A citation-based method for searching scientific literature

Miranda L Scalabrino, Sanford L Boye, Kathryn M H Fransen, Jennifer M Noel, Frank M Dyka, Seok Hong Min, Qing Ruan, Charles N De Leeuw, Elizabeth M Simpson, Ronald G Gregg, Maureen A McCall, Neal S Peachey, Shannon E Boye. Hum Mol Genet 2015
Times Cited: 37







List of co-cited articles
448 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


In vivo-directed evolution of a new adeno-associated virus for therapeutic outer retinal gene delivery from the vitreous.
Deniz Dalkara, Leah C Byrne, Ryan R Klimczak, Meike Visel, Lu Yin, William H Merigan, John G Flannery, David V Schaffer. Sci Transl Med 2013
344
45

Targeting channelrhodopsin-2 to ON-bipolar cells with vitreally administered AAV Restores ON and OFF visual responses in blind mice.
Emilie Macé, Romain Caplette, Olivier Marre, Abhishek Sengupta, Antoine Chaffiol, Peggy Barbe, Mélissa Desrosiers, Ernst Bamberg, Jose-Alain Sahel, Serge Picaud,[...]. Mol Ther 2015
93
35

Efficient transduction and optogenetic stimulation of retinal bipolar cells by a synthetic adeno-associated virus capsid and promoter.
Therese Cronin, Luk H Vandenberghe, Péter Hantz, Josephine Juttner, Andreas Reimann, Agota-Enikő Kacsó, Rachel M Huckfeldt, Volker Busskamp, Hubertus Kohler, Pamela S Lagali,[...]. EMBO Mol Med 2014
91
32

Safety and efficacy of gene transfer for Leber's congenital amaurosis.
Albert M Maguire, Francesca Simonelli, Eric A Pierce, Edward N Pugh, Federico Mingozzi, Jeannette Bennicelli, Sandro Banfi, Kathleen A Marshall, Francesco Testa, Enrico M Surace,[...]. N Engl J Med 2008
29

Targeting photoreceptors via intravitreal delivery using novel, capsid-mutated AAV vectors.
Christine N Kay, Renee C Ryals, George V Aslanidi, Seok Hong Min, Qing Ruan, Jingfen Sun, Frank M Dyka, Daniel Kasuga, Andrea E Ayala, Kim Van Vliet,[...]. PLoS One 2013
114
29

Light-activated channels targeted to ON bipolar cells restore visual function in retinal degeneration.
Pamela S Lagali, David Balya, Gautam B Awatramani, Thomas A Münch, Douglas S Kim, Volker Busskamp, Constance L Cepko, Botond Roska. Nat Neurosci 2008
335
29

Long-term effect of gene therapy on Leber's congenital amaurosis.
James W B Bainbridge, Manjit S Mehat, Venki Sundaram, Scott J Robbie, Susie E Barker, Caterina Ripamonti, Anastasios Georgiadis, Freya M Mowat, Stuart G Beattie, Peter J Gardner,[...]. N Engl J Med 2015
403
27

Retinal gene therapy in patients with choroideremia: initial findings from a phase 1/2 clinical trial.
Robert E MacLaren, Markus Groppe, Alun R Barnard, Charles L Cottriall, Tanya Tolmachova, Len Seymour, K Reed Clark, Matthew J During, Frans P M Cremers, Graeme C M Black,[...]. Lancet 2014
484
27

Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years.
Samuel G Jacobson, Artur V Cideciyan, Ramakrishna Ratnakaram, Elise Heon, Sharon B Schwartz, Alejandro J Roman, Marc C Peden, Tomas S Aleman, Sanford L Boye, Alexander Sumaroka,[...]. Arch Ophthalmol 2012
415
27

Inner limiting membrane barriers to AAV-mediated retinal transduction from the vitreous.
Deniz Dalkara, Kathleen D Kolstad, Natalia Caporale, Meike Visel, Ryan R Klimczak, David V Schaffer, John G Flannery. Mol Ther 2009
178
27

