PhenoDB, a phenotypic and genomic database, and created PhenoDB Variant Analysis Tool used worldwide. She is also one of the creators of GeneMatcher, VariantMatcher, and one of the co-founders of the Matchmaker Exchange, all intended to share next-generation sequencing data. She has also worked extensively on functional studies that evaluate the possible pathogenic effects of the candidate causative variants. Recent News Articles and Media Coverage Living the Hopkins Mission Honorees, Johns Hopkins Medicine Successes in Characterizing Genes through GeneMatcher with Nara L. M. Sobreira, MD, PhD, Ambry Genetics (April 30, 2018) Enfermedades raras: el desafio es encontrar otros pacientes que tienen el mismo mal, Lun (26 de septiembre de 2019) 2021 Science Writers' Boot Camp, Johns Hopkins Medicine (June 7, 2021) Making the Perfect Match, Johns Hopkins Medicine (February 1, 2020). Dr. De Macena Sobreira is rated as an Experienced provider by MediFind in the treatment of Infantile Neutropenia. Her top areas of expertise are Spondyloepimetaphyseal Dysplasia Strudwick Type, Greenberg Dysplasia, Blepharophimosis, and Early Infantile Epileptic Encephalopathy.