
Overview
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 Ectodermal Dysplasias. Her top areas of expertise are Spondyloepimetaphyseal Dysplasia Strudwick Type, Greenberg Dysplasia, Blepharophimosis, and Early Infantile Epileptic Encephalopathy.
Her clinical research consists of co-authoring 105 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Ectodermal Dysplasias.
Insurance
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Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- INSURANCE PLAN
- MEDICARE PDP
- PPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
Locations
Rubenstein BLDG Lower Level, Baltimore, MD 21287
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.
1 Clinical Trials
Gabriele Richard is a Medical Genetics provider in Gaithersburg, Maryland. Dr. Richard is rated as an Advanced provider by MediFind in the treatment of Ectodermal Dysplasias. Her top areas of expertise are Naegeli-Franceschetti-Jadassohn Syndrome, Chondrodysplasia Punctata with Steroid Sulfatase Deficiency, Microphthalmia, and Cortical Dysplasia.
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 Ectodermal Dysplasias. Her top areas of expertise are Polyhydramnios, Bilateral Renal Agenesis Dominant Type, Lung Agenesis, and Atresia of Small Intestine.
Roger Packer is a Neurologist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Packer is rated as an Elite provider by MediFind in the treatment of Ectodermal Dysplasias. His top areas of expertise are Brain Tumor, Diffuse Midline Glioma H3 K27M-Mutant, Medulloblastoma, and Gliomatosis Cerebri.
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
- Elite
- Spondyloepimetaphyseal Dysplasia Strudwick TypeDr. De Macena Sobreira isElite. Learn about Spondyloepimetaphyseal Dysplasia Strudwick Type.
- Distinguished
- BlepharophimosisDr. De Macena Sobreira isDistinguished. Learn about Blepharophimosis.
- Early Infantile Epileptic EncephalopathyDr. De Macena Sobreira isDistinguished. Learn about Early Infantile Epileptic Encephalopathy.
- Greenberg DysplasiaDr. De Macena Sobreira isDistinguished. Learn about Greenberg Dysplasia.
- Advanced
- Achalasia Microcephaly SyndromeDr. De Macena Sobreira isAdvanced. Learn about Achalasia Microcephaly Syndrome.
- Acrofacial Dysostosis Rodriguez TypeDr. De Macena Sobreira isAdvanced. Learn about Acrofacial Dysostosis Rodriguez Type.
- Acrofrontofacionasal Dysostosis SyndromeDr. De Macena Sobreira isAdvanced. Learn about Acrofrontofacionasal Dysostosis Syndrome.
- Brachydactyly Mononen TypeDr. De Macena Sobreira isAdvanced. Learn about Brachydactyly Mononen Type.
- Cardiomyopathy Hypogonadism Metabolic AnomaliesDr. De Macena Sobreira isAdvanced. Learn about Cardiomyopathy Hypogonadism Metabolic Anomalies.
- ChondrodystrophyDr. De Macena Sobreira isAdvanced. Learn about Chondrodystrophy.
- Experienced
- AchondroplasiaDr. De Macena Sobreira isExperienced. Learn about Achondroplasia.
- AcrocephalopolydactylyDr. De Macena Sobreira isExperienced. Learn about Acrocephalopolydactyly.
- Acromicric DysplasiaDr. De Macena Sobreira isExperienced. Learn about Acromicric Dysplasia.
- AniridiaDr. De Macena Sobreira isExperienced. Learn about Aniridia.
- Anophthalmia Plus SyndromeDr. De Macena Sobreira isExperienced. Learn about Anophthalmia Plus Syndrome.
- Apert SyndromeDr. De Macena Sobreira isExperienced. Learn about Apert Syndrome.
