• 9034 Citations
  • 37 h-Index
1986 …2019
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Fingerprint Dive into the research topics where Thomas M Glaser is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 4 Similar Profiles
Aniridia Medicine & Life Sciences
Genes Medicine & Life Sciences
Chromosomes, Human, Pair 11 Medicine & Life Sciences
Wilms Tumor Medicine & Life Sciences
Retinal Ganglion Cells Medicine & Life Sciences
Mutation Medicine & Life Sciences
Human Chromosomes Medicine & Life Sciences
Anophthalmos Medicine & Life Sciences

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Projects 1997 2015

Anophthalmos
Microphthalmos
Coloboma
Mutation
Penetrance
Diamond-Blackfan Anemia
Tail
Mutation
Phenotype
Ribosomes
Ribosomal Proteins
Tail
Mutation
Phenotype
Diamond-Blackfan Anemia
Retinal Ganglion Cells
Retinal Neurons
Optic Nerve
Glaucoma
Tail
Anophthalmos
Mutation
Ambystoma mexicanum
Genes
Spalax

Research Output 1986 2019

  • 9034 Citations
  • 37 h-Index
  • 71 Article

Considerations for the use of Cre recombinase for conditional gene deletion in the mouse lens

Lam, P. T., Padula, S. L., Hoang, T. V., Poth, J. E., Liu, L., Liang, C., LeFever, A. S., Wallace, L. M., Ashery-Padan, R., Riggs, P. K., Shields, J. E., Shaham, O., Rowan, S., Brown, N. L., Glaser, T. M. & Robinson, M. L., Feb 15 2019, In : Human genomics. 13, 1, 1 p.

Research output: Contribution to journalArticle

Gene Deletion
Lenses
Transgenes
Transgenic Mice
Eye Abnormalities
2 Citations (Scopus)

NAA10 polyadenylation signal variants cause syndromic microphthalmia

Johnston, J. J., Williamson, K. A., Chou, C. M., Sapp, J. C., Ansari, M., Chapman, H. M., Cooper, D. N., Dabir, T., Dudley, J. N., Holt, R. J., Ragge, N. K., Schäffer, A. A., Sen, S. K., Slavotinek, A. M., Fitzpatrick, D. R., Glaser, T. M., Stewart, F., Black, G. C. M. & Biesecker, L. G., Jan 1 2019, In : Journal of medical genetics.

Research output: Contribution to journalArticle

Microphthalmos
Polyadenylation
Exome
Anophthalmos
Genes
4 Citations (Scopus)

Maternal Inheritance of a Recessive RBP4 Defect in Canine Congenital Eye Disease

Kaukonen, M., Woods, S., Ahonen, S., Lemberg, S., Hellman, M., Hytönen, M. K., Permi, P., Glaser, T. M. & Lohi, H., May 29 2018, In : Cell Reports. 23, 9, p. 2643-2652 10 p.

Research output: Contribution to journalArticle

Eye Diseases
Vitamin A
Canidae
Defects
Placenta
3 Citations (Scopus)

The dynamics of native Atoh7 protein expression during mouse retinal histogenesis, revealed with a new antibody

Miesfeld, J. B., Glaser, T. M. & Brown, N. L., Jan 1 2018, In : Gene Expression Patterns. 27, p. 114-121 8 p.

Research output: Contribution to journalArticle

Retinal Ganglion Cells
Antibodies
Neurogenesis
Knockout Mice
Transgenic Mice
2 Citations (Scopus)

Arap1 deficiency causes photoreceptor degeneration in mice

Moshiri, A., Humpal, D., Leonard, B. C., Imai, D., Tham, A., Bower, L., Clary, D., Glaser, T. M., Lloyd, K. C. K. & Murphy, C. J., Mar 1 2017, In : Investigative Ophthalmology and Visual Science. 58, 3, p. 1709-1718 10 p.

Research output: Contribution to journalArticle

Retina
Guanosine
Knockout Mice
Neuroglia
Eye Abnormalities