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Julie Elizabeth Hoover-Fong, M.D., Ph.D.

Headshot of Julie Elizabeth Hoover-Fong
  • Director, Greenberg Center for Skeletal Dysplasias
  • Professor of Genetic Medicine

Specializes in: Adolescents (12-18 years), Adults (18+ years), Children (1-11 years), Infants (up to 1 year)

Female

Expertise

Achondroplasia, Genetics, Medical Genetics, Skeletal Dysplasias ...read more

Research Interests

Achondroplasia; Skeletal Dysplasias; Genetic Skeletal Disorders; Autism; Clinical Genetics; Bone Health; Natural History Skeletal Dysplasias; Nail Patella Syndrome; Craniofacial Malformations; Orofacial Clefting; Clinical Research ...read more

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Insurance Information

Main Phone

410-955-3071

Outside of Maryland

410-464-6641
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International Patients

+1-410-502-7683
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Locations

The Johns Hopkins Hospital

Appointment Phone: 410-955-3071
600 N. Wolfe Street
Blalock 1008
Baltimore, MD 21287 map
Phone: 410-955-3071 | Fax: 410-502-2375

Background

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 PhD 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.

As a board certified clinical geneticist, 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. 

...read more

Titles

  • Director, Greenberg Center for Skeletal Dysplasias
  • Professor of Genetic Medicine
  • Professor of Pediatrics

Departments / Divisions

Centers & Institutes

Education

Degrees

  • MD; The Ohio State University Wexner Medical Center (1995)

Residencies

  • Pediatrics; Washington University School of Medicine -St Louis Children's Hospital (1998)

Fellowships

  • Genetics; Johns Hopkins University School of Medicine (2002)

Board Certifications

  • American Board of Medical Genetics and Genomics (Clinical Genetics (MD)) (2002)

Research & Publications

Clinical Trial Keywords

Achondroplasia; Skeletal dysplasisa; Craniofacial Malformations

Clinical Trials

Achondroplasia, Hypophosphatasia

Selected Publications

View all on PubMed

Hoover-Fong J, Cheung MS, Fano V, Hagenas L, Hecht JT, Ireland P, Irving M, Mohnike K, Offiah AC, Okenfuss E, Ozono K, Raggio C, Tofts L, Kelly D, Shediac R, Pan W, Savarirayan R., Lifetime impact of achondroplasia: Current evidence and perspectives on the natural history. Bone. 2021 Feb 3;146:115872. doi: 10.1016/j.bone.2021.115872. Online ahead of print. PMID: 33545406 Review. PMID: 33545406

Hoover-Fong J, Scott CI, Jones MC; COMMITTEE ON GENETICS.Health Supervision for People With Achondroplasia. Pediatrics. 2020 Jun;145(6):e20201010. doi: 10.1542/peds.2020-1010. PMID: 32457214 Review.  PMID: 32457214

Hoover-Fong J, Alade AY, Ain M, Berkowitz I, Bober M, Carter E, Hecht J, Hoerschemeyer D, Krakow D, MacCarrick G, Mackenzie WG, Mendoza R, Okenfuss E, Popplewell D, Raggio C, Schulze K, McGready J. Blood pressure in adults with short stature skeletal dysplasias. Am J Med Genet A. 2020 Jan;182(1):150-161. doi: 10.1002/ajmg.a.61402. Epub 2019 Nov 15. PMID: 31729121

Savarirayan R, Irving M, Bacino CA, Bostwick B, Charrow J, Cormier-Daire V, Le Quan Sang KH, Dickson P, Harmatz P, Phillips J, Owen N, Cherukuri A, Jayaram K, Jeha GS, Larimore K, Chan ML, Huntsman Labed A, Day J, Hoover-Fong J. C-Type Natriuretic Peptide Analogue Therapy in Children with Achondroplasia. N Engl J Med. 2019 Jul 4;381(1):25-35. doi: 10.1056/NEJMoa1813446. Epub 2019 Jun 18. PMID: 31269546 Clinical Trial.

You J, Sobreira NL, Gable DL, Jurgens J, Grange DK, Belnap N, Siniard A, Szelinger S, Schrauwen I, Richholt RF, Vallee SE, Dinulos MBP, Valle D, Armanios M, Hoover-Fong J. A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2, a Gene Encoding a Component of the TTT Complex. Am J Hum Genet. 2016 May 5;98(5):909-918. doi: 10.1016/j.ajhg.2016.03.014. Epub 2016 Apr 28. PMID: 27132593 Free PMC article

Contact for Research Inquiries

Johns Hopkins Hospital, Broadway Research Building
733 N. Broadway
Broadway Research Building
Baltimore, MD 21205 map
Phone: 410-614-0977

Academic Affiliations & Courses

Graduate Program Affiliation

Graduate Training Program in Clinical Investigation

Activities & Honors

Honors

  • The Miller-Coulson Academy of Clinical Excellence, Johns Hopkins University, 2017
  • The David Valle Clinical Teaching Appreciation Award for Genetic Faculty, Johns Hopkins University, 2016
  • Top Doctor in Baltimore, Maryland in Genetics, Baltimore Magazine, 2016
  • Little People of America Lifetime Achievement Award, Little People of America, 2016

Memberships

  • American Society of Human Genetics (ASHG)
  • Johns Hopkins Medical and Surgical Association
  • American College of Medical Genetics (ACMG), fellow
  • International Skeletal Dysplasia Society (ISDS)
  • American Cleft Palate-Craniofacial Association (ACPA)

Professional Activities

  • Member, Associate Professor Promotions Committee
  • Medical Advisory Board, Little People of America
  • Advisory Committee, Graduate Training Program in Clinical Investigation

Patient Ratings & Comments

The Patient Rating score is an average of all responses to physician related questions on the national CG-CAHPS Medical Practice patient experience survey through Press Ganey. Responses are measured on a scale of 1 to 5, with 5 being the best score. Comments are also gathered from our CG-CAHPS Medical Practice Survey through Press Ganey and displayed in their entirety. Patients are de-identified for confidentiality and patient privacy.

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