Effect of gene therapy on visual function in Leber's congenital amaurosis.
James W B Bainbridge, Alexander J Smith, Susie S Barker, Scott Robbie, Robert Henderson, Kamaljit Balaggan, Ananth Viswanathan, Graham E Holder, Andrew Stockman, Nick Tyler,[...]. N Engl J Med 2008
27

Targeted CNS Delivery Using Human MiniPromoters and Demonstrated Compatibility with Adeno-Associated Viral Vectors.
Charles N de Leeuw, Frank M Dyka, Sanford L Boye, Stéphanie Laprise, Michelle Zhou, Alice Y Chou, Lisa Borretta, Simone C McInerny, Kathleen G Banks, Elodie Portales-Casamar,[...]. Mol Ther Methods Clin Dev 2014
29
31


Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics.
Artur V Cideciyan, Tomas S Aleman, Sanford L Boye, Sharon B Schwartz, Shalesh Kaushal, Alejandro J Roman, Ji-Jing Pang, Alexander Sumaroka, Elizabeth A M Windsor, James M Wilson,[...]. Proc Natl Acad Sci U S A 2008
522
21

Dosage thresholds for AAV2 and AAV8 photoreceptor gene therapy in monkey.
Luk H Vandenberghe, Peter Bell, Albert M Maguire, Cassia N Cearley, Ru Xiao, Roberto Calcedo, Lili Wang, Michael J Castle, Alexandra C Maguire, Rebecca Grant,[...]. Sci Transl Med 2011
134
21


Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
N T Bech-Hansen, M J Naylor, T A Maybaum, R L Sparkes, B Koop, D G Birch, A A Bergen, C F Prinsen, R C Polomeno, A Gal,[...]. Nat Genet 2000
234
21

Ectopic expression of a microbial-type rhodopsin restores visual responses in mice with photoreceptor degeneration.
Anding Bi, Jinjuan Cui, Yu-Ping Ma, Elena Olshevskaya, Mingliang Pu, Alexander M Dizhoor, Zhuo-Hua Pan. Neuron 2006
403
18

Novel adeno-associated viral vectors for retinal gene therapy.
L H Vandenberghe, A Auricchio. Gene Ther 2012
89
18

Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial.
William W Hauswirth, Tomas S Aleman, Shalesh Kaushal, Artur V Cideciyan, Sharon B Schwartz, Lili Wang, Thomas J Conlon, Sanford L Boye, Terence R Flotte, Barry J Byrne,[...]. Hum Gene Ther 2008
688
18

Restoration of Vision with Ectopic Expression of Human Rod Opsin.
Jasmina Cehajic-Kapetanovic, Cyril Eleftheriou, Annette E Allen, Nina Milosavljevic, Abigail Pienaar, Robert Bedford, Katherine E Davis, Paul N Bishop, Robert J Lucas. Curr Biol 2015
74
18

Optogenetic Vision Restoration Using Rhodopsin for Enhanced Sensitivity.
Benjamin M Gaub, Michael H Berry, Amy E Holt, Ehud Y Isacoff, John G Flannery. Mol Ther 2015
60
18

Virally delivered channelrhodopsin-2 safely and effectively restores visual function in multiple mouse models of blindness.
M Mehdi Doroudchi, Kenneth P Greenberg, Jianwen Liu, Kimberly A Silka, Edward S Boyden, Jennifer A Lockridge, A Cyrus Arman, Ramesh Janani, Shannon E Boye, Sanford L Boye,[...]. Mol Ther 2011
166
18

Restoration of visual function by expression of a light-gated mammalian ion channel in retinal ganglion cells or ON-bipolar cells.
Benjamin M Gaub, Michael H Berry, Amy E Holt, Andreas Reiner, Michael A Kienzler, Natalia Dolgova, Sergei Nikonov, Gustavo D Aguirre, William A Beltran, John G Flannery,[...]. Proc Natl Acad Sci U S A 2014
63
18

