
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 Experienced provider by MediFind in the treatment of Hypochondroplasia. 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 Hypochondroplasia.
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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.
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 Hypochondroplasia. Her top areas of expertise are Achondroplasia, Rhizomelic Syndrome, Spondyloepimetaphyseal Dysplasia Strudwick Type, Adenoidectomy, and Myringotomy.
Gynecology And Obstetrics - Nelson/Harvey Building
Dr. Angie Jelin is the assistant director of prenatal genetics at the Prenatal Diagnostic Center in the Division of Maternal-Fetal Medicine and an assistant professor in the Johns Hopkins Medicine Department of Gynecology and Obstetrics. Her areas of clinical expertise include prenatal genetic counseling, fetal imaging, chorionic villus sampling and amniocentesis, with a focus on fetal complications in pregnancy. Dr. Jelin earned her medical degree from Harvard Medical School. She did her residency in obstetrics and gynecology at the University of California, San Francisco, and then remained there to complete a maternal-fetal medicine and genetics fellowship. In 2015, Dr. Jelin joined the Johns Hopkins faculty, at which time she also received a Building Interdisciplinary Research Careers in Women’s Health grant to study fetal genetic disorders. Dr. Jelin’s research involves fetal imaging and genetic diagnoses, including whole exome sequencing. Dr. Jelin is a member of the American College of Obstetricians and Gynecologists, the Society of Maternal-Fetal Medicine and the International Society of Prenatal Diagnosis. She currently serves on the IRB committee of the American Board of Obstetrics and Gynecology. Dr. Jelin has published many articles in obstetrics and maternal-fetal medicine journals. Dr. Jelin is rated as a Distinguished provider by MediFind in the treatment of Hypochondroplasia. Her top areas of expertise are Polyhydramnios, Bilateral Renal Agenesis Dominant Type, Lung Agenesis, and Atresia of Small Intestine.
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).

