A citation-based method for searching scientific literature

Sui Wang, Constance L Cepko. Invest Ophthalmol Vis Sci 2016
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


Photoreceptor cell fate specification in vertebrates.
Joseph A Brzezinski, Thomas A Reh. Development 2015
75
50

The Determination of Rod and Cone Photoreceptor Fate.
Constance L Cepko. Annu Rev Vis Sci 2015
18
30


Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa.
Frauke Coppieters, Bart P Leroy, Diane Beysen, Jan Hellemans, Karolien De Bosscher, Guy Haegeman, Kirsten Robberecht, Wim Wuyts, Paul J Coucke, Elfride De Baere. Am J Hum Genet 2007
80
30

Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family.
Pascal Escher, Peter Gouras, Raphaël Roduit, Leila Tiab, Sylvain Bolay, Tania Delarive, Shiming Chen, Chih-Cheng Tsai, Masanori Hayashi, Jana Zernant,[...]. Hum Mutat 2009
47
30

Transcriptional regulation of photoreceptor development and homeostasis in the mammalian retina.
Anand Swaroop, Douglas Kim, Douglas Forrest. Nat Rev Neurosci 2010
322
30

Searching for SNPs with cloud computing.
Ben Langmead, Michael C Schatz, Jimmy Lin, Mihai Pop, Steven L Salzberg. Genome Biol 2009
20

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome.
Ben Langmead, Cole Trapnell, Mihai Pop, Steven L Salzberg. Genome Biol 2009
20

Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration.
Dror Sharon, Michael A Sandberg, Rafael C Caruso, Eliot L Berson, Thaddeus P Dryja. Arch Ophthalmol 2003
122
20

Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors.
Edwin C T Oh, Hong Cheng, Hong Hao, Lin Jia, Naheed Wali Khan, Anand Swaroop. Brain Res 2008
83
20

Nrl is required for rod photoreceptor development.
A J Mears, M Kondo, P K Swain, Y Takada, R A Bush, T L Saunders, P A Sieving, A Swaroop. Nat Genet 2001
655
20

Modifier genes as therapeutics: the nuclear hormone receptor Rev Erb alpha (Nr1d1) rescues Nr2e3 associated retinal disease.
Nelly M Cruz, Yang Yuan, Barrett D Leehy, Rinku Baid, Uday Kompella, Margaret M DeAngelis, Pascal Escher, Neena B Haider. PLoS One 2014
25
20

An Arg311Gln NR2E3 mutation in a family with classic Goldmann-Favre syndrome.
S H Chavala, A Sari, H Lewis, G J T Pauer, E Simpson, S A Hagstrom, E I Traboulsi. Br J Ophthalmol 2005
30
20

Vax2 regulates retinoic acid distribution and cone opsin expression in the vertebrate eye.
Giovanna Alfano, Ivan Conte, Tiziana Caramico, Raffaella Avellino, Benedetta Arnò, Maria Teresa Pizzo, Naoyuki Tanimoto, Susanne C Beck, Gesine Huber, Pascal Dollé,[...]. Development 2011
31
20

Nr2e3-directed transcriptional regulation of genes involved in photoreceptor development and cell-type specific phototransduction.
Neena B Haider, Nissa Mollema, Meghan Gaule, Yang Yuan, Andrew J Sachs, Arne M Nystuen, Jürgen K Naggert, Patsy M Nishina. Exp Eye Res 2009
57
20

The major cell populations of the mouse retina.
C J Jeon, E Strettoi, R H Masland. J Neurosci 1998
882
20

Making the gradient: thyroid hormone regulates cone opsin expression in the developing mouse retina.
Melanie R Roberts, Maya Srinivas, Douglas Forrest, Gabriella Morreale de Escobar, Thomas A Reh. Proc Natl Acad Sci U S A 2006
169
20

Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome.
Alan F Wright, Adam C Reddick, Sharon B Schwartz, Julie S Ferguson, Tomas S Aleman, Ulrich Kellner, Bernhard Jurklies, Andreas Schuster, Eberhart Zrenner, Bernd Wissinger,[...]. Hum Mutat 2004
80
20

The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation.
Neena B Haider, Paul Demarco, Arne M Nystuen, Xiaona Huang, Richard S Smith, Maureen A McCall, Jürgen K Naggert, Patsy M Nishina. Vis Neurosci 2006
55
20

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.
N B Haider, S G Jacobson, A V Cideciyan, R Swiderski, L M Streb, C Searby, G Beck, R Hockey, D B Hanna, S Gorman,[...]. Nat Genet 2000
341
20

Nuclear receptor Rev-erb alpha (Nr1d1) functions in concert with Nr2e3 to regulate transcriptional networks in the retina.
Nissa J Mollema, Yang Yuan, Austin S Jelcick, Andrew J Sachs, Désirée von Alpen, Daniel Schorderet, Pascal Escher, Neena B Haider. PLoS One 2011
44
20

Efficient generation of retinal progenitor cells from human embryonic stem cells.
Deepak A Lamba, Mike O Karl, Carol B Ware, Thomas A Reh. Proc Natl Acad Sci U S A 2006
449
20

Generation of three-dimensional retinal tissue with functional photoreceptors from human iPSCs.
Xiufeng Zhong, Christian Gutierrez, Tian Xue, Christopher Hampton, M Natalia Vergara, Li-Hui Cao, Ann Peters, Tea Soon Park, Elias T Zambidis, Jason S Meyer,[...]. Nat Commun 2014
401
20

