• 568 Citations
  • 12 h-Index
19982020
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Fingerprint Fingerprint is based on mining the text of the experts' scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 9 Similar Profiles
Macular Degeneration Medicine & Life Sciences
Diabetic Retinopathy Medicine & Life Sciences
Retinitis Pigmentosa Medicine & Life Sciences
Mutation Medicine & Life Sciences
Complement Factor H Medicine & Life Sciences
Electroretinography Medicine & Life Sciences
Scotoma Medicine & Life Sciences
Genes Medicine & Life Sciences

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Projects 2008 2020

Diabetic Retinopathy
Leukocytes
Biomarkers
Inflammation Mediators
Blood Vessels

Genomic and Genetic Studies of Diabetic Retinopathy

Grassi, M.

National Institutes of Health

9/15/088/31/13

Project: Research projectClinical Investigator Award (CIA)

Diabetic Retinopathy
Eye Diseases
Genes
Single Nucleotide Polymorphism
Genome

Research Output 1998 2018

  • 568 Citations
  • 12 h-Index
  • 32 Article
  • 1 Conference contribution
  • 1 Comment/debate

MACULAR DETACHMENT ASSOCIATED WITH ANOMALOUS OPTIC NERVES AND DURAL ECTASIA IN 49, XXXXY SYNDROME

Hajrasouliha, A. R., Moss, H. E., Maralani, P. J., Kaufman, L. & Grassi, M., Dec 1 2018, In : Retinal cases & brief reports. 12, 1, p. 39-41 3 p.

Research output: Contribution to journalArticle

Klinefelter Syndrome
Pathologic Dilatations
Optic Nerve
Eye Abnormalities
Intracranial Hypertension

Mutations in MERTK are not associated with age-related macular degeneration

Al-khersan, H., Kwong, A. & Grassi, M. A., Jan 3 2018, (Accepted/In press) In : International Ophthalmology. p. 1-5 5 p.

Research output: Contribution to journalArticle

Macular Degeneration
Protein-Tyrosine Kinases
Mutation
Genome
Propensity Score

Night Blindness, Ring Scotoma, and a Nonrecordable Electroretinogram in an Elderly Woman

Grassi, M., Maker, M. P. & Marmor, M. F., Jan 1 2018, (Accepted/In press) In : JAMA ophthalmology.

Research output: Contribution to journalArticle

Night Blindness
Scotoma
2 Citations

A novel MERTK mutation causing retinitis pigmentosa

Al-khersan, H., Shah, K. P., Jung, S. C., Rodriguez, A., Madduri, R. K. & Grassi, M. A., May 1 2017, (Accepted/In press) In : Graefe's Archive for Clinical and Experimental Ophthalmology. p. 1-7 7 p.

Research output: Contribution to journalArticle

Retinitis Pigmentosa
Mutation
Exome
Siblings
Nonsense Codon

PERIPHERAL RETINOPATHY ASSOCIATED with APLASTIC ANEMIA

Metelitsina, T. I., Sheth, V. S., Patel, S. B. & Grassi, M., 2017, In : Retinal Cases and Brief Reports. 11, 2, p. 108-110 3 p.

Research output: Contribution to journalArticle

Aplastic Anemia
Pancytopenia
Bone Marrow
Vitreous Hemorrhage
Telangiectasis