Works matching AU Cideciyan, Artur V.

Results: 59

Canine and human visual cortex intact and responsive despite early retinal blindness from RPE65 mutation.

Published in:

2007

By:

Aguirre, Geoffrey K.;
Komáromy, András M.;
Cideciyan, Artur V.;
Brainard, David H.;
Aleman, Tomas S.;
Roman, Alejandro J.;
Avants, Brian B.;
Gee, James C.;
Korczykowski, Marc;
Hauswirth, William W.;
Acland, Gregory M.;
Aguirre, Gustavo D.;
Jacobson, Samuel G.;
Komáromy, András M

Publication type:

journal article

Lentiviral expression of retinal guanylate cyclase-1 (RetGC1) restores vision in an avian model of childhood blindness.

Published in:

2006

By:

Williams, Melissa L.;
Coleman, Jason E.;
Haire, Shannon E.;
Aleman, Tomas S.;
Cideciyan, Artur V.;
Sokal, Izabel;
Palczewski, Krzysztof;
Jacobson, Samuel G.;
Semple-Rowland, Susan L.

Publication type:

journal article

Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis.

Published in:

Human Mutation, 2007, v. 28, n. 11, p. 1074, doi. 10.1002/humu.20565

By:

Cideciyan, Artur V.;
Aleman, Tomas S.;
Jacobson, Samuel G.;
Khanna, Hemant;
Sumaroka, Alexander;
Aguirre, Geoffrey K.;
Schwartz, Sharon B.;
Windsor, Elizabeth A.M.;
He, Shirley;
Chang, Bo;
Stone, Edwin M.;
Swaroop, Anand

Publication type:

Article

Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome.

Published in:

Human Mutation, 2004, v. 24, n. 5, p. 439, doi. 10.1002/humu.9285

By:

Wright, Alan F.;
Reddick, Adam C.;
Schwartz, Sharon B.;
Ferguson, Julie S.;
Aleman, Tomas S.;
Kellner, Ulrich;
Jurklies, Bernhard;
Schuster, Andreas;
Zrenner, Eberhart;
Wissinger, Bernd;
Lennon, Alan;
Shu, Xinhua;
Cideciyan, Artur V.;
Stone, Edwin M.;
Jacobson, Samuel G.;
Swaroop, Anand

Publication type:

Article

EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease Progression.

Published in:

Genes, 2017, v. 8, n. 7, p. 178, doi. 10.3390/genes8070178

By:

McGuigan, David B.;
Heon, Elise;
Cideciyan, Artur V.;
Ratnapriya, Rinki;
Lu, Monica;
Sumaroka, Alexander;
Roman, Alejandro J.;
Batmanabane, Vaishnavi;
Garafalo, Alexandra V.;
Stone, Edwin M.;
Swaroop, Anand;
Jacobson, Samuel G.

Publication type:

Article

ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 7, p. 812, doi. 10.1038/ejhg.2008.23

By:

Kitiratschky, Veronique B. D.;
Grau, Tanja;
Bernd, Antje;
Zrenner, Eberhart;
Jägle, Herbert;
Renner, Agnes B.;
Kellner, Ulrich;
Rudolph, Günther;
Jacobson, Samuel G.;
Cideciyan, Artur V.;
Schaich, Simone;
Kohl, Susanne;
Wissinger, Bernd

Publication type:

Article

Lifespan and mitochondrial control of neurodegeneration.

Published in:

Nature Genetics, 2004, v. 36, n. 11, p. 1153, doi. 10.1038/ng1448

By:

Wright, Alan F.;
Jacobson, Samuel G.;
Cideciyan, Artur V.;
Roman, Alejandro J;
Shu, Xinhua;
Vlachantoni, Dafni;
McInnes, Roderick R.;
Riemersma, Rudolph A.

Publication type:

Article

Gene therapy restores vision in a canine model of childhood blindness.

