A citation-based method for searching scientific literature

Bo Chang, Mark S Dacey, Norm L Hawes, Peter F Hitchcock, Ann H Milam, Pelin Atmaca-Sonmez, Steven Nusinowitz, John R Heckenlively. Invest Ophthalmol Vis Sci 2006
Times Cited: 118







List of co-cited articles
1109 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Phototransduction in transgenic mice after targeted deletion of the rod transducin alpha -subunit.
P D Calvert, N V Krasnoperova, A L Lyubarsky, T Isayama, M Nicoló, B Kosaras, G Wong, K S Gannon, R F Margolskee, R L Sidman,[...]. Proc Natl Acad Sci U S A 2000
271
30

Restoration of cone vision in a mouse model of achromatopsia.
John J Alexander, Yumiko Umino, Drew Everhart, Bo Chang, Seok H Min, Qiuhong Li, Adrian M Timmers, Norman L Hawes, Ji-Jing Pang, Robert B Barlow,[...]. Nat Med 2007
160
24

Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3.
M Biel, M Seeliger, A Pfeifer, K Kohler, A Gerstner, A Ludwig, G Jaissle, S Fauser, E Zrenner, F Hofmann. Proc Natl Acad Sci U S A 1999
224
20

Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia.
Susanne Kohl, Britta Baumann, Thomas Rosenberg, Ulrich Kellner, Birgit Lorenz, Maria Vadalà, Samuel G Jacobson, Bernd Wissinger. Am J Hum Genet 2002
183
20

A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene.
Bo Chang, Tanja Grau, Susann Dangel, Ron Hurd, Bernhard Jurklies, E Cumhur Sener, Sten Andreasson, Helene Dollfus, Britta Baumann, Sylvia Bolz,[...]. Proc Natl Acad Sci U S A 2009
127
19

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
16

Retinal degeneration mutants in the mouse.
B Chang, N L Hawes, R E Hurd, M T Davisson, S Nusinowitz, J R Heckenlively. Vision Res 2002
549
16

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
15

Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21.
S Kohl, B Baumann, M Broghammer, H Jägle, P Sieving, U Kellner, R Spegal, M Anastasi, E Zrenner, L T Sharpe,[...]. Hum Mol Genet 2000
214
15

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
14

Dark light, rod saturation, and the absolute and incremental sensitivity of mouse cone vision.
Frank Naarendorp, Tricia M Esdaille, Serenity M Banden, John Andrews-Labenski, Owen P Gross, Edward N Pugh. J Neurosci 2010
95
14

Gene therapy restores vision in a canine model of childhood blindness.
G M Acland, G D Aguirre, J Ray, Q Zhang, T S Aleman, A V Cideciyan, S E Pearce-Kelling, V Anand, Y Zeng, A M Maguire,[...]. Nat Genet 2001
838
13

CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
Susanne Kohl, Balazs Varsanyi, Gesine Abadin Antunes, Britta Baumann, Carel B Hoyng, Herbert Jägle, Thomas Rosenberg, Ulrich Kellner, Birgit Lorenz, Roberto Salati,[...]. Eur J Hum Genet 2005
160
13

Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel.
S Kohl, T Marx, I Giddings, H Jägle, S G Jacobson, E Apfelstedt-Sylla, E Zrenner, L T Sharpe, B Wissinger. Nat Genet 1998
242
13

Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders.
Alberta A H J Thiadens, Anneke I den Hollander, Susanne Roosing, Sander B Nabuurs, Renate C Zekveld-Vroon, Rob W J Collin, Elfride De Baere, Robert K Koenekoop, Mary J van Schooneveld, Tim M Strom,[...]. Am J Hum Genet 2009
140
13

Speed, spatial, and temporal tuning of rod and cone vision in mouse.
Yumiko Umino, Eduardo Solessio, Robert B Barlow. J Neurosci 2008
147
13

Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle.
T M Redmond, S Yu, E Lee, D Bok, D Hamasaki, N Chen, P Goletz, J X Ma, R K Crouch, K Pfeifer. Nat Genet 1998
721
13

Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).
Ji-Jing Pang, Bo Chang, Norman L Hawes, Ronald E Hurd, Muriel T Davisson, Jie Li, Syed M Noorwez, Ritu Malhotra, J Hugh McDowell, Shalesh Kaushal,[...]. Mol Vis 2005
154
13

Physiological features of the S- and M-cone photoreceptors of wild-type mice from single-cell recordings.
Sergei S Nikonov, Roman Kholodenko, Janis Lem, Edward N Pugh. J Gen Physiol 2006
207
13

Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3.
Duska J Sidjanin, Jennifer K Lowe, John L McElwee, Bruce S Milne, Taryn M Phippen, David R Sargan, Gustavo D Aguirre, Gregory M Acland, Elaine A Ostrander. Hum Mol Genet 2002
136
12

Impaired opsin targeting and cone photoreceptor migration in the retina of mice lacking the cyclic nucleotide-gated channel CNGA3.
Stylianos Michalakis, Heidi Geiger, Silke Haverkamp, Franz Hofmann, Andrea Gerstner, Martin Biel. Invest Ophthalmol Vis Sci 2005
99
12


Retinopathy induced in mice by targeted disruption of the rhodopsin gene.
M M Humphries, D Rancourt, G J Farrar, P Kenna, M Hazel, R A Bush, P A Sieving, D M Sheils, N McNally, P Creighton,[...]. Nat Genet 1997
424
11

CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina.
Adrienne K Mehalow, Shuhei Kameya, Richard S Smith, Norman L Hawes, James M Denegre, James A Young, Lesley Bechtold, Neena B Haider, Ulrich Tepass, John R Heckenlively,[...]. Hum Mol Genet 2003
269
11

Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy.
Livia S Carvalho, Jianhua Xu, Rachael A Pearson, Alexander J Smith, James W Bainbridge, Lynsie M Morris, Steven J Fliesler, Xi-Qin Ding, Robin R Ali. Hum Mol Genet 2011
115
11

Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2).
I A Aligianis, T Forshew, S Johnson, M Michaelides, C A Johnson, R C Trembath, D M Hunt, A T Moore, E R Maher. J Med Genet 2002
84
11


Scotopic and photopic visual thresholds and spatial and temporal discrimination evaluated by behavior of mice in a water maze.
Janaki Nathan, Rebecca Reh, Irina Ankoudinova, Genie Ankoudinova, Bo Chang, John Heckenlively, James B Hurley. Photochem Photobiol 2006
29
34

Microcircuits for night vision in mouse retina.
Y Tsukamoto, K Morigiwa, M Ueda, P Sterling. J Neurosci 2001
224
10

Melanopsin-expressing retinal ganglion-cell photoreceptors: cellular diversity and role in pattern vision.
Jennifer L Ecker, Olivia N Dumitrescu, Kwoon Y Wong, Nazia M Alam, Shih-Kuo Chen, Tara LeGates, Jordan M Renna, Glen T Prusky, David M Berson, Samer Hattar. Neuron 2010
381
10

A novel signaling pathway from rod photoreceptors to ganglion cells in mammalian retina.
E Soucy, Y Wang, S Nirenberg, J Nathans, M Meister. Neuron 1998
212
10

Gene therapy rescues cone function in congenital achromatopsia.
András M Komáromy, John J Alexander, Jessica S Rowlan, Monique M Garcia, Vince A Chiodo, Asli Kaya, Jacqueline C Tanaka, Gregory M Acland, William W Hauswirth, Gustavo D Aguirre. Hum Mol Genet 2010
169
10

Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.
B Chang, N L Hawes, M T Pardue, A M German, R E Hurd, M T Davisson, S Nusinowitz, K Rengarajan, A P Boyd, S S Sidney,[...]. Vision Res 2007
233
10

