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Benjamin Bakall

college of medicine

21H指数
64论文数
2.4K被引数
收录论文 17
发表时间
Validation of a novel multi-luminance shape discrimination test for assessment of functional vision一种新型多亮度形状辨别测试的功能性视力评估验证
err2026-03-13
err0
PREAI
errAndres Emanuelli; Benjamin Bakall; Byron L. Lam; Charles C. Wykoff; David Liao; Lance Bergstrom; Zak Vitaliy; Michael Carlson; Sanghoon Kim; Subrata Batabyal; Jean Chang; John Koester; Mark Von Tress; Mark Kosinski; Samuel B. Barone; Samarendra K. Mohanty
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A novel modifier gene therapy to treat Stargardt disease: Phase 1 GARDian1 Trial Insights
errEye
IF3.2
err2026-01-10
err0
errOAAI
errArshad M. Khanani; Lejla Vajzovic; Benjamin Bakall; Venkata Ramana Murthy Chavali; Huma Qamar
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Variants in CFAP410 cause a range of retinal and skeletal phenotypesCFAP410基因的变异导致一系列视网膜和骨骼表型。
err2025-04-17
err0
errOAAI
errSchmidt, Ryan E.; Pohodich, Amy E.; Birch, David; Jones, Kaylie; Lam, Byron L.; Jung, Emily H.; Jain, Nieraj; Georgiou, Michalis; Mahroo, Omar A.; Webster, Andrew R.; Michaelides, Michel; Bakall, Benjamin; Iannaccone, Alessandro; Vincent, Ajoy; Parameswarappa, Deepika C.; Heon, Elise; Scholl, Hendrik P. N.; Janeschitz-Kriegl, Lucas; Traboulsi, Elias I.; Zein, Wadih; Brooks, Brian P.; Cukras, Catherine; Hufnagel, Robert; Aleman, Tomas S.; Sylla, Mohamed M.; Tsang, Stephen H.; Alabek, Michelle; Sahel, Jose; Gorin, Michael B.; van Genderen, Maria M.; Stingl, Katarina; Reith, Milda; Kohl, Susanne; Amaral, Rebeca Azevedo Souza; Sallum, Juliana Maria Ferraz; Vincent, Andrea L.; Hull, Sarah; Duncan, Jacque L.; Hanson, James V. M.; Tedeus, Matthias; Maggi, Jordi; Graf, Urs; Koller, Samuel; Berger, Wolfgang; Gerth-Kahlert, Christina; Marra, Molly; Everett, Lesley A.; Yang, Paul; Pennesi, Mark E.
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A Phase I, Single Ascending Dose Study of GEM103 (Recombinant Human Complement Factor H) in Patients with Geographic Atrophy
err2022-06-01
err10
errOAAI
errKhanani, Arshad M.; Maturi, Raj K.; Bagheri, Nika; Bakall, Benjamin; Boyer, David S.; Couvillion, Stephen S.; Dhoot, Dilsher S.; Holekamp, Nancy M.; Jamal, Karim N.; Marcus, Dennis M.; Pieramici, Dante; Aziz, Aamir A.; Patki, Kiran C.; Bridges Jr, William Z.; Barone, Samuel B.
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Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis通过全基因组序列分析破译三个种族人群中IRD的遗传结构和人种学分布
err2021-10-18
err21
errOAAI
errBiswas, Pooja; Villanueva, Adda L.; Soto-Hermida, Angel; Duncan, Jacque L.; Matsui, Hiroko; Borooah, Shyamanga; Kumarov, Berzhan; Richard, Gabriele; Khan, Shahid Yar; Branham, Kari; Huang, Bonnie; Suk, John; Bakall, Benjamin; Goldberg, Jeffrey L.; Gabriel, Luis; Khan, Naheed W.; Raghavendra, Pongali B.; Zhao, Jason; Devalaraja, Sindhu; Huynh, Andrew; Alapati, Akhila; Zawaydeh, Qais; Weleber, Richard G.; Heckenlively, John R.; Hejtmancik, J. Fielding; Riazuddin, Sheikh; Sieving, Paul A.; Riazuddin, S. Amer; Frazer, Kelly A.; Ayyagari, Radha
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Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome
err2021-06-29
err18
errOAAI
errda Palma, Mariana Matioli; Igelman, Austin D.; Ku, Cristy; Burr, Amanda; You, Jia Yue; Place, Emily M.; Wang, Nan-Kai; Oh, Jin Kyun; Branham, Kari E.; Zhang, Xinxin; Ahn, Jeeyun; Gorin, Michael B.; Lam, Byron L.; Ronquillo, Cecinio C.; Bernstein, Paul S.; Nagiel, Aaron; Huckfeldt, Rachel; Cabrera, Michelle T.; Kelly, John P.; Bakall, Benjamin; Iannaccone, Alessandro; Hufnagel, Robert B.; Zein, Wadih M.; Koenekoop, Robert K.; Birch, David G.; Yang, Paul; Fahim, Abigail T.; Pennesi, Mark E.