Published in:

Nature Genetics, 2001, v. 28, n. 1, p. 92, doi. 10.1038/88327

By:

Acland, Gregory M.;
Aguirre, Gustavo D.;
Ray, Jharna;
Zhang, Qi;
Aleman, Tomas S.;
Cideciyan, Artur V.;
Pearce-Kelling, Susan E.;
Anand, Vibha;
Zeng, Yong;
Maguire, Albert M.;
Jacobson, Samuel G.;
Hauswirth, William W.;
Bennett, Jean

Publication type:

Article

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 127, doi. 10.1038/72777

By:

Haider, Neena B.;
Jacobson, Samuel G.;
Cideciyan, Artur V.;
Swiderski, Ruth;
Streb, Luan M.;
Searby, Charles;
Beck, Gretel;
Hockey, Robin;
Hanna, David B.;
Gorman, Susan;
Duhl, David;
Carmi, Rivka;
Bennett, Jean;
Weleber, Richard G.;
Fishman, Gerald A.;
Wright, Alan F.;
Stone, Edwin M.;
Sheffield, Val C.

Publication type:

Article

Retinal prolactin isoform PRLΔE1 sustains rod disease in inherited retinal degenerations.

Published in:

Cell Death & Disease, 2024, v. 15, n. 9, p. 1, doi. 10.1038/s41419-024-07070-1

By:

Sudharsan, Raghavi;
Kwok, Jennifer;
Swider, Malgorzata;
Sumaroka, Alexander;
Aguirre, Gustavo D.;
Cideciyan, Artur V.;
Beltran, William A.

Publication type:

Article

Blue Cone Monochromacy: Visual Function and Efficacy Outcome Measures for Clinical Trials.

Published in:

PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0125700

By:

Luo, Xunda;
Cideciyan, Artur V.;
Iannaccone, Alessandro;
Roman, Alejandro J.;
Ditta, Lauren C.;
Jennings, Barbara J.;
Yatsenko, Svetlana A.;
Sheplock, Rebecca;
Sumaroka, Alexander;
Swider, Malgorzata;
Schwartz, Sharon B.;
Wissinger, Bernd;
Kohl, Susanne;
Jacobson, Samuel G.

Publication type:

Article

Natural History of Cone Disease in the Murine Model of Leber Congenital Amaurosis Due to <i>CEP290</i> Mutation: Determining the Timing and Expectation of Therapy.

Published in:

PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0092928

By:

Boye, Shannon E.;
Huang, Wei-Chieh;
Roman, Alejandro J.;
Sumaroka, Alexander;
Boye, Sanford L.;
Ryals, Renee C.;
Olivares, Melani B.;
Ruan, Qing;
Tucker, Budd A.;
Stone, Edwin M.;
Swaroop, Anand;
Cideciyan, Artur V.;
Hauswirth, William W.;
Jacobson, Samuel G.

Publication type:

Article

Canine Retina Has a Primate Fovea-Like Bouquet of Cone Photoreceptors Which Is Affected by Inherited Macular Degenerations.

Published in:

PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0090390

By:

Beltran, William A.;
Cideciyan, Artur V.;
Guziewicz, Karina E.;
Iwabe, Simone;
Swider, Malgorzata;
Scott, Erin M.;
Savina, Svetlana V.;
Ruthel, Gordon;
Stefano, Frank;
Zhang, Lingli;
Zorger, Richard;
Sumaroka, Alexander;
Jacobson, Samuel G.;
Aguirre, Gustavo D.

Publication type:

Article

Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degeneration.

Published in:

FASEB Journal, 2011, v. 25, n. 9, p. 3157, doi. 10.1096/fj.11-186767

By:

Mustafi, Debarshi;
Kevany, Brian M.;
Genoud, Christel;
Okano, Kiichiro;
Cideciyan, Artur V.;
Sumaroka, Alexander;
Roman, Alejandro J.;
Jacobson, Samuel G.;
Engel, Andreas;
Adams, Mark D.;
Palczewski, Krzysztof

Publication type:

Article

Nonhuman primate models for diabetic ocular neovascularization using AAV2-mediated overexpression of vascular endothelial growth factor.

