A citation-based method for searching scientific literature

R E Kelsell, K Gregory-Evans, A M Payne, I Perrault, J Kaplan, R B Yang, D L Garbers, A C Bird, A T Moore, D M Hunt. Hum Mol Genet 1998
Times Cited: 173







List of co-cited articles
1075 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Retinal-specific guanylate cyclase gene mutations in Leber's congenital amaurosis.
I Perrault, J M Rozet, P Calvas, S Gerber, A Camuzat, H Dollfus, S Châtelin, E Souied, I Ghazi, C Leowski,[...]. Nat Genet 1996
309
42

Biochemical analysis of a dimerization domain mutation in RetGC-1 associated with dominant cone-rod dystrophy.
C L Tucker, S C Woodcock, R E Kelsell, V Ramamurthy, D M Hunt, J B Hurley. Proc Natl Acad Sci U S A 1999
83
38

Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1.
S M Downes, A M Payne, R E Kelsell, F W Fitzke, G E Holder, D M Hunt, A T Moore, A C Bird. Arch Ophthalmol 2001
74
35


Cone rod dystrophies.
Christian P Hamel. Orphanet J Rare Dis 2007
237
26

Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degeneration.
Veronique B D Kitiratschky, Robert Wilke, Agnes B Renner, Ulrich Kellner, Maria Vadalà, David G Birch, Bernd Wissinger, Eberhart Zrenner, Susanne Kohl. Invest Ophthalmol Vis Sci 2008
52
50

A retGC-1 mutation in autosomal dominant cone-rod dystrophy.
I Perrault, J M Rozet, S Gerber, R E Kelsell, E Souied, A Cabot, D M Hunt, A Munnich, J Kaplan. Am J Hum Genet 1998
63
39


Cloning and expression of a second photoreceptor-specific membrane retina guanylyl cyclase (RetGC), RetGC-2.
D G Lowe, A M Dizhoor, K Liu, Q Gu, M Spencer, R Laura, L Lu, J B Hurley. Proc Natl Acad Sci U S A 1995
166
25

A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1.
A M Payne, S M Downes, D A Bessant, R Taylor, G E Holder, M J Warren, A C Bird, S S Bhattacharya. Hum Mol Genet 1998
160
24

Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies.
A M Payne, A G Morris, S M Downes, S Johnson, A C Bird, A T Moore, S S Bhattacharya, D M Hunt. J Med Genet 2001
44
52

Cloning, sequencing, and expression of a 24-kDa Ca(2+)-binding protein activating photoreceptor guanylyl cyclase.
A M Dizhoor, E V Olshevskaya, W J Henzel, S C Wong, J T Stults, I Ankoudinova, J B Hurley. J Biol Chem 1995
232
22

Molecular cloning and characterization of retinal photoreceptor guanylyl cyclase-activating protein.
K Palczewski, I Subbaraya, W A Gorczyca, B S Helekar, C C Ruiz, H Ohguro, J Huang, X Zhao, J W Crabb, R S Johnson. Neuron 1994
243
21

Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase.
K Gregory-Evans, R E Kelsell, C Y Gregory-Evans, S M Downes, F W Fitzke, G E Holder, M Simunovic, J D Mollon, R Taylor, D M Hunt,[...]. Ophthalmology 2000
54
38

Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophy.
S E Wilkie, R J Newbold, E Deery, C E Walker, I Stinton, V Ramamurthy, J B Hurley, S S Bhattacharya, M J Warren, D M Hunt. Hum Mol Genet 2000
67
29

Two membrane forms of guanylyl cyclase found in the eye.
R B Yang, D C Foster, D L Garbers, H J Fülle. Proc Natl Acad Sci U S A 1995
160
20

The function of guanylate cyclase 1 and guanylate cyclase 2 in rod and cone photoreceptors.
Wolfgang Baehr, Sukanya Karan, Tadao Maeda, Dong-Gen Luo, Sha Li, J Darin Bronson, Carl B Watt, King-Wai Yau, Jeanne M Frederick, Krzysztof Palczewski. J Biol Chem 2007
121
20

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
377
19

Prevalence of AIPL1 mutations in inherited retinal degenerative disease.
M M Sohocki, I Perrault, B P Leroy, A M Payne, S Dharmaraj, S S Bhattacharya, J Kaplan, I H Maumenee, R Koenekoop, F M Meire,[...]. Mol Genet Metab 2000
120
18

Disruption of a retinal guanylyl cyclase gene leads to cone-specific dystrophy and paradoxical rod behavior.
R B Yang, S W Robinson, W H Xiong, K W Yau, D G Birch, D L Garbers. J Neurosci 1999
123
18

Ultrastructural localization of retinal guanylate cyclase in human and monkey retinas.
X Liu, K Seno, Y Nishizawa, F Hayashi, A Yamazaki, H Matsumoto, T Wakabayashi, J Usukura. Exp Eye Res 1994
93
19

Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy.
S E Wilkie, Y Li, E C Deery, R J Newbold, D Garibaldi, J B Bateman, H Zhang, W Lin, D J Zack, S S Bhattacharya,[...]. Am J Hum Genet 2001
74
24

Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1.
S M Downes, G E Holder, F W Fitzke, A M Payne, M J Warren, S S Bhattacharya, A C Bird. Arch Ophthalmol 2001
76
22

Role of guanylate cyclase-activating proteins (GCAPs) in setting the flash sensitivity of rod photoreceptors.
A Mendez, M E Burns, I Sokal, A M Dizhoor, W Baehr, K Palczewski, D A Baylor, J Chen. Proc Natl Acad Sci U S A 2001
191
17


Guanylate cyclases and associated activator proteins in retinal disease.
David M Hunt, Prateek Buch, Michel Michaelides. Mol Cell Biochem 2010
48
35

Enzymatic properties and regulation of the native isozymes of retinal membrane guanylyl cyclase (RetGC) from mouse photoreceptors.
Igor V Peshenko, Elena V Olshevskaya, Andrey B Savchenko, Sukanya Karan, Krzysztof Palczewski, Wolfgang Baehr, Alexander M Dizhoor. Biochemistry 2011
66
25




Progressive cone and cone-rod dystrophies: phenotypes and underlying molecular genetic basis.
Michel Michaelides, Alison J Hardcastle, David M Hunt, Anthony T Moore. Surv Ophthalmol 2006
145
16

Spectrum of retGC1 mutations in Leber's congenital amaurosis.
I Perrault, J M Rozet, S Gerber, I Ghazi, D Ducroq, E Souied, C Leowski, M Bonnemaison, J L Dufier, A Munnich,[...]. Eur J Hum Genet 2000
82
19

Codons 837 and 838 in the retinal guanylate cyclase gene on chromosome 17p: hot spots for mutations in autosomal dominant cone-rod dystrophy?
M Weigell-Weber, S Fokstuen, B Török, G Niemeyer, A Schinzel, M Hergersberg. Arch Ophthalmol 2000
35
42

Leber congenital amaurosis: genes, proteins and disease mechanisms.
Anneke I den Hollander, Ronald Roepman, Robert K Koenekoop, Frans P M Cremers. Prog Retin Eye Res 2008
483
15



Identification of GUCY2D gene mutations in CORD5 families and evidence of incomplete penetrance.
Nitin Udar, Svetlana Yelchits, Meenal Chalukya, Vivek Yellore, Steve Nusinowitz, Rosamaria Silva-Garcia, Tamara Vrabec, Irene Hussles Maumenee, Larry Donoso, Kent W Small. Hum Mutat 2003
26
53

The Y99C mutation in guanylyl cyclase-activating protein 1 increases intracellular Ca2+ and causes photoreceptor degeneration in transgenic mice.
Elena V Olshevskaya, Peter D Calvert, Michael L Woodruff, Igor V Peshenko, Andrey B Savchenko, Clint L Makino, Ye-Shih Ho, Gordon L Fain, Alexander M Dizhoor. J Neurosci 2004
80
17

Characterization of retinal guanylate cyclase-activating protein 3 (GCAP3) from zebrafish to man.
Yoshikazu Imanishi, Ning Li, Izabela Sokal, Mathew E Sowa, Olivier Lichtarge, Theodore G Wensel, David A Saperstein, Wolfgang Baehr, Krzysztof Palczewski. Eur J Neurosci 2002
84
16

Measurement of cytoplasmic calcium concentration in the rods of wild-type and transducin knock-out mice.
Michael L Woodruff, A P Sampath, Hugh R Matthews, N V Krasnoperova, J Lem, Gordon L Fain. J Physiol 2002
154
14


Photoreceptor guanylate cyclases: a review.
E N Pugh, T Duda, A Sitaramayya, R K Sharma. Biosci Rep 1997
119
14


Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutants.
Samuel G Jacobson, Artur V Cideciyan, Igor V Peshenko, Alexander Sumaroka, Elena V Olshevskaya, Lihui Cao, Sharon B Schwartz, Alejandro J Roman, Melani B Olivares, Sam Sadigh,[...]. Hum Mol Genet 2013
68
20

GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophy.
I Sokal, N Li, I Surgucheva, M J Warren, A M Payne, S S Bhattacharya, W Baehr, K Palczewski. Mol Cell 1998
106
13

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
201
13

Mutations in the GUCA1A gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase.
Veronique B D Kitiratschky, Petra Behnen, Ulrich Kellner, John R Heckenlively, Eberhart Zrenner, Herbert Jägle, Susanne Kohl, Bernd Wissinger, Karl-Wilhelm Koch. Hum Mutat 2009
59
22


X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15.
F Yesim K Demirci, Brian W Rigatti, Gaiping Wen, Amy L Radak, Tammy S Mah, Corrine L Baic, Elias I Traboulsi, Tiina Alitalo, Juliane Ramser, Michael B Gorin. Am J Hum Genet 2002
123
12

Complete abolition of the retinal-specific guanylyl cyclase (retGC-1) catalytic ability consistently leads to leber congenital amaurosis (LCA).
J M Rozet, I Perrault, S Gerber, S Hanein, F Barbet, D Ducroq, E Souied, A Munnich, J Kaplan. Invest Ophthalmol Vis Sci 2001
32
37


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.