Retinal Organoids from Pluripotent Stem Cells Efficiently Recapitulate Retinogenesis.
Manuela Völkner, Marlen Zschätzsch, Maria Rostovskaya, Rupert W Overall, Volker Busskamp, Konstantinos Anastassiadis, Mike O Karl. Stem Cell Reports 2016
123
20

Quantification of Retinogenesis in 3D Cultures Reveals Epigenetic Memory and Higher Efficiency in iPSCs Derived from Rod Photoreceptors.
Daniel Hiler, Xiang Chen, Jennifer Hazen, Sergey Kupriyanov, Patrick A Carroll, Chunxu Qu, Beisi Xu, Dianna Johnson, Lyra Griffiths, Sharon Frase,[...]. Cell Stem Cell 2015
58
20


Stimulation of functional neuronal regeneration from Müller glia in adult mice.
Nikolas L Jorstad, Matthew S Wilken, William N Grimes, Stefanie G Wohl, Leah S VandenBosch, Takeshi Yoshimatsu, Rachel O Wong, Fred Rieke, Thomas A Reh. Nature 2017
171
20

Role of topoisomerase IIbeta in the expression of developmentally regulated genes.
Yi Lisa Lyu, Chao-Po Lin, Anna M Azarova, Li Cai, James C Wang, Leroy F Liu. Mol Cell Biol 2006
120
10


Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation.
Cole Trapnell, Brian A Williams, Geo Pertea, Ali Mortazavi, Gordon Kwan, Marijke J van Baren, Steven L Salzberg, Barbara J Wold, Lior Pachter. Nat Biotechnol 2010
10

Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin.
C J Weitz, Y Miyake, K Shinzato, E Montag, E Zrenner, L N Went, J Nathans. Am J Hum Genet 1992
75
10

Delayed expression of the Crx gene and photoreceptor development in the Chx10-deficient retina.
Adam D Rutherford, Nathalie Dhomen, Hazel K Smith, Jane C Sowden. Invest Ophthalmol Vis Sci 2004
21
10

Vesicular neurotransmitter transporter expression in developing postnatal rodent retina: GABA and glycine precede glutamate.
Juliette Johnson, Ning Tian, Matthew S Caywood, Richard J Reimer, Robert H Edwards, David R Copenhagen. J Neurosci 2003
145
10

Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2.
José L Badano, Stephen J Ansley, Carmen C Leitch, Richard Alan Lewis, James R Lupski, Nicholas Katsanis. Am J Hum Genet 2003
160
10

Helium Ion Microscopy (HIM) for the imaging of biological samples at sub-nanometer resolution.
Matthew S Joens, Chuong Huynh, James M Kasuboski, David Ferranti, Yury J Sigal, Fabian Zeitvogel, Martin Obst, Claus J Burkhardt, Kevin P Curran, Sreekanth H Chalasani,[...]. Sci Rep 2013
52
10

Target genes of Topoisomerase IIβ regulate neuronal survival and are defined by their chromatin state.
Vijay K Tiwari, Lukas Burger, Vassiliki Nikoletopoulou, Ruben Deogracias, Sudhir Thakurela, Christiane Wirbelauer, Johannes Kaut, Remi Terranova, Leslie Hoerner, Christian Mielke,[...]. Proc Natl Acad Sci U S A 2012
92
10

A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13.
S Gerber, J M Rozet, D Bonneau, E Souied, A Camuzat, J L Dufier, P Amalric, J Weissenbach, A Munnich, J Kaplan. Am J Hum Genet 1995
57
10


Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis.
M W Seeliger, H K Biesalski, B Wissinger, H Gollnick, S Gielen, J Frank, S Beck, E Zrenner. Invest Ophthalmol Vis Sci 1999
115
10

Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin.
Edgar A Otto, Bart Loeys, Hemant Khanna, Jan Hellemans, Ralf Sudbrak, Shuling Fan, Ulla Muerb, John F O'Toole, Juliana Helou, Massimo Attanasio,[...]. Nat Genet 2005
276
10

Disc morphogenesis in vertebrate photoreceptors.
R H Steinberg, S K Fisher, D H Anderson. J Comp Neurol 1980
271
10

Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome.
Yanli Fan, Muneer A Esmail, Stephen J Ansley, Oliver E Blacque, Keith Boroevich, Alison J Ross, Susan J Moore, Jose L Badano, Helen May-Simera, Deanna S Compton,[...]. Nat Genet 2004
238
10


Molecular cloning of partial cDNAs for rat DNA topoisomerase II isoforms and their differential expression in brain development.
K Tsutsui, K Tsutsui, S Okada, M Watanabe, T Shohmori, S Seki, Y Inoue. J Biol Chem 1993
57
10


AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis.
Carrie M Louie, Gianluca Caridi, Vanda S Lopes, Francesco Brancati, Andreas Kispert, Madeline A Lancaster, Andrew M Schlossman, Edgar A Otto, Michael Leitges, Hermann-Josef Gröne,[...]. Nat Genet 2010
133
10

Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy.
A Maugeri, B J Klevering, K Rohrschneider, A Blankenagel, H G Brunner, A F Deutman, C B Hoyng, F P Cremers. Am J Hum Genet 2000
229
10



Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration.
P K Swain, S Chen, Q L Wang, L M Affatigato, C L Coats, K D Brady, G A Fishman, S G Jacobson, A Swaroop, E Stone,[...]. Neuron 1997
214
10


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.