Published in:

2005

By:

Lebherz, Corinna;
Maguire, Albert M.;
Auricchio, Alberto;
Tang, Waixing;
Aleman, Tomas S.;
Wei, Zhangyong;
Grant, Rebecca;
Cideciyan, Artur V.;
Jacobson, Samuel G.;
Wilson, James M.;
Bennett, Jean

Publication type:

journal article

Detailed phenotype and long-term follow-up of RAB28-associated cone-rod dystrophy.

Published in:

Ophthalmic Genetics, 2024, v. 45, n. 5, p. 506, doi. 10.1080/13816810.2024.2362204

By:

Rao, Nitya T.;
Sumaroka, Alexander;
Santos, Arlene J.;
Parchinski, Kelsey M.;
Weber, Mariejel L.;
Maguire, Albert M.;
Cideciyan, Artur V.;
Aleman, Tomas S.

Publication type:

Article

SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosa.

Published in:

Ophthalmic Genetics, 2016, v. 37, n. 3, p. 333, doi. 10.3109/13816810.2015.1130154

By:

Matsui, Rodrigo;
McGuigan III, David B.;
Gruzensky, Michaela L.;
Aleman, Tomas S.;
Schwartz, Sharon B.;
Sumaroka, Alexander;
Koenekoop, Robert K.;
Cideciyan, Artur V.;
Jacobson, Samuel G.

Publication type:

Article

RPGR isoform imbalance causes ciliary defects due to exon ORF15 mutations in X-linked retinitis pigmentosa (XLRP).

Published in:

Human Molecular Genetics, 2020, v. 29, n. 22, p. 3706, doi. 10.1093/hmg/ddaa269

By:

Moreno-Leon, Laura;
West, Emma L;
O'Hara-Wright, Michelle;
Li, Linjing;
Nair, Rohini;
He, Jie;
Anand, Manisha;
Sahu, Bhubanananda;
Chavali, Venkat Ramana Murthy;
Smith, Alexander J;
Ali, Robin R;
Jacobson, Samuel G;
Cideciyan, Artur V;
Khanna, Hemant

Publication type:

Article

Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.

Published in:

Human Molecular Genetics, 2019, v. 28, n. 1, p. 175, doi. 10.1093/hmg/ddy342

By:

Charng, Jason;
Cideciyan, Artur V;
Jacobson, Samuel G;
Sumaroka, Alexander;
Schwartz, Sharon B;
Swider, Malgorzata;
Roman, Alejandro J;
Sheplock, Rebecca;
Anand, Manisha;
Peden, Marc C;
Khanna, Hemant;
Heon, Elise;
Wright, Alan F;
Swaroop, Anand

Publication type:

Article

REEP6 mediates trafficking of a subset of Clathrin-coated vesicles and is critical for rod photoreceptor function and survival.

Published in:

Human Molecular Genetics, 2017, v. 26, n. 12, p. 2218, doi. 10.1093/hmg/ddx111

By:

Veleri, Shobi;
Nellissery, Jacob;
Mishra, Bibhudatta;
Manjunath, Souparnika H.;
Brooks, Matthew J.;
Lijin Dong;
Kunio Nagashima;
Haohua Qian;
Chun Gao;
Sergeev, Yuri V.;
Xiu-Feng Huang;
Jia Qu;
Fan Lu;
Cideciyan, Artur V.;
Tiansen Li;
Zi-Bing Jin;
Fariss, Robert N.;
Ratnapriya, Rinki;
Jacobson, Samuel G.;
Swaroop, Anand

Publication type:

Article

Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 24, p. 5444, doi. 10.1093/hmg/ddw361

By:

Charng, Jason;
Cideciyan, Artur V.;
Jacobson, Samuel G.;
Sumaroka, Alexander;
Schwartz, Sharon B.;
Swider, Malgorzata;
Roman, Alejandro J.;
Sheplock, Rebecca;
Anand, Manisha;
Peden, Marc C.;
Khanna, Hemant;
Heon, Elise;
Wright, Alan F.;
Swaroop, Anand

Publication type:

Article

Overlap of abnormal photoreceptor development and progressive degeneration in Leber congenital amaurosis caused by NPHP5 mutation.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 19, p. 4211, doi. 10.1093/hmg/ddw254

By:

Downs, Louise M.;
Scott, Erin M.;
Cideciyan, Artur V.;
Iwabe, Simone;
Dufour, Valerie;
Gardiner, Kristin L.;
Genini, Sem;
Marinho, Luis Felipe;
Sumaroka, Alexander;
Kosyk, Mychajlo S.;
Swider, Malgorzata;
Aguirre, Geoffrey K.;
Jacobson, Samuel G.;
Beltran, William A.;
Aguirre, Gustavo D.

