Carly will present her research in the genetic basis of glaucoma in patients of African heritage at the biennial meeting of the International Society for Eye Research (ISER) in Belfast, Northern Ireland. She was awarded a travel fellowship from ISER and from the Knights Templar Eye Foundation to support her travel to share her research at this important meeting.
Lab Graduate Student, Carly Van der Heide wins Travel Fellowship to Research Meeting in Belfast, Northern IrelandFingert Lab NewsWednesday, July 18, 2018 - 13:45
Fingert Lab NewsThursday, July 5, 2018 - 11:15
The Glaucoma Genetics Lab is thrilled to announce that Ankur Jain PHD will be joining the team as a post-doctoral fellow. Ankur completed his PHD training with Dr. Abbot Clark at the University of Northern Texas and his first post-doctoral fellowship with Dr. Val Sheffield, our close collaborator here at the Institute for Vision Research. Ankur will work with Budd Tucker in his stem cell facility and take the lead in the Glaucoma Center’s stem cell biology efforts to study optic atrophy and glaucoma.
Fingert Lab NewsWednesday, February 21, 2018 - 12:15
Dr. John Fingert, Dr. Todd Scheetz, and Dr. Michael Anderson were awarded an R21 grant to search for the genes that cause glaucoma associated with pigment release from the iris. This award will provide support ($419,000 over two years) for studying whole exomes from 550 pigmentary glaucoma patients and normal subjects.
Fingert Lab NewsFriday, January 19, 2018 - 09:45
The Glaucoma Genetics Lab identified a defect in the OPA1 gene that causes optic nerve atrophy that is dominantly inherited in a large family. We created a model of the protein encoded by the OPA1 gene (shown above) and we studied the effects of the disease-causing mutation on the protein structure and function. Read more about the discovery here.
Fingert Lab NewsThursday, January 11, 2018 - 15:00
In partnership with Dr. Alward, Dr. Kwon, Dr. Bettis, and Dr. Sears, the Fingert Lab has collected skin biopsies from over 50 patients with exfoliation glaucoma. The Glaucoma Foundation has provided funds for the lab to study these skin cells to identify abnormalities in function (i.e. energy production or waste management) and their role in exfoliation syndrome.
Fingert Lab NewsThursday, December 7, 2017 - 07:15
In a world-wide collaboration, we used genome-sequencing approaches to precisely define the extent and organization of TBK1 gene duplications and triplications in glaucoma patients. Read more about it here.
Fingert Lab NewsWednesday, July 26, 2017 - 14:45
The Glaucoma Genetics Lab joined Tin Aung, CC Khor, and our colleagues around the world in conducting a genome-wide association study (GWAS) of exfoliation syndrome and glaucoma. This huge multi-center study of 13,620 patients and 109,837 control subjects identified five new genetic risk factors for exfoliation syndrome: POMP, TMEM136, AGPAT1, RBMS3, and SEMA6A. Read more about this discovery here (11.8 MB).
Fingert Lab NewsWednesday, July 12, 2017 - 16:00
We recently published a report about the different types of inherited glaucoma that have an onset during childhood. Read more about this report here.
Fingert Lab NewsThursday, March 30, 2017 - 12:15
The Glaucoma Genetics Lab discovers mutation of the TP63 gene in a patient with Lacrimo-Auriculo-Dento-Digital (LADD) syndrome, which is a condition that causes malformation of ears, teeth, and hands as well as problems with tear formation and dry eye. In this manuscript, we report the genetic cause of the first case of LADD syndrome with glaucoma and thin corneas. Read more about this discovery here.
Fingert Lab NewsFriday, February 17, 2017 - 21:45