Intravitreal injection of AAV2 transduces macaque inner retina.
Lu Yin, Kenneth Greenberg, Jennifer J Hunter, Deniz Dalkara, Kathleen D Kolstad, Benjamin D Masella, Robert Wolfe, Meike Visel, Daniel Stone, Richard T Libby,[...]. Invest Ophthalmol Vis Sci 2011
123
18

Novel adeno-associated virus serotypes efficiently transduce murine photoreceptors.
Mariacarmela Allocca, Claudio Mussolino, Maria Garcia-Hoyos, Daniela Sanges, Carolina Iodice, Marco Petrillo, Luk H Vandenberghe, James M Wilson, Valeria Marigo, Enrico M Surace,[...]. J Virol 2007
165
18


The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
C M Pusch, C Zeitz, O Brandau, K Pesch, H Achatz, S Feil, C Scharfe, J Maurer, F K Jacobi, A Pinckers,[...]. Nat Genet 2000
183
18

Restoring the ON Switch in Blind Retinas: Opto-mGluR6, a Next-Generation, Cell-Tailored Optogenetic Tool.
Michiel van Wyk, Justyna Pielecka-Fortuna, Siegrid Löwel, Sonja Kleinlogel. PLoS Biol 2015
87
16

Restoration of visual function in retinal degeneration mice by ectopic expression of melanopsin.
Bin Lin, Amane Koizumi, Nobushige Tanaka, Satchidananda Panda, Richard H Masland. Proc Natl Acad Sci U S A 2008
180
16

AAV2 gene therapy readministration in three adults with congenital blindness.
Jean Bennett, Manzar Ashtari, Jennifer Wellman, Kathleen A Marshall, Laura L Cyckowski, Daniel C Chung, Sarah McCague, Eric A Pierce, Yifeng Chen, Jeannette L Bennicelli,[...]. Sci Transl Med 2012
268
16

Novel properties of tyrosine-mutant AAV2 vectors in the mouse retina.
Hilda Petrs-Silva, Astra Dinculescu, Qiuhong Li, Wen-Tao Deng, Ji-Jing Pang, Seok-Hong Min, Vince Chiodo, Andy W Neeley, Lakshmanan Govindasamy, Antonette Bennett,[...]. Mol Ther 2011
164
16

Identification of the gene and the mutation responsible for the mouse nob phenotype.
Ronald G Gregg, Suparna Mukhopadhyay, Sophie I Candille, Sherry L Ball, Machelle T Pardue, Maureen A McCall, Neal S Peachey. Invest Ophthalmol Vis Sci 2003
83
16

A role for nyctalopin, a small leucine-rich repeat protein, in localizing the TRP melastatin 1 channel to retinal depolarizing bipolar cell dendrites.
Jillian N Pearring, Pasano Bojang, Yin Shen, Chieko Koike, Takahisa Furukawa, Scott Nawy, Ronald G Gregg. J Neurosci 2011
61
16

GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.
Neal S Peachey, Thomas A Ray, Ralph Florijn, Lucy B Rowe, Trijntje Sjoerdsma, Susana Contreras-Alcantara, Kenkichi Baba, Gianluca Tosini, Nikita Pozdeyev, P Michael Iuvone,[...]. Am J Hum Genet 2012
90
16

High-efficiency transduction of the mouse retina by tyrosine-mutant AAV serotype vectors.
Hilda Petrs-Silva, Astra Dinculescu, Qiuhong Li, Seok-Hong Min, Vince Chiodo, Ji-Jing Pang, Li Zhong, Sergei Zolotukhin, Arun Srivastava, Alfred S Lewin,[...]. Mol Ther 2009
269
13

Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with Leber congenital Amaurosis type 2.
Francesco Testa, Albert M Maguire, Settimio Rossi, Eric A Pierce, Paolo Melillo, Kathleen Marshall, Sandro Banfi, Enrico M Surace, Junwei Sun, Carmela Acerra,[...]. Ophthalmology 2013
215
13