Publication type:

Article

Protein misfolding and the pathogenesis of ABCA4-associated retinal degenerations.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 11, p. 3220, doi. 10.1093/hmg/ddv073

By:

Ning Zhang;
Tsybovsky, Yaroslav;
Kolesnikov, Alexander V.;
Rozanowska, Malgorzata;
Swider, Malgorzata;
Schwartz, Sharon B.;
Stone, Edwin M.;
Palczewska, Grazyna;
Maeda, Akiko;
Kefalov, Vladimir J.;
Jacobson, Samuel G.;
Cideciyan, Artur V.;
Palczewski, Krzysztof

Publication type:

Article

Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 25, p. 5136, doi. 10.1093/hmg/ddt367

By:

Braun, 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.

Publication type:

Article

Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutants.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 1, p. 168, doi. 10.1093/hmg/dds421

By:

Jacobson, Samuel G.;
Cideciyan, Artur V.;
Peshenko, Igor V.;
Sumaroka, Alexander;
Olshevskaya, Elena V.;
Cao, Lihui;
Schwartz, Sharon B.;
Roman, Alejandro J.;
Olivares, Melani B.;
Sadigh, Sam;
Yau, King-Wai;
Heon, Elise;
Stone, Edwin M.;
Dizhoor, Alexander M.

Publication type:

Article

A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locus.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 8, p. 1541, doi. 10.1093/hmg/8.8.1541

By:

Guillonneau, Xavier;
Piriev, Natik I.;
Danciger, Michael;
Kozak, Christine A.;
Cideciyan, Artur V.;
Jacobson, Samuel G.;
Farber, Debora B.

Publication type:

Article

Rod function deficit in retained photoreceptors of patients with class B Rhodopsin mutations.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-69456-3

By:

Cideciyan, Artur V.;
Jacobson, Samuel G.;
Roman, Alejandro J.;
Sumaroka, Alexander;
Wu, Vivian;
Charng, Jason;
Lisi, Brianna;
Swider, Malgorzata;
Aguirre, Gustavo D.;
Beltran, William A.

Publication type:

Article

Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathy.

Published in:

Human Molecular Genetics, 2011, v. 20, n. 7, p. 1411, doi. 10.1093/hmg/ddr022

By:

Cideciyan, Artur V.;
Rachel, Rivka A.;
Aleman, Tomas S.;
Swider, Malgorzata;
Schwartz, Sharon B.;
Sumaroka, Alexander;
Roman, Alejandro J.;
Stone, Edwin M.;
Jacobson, Samuel G.;
Swaroop, Anand

Publication type:

Article

Loss of cone photoreceptors caused by chromophore depletion is partially prevented by the artificial chromophore pro-drug, 9-cis-retinyl acetate.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 12, p. 2277, doi. 10.1093/hmg/ddp163

By:

Maeda, Tadao;
Cideciyan, Artur V.;
Maeda, Akiko;
Golczak, Marcin;
Aleman, Tomas S.;
Jacobson, Samuel G.;
Palczewski, Krzysztof

Publication type:

Article

ABCA4 disease progression and a proposed strategy for gene therapy.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 5, p. 931, doi. 10.1093/hmg/ddn421

By:

Cideciyan, Artur V.;
Swider, Malgorzata;
Aleman, Tomas S.;
Tsybovsky, Yaroslav;
Schwartz, Sharon B.;
Windsor, Elizabeth A.M.;
Roman, Alejandro J.;
Sumaroka, Alexander;
Steinberg, Janet D.;
Jacobson, Samuel G.;
Stone, Edwin M.;
Palczewski, Krzysztof

