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Jared Marks, M.D.

Jared Joseph Marks, M.D.


Appointment Phone


Main Location

The Johns Hopkins Hospital

Out-of-State & International Patients +
Out of State Patients

Call 410-464-6641 (8a.m. to 6p.m., EST, Mon-Fri)

Learn more about our out-of-state patient services »

International Patients

Call +1-410-502-7683 (7a.m. to 6p.m., EST, Mon-Fri)

Learn more about our international patient services »

Centers & Institutes


  • Neurosurgery


The Johns Hopkins Hospital

Appointment Phone: 410-955-4424

600 N. Wolfe Street
Sheikh Zayed Tower
Baltimore, MD 21287 map
Phone: 410-955-4424

The Johns Hopkins Hospital

600 N. Wolfe Street
Carnegie 446D1
Baltimore, MD 21287 map

Johns Hopkins Bayview Medical Center

Appointment Phone: 410-550-0939

4940 Eastern Avenue
Baltimore, MD 21224 map
Phone: 410-550-0939

Johns Hopkins Bayview Medical Center

GI Clinic
4940 Eastern Avenue
A Building, 5th floor
Baltimore, MD 21224 map

Johns Hopkins Bayview Medical Center

4940 Eastern Avenue
Oculoplastics, Room A623
Baltimore, MD 21224 map


Neurosurgery, Spinal Trauma, Spine, Spine and Spinal Deformities, Spine Surgery


Dr. Jared Marks is a spine instructor in the Johns Hopkins Neurosurgical Spine Center. He sees patients at Johns Hopkins Bayview Medical Center. more

    Additional Information

  • Education +


    • Temple University School of Medicine / MD; Medicine (2005)


    • University of Mississippi Medical Center / Neurosurgery (2012)
  • Research & Publications +

    Selected Publications

    Ferreiro A, Ceuterick-De Groote C, Marks JJ, Goemans N, Schreiber G, Hanefeld F, Fardeau M, Martin JJ, Goebel HH, Richard P, Guicheney P, Bonnemann CG. (2004) Desmin-related myopathy with mallory body-like inclusions is caused by mutations of the selenoprotein N gene. Ann Neurol. 55(5):676-86.

    Hart TC, Zhang Y, Gorry MC, Hart PS, Cooper M, Marazita ML, Marks JM*, Cortelli JR, Pallos D. (2002) A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1. Am J Hum Genet. 70(4):943-54. (* = publisher’s typographical error)

    Zhang Y, Gorry MC, Hart PS, Pettenati MJ, Wang L, Marks JJ, Lu X, Hart TC. (2001) Localization, genomic organization, and alternative transcription of a novel human SAM-dependent methyltransferase gene on chromosome 2p22-->p21. Cytogenet Cell Genet. 95(3-4):146-52.

    Zhang Y, Lundgren T, Renvert S, Tatakis DN, Firatli E, Uygur C, Hart PS, Gorry MC, Marks JJ, Hart TC. (2001) Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefevre syndrome patients. J Med Genet. 38(2):96-101.

    Hart PS, Zhang Y, Firatli E, Uygur C, Lotfazar M, Michalec MD, Marks JJ, Lu X, Coates BJ, Seow WK, Marshall R, Williams D, Reed JB, Wright JT, Hart TC. (2000) Identification of cathepsin C mutations in ethnically diverse papillon-Lefevre syndrome patients. J Med Genet. 37(12):927-32.

  • Academic Affiliations & Courses +
  • Activities & Honors +


    • American Association of Neurological Surgeons (AANS)
    • Congress of Neurological Surgeons (CNS)
  • Videos & Media +
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