Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Benjamin T Whigham"'
Autor:
Megan Ulmer Carnes, Yangfan P Liu, R Rand Allingham, Benjamin T Whigham, Shane Havens, Melanie E Garrett, Chunyan Qiao, NEIGHBORHOOD Consortium Investigators, Nicholas Katsanis, Janey L Wiggs, Louis R Pasquale, Allison Ashley-Koch, Edwin C Oh, Michael A Hauser
Publikováno v:
PLoS Genetics, Vol 10, Iss 5, p e1004372 (2014)
Glaucoma is a leading cause of blindness worldwide. Primary open-angle glaucoma (POAG) is the most common subtype and is a complex trait with multigenic inheritance. Genome-wide association studies have previously identified a significant association
Externí odkaz:
https://doaj.org/article/09a059fa35e943d39c6a161436730c9a
Publikováno v:
Current Ophthalmology Reports. 7:136-142
The goal of this review is to highlight the application of artificial intelligence (AI) in the diagnosis and management of glaucoma. Numerous AI strategies have been reported that could potentially help interpret clinical data and imaging studies rel
Publikováno v:
Asia-Pacific journal of ophthalmology (Philadelphia, Pa.). 8(2)
This review article aimed to highlight the application and use of artificial intelligence (AI) in optical coherence tomography (OCT) imaging in ophthalmology. Artificial intelligence programs seek to simulate intelligent human behavior in computers.
Autor:
Benjamin T, Whigham, R Rand, Allingham
Publikováno v:
Asia-Pacific Journal of Ophthalmology. 2:177-186
The purpose of this study was to summarize major developments in ocular genetics over the past year.A literature review was performed for articles relating to the genetics of eye diseases and morphology. The search focused on articles published betwe
Autor:
Karen G. Hales, Levi P Benson, R. Steven Stowers, Monica M Siegenthaler, Amanda C. Aldridge, Benjamin T Whigham
Publikováno v:
Fly. 1:38-46
Mitochondria undergo dramatic rearrangement during Drosophila spermatogenesis. In wild type testes, the many small mitochondria present in pre-meiotic spermatocytes later aggregate, fuse, and interwrap in post-meiotic haploid spermatids to form the s
Autor:
Kazunori Miyata, André Reis, Ken Hayashi, Takanori Mizoguchi, Ari Ziskind, W. Daniel Stamer, Shin-ichi Manabe, Michael A. Hauser, Eranga N. Vithana, Pratap Challa, Yosai Mori, Tin Aung, Francesca Pasutto, Chiea Chuen Khor, Michèle Ramsay, Alexias Safi, Susan Williams, Mineo Ozaki, Trevor R. Carmichael, Nagahisa Yoshimura, Joshua Wheeler, Xuejun Qin, Robyn M. Rautenbach, Andrew M. Williams, Lingyun Song, Shigeyasu Kazama, Allison E. Ashley-Koch, Benjamin T. Whigham, R. Rand Allingham, Inas F. Aboobakar, Steffen Uebe, Gregory E. Crawford, Cecelia Santiago-Turla, Shiroh Miura, Satoko Nakano, Yutao Liu, Toshiaki Kubota
Publikováno v:
Human molecular genetics. 24(22)
Exfoliation syndrome (XFS) is a common, age-related, systemic fibrillinopathy. It greatly increases risk of exfoliation glaucoma (XFG), a major worldwide cause of irreversible blindness. Coding variants in the lysyl oxidase-like 1 (LOXL1) gene are st
Autor:
Hemin R. Chin, Donald J. Zack, Yangfan P. Liu, Kang Zhang, Richard K. Lee, Edwin C. Oh, Robert N. Weinreb, Jonathan L. Haines, Terry Gaasterland, David S. Friedman, Douglas Vollrath, Louis R. Pasquale, Nicholas Katsanis, Kuldev Singh, Paul R. Lichter, Benjamin T. Whigham, Allison E. Ashley-Koch, Brian L. Yaspan, Janey L. Wiggs, Douglas E. Gaasterland, Megan U. Carnes, Jessica N. Cooke Bailey, Chunyan Qiao, Jae H. Kang, William K. Scott, Cathy Essentia McCarty, Sayoko E. Moroi, Donald L. Budenz, Stephanie Loomis, Arthur J. Sit, Michael A. Hauser, Melanie E. Garrett, Anthony Realini, Margaret A. Pericak-Vance, Gadi Wollstein, R. Rand Allingham, Julia E. Richards, Shane J. Havens, Murray H. Brilliant, Joel S. Schuman, John H. Fingert, Yutao Liu
Publikováno v:
PLoS genetics, vol 10, iss 5
PLoS Genetics, Vol 10, Iss 5, p e1004372 (2014)
PLoS Genetics
PLoS Genetics, Vol 10, Iss 5, p e1004372 (2014)
PLoS Genetics
Glaucoma is a leading cause of blindness worldwide. Primary open-angle glaucoma (POAG) is the most common subtype and is a complex trait with multigenic inheritance. Genome-wide association studies have previously identified a significant association
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb8177ed75c16a3fd6be331c812b4daa
https://escholarship.org/uc/item/8gv231gq
https://escholarship.org/uc/item/8gv231gq
Autor:
Yutao, Liu, Benjamin T, Whigham, Joshua, Wheeler, Susan E I, Williams, Robyn M, Rautenbach, Ari, Ziskind, Michele, Ramsay, Trevor R, Carmichael, Allison E, Ashley-Koch, R Rand, Allingham, Michael A, Hauser
Publikováno v:
Molecular Vision
Purpose To investigate whether DNA copy number variants (CNVs) in the lysyl oxidase-like 1 (LOXL1) gene are associated with exfoliation glaucoma (XFG) in black South Africans. Methods Black South African subjects with XFG and age-matched unaffected c
Autor:
R. Rand Allingham, Benjamin T. Whigham
Publikováno v:
Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society. 25(4)
Exfoliation syndrome is a common cause of open-angle glaucoma. It is characterized by microscopic flakes of protein-rich material being deposited in both ocular and non-ocular tissues. While its mechanism is poorly understood, family- and population-