Publication type:

Article

Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 15, p. 2405, doi. 10.1093/hmg/ddn140

By:

Jacobson, Samuel G.;
Cideciyan, Artur V.;
Aleman, Tomas S.;
Sumaroka, Alexander;
Roman, Alejandro J.;
Gardner, Leigh M.;
Prosser, Haydn M.;
Mishra, Monalisa;
Bech-Hansen, N. Torben;
Herrera, Waldo;
Schwartz, Sharon B.;
Liu, Xue-Zhong;
Kimberling, William J.;
Steel, Karen P.;
Williams, David S.

Publication type:

Article

In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 17, p. 2588, doi. 10.1093/hmg/ddl185

By:

Cheng, Hong;
Aleman, Tomas S.;
Cideciyan, Artur V.;
Khanna, Ritu;
Jacobson, Samuel G.;
Swaroop, Anand

Publication type:

Article

Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 17, p. 1893, doi. 10.1093/hmg/ddh198

By:

Jacobson, Samuel G.;
Sumaroka, Alexander;
Aleman, Tomas S.;
Cideciyan, Artur V.;
Schwartz, Sharon B.;
Roman, Alejandro J.;
McInnes, Roderick R.;
Sheffield, Val C.;
Stone, Edwin M.;
Swaroop, Anand;
Wright, Alan F.

Publication type:

Article

Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 5, p. 525, doi. 10.1093/hmg/ddh048

By:

Cideciyan, Artur V.;
Aleman, Tomas S.;
Swider, Malgorzata;
Schwartz, Sharon B.;
Steinberg, Janet D.;
Brucker, Alexander J.;
Maguire, Albert M.;
Bennett, Jean;
Stone, Edwin M.;
Jacobson, Samuel G.

Publication type:

Article

Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 20, p. 2657, doi. 10.1093/hmg/ddg289

By:

Hayward, Caroline;
Shu, Xinhua;
Cideciyan, Artur V.;
Lennon, Alan;
Barran, Perdita;
Zareparsi, Sepideh;
Sawyer, Lindsay;
Hendry, Grace;
Dhillon, Baljean;
Milam, Ann H.;
Luthert, Philip J.;
Swaroop, Anand;
Hastie, Nicholas D.;
Jacobson, Samuel G.;
Wright, Alan F.

Publication type:

Article

Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 9, p. 1073, doi. 10.1093/hmg/ddg117

By:

Jacobson, Samuel G.;
Cideciyan, Artur V.;
Aleman, Tomas S.;
Pianta, Michael J.;
Sumaroka, Alexander;
Schwartz, Sharon B.;
Smilko, Elaine E.;
Milam, Ann H.;
Sheffield, Val C.;
Stone, Edwin M.

Publication type:

Article

881. Safety, Efficacy and Biodistribution of Recombinant AAV2-RPE65 Vector Delivered by Ocular Subretinal Injection.

Published in:

Molecular Therapy, 2006, v. 13, p. S339, doi. 10.1016/j.ymthe.2006.08.970

By:

Jacobson, Samuel G.;
Acland, Gregory M.;
Aguirre, Gustavo D.;
Aleman, Tomas S.;
Boye, Sanford L.;
Schwartz, Sharon B.;
Cideciyan, Artur V.;
Zeiss, Caroline J.;
Komaromy, Andras M.;
Roman, Alejandro J.;
Windsor, Elizabeth A. M.;
Sumaroka, Alexander;
Pearce-Kelling, Susan E.;
Conlon, Thomas J.;
Quihong Li;
Chiodo, Vincent A.;
Flotte, Terence R.;
Maguire, Albert M.;
Bennett, Jean;
Hauswirth, William W.

Publication type:

Article

Safety of Recombinant Adeno-Associated Virus Type 2–RPE65 Vector Delivered by Ocular Subretinal Injection.

