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UC Davis Eye Center at UC Davis Health seeks a Genetic Counselor to provide specialized genetic counseling and testing support across multiple ophthalmic subspecialties, including IRD, glaucoma, and pediatric conditions. The role partners with faculty to assess risk, obtain histories, coordinate testing, and communicate results to patients and families.
The counselor will integrate genetic information into diagnosis, treatment planning, and clinical decision making, ensuring access to services
Genetic testing and counseling are now the standard of care for a substantial number of patients seen at the UC Davis Eye Center. The Department of Ophthalmology & Vision Science seeks a Genetic Counselor to provide specialized genetic counseling and testing support across multiple ophthalmic subspecialties, including inherited retinal diseases, glaucoma, optic neuropathies, ocular tumors, retinal and inflammatory eye diseases, pediatric ophthalmic conditions, and corneal dystrophies.
Genetic testing and counseling are now the standard of care for a substantial number of patients seen at the UC Davis Eye Center. The Department of Ophthalmology & Vision Science seeks a Genetic Counselor to provide specialized genetic counseling and testing support across multiple ophthalmic subspecialties, including inherited retinal diseases, glaucoma, optic neuropathies, ocular tumors, retinal and inflammatory eye diseases, pediatric ophthalmic conditions, and corneal dystrophies.
The Genetic Counselor will collaborate with faculty and clinical teams to assess genetic risk, obtain and evaluate family histories, coordinate appropriate genetic testing, interpret and communicate results, and counsel patients and families regarding inheritance, prognosis, screening, and implications for at-risk relatives.
Serving as a department-wide resource, the Genetic Counselor will support the integration of genetic information into diagnosis, treatment planning, and clinical decision making while ensuring coordinated access to genetic services as precision and genomic medicine become increasingly important in ophthalmic care.
Complex Ophthalmology and Vision Science based department. 20 + clinical and research faculty, 12 residents, 5 fellows. Dept consists of 4 locations located across the greater Sacramento area and covers Yolo and Placer Counties.
Genetic testing and counseling have become an increasingly important standard of care across multiple specialties within the UC Davis Eye Center. Prior to joining UC Davis, Dr. Jayasundera supervised three health-system-employed genetic counselors at the University of Michigan, reflecting the integral role genetic counseling plays within a comprehensive academic ophthalmology program. As he assumes Dr. Sieving’s practice and continues to expand UC Davis’ established Inherited Retinal Disease (IRD) program, the need for dedicated genetic counseling support is expected to grow.
This need extends well beyond the IRD service. The expanding glaucoma division will incorporate Polygenic Risk Score (PRS) assessments to better identify inherited susceptibility to glaucoma and disease progression. Genetic evaluation is also particularly important for pediatric and juvenile glaucoma, where hereditary conditions can influence diagnosis, prognosis, family screening, treatment planning, and, in some cases, surgical decision-making.
Genetic testing is similarly relevant across several other Eye Center specialties. Neuro-ophthalmology evaluates inherited and mitochondrial optic neuropathies, including Leber’s Hereditary Optic Neuropathy and Dominant Optic Atrophy. Ocular oncology and retina manage conditions with established genetic associations, while the uveitis service evaluates monogenic and autoinflammatory disorders such as Blau syndrome, ROSAH, and ADNIV. Genetic evaluation can also help distinguish inflammatory disease from inherited retinal disorders, potentially preventing unnecessary immunosuppression and directing patients toward appropriate treatment.
Pediatric ophthalmology frequently evaluates children with poor vision, nystagmus, pathologic myopia, and suspected inherited or syndromic disorders, including Stickler, Neurofibromatosis, DiGeorge, and Goldenhar syndromes. Likewise, the cornea service manages patients with corneal dystrophies for whom genetic confirmation can assist with diagnosis, prognosis, and counseling regarding familial risk.
Collectively, these services demonstrate that genetic testing is no longer limited to a single ophthalmic subspecialty. Dedicated genetic counseling support would provide a centralized resource across the Eye Center to facilitate appropriate test selection and coordination, interpretation of results, patient and family counseling, identification of at-risk relatives, and integration of genetic findings into clinical management.
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