A citation-based method for searching scientific literature

Guang-Hua Peng, Omar Ahmad, Faisel Ahmad, Jianfeng Liu, Shiming Chen. Hum Mol Genet 2005
Times Cited: 179







List of co-cited articles
1017 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
48


Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors.
Hong Cheng, Hemant Khanna, Edwin C T Oh, David Hicks, Kenneth P Mitton, Anand Swaroop. Hum Mol Genet 2004
176
46

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
46

Transcriptional regulation of photoreceptor development and homeostasis in the mammalian retina.
Anand Swaroop, Douglas Kim, Douglas Forrest. Nat Rev Neurosci 2010
322
36


Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes.
S Chen, Q L Wang, Z Nie, H Sun, G Lennon, N G Copeland, D J Gilbert, N A Jenkins, D J Zack. Neuron 1997
536
32

Otx2 homeobox gene controls retinal photoreceptor cell fate and pineal gland development.
Akihiro Nishida, Akiko Furukawa, Chieko Koike, Yasuo Tano, Shinichi Aizawa, Isao Matsuo, Takahisa Furukawa. Nat Neurosci 2003
400
32

Retinopathy and attenuated circadian entrainment in Crx-deficient mice.
T Furukawa, E M Morrow, T Li, F C Davis, C L Cepko. Nat Genet 1999
406
30


A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse.
N B Akhmedov, N I Piriev, B Chang, A L Rapoport, N L Hawes, P M Nishina, S Nusinowitz, J R Heckenlively, T H Roderick, C A Kozak,[...]. Proc Natl Acad Sci U S A 2000
167
25

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
30

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
24


Identification of a photoreceptor cell-specific nuclear receptor.
M Kobayashi, S Takezawa, K Hara, R T Yu, Y Umesono, K Agata, M Taniwaki, K Yasuda, K Umesono. Proc Natl Acad Sci U S A 1999
166
24

A thyroid hormone receptor that is required for the development of green cone photoreceptors.
L Ng, J B Hurley, B Dierks, M Srinivas, C Saltó, B Vennström, T A Reh, D Forrest. Nat Genet 2001
381
24

In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development.
Hong Cheng, Tomas S Aleman, Artur V Cideciyan, Ritu Khanna, Samuel G Jacobson, Anand Swaroop. Hum Mol Genet 2006
83
27

The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration.
Ann H Milam, Linda Rose, Artur V Cideciyan, Mark R Barakat, Wai-Xing Tang, Nisha Gupta, Tomas S Aleman, Alan F Wright, Edwin M Stone, Val C Sheffield,[...]. Proc Natl Acad Sci U S A 2002
166
23

Retinoid-related orphan nuclear receptor RORbeta is an early-acting factor in rod photoreceptor development.
Li Jia, Edwin C T Oh, Lily Ng, Maya Srinivas, Matthew Brooks, Anand Swaroop, Douglas Forrest. Proc Natl Acad Sci U S A 2009
90
25

Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors.
Masayuki Akimoto, Hong Cheng, Dongxiao Zhu, Joseph A Brzezinski, Ritu Khanna, Elena Filippova, Edwin C T Oh, Yuezhou Jing, Jose-Luis Linares, Matthew Brooks,[...]. Proc Natl Acad Sci U S A 2006
227
23

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
27

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.
C L Freund, C Y Gregory-Evans, T Furukawa, M Papaioannou, J Looser, L Ploder, J Bellingham, D Ng, J A Herbrick, A Duncan,[...]. Cell 1997
434
22

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
44


CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors.
Joseph C Corbo, Karen A Lawrence, Marcus Karlstetter, Connie A Myers, Musa Abdelaziz, William Dirkes, Karin Weigelt, Martin Seifert, Vladimir Benes, Lars G Fritsche,[...]. Genome Res 2010
124
21


Retinoid X receptor (gamma) is necessary to establish the S-opsin gradient in cone photoreceptors of the developing mouse retina.
Melanie R Roberts, Anita Hendrickson, Christopher R McGuire, Thomas A Reh. Invest Ophthalmol Vis Sci 2005
147
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
34

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
33

Transformation of cone precursors to functional rod photoreceptors by bZIP transcription factor NRL.
Edwin C T Oh, Naheed Khan, Elena Novelli, Hemant Khanna, Enrica Strettoi, Anand Swaroop. Proc Natl Acad Sci U S A 2007
109
19

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
22


Transcriptional regulation of rod photoreceptor homeostasis revealed by in vivo NRL targetome analysis.
Hong Hao, Douglas S Kim, Bernward Klocke, Kory R Johnson, Kairong Cui, Norimoto Gotoh, Chongzhi Zang, Janina Gregorski, Linn Gieser, Weiqun Peng,[...]. PLoS Genet 2012
72
25

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
17

Functional roles of Otx2 transcription factor in postnatal mouse retinal development.
Chieko Koike, Akihiro Nishida, Shinji Ueno, Hiromitsu Saito, Rikako Sanuki, Shigeru Sato, Akiko Furukawa, Shinichi Aizawa, Isao Matsuo, Noboru Suzuki,[...]. Mol Cell Biol 2007
126
17


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
36

Expression of photoreceptor-specific nuclear receptor NR2E3 in rod photoreceptors of fetal human retina.
Keely M Bumsted O'Brien, Hong Cheng, Yibin Jiang, Dorothea Schulte, Anand Swaroop, Anita E Hendrickson. Invest Ophthalmol Vis Sci 2004
58
25

Activation of the blue opsin gene in cone photoreceptor development by retinoid-related orphan receptor beta.
Maya Srinivas, Lily Ng, Hong Liu, Li Jia, Douglas Forrest. Mol Endocrinol 2006
80
18

Pias3-dependent SUMOylation directs rod photoreceptor development.
Akishi Onishi, Guang-Hua Peng, Chengda Hsu, Uel Alexis, Shiming Chen, Seth Blackshaw. Neuron 2009
88
17

The cis-regulatory logic of the mammalian photoreceptor transcriptional network.
Timothy H-C Hsiau, Claudiu Diaconu, Connie A Myers, Jongwoo Lee, Constance L Cepko, Joseph C Corbo. PLoS One 2007
106
15


Phenotypic variation in enhanced S-cone syndrome.
Isabelle Audo, Michel Michaelides, Anthony G Robson, Marko Hawlina, Veronika Vaclavik, Jennifer M Sandbach, Magella M Neveu, Chris R Hogg, David M Hunt, Anthony T Moore,[...]. Invest Ophthalmol Vis Sci 2008
73
19


De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis.
C L Freund, Q L Wang, S Chen, B L Muskat, C D Wiles, V C Sheffield, S G Jacobson, R R McInnes, D J Zack, E M Stone. Nat Genet 1998
233
14

Dual role of Nr2e3 in photoreceptor development and maintenance.
Andrea L Webber, Paul Hodor, Catherine J Thut, Thomas F Vogt, Theresa Zhang, Daniel J Holder, Konstantin Petrukhin. Exp Eye Res 2008
29
48

Diagnostic clinical findings of a new syndrome with night blindness, maculopathy, and enhanced S cone sensitivity.
M F Marmor, S G Jacobson, M H Foerster, U Kellner, R G Weleber. Am J Ophthalmol 1990
119
13

Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration.
Samuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, Artur V Cideciyan, Sharon B Schwartz, Alejandro J Roman, Roderick R McInnes, Val C Sheffield, Edwin M Stone, Anand Swaroop,[...]. Hum Mol Genet 2004
78
16



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.