Published in:

Molecular Therapy, 2006, v. 13, n. 6, p. 1074, doi. 10.1016/j.ymthe.2006.03.005

By:

Jacobson, Samuel G.;
Acland, Gregory M.;
Aguirre, Gustavo D.;
Aleman, Tomas S.;
Schwartz, Sharon B.;
Cideciyan, Artur V.;
Zeiss, Caroline J.;
Komaromy, Andras M.;
Kaushal, Shalesh;
Roman, Alejandro J.;
Windsor, Elizabeth A.M.;
Sumaroka, Alexander;
Pearce-Kelling, Susan E.;
Conlon, Thomas J.;
Chiodo, Vincent A.;
Boye, Sanford L.;
Flotte, Terence R.;
Maguire, Albert M.;
Bennett, Jean;
Hauswirth, William W.

Publication type:

Article

Long-Term Restoration of Rod and Cone Vision by Single Dose rAAV-Mediated Gene Transfer to the Retina in a Canine Model of Childhood Blindness

Published in:

Molecular Therapy, 2005, v. 12, n. 6, p. 1072, doi. 10.1016/j.ymthe.2005.08.008

By:

Acland, Gregory M.;
Aguirre, Gustavo D.;
Bennett, Jean;
Aleman, Tomas S.;
Cideciyan, Artur V.;
Bennicelli, Jeannette;
Dejneka, Nadine S.;
Pearce-Kelling, Susan E.;
Maguire, Albert M.;
Palczewski, Krzysztof;
Hauswirth, William W.;
Jacobson, Samuel G.

Publication type:

Article

In Utero Gene Therapy Rescues Vision in a Murine Model of Congenital Blindness

Published in:

Molecular Therapy, 2004, v. 9, n. 2, p. 182, doi. 10.1016/j.ymthe.2003.11.013

By:

Dejneka, Nadine S.;
Surace, Enrico M.;
Aleman, Tomas S.;
Cideciyan, Artur V.;
Lyubarsky, Arkady;
Savchenko, Andrey;
Redmond, T. Michael;
Tang, Waixing;
Wei, Zhangyong;
Rex, Tonia S.;
Glover, Ernest;
Maguire, Albert M.;
Pugh Jr., Edward N.;
Jacobson, Samuel G.;
Bennett, Jean

Publication type:

Article

Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 12-Month Period: ProgStar Report No. 11.

Published in:

JAMA Ophthalmology, 2019, v. 137, n. 10, p. 1134, doi. 10.1001/jamaophthalmol.2019.2885

By:

Strauss, Rupert W.;
Kong, Xiangrong;
Ho, Alexander;
Jha, Anamika;
West, Sheila;
Ip, Michael;
Bernstein, Paul S.;
Birch, David G.;
Cideciyan, Artur V.;
Michaelides, Michel;
Sahel, José-Alain;
Sunness, Janet S.;
Traboulsi, Elias I.;
Zrenner, Eberhart;
Pitetta, Sean;
Jenkins, Dennis;
Hariri, Amir Hossein;
Sadda, SriniVas;
Scholl, Hendrik P. N.

Publication type:

Article

Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 12-Month Period: ProgStar Report No. 11.

Published in:

2019

By:

Strauss, Rupert W;
Kong, Xiangrong;
Ho, Alexander;
Jha, Anamika;
West, Sheila;
Ip, Michael;
Bernstein, Paul S;
Birch, David G;
Cideciyan, Artur V;
Michaelides, Michel;
Sahel, José-Alain;
Sunness, Janet S;
Traboulsi, Elias I;
Zrenner, Eberhart;
Pitetta, Sean;
Jenkins, Dennis;
Hariri, Amir Hossein;
Sadda, SriniVas;
Scholl, Hendrik P N;
ProgStar Study Group

Publication type:

journal article

Visual Acuity Change Over 24 Months and Its Association With Foveal Phenotype and Genotype in Individuals With Stargardt Disease: ProgStar Study Report No. 10.