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Indirect Traumatic Optic Neuropathy in Mild Chronic Traumatic Brain Injury
err2019-05-08
err25
errOAAI
errChan, Jane W.; Hills, Nancy K.; Bakall, Benjamin; Fernandez, Brian
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Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy
err2017-06-06
err42
errOAAI
errKhan, Kamron N.; El-Asrag, Mohammed E.; Ku, Cristy A.; Holder, Graham E.; McKibbin, Martin; Arno, Gavin; Poulter, James A.; Carss, Keren; Bommireddy, Tejaswi; Bagheri, Saghar; Bakall, Benjamin; Scholl, Hendrik P.; Raymond, F. Lucy; Toomes, Carmel; Inglehearn, Chris F.; Pennesi, Mark E.; Moore, Anthony T.; Michaelides, Michel; Webster, Andrew R.; Ali, Manir
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Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease
err2013-08-04
err166
errOAAI
errBraun, Terry A.; Mullins, Robert F.; Wagner, Alex H.; Andorf, Jeaneen L.; Johnston, Rebecca M.; Bakall, Benjamin B.; Deluca, Adam P.; Fishman, Gerald A.; Lam, Byron L.; Weleber, Richard G.; Cideciyan, Artur V.; Jacobson, Samuel G.; Sheffield, Val C.; Tucker, Budd A.; Stone, Edwin M.
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Aflibercept Therapy for Exudative Age-related Macular Degeneration Resistant to Bevacizumab and Ranibizumab
err2013-07-01
err202
PREAI
errBakall, Benjamin; Folk, James C.; Boldt, H. Culver; Sohn, Elliott H.; Stone, Edwin M.; Russell, Stephen R.; Mahajan, Vinit B.
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Bestrophin-2 is involved in the generation of intraocular pressure
err2008-04-01
err61
errOAAI
errBakall, Benjamin; McLaughlin, Precious; Stanton, J. Brett; Zhang, Youwen; Hartzell, H. Criss; Marmorstein, Lihua Y.; Marmorstein, Alan D.
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Lack of fibulin-3 causes early aging and herniation, but not macular degeneration in mice
err2007-09-13
err152
errOAAI
errMcLaughlin, Precious J.; Bakall, Benjamin; Choi, Jiwon; Liu, Zhonglin; Sasaki, Takako; Davis, Elaine C.; Marmorstein, Alan D.; Marmorstein, Lihua Y.
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Enhanced accumulation of A2E in individuals homozygous or heterozygous for mutations in BEST1 (VMD2)
err2007-07-01
err82
PREAI
errBakall, B.; Radu, R. A.; Stanton, J. B.; Burke, J. M.; Mckay, B. S.; Wadelius, C.; Mullins, R. F.; Stone, E. M.; Travis, G. H.; Marmorstein, A. D.
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Expression of bestrophin-1, the product of the VMD2 gene, modulates voltage-dependent Ca2+ channels in retinal pigment epithelial cells
err2006-01-01
err168
PREAI
errRosenthal, R; Bakall, B; Kinnick, T; Peachey, N; Wimmers, S; Wadelius, C; Marmorstein, A; Strauss, O
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A model of best vitelliform macular dystrophy in rats
err2004-10-01
err55
errOAAI
errMarmorstein, AD; Stanton, JB; Yocom, J; Bakall, B; Schiavone, MT; Wadelius, C; Marmorstein, LY; Peachey, NS
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Expression and localization of bestrophin during normal mouse development
err2003-08-01
err97
PREAI
errBakall, B; Marmorstein, LY; Hoppe, G; Peachey, NS; Wadelius, C; Marmorstein, AD
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The mutation spectrum of the bestrophin protein - functional implications
err1999-06-02
err95
PREAI
errBakall, B; Marknell, T; Ingvast, S; Koisti, MJ; Sandgren, O; Li, W; Bergen, AAB; Andreasson, S; Rosenberg, T; Petrukhin, K; Wadelius, C
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