Impaired cone function and cone degeneration resulting from CNGB3 deficiency: down-regulation of CNGA3 biosynthesis as a potential mechanism.
Xi-Qin Ding, Cynthia S Harry, Yumiko Umino, Alexander V Matveev, Steven J Fliesler, Robert B Barlow. Hum Mol Genet 2009
57
17

Rod photoreceptors drive circadian photoentrainment across a wide range of light intensities.
Cara M Altimus, Ali D Güler, Nazia M Alam, A Cyrus Arman, Glen T Prusky, Alapakkam P Sampath, Samer Hattar. Nat Neurosci 2010
156
10

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
9

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.
Gregory M Acland, Gustavo D Aguirre, Jean Bennett, Tomas S Aleman, Artur V Cideciyan, Jeannette Bennicelli, Nadine S Dejneka, Susan E Pearce-Kelling, Albert M Maguire, Krzysztof Palczewski,[...]. Mol Ther 2005
326
9

CNGA3 mutations in hereditary cone photoreceptor disorders.
B Wissinger, D Gamer, H Jägle, R Giorda, T Marx, S Mayer, S Tippmann, M Broghammer, B Jurklies, T Rosenberg,[...]. Am J Hum Genet 2001
213
9

The cone dysfunction syndromes.
M Michaelides, D M Hunt, A T Moore. Br J Ophthalmol 2004
149
9

Convergence and segregation of the multiple rod pathways in mammalian retina.
Béla Völgyi, Michael R Deans, David L Paul, Stewart A Bloomfield. J Neurosci 2004
124
9

Phototransduction by retinal ganglion cells that set the circadian clock.
David M Berson, Felice A Dunn, Motoharu Takao. Science 2002
9

Connexin36 is essential for transmission of rod-mediated visual signals in the mammalian retina.
Michael R Deans, Bela Volgyi, Daniel A Goodenough, Stewart A Bloomfield, David L Paul. Neuron 2002
300
9

Rapid quantification of adult and developing mouse spatial vision using a virtual optomotor system.
Glen T Prusky, Nazia M Alam, Steven Beekman, Robert M Douglas. Invest Ophthalmol Vis Sci 2004
495
9

Melanopsin and rod-cone photoreceptive systems account for all major accessory visual functions in mice.
S Hattar, R J Lucas, N Mrosovsky, S Thompson, R H Douglas, M W Hankins, J Lem, M Biel, F Hofmann, R G Foster,[...]. Nature 2003
749
9

Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial.
Albert M Maguire, Katherine A High, Alberto Auricchio, J Fraser Wright, Eric A Pierce, Francesco Testa, Federico Mingozzi, Jeannette L Bennicelli, Gui-shuang Ying, Settimio Rossi,[...]. Lancet 2009
567
9

Morphological, physiological, and biochemical changes in rhodopsin knockout mice.
J Lem, N V Krasnoperova, P D Calvert, B Kosaras, D A Cameron, M Nicolò, C L Makino, R L Sidman. Proc Natl Acad Sci U S A 1999
312
9


Progressive loss of cones in achromatopsia: an imaging study using spectral-domain optical coherence tomography.
Alberta A H J Thiadens, Ville Somervuo, L Ingeborgh van den Born, Susanne Roosing, Mary J van Schooneveld, Robert W A M Kuijpers, Norka van Moll-Ramirez, Frans P M Cremers, Carel B Hoyng, Caroline C W Klaver. Invest Ophthalmol Vis Sci 2010
109
9

The Rd8 mutation of the Crb1 gene is present in vendor lines of C57BL/6N mice and embryonic stem cells, and confounds ocular induced mutant phenotypes.
Mary J Mattapallil, Eric F Wawrousek, Chi-Chao Chan, Hui Zhao, Jayeeta Roychoudhury, Thomas A Ferguson, Rachel R Caspi. Invest Ophthalmol Vis Sci 2012
428
9



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.