Improvement and decline in vision with gene therapy in childhood blindness.
Samuel G Jacobson, Artur V Cideciyan, Alejandro J Roman, Alexander Sumaroka, Sharon B Schwartz, Elise Heon, William W Hauswirth. N Engl J Med 2015
220
13

A comprehensive review of retinal gene therapy.
Shannon E Boye, Sanford L Boye, Alfred S Lewin, William W Hauswirth. Mol Ther 2013
183
13

A regulatory toolbox of MiniPromoters to drive selective expression in the brain.
Elodie Portales-Casamar, Douglas J Swanson, Li Liu, Charles N de Leeuw, Kathleen G Banks, Shannan J Ho Sui, Debra L Fulton, Johar Ali, Mahsa Amirabbasi, David J Arenillas,[...]. Proc Natl Acad Sci U S A 2010
53
13

The human rhodopsin kinase promoter in an AAV5 vector confers rod- and cone-specific expression in the primate retina.
Shannon E Boye, John J Alexander, Sanford L Boye, Clark D Witherspoon, Kristen J Sandefer, Thomas J Conlon, Kirsten Erger, Jingfen Sun, Renee Ryals, Vince A Chiodo,[...]. Hum Gene Ther 2012
77
13

AAV9 targets cone photoreceptors in the nonhuman primate retina.
Luk H Vandenberghe, Peter Bell, Albert M Maguire, Ru Xiao, Tim B Hopkins, Rebecca Grant, Jean Bennett, James M Wilson. PLoS One 2013
59
13

Safety and durability of effect of contralateral-eye administration of AAV2 gene therapy in patients with childhood-onset blindness caused by RPE65 mutations: a follow-on phase 1 trial.
Jean Bennett, Jennifer Wellman, Kathleen A Marshall, Sarah McCague, Manzar Ashtari, Julie DiStefano-Pappas, Okan U Elci, Daniel C Chung, Junwei Sun, J Fraser Wright,[...]. Lancet 2016
222
13

Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB).
Marion Neuillé, Said El Shamieh, Elise Orhan, Christelle Michiels, Aline Antonio, Marie-Elise Lancelot, Christel Condroyer, Kinga Bujakowska, Olivier Poch, José-Alain Sahel,[...]. PLoS One 2014
35
14

Specific deficit of the ON response in visual transmission by targeted disruption of the mGluR6 gene.
M Masu, H Iwakabe, Y Tagawa, T Miyoshi, M Yamashita, Y Fukuda, H Sasaki, K Hiroi, Y Nakamura, R Shigemoto. Cell 1995
364
13

Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
347
13

TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
Isabelle Audo, Susanne Kohl, Bart P Leroy, Francis L Munier, Xavier Guillonneau, Saddek Mohand-Saïd, Kinga Bujakowska, Emeline F Nandrot, Birgit Lorenz, Markus Preising,[...]. Am J Hum Genet 2009
155
13

Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.
Maria M van Genderen, Mieke M C Bijveld, Yvonne B Claassen, Ralph J Florijn, Jillian N Pearring, Francoise M Meire, Maureen A McCall, Frans C C Riemslag, Ronald G Gregg, Arthur A B Bergen,[...]. Am J Hum Genet 2009
141
13

Present Molecular Limitations of ON-Bipolar Cell Targeted Gene Therapy.
Michiel van Wyk, Elmar C Hulliger, Lara Girod, Andreas Ebneter, Sonja Kleinlogel. Front Neurosci 2017
14
35

Highly Efficient Delivery of Adeno-Associated Viral Vectors to the Primate Retina.
Shannon E Boye, John J Alexander, C Douglas Witherspoon, Sanford L Boye, James J Peterson, Mark E Clark, Kristen J Sandefer, Chris A Girkin, William W Hauswirth, Paul D Gamlin. Hum Gene Ther 2016
45
13


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.