Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Benjamin R. Roos"'
Autor:
Joshua Hagedorn, Armin Avdic, Michael J. Schnieders, Benjamin R. Roos, Young H. Kwon, Arlene V. Drack, Erin A. Boese, John H. Fingert
Publikováno v:
BMC Ophthalmology, Vol 20, Iss 1, Pp 1-6 (2020)
Abstract Background Nanophthalmos has a significant genetic background and disease-causing mutations have been recently been reported in the myelin regulatory factor (MYRF) gene. We report clinical features in a patient with nanophthalmos and a Thr51
Externí odkaz:
https://doaj.org/article/a773c18c5d8f47cd81a2c7d263d78637
Autor:
Elliott H. Sohn, MD, Ian C. Han, MD, Benjamin R. Roos, BS, Benjamin Faga, BS, Meagan A. Luse, BS, Elaine M. Binkley, MD, H. Culver Boldt, MD, James C. Folk, MD, Stephen R. Russell, MD, Robert F. Mullins, PhD, John H. Fingert, MD, PhD, Edwin M. Stone, MD, PhD, Todd E. Scheetz, PhD
Publikováno v:
Ophthalmology Science, Vol 1, Iss 1, Pp 100002- (2021)
Purpose: To evaluate the first association specific to exudative age-related macular degeneration (AMD) located near the matrix metalloproteinase 9 (MMP9) gene. Design: Genetic association study. Participants: One thousand seven hundred twelve patien
Externí odkaz:
https://doaj.org/article/e464e9fd67834a58a547928b16aa7e00
Autor:
Malan Holm, Henrik Vorum, Benjamin R. Roos, Allie Simpson, Kaj Vilhelmsen, Thomas Rosenberg, John H. Fingert, Gudrid Andorsdottir, Elin Holm
Publikováno v:
J Glaucoma
Holm, E, Holm, M, Vilhelmsen, K, Andorsdottir, G, Vorum, H, Simpson, A, Roos, B R, Fingert, J H & Rosenberg, T 2022, ' Prevalence of Open-angle Glaucoma in the Faroese Population ', Journal of glaucoma, vol. 31, no. 2, pp. 72-78 . https://doi.org/10.1097/IJG.0000000000001921
Holm, E, Holm, M, Vilhelmsen, K, Andorsdottir, G, Vorum, H, Simpson, A, Roos, B R, Fingert, J H & Rosenberg, T 2022, ' Prevalence of Open-angle Glaucoma in the Faroese Population ', Journal of glaucoma, vol. 31, no. 2, pp. 72-78 . https://doi.org/10.1097/IJG.0000000000001921
PURPOSE: The Faroe Islands are home to 50,000 genetically isolated people in the North Atlantic. The prevalence of open-angle glaucoma (OAG) in the Faroese population is unknown. Consequently, we conducted a survey to determine the prevalence of OAG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::650fb8c771ee3afcd9b839a0edee8211
https://doi.org/10.1097/ijg.0000000000001921
https://doi.org/10.1097/ijg.0000000000001921
Autor:
Young H. Kwon, Joshua Hagedorn, John H. Fingert, Erin A. Boese, Armin Avdic, Arlene V. Drack, Benjamin R. Roos, Michael J. Schnieders
Publikováno v:
BMC Ophthalmology, Vol 20, Iss 1, Pp 1-6 (2020)
Background Nanophthalmos has a significant genetic background and disease-causing mutations have been recently been reported in the myelin regulatory factor (MYRF) gene. We report clinical features in a patient with nanophthalmos and a Thr518Met MYRF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c07a635f3c0fe27175bc31023a2f748
https://doi.org/10.1186/s12886-020-01659-8
https://doi.org/10.1186/s12886-020-01659-8
Autor:
H. Culver Boldt, Edwin M. Stone, Elliott H. Sohn, Robert F. Mullins, Todd E. Scheetz, Benjamin Faga, Ian C. Han, Meagan A Luse, Stephen R. Russell, Benjamin R. Roos, Elaine M. Binkley, John H. Fingert, James C. Folk
Publikováno v:
Ophthalmology Science, Vol 1, Iss 1, Pp 100002-(2021)
Purpose To evaluate the first association specific to exudative age-related macular degeneration (AMD) located near the matrix metalloproteinase 9 (MMP9) gene. Design Genetic association study. Participants One thousand seven hundred twelve patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22973a1d7a80a4950fa1cbd7a90ef50d
https://doi.org/10.1016/j.xops.2020.100002
https://doi.org/10.1016/j.xops.2020.100002
Autor:
Michael A. Grassi, Robert F. Mullins, Edwin M. Stone, Abdirashid M. Shire, Robert Ritch, Kazuhide Kawase, Benjamin R. Roos, John H. Fingert, Todd E. Scheetz, Sheila K. West
Publikováno v:
Human Mutation. 27:921-925
Age-related macular degeneration (AMD) is the most common cause of irreversible visual loss in the developed world. Previous studies have demonstrated that the c.1204T>C, p.Tyr402His allelic variant in the complement factor H (CFH) gene is associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10bc711a2b0f770b127a46384ad02814
https://doi.org/10.1002/humu.20359
https://doi.org/10.1002/humu.20359
Autor:
Kazuhide Kawase, Val C. Sheffield, Cheryl L. Khanna, Benjamin R. Roos, Young H. Kwon, Jamie E Craig, Edwin M. Stone, Sohan Singh Hayreh, Wallace L.M. Alward, David A. Mackey, Tetsuya Yamamoto, A. Tim Johnson, Louisa M. Affatigato
Publikováno v:
American Journal of Ophthalmology. 136:904-910
Purpose To investigate the association of sequence variations in the optineurin (OPTN) gene in patients with open-angle glaucoma. Design Prospective case control study. Methods The OPTN gene was screened for sequence variations using a combination of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68295f07126c9b99ab9a380de8718525
https://doi.org/10.1016/s0002-9394(03)00577-4
https://doi.org/10.1016/s0002-9394(03)00577-4
Autor:
Boese, Erin A., Drack, Arlene V., Roos, Benjamin R., Alward, Wallace L. M., Tollefson, Mallory R., Schnieders, Michael J., Scheetz, Todd E., Boldt, H. Culver, Stone, Edwin M., Fingert, John H.
Publikováno v:
JAMA Ophthalmology; Sep2023, Vol. 141 Issue 9, p872-879, 8p
Autor:
Holm, Elin, Holm, Malan, Vilhelmsen, Kaj, Andorsdottir, Gudrid, Vorum, Henrik, Simpson, Allie, Roos, Benjamin R., Fingert, John H., Rosenberg, Thomas
Publikováno v:
Journal of Glaucoma; Feb2022, Vol. 31 Issue 2, p72-78, 7p
Autor:
Hagedorn, Joshua, Avdic, Armin, Schnieders, Michael J., Roos, Benjamin R., Kwon, Young H., Drack, Arlene V., Boese, Erin A., Fingert, John H.
Publikováno v:
BMC Ophthalmology; 10/1/2020, Vol. 20 Issue 1, p1-6, 6p