Published in:

2018

By:

Kong, Xiangrong;
Fujinami, Kaoru;
Strauss, Rupert W.;
Munoz, Beatriz;
West, Sheila K.;
Cideciyan, Artur V.;
Michaelides, Michel;
Ahmed, Mohamed;
Ervin, Ann-Margret;
Schönbach, Etienne;
Cheetham, Janet K.;
Scholl, Hendrik P. N.;
Schönbach, Etienne;
ProgStar Study Group

Publication type:

journal article

Progression of Stargardt Disease as Determined by Fundus Autofluorescence in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 9).

Published in:

2017

By:

Strauss, Rupert W.;
Muñoz, Beatriz;
Ho, Alexander;
Jha, Anamika;
Michaelides, Michel;
Cideciyan, Artur V.;
Audo, Isabelle;
Birch, David G.;
Hariri, Amir H.;
Nittala, Muneeswar G.;
Sadda, SriniVas;
West, Sheila;
Scholl, Hendrik P. N.;
ProgStar Study Group

Publication type:

journal article

Macular Sensitivity Measured With Microperimetry in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study: Report No. 7.

Published in:

2017

By:

Schönbach, Etienne M.;
Wolfson, Yulia;
Strauss, Rupert W.;
Ibrahim, Mohamed A.;
Xiangrong Kong;
Muñoz, Beatriz;
Birch, David G.;
Cideciyan, Artur V.;
Hahn, Gesa-Astrid;
Nittala, Muneeswar;
Sunness, Janet S.;
Sadda, SriniVas R.;
West, Sheila K.;
Scholl, Hendrik P. N.;
Kong, Xiangrong;
ProgStar Study Group

Publication type:

journal article

Incidence of Atrophic Lesions in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study: Report No. 5.

Published in:

2017

By:

Strauss, Rupert W.;
Muñoz, Beatriz;
Ho, Alex;
Jha, Anamika;
Michaelides, Michel;
Mohand-Said, Saddek;
Cideciyan, Artur V.;
Birch, David;
Hariri, Amir H.;
Nittala, Muneeswar G.;
Sadda, Srini Vas;
Scholl, Hendrik P. N.;
Sadda, SriniVas;
ProgStar Study Group

Publication type:

journal article

Late-Onset Retinal Degeneration Caused by C1QTNF5 Mutation: Sub-Retinal Pigment Epithelium Deposits and Visual Consequences.

Published in:

JAMA Ophthalmology, 2014, v. 132, n. 10, p. 1252, doi. 10.1001/jamaophthalmol.2014.2059

By:

Jacobson, Samuel G.;
Cideciyan, Artur V.;
Sumaroka, Alexander;
Roman, Alejandro J.;
Wright, Alan F.

Publication type:

Article

Mobility test to assess functional vision in dark-adapted patients with Leber congenital amaurosis.

Published in:

2022

By:

Roman, Alejandro J.;
Cideciyan, Artur V.;
Wu, Vivian;
Mascio, Abraham A.;
Krishnan, Arun K.;
Garafalo, Alexandra V.;
Jacobson, Samuel G.

Publication type:

journal article

Patterns of Individual Variation in Visual Pathway Structure and Function in the Sighted and Blind.

Published in:

PLoS ONE, 2016, v. 11, n. 11, p. 1, doi. 10.1371/journal.pone.0164677

By:

Aguirre, Geoffrey K.;
Datta, Ritobrato;
Benson, Noah C.;
Prasad, Sashank;
Jacobson, Samuel G.;
Cideciyan, Artur V.;
Bridge, Holly;
Watkins, Kate E.;
Butt, Omar H.;
Dain, Aleksandra S.;
Brandes, Lauren;
Gennatas, Efstathios D.

Publication type:

Article

Drusen and Photoreceptor Abnormalities in African-Americans with Intermediate Non-neovascular Age-related Macular Degeneration.

Published in:

Current Eye Research, 2015, v. 40, n. 4, p. 398, doi. 10.3109/02713683.2014.925934

By:

Sadigh, Sam;
Luo, Xunda;
Cideciyan, Artur V.;
Sumaroka, Alexander;
Boxley, Stacy L.;
Hall, Laura M.;
Sheplock, Rebecca;
Feuer, William J.;
Stambolian, Dwight S.;
Jacobson, Samuel G.

Publication type:

Article