
Overview
Karin Blakemore, M.D., is the director of prenatal genetics at the prenatal diagnostic center in the Johns Hopkins Department of Gynecology and Obstetrics, and she is a member of the McKusick-Nathans Institute of Genetic Medicine. Her areas of clinical expertise include fetal imaging and fetal genetic disorders. Dr. Blakemore also serves as a professor of oncology and of gynecology and obstetrics in the Johns Hopkins University School of Medicine. Dr. Blakemore earned her medical degree from the Medical College of Ohio at Toledo. She completed her residency at New York University Medical Center and performed fellowships in genetics at Yale University School of Medicine and in maternal and fetal medicine at Washington University School of Medicine. Her research interests include Fetal Genetic Disorders; Prenatal Diagnosis and Fetal Treatment; In Utero Hematopoietic Stem Cell Transplantation; Hemoglobinopathies; Red cell and platelet alloimmunization; Intrapartum physiology and outcomes; Placental development and abnormalities.
Dr. Blakemore is rated as an Advanced provider by MediFind in the treatment of Desbuquois Syndrome. Her top areas of expertise are HELLP Syndrome, Desbuquois Syndrome, Atypical Hemolytic Uremic Syndrome (aHUS), and Hypochondroplasia.
Her clinical research consists of co-authoring 39 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Desbuquois Syndrome.
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Locations
10753 Falls Road, Pavilion II Suite 245, Pavilion II Suite 245, Lutherville, MD 21093
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
The Johns Hopkins Hospital
Dr. Ahmet Baschat is director of the Center for Fetal Therapy and professor in the Johns Hopkins Medicine Department of Gynecology and Obstetrics. His areas of clinical expertise include prenatal diagnosis and therapy of a wide range of fetal conditions including congenital diaphragmatic hernia, intrauterine growth restriction, twin-to-twin transfusion syndrome (TTTS), as well as other complications of monochorionic twin pregnancies. Dr. Baschat received his undergraduate and medical degrees from The Royal College of Surgeons in Ireland. He earned his doctorate in medicine (Dr. Med) from the University of Lübeck, where he also completed a residency in obstetrics and gynecology. Dr. Baschat also completed residencies at Newton-Wellesley Hospital and at University of Maryland Medical Center. He performed a fellowship in maternal-fetal medicine at University of Maryland Medical Center and went on to develop its Center for Advanced Fetal Care. Dr. Baschat joined the Johns Hopkins faculty in 2014. Prior to joining Johns Hopkins, Dr. Baschat was professor and director of Maternal-Fetal Medicine and the Section of Fetal Therapy at the University of Maryland School of Medicine. Dr. Baschat’s research interests include interventions and management techniques for fetal growth restriction and placental insufficiency. He has also done extensive research on the use of high resolution prenatal ultrasound techniques, including Doppler and fetal echocardiography, to predict and detect fetal complications. Dr. Baschat serves on a variety of boards and is a member of the American Congress of Obstetricians and Gynecologists (ACOG), the International Society of Ultrasound in Obstetrics & Gynecology and the International Fetal Medicine and Surgery Society. He has been recognized with several awards and honors, including the 2010 Award for Excellence in Research by the Society for Maternal-Fetal Medicine. Dr. Baschat’s passion for developing an individualized care plan for each of his patients has been the hallmark of his practice. Dr. Baschat is rated as a Distinguished provider by MediFind in the treatment of Desbuquois Syndrome. His top areas of expertise are Twin-To-Twin Transfusion Syndrome, Intrauterine Growth Restriction, Bilateral Renal Agenesis Dominant Type, Diaphragmatic Hernia, and Endoscopy.
Rubenstein Child Health Building
Dr. Julie Hoover-Fong is a Professor of Genetic Medicine and Pediatrics and Director of the Greenberg Center for Skeletal Dysplasias at Johns Hopkins University. Dr. Hoover-Fong holds a bachelor’s degree in Human Nutrition from The Ohio State University, where she also completed her medical degree. She received her Ph.D. in the Graduate Training Program in Clinical Investigation at the Johns Hopkins University School of Medicine and Bloomberg School of Public Health. Dr. Hoover-Fong completed a pediatric internship and residency at Washington University in St. Louis and a fellowship in medical genetics at Johns Hopkins University in Baltimore. She joined the Johns Hopkins University faculty in 2002 and progressed to Professor of Genetic Medicine and Pediatrics in 2019. She practices and oversees the clinical operations, research and educational ventures for the patients, families and healthcare providers served by the Greenberg Center. Her clinical team develops and improves diagnostic and treatment guidelines for comprehensive care of patients with all types of bone conditions including dwarfism, orofacial clefting, craniosynostosis and more. Dr. Hoover-Fong also mentors and teaches medical students, residents and genetic medicine trainees. As an active clinical researcher, Dr. Hoover-Fong is the Principal Investigator of multiple global clinical trials for achondroplasia, the first multi-center, investigator-initiated natural history study for achondroplasia, and multiple clinical studies for patients with orofacial clefting, hypophosphatasia and other conditions. She is also a co-investigator on the ELSI and Phenotype Review Committees for the Mendel Project, a whole exome sequencing venture to identify the genetic cause of Mendelian conditions. From an institutional service perspective, Dr. Hoover-Fong serves on the Johns Hopkins Associate Professor Promotions Committee and the Advisory Committee for the Graduate Training Program in Clinical Investigation. She serves on the Medical Advisory Board of the Little People of America, is a member of the Miller-Coulson Academy of Clinical Excellence at Johns Hopkins University and is a charter member of the International Skeletal Dysplasia Management Consortium, publishing best practice guidelines for patients with skeletal dysplasias. Dr. Hoover is rated as an Elite provider by MediFind in the treatment of Desbuquois Syndrome. Her top areas of expertise are Achondroplasia, Rhizomelic Syndrome, Spondyloepimetaphyseal Dysplasia Strudwick Type, Adenoidectomy, and Myringotomy.
Luis Franco is a Medical Genetics provider in Bethesda, Maryland. Dr. Franco is rated as an Experienced provider by MediFind in the treatment of Desbuquois Syndrome. His top area of expertise is Desbuquois Syndrome.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- Desbuquois SyndromeDr. Blakemore isAdvanced. Learn about Desbuquois Syndrome.
- HELLP SyndromeDr. Blakemore isAdvanced. Learn about HELLP Syndrome.
- Experienced
- Achalasia Microcephaly SyndromeDr. Blakemore isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Atypical Hemolytic Uremic Syndrome (aHUS)Dr. Blakemore isExperienced. Learn about Atypical Hemolytic Uremic Syndrome (aHUS).
- HypochondroplasiaDr. Blakemore isExperienced. Learn about Hypochondroplasia.
- Methimazole Antenatal ExposureDr. Blakemore isExperienced. Learn about Methimazole Antenatal Exposure.
- OmphaloceleDr. Blakemore isExperienced. Learn about Omphalocele.
- Paroxysmal Nocturnal Hemoglobinuria (PNH)Dr. Blakemore isExperienced. Learn about Paroxysmal Nocturnal Hemoglobinuria (PNH).

