A citation-based method for searching scientific literature

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, D Duhl, R Carmi, J Bennett, R G Weleber, G A Fishman, A F Wright, E M Stone, V C Sheffield. Nat Genet 2000
Times Cited: 354







List of co-cited articles
1143 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
172
36

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
125
28

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
190
27

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
682
27



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
79
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
124
22

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
62
35

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
82
25


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
170
18

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
58
31

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
81
22

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
83
20

SWS (blue) cone hypersensitivity in a newly identified retinal degeneration.
S G Jacobson, M F Marmor, C M Kemp, R W Knighton. Invest Ophthalmol Vis Sci 1990
108
17

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
89
17

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
169
16


Expanded clinical spectrum of enhanced S-cone syndrome.
Suzanne Yzer, Irene Barbazetto, Rando Allikmets, Mary J van Schooneveld, Arthur Bergen, Stephen H Tsang, Samuel G Jacobson, Lawrence A Yannuzzi. JAMA Ophthalmol 2013
38
42

Transcriptional regulation of photoreceptor development and homeostasis in the mammalian retina.
Anand Swaroop, Douglas Kim, Douglas Forrest. Nat Rev Neurosci 2010
350
16

Clinical and molecular characterization of enhanced S-cone syndrome in children.
Sarah Hull, Gavin Arno, Panagiotis I Sergouniotis, Peter Tiffin, Arundhati Dev Borman, Aman Chandra, Anthony G Robson, Graham E Holder, Andrew R Webster, Anthony T Moore. JAMA Ophthalmol 2014
26
61

Enhanced S cone syndrome: evidence for an abnormally large number of S cones.
D C Hood, A V Cideciyan, A J Roman, S G Jacobson. Vision Res 1995
74
21


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
420
15

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
50
26

ISCEV Standard for full-field clinical electroretinography (2015 update).
Daphne L McCulloch, Michael F Marmor, Mitchell G Brigell, Ruth Hamilton, Graham E Holder, Radouil Tzekov, Michael Bach. Doc Ophthalmol 2015
901
13


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
27
48

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
49
24

Relatively enhanced S cone function in the Goldmann-Favre syndrome.
S G Jacobson, A J Román, M I Román, J D Gass, J A Parker. Am J Ophthalmol 1991
61
19


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
30
36


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
115
11


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
393
11

Photoreceptor cell fate specification in vertebrates.
Joseph A Brzezinski, Thomas A Reh. Development 2015
88
12

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
552
11

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
95
11

Retinitis pigmentosa.
Dyonne T Hartong, Eliot L Berson, Thaddeus P Dryja. Lancet 2006
11

The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition.
S Gerber, J M Rozet, S I Takezawa, L C dos Santos, L Lopes, O Gribouval, C Penet, I Perrault, D Ducroq, E Souied,[...]. Hum Genet 2000
64
17

The crystal structure of the orphan nuclear receptor NR2E3/PNR ligand binding domain reveals a dimeric auto-repressed conformation.
M H Eileen Tan, X Edward Zhou, Fen-Fen Soon, Xiaodan Li, Jun Li, Eu-Leong Yong, Karsten Melcher, H Eric Xu. PLoS One 2013
26
38

Treatment of adult-onset acute macular retinoschisis in enhanced s-cone syndrome with oral acetazolamide.
Alessandro Iannaccone, Kenneth H Fung, Mari E Eyestone, Edwin M Stone. Am J Ophthalmol 2009
28
32

Macular function assessed by microperimetry in patients with enhanced S-cone syndrome.
Elliott H Sohn, Fred K Chen, Gary S Rubin, Anthony T Moore, Andrew R Webster, Robert E MacLaren. Ophthalmology 2010
32
28

The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa.
Anisa I Gire, Lori S Sullivan, Sara J Bowne, David G Birch, Dianna Hughbanks-Wheaton, John R Heckenlively, Stephen P Daiger. Mol Vis 2007
44
20

Pathognomonic (diagnostic) ERGs. A review and update.
Ajoy Vincent, Anthony G Robson, Graham E Holder. Retina 2013
53
16

Cell fate determination in the vertebrate retina.
C L Cepko, C P Austin, X Yang, M Alexiades, D Ezzeddine. Proc Natl Acad Sci U S A 1996
771
9

Atypical mild enhanced S-cone syndrome with novel compound heterozygosity of the NR2E3 gene.
Byron L Lam, Jeffrey L Goldberg, Kristen L Hartley, Edwin M Stone, Mu Liu. Am J Ophthalmol 2007
28
32

Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function.
Koji M Nishiguchi, James S Friedman, Michael A Sandberg, Anand Swaroop, Eliot L Berson, Thaddeus P Dryja. Proc Natl Acad Sci U S A 